ISOHELIX PUBLICATIONS

Bulik, Cynthia M., et al. “The Eating Disorders Genetics Initiative (EDGI): study protocol.” BMC psychiatry 21.1 (2021): 1-9. https://doi.org/10.1186/s12888-021-03212-3

Byrne, Enda M., et al. “Cohort profile: the Australian genetics of depression study.” BMJ open 10.5 (2020): e032580. http://dx.doi.org/10.1136/bmjopen-2019-032580

Campos, Adrián I., et al. “Genetic risk for chronic pain is associated with lower antidepressant effectiveness: Converging evidence for a depression subtype.” Australian & New Zealand Journal of Psychiatry (2021): 00048674211031491. https://doi.org/10.1177/00048674211031491

Campos, Adrian I., et al. “Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression Study.” The Pharmacogenomics Journal 22.2 (2022): 130-135. https://doi.org/10.1038/s41397-022-00267-7

Davies, Molly R., et al. “The Genetic Links to Anxiety and Depression (GLAD) Study: Online recruitment into the largest recontactable study of depression and anxiety.” Behaviour research and therapy 123 (2019): 103503. https://doi.org/10.1016/j.brat.2019.103503

Devereux-Cooke, Andy, et al. “DecodeME: community recruitment for a large genetics study of myalgic encephalomyelitis/chronic fatigue syndrome.” Bmc neurology 22.1 (2022): 269. https://doi.org/10.1186/s12883-022-02763-6

McEwen, Fiona S., et al. “Cohort profile: biological pathways of risk and resilience in Syrian refugee children (BIOPATH).” Social psychiatry and psychiatric epidemiology 57.4 (2022): 873-883.

https://doi.org/10.1007/s00127-022-02228-8

Monssen, Dina, et al. “The Eating Disorders Genetics Initiative (EDGI) United Kingdom.” medRxiv (2022): 2022-11. https://doi.org/10.1101/2022.11.11.22282083

Gomez, Lina, et al. “Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study.” European Archives of Psychiatry and Clinical Neuroscience (2022): 1 https://doi.org/10.1007/s00406-022-01527-0

Habota, Tina, et al. “Cohort profile for the STRADL study: A depression-focused investigation of Generation Scotland, using detailed clinical, cognitive, and neuroimaging assessments.” Wellcome Open Research (2021) https://doi.org/10.12688/wellcomeopenres.15538.2

Lacourt, Aude, et al. “ETIOSARC study: environmental aetiology of sarcomas from a French prospective multicentric population-based case–control study—study protocol.” BMJ open 9.6 (2019): e030013. http://dx.doi.org/10.1136/bmjopen-2019-030013

Mitchell, Brittany L., et al. “Polygenic risk scores derived from varying definitions of depression and risk of depression.” JAMA psychiatry 78.10 (2021): 1152-1160. https://doi.org/10.1001/jamapsychiatry.2021.1988

Zatońska, Katarzyna, et al. “population cohort Study of Wroclaw citizens (pictUre)–study protocol.” Journal of Health Inequalities 8.1. https://doi.org/10.5114/jhi.2022.115930

Boshnjaku, Arben, et al. “ACTN3 Genotypes and Their Relationship with Muscle Mass and Function of Kosovan Adults.” International Journal of Environ     mental Research and Public Health 18.17 (2021): 9135. https://doi.org/10.3390/ijerph18179135

Bulik, Cynthia M., et al. “The Eating Disorders Genetics Initiative (EDGI): study protocol.” BMC psychiatry 21.1 (2021): 1-9. https://doi.org/10.1186/s12888-021-03212-3

Butler, Tony, et al. “Sertraline hydrochloride for reducing impulsive behaviour in male, repeat-violent offenders (ReINVEST): protocol for a phase IV, double-blind, placebo-controlled, randomised clinical trial.” BMJ open 11.9 (2021): e044656. https://doi.org/10.1136/bmjopen-2020-044656

Campos, Adrian I., et al. “Understanding genetic risk factors for common side effects of antidepressant medications.” Communications Medicine 1.1 (2021): 1-10. https://doi.org/10.1038/s43856-021-00046-8

Garcia, Sara L., et al. “Prediction of nephrotoxicity associated with cisplatin-based chemotherapy in testicular cancer patients.” JNCI cancer spectrum 4.3 (2020): pkaa032. https://doi.org/10.1093/jncics/pkaa032

Graham, Catherine AM, et al. “The association of parental genetic, lifestyle, and social determinants of health with offspring overweight.” Lifestyle genomics 13.2 (2020): 99-106.      https://doi.org/10.1159/000505749

Graham, Catherine AM, et al. “Genetic differences in fat taste sensitivity and dietary intake in a UK female cohort.” Food Quality and Preference 92 (2021): 104202. https://doi.org/10.1016/j.foodqual.2021.104202

Grossmann, Leoni, et al. “Generation of integration-free induced pluripotent stem cell lines from four pediatric ADHD patients.” Stem Cell Research 53 (2021): 102268. https://doi.org/10.1016/j.scr.2021.102268

Hall, Elliott CR, et al. “The genetic association with injury risk in male academy soccer players depends on maturity status.” Scandinavian Journal of Medicine & Science in Sports 32.2 (2022): 338-350.

https://doi.org/10.1111/sms.14077

Li, Song, et al. “Pain predict genetics: protocol for a prospective observational study of clinical and genetic factors to predict the development of postoperative pain.” BMJ open 12.11 (2022): e066134. https://doi.org/10.1136/bmjopen-2022-066134

McCallum, Linsay, et al. “Rationale and design of the genotype-blinded trial of torasemide for the treatment of hypertension (BHF UMOD).” American Journal of Hypertension (2020). https://doi.org/10.1093/ajh/hpaa166   

Murtagh, Conall F., et al. “The genetic profile of elite youth soccer players and its association with power and speed depends on maturity status.” PloS one 15.6 (2020): e0234458. https://doi.org/10.1371/journal.pone.0234458

Ohki, Cristine Marie Yde, et al. “Generation of integration-free induced pluripotent stem cells from healthy individuals.” Stem Cell Research 53 (2021): 102269. https://doi.org/10.1016/j.scr.2021.102269

Ramesh, S., et al. “Incidence of major adverse cardiovascular events with genotype test guided antiplatelet treatment strategy after percutaneous coronary intervention.” Indian Heart Journal (2020). https://doi.org/10.1016/j.ihj.2020.09.002

Robino, Antonietta, et al. “Combined influence of TAS2R38 genotype and PROP phenotype on the intensity of basic tastes, astringency and pungency in the Italian taste project.” Food Quality and Preference 95 (2022): 104361. https://doi.org/10.1016/j.foodqual.2021.104361

Ruffles, Tom, et al. “Asthma prescribing according to Arg16Gly beta-2 genotype: a randomised trial in adolescents.” European Respiratory Journal (2021). https://doi.org/10.1183/13993003.04107-2020

Sugrue, Jamie A., et al. “Enhanced TLR3 responsiveness in hepatitis C virus resistant women from the Irish anti-D cohort.” Cell Reports Medicine 3.11 (2022): 100804. https://doi.org/10.1016/j.xcrm.2022.100804

Wiley, Laura K., et al. “Building a Vertically-Integrated Genomic Learning Health System: The Colorado Center for Personalized Medicine Biobank.” medRxiv (2022): 2022-06. https://doi.org/10.1101/2022.06.09.22276222

Hansen, Marcus Høy, and Charlotte Guldborg Nyvold. “Replicate whole-genome next-generation sequencing data derived from Caucasian donor saliva samples.” Data in Brief 38 (2021): 107349. https://doi.org/10.1016/j.dib.2021.107349

Sato, Mitra S., et al. “Hemizygous mutations in L1CAM in two unrelated male probands with childhood onset psychosis.” Psychiatric genetics 30.3 (2020): 73-82. https://doi.org/10.1097/YPG.0000000000000253

Yu, Miao, et al. “KDF1 Novel Variant Causes Unique Dental and Oral Epithelial Defects.” International Journal of Molecular Sciences 23.20 (2022): 12465. https://doi.org/10.3390/ijms232012465

Ahrens, Angelica P., et al. “Saliva microbiome, dietary, and genetic markers are associated with suicidal ideation in university students.” Scientific reports 12.1 (2022): 14306. https://doi.org/10.1038/s41598-022-18020-2

Gopinath, Divya, et al. “Salivary bacterial shifts in oral leukoplakia resemble the dysbiotic oral cancer bacteriome.” Journal of oral microbiology 13.1 (2021): 1857998. https://doi.org/10.1080/20002297.2020.1857998

Gopinath, Divya, et al. “Differences in the bacteriome of swab, saliva, and tissue biopsies in oral cancer.” Scientific reports 11.1 (2021): 1-13. https://doi.org/10.1038/s41598-020-80859-0

Lee, Yeon-Hee, Ji-Youn Hong, and Gi-Ja Lee. “Composition and Diversity of Salivary Microbiome Affected by Sample Collection Method.” Journal of Oral Medicine and Pain 47.1 (2022): 10-26. https://doi.org/10.14476/jomp.2022.47.1.10

Roesch, Luiz Fernando W., et al. “PIME: a package for discovery of novel differences among microbial communities.” Molecular ecology resources 20.2 (2020): 415-428. https://doi.org/10.1111/1755-0998.13116

Ruffell, Simon GD, et al. “Ceremonial Ayahuasca in Amazonian Retreats—Mental Health and Epigenetic Outcomes From a Six-Month Naturalistic Study.” Frontiers in Psychiatry 12 (2021): 898. https://doi.org/10.3389/fpsyt.2021.687615

Zhang, Jun, et al. “Exploring Effect of Postdischarge Developmental Support Program on Preterm Infant Neurodevelopment and BDNF Gene DNA Methylation.” Advances in Neonatal Care (2022): 10-1097. https://doi.org/10.1097/ANC.0000000000001046B

Alexis, N. E., et al. “A Validation Study on a Sputum Home Collection Method with Immediate Freezing and Delayed Processing: Impact on Proteomic, Mucin and RNA/DNA Endpoints.” American Thoracic Society, 2022. A1155-A1155. https://www.atsjournals.org/doi/pdf/10.1164/ajrccm-conference.2022.205.1_MeetingAbstracts.A1155

Nikolaou, Elissavet, et al. “Experimental Human Challenge Defines Distinct Pneumococcal Kinetic Profiles and Mucosal Responses between Colonized and Non-Colonized Adults.” Mbio 12.1 (2021). https://doi.org/10.1128/mBio.02020-20.

Potocka, Natalia, et al. “Association of ACTN3 Polymorphism with Body Somatotype and Cardiorespiratory Fitness in Young Healthy Adults.” International journal of environmental research and public health 16.9 (2019): 1489. https://doi.org/10.3390/ijerph16091489

Bankvall, Maria, et al. “A family‐based genome‐wide association study of recurrent aphthous stomatitis.” Oral Diseases 26.8 (2020): 1696-1705.              https://doi.org/10.1111/odi.13490

Bernardi J.R., Ferreira C.F., Nunes M., da Silva C.H., Bosa V.L., Silveira P.P., and Goldani M.Z. (2012) Impact of perinatal different intrauterine environments on child growth and development in the first six months of life-IVAPSA birth cohort: Rationale, design, and methods. BMC Pregnancy and Childbirth 12: 25. https://doi.org/10.1186/1471-2393-12-25

Hourihane, Jonathan, et al. “Early initiation of short-term emollient use for the prevention of atopic dermatitis in high risk infants–the STOP AD randomised controlled trial.” Authorea Preprints (2022).

https://doi.org/10.22541/au.164940311.12725370/v1

Jabbar-Lopez ZK, Gurung N, Greenblatt D, et al. Protocol for an outcome assessor-blinded pilot randomised controlled trial of an ion-exchange water softener for the prevention of atopic eczema in neonates, with an embedded mechanistic study: the Softened Water for Eczema Prevention (SOFTER) trial. BMJ Open 2019;9:e027168. https://doi.org/10.1136/bmjopen-2018-027168

Kvist, Tuomas, et al. “Cohort profile: Cohort profile: InTraUterine sampling in early pregnancy (ITU), a prospective pregnancy cohort study in Finland: study design and baseline characteristics.” BMJ Open 12.1 (2022). https://doi.org/10.1136/bmjopen-2021-049231

Marsaux, C.F., Celis-Morales, C., Fallaize, R., Macready, A.L., Kolossa, S., Woolhead, C., et al. (2015) Effects of a Web-Based Personalized Intervention on Physical Activity in European Adults: A Randomized Controlled Trial. Journal of medical Internet research 17: e231. https://doi.org/10.2196/jmir.4660

Wienholtz, Nita Katarina Frifelt, et al. “Cohort profile: COpenhagen ROsacea COhort (COROCO) and COpenhagen MIgraine COhort (COMICO).” BMJ open 10.8 (2020): e039445. https://doi.org/10.1136/bmjopen-2020-039445

Almomani B., Hawwa A.F., Millership J.S., Heaney L., Douglas I., McElnay J.C., and Shields M.D. (2013) Can certain genotypes predispose to poor asthma control in children? A pharmacogenetic study of 9 candidate genes in children with difficult asthma. PloS One 8: e60592. https://doi.org/10.1371/journal.pone.0060592

Ammerdorffer, Anne, et al. “Genetic variation in TLR10 is not associated with chronic Q fever, despite the inhibitory effect of TLR10 on Coxiella burnetii-induced cytokines in vitro.” Cytokine 77 (2016): 196-202 https://doi.org/10.1016/j.cyto.2015.09.005

Andersson, Anna Maria, et al. “Assessment of biomarkers in pediatric atopic dermatitis by tape strips and skin biopsies.” Allergy (2021) https://doi.org/10.1111/all.15153

Bakeberg, Megan C., et al. “The TOMM40 ‘523’polymorphism in disease risk and age of symptom onset in two independent cohorts of Parkinson’s disease.” Scientific reports 11.1 (2021): 1-9. https://doi.org/10.1038/s41598-021-85510-0

Bartik, Zsuzsa, et al. “A genome‑wide scan to locate regions associated with familial vesicoureteral reflux.” Experimental and Therapeutic Medicine 23.1 (2022): 1-12. https://doi.org/10.3892/etm.2021.11015

Bhatt, Ishan Sunilkumar, et al. “Association Analysis of Candidate Gene Polymorphisms and Audiometric Measures of Noise-Induced Hearing Loss in Young Musicians.” Otology & neurotology: official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 41.5 (2020): e538.     https://doi.org/10.1097/MAO.0000000000002615

Bowler F.R., Reid P.A., Boyd A.C., Diaz-Mochon J.J., and Bradley M. (2011) Dynamic chemistry for enzyme-free allele discrimination in genotyping by MALDI-TOF mass spectrometry. Analytical Methods 3: 1656-1663. https://doi.org/10.1039/c1ay05176h

Buijs, S. B., et al. “Single nucleotide polymorphism (SNP) rs3751143 in P2RX7 is associated with therapy failure in chronic Q fever while rs7125062 in MMP1 is associated with fewer complications.” Clinical Microbiology and Infection (2020). https://doi.org/10.1016/j.cmi.2020.06.016

Capalbo, Antonio, et al. “Artificial oocyte activation with calcium ionophore does not cause a widespread increase in chromosome segregation errors in the second meiotic division of the oocyte.” Fertility and sterility 105.3 (2016): 807-814. https://doi.org/10.1016/j.fertnstert.2015.11.017

Celis-Morales, C., Livingstone, K.M., Marsaux, C.F., Forster, H., O’Donovan, C.B., Woolhead, C., et al. (2015) Design and baseline characteristics of the Food4Me study: a web-based randomised controlled trial of personalised nutrition in seven European countries. Genes & Nutrit 10: 1-13. http://dx.doi.org/10.1007/s12263-014-0450-2

Celis-Morales, C., Livingstone, K.M., Woolhead, C., Forster, H., O’Donovan, C.B., Macready, A.L., et al. (2015) How reliable is internet-based self-reported identity, socio-demographic and obesity measures in European adults? Genes & Nutrit 10: 1-10. https://doi.org/10.1007/s12263-015-0476-0

Celis‐Morales, Carlos, et al. “Physical activity attenuates the effect of the FTO genotype on obesity traits in European adults: the Food4Me study.” Obesity 24.4 (2016): 962-969. https://doi.org/10.1002/oby.21422

Centanni, T., Green, J.R., Iuzzini-Seigel, J., Bartlett, C.W., and Hogan, T.P. (2015) Evidence for the multiple hits genetic theory for inherited language impairment: a case study. Front Genet 6: 272. https://doi.org/10.3389/fgene.2015.00272

Centanni, T., Sanmann, J., Green, J., Iuzzini‐Seigel, J., Bartlett, C., Sanger, W., and Hogan, T. (2015) The role of candidate‐gene CNTNAP2 in childhood apraxia of speech and specific language impairment. Am. J. Med. Genet 168: 536-543. https://doi.org/10.1002/ajmg.b.32325

Chaoimh, Carol Ní, et al. “Early initiation of short‐term emollient use for the prevention of atopic dermatitis in high‐risk infants—The STOP‐AD randomised controlled trial.” Allergy (2022). https://doi.org/10.1111/all.15491

Chiu, Christine L., Nerissa L. Hearn, and Joanne M. Lind. “Development of a Risk Score for Extraintestinal Manifestations of Coeliac Disease.” Medicine 95.15 (2016). https://doi.org/10.1097/MD.0000000000003286

Cimino, Silvia, et al. “The μ‐opioid receptor gene A118G polymorphism is associated with insecure attachment in children with disruptive mood regulation disorder and their mothers.” Brain and behavior 10.7 (2020): e01659. https://doi.org/10.1002/brb3.1659

Colbert, Lauren E., et al. “Expansion of Candidate HPV-Specific T Cells in the Tumor Microenvironment during Chemoradiotherapy Is Prognostic in HPV16+ Cancers.” Cancer immunology research 10.2 (2022): 259-271. http://doi.org/10.1158/2326-6066.CIR-21-0119

Concas, Maria Pina, et al. “Genetic variations associated with the soapy flavor perception in Gorgonzola PDO cheese.” Food Quality and Preference 99 (2022): 104569. https://doi.org/10.1016/j.foodqual.2022.104569

Fallaize, Rosalind, et al. “The effect of the apolipoprotein E genotype on response to personalized dietary advice intervention: findings from the Food4Me randomized controlled trial.” The American journal of clinical nutrition 104.3 (2016): 827-836. https://doi.org/10.3945/ajcn.116.135012

Fishe, Jennifer N., et al. “Methods and implementation of a pediatric asthma pharmacogenomic study in the emergency department setting.” Pharmacogenetics and Genomics 30.9 (2020): 201-207. https://doi.org/10.31487/j.JDOA.2020.02.04

Fishe, Jennifer N., et al. “SNPs in PRKG1 & SPATA13-AS1 are associated with bronchodilator response: a pilot study during acute asthma exacerbations in African American children.” Pharmacogenetics and Genomics 31.7 (2021): 146-154. https://doi.org/10.1097/FPC.0000000000000434

Gerner, Trine, et al. “‘Barrier dysfunction in Atopic newBorns studY’(BABY): protocol of a Danish prospective birth cohort study.” BMJ open 10.7 (2020): e033801. http://dx.doi.org/10.1136/bmjopen-2019-033801

Gerner, Trine, et al. “Differences in Occurrence, Risk Factors and Severity of Early-onset Atopic Dermatitis among Preterm and Term Children.” Acta Dermato-Venereologica 102 (2022): adv00737-adv00737. http:// https://doi.org/10.2340/actadv.v102.575

Gielis, Els M., et al. “The use of plasma donor-derived, cell-free DNA to monitor acute rejection after kidney transplantation.” Nephrology Dialysis Transplantation 35.4 (2020): 714-721. https://doi.org/10.1093/ndt/gfz091

Gilbert-Diamond, Diane, et al. “Television food advertisement exposure and FTO rs9939609 genotype in relation to excess consumption in children.” International journal of obesity 41.1 (2017): 23-29. https://doi.org/10.1038/ijo.2016.163

Gorecki, Anastazja M., et al. “Single nucleotide polymorphisms associated with gut homeostasis influence risk and age-at-onset of Parkinson’s disease.” Frontiers in Aging Neuroscience 12 (2020). https://doi.org/10.3389/fnagi.2020.603849

Gosadi, I.M., Goyder, E.C., and Teare, M.D. (2014) Investigating the potential effect of consanguinity on type 2 diabetes susceptibility in a Saudi population. Hum Hered 77: 197-206. https://doi.org/10.1159/000362447

Grgic, Jozo, et al. “ADOR2A C allele carriers exhibit ergogenic responses to caffeine supplementation.” Nutrients 12.3 (2020): 741. https://doi.org/10.3390/nu12030741

Grgic, Jozo, et al. “CYP1A2 genotype and acute effects of caffeine on resistance exercise, jumping, and sprinting performance.” Journal of the International Society of Sports Nutrition 17 (2020): 1-11. https://doi.org/10.1186/s12970-020-00349-6

Harker, M., Carvell, A., Marti, V.P., Riazanskaia, S., Kelso, H., Taylor, D., et al.(2014) Functional characterisation of a SNP in the ABCC11 allele—effects on axillary skin metabolism, odour generation and associated behaviours. J Dermatol Sci 73: 23-30. https://doi.org/10.1016/j.jdermsci.2013.08.016

Huang, Wei-Hsin, et al. “Study of seven single-nucleotide polymorphisms identified in East Asians for association with obesity in a Taiwanese population.” BMJ open 6.8 (2016): e011713. http://dx.doi.org/10.1136/bmjopen-2016-011713

Ibiyemi, Olushola, et al. “Single Nucleotide Polymorphisms in COL1A2 gene and dental fluorosis among 4-and 8-year old Nigerian children.” Journal of Dentistry (2020). https://doi.org/10.31487/j.JDOA.2020.02.04

Jacob, Ysabel, et al. “ACTN3 (R577X) genotype is associated with Australian football league players.” Journal of strength and conditioning research 36.2 (2022): 573-576. https://doi.org/10.1519/JSC.0000000000003458

Jenkins, Luke C., et al. “Cortical function and sensorimotor plasticity are prognostic factors associated with future low back pain after an acute episode: the UPWaRD prospective cohort study.” Pain (2022): 10-1097.

https://doi.org/10.1097/j.pain.0000000000002684

Jenkins, Luke C., et al. “Low somatosensory cortex excitability in the acute stage of low back pain causes chronic pain.” The Journal of Pain 23.2 (2022): 289-304. https://doi.org/10.1016/j.jpain.2021.08.003

Jilani, M., Mohamed, A.A., Zeglam, H.B., Alhudiri, I.M., Ramadan, A.M., Saleh, S.S., et al. (2015) Association between vitamin D receptor gene polymorphisms and chronic periodontitis among Libyans. Libyan J of Med 10: 1. https://doi.com/10.3402/ljm.v10.26771

Johnson, Leslie Weaver, et al. “Factors influencing recovery from mild traumatic brain injury.” Brain injury 34.9 (2020): 1202-1212. https://doi.org/10.1080/02699052.2020.1795719

Jones, N., et al. “A genetic-based algorithm for personalized resistance training.” Biology of sport 33.2 (2016): 117. https://doi.org/10.5604/20831862.1198210

Kaur, Kiranjit, et al. “A Cross-Sectional Study of Bitter-Taste Receptor Genotypes, Oral Health, and Markers of Oral Inflammation.” Oral 1.2 (2021): 122-138. https://doi.org/10.3390/oral1020013

Khodakov, Dmitriy, et al. “Highly multiplexed rapid DNA detection with single-nucleotide specificity via convective PCR in a portable device.” Nature Biomedical Engineering 5.7 (2021): 702-712. https://doi.org/10.1038/s41551-021-00755-4

Klumpers, Marije J., et al. “Contribution of common and rare genetic variants in CEP72 on vincristine‐induced peripheral neuropathy in brain tumour patients.” British Journal of Clinical Pharmacology 88.7 (2022): 3463-3473. https://doi.org/10.1111/bcp.15267

Klumpers, Marije J., et al. “Genome-wide analyses of nephrotoxicity in platinum-treated cancer patients identify association with genetic variant in RBMS3 and acute kidney injury.” Journal of Personalized Medicine 12.6 (2022): 892. https://doi.org/10.3390/jpm12060892

Krueger F., Parasuraman R., Iyengar V., Thornburg M., Weel J., Lin M., et al.(2012) Oxytocin receptor genetic variation promotes human trust behavior. Front Hum Neurosci 6: 4. https://doi.org/10.3389/fnhum.2012.00004

Lancaster, Claire, et al. “Prospective Memory: Age related change is influenced by APOE genotype.” Aging, Neuropsychology, and Cognition 27.5 (2020): 710-728.   https://doi.org/10.1080/13825585.2019.1671305

Lancaster T., Linden D., and Heerey E. (2012) COMT val158met predicts reward responsiveness in humans. Genes, Brain and Behavior 11: 986-992. https://doi.org/10.1111/j.1601-183X.2012.00838.x

Li, Katherine, et al. “HLA-C* 06: 02 allele and response to IL-12/23 inhibition: results from the ustekinumab phase 3 psoriasis program.” Journal of Investigative Dermatology 136.12 (2016): 2364-2371. https://doi.org/10.1016/j.jid.2016.06.631

Lin, Siying, et al. “Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B).” NPJ Genomic Medicine 7.1 (2022): 2. https://doi.org/10.1038/s41525-021-00275-9

Livingstone, Katherine M., et al. “Fat mass-and obesity-associated genotype, dietary intakes and anthropometric measures in European adults: the Food4Me study.” British Journal of Nutrition 115.03 (2016): 440-448. https://doi.org/10.1017/S0007114515004675

Livingstone, Katherine M., et al. “Weekday sunlight exposure, but not vitamin D intake, influences the association between vitamin D receptor genotype and circulating concentration 25‐hydroxyvitamin D in a pan‐European population: the Food4Me study.” Molecular nutrition & food research 61.2 (2017): 1600476 https://doi.org/10.1002/mnfr.201600476

Livingstone, Katherine M., et al. “Characteristics of European adults who dropped out from the Food4Me Internet-based personalised nutrition intervention.” Public health nutrition 20.1 (2017): 53-63. http://dx.doi.org/10.1017/S1368980016002020

Livingstone, Katherine M., et al. “Characteristics of participants who benefit most from personalised nutrition: findings from the pan-European Food4Me randomised controlled trial.” British Journal of Nutrition 123.12 (2020): 1396-1405. https://doi.org/10.1017/S0007114520000653

Livingstone, Katherine M., et al. “Associations between dietary patterns, FTO genotype and obesity in adults from seven European countries.” European Journal of Nutrition 61.6 (2022): 2953-2965. https://doi.org/10.1007/s00394-022-02858-3

Marsaux, Cyril FM, et al. “Changes in physical activity following a genetic-based internet-delivered personalized intervention: randomized controlled trial (Food4Me).” Journal of medical Internet research 18.2 (2016). https://doi.org/10.2196/jmir.5198

McCarty, Matt, and Keqin Gregg. “Methods of detecting synthetic urine and matching a urine sample to a subject.” U.S. Patent Application No. 14/752,511.

McDonnell M.N., Buckley J.D., Opie G.M., Ridding M.C., and Semmler J.G. (2013) A single bout of aerobic exercise promotes motor cortical neuroplasticity. J Appl Physiol (1985) 114: 1174-1182. https://doi.org/10.1152/japplphysiol.01378.2012

McMichael G.L., Gibson C.S., O’Callaghan M.E., Goldwater P.N., Dekker G.A., Haan E.A., et al. (2009) DNA from buccal swabs suitable for high-throughput SNP multiplex analysis. J Biomol Tech 20: 232-235. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777348/

Miller, L., Sajdler, C., and Chauhan, N. (2015) The impact of chronic pain in patients on the acute pain service British Journal of Pain 9: 5-75. https://doi.org/10.1177/2049463715579924

Morgan, A.R., Han, D Y., Wickens, K., Barthow, C., Mitchell, E.A., Stanley, T.V. et al. (2014) Differential modification of genetic susceptibility to childhood eczema by two probiotics. Clinical & Experimental Allergy 44(10): 1255-1265 https://doi.org/10.1111/cea.12394

Moskowitz, Simon, et al. “Is impaired dopaminergic function associated with mobility capacity in older adults?.” GeroScience (2020): 1-22. https://doi.org/10.1007/s11357-020-00303-z

Mueckenhausen, Raphaela, et al. “Heparanase wildtype is associated with a reduced incidence of transplant-associated systemic vasculopathies.” Hematology/Oncology and Stem Cell Therapy (2021). https://doi.org/10.1016/j.hemonc.2021.10.003

Mulligan, Connie J., et al. “Novel GxE effects and resilience: A case: control longitudinal study of psychosocial stress with war-affected youth.” Plos one 17.4 (2022): e0266509. https://doi.org/10.1371/journal.pone.0266509

Nor, Nurfarhana Diana Mohd, et al. “The effects of taste sensitivity and repeated taste exposure on children’s intake and liking of turnip (Brassica rapa subsp. rapa); a bitter Brassica vegetable.” Appetite 157 (2021): 104991. https://doi.org/10.1016/j.appet.2020.104991

O’Donovan, Clare B., et al. “The impact of MTHFR 677C→ T risk knowledge on changes in folate intake: findings from the Food4Me study.” Genes & Nutrition 11.1 (2016): 25. https://doi.org/10.1186/s12263-016-0539-x

Ottolini, Christian S., et al. “Genome-wide maps of recombination and chromosome segregation in human oocytes and embryos show selection for maternal recombination rates.” Nature genetics 47.7 (2015): 727-735. https://doi.org/10.1038/ng.3306

Paladino T., Mendoza E., Jin Y., Stoerker J., Dobb M., Farkas D., Oeth P. (2011) Evaluation Of Buccal Swabs As Source Of DNA For Multiplexed Genotyping Of AMD Associated Markers. ARVO 2011. http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=7de7e149-869f-4f57-b973-50ae74ccda44&cKey=e9fc6bc6-6ab3-4c8a-93cf-6c23e88e01b2&mKey=6f224a2d-af6a-4533-8bbb-6a8d7b26edb3

Pascale, Esterina, et al. “Disordered eating in early childhood: DRD4 and DAT1 gene polymorphisms and quality of mother–child interaction.” Eating and Weight Disorders-Studies on Anorexia, Bulimia and Obesity 27.7 (2022): 2605-2616. https://doi.org/10.1007/s40519-022-01408-4

Pellicano, Gaia Romana, et al. “Beyond the dyad: the role of mother and father in newborns’ global DNA methylation during the first month of life—a pilot study.” Developmental Psychobiology (2020). https://doi.org/10.1002/dev.22072

Phillips, S.L., Richter, S.J., Teglas, S.L., Bhatt, I.S., Morehouse, R.C., Hauser, E.R., and Henrich, V.C. (2015) Feasibility of a bilateral 4000–6000 Hz notch as a phenotype for genetic association analysis1-8. Int J Audiol 19: 1-8. https://doi.org/10.3109/14992027.2015.1030512

Reavis, Eric A., Sebastian M. Frank, and U. Tse Peter. “Caudate nucleus reactivity predicts perceptual learning rate for visual feature conjunctions.” NeuroImage 110 (2015): 171-181. https://doi.org/10.1016/j.neuroimage.2015.01.051

Runge, Christina L., et al. “Association of TMTC2 with human nonsyndromic sensorineural hearing loss.” JAMA Otolaryngology–Head & Neck Surgery 142.9 (2016): 866-872. https://doi.org/10.1001/jamaoto.2016.1444

Schoffelen, T., Ammerdorffer, A., Hagenaars, J.C., Bleeker-Rovers, C.P., Wegdam-Blans, M.C., Wever, P.C., et al. (2015) Genetic Variation in Pattern Recognition Receptors and Adaptor Proteins Associated With Development of Chronic Q Fever. J Infect Dis 212: 818-829. https://doi.org/10.1093/infdis/jiv113

Scutt, Greg, et al. “The association of a single-nucleotide polymorphism in the nuclear factor (erythroid-derived 2)-like 2 gene with adverse drug reactions, multimorbidity, and frailty in older people.” The Journals of Gerontology: Series A 75.6 (2020): 1050-1057. https://doi.org/10.1093/gerona/glz131

Senzaki, Sawa, et al. “Roles of culture and COMT Val58Met gene on neural basis of executive function: A comparison between Japanese and American children.” Developmental Psychobiology (2021). https://doi.org/10.1002/dev.22087

Shindler, A. E., et al. “A preliminary study of pharmacogenetic biomarkers for individuals with autism and gastrointestinal dysfunction.” Research in Autism Spectrum Disorders 71 (2020): 101516. https://doi.org/10.1016/j.rasd.2020.101516

Shindler, A. E., et al. “Towards Identifying Genetic Biomarkers f or Gastrointestinal Dysfunction in Autism.” Journal of autism and developmental disorders 50.1 (2020): 76-86.                                https://doi.org/10.1007/s10803-019-04231-6

Shoeb, D., Dearden, J., Weatherall, A., Bargery, C., Moreea, S., Alam, S., et al.(2014) Extended duration therapy with pegylated interferon and ribavirin for patients with genotype 3 hepatitis C and advanced fibrosis: final results from the STEPS trial. J Hepatol 60: 699-705. https://doi.org/10.1016/j.jhep.2013.11.011

ŠIMONEK, JAROMÍR, and RADOSLAV ŽIDEK. “Sports talent identification based on motor tests and genetic analysis.” Trends in Sport Sciences25.4 (2018) https://doi.org/10.23829/TSS.2018.25.4-5

Startin, C.M., Fiorentini, C., de Haan, M., and Skuse, D.H. (2015) Variation in the X-Linked EFHC2 Gene Is Associated with Social Cognitive Abilities in Males. PLoS One 10: e0131604. https://doi.org/10.1371/journal.pone.0131604

Tenhu, Elina, et al. “Gene Polymorphisms of TLR4 and TLR9 and Haemophilus influenzae Meningitis in Angolan Children.” Genes 11.9 (2020): 1099. https://doi.org/10.3390/genes11091099

Tovar, Alison, et al. “An FTO Gene Variant Moderates the Association between Parental Restriction and Child BMI.” PloS one 11.5 (2016): e0155521.  https://doi.org/10.1371/journal.pone.0155521

Yang, Qian, et al. “Exploring the relationships between taste phenotypes, genotypes, ethnicity, gender and taste perception using Chi-square and regression tree analysis.” Food Quality and Preference 83 (2020): 103928. https://doi.org/10.1016/j.foodqual.2020.103928

Valdes A.M., Arden N.K., Vaughn F.L., Doherty S.A., Leaverton P.E., Zhang W., et al. (2011) Role of the Nav1. 7 R1150W amino acid change in susceptibility to symptomatic knee osteoarthritis and multiple regional pain. Arthritis Care & Research 63: 440-444. https://doi.org/10.1002/acr.20375

Wachman, Elisha M., et al. “Association of maternal and infant variants in PNOC and COMT genes with neonatal abstinence syndrome severity.” The American Journal on Addictions 26.1 (2017): 42-49. https://doi.org/10.1111/ajad.12483

Ye, Zimeng, et al. “Mosaicism in tuberous sclerosis complex: Lowering the threshold for clinical reporting.” Human Mutation 43.12 (2022): 1956-1969. https://doi.org/10.1002/humu.24454

Andrianova, Maria A., et al. “Extended family with germline pathogenic variant in polymerase delta provides strong evidence for recessive effect of proofreading inactivation.” bioRxiv (2022): 2022-07. https://doi.org/10.1101/2022.07.20.500591

Andrew T., Calloway C.D., Stuart S., Lee S.H., Gill R., Clement G., et al. (2011) A twin study of mitochondrial DNA polymorphisms shows that heteroplasmy at multiple sites is associated with mtDNA variant 16093 but not with zygosity. PloS One 6: e22332.  https://doi.org/10.1371/journal.pone.0022332

Aguilera-Diaz, Almudena, et al. “Strategy for identification of a potential inherited leukemia predisposition in a 299 patient’s cohort with tumor-only sequencing data.” Leukemia Research 95 (2020): 106386. https://doi.org/10.1016/j.leukres.2020.106386

Bartik, Zsuzsa I., et al. “Whole exome sequencing identifies KIF26B, LIFR and LAMC1 mutations in familial vesicoureteral reflux.” Plos one 17.11 (2022): e0277524. https://doi.org/10.1371/journal.pone.0277524

Bernardi, Simona, et al. “ETV6: A candidate gene for predisposition to “Blend Pedigrees”? A case report from the NEXT-famly clinical trial.” Case reports in hematology 2020 (2020). https://doi.org/10.1155/2020/2795656

Bronk, Julianna K., et al. “Feasibility of a novel non-invasive swab technique for serial whole-exome sequencing of cervical tumors during chemoradiation therapy.” Plos one 17.10 (2022): e0274457. https://doi.org/10.1371/journal.pone.0274457

Chen, Yi, et al. “CHST15 gene germline mutation is associated with the development of familial myeloproliferative neoplasms and higher transformation risk.” Cell Death & Disease 13.7 (2022): 586. https://doi.org/10.1038/s41419-022-05035-w

Dawson P.A., Sim P., Mudge D.W., and Cowley D. (2013) Human SLC26A1 gene variants: A pilot study. The Scientific World Journal 2013: ID 541710. https://doi.org/10.1155/2013/541710

Duc T.T.T., Farnir F., Michaux C., Desmecht D., and Cornet A. (2012) Detection of new biallelic polymorphisms in the human MxA gene. Mol Biol Rep 39: 8533-8538. https://doi.org/10.1007/s11033-012-1708-7

Duy, Phan Q., et al. “Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus.” Nature neuroscience 25.4 (2022): 458-473. https://doi.org/10.1038/s41593-022-01043-3

El-Kordi A., Kästner A., Grube S., Klugmann M., Begemann M., Sperling S., et al.(2013) A single gene defect causing claustrophobia. Translational Psychiatry 3: e254. https://doi.org/10.1038/tp.2013.28

Fonteles, C. S., et al. “De novo ALX4 variant detected in child with non-syndromic craniosynostosis.” Brazilian Journal of Medical and Biological Research 54 (2021). https://doi.org/10.1590/1414-431X2021e11396

Gale G., Östman S., Rekabdar E., Naluai Å.T., Högkil K., Hasséus B., et al. (2015) Characterisation of a Swedish cohort with orofacial granulomatosis with or without Crohn’s disease. Oral diseases 21 (1): e98-e104. https://doi.org/10.1111/odi.12236

Harker M., Carvell A., Marti V.P., Riazanskaia S., Kelso H., Taylor D., et al.(2014) Functional characterisation of a SNP in the ABCC11 allele—Effects on axillary skin metabolism, odour generation and associated behaviours. J Dermatol Sci 73: 23-30. https://doi.org/10.1016/j.jdermsci.2013.08.016

Hofman, Jagoda, et al. “Case report: Rare among ultrarare—Clinical odyssey of a new patient with Ogden syndrome.” Frontiers in Genetics 13 (2022). https://doi.org/10.3389/fgene.2022.979377

Jin, Sheng Chih, et al. “Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus.” Nature medicine 26.11 (2020): 1754-1765. https://doi.org/10.1038/s41591-020-1090-2

Pham, Kala T., Tatiana Cisneros Napravnik, and Ann H. Klopp. “HPV-Reactive T-Cell Receptor Expand in Combination Therapy.” (2022). https://openworks.mdanderson.org/cgi/viewcontent.cgi?article=1001&context=sumexp22

Polcari, I., Becker, L., Stein, S. L., Smith, M. S., & Paller, A. S. (2014). Filaggrin Gene Mutations in African Americans with Both Ichthyosis Vulgaris and Atopic Dermatitis. Pediatric dermatology 31 (4): 489-492. https://doi.org/10.1111/pde.12355

Porter T.R., Li X., Stephensen C.B., Mulligan K., Rutledge B., Flynn P.M., et al.(2013) Genetic associations with 25-hydroxyvitamin D deficiency in HIV-1-infected youth: Fine-mapping for the GC/DBP gene that encodes the vitamin D-binding protein. Frontiers in Genetics 4: 234. https://doi.org/10.3389/fgene.2013.00234

Schmidt B.L., Kuczynski, J., Bhattacharya A., Huey B. Corby, P. M. Queiroz, et al.(2014). Changes in Abundance of Oral Microbiota Associated with Oral Cancer. PLoS One, 9(6): e98741. https://doi.org/10.1371/journal.pone.0098741

Schroeder K.B., McElreath R., and Nettle D. (2013) Variants at serotonin transporter and 2A receptor genes predict cooperative behavior differentially according to presence of punishment. Proc Natl Acad Sci U S A 110: 3955-3960. https://doi.org/10.1073/pnas.1216841110

Schultz J.M., Bhatti R., Madeo A.C., Turriff A., Muskett J.A., Zalewski C.K., et al. (2011) Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or usher syndrome USH1D in compound heterozygotes. J Med Genet 48: 767-775. http://dx.doi.org/10.1136/jmedgenet-2011-100262

Serra, Eva Gonçalves, et al. “Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease.” Nature communications 11.1 (2020): 1-15. https://doi.org/10.1038/s41467-019-14275-y

Simon C., Chagraoui J., Krosl J., Gendron P., Wilhelm B., Lemieux S., et al.(2012) A key role for EZH2 and associated genes in mouse and human adult T-cell acute leukemia. Genes Dev 26: 651-656.

Smith K.E., Porges E.C., Norman G.J., Connelly J.J., and Decety J. (2014) Oxytocin receptor gene variation predicts empathic concern and autonomic arousal while perceiving harm to others. Social Neuroscience 9: 1-9. https://doi.org/10.1080/17470919.2013.863223

Stephensen C.B., Armstrong P., Newman J.W., Pedersen T.L., Legault J., Schuster G.U., et al. (2011) ALOX5 gene variants affect eicosanoid production and response to fish oil supplementation. J Lipid Res 52: 991-1003. https://doi.org/10.1194/jlr.P012864

Timberlake, Andrew T., et al. “Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles.” Elife 5 (2016): e20125 https://doi.org/10.7554/eLife.20125

Topka, S., Vijai, J., Walsh, M.F., Jacobs, L., Maria, A., Villano, D., et al. (2015) Germline ETV6 mutations confer susceptibility to acute lymphoblastic leukemia and thrombocytopenia. PLoS Gen 11: e1005262. https://doi.org/10.1371/journal.pgen.1005262

Yin, Le, et al. “Novel germline mutation KMT2A G3131S confers genetic susceptibility to familial myeloproliferative neoplasms.” Annals of Hematology 100.9 (2021): 2229-2240. https://doi.org/10.1007/s00277-021-04562-4

Archer, Nicholas Steven, et al. “A comparison of collection techniques for gene expression analysis of human oral taste tissue.” PloS one 11.3 (2016): e0152157.   https://doi.org/10.1371/journal.pone.0152157

Robino, Antonietta, et al. “Taste perception and expression in stomach of bitter taste receptor tas2r38 in obese and lean subjects.” Appetite 166 (2021): 105595. https://doi.org/10.1016/j.appet.2021.105595

Adams E.R., Gomez M.A., Scheske L., Rios R., Marquez, R., Cossio, A., et al. (2014). Sensitive diagnosis of cutaneous leishmaniasis by lesion swab sampling coupled to qPCR. Parasitology 141:1891-1897. https://doi.org/10.1017/S0031182014001280

Al Bataineh, Mohammad Tahseen, et al. “Revealing oral microbiota composition and functionality associated with heavy cigarette smoking.” Journal of translational medicine 18.1 (2020): 1-10. https://doi.org/10.1186/s12967-020-02579-3

Al Bataineh, Mohammad Tahseen, et al. “Altered composition of the oral microbiota in depression among cigarette smokers: A pilot study.” Frontiers in Psychiatry 13 (2022). https://doi.org/10.3389/fpsyt.2022.902433

Bahig, Houda, et al. “Longitudinal characterization of the tumoral microbiome during radiotherapy in HPV-associated oropharynx cancer.” Clinical and translational radiation oncology 26 (2021): 98-103. https://doi.org/10.1016/j.ctro.2020.11.007

Bankvall, M., Sjöberg, F., Gale, G., Wold, A., Jontell, M., and Östman, S. (2014) The oral microbiota of patients with recurrent aphthous stomatitis. J Oral Microb6: 10. https://doi.org/10.3402/jom.v6.25739

Biegert, Greyson, et al. “Diversity and composition of gut microbiome of cervical cancer patients: Do results of 16S rRNA sequencing and whole genome sequencing approaches align?.” Journal of Microbiological Methods 185 (2021): 106213. https://doi.org/10.1016/j.mimet.2021.106213

Brzychcy, Karolina, et al. “Gut microbiota in alopecia areata.” Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii 39.6 (2022): 1162-1170. https://doi.org/10.5114/ada.2022.120453

Charalambous, Eleftheria G., et al. “Early-Life Adversity Leaves Its Imprint on the Oral Microbiome for More Than 20 Years and Is Associated with Long-Term Immune Changes.” International Journal of Molecular Sciences 22.23 (2021): 12682. https://doi.org/10.3390/ijms222312682

Chang, Chih-Chiun J., et al. “Topical glaucoma therapy is associated with alterations of the ocular surface microbiome.” Investigative Ophthalmology & Visual Science 63.9 (2022): 32-32. https://doi.org/10.1167/iovs.63.9.32

Coker, Modupe O., et al. “Dental caries and its association with the oral microbiomes and HIV in young children—Nigeria (DOMHaIN): a cohort study.” BMC oral health 21.1 (2021): 1-15. https://doi.org/10.1186/s12903-021-01944-y

Colbert, Lauren E., et al. “Cancer-associated Lactobacillus iners are genetically distinct and associated with chemoradiation resistance in cervical cancer.” medRxiv (2022): 2022-04. https://doi.org/10.1101/2022.04.26.22274346

Conte, Ianina, et al. “A comparison of community based preventative services to improve child dental health.” NIHR Open Res 2.8 (2022): 8. https://doi.org/10.3310/nihropenres.1115174.1

Danko, David, et al. “A global metagenomic map of urban microbiomes and antimicrobial resistance.” Cell (2021). https://doi.org/10.1016/j.cell.2021.05.002

Divya, Gopinath, et al. “Differences in the bacteriome of swab, saliva, and tissue biopsies in oral cancer.” Scientific Reports (Nature Publisher Group) 11.1 (2021).    https://doi.org/10.1038/s41598-020-80859-0

El Alam, Molly B., et al. “A prospective study of the adaptive changes in the gut microbiome during standard-of-care chemoradiotherapy for gynecologic cancers.” PloS one 16.3 (2021): e0247905. https://doi.org/10.1371/journal.pone.0247905

Fabian Cieplik, Egija Zaura, Bernd W. Brandt, Mark J. Buijs, Wolfgang Buchalla, Wim Crielaard, Marja L. Laine, Dong Mei Deng & Rob A. M. Exterkate (2019) Microcosm biofilms cultured from different oral niches in periodontitis patients, Journal of Oral Microbiology, 11:1 https://doi.org/10.1080/20022727.2018.1551596

Gopinath, Divya, et al. “Compositional profile of mucosal bacteriome of smokers and smokeless tobacco users.” Clinical Oral Investigations (2021): 1-10. https://doi.org/10.1007/s00784-021-04137-7

Grant-Beurmann, Silvia, et al. “Dynamics of the infant gut microbiota in the first 18 months of life: the impact of maternal HIV infection and breastfeeding.” Microbiome 10.1 (2022): 61. https://doi.org/10.1186/s40168-022-01230-1

Guevarra, Robin B., et al. “Metagenomic characterization of bacterial community and antibiotic resistance genes found in the mass transit system in Seoul, South Korea.” Ecotoxicology and Environmental Safety 246 (2022): 114176. https://doi.org/10.1016/j.ecoenv.2022.114176

Hernández, Miguel, et al. “Microbiology of molar–incisor hypomineralization lesions. A pilot study.” Journal of Oral Microbiology 12.1 (2020): 1766166. https://doi.org/10.1080/20002297.2020.1766166

HERNÁNDEZ, MIGUEL, Miguel Carda, and Alex Mira. “Comparative pilot study on the qualitative differences in dental biofilm between teeth with molar-incisor hypomineralization and their healthy counterparts.” ODONTOL PEDIÁTR 28.3 (2020): 133-142. https://dialnet.unirioja.es/servlet/articulo?codigo=7705129

Kaiser, Hannah, et al. “Multiscale biology of cardiovascular risk in psoriasis: Protocol for a case-control study.” JMIR research protocols 10.9 (2021): e28669. https://doi.org/10.2196/28669

Kalyan, S., Wang, J., Quabius, E.S., Huck, J., Wiltfang, J., Baines, J.F., and Kabelitz, D. (2015) Systemic immunity shapes the oral microbiome and susceptibility to bisphosphonate-associated osteonecrosis of the jaw. J Transl Med 13: 212-015-0568-z. https://doi.org/10.1186/s12967-015-0568-z

Karpinets, Tatiana V., et al. “Metagenomes of rectal swabs in larger, advanced stage cervical cancers have enhanced mucus degrading functionalities and distinct taxonomic structure.” BMC cancer 22.1 (2022): 945.

https://doi.org/10.1186/s12885-022-09997-0

Kaspar, U., Kriegeskorte, A., Schubert, T., Peters, G., Rudack, C., Pieper, D.H., et al. (2015) The Culturome of the Human Nose Habitats Reveals Individual Bacterial Fingerprint Patterns. Environ Microbiol (in press). https://doi.org/10.1111/1462-2920.12891

Kim, Jeongwon, Sang Jun Han, and Keunje Yoo. “Dust-Associated Bacterial and Fungal Communities in Indoor Multiple-Use and Public Transportation Facilities.” Atmosphere 13.9 (2022): 1373. https://doi.org/10.3390/atmos13091373

Kim, Ji Heui, et al. “Association between the sinus microbiota with eosinophilic inflammation and prognosis in chronic rhinosinusitis with nasal polyps.” Experimental & molecular medicine 52.6 (2020): 978-987. https://doi.org/10.1038/s12276-020-0458-1

Lin, Daniel, et al. “Microbiome Dynamics During Chemoradiation Therapy for Anal Cancer.” International Journal of Radiation Oncology* Biology* Physics (2022). https://doi.org/10.1016/j.ijrobp.2022.04.037

Lin, Dongjia, et al. “The niche-specialist and age-related oral microbial ecosystem: crosstalk with host immune cells in homeostasis.” Microbial Genomics 8.6 (2022): 000811. https://doi.org/10.1099/mgen.0.000811

López-Santacruz, Hiram D., et al. “Streptococcus dentisani is a common inhabitant of the oral microbiota worldwide and is found at higher levels in caries-free individuals.” International Microbiology 24.4 (2021): 619-629. https://doi.org/10.1007/s10123-021-00222-9

Low, Liying, et al. “Evaluation of full-length nanopore 16S sequencing for detection of pathogens in microbial keratitis.” PeerJ 9 (2021): e10778. https://doi.org/10.7717/peerj.10778

Magiopoulos, I., et al. “A multi-parametric assessment of decontamination protocols for the subglacial Lake Ellsworth probe.” Journal of microbiological methods 123 (2016): 87-93. https://doi.org/10.1016/j.mimet.2016.02.012

McFrederick, Quinn S., et al. “Flowers and Wild Megachilid Bees Share Microbes.” Microbial Ecology 73.1 (2017): 188-200. https://doi.org/10.1007/s00248-016-0838-1

McQuillan, Jonathan S., et al. “Buzz off! An evaluation of ultrasonic acoustic vibration for the disruption of marine micro‐organisms on sensor‐housing materials.” Letters in applied microbiology 63.6 (2016): 393-399. https://doi.org/10.1111/lam.12671

Mitra, Aparna, et al. “Microbial diversity and composition is associated with patient-reported toxicity during chemoradiation therapy for cervical cancer.” International Journal of Radiation Oncology* Biology* Physics 107.1 (2020): 163-171.               https://doi.org/10.1016/j.ijrobp.2019.12.040

Neckovic, Ana, et al. “Investigation of direct and indirect transfer of microbiomes between individuals.” Forensic Science International: Genetics 45 (2020): 102212. https://doi.org/10.1016/j.fsigen.2019.102212

Ninomiya, Kazunori, et al. “Effect of Systemic Administration of Amitriptyline on Oral Microbes in Rats.” in vivo 36.5 (2022): 2134-2142. https://doi.org/10.21873/invivo.12939

Older, Caitlin E., Diesel, Alison B., Lawhon, Sara D., Queiroz, Cintia R. R., Henker, Luan C., Rodrigues Hoffmann, Aline. “The feline cutaneous and oral microbiota are influenced by breed and environment   https://doi.org/10.1371/journal.pone.0220463

Ortiz, Katlyn, Jess W. Jones, and Eric M. Hallerman. “Development and Characterization of Microsatellite Loci in the Endangered Catspaw, Epioblasma Obliquata (Bivalvia: Unionidae).” Freshwater Mollusk Biology and Conservation 25.1 (2022): 1-6. https://doi.org/10.31931/fmbc-d-21-00002

Paudel, Durga, et al. “Proteomic and microbiota analyses of the oral cavity during psychological stress.” Plos one 17.5 (2022): e0268155. https://doi.org/10.1371/journal.pone.0268155

Pearce, D. A., et al. “Microbiology: lessons from a first attempt at Lake Ellsworth.” Philosophical transactions. Series A, Mathematical, physical, and engineering sciences 374.2059 (2016). https://doi.org/10.1098/rsta.2014.0291

Rautava, J., Pinnell, L.J., Vong, L., Akseer, N., Assa, A., and Sherman, P.M. (2015) Oral microbiome composition changes in mouse models of colitis. J Gastroenterol Hepatol 30: 521-527. https://doi.org/10.1111/jgh.12713

Saifon, Woraseth, et al. “Gastrointestinal microbiota profile and clinical correlations in advanced EGFR-WT and EGFR-mutant non-small cell lung cancer.” BMC cancer 22.1 (2022): 1-15. https://doi.org/10.1186/s12885-022-10050-3

Schmidt, B.L., Kuczynski, J., Bhattacharya, A., Huey, B., Corby, P.M., Queiroz, E.L., et al. (2014) Changes in abundance of oral microbiota associated with oral cancer. PlosOne 9 (6): e98741.   https://doi.org/10.1371/journal.pone.0098741

Shivaji, Sisinthy, et al. “Alterations in the conjunctival surface bacterial microbiome in bacterial keratitis patients.” Experimental Eye Research 203 (2021): 108418. https://doi.org/10.1016/j.exer.2020.108418

Siegal, Nora, et al. “Elevated levels of Merkel cell polyoma virus in the anophthalmic conjunctiva.” Scientific Reports 11.1 (2021): 1-9. https://doi.org/10.1038/s41598-021-92642-w

Sims, Travis T., et al. “Tumor microbial diversity and compositional differences among women in Botswana with high-grade cervical dysplasia and cervical cancer.” International Journal of Gynecologic Cancer 30.8 (2020).                 http://dx.doi.org/10.1136/ijgc-2020-001547

Sims, Travis T., et al. “Gut microbiome diversity is an independent predictor of survival in cervical cancer patients receiving chemoradiation.” Communications biology 4.1 (2021): 1-10. https://doi.org/10.1038/s42003-021-01741-x

Somineni, Hari K., et al. “Site-and Taxa-Specific Disease-Associated Oral Microbial Structures Distinguish Inflammatory Bowel Diseases.” Inflammatory Bowel Diseases (2021). https://doi.org/10.1093/ibd/izab082

Sotozono, Maki, et al. “Impact of sleep on the microbiome of oral biofilms.” Plos one 16.12 (2021): e0259850. https://doi.org/10.1371/journal.pone.0259850

Su, Shih-Chi, et al. “Oral microbial dysbiosis and its performance in predicting oral cancer.” Carcinogenesis (2020).                 https://doi.org/10.1093/carcin/bgaa062

Vidović, B., et al. “The effect of the octenidine-based oral antiseptic on the structure of microbial communities and periodontal status in patients with fixed orthodontic treatments.” European Review for Medical and Pharmacological Sciences 23 (2019): 8598-8605. https://doi.org/10.26355/eurrev_201910_19176

Aghagoli, Ghazal, et al. “Epigenome-wide analysis identifies genes and pathways linked to acoustic cry variation in preterm infants.” Pediatric Research (2020): 1-7. https://doi.org/10.1038/s41390-020-01172-0

Auvinen, Pauliina, et al. “Chromatin modifier developmental pluripotency associated factor 4 (DPPA4) is a candidate gene for alcohol-induced developmental disorders.” BMC medicine 20.1 (2022): 495. https://doi.org/10.1186/s12916-022-02699-1

Azzi S., Blaise A., Steunou V., Harbison M.D., Salem J., Brioude, F., et al. (2014). Complex Tissue‐Specific Epigenotypes in Russell–Silver Syndrome Associated with 11p15 ICR1 Hypomethylation. Human mutation 35 (10): 1211-1220. https://doi.org/10.1002/humu.22623

Carola, Valeria, et al. “Children with disruptive mood dysregulation disorder and psychopathological risk in their mothers: the function of global DNA methylation.” Frontiers in psychiatry 12 (2021). https://doi.org/10.3389/fpsyt.2021.593500

Carpentieri, Valentina, et al. “Epigenetic regulation of DAT gene promoter modulates the risk of externalizing and internalizing behaviors on a normative population: An explorative study.” Behavioural Brain Research 406 (2021): 113246. https://doi.org/10.1016/j.bbr.2021.113246

Carpentieri, Valentina, et al. “Methylation patterns within 5′-UTR of DAT1 gene as a function of allelic 3′-UTR variants and their maternal or paternal origin: May these affect the psychopathological phenotypes in children? An explorative study.” Neurosci https://doi.org/10.1016/j.neulet.2022.136916

Cerniglia, Luca, et al. “Patterns of DNA methylation at specific loci of the dopamine transporter 1 gene and psychopathological risk in trios of mothers, fathers and children.” European Journal of Developmental Psychology (2020): 1-28. https://doi.org/10.3390/bs11010009

Cimino, S., et al. “DNA Methylation and Allelic Polymorphism at the Dopamine Transporter Promoter Affect Internalizing and Externalizing Symptoms in Preschoolers.” Child Psychiatry & Human Development (2020): 1-10. https://doi.org/10.1007/s10578-020-01009-1

Cimino, Silvia, et al. “DAT1 and Its Psychological Correlates in Children with Avoidant/Restrictive Food Intake Disorder: A Cross-Sectional Pilot Study.” Behavioral Sciences 11.1 (2021): 9. https://doi.org/10.3390/bs11010009

Coppens, Grégoire, et al. “Assessment of aberrant DNA methylation two years after paediatric critical illness: a pre-planned secondary analysis of the international PEPaNIC trial.” Epigenetics (2022): 1-12. https://doi.org/10.1080/15592294.2022.2146966

Essex M.J., Thomas Boyce W., Hertzman C., Lam L.L., Armstrong J.M., Neumann S., and Kobor M.S. (2013) Epigenetic vestiges of early developmental adversity: Childhood stress exposure and DNA methylation in adolescence. Child Dev 84: 58-75. https://doi.org/10.1111/j.1467-8624.2011.01641.x

Everson, Todd M., et al. “Serious neonatal morbidities are associated with differences in DNA methylation among very preterm infants.” Clinical epigenetics 12.1 (2020): 1-15.               https://doi.org/10.1186/s13148-020-00942-1

Gomaa, Noha, et al. “Association of Pediatric Buccal Epigenetic Age Acceleration With Adverse Neonatal Brain Growth and Neurodevelopmental Outcomes Among Children Born Very Preterm With a Neonatal Infection.” JAMA Network Open 5.11 (2022): e2239796-e22397 https://doi.org/10.1001/jamanetworkopen.2022.39796

Jones M.J., Farré P., McEwen L.M., MacIsaac J.L., Watt K., Neumann S.M., et al.(2013) Distinct DNA methylation patterns of cognitive impairment and trisomy 21 in down syndrome. BMC Medical Genomics 6: 58. https://doi.org/10.1186/1755-8794-6-58

Kim, Youl-Ri, et al. “Differential methylation of the oxytocin receptor gene in patients with anorexia nervosa: a pilot study.” PloS one 9.2 (2014): e88673.   https://doi.org/10.1371/journal.pone.0088673

Marzilli, Eleonora, et al. “Children’s ADHD and Dysregulation Problems, DAT1 Genotype and Methylation, and Their Interplay with Family Environment.” Child & Youth Care Forum. New York: Springer US, 2022.

https://doi.org/10.1007/s10566-022-09687-9

Mavioglu, Rezan Nehir, et al. “A history of childhood maltreatment is associated with altered DNA methylation levels of DNA methyltransferase 1 in maternal but not neonatal mononuclear immune cells.” Frontiers in psychiatry 13 (2022). https://doi.org/10.3389/fpsyt.2022.945343

McGill, Megan G., et al. “Maternal prenatal anxiety and the fetal origins of epigenetic aging.” Biological psychiatry (2021) https://doi.org/10.1016/j.biopsych.2021.07.025

Non, A.L., and Thayer, Z.M. (2015) Epigenetics for anthropologists: An introduction to methods. Am J Hum Biol 27: 295-303. https://doi.org/10.1002/ajhb.22679

Portales-Casamar, Elodie, et al. “DNA methylation signature of human fetal alcohol spectrum disorder.” Epigenetics & Chromatin 9.1 (2016): 25. https://doi.org/10.1186/s13072-016-0074-4

Price M.E., Cotton A.M., Lam L.L., Farre P., Emberly E., Brown C.J., et al. (2013) Additional annotation enhances potential for biologically-relevant analysis of the illumina infinium HumanMethylation450 BeadChip array. Epigenetics Chromatin 6: 4-8935-6-4. https://doi.org/10.1186/1756-8935-6-4

Raffington, Laurel, et al. “Associations of Socioeconomic Disparities With Buccal DNA-Methylation Measures Of Biological Aging.” bioRxiv (2022): 2022-12.

https://www.biorxiv.org/content/10.1101/2022.12.07.519438v1

Richter, Anne E., et al. “Altered neurodevelopmental DNA methylation status after fetal growth restriction with brain-sparing.” Journal of developmental origins of health and disease 13.3 (2022): 378-389. https://doi.org/10.1017/S2040174421000374

Ross, Jason P., et al. “Batch-effect detection, correction and characterisation in Illumina HumanMethylation450 and MethylationEPIC BeadChip array data.” Clinical Epigenetics 14.1 (2022): 1-28.

https://doi.org/10.1186/s13148-022-01277-9

Sommerer, Yasmine, et al. “A correlation map of genome-wide DNA methylation patterns between paired human brain and buccal samples.” Clinical Epigenetics 14.1 (2022): 1-10. https://doi.org/10.1186/s13148-022-01357-w

Sommerer, Yasmine, et al. “Epigenome-Wide Association Study in Peripheral Tissues Highlights DNA Methylation Profiles Associated with Episodic Memory Performance in Humans.” Biomedicines 10.11 (2022): 2798. https://doi.org/10.3390/biomedicines10112798

Taylor, Rachael M., et al. “Global DNA methylation and cognitive and behavioral outcomes at 4 years of age: A cross‐sectional study.” Brain and behavior 10.4 (2020): e01579. https://doi.org/10.1002/brb3.1579

Teh, Ai Ling, et al. “Comparison of Methyl-capture Sequencing vs. Infinium 450K methylation array for methylome analysis in clinical samples.” Epigenetics 11.1 (2016): 36-48. https://doi.org/10.1080/15592294.2015.1132136

Viet, Chi T., et al. “Brush swab as a noninvasive surrogate for tissue biopsies in epigenomic profiling of oral cancer.” Biomarker research 9.1 (2021): 1-10. https://doi.org/10.1186/s40364-021-00349-x

Al-Ghafri, Mataab K., et al. “Genetic diversity of the Nubian ibex in Oman as revealed by mitochondrial DNA.” Royal Society open science 8.5 (2021): 210125. https://doi.org/10.1098/rsos.210125

Baciu, Iulia, Ancuta Fedorca, and Georgeta Ionescu. “Noninvasive Genetics Knowledge from the Brown Bear Populations to Assist Biodiversity Conservation.” Diversity 14.2 (2022): 121. https://doi.org/10.3390/d14020121

Balázs, Gergely, et al. “A new non-invasive in situ underwater DNA sampling method for estimating genetic diversity.” Evolutionary Ecology 34.4 (2020): 633-644.          https://doi.org/10.1007/s10682-020-10053-1

Cano, Irene, et al. “Non‐lethal loop‐mediated isothermal amplification assay as a point‐of‐care diagnostics tool for Neoparamoeba perurans, the causative agent of amoebic gill disease.” Journal of fish diseases 43.7 (2020): 779-790. https://doi.org/10.1111/jfd.13175

Cano, Irene, et al. “Seroconversion and Skin Mucosal Parameters during Koi Herpesvirus Shedding in Common Carp, Cyprinus carpio.” International journal of molecular sciences 21.22 (2020): 8482. https://doi.org/10.3390/ijms21228482

Cano, Irene, et al. “A Seasonal Study of Koi Herpesvirus and Koi Sleepy Disease Outbreaks in the United Kingdom in 2018 Using a Pond-Side Test.” Animals 11.2 (2021): 459. https://doi.org/10.3390/ani11020459

Cheallaigh, Clíona Ní, et al. “A common variant in the adaptor mal regulates interferon gamma signalling.” Immunity 44.2 (2016): 368-379. https://doi.org/10.1016/j.immuni.2016.01.019

Ciucani, Marta Maria, et al. “Genomes of the extinct Sicilian wolf reveal a complex history of isolation and admixture with ancient dogs.” bioRxiv (2022): 2022-01. https://doi.org/10.1101/2022.01.21.47728

Darden JE, Scott EM, Arnold C, Scallan EM, Simon BT, et al. (2019) Evaluation of the bacterial ocular surface microbiome in clinically normal cats before and after treatment with topical erythromycin. PLOS ONE 14(10): e0223859. https://doi.org/10.1371/journal.pone.0223859

Des Roches, S., et al. “Survival by genotype: patterns at Mc1r are not black and white at the W hite S ands ecotone.” Molecular ecology 26.1 (2017): 320-329. https://doi.org/10.1111/mec.13894

Doubleday, Molly, and Capercaillie Advisory Officer. “Developing a new approach to estimating the size of the UK capercaillie population using genetic material.” (2022). https://cairngormscapercaillie.scot/wp-content/uploads/2022/08/Phase-1-sample-collection-report-Developing-a-new-approach-to-estimating-the-size-of-the-UK-capercaillie-population-using-genetic-material.pdf

Dutra, Luísa, et al. “Validating the use of oral swabs for telomere length assessment in dogs.” Journal of Veterinary Behavior 40 (2020): 16-20. https://doi.org/10.1016/j.jveb.2020.07.011

Fernandez‐Senac, Carolina, et al. “A comparison of the use of different swab materials for optimal diagnosis of amoebic gill disease (AGD) in Atlantic salmon (Salmo salar L.).” Journal of Fish Diseases 43.11 (2020): 1463-1472. https://doi.org/10.1111/jfd.13243

Finlay, Margaret, et al. “The detection of Bovine Papillomavirus type 1 DNA in flies.” Virus research 144.1-2 (2009): 315-317. https://doi.org/10.1016/j.virusres.2009.04.015

Gadoin, Elsa, et al. “Fishing for the Virome of Tropical Tuna.” Viruses 13.7 (2021): 1291 https://doi.org/10.3390/v13071291

Gladstone, Nicholas S., et al. “Population genomics reveal low differentiation and complex demographic histories in a highly fragmented and endangered freshwater mussel.” Aquatic Conservation: Marine and Freshwater Ecosystems 32.8 (2022): 1235-1248. https://doi.org/10.1002/aqc.3849

Hardwick R.J., Machado L.R., Zuccherato L.W., Antolinos S., Xue Y., Shawa N., et al. (2011) A worldwide analysis of beta‐defensin copy number variation suggests recent selection of a high‐expressing DEFB103 gene copy in east asia. Hum Mutat 32: 743-750. https://doi.org/10.1002/humu.21491

Klymus, Katy E., et al. “Metabarcoding assays for the detection of freshwater mussels (Unionida) with environmental DNA.” Environmental DNA (2020). https://doi.org/10.1002/edn3.166

Kolomyjec, Stephen H., et al. “Regional population structuring and conservation units in the platypus (Ornithorhynchus anatinus).” Australian Journal of Zoology 61.5 (2014): 378-385. https://doi.org/10.1071/ZO13029

Kropatsch, R., Melis, C., Stronen, A.V., Jensen, H., and Epplen, J.T. (2015) Molecular Genetics of Sex Identification, Breed Ancestry and Polydactyly in the Norwegian Lundehund Breed. J Hered 106 (4): 403-406. https://doi.org/10.1093/jhered/esv031

Laguardia, Alice, et al. “Assessing the feasibility of density estimation methodologies for African forest elephant at large spatial scales.” Global Ecology and Conservation 27 (2021): e01550. https://doi.org/10.1016/j.gecco.2021.e01550

Lane, Timothy W., E. M. Hallerman, and J. W. Jones. “Phylogenetic and taxonomic assessment of the endangered Cumberland bean, Villosa trabalis and purple bean, Villosa perpurpurea (Bivalvia: Unionidae).” Conservation genetics 17.5 (2016): 1109-1124. https://doi.org/10.1007/s10592-016-0847-0

Ma, Gemma C., et al. “New insights on the epidemiology of Coxiella burnetii in pet dogs and cats from New South Wales, Australia.” Acta tropica 205 (2020): 105416. https://doi.org/10.1016/j.actatropica.2020.105416

Macfarlane, C.M., and Badge, R.M. (2015) Genome-wide amplification of proviral sequences reveals new polymorphic HERV-K(HML-2) proviruses in humans and chimpanzees that are absent from genome assemblies. Retrovirology 12: 35-015-0162-8. https://doi.org/10.1186/s12977-015-0162-8

Meason-Smith, C., Diesel, A., Patterson, A.P., Older, C.E., Mansell, J.M., Suchodolski, J.S., and Rodrigues Hoffmann, A. (2015) What is living on your dog’s skin? Characterization of the canine cutaneous mycobiota and fungal dysbiosis in canine allergic dermatitis. FEMS Microbiol Ecol 91 (12): (in press).  https://doi.org/10.1093/femsec/fiv139

Meason-Smith, Courtney, et al. “Malassezia species dysbiosis in natural and allergen-induced atopic dermatitis in dogs.” Medical mycology 58.6 (2020): 756-765. https://doi.org/10.1093/mmy/myz118

Melis C., Borg Å.A., Espelien I.S., and Jensen H. (2013) Low neutral genetic variability in a specialist puffin hunter: The norwegian lundehund. Anim Genet 44: 348-351. https://doi.org/10.1111/age.12000

Melis, Claudia, et al. “Genetic rescue of the highly inbred Norwegian Lundehund.” Genes 13.1 (2022): 163.

https://doi.org/10.3390/genes13010163

Mellanby R.J., Ogden R., Clements D.N., French A.T., Gow A.G., Powell R., et al.(2013) Population structure and genetic heterogeneity in popular dog breeds in the UK. The Veterinary Journal 196: 92-97. https://doi.org/10.1016/j.tvjl.2012.08.009

Monteiro, N. M., et al. “Validating the use of colouration patterns for individual recognition in the worm pipefish using a novel set of microsatellite markers.” Molecular ecology resources 14.1 (2014): 150-156. https://doi.org/10.1111/1755-0998.12151

Myers, Alexandra N., et al. “Characterization of the cutaneous mycobiota in Persian cats with severe dermatophytosis.” Veterinary Dermatology (2021). https://doi.org/10.1111/vde.12969

Older, Caitlin E., et al. “The feline cutaneous and oral microbiota are influenced by breed and environment.” PloS one 14.7 (2019): e0220463.  https://doi.org/10.1371/journal.pone.0220463

Older, Caitlin E., et al. “Characterization of Cutaneous Bacterial Microbiota from Superficial Pyoderma Forms in Atopic Dogs.” Pathogens 9.8 (2020): 638. https://doi.org/10.3390/pathogens9080638

Older, Caitlin E., et al. “Characterization of staphylococcal communities on healthy and allergic feline skin.” Veterinary Dermatology (2020). https://doi.org/10.1111/vde.12885

Older, Caitlin E., et al. “Influence of the FIV Status and Chronic Gingivitis on Feline Oral Microbiota.” Pathogens 9.5 (2020): 383. https://doi.org/10.3390/pathogens9050383

Persson, Mia E., et al. “Genomic regions associated with interspecies communication in dogs contain genes related to human social disorders.” Scientific reports 6 (2016). https://doi.org/10.1038/srep33439

Petchey, Alex, et al. “Characterisation of 9 polymorphic microsatellite markers for the Critically Endangered lemur leaf frog Agalychnis lemur.” Conservation genetics resources 6.4 (2014): 971-973. https://doi.org/10.1007/s12686-014-0261-1

Pierezan, Felipe, et al. “The skin microbiome in allergen‐induced canine atopic dermatitis.” Veterinary Dermatology 27.5 (2016): 332 https://doi.org/10.1111/vde.12366

Robinson, Chloe Victoria, and Hanna Katariina Nuuttila. “Don’t Hold Your Breath: Limited DNA Capture Using Non-Invasive Blow Sampling for Small Cetaceans.” Aquatic Mammals 46.1 (2020): 32-41. https://doi.org/10.1578/AM.46.1.2020.32

Rogers, Callie M., et al. “Evaluation of the bacterial ocular surface microbiome in ophthalmologically normal dogs prior to and following treatment with topical neomycin-polymyxin-bacitracin.” PloS one 15.6 (2020): e0234313. https://doi.org/10.1371/journal.pone.0234313

Ross, Steven, et al. “First evaluation of the population structure, genetic diversity and landscape connectivity of the Endangered Arabian tahr.” Mammalian Biology 100.6 (2020): 659-673. https://doi.org/10.1007/s42991-020-00072-4

Sánchez-Molano, E., Pong-Wong, R., Clements, D.N., Blott, S.C., Wiener, P., and Woolliams, J.A. (2015) Genomic prediction of traits related to canine hip dysplasia 6: 97. https://doi.org/10.3389/fgene.2015.00097

Santoro, Domenico, et al. “Clinical efficacy of spray‐based heat‐treated lactobacilli in canine atopic dermatitis: a preliminary, open‐label, uncontrolled study.” Veterinary dermatology (2020). https://doi.org/10.1111/vde.12915

Seyer, Lindsay D., et al. “Description of non‐brachycephalic canine conjunctival microbiome before and after application of an antiseptic preparation.” Veterinary Ophthalmology (2022). https://doi.org/10.1111/vop.12992

Showering, Alicia, et al. “Skin microbiome alters attractiveness to Anopheles mosquitoes.” BMC microbiology 22.1 (2022): 98. https://doi.org/10.1186/s12866-022-02502-4

Sima, C., et al. “Identification of quantitative trait loci influencing inflammation‐mediated alveolar bone loss: insights into polygenic inheritance of host–biofilm disequilibria in periodontitis.” Journal of periodontal research 51.2 (2016): 237-249. https://doi.org/10.1111/jre.12303

Simpson, Siobhan, et al. “Multiple genetic associations with Irish wolfhound dilated cardiomyopathy.” BioMed Research International 2016 (2016). https://doi.org/10.1155/2016/6374082

Simpson, Siobhan, et al. “Molecular characterisation of canine osteosarcoma in high risk breeds.” Cancers 12.9 (2020): 2405. https://doi.org/10.3390/cancers12092405

Smith, Chase H., et al. “Resolving species boundaries in the critically imperiled freshwater mussel species, Fusconaia mitchelli (Bivalvia: Unionidae).” Journal of Zoological Systematics and Evolutionary Research 59.1 (2021): 60-77. https://doi.org/10.1111/jzs.12412

Thomas, Sarah, et al. “DNA Yield and Turtle Handling Time: Buccal Swabs Versus Blood Samples from Red-Eared Sliders and Eastern Musk Turtles.” Southeastern Naturalist 19.2 (2020): 355-362. https://doi.org/10.1656/058.019.0216

Vladimir, Dimitrijević, et al. “Use of Microsatellites in Genetic Diversity Assessment, Parentage Testing and Individual Identification of the Kangal Shepherd Dog.” Acta Veterinaria 70.2 (2020): 170-181. https://doi.org/10.2478/acve-2020-0012

Walsh, Mary L., et al. “Evaluation of the ocular surface mycobiota in clinically normal horses.” Plos one 16.2 (2021): e0246537. https://doi.org/10.1371/journal.pone.0246537

Weigand, Hannah, Jennifer Cross Lopez de Llergo, and Alain C. Frantz. “Genomic basis for an informed conservation management of Pelophylax water frogs in Luxembourg.” Ecology and Evolution 12.4 (2022): e8810. https://doi.org/10.1002/ece3.8810

Werhahn G,Senn H,Kaden J, Joshi J,Bhattarai S, Kusi N, Sillero-Zubiri C, Macdonald DW. 2017 Phylogenetic evidence for the ancient Himalayan wolf : towards a clarification of its taxonomic status based on genetic sampling from western Nepal. R.Soc. opensci.4:170186. https://doi.org/10.1098/rsos.170186

Werhahn, Geraldine, et al. “Himalayan wolf foraging ecology and the importance of wild prey.” Global Ecology and Conservation 20 (2019): e00780. https://doi.org/10.1016/j.gecco.2019.e00780

Willsie, Julia A., Todd J. Morris, and David T. Zanatta. “Morphometric Analyses Distinguish Wabash Pigtoe (Fusconaia flava) and Round Pigtoe (Pleurobema sintoxia) Mussels.” Diversity 12.9 (2020): 337. https://doi.org/10.3390/d12090337

Yergeau, Donald A., et al. “Forward genetic screens in Xenopus using transposon-mediated insertional mutagenesis.” Xenopus Protocols. Humana Press, Totowa, NJ, 2012. 111-127. https://doi.org/10.1007/978-1-61779-992-1_6

Alsaleh, Abrar B., et al. “The impact of chimerism on DNA-based human identification from skin surface cells of post-allogenic hematopoietic stem cell transplantation (HCST) patients.” Forensic Science International 318 (2021): 110636. https://doi.org/10.1016/j.forsciint.2020.110636

Bakeberg, Megan, et al. “The TOMM40 ‘523’polymorphism in disease risk and age of symptom onset in two independent cohorts of Parkinson’s disease.” (2020). https://doi.org/10.21203/rs.3.rs-119345/v1

Bonsu, Dan OM, et al. “Evaluation of the efficiency of Isohelix™ and Rayon swabs for recovery of DNA from metal surfaces.” Forensic Science, Medicine and Pathology (2020): 1-9.                https://doi.org/10.1007/s12024-020-00329-x

Bonsu, Dan Osei Mensah, Denice Higgins, and Jeremy J. Austin. “Forensic touch DNA recovery from metal surfaces–A review.” Science & Justice 60.3 (2020): 206-215. https://doi.org/10.1016/j.scijus.2020.01.002

Bonsu, Dan OM, et al. “Comparison of Isohelix™ and Rayon swabbing systems for touch DNA recovery from metal surfaces.” Forensic Science, Medicine and Pathology 17.4 (2021): 577-584. https://doi.org/10.1007/s12024-021-00423-8

Carson, Sasha, et al. “The potential for investigator-mediated contamination to occur during routine search activities.” Forensic Science, Medicine and Pathology 18.3 (2022): 299-310. https://doi.org/10.1007/s12024-022-00465-6

Chan, Kamfai, et al. “A rapid and low-cost PCR thermal cycler for infectious disease diagnostics.” PloS one 11.2 (2016): e0149150. https://doi.org/10.1371/journal.pone.0149150

Cirillo J., Hughes J., Ridding M., Thomas P.Q., and Semmler J.G. (2012) Differential modulation of motor cortex excitability in BDNF met allele carriers following experimentally induced and use‐dependent plasticity. Eur J Neurosci 36: 2640-2649. https://doi.org/10.1111/j.1460-9568.2012.08177.x

Cook, Russell, Natasha Mitchell, and Julianne Henry. “Assessment of Diamond™ Nucleic Acid Dye for the identification and targeted sampling of latent DNA in operational casework.” Forensic Science International: Genetics 55 (2021): 102579. https://doi.org/10.1016/j.fsigen.2021.102579

Crauciuc, George Andrei, et al. “Significant Associations between AXIN1 rs1805105, rs12921862, rs370681 Haplotypes and Variant Genotypes of AXIN2 rs2240308 with Risk of Congenital Heart Defects.” International Journal of Environmental Research and Public Health 17.20 (2020): 7671. https://doi.org/10.3390/ijerph17207671

Devesse, L., Syndercombe Court, D., and Cowan, D. (2015) Determining the authenticity of athlete urine in doping control by DNA analysis. Drug Test. Analysis 7: 912-18 https://doi.org/10.1002/dta.1785

Dlouhá, Lucie, et al. “Five genetic polymorphisms of cytochrome P450 enzymes in the Czech non-Roma and Czech Roma population samples.” Drug metabolism and personalized therapy 1.ahead-of-print (2020). https://doi.org/10.1515/dmdi-2020-0103

Griffin, Amy, et al. “DNA on drugs! A preliminary investigation of DNA deposition during the handling of illicit drug capsules.” Forensic Science International: Genetics 54 (2021): 102559. https://doi.org/10.1016/j.fsigen.2021.102559

Griffin, Amy, et al. “DNA on drugs.” Forensic Science International: Genetics Supplement Series 8 (2022): 3-4.

https://doi.org/10.1016/j.fsigss.2022.09.001

Griffin, Amy, et al. “DNA on drugs (part 2): An extended study into the transfer and persistence of DNA onto illicit drug capsules using realistic scenarios.” Forensic Science International: Genetics 60 (2022): 102740. https://doi.org/10.1016/j.fsigen.2022.102740

Griffin, Amy, et al. “Recovery of integrated and surface trace DNA from illicit drug tablets.” Forensic Science International: Genetics 61 (2022): 102772. https://doi.org/10.1016/j.fsigen.2022.102772

Henst, R.H., Jaspers, R.T., Roden, L.C., and Rae, D.E. (2015) A chronotype comparison of South African and Dutch marathon runners: The role of scheduled race start times and effects on performance. Chronobiol Int 32: 858-868. https://doi.org/10.3109/07420528.2015.1048870

Hubáček, Jaroslav A., et al. “Different prevalence of T2DM risk alleles in Roma population in comparison with the majority Czech population.” Molecular Genetics & Genomic Medicine 8.9 (2020): e1361. https://doi.org/10.1002/mgg3.1361

Hubáček, Jaroslav A., et al. “Increased prevalence of the CVD-associated ANRIL allele in the Roma/Gypsy population in comparison with the majority Czech population.” Genetics and Molecular Biology 44 (2021). https://doi.org/10.1590/1678-4685-GMB-2020-0405

Kanokwongnuwut, Piyamas, et al. “How many cells are required for successful DNA profiling?.” Forensic Science International: Genetics 51 (2021): 102453. https://doi.org/10.1016/j.fsigen.2020.102453

Khalil, Dalia, et al. “Recruiting Immigrant and Refugee Arab American Mother–Father–Infant Triads Resettling in the United States: A Feasibility Study.” Canadian Journal of Nursing Research 52.2 (2020): 139-148. https://doi.org/10.1177/0844562120910856

Li, Jiyu, et al. “Selective single-bacteria extraction based on capture and release of microemulsion droplets.” Scientific Reports 12.1 (2022): 1-12. https://doi.org/10.1038/s41598-022-19844-8

Lian, M., Rajan-Babu, I., Singh, K., Lee, C.G., Law, H., and Chong, S.S. (2015) Efficient and Highly Sensitive Screen for Myotonic Dystrophy Type 1 Using a One-Step Triplet-Primed PCR and Melting Curve Assay 17: 128-135. https://doi.org/10.1016/j.jmoldx.2014.10.001

Puliatti, Lucas, Oliva Handt, and Duncan Taylor. “The level of DNA an individual transfers to untouched items in their immediate surroundings.” Forensic Science International: Genetics 54 (2021): 102561. https://doi.org/10.1016/j.fsigen.2021.102561

Quabius, Elgar Susanne, et al. “Tonsillar swabs and sputum predict SLPI‑and AnxA2 expression in tonsils: A prospective study on smoking dependent SLPI‑and AnxA2‑expression, and tonsillar HPV infection.” Oncology Letters 23.5 (2022): 1-13. https://doi.org/10.3892/ol.2022.13284

Quinonez, Shane C., and Zewdu Terefework. “The introduction of clinical genetic testing in Ethiopia: Experiences and lessons learned.” American Journal of Medical Genetics Part A 185.10 (2021): 2995-3004. https://doi.org/10.1002/ajmg.a.62396

Roher A.E., Debbins J.P., Malek-Ahmadi M., Chen K., Pipe J.G., Maze S., et al.(2012) Cerebral blood flow in alzheimer’s disease. Vasc Health Risk Manag 8: 599-611. https://doi.org/10.2147/VHRM.S34874

Rowles J., Karr S., Gurney M.K., Brownlow W., Garza M., and Olsen M. (2012) Description of a facile, rapid, and inexpensive method to profile for the organic cation transporter (oct1) del420 variant. Int J LifeSc Bt & Pharm Res. 1: 36-41. http://www.ijlbpr.com/index.php?m=content&c=index&a=show&catid=116&id=371

Senzaki, Sawa, et al. “Roles of culture and COMT Val58Met gene on neural basis of executive function: A comparison between Japanese and American children.” Developmental Psychobiology. https://doi.org/10.1002/dev.22087

Shawa, Nyambura, and Laura Catherine Roden. “Chronotype of South African adults is affected by solar entrainment.” Chronobiology international 33.3 (2016): 315-323. https://doi.org/10.3109/07420528.2016.1144608

Shi, Q., Wang, X.S., Li, G., Shah, N.D., Orlowski, R.Z., Williams, L.A., et al.(2015) Racial/ethnic disparities in inflammatory gene single‐nucleotide polymorphisms as predictors of a high risk for symptom burden in patients with multiple myeloma 1 year after diagnosis. Cancer 121: 1138-1146. https://doi.org/10.1002/cncr.29154

Stark, Christina Runow, et al. “Brush Samples of Oral Lesions to FTA Elute Card for High-risk Human Papilloma Virus Diagnosis.” Anticancer Research 41.1 (2021): 269-277. https://doi.org/10.21873/anticanres.14773

Van Breda, K., Collins, M., Stein, D.J., and Rauch, L. (2015) The COMT val 158 met polymorphism in ultra-endurance athletes. Physiol Behav 151: 279-283. https://doi.org/10.1016/j.physbeh.2015.07.039

Wagaiyu, E.G., and Bulimo, W.D. (2014) Genetic polymorphisms in IL-1A and IL-1B isoforms and their associations with chronic periodontitis in the Swahili people of Kenya. IOSR-JDMS 13 (11): 7-15 http://erepository.uonbi.ac.ke/handle/11295/77369

Wong, G., Wong, I., Chan, K., Hsieh, Y., and Wong, S. (2015) A Rapid and Low-Cost PCR Thermal Cycler for Low Resource Settings. PLoS One 10: e0131701.   https://doi.org/10.1371/journal.pone.0131701

Zijlmans, Wilco, et al. “Cohort profile: Caribbean Consortium for Research in Environmental and Occupational Health (CCREOH) Cohort Study: influences of complex environmental exposures on maternal and child health in Suriname.” BMJ Open 10.9 (2020). https://doi.org/10.1136/bmjopen-2019-034702

Asok A., Bernard K., Roth T., Rosen J., and Dozier M. (2013) Parental responsiveness moderates the association between early-life stress and reduced telomere length. Dev Psychopathol 25: 577-585. https://doi.org/10.1017/S0954579413000011

Barha, Cindy K., et al. “Number of children and telomere length in women: a prospective, longitudinal evaluation.” PloS one 11.1 (2016): e0146424. https://doi.org/10.1371/journal.pone.0146424

Bordas-Martínez, Jaume, et al. “Idiopathic pulmonary fibrosis cluster analysis highlights diagnostic delay and cardiovascular comorbidity association with outcome.” ERJ open research 7.2 (2021). https://doi.org/10.1183/23120541.00897-2020

Drury S.S., Mabile E., Brett Z.H., Esteves K., Jones E., Shirtcliff E.A., and Theall, K.P. (2014). The association of telomere length with family violence and disruption. Pediatrics, 134(1): peds-2013-3415. https://doi.org/10.1542/peds.2013-3415

Drury S. S., Shirtcliff E.A., Shachet A., Phan J., Mabile, E., Brett, Z.H., and Theall, K. P. (2014). Growing up or growing old? Cellular aging linked with testosterone reactivity to stress in youth. The American journal of the medical sciences 348(2): 92-100. https://doi.org/10.1097/MAJ.0000000000000299

Esteves, Kyle C., et al. “Adverse childhood experiences: implications for offspring telomere length and psychopathology.” American Journal of Psychiatry 177.1 (2020): 47-57. https://doi.org/10.1176/appi.ajp.2019.18030335

Hautekiet, Pauline, et al. “Child buccal telomere length and mitochondrial DNA content as biomolecular markers of ageing in association with air pollution.” Environment International 147 (2021): 106332. https://doi.org/10.1016/j.envint.2020.106332

Howell, Meghan P., et al. “Impact of prenatal tobacco smoking on infant telomere length trajectory and ADHD symptoms at 18 months: a longitudinal cohort study.” BMC medicine 20.1 (2022): 153. https://doi.org/10.1186/s12916-022-02340-1

Humphreys, Kathryn L., et al. “Accelerated telomere shortening: Tracking the lasting impact of early institutional care at the cellular level.” Psychiatry Research 246 (2016): 95-100. https://doi.org/10.1016/j.psychres.2016.09.023

Küffer, Andreas Lorenz, et al. “Posttraumatic stress disorder, adverse childhood events, and buccal cell telomere length in elderly swiss former indentured child laborers.” Frontiers in Psychiatry 7 (2016). https://doi.org/10.3389/fpsyt.2016.00147

Merino, Ana, et al. “Membrane particles from mesenchymal stromal cells reduce the expression of fibrotic markers on pulmonary cells.” PloS one 16.3 (2021): e0248415. https://doi.org/10.1371/journal.pone.0248415

Nickels, Matt, et al. “Elite swimmers possess shorter telomeres than recreationally active controls.” Gene 769 (2021): 145242. https://doi.org/10.1016/j.gene.2020.145242

Planas-Cerezales, Lurdes, et al. “Lung Transplant Improves Survival and Quality of Life Regardless of Telomere Dysfunction.” Frontiers in medicine 8 (2021). https://doi.org/10.3389/fmed.2021.695919

Wade, Mark, et al. “Telomere length and psychopathology: specificity and direction of effects within the Bucharest Early Intervention Project.” Journal of the American Academy of Child & Adolescent Psychiatry 59.1 (2020): 140-148. https://doi.org/10.1016/j.jaac.2019.02.013

Wong L.S., Huzen J., de Boer R.A., van Gilst W.H., van Veldhuisen D.J., and van der Harst P. (2011) Telomere length of circulating leukocyte subpopulations and buccal cells in patients with ischemic heart failure and their offspring. PloS One 6: e23118.  https://doi.org/10.1371/journal.pone.0023118

Hautekiet, Pauline, et al. “Higher buccal mtDNA content is associated with residential surrounding green in a panel study of primary school children.” Environmental Research 213 (2022): 113551.

https://doi.org/10.1016/j.envres.2022.113551