1. Saliva

COVID-19

Beetz, Christian, et al. “Rapid large-scale COVID-19 testing during shortages.” Diagnostics 10.7 (2020): 464. https://doi.org/10.3390/diagnostics10070464

GWAS/Cohort Studies

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

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

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

SNP’s/Genotyping

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

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

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

Sequencing

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

Microbiome

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

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

PCR/qPCR/STR/RFLP

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

2. Swabs

COVID-19

Parker, Ceth W., et al. “End-to-End Protocol for the Detection of SARS-CoV-2 from Built Environments.” Msystems 5.5 (2020). https://doi.org/10.1128/mSystems.00771-20.

GWAS/Cohort Studies

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

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

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

SNP’s/Genotyping

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

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

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

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

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

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

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

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

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

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

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

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

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 for 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

Sequencing

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

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

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

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

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

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

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

RNA/Gene Expression

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

Microbiome

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

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

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

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

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

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

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, 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

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

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

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

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

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

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

Epigenetics/Methylation

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

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

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

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

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

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

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

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

Animal Applications

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

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

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

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

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

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

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

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

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

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

PCR/qPCR/STR/RFLP

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

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

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

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

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

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

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

Telomere Length Studies

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

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