Scientific Publications
2015 [ view all publications ⌂ ]
Abdolmaleky HM et al. Antipsychotic drugs attenuate aberrant DNA methylation of DTNBP1 (dysbindin) promoter in saliva and post-mortem brain of patients with schizophrenia and Psychotic bipolar disorder. Am J Med Genet B Neuropsychiatr Genet. 168(8):687-696 (2015).
Adams SV et al. Genetic variation in metallothionein and metal-regulatory transcription factor 1 in relation to urinary cadmium, copper, and zinc. Toxicol Appl Pharmacol. 289(3):381-388 (2015).
Adkins DE et al. Genome-wide meta-analysis of longitudinal alcohol consumption across youth and early adulthood. Twin Res Hum Genet. 18(4):335-347 (2015).
Adrian M et al. Examining gene-environment interactions in comorbid depressive and disruptive behavior disorders using a Bayesian approach. J Psychiatr Res. 68:125-133 (2015).
Alemany S et al. New Suggestive Genetic Loci and Biological Pathways for Attention Function in Adult Attention-Deficit/Hyperactivity Disorder. Am J Med Genet B Neuropsychiatr Genet. Epub ahead of print (2015).
AlFawaz S et al. A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesis. Arch Oral Biol. 60(7):982-988 (2015).
Alhmoudi OA et al. Population genetics data for 21 autosomal STR loci for United Arab Emirates (UAE) population using next generation multiplex STR kit. Foresic Sci Int Genet. 19:190-191 (2015).
Almoguera B et al. Application of Whole Exome Sequencing in Six Families with an Initial Diagnosis of Autosomal Dominant Retinitis Pigmentosa: Lessons Learned. PLOS One. 10(7):e0133624 (2015).
Alsafar H et al. Association of Angiotensin Converting Enzyme Insertion-Deletion Polymorphism with Hypertension in Emiratis with Type 2 Diabetes Mellitus and Its Interaction with Obesity Status. Dis Markers. 2015:536041 (2015).
Anderson D et al. First genome-wide association study in an australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes. PLoS One. 10(3):e0119333 (2015).
Andersson E et al. Filtration device for on-site collection, storage and shipment of cells from urine and its application to DNA-based detection of bladder cancer. PLoS One. 10(7):e0131889 (2015).
Andraweera PH et al. Insulin family polymorphisms in pregnancies complicated by small for gestational age infants. Mol Hum Reprod. 21(9):745-752 (2015).
Anjomshoaa I et al. Aquaporin 5 Interacts with Fluoride and Possibly Protects against Caries. PLoS One. 10(12):e0143068 (2015).
Applebaum E et al. Genetic variants in cyclooxygenase-2 contribute to post-treatment pain among endodontic patients. J Endod. 41(8):1214-1218 (2015).
Arab AH and Elhawary NA. Association between ANKK11 (rs1800497) and LTA (rs909253) genetic variants and risk of schizophrenia. Biomed Res Int. 2015:821827 (2015).
Arantes LM et al. Validation of methylation markers for diagnosis of oral cavity cancer. Eur J Cancer. 51(5):632-641 (2015).
Archer NS et al. A Comparison of Collection Techniques for Gene Expression Analysis of Human Oral Taste Tissue. PLoS One. 11(3):e0152157 (2016).
Armingohar Z et al. Polymorphisms in the interleukin-10 gene and chronic periodontitis in patients with atherosclerotic and aortic aneurysmal vascular diseases. J Oral Microbiol. 7: 26051 (2015).
Arnott ER et al. Strong selection for behavioural resilience in Australian stock working dogs identified by selective sweep analysis. Canine Genet Epidemiol. 2:6 (2015).
Arrieta-Bolaños E, Madrigal JA and Shaw BE. Novel alleles of the transforming growth factor β-1 regulatory region and exon 1. Tissue Antigens. 85(6):484-491 (2015).
Askenazi DJ et al. Genetic polymorphisms of heme-oxygenase 1 (HO-1) may impact on acute kidney injury, bronchopulmonary dysplasia, and mortality in premature infants. Pediatr Res. 77(6):793-798 (2015).
Atencia-Fernandez S et al. Muscular dystrophy in the Japanese Spitz: an inversion disrupts the DMD and RPGR genes. Anim Genet. 46(2):175-184 (2015).
Baetu I et al. Commonly-occurring polymorphisms in the COMT, DRD1 and DRD2 genes influence different aspects of motor sequence learning in humans. Neurobiol Learn Mem. 125:176-188 (2015).
Bahmanimehr A, Eskandari G and Nikmanesh F. The congruence between matrilineal genetic (mtDNA) and geographic diversity of Iranians and the territorial populations. Iran J Basic Med Sci. 18(1):30-37 (2015).
Bailey HR et al. APOE ε4 genotype predicts memory for everyday activities. Neuropsychol Dev Cogn B Aging Neuropsychol Cogn. 10:46753 (2015).
Basso TR et al. Genomic profile of a Li-Fraumeni-like syndrome patient with a 45,X/46,XX karyotype, presenting neither mutations in TP53 nor clinical stigmata of Turner syndrome. Cancer Genet. 208(6):341-344 (2015).
Bassuk AG et al. Structural modeling of a novel CAPN5 mutation that causes uveitis and neovascular retinal detachment. PLoS One. 10(4):e0122352 (2015).
Bayram M et al. Genetic influences on dental enamel that impact caries differ between the primary and permanent dentitions. Eur J Oral Sci. Epub ahead of print (2015).
Berlin NL et al. Family history of skin cancer is associated with early-onset basal cell carcinoma independent of MC1R genotype. Cancer Epidemiol. 39(6):1078-1083 (2015).
Bienkowski P et al. Functional polymorphism of matrix metalloproteinase-9 (MMP9) gene 4 is not associated with schizophrenia and with its deficit subtype. Pharmacol Rep. 67(3):442-445 (2015).
Bijttebier S et al. The Vulnerability to Suicidal Behavior is Associated with Reduced Connectivity Strength. Front Hum Neurosci. 9: 632 (2015).
Bing D et al. Cochlear NMDA receptors as a therapeutic target of noise-induced tinnitus. Cell Physiol Biochem. 35(5):1905-1923 (2015).
Blair C et al. Catechol-O-methyltransferase Val158met Polymorphism Interacts With Early Experience to Predict Executive Functions in Early Childhood. Dev Psychobiol. 57(7):833-841 (2015).
Henje Blom E et al. Peripheral telomere length and hippocampal volume in adolescents with major depressive disorder. Transl Psychiatry. 5:e676 (2015).
Blum S, Csurhes P and McCombe P. The frequencies of Killer immunoglobulin-like receptors and their HLA ligands in chronic inflammatory demyelinating polyradiculoneuropathy are similar to those in Guillian Barre syndrome but differ from those of controls, suggesting a role for NK cells in pathogenesis. J Neuroimmunol. 285:53-56 (2015).
Boardman JD, Domingue BW and Daw J. What can genes tell us about the relationship between education and health? Soc Sci Med. 127:171-180 (2015).
Boles RG et al. Hurt, tired and queasy: Specific variants in the ATPase domain of the TRAP1 mitochondrial chaperone are associated with common, chronic “functional” symptomatology including pain, fatigue and gastrointestinal dysmotility. Mitochondrion. 23:64-70 (2015).
Boone PM et al. Hutterite-type cataract maps to chromosome 6p21.32-p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death. Mol Genet Genomic Med. 14(1):77-94 (2015).
Borel P et al. A Combination of Single-Nucleotide Polymorphisms Is Associated with Interindividual Variability in Dietary Beta-Carotene in Healthy Men. J Nutr. 145(8):1740-1747 (2015).
Borel P et al. Can genetic variability in a-tocopherol bioavailability explain the heterogeneous response to α-tocopherol supplements? Antioxid Redox Signal. 22(8):669-678 (2015).
Borel P et al. Lycopene bioavailability is associated with a combination of geneticvariants. Free Radic Biol Med. 83:238-244 (2015).
Borghini A et al. Chronic and acute effects of endurance training on telomere length. Mutagenesis. 30(5):711-716 (2015).
Bosten JM et al. A population study of binocular function. Vision Res. 110:34-50 (2015).
Bowers H et al. COMT polymorphism modulates the resting-state EEG alpha oscillatory response to acute nicotine in male non-smokers. Genes Brain Behav. 14(6):466-476 (2015).
Brehm JM et al. Stress and bronchodilator response in children with asthma. Am J Respir Crit Care Med. 192(1):47-56 (2015).
Brissenden JE et al. Mongolians in the Genetic Landscape of Central Asia: Exploring the Genetic Relations among Mongolians and Other World Populations. Hum Biol. 87(2):73-91 (2015).
Brody GH, Yu T and Beach SRH. A differential susceptibility analysis reveals the “who and how” about adolescents’ responses to preventive interventions: Tests of first- and second-generation Gene x Intervention hypotheses. Dev Psychopathol. 27(1):37-49 (2015).
Brown LM et al. Evaluation of glycogen storage disease as a cause of ketotic hypoglycemia in children. J Inherit Metab Dis. 38(3):489-493 (2015).
Bruno C et al. Germline correction of an epimutation related to Silver–Russell syndrome. Hum Mol Genet. 24(12):3314-3321 (2015).
Bujarski S et al. Genetic and Environmental Predictors of Alcohol Use in Asian American Young Adults. 76(5):690-699 (2015).
Cadamuro VC et al. Determined about sex: sex-testing in 45 primate species using a 2Y/1X sex-typing assay. Forensic Sci Int Genet. 14:69-107 (2015).
Cai N et al. Molecular Signatures of Major Depression. Curr Biol. 25:1146-1156 (2015).
Cannon DS et al. CYP2A6 Effects on Subjective Reactions to Initial Smoking Attempt. Nicotine Tob Res. 18(5): 637-641 (2015).
Carlson MD et al. Interactions Between DRD4 and Developmentally Specific Environments in Alcohol-Dependence Symptoms. J Abnorm Psychol. 124(4):1043-1049 (2015).
Caruana G et al. Copy-number variation associated with congenital anomalies of the kidney and urinary tract. Pediatr Nephrol. 30(3):487-495 (2015).
Caseras X et al. Association between genetic risk scoring for schizophrenia and bipolar disorder with regional subcortical volumes. Transl Psychiatry. 5:e692 (2015).
Castaño-Vinyals G et al. Population-based multicase-control study in common tumors in Spain (MCC-Spain): rationale and study design. Gac Sanit. 29(4):308-315 (2015).
Castillejo A et al. Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer. J Med Genet. 52(7):498-502 (2015).
Chagnon YC et al. DNA methylation and single nucleotide variants in the brain-derived neurotrophic factor (BDNF) and oxytocin receptor (OXTR) genes are associated with anxiety/depression in older women. Front Genet. 6:230 (2015).
Chau CMY et al. The Val66Met Brain-Derived Neurotrophic Factor Gene Variant Interacts with Early Pain Exposure to Predict Cortisol Dysregulation in 7-year-old Children Born Very Preterm: Implications for Cognition. Neuroscience. Epub ahead of print (2015).
Chen FS et al. Genetic modulation of oxytocin sensitivity: a pharmacogenetic approach. Transl Psychiatry. 5:e664 (2015).
Chen H et al. Association study of stuttering candidate genes GNPTAB, GNPTG and NAGPA with dyslexia in Chinese population. BMC Genet. 16:7 (2015).
Chen J et al. BDNF Val66Met, stress, and positive mothering: Differential susceptibility model of adolescent trait anxiety. J Anxiety Disord. 34:68-75 (2015).
Chen X et al. Smoking and perceived stress in relation to short salivary telomere length among caregivers of children with disabilities. Stress. 18(1):20-28 (2015).
Chen YF and Brody GH. Family Economic Hardship, Corticotropin-Releasing Hormone Receptor Polymorphisms, and Depressive Symptoms in Rural African-American Youths. J Adolesc Health. 57(2):235-240 (2015).
Cheon BK et al. Contribution of serotonin transporter polymorphism (5-HTTLPR) to automatic racial bias. Pers Individ Dif. 79:35-38 (2015).
Chester DS et al. Looking for reward in all the wrong places: dopamine receptor gene polymorphisms indirectly affect aggression through sensation-seeking. Soc Neurosci. Epub ahead of print (2015).
Chester DS et al. Monoamine oxidase A (MAOA) genotype predicts greater aggression through impulsive reactivity to negative affect. Behav Brain Res. 283:97-101 (2015).
Chettier R et al. Haplotypes at LBX1 have distinct inheritance patterns with opposite effects in adolescent idiopathic scoliosis. PLoS One. 10(2):e0117708 (2015).
Cheung J and Bryant RA. FKBP5 risk alleles and the development of intrusive memories. Neurobiol Learn Mem. 125:258-264 (2015).
Ching-López A et al. Epidemiological support for genetic variability at hypothalamic–pituitary–adrenal axis and serotonergic system as risk factors for major depression. Neuropsychiatr Dis Treat. 11:2743-2754 (2015).
Choo JM, Leong LEX and Rogers GB. Sample storage conditions significantly influence faecal microbiome profiles. Sci Rep. 5:16350 (2015).
Christiaens I et al. Two novel genetic variants in the mineralocorticoid receptor gene associated with spontaneous preterm birth. BMC Med Genet. 16:59 (2015).
Christou AI et al. BDNF Val(66)Met and 5-HTTLPR Genotype are Each Associated with Visual Scanning Patterns of Faces in Young Children. Front Behav Neurosci. 9:175 (2015).
Cicchetti D, Handley ED and Rogosch FA. Child maltreatment, inflammation, and internalizing symptoms: Investigating the roles of C-reactive protein, gene variation, and neuroendocrine regulation. Dev Psychopathol. 27(2):553-566 (2015).
Clavel-Chapelon F and E3N Study Group. Cohort profile: The french E3N cohort study. Int J Epidemiol. 44(3):801-809 (2015).
Coller JK et al. Predictive model for risk of severe gastrointestinal toxicity following chemotherapy using patient immune genetics and type of cancer: a pilot study. Support Care Cancer. 23(5):1233-1236 (2015).
Comasco E et al. Psychiatric symptoms in adolescents: FKBP5 genotype—early life adversity interaction effects. Eur Child Adolesc Psychiatry. 24(12):1473-1483 (2015).
Conti V et al. Focal dysplasia of the cerebral cortex and infantile spasms associated with somatic 1q21.1-q44 duplication including the AKT3 gene. Clin Genet. 88(3):241-247 (2015).
Corpas M et al. Crowdsourced direct-to-consumer genomic analysis of a family quartet. BMC Genomics. 16:910 (2015).
Cotterchio M et al. Association between variants in atopy- related immunologic candidate genes and pancreatic cancer risk. PLoS One. 10(5):e0125273 (2015).
Courtney KE, Chahremani DG and Ray LA. The Effect Of Alcohol Priming On Neural Markers Of Alcohol Cue-Reactivity. Am J Drug Alcohol Abuse. 41(4):300-308 (2015).
Crawford RR et al. Multiple lithium-dependent Brugada syndrome unmasking events in a bipolar patient. Clin Case Rep. 3(1):14-18 (2015).
Cremers RG et al. Known susceptibility SNPs for sporadic prostate cancer show a similar association with ‘‘hereditary’’ prostate cancer. Prostate. 75(5):474-483 (2015).
Currier RL et al. Innate Susceptibility to Norovirus Infections Influenced by FUT2 Genotype in a United States Pediatric Population. Clin Infect Dis. 60(11):1631-1638 (2015).
da Fontoura CS et al. Candidate Gene Analyses of Skeletal Variation in Malocclusion. J Dental Res. 94(7):913-920 (2015).
Dadds MR et al. Individual Differences in Childhood Behavior Disorders Associated With Epigenetic Modulation of the Cortisol Receptor Gene. Child Dev. 86(5):1311-1320 (2015).
Davies AK et al. Effectiveness of a self-management intervention with personalised genetic and lifestyle-related risk information on coronary heart disease and diabetes-related risk in type 2 diabetes (CoRDia): study protocol for a randomised controlled trial. Trials. 16:547 (2015).
Dávila-Fajardo CL et al. FcGR genetic polymorphisms and the response to adalimumab in patients with rheumatoid arthritis. Pharmacogenomics. 16(4):373-381 (2015).
Davis CR et al. A randomised controlled intervention trial evaluating the efficacy of an Australianised Mediterranean diet compared to the habitual Australian diet on cognitive function, psychological wellbeing and cardiovascular health in healthy older adults (MedLey study): protocol paper. BMC Nutri. 1:35 (2015).
Costa LS et al. Cytogenomic delineation and clinical follow-up of 10 Brazilian patients with Pallister-Killian syndrome. Mol Cytogenet. 8:42 (2015).
Dean M et al. Addressing health disparities in Hispanic breast cancer: accurate and inexpensive sequencing of BRCA1 and BRCA2. GigaScience. 4:50 (2015).
Dees EW et al. The influence of L-opsin gene polymorphisms and neural ageing on spatio-chromatic contrast sensitivity in 20–71 year olds. Vision Res. 116(Pt A):13-24 (2015).
DeLorenze GN et al. Polymorphisms in HLA Class II Genes Are Associated With Susceptibility to Staphylococcus aureus Infection in a White Population. J Infect Dis. 213(5):816-823 (2016).
Dincheva I et al. FAAH genetic variation enhances fronto-amygdala function in mouse and human. Nat Commun. 6:6935 (2015).
Domingue BW et al. Polygenic Influence on Educational Attainment: New Evidence From the National Longitudinal Study of Adolescent to Adult Health. AERA Open. 1(3):41275 (2015).
Drake CL et al. Length polymorphism in the Period 3 gene is associated with sleepiness and maladaptive circadian phase in night-shift workers. J Sleep Res. 24(3):254-261 (2015).
Dudakova L et al. Validation of rs2956540:G>C and rs3735520:G>A association with keratoconus in a population of European descent. Eur J Hum Genet. 23(11):1581-1583 (2015).
Dworshak GC et al. Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalities. Birth Defects Res A Clin Mol Teratol. 103(4):235-242 (2015).
Eaton K et al. Association study confirms the role of two OCA2 polymorphisms in normal skin pigmentation variation in east asian populations. Am J Hum Biol. 27(4):520-525 (2015).
Ebstein RP et al. Association between the dopamine D4 receptor gene exon III variable number of tandem repeats and political attitudes in female Han Chinese. Proc Biol Soc. 282(1813):20151360 (2015).
Edea Z et al. Genome-wide genetic diversity, population structure and admixture analysis in African and Asian cattle breeds. Animal. 9(2):218-226 (2015).
Edea Z et al. Genome-wide linkage disequilibrium analysis of indigenous cattle breeds of Ethiopia and Korea using different SNP genotyping BeadChips. Genes Genom. 37:759-765 (2015).
Edelman D et al. Genetic analysis of nonalcoholic fatty liver disease within a Caribbean–Hispanic population. Mol Gen Genom Med. 3(6):558-569 (2015).
Edwards M et al. Iris pigmentation as a quantitative trait: variation in populations of European, East Asian and South Asian ancestry and association with candidate gene polymorphisms. Pigment Cell Melanoma Res. 29(2):141-162 (2015).
Ellervik C and Vaught J. Preanalytical variables affecting the integrity of human biospecimens in biobanking. Clin Chem. 61(7):914-934 (2015).
Ellis KL et al. Genetic variation at glucose and insulin trait loci and response to glucose-insulin-potassium (GIK) therapy: the IMMEDIATE trial. Pharmacogenomics J. 15(1):55-62 (2015).
Erasmus JC, Klingenberg A and Greeff JM. Allele frequencies of AVPR1A and MAOA in the Afrikaner population. South African J Sci. 111:42589 (2015).
Etzold A. Further evidence for pathogenicity of the TP53 tetramerization domain mutation p.Arg342Pro in Li-Fraumeni syndrome. Fam Cancer. 14(1):161-165 (2015).
Evans CJ et al. Identification of six novel mutations in ZEB1 and description of the associated phenotypes in patients with posterior polymorphous corneal dystrophy 3. Ann Hum Genet. 79(1):1-9 (2015).
Evans PD et al. A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13. Genes Brain Behav. 14(5):387-397 (2015).
Adel Fahmideh M et al. CCDC26, CDKN2BAS, RTEL1 and TERT Polymorphisms in pediatric brain tumor susceptibility. Carcinogensis. 36(8):876-882 (2015).
Feng C et al. A common oxytocin receptor gene (OXTR) polymorphism modulates intranasal oxytocin effects on the neural response to social cooperation in humans. Genes Brain Behav. 14(7):516-525 (2015).
Fernández-Jaén A et al. Cortical thickness differences in the prefrontal cortex in children and adolescents with ADHD in relation to dopamine transporter (DAT1) genotype. Psychiatry Res. 233(3):409-417 (2015).
Fernandes-Lima ZS et al. Ocular and craniofacial phenotypes in a large Brazilian family with congenital aniridia. Clin Genet. 87(1):68-73 (2015).
Fernandez-Navarro P et al. Genome wide association study identifies a novel putative mammographic density locus at 1q12-q21. Int J Cancer. 136(10):2427-2436 (2015).
Fonseca CLW et al. Project REENCONTRO: ethical aspects of genetic identification in families separated by the compulsory isolation of leprosy patients in Brazil. J Community Genet. 6(3):215-222 (2015).
Fontoura C et al. Association of WNT9B gene polymorphisms with nonsyndromic cleft lip with or without cleft palate in brazilian nuclear families. Cleft Palate Craniofac J. 52(1):44-48 (2015).
Franz EA et al. Congenital mirror movements: Phenotypes associated with DCC and RAD51 mutations. J Nerurol Sci. 351(1-2):140-145 (2015).
Frokjaer VG et al. Role of serotonin transporter changes in depressive responses to sex-steroid hormone manipulation: a positron emission tomography study. Biol Psychiatry. 78(8):534-543 (2015).
Gaedigk A et al. SNP genotyping using TaqMan technology: the CYP2D6*17 assay conundrum. Sci Rep. 5:9257 (2015).
Gardner KR, Sapienza C and FIsher JO. Genetic and epigenetic associations to obesity-related appetite phenotypes among African–American children. Pediatr Obes. 10(6):476-482 (2015).
Gatto NM et al. Vitamin D receptor gene polymorphisms and Parkinson's disease in a population with high ultraviolet radiation exposure. J Nerurol Sci. 352(1-2):88-93 (2015).
Gee JA et al. Identification of novel PIKFYVE gene mutations associated with Fleck corneal dystrophy. Mol Vis. 21:1093-1100 (2015).
Geraskina NV et al. The dtd gene from Bacillus amyloliquefaciens encodes a putative D-tyrosyl-tRNATyr deacylase and is a selectable marker for Bacillus subtilis. Microbiol Res. 171:90-96 (2015).
Gerritsen KEH et al. Full-length HLA-DRB1 coding sequences generated by a hemizygous RNA-SBT approach. Tissue Antigens. 86(5):333-342 (2015).
Gilman TL et al. Variation of 5-HTTLPR and Deficits in Emotion Regulation: A Pathway to Risk? Psych Neurosci. 8(3):397-413 (2015).
Godderis L et al. Global methylation and hydroxymethylation in DNA from blood and saliva in healthy volunteers. Biomed Res Int. 2015:845041 (2015).
Goenjian AK et al. Association of COMT and TPH-2 genes with DSM-5 based PTSD symptoms. J Affect Dis. 172:472-478 (2015).
Gong Z et al. Genetic variants in one-carbon metabolism genes and breast cancer risk in European American and African American women. Int J Cancer. 137(3):666-677 (2015).
Goni L et al. A genetic risk tool for obesity predisposition assessment and personalized nutrition implementation based on macronutrient intake. Genes Nutr. 10(1):445 (2015).
González-Santos M et al. Genome-Wide SNP Analysis of Southern African Populations Provides New Insights into the Dispersal of Bantu-Speaking Groups. Genome Biol Evol. 7(9):2560-2568 (2015).
Gordon EM et al. Resting-state striato-frontal functional connectivity is sensitive to DAT1 genotype and predicts executive function. Cereb Cortex. 25(2):336-345 (2015).
Goswami Y et al. Salivary Biomarkers - A Review of Powerful Diagnostic tool. J Dental Med Sci. 14(3):80-87 (2015).
Gotlib IH et al. Telomere length and cortisol reactivity in children of depressed mothers. Mol Psychiatry. 20(5):615-620 (2015).
Gottfredson NC et al. Genetic heterogeneity in adolescents' depressive symptoms in response to victimization. J Clin Child Adolesc Psychol. 44(5):762-774 (2015).
Greenop KR et al. Folate pathway gene polymorphisms and risk of childhood brain tumors: results from an Australian case-control study. Cancer Epidemiol Biomarkers Prev. 24(6):931-937 (2015).
Groth SW and Morrison-Beedy D. GNB3 and FTO polymorphisms and pregnancy weight gain in black women. Biol Res Nurs. 17(4):405-412 (2015).
Gruber R et al. Sebaceous gland, hair shaft, and epidermal barrier abnormalities in keratosis pilaris with and without filaggrin deficiency. Am J Pathol. 185(4):1012-1021 (2015).
Guay-Bélanger S et al. Detection of SQSTM1/P392L post-zygotic mutations in Paget's disease of bone. Hum Genet. 134(1):53-56 (2015).
Gumenyk V et al. Differential sleep, sleepiness, and neurophysiology in the insomnia phenotypes of shift work disorder. Sleep. 38(1):119-126 (2015).
Gunderson EP et al. The study of women, infant feeding and type 2 diabetes after GDM pregnancy and growth of their offspring (SWIFT Offspring study): prospective design, methodology and baseline characteristics. BMC Pregnancy Childbirth. 15:150 (2015).
Gunst A et al. A study of possible associations between single nucleotide polymorphisms in the estrogen receptor 2 gene and female sexual desire. J Sex Med. 12(3):676-684 (2015).
Guo G et al. Peer influence, genetic propensity, and binge drinking: A natural experiment and a replication. AJS. 121(3):914-954 (2015).
Gupta A et al. Interactions of early adversity with stress-related gene polymorphisms impact regional brain structure in females. Brain Struct Funct. 221(3):1667-1679 (2016).
Gurung N et al. Mutations in PTF1A are not a common cause for human VATER/VACTERL association or neural tube defects mirroring Danforth's short tail mouse. Mol Med Rep. 12(1):1579-1583 (2015).
Haas DM et al. Steroid Pathway Genes and Neonatal Respiratory Distress After Betamethasone Use in Anticipated Preterm Birth. Reprod Sci. 23(5):680-686 (2015).
Haase CM et al. Short alleles, bigger smiles? The effect of 5-HTTLPR on positive emotional expressions. Emotion. 15(4):438-448 (2015).
Haberstick BC et al. Population frequencies of the triallelic 5-HTTLPR in six ethnicially diverse samples from north america, southeast asia, and africa. Behav Genet. 45(2):255-261 (2015).
Hadchouel A et al. Salivary Telomere Length and Lung Function in Adolescents Born Very Preterm: A Prospective Multicenter Study. PLoS One. 10(9):e0136123 (2015).
Hadifar S et al. Molecular typing of Iranian mycobacteria isolates by polymerase chain reaction‑restriction fragment length polymorphism analysis of 360‑bp rpoB gene. Adv Biomed Res. 4:152 (2015).
Hafrén L et al. Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus. PLoS One. 10(7):e0132551 (2015).
Hagleitner MM et al. A first step towards personalized medicine in osteosarcoma: Pharmacogenetics as predictive marker of outcome after chemotherapy based treatment. Clin Cancer Res. 21(15):3436-3441 (2015).
Hallak JA et al. Single Nucleotide Polymorphisms in the BDNF, VDR, and DNASE 1 Genes in Dry Eye Disease Patients: A Case-Control Study. Invest Ophthalmol Vis Sci. 56(10):5990-5996 (2015).
Hallast P et al. The Y-chromosome tree bursts into leaf: 13,000 high-confidence snps covering the majority of known clades. Mol Biol Evol. 32(3):661-673 (2015).
Han J et al. X-linked megalocornea associated with the novel CHRDL1 gene mutation p.(Pro56Leu*8). Ophthalmic Genet. 36(2):145-148 (2015).
Han MR et al. Evaluating 17 breast cancer susceptibility loci in the Nashville breast health study. Breast Cancer. 22(5):544-551 (2015).
Hankin BL et al. 5-HTTLPR×interpersonal stress interaction and nonsuicidal self-injury in general community sample of youth. Psychiatry Res. 225(3):609-612 (2015).
Hankin BL et al. Cortisol reactivity to stress among youth: stability over time and genetic variants for stress sensitivity. J Abnorm Psychol. 124(1):54-67 (2015).
Harden KP et al. Childhood sexual abuse and impulsive personality traits: Mixed evidence for moderation by DRD4 genotype. J Res Pers. 55:30-40 (2015).
Harkness KL et al. Childhood emotional and sexual maltreatment moderate the relation of the serotonin transporter gene to stress generation. J Abnorm Psychol. 124(2):275-287 (2015).
Hassan AA et al. Comparison of ORAGENE® and Mouthwashed-Based Saliva Collection Methods for Genomic DNA Isolation. J Student Sci Tech. 8(2):15-20 (2015).
Hayes JE et al. Quinine Bitterness and Grapefruit Liking Associate with Allelic Variants in TAS2R31. Chem Senses. 40(6):437-443 (2015).
Henningsson S et al. Association between polymorphisms in NOS3 and KCNH2 and social memory. Front Neurosci. 9:393 (2015).
Hiippala A et al. Expanding the phenotype of timothy syndrome type 2: an adolescent with ventricular fibrillation but normal development. Am J Med Genet A. 167A(3):629-634 (2015).
Hino-Fukuyo N et al. Genomic analysis identifies candidate pathogenic variants in of 18 patients with unexplained West syndrome. Hum Genet. 134(6):649-658 (2015).
Holmes AJ et al. Brain Genomics Superstruct Project initial data release with structural, functional, and behavioral measures. Sci Data. 2:150031 (2015).
Hosseini SS et al. Association between respiratory viruses and exacerbation of COPD: a case-control study. Infect Dis (Lond). 47(8):523-529 (2015).
Huang HJ et al. Imaging Pulmonary Inducible Nitric Oxide Synthase Expression with PET. J Nucl Med. 56(1):76-81 (2015).
Hubbard AR, Guatelli-Steinberg D and Irish JD. Do nuclear DNA and dental nonmetric data produce similar reconstructions of regional population history? An example from modern coastal Kenya. Am J Phys Anthropol. 157(2):295-304 (2015).
Huckert M et al. Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta. Hum Mol Genet. 24(11):3038-3049 (2015).
Hygen BW et al. Child exposure to serious life events, COMT, and aggression: Testing differential susceptibility theory. Dev Psychol. 51(8):1098-1104 (2015).
Ito T et al. Effect of CYP2A6*4 Genetic Polymorphisms On Smoking Behaviours and Nicotine Dependence in a General Population of Japanese Men. Fukushima J Med Sci. 61(2):125-130 (2015).
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