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  • Support → Scientific Publications → 2014

    Scientific Publications

    2014

    Abdolmaleky HM et al. DNA hypermethylation of serotonin transporter gene promoter in drug naïve patients with schizophrenia. Schizophr Res. 152(2-3):373-380 (2014).

    Abugattas J et al. Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from Peru. Clin Genet. 88(4):371-375 (2014).

    Adam Y et al. Dissociable genetic contributions to error processing: a multimodal neuroimaging study. PLoS One. 9(7):e101784 (2014).

    Addis L et al. Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci. Genes Brain Behav. 13(3):333-340 (2014).

    Agler C et al. Canine hereditary ataxia in Old English Sheepdogs and Gordon Setters is associated with a defect in the autophagy gene encoding RAB24. PLoS Genet. 10(2):e1003991 (2014).

    Agopian AJ et al. Genome-wide association study of maternal and inherited loci for conotruncal heart defects. PLoS One. 9(5):e96057 (2014).

    Ahmed I et al. Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease. PLoS Genet. 10(11):e1004788 (2014).

    Akbari MR et al. The spectrum of BRCA1 and BRCA2 mutations in breast cancer patients in the Bahamas. Clin Genet. 85(1):64-67 (2014).

    Akutagava-Martins GC et al. Glutamatergic copy number variants and their role in attention-deficit/hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet. 165B(6):502-509 (2014).

    Alexander ES et al. Twin and family studies reveal strong environmental and weaker genetic cues explaining heritability of eosinophilic esophagitis. J Allergy Clin Immunol. 134(5):1084-1092 (2014).

    Algoe SB and Way BM. Evidence for a role of the oxytocin system, indexed by genetic variation in CD38, in the social bonding effects of expressed gratitude. Soc Cogn Affect Neurosci. 9(12):1855-1861 (2014).

    Alkorta-Aranburu G et al. Phenotypic heterogeneity in monogenic diabetes: the clinical and diagnostic utility of a gene panel-based next-generation sequencing approach. Mol Genet Metab. 113(4):315-320 (2014).

    Allen AL, McGeary JE and Hayes JE. Polymorphisms in TRPV1 and TAS2Rs associate with sensations from sampled ethanol. Alcohol Clin Exp Res. 38(10):2550-2560 (2014).

    Al-Malky G et al. Normal hearing in a child with the m.1555A>G mutation despite repeated exposure to aminoglycosides. Has the penetrance of this pharmacogenetic interaction been overestimated? Int J Pediatr Otorhinolaryngol. 78(6):969-973 (2014).

    Alvarado DM et al. Multiplexed direct genomic selection (MDiGS): a pooled BAC capture approach for highly accurate CNV and SNP/INDEL detection. Nucleic Acids Res. 42(10):e82 (2014).

    Angstadt AY et al. The effect of UGT1A and UGT2B polymorphisms on colorectal cancer risk: haplotype associations and gene–environment interactions. Genes Chromosomes Cancer. 53(6):454-466 (2014).

    Archer NP et al. Genetic, psychosocial, and demographic factors associated with social disinhibition in Mexican-origin youth. Brain Behav. 4(4):521-530 (2014).

    Armingohar Z et al. Polymorphisms in the interleukin-1 gene locus and chronic periodontitis in patients with atherosclerotic and aortic aneurysmal vascular diseases. Scand J Immunol. 79(5):338-345 (2014).

    Armstrong DA et al. Global and gene-specific DNA methylation across multiple tissues in early infancy: implications for children's health research. FASEB J. 28(5):2088-2097 (2014).

    Arrieta-Bolaños E et al. The frequency of HLA-B(∗)57:01 and the risk of abacavir hypersensitivity reactions in the majority population of Costa Rica. Hum Immunol. 75(11):1092-1096 (2014).

    Asarnow LD et al. Children at risk for depression: memory biases, self-schemas, and genotypic variation. J Affect Disor. 159:66-72 (2014).

    Audenet F et al. Germline genetic variations at 11q13 and 12p11 locus modulate age at onset for renal cell carcinoma. J Urol. 191(2):487-492 (2014).

    Avgan N et al. Variation H452Y in HTR2A Gene Effects Immediate Visual Memory. J Genet Genome Res. 1(1):007 (2014).

    Baird AE et al. Genetic basis of cranial cruciate ligament rupture (CCLR) in dogs. Connect Tissue Res. 55(4):275-281 (2014).

    Baird AE et al. Genome-wide association study identifies genomic regions of association for cruciate ligament rupture in Newfoundland dogs. Anim Genet. 45(4):542-549 (2014).

    Bakker JM et al. Therapygenetics in mindfulness-based cognitive therapy: do genes have an impact on therapy-induced change in real-life positive affective experiences? Transl Psychiatry. 4:e384 (2014).

    Banducci et al. Preliminary examination of the relationship between the 5-HTTLPR and childhood emotional abuse on depressive symptoms in 10-12-year-old youth. Psychol Trauma. 6(1):1-7 (2014).

    Baquero-Montoya C et al. Severe ipsilateral musculoskeletal involvement in a Cornelia de Lange patient with a novel NIPBL mutation. Eur J Med Genet. 57(9):503-509 (2014).

    Barfield RT et al. Accounting for population stratification in DNA methylation studies. Genet Epidemiol. 38(3):231-241 (2014).

    Bar-Shira A et al. CHRNB3 c.-57A>G functional promoter change affects Parkinson's disease and smoking. Neurobiol Aging. 35(9):2179.e1-6 (2014).

    Bartling CM et al. A next-generation sequencing approach to epignetic-based tissue source attribution. Electrophoresis. 35(21-22):3096-3101 (2014).

    Bastiaansen JA et al. Filling the gap: relationship between the serotonin-transporter-linked polymorphic region and amygdala activation. Psychol Sci. 25(11):2058-2066 (2014).

    Beach SR et al. Is serotonin transporter genotype associated with epigenetic susceptibility or vulnerability? Examination of the impact of socioeconomic status risk on African American youth. Dev Psychopathol. 26(2):289-304 (2014).

    Ben Khelifa M et al. Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella. Am J Hum Genet. 94(1):95-104 (2014).

    Berenguer A et al. Genetic polymorphisms and asthma: findings from a case-control study in the Madeira island population. Biol Res. 47(1):40 (2014).

    Bhandari R et al. Salivary oxytocin mediates the association between emotional maltreatment and responses to emotional infant faces. Physiol Behav. 131:123-128 (2014).

    Biagini Myers JM et al. Epistasis between serine protease inhibitor Kazal-type 5 (SPINK5) and thymic stromal lymphopoietin (TSLP) genes contributes to childhood asthma. J Allergy Clin Immuno. 134(4):891-899 (2014).

    Bider-Canfield Z and Cotterchio M. Self-reported ABO blood type compared with DNA-derived blood group. Epidemiology. 25(6):936-937 (2014).

    Bitner-Glindzicz M et al. Gentamicin, genetic variation and deafness in preterm children. BMC Pediatr. 14:66 (2014).

    Blum S et al. Killer immunoglobulin-like receptor and their HLA ligands in Guillain-Barré Syndrome. J Neuroimmunol. 267(1-2):92-96 (2014).

    Boardman JP et al. Common genetic variants and risk of brain injury after preterm birth. Pediatrics. 133(6):e1655-1663 (2014).

    Bogdan R et al. Serotonin transporter-linked polymorphic region (5-HTTLPR) genotype and stressful life events interact to predict preschool-onset depression: a replication and developmental extension. J Child Psychol Psychiatry. 55(5):448-457 (2014).

    Bortoluzzi A et al. Anxiety disorders and anxiety-related traits and serotonin transporter gene-linked polymorphic region (5-HTTLPR) in adolescents: case-control and trio studies. Psychiatr Genet. 24(4):176-180 (2014).

    Bosch J et al. In search of genetic markers for nonsyndromic deafness in Africa: a study in Cameroonians and Black South Africans with the GJB6 and GJA1 candidate genes. OMICS. 18(7):481-485 (2014).

    Bosten JM et al. Suggestive association with ocular phoria at chromosome 6p22. Invest Ophthalmol Vis Sci. 55(1):345-352 (2014).

    Bousman CA et al. Effects of neuregulin-1 genetic variation and depression symptom severity on longitudinal patterns of psychotic symptoms in primary care attendees. Am J Med Genet B Neuropsychiatr Genet. 165B(1):62-67 (2014).

    Bousman CA et al. Methylenetetrahydrofolate reductase (MTHFR) genetic variation and major depressive disorder prognosis: A five-year prospective cohort study of primary care attendees. Am J Med Genet B Neuropsychiatr Genet. 165B(1):68-76 (2014).

    Briley AL et al. A complex intervention to improve pregnancy outcome in obese women; the UPBEAT randomised controlled trial. BMC Pregnancy Childbirth. 14:74 (2014).

    Brody GH et al. Differential sensitivity to prevention programming: a dopaminergic polymorphism-enhanced prevention effect on protective parenting and adolescent substance use. Health Psychol. 33(2):182-191 (2014).

    Brody GH et al. Harsh parenting and adolescent health: A longitudinal analysis with genetic moderation. Health Psychol. 33(5):401-409 (2014).

    Brown GW et al. Functional polymorphism in the brain-derived neurotrophic factor gene interacts with stressful life events but not childhood maltreatment in the etiology of depression. Depress Anxiety. 31(4):326-334 (2014).

    Bruenig D et al. Subclinical psychotic experiences in healthy young adults: associations with stress and genetic predisposition. Genet Test Mol Biomarkers. 18(10):683-689 (2014).

    Bruwer Z et al. Predictive genetic testing in children: Constitutional mismatch repair deficiency cancer predisposing syndrome. J Genet Couns. 23(2):147-155 (2014).

    Bühler KM et al. Risky alcohol consumption in young people is associated with the fatty acid amide hydrolase gene polymorphism C385A and affective rating of drug pictures. Mol Genet Genomics. 289(3):279-289 (2014).

    Butali A et al. Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan Africa. Mol Genet Genomic Med. 2(3):254-260 (2014).

    Calderwood L et al. Collecting saliva samples for DNA extraction from children and parents: findings from a pilot study using lay interviewers in the UK. SMIF. Epub ahead of print (2014).

    Canault M et al. Human CalDAG-GEFI gene (RASGRP2) mutation affects platelet function and causes severe bleeding. J Exp Med. 211(7):1349-1362 (2014).

    Cao C et al. TPH2 genotype is associated with PTSD's avoidance symptoms in Chinese female earthquake survivors. Psychiatr Genet. 24(6):257-261 (2014).

    Cao-Lei L et al. DNA methylation signatures triggered by prenatal maternal stress exposure to a natural disaster: Project Ice Storm. PLoS One. 9(9):e107653 (2014).

    Cappi C et al. An inherited small microdeletion at 15q13.3 in a patient with early-onset obsessive-compulsive disorder. PLoS One. 9(10):e110198 (2014).

    Castronovo C et al. Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome. Hum Reprod. 29(2):368-379 (2014).

    Cavanagh JF et al. Conflict acts as an implicit cost in reinforcement learning. Nat Commun. 5:5394 (2014).

    Chan TW et al. Impulsivity and genetic variants in DRD2 and ANKK1 moderate longitudinal associations between sleep problems and overweight from ages 5 to 11. Int J Obes (Lond). 38(3):404-410 (2014).

    Chau CM et al. Neonatal pain and COMT Val158Met genotype in relation to serotonin transporter (SLC6A4) promoter methylation in very preterm children at school age. Front Behav Neurosci. 8:409 (2014).

    Chaussain C et al. Dental caries and enamelin haplotype. J Dent Res. 93(4):360-365 (2014).

    Chen H et al. Stuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia in Chinese population. Behav Brain Funct. 10(1):29 (2014).

    Cheon BK et al. Gene x environment interaction on intergroup bias: the role of 5-HTTLPR and perceived outgroup threat. Soc Cogn Affect Neurosci. 9(9):1268-1275 (2014).

    Chew GYJ et al. TNFRSF13B variants in SLE and immunodeficiency.  J Clin Cell Immunol. 5:233 (2014).

    Choe DE et al. Interactions between monoamine oxidase A and punitive discipline in African American and Caucasian men’s antisocial behavior. Clin Psych Sci. 2(5):591-601 (2014).

    Chumbley J et al. BDNF Val66Met polymorphism influence on striatal blood-level-dependent response to monetary feedback depends on valence and agency. Neuroscience. 280:130-141 (2014).

    Ci H, Wu N and Su Y. Clock gene modulates roles of OXTR and AVPR1b genes in prosociality. PLoS One. 9(10):e109086 (2014).

    Cividanes G et al. Lack of association between the 5-HTTLPR and positive screening for mental disorders among children exposed to urban violence and maltreatment. Rev Bras Psiquiatr. 36(4):277-284 (2014).

    Coghlan MA et al. Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations. BMJ Open Respir Res. 1(1):e000057 (2014).

    Colzato LS, van den Wildenberg WPM and Hommel B. Cognitive control and the COMT Val158Met polymorphism: Genetic modulation of videogame training and transfer to task-switching efficiency. Psychol Res. 78(5):670-678 (2014).

    Concepcion JP et al. Neonatal diabetes, gallbladder agenesis, duodenal atresia, and intestinal malrotation caused by a novel homozygous mutation in RFX6. Pediatr Diabetes. 15(1):67-72 (2014).

    Conway CC, Slavich GM and Hammen C. Daily stress reactivity and serotonin transporter gene (5-HTTLPR) variation: internalizing responses to everyday stress as a possible transdiagnostic phenotype. Biol Mood Anxiety Disord. 4(1):2 (2014).

    Cook GR et al. Quantitative measurement of odor detection thresholds using an air dilution olfactometer, and association with genetic variants in a sample of diverse ancestry. PeerJ. 2:e643 (2014).

    Coon H et al. Association of the CHRNA4 neuronal nicotinic receptor subunit gene with frequency of binge drinking in young adults. Alcohol Clin Exp Res. 38(4):930-937 (2014).

    Cormier C et al. A pooling-based genomewide association study identifies genetic variants associated with Staphylococcus aureus colonization in chronic rhinosinusitis patients. Int Forum Allergy Rhinol. 4(3):207-215 (2014).

    Cotterchio M et al. Active cigarette smoking, variants in carcinogen metabolism genes and breast cancer risk among pre- and postmenopausal women in Ontario, Canada. Breast J. 20(5):468-480 (2014).

    Couthouis J et al. Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy. Neuromuscul Disord. 24(5):431-435 (2014).

    Cragun D et al. Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory. Clin Genet. 86(6):510-520 (2014).

    Cummins TD et al. Alpha-2A adrenergic receptor gene variants are associated with increased intra-individual variability in response time. Mol Psychiatry. 19(9):1031-1036 (2014).

    Dadds MR et al. Polymorphisms in the oxytocin receptor gene are associated with the development of psychopathy. Dev Psychopathol. 26(1):21-31 (2014).

    Dale RC et al. Antibodies to MOG have a demyelination phenotype and affect oligodendrocyte cytoskeleton. Neurol Neuroimmunol Neuroinflamm. 1(1):e12 (2014).

    Damiano CR et al. Association between the oxytocin receptor (OXTR) gene and mesolimbic responses to rewards. Mol Autism. 5(1):7 (2014).

    Davis EE et al. Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes spondyloepiphyseal dysplasia tarda (SEDT). Clin Genet. 85(4):359-364 (2014).

    Davydow DS et al. A pilot investigation of the association of genetic polymorphisms regulating corticotrophin-releasing hormone with posttraumatic stress and depressive symptoms in medical-surgical intensive care unit survivors. J Crit Care. 29(1):101-106 (2014).

    Daw J and Boardman JD. The long arm of adolescence: school health behavioral environments, tobacco and alcohol co-use, and the 5HTTLPR gene. Biodemography Soc Biol. 60(2):117-136 (2014).

    Daw J et al. The interactive effect of neighborhood peer cigarette use and 5HTTLPR genotype on individual cigarette use. Addict Behav. 39(12):1804-1810 (2014).

    de Kock L et al. Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations. Acta Neuropathol. 128(1):111-122 (2014).

    Dean M et al. Increased incidence and disparity of diagnosis of retinoblastoma patients in Guatemala. Cancer Lett. 351(1):59-63 (2014).

    Delicado A et al. Familial imbalance in 16p13.11 leads to a dosage compensation rearrangement in an unaffected carrier. BMC Med Genet. 15(1):116 (2014).

    Delport D et al. Significance of dietary folate intake, homocysteine levels and MTHFR 677 C>T genotyping in South African patients diagnosed with depression: test development for clinical application. Metab Brain Dis. 29(2):377-384 (2014).

    Desmarchelier C et al. The postprandial chylomicron triacylglycerol response to dietary fat in healthy male adults is significantly explained by a combination of single nucleotide polymorphisms in genes involved in triacylglycerol metabolism. J Clin Endocrinol Metab. 99(3):E484-488 (2014).

    Dick DM et al. Spit for Science: launching a longitudinal study of genetic and environmental influences on substance use and emotional health at a large US university. Front Genet. 5:47 (2014).

    Dixon RA et al. APOE and COMT polymorphisms are complementary biomarkers of status, stability, and transitions in normal aging and early mild cognitive impairment. Front Aging Neurosci. 6:236 (2014).

    Do KT et al. Estimation of effective population size using single-nucleotide polymorphism (SNP) data in Jeju horse. J Anim Sci Technol. 56:28 (2014).

    Domingue BW et al. Genetic and educational assortative mating among US adults. Proc Natl Acad Sci USA. 111(22):7996-8000 (2014).

    Domingue BW et al. Polygenic risk predicts obesity in both white and black young adults. PLoS One. 9(7):e101596 (2014).

    Donahue MJ et al. Vessel-encoded arterial spin labeling (VE-ASL) reveals elevated flow territory asymmetry in older adults with substandard verbal memory performance. J Magn Reson Imaging. 39(2):377-386 (2014).

    Dunn EC et al. Interaction between genetic variants and exposure to Hurricane Katrina on post-traumatic stress and post-traumatic growth: a prospective analysis of low income adults. J Affect Disord. 152-154:243-249 (2014).

    Dutra CG et al. Lack of association between thrombophilic gene variants and recurrent pregnancy loss. Hum Fertil (Camb). 17(2):99-105 (2014).

    Edea Z et al. Linkage disequilibrium and genomic scan to detect selective loci in cattle populations adapted to different ecological conditions in Ethiopia. J Anim Breed Genet. 131(5):358-366 (2014).

    Ellingjord-Dale M et al. Breast cancer susceptibility variants and mammographic density phenotypes in norwegian postmenopausal women. Cancer Epidemiol Biomarkers Prev. 23(9):1752-1763 (2014).

    Ellyard JI et al. Identification of a pathogenic variant in TREX1 in early-onset cerebral systemic lupus erythematosus by Whole-exome sequencing. Arthritis Rheumatol. 66(12):3382-3386 (2014).

    Emerenciano M et al. ARID5B polymorphism confers an increased risk to acquire specific MLL rearrangements in early childhood leukemia. BMC Cancer. 14:127 (2014).

    Ergöz N et al. Genetic variation in Ameloblastin is associated with caries in asthmatic children. Eur Arch Paediatr Dent. 15(3):211-216 (2014).

    Ernst M et al. Loss aversion and 5HTT gene variants in adolescent anxiety. Dev Cogn Neurosci. 8:77-85 (2014).

    Eytan O et al. A novel splice-site mutation in the AAGAB gene segregates with hereditary punctate palmoplantar keratoderma and congenital dysplasia of the hip in a large family. Clin Exp Dermatol. 39(2):182-186 (2014).

    Feeney EL and Haves JE. Exploring associations between taste perception, oral anatomy and polymorphisms in the carbonic anhydrase (gustin) gene CA6. Physiol Behav. 128:148-154 (2014).

    Feigl B et al. The relationship between BCMO1 gene variants and macular pigment optical density in persons with and without age-related macular degeneration. PLoS One. 9(2):e89069 (2014).

    Feng P et al. Genome wide association scan for chronic periodontitis implicates novel locus. BMC Oral Health. 14:84 (2014).

    Fidancı ID et al. A Polymorphism in the IL-5 Gene is Associated with Inhibitor Development in Severe Hemophilia A Patients. Turk J Haematol. 31(1):17-24 (2014).

    Figueiredo JC et al. Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians. Am J Med Genet A. 164A(10):2572-2580 (2014).

    Fiorentino A et al. Analysis of ANK3 and CACNA1C variants identified in bipolar disorder whole genome sequence data. Bipolar Disord. 16(6):583-591 (2014).

    Flak MM et al. The Memory Aid study: protocol for a randomized controlled clinical trial evaluating the effect of computer-based working memory training in elderly patients with mild cognitive impairment (MCI). Trials. 15:156 (2014).

    Ford BQ et al. Emotion regulation moderates the risk associated with the 5-HTT gene and stress in children. Emotion. 14(5):930-939 (2014).

    Foshee VA et al. Self-regulatory failure and the perpetration of adolescent dating violence: Examining an alcohol use by gene explanation. Aggress Behav. 41(2):189-203 (2014).

    Foxman B et al. Exploring the effect of dentition, dental decay and familiality on oral health using metabolomics. Infect Genet Evol. 22:201-207 (2014).

    Fraga LR et al. p53 signaling pathway polymorphisms associated to recurrent pregnancy loss. Mol Biol Rep. 41(3):1871-1877 (2014).

    Franzosa EA et al. Relating the metatranscriptome and metagenome of the human gut. Proc Natl Acad Sci USA. 111(22):e2329-2338 (2014).

    Frazier-Bowers SA et al. Novel mutations in PTH1R associated with primary failure of eruption and osteoarthritis. J Dent Res. 93(2):134-139 (2014).

    Gan W et al. A filter paper-based microdevice for low-cost, rapid, and automated DNA extraction and amplification from diverse sample types. Lab Chip. 14(19):3719-3728 (2014).

    Gassó P et al. The effect of age on DNA concentration from whole saliva: implications for the standard isolation method. Am J Hum Biol. 26(6):859-862 (2014).

    Gianfrancesco MA et al. Obesity during childhood and adolescence increases susceptibility to multiple sclerosis after accounting for established genetic and environmental risk factors. Obes Res Clin Pract. 8(5):e435-447 (2014).

    Gijsen VM et al. P450 oxidoreductase *28 (POR*28) and tacrolimus disposition in pediatric kidney transplant recipients--a pilot study. Ther Drug Monit. 36(2):152-158 (2014).

    Gill R et al. Whole-Exome sequencing identifies novel LEPR mutations in individuals with severe early onset obesity. Obesity (Silver Spring). 22(2):576-584 (2014).

    Girotto G et al. Expression and replication studies to identify new candidate genes involved in normal hearing function. PLoS One. 9(1):e85352 (2014).

    Gonçalves H et al. Cohort Profile update: The 1993 Pelotas (Brazil) Birth Cohort follow-up visits in adolescence. Int J Epidemiol. 43(4):1082-1088 (2014).

    Goodbourn PT et al. Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia. Genes Brain Behav. 13(2):144-151 (2014).

    Gorzkowska I et al. An interaction between a polymorphism of the serotonin transporter (5HTT) gene and the clinical picture of adolescents with combined ype of ADHD (hyperkinetic disorder) and youth drinking. Psychiatr Pol. 48(3):541-551 (2014).

    Graham EA et al. Defining background DNA levels found on the skin of children aged 0-5 years. Int J Legal Med. 128(2):251-258 (2014).

    Gray JC and MacKillop J. Genetic basis of delay discounting in frequent gamblers: examination of a priori candidates and exploration of a panel of dopamine-related loci. Brain Behav. 4(6):812-821 (2014).

    Guo G et al. Genetic bio-ancestry and social construction of racial classification in social surveys in the contemporary United States. Demography. 51(1):141-172 (2014).

    Gutierrez-Camino A et al. Noncoding RNA-related polymorphisms in pediatric acute lymphoblastic leukemia susceptibility. Pediatr Res. 75(6):767-773 (2014).

    Haahr ME et al. Central 5-HT4 receptor binding as biomarker of serotonergic tonus in humans: a [11C]SB207145 PET study. Mol Psychiatry. 19(4):427-432 (2014).

    Haberstick BC et al. Simple sequence repeats in the National Longitudinal Study of Adolescent Health: an ethnically diverse resource for genetic analysis of health and behavior. Behav Genet. 44(5):487-497 (2014).

    Hagleitner MM et al. The role of the MTHFR 677C>T polymorphism in methotrexate-induced liver toxicity: a meta-analysis in patients with cancer. Pharmacogenomics J. 14(2):115-119 (2014).

    Harrisberger F et al. The association of the BDNF Val66Met polymorphism and the hippocampal volumes in healthy humans: a joint meta-analysis of published and new data. Neurosci Biobehav Rev. 42:267-278 (2014).

    Hasan NA et al. Microbial community profiling of human saliva using shotgun metagenomic sequencing. PLoS One. 9(5):e97699 (2014).

    Hendershot CS, Claus ED and Ramchandani VA. Associations of OPRM1 A118G and alcohol sensitivity with intravenous alcohol self-administration in young adults. Addict Biol. 21(1):125-135 (2014).

    Herd P, Carr D and Roan C. Cohort profile: Wisconsin longitudinal study (WLS). Int J Epidemiol. 43(1):34-41 (2014).

    Hiemstra M et al. Environmental smoking and smoking onset in adolescence: the role of dopamine-related genes. Findings from two longitudinal studies. PLoS One. 9(1):e86497 (2014).

    Hodgson JA et al. Early back-to-Africa migration into the Horn of Africa. PLoS Genet. 10(6):e1004393 (2014).

    Hoogman M et al. Assessing the effects of common variation in the FOXP2 gene on human brain structure. Front Hum Neurosci. 8:473 (2014).

    Hoogstraat M et al. Genomic and transcriptomic plasticity in treatment-naive ovarian cancer. Genome Res. 24(2):200-211 (2014).

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