Scientific Publications
2012 [ view all publications ⌂ ]
Abraham JE et al. Saliva samples are a viable alternative to blood samples as a source of DNA for high throughput genotyping. BMC Med Genomics. 5(1):19 (2012).
Agren T et al. Human fear reconsolidation and allelic differences in serotonergic and dopaminergic genes. Transl Psychiatry. 7(2):e76 (2012).
Ahmed I et al. Association between Parkinson's disease and the HLA-DRB1 locus. Mov Disord. 27(9):1104-1110 (2012).
Alkorta-Aranburu G et al. The genetic architecture of adaptations to high altitude in ethiopia. PLoS Genet. 8(12):e1003110 (2012).
Allen-Hall A and McNevin D. Human tissue preservation for disaster victim identification (DVI) in tropical climates. Forensic Sci Int Genet. 6(5):653-657 (2012).
Allou L et al. 14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements. Eur J Hum Genet. 20(12):1216-1223 (2012).
Amstadter AB et al. Genetic associations with performance on a behavioral measure of distress intolerance. J Psychiatr Res. 46(1):87-94 (2012).
Amstadter AB et al. The relationship between risk-taking propensity and the COMT Val158Met polymorphism among early adolescents as a function of sex. J Psychiatr Res. 46(7):940-945 (2012).
Anderson LN et al. Passive cigarette smoke exposure during various periods of life, genetic variants, and breast cancer risk among never smokers. Am J Epidemiol. 175(4):289-301 (2012).
Andraweera PH et al. A functional variant in ANGPT1 and the risk of pregnancies with hypertensive disorders and small-for-gestational-age infants. Mol Hum Reprod. 18(6):325-332 (2012).
Aneji CN, Northrup H and Au KS. Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningocele. Birth Defects Res A Clin Mol Teratol. 94(2):84-90 (2012).
Ang KC et al. Skin color variation in Orang Asli tribes of Peninsular Malaysia. PLoS One. 7(8):e42752 (2012).
Anic GM et al. An exploratory analysis of common genetic variants in the vitamin D pathway including genome-wide associated variants in relation to glioma risk and outcome. Cancer Causes Control. 23(9):1443-1449 (2012).
Athanasoulia AP et al. Polymorphisms of the drug transporter gene ABCB1 predict side effects of treatment with cabergoline in patients with PRL adenomas. Eur J Endocrinol. 167(3):327-335 (2012).
Baker ME et al. Polymorphisms in the Gene That Encodes the Iron Transport Protein Ferroportin 1 Influence Susceptibility to Tuberculosis. J Infect Dis. 205(7):1043–1047 (2012).
Bartolome N et al. Genetic polymorphisms, inside and outside the MHC, improve prediction of AS radiographic severity in addition to clinical variables. Rheumatology (Oxford). 51(8):1471-1478 (2012).
Bayat V et al. Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans. PLoS Biol. 10(3):e1001288 (2012).
Bee KJ et al. TGFβRIIb Mutations Trigger Aortic Aneurysm Pathogenesis by Altering Transforming Growth Factor β2 Signal Transduction. Circ Cardiovasc Genet. 5(6):621-629 (2012).
Beitchman JH et al. Childhood aggression, callous-unemotional traits and oxytocin genes. Eur Child Adolesc Psychiatry. 21:125–132 (2012).
Ben Khelifa M et al. Identification of a new recurrent Aurora kinase C mutation in both European and African men with macrozoospermia. Hum Reprod. 27(11):3337-3346 (2012).
Bergen AW et al. Chronic psychosocial stressors and salivary biomarkers in emerging adults. Psychoneuroendocrinology. 37(8):1158-1170 (2012).
Best LG et al. Genetic variants, endothelial function, and risk of preeclampsia among American Indians. Hypertens Pregnancy. 31(1):1-10 (2012).
Best LG et al. Genetic variants, immune function, and risk of pre-eclampsia among American indians. Am J Reprod Immunol. 67(2):152-159 (2012).
Binder G et al. Health and quality of life in adults with Noonan syndrome. J Pediatr. 161(3):501-505 (2012).
Blanco JG et al. Anthracycline-related cardiomyopathy after childhood cancer: role of polymorphisms in carbonyl reductase genes--a report from the Children's Oncology Group. J Clin Oncol. 30(13):1415-1421 (2012).
Bödör C et al. Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival. Haematologica. 97(6):890-894 (2012).
Boettler U et al. Induction of antioxidative Nrf2 gene transcription by coffee in humans: depending on genotype. Mol Biol Rep. 39:7155–7162 (2012).
Bogdan R, Williamson DE and Hariri AR. Mineralocorticoid receptor Iso/Val (rs5522) genotype moderates the association between previous childhood emotional neglect and amygdala reactivity. Am J Psychiatry. 169(5):515-522 (2012).
Bornman DM et al. Short-read, high-throughput sequencing technology for STR genotyping. Biotechniques. 0(0):1-6 (2012).
Brody GH et al. Life stress, the dopamine receptor gene, and emerging adult drug use trajectories: a longitudinal, multilevel, mediated moderation analysis. Dev Psychopathol. 24(3):941-951 (2012).
Broos S et al. Role of alpha-actinin-3 in contractile properties of human single muscle fibers: a case series study in paraplegics. PLoS One. 7(11):e49281 (2012).
Carreño O et al. SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish population. Am J Med Genet B Neuropsychiatr Genet. 159B(1):94-103 (2012).
Carroll CL et al. Beta-Adrenergic receptor polymorphisms associated with length of ICU stay in pediatric status asthmaticus. Pediatr Pulmonol. 47(3):233-239 (2012).
Chabris CF et al. Most reported genetic associations with general intelligence are probably false positives. Psychol Sci. 23(11):1314-1323 (2012).
Chen H et al. The MAOA gene predicts happiness in women. Prog Neuropsychopharmacol Biol Psychiatry. 40:122-125 (2012).
Chen J, Li X and McGue M. Interacting effect of BDNF Val66Met polymorphism and stressful life events on adolescent depression. Genes Brain Behav. Epub ahead of print (2012).
Chew GY et al. Autoimmunity in primary antibody deficiency is associated with protein tyrosine phosphatase nonreceptor type 22 (PTPN22). J Allergy Clin Immunol. 131(4):1130-1135 (2012).
Collins AG and Frank MJ. How much of reinforcement learning is working memory, not reinforcement learning? A behavioral, computational, and neurogenetic analysis. Eur J Neurosci. 35(7):1024-1035 (2012).
Corso-Díaz X et al. Absence of NR2E1 mutations in patients with aniridia. Mol Vis. 18:2770-2782 (2012).
Coutton C et al. MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia. Hum Reprod. 27(8):2549-2558 (2012).
Cozen W et al. A genome-wide meta-analysis of nodular sclerosing Hodgkin lymphoma identifies risk loci at 6p21.32. Blood. 119(2):469-475 (2012).
Creswell KG et al. DRD4 Polymorphism Moderates the Effect of Alcohol Consumption on Social Bonding. PLoS One. 7(2):e28914 (2012).
Cukier HN et al. The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1. Autism Res. 5(6):385-397 (2012).
Cummins TDR et al. Dopamine transporter genotype predicts behavioural and neural measures of response inhibition. Mol Psychiatry. 17(11):1086-1092 (2012).
Curchin C et al. Dermoscopy, reflectance confocal microscopy and histopathology of an amelanotic melanoma from an individual heterozygous for MC1R and tyrosinase variant alleles. Australas J Dermatol. 53(4):291-294 (2012).
Dalle Molle R et al. Associations between parenting behavior and anxiety in a rodent model and a clinical sample: relationship to peripheral BDNF levels. Transl Psychiatry. 2:e195 (2012).
David AC et al. Symptom persistence and memory performance in posttraumatic stress disorder: a gene X environment pilot study. Behav Sci. 2012(2):103-114 (2012).
de Aguiar Gonçalves BA et al. NQO1 rs1800566 (C609T), PON1 rs662 (Q192R), and PON1 rs854560 (L55M) polymorphisms segregate the risk of childhood acute leukemias according to age range distribution. Cancer Causes Control. 23(11):1811-1819 (2012).
De Beaumont L et al. Altered bidirectional plasticity and reduced implicit motor learning in concussed athletes. Cereb Cortex. 22(1):112-121 (2012).
de Koning MB et al. Startle reactivity and prepulse inhibition of the acoustic startle response are modulated by catechol-O-methyl-transferase Val(158) Met polymorphism in adults with 22q11 deletion syndrome. J Psychopharmacol. 26(12):1548-1560 (2012).
de Quervain DJ et al. PKCα is genetically linked to memory capacity in healthy subjects and to risk for posttraumatic stress disorder in genocide survivors. Proc Natl Acad Sci USA. 109(22):8746-8751 (2012).
Dongés B et al. Role of the apolipoprotein E and catechol-O-methyltransferase genes in prospective and retrospective memory traits. Gene. 506(1):135-140 (2012).
Doros L et al. DICER1 mutations in embryonal rhabdomyosarcomas from children with and without familial PPB-tumor predisposition syndrome. Pediatr Blood Cancer. 59(3):558-560 (2012).
Dussaillant C et al. APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family. BMC Med Genet. 13:106 (2012).
Edwards TL et al. A study of prostaglandin pathway genes and interactions with current nonsteroidal anti-inflammatory drug use in colorectal adenoma. Cancer Prev Res (Phila). 5(6):855-863 (2012).
Ellnati E et al. Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots. Hum Mol Genet. 21(16):3695-3702 (2012).
Enter D, Colzato LS and Roelofs K. Dopamine transporter polymorphisms affect social approach–avoidance tendencies. Genes Brain Behav. 11(6):671-676 (2012).
Epstein TG et al. Genetic variation in small proline rich protein 2B as a predictor for asthma among children with eczema. Ann Allergy Asthma Immunol. 108(3):145-150 (2012).
Evans DG et al. Assessing individual breast cancer risk within the U.K. National Health Service Breast Screening Program: a new paradigm for cancer prevention. Cancer Prev Res (Phila). 5(7):943-951 (2012).
Everaerd D et al. Sex Modulates the Interactive Effect of the Serotonin Transporter Gene Polymorphism and Childhood Adversity on Hippocampal Volume. Neuropsychopharmacology. 37(8):1848-1855 (2012).
Fandiño-Losada A et al. Influence of serotonin transporter promoter variation on the effects of separation from parent/partner on depression. J Affect Disord. 144(3):216-224 (2012).
Favaro A et al. Catechol-O-methyltransferase genotype modifies executive functioning and prefrontal functional connectivity in women with anorexia nervosa. J Psychiatry Neurosci. 37(6):120068 (2012).
Fergusson DM et al. Moderating role of the MAOA genotype in antisocial behaviour. Br J Psychiatry. 200(2):116-123 (2012).
Fernández L et al. Additional case of an uncommon 22q11.2 reciprocal rearrangement in a phenotypically normal mother of children with 22q11.2 deletion and 22q11.2 duplication syndromes. Am J Med Genet A. 158A(11):2963-2968 (2012).
Fernàndez-Castillo N et al. Candidate pathway association study in cocaine dependence: the control of neurotransmitter release. World J Biol Psychiatry. 13(2):126-134 (2012).
Fernandez-Navarro P et al. Association analysis between breast cancer genetic variants and mammographic density in a large population-based study (Determinants of Density in Mammographies in Spain) identifies susceptibility loci in TOX3 gene. Eur J Cancer. 49(2):474-481 (2012).
Fontoura C et al. Further evidence of association of the ABCA4 gene with cleft lip/palate. Eur J Oral Sci. 120(6):553-557 (2012).
Fuchs-Telem D et al. Familial pityriasis rubra pilaris Is caused by mutations in CARD14. Am J Hum Genet. 91(1):163-170 (2012).
Funk-Keenan J et al. Evaluation of polymorphisms in the sulfonamide detoxification genes CYB5A and CYB5R3 in dogs with sulfonamide hypersensitivity. J Vet Intern Med. 26(5):1126-1133 (2012).
Galetzka D et al. Monozygotic twins discordant for constitutive BRCA1 promoter methylation, childhood cancer and secondary cancer. Epigenetics. 7(1):47-54 (2012).
Gan-Or Z et al. Association of sequence alterations in the putative promoter of RAB7L1 with a reduced parkinson disease risk. Arch Neurol. 69(1):105-110 (2012).
Gatt JM et al. The TWIN-E project in emotional wellbeing: study protocol and preliminary heritability results across four MRI and DTI measures. Twin Res Hum Genet. 15(3):419-441 (2012).
Gerritsen L et al. BDNF Val66Met genotype modulates the effect of childhood adversity on subgenual anterior cingulate cortex volume in healthy subjects. Mol Psychiatry. 17(6):597-603 (2012).
Gibbons FX et al. The impact of stress on the life history strategies of African American adolescents: cognitions, genetic moderation, and the role of discrimination. Dev Psychol. 48(3):722-739 (2012).
Gibson WT et al. Mutations in EZH2 cause Weaver Syndrome. Am J Hum Genet. 90(1):110-118 (2012).
Gordon EM et al. Effect of dopamine transporter genotype on intrinsic functional connectivity depends on cognitive state. Cereb Cortex. 22(9):2182-2196 (2012).
Grealy R et al. The genetics of endurance: Frequency of the ACTN3 R577X variant in Ironman World Championship athletes. J Sci Med Sport. S1440-2440(12):00187-00189 (2012).
Groom A et al. Postnatal growth and DNA methylation are associated with differential gene expression of the TACSTD2 gene and childhood fat mass. Diabetes. 61(2):391-400 (2012).
Guntheroth W et al. Wenckebach periodicity at rest that normalizes with tachycardia in a family with a NKX2.5 mutation. Am J Cardiol. 110(11):1646-1650 (2012).
Haas DM et al. The impact of drug metabolizing enzyme polymorphisms on outcomes after antenatal corticosteroid use. Am J Obstet Gynecol. 206(5):447.e17-447.e24 (2012).
Haeffela GJ, Eastman M and Grigorenko EL. Using a cognitive endophenotype to identify risk genes for depression. Neurosci Lett. 510(1):10-13 (2012).
Hampson E and Sankar JS. Hand preference in humans is associated with testosteronel evels and androgen receptor gene polymorphism. Neuropsychologia. 50(8):2018-2025 (2012).
Harding K et al. Genotype–phenotype correlation for non-HLA disease associated risk alleles in multiple sclerosis. Neurosci Lett. 526(1):15-19 (2012).
Hartley CA et al. Serotonin transporter polyadenylation polymorphism modulates the retention of fear extinction memory. Proc Natl Acad Sci USA. 109(14):5493–5498 (2012).
Hayden KM et al. A homopolymer polymorphism in the TOMM40 gene contributes to cognitive performance in aging. Alzheimers Dement. 8(5):381-388 (2012).
Hedges DJ et al. Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci. Mol Autism. 3:2 (2012).
Herbert J et al. Interaction between the BDNF gene Val/66/Met polymorphism and morning cortisol levels as a predictor of depression in adult women. Br J Psychiatry. 201(4):313-319 (2012).
Hobbs A et al. Exclusion of CTSB and FDFT1 as positional and functional candidate genes for keratolytic winter erythema (KWE). J Dermatol Sci. 65(1):58-62 (2012).
Holman EA. Acute stress and cardiovascular health: is there an ACE gene connection? J Trauma Stress. 25(5):592-597 (2012).
Hooper DK et al. Risk of tacrolimus toxicity in CYP3A5 nonexpressors treated with intravenous nicardipine after kidney transplantation. Transplantation. 93(8):806-812 (2012).
Hopkins ME et al. Differential effects of acute and regular physical exercise on cognition and affect. Neuroscience. 215:59-68 (2012).
Hu Y et al. Genotyping performance between saliva and blood-derived genomic DNAs on the DMET array: a comparison. PLoS One. 7(3):e33968 (2012).
Huertas E et al. C957T polymorphism of the dopamine D2 receptor gene is associated with motor learning and heart rate. Genes Brain Behav. 11(6):677-683 (2012).
Huizink AC et al. Youth in the Netherlands Study (JOiN): study design. BMC Public Health. 12(1):350 (2012).
Idkowiak J et al. A missense mutation in the human cytochrome b5 gene causes 46,XY disorder of sex development due to true isolated 17,20 lyase deficiency. J Clin Endocrinol Metab. 97(3):e465-e475 (2012).
Jackling FC, Johnson WE and Appleton BR. The Genetic Inheritance of the Blue-eyed White Phenotype in Alpacas (Vicugna pacos). J Hered. Epub ahead of print (2012).
Jasinska AJ et al. Amygdala response to smoking-cessation messages mediates the effects of serotonin transporter gene variation on quitting. Neuroimage. 60(1):766-773 (2012).
Jasinska AJ et al. Influence of threat and serotonin transporter genotype on interference effects. Front Psychol. 3:139 (2012).
Jern P et al. A study of possible associations between single nucleotide polymorphisms in the serotonin receptor 1A, 1B, and 2C genes and self-reported ejaculation latency time. J Sex Med. 9(3):866-872 (2012).
Jin Y et al. Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. Nat Genet. 44(6):676-681 (2012).
Johansson A et al. Alcohol and aggressive behavior in men–moderating effects of oxytocin receptor gene (OXTR) polymorphisms. Genes Brain Behav. 11(2):214-221 (2012).
Johansson A et al. Associations between oxytocin receptor gene (OXTR) polymorphisms and self-reported aggressive behavior and anger: Interactions with alcohol consumption. Psychoneuroendocrinology. 37(9):1546-1556 (2012).
Josephs RA et al. Genetic and hormonal sensitivity to threat: Testing a serotonin transporter genotype x testosterone interaction. Psychoneuroendocrinology. 37(6):752-761 (2012).
Justice CM et al. A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9. Nat Genet. 44(12):1360-1364 (2012).
Kase BA et al. Association of copper-zinc superoxide dismutase (SOD1) and manganese superoxide dismutase (SOD2) genes with nonsyndromic myelomeningocele. Birth Defects Res A Clin Mol Teratol. 94(10):762-769 (2012).
Keller KL et al. Common variants in the CD36 gene are associated with oral fat perception, fat preferences, and obesity in African Americans. Obesity (Silver Spring). 20(5):1066-1073 (2012).
Kelly BN et al. Quantification of growth hormone mRNA in blood. Clin Chim Acta. 414:206-210 (2012).
Kharagjitsingh A et al. Genetic correlates of early accelerated infant growth associated with juvenile-onset type 1 diabetes. Pediatr Diabetes. 13(3):266-271 (2012).
Kim JH et al. Association between FGFR1OP2/wit3.0 polymorphisms and residual ridge resorption of mandible in Korean population. PLoS One. 7(8):e42734 (2012).
Kim SD et al. Leucine-rich repeat, immunoglobulin-like and transmembrane domain 3 (LRIT3) is a modulator of FGFR1. FEBS Lett. 586(10):1516-1521 (2012).
Kitzman JO et al. Noninvasive whole-genome sequencing of a human fetus. Sci Transl Med. 4(137):137ra76 (2012).
Klengel T et al. Allele-specific FKBP5 DNA demethylation mediates gene-childhood trauma interactions. Nat Neurosci. 16(1):33-41 (2012).
Klockars T, Kyttanen S and Ellonen P. TBX22 and tongue-tie. Cleft Palate Craniofac J. 49(3):378-379 (2012).
Knaapila A et al. A genome-wide study on the perception of the odorants androstenone and galaxolide. Chem Senses. 37(6):541-552 (2012).
Knowles JW et al. Randomized trial of personal genomics for preventive cardiology: design and challenges. Circ Cardiovasc Genet. 5(3):368-376 (2012).
Kos M et al. CNTNAP2 and language processing in healthy individuals as measured with ERPs. PLoS One. 7(10):e46995 (2012).
Kranzler HR et al. The 5-HTTLPR polymorphism moderates the effect of stressful life events on drinking behavior in college students of African descent. Am J Med Genet B Neuropsychiatr Genet. 159B(5):484-490 (2012).
Kristiansen W et al. Gene variations in sex hormone pathways and the risk of testicular germ cell tumour: a case–parent triad study in a Norwegian–Swedish population. Hum Reprod. 27(5):1525-1535 (2012).
Kwee LC et al. A high-density genome-wide association screen of sporadic ALS in US veterans. PLoS One. 7(3):e32768 (2012).
Lackner C et al. Dopamine receptor D4 gene variation predicts preschoolers’ developing theory of mind. Dev Sci. 15(2):272-280 (2012).
Lahey BB et al. Preliminary genetic imaging study of the association between estrogen receptor-α gene polymorphisms and harsh human maternal parenting. Neurosci Lett. 525(1):17-22 (2012).
Lauria F et al. Prospective analysis of the association of a common variant of FTO (rs9939609) with adiposity in children: results of the IDEFICS study. PLoS One. 7(11):e48876 (2012).
Lawford BR et al. NOS1AP is associated with increased severity of PTSD and depression in untreated combat veterans. J Affect Disord. S0165-0327(12):00692-1 (2012).
Lee JH et al. De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly. Nat Genet. 44(8):941-945 (2012).
Lee SM et al. Is double inactivation of the Nf1 gene responsible for the development of congenital pseudarthrosis of the tibia associated with NF1. J Orthop Res. 30(10):1535-40 (2012).
Lewis G et al. Maternal depression and child and adolescent depression symptoms: an exploratory test for moderation by CRHR1, FKBP5 and NR3C1 gene variants. Behav Genet. 42(1):121-132 (2012).
Li JJ and Lee SS. Association of Positive and Negative Parenting Behavior with Childhood ADHD: Interactions with Offspring Monoamine Oxidase A (MAO-A) Genotype. J Abnorm Child Psychol. 40(2):165-175 (2012).
Li X, McGue M and Gottesman II. Two sources of genetic liability to depression: interpreting the relationship between stress sensitivity and depression under a multifactorial polygenic model. Behav Genet. 42(2):268-277 (2012).
Lim J et al. Dopaminergic polymorphisms associated with time-on-task declines and fatigue in the psychomotor vigilance test. PLoS One. 7(3):e33767 (2012).
Lim WY et al. Female reproductive factors, gene polymorphisms in the estrogen metabolism pathway, and risk of lung cancer in Chinese women. Am J Epidemiol. 175(6):492–503 (2012).
Linnertz C et al. Characterization of the poly-T variant in the TOMM40 gene in diverse populations. PLoS One. 7(2):e30994 (2012).
Lipchock SV, Reed, DR and Mennella JA. Relationship between bitter-taste receptor genotype and solid medication formulation usage among young children: a retrospective analysis. Clin Ther. 34(3):728-733 (2012).
Liu JZ et al. Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. Nat Genet. 44(10):1137-1141 (2012).
Louttit MD et al. A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability. Cornea. 31(1):26-35 (2012).
Lu W et al. Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfoot. Am J Med Genet A. 158A(7):1620-1627 (2012).
Lundwall RA, Guo DC and Dannemiller JL. Exogenous Visual Orienting Is Associated with Specific Neurotransmitter Genetic Markers: A Population-Based Genetic Association Study. PLoS One. 7(2):e30731 (2012).
Malik AI et al. The role of oxytocin and oxytocin receptor gene variants in childhood-onset aggression. Genes Brain Behav. 11(5):545-551 (2012).
Marinho S et al. 17q12-21 variants are associated with asthma and interact with active smoking in an adult population from the United Kingdom. Ann Allergy Asthma Immunol. 108(6):402-411 (2012).
Markljung E et al. A rare microduplication in a familial case of annular pancreas and duodenal stenosis. J Pediatr Surg. 47(11):2039-2043 (2012).
Marks SJ et al. Migration distance rather than migration rate explains genetic diversity in human patrilocal groups. Mol Ecol. 21(20):4958-4969 (2012).
Marsh AA et al. The influence of oxytocin administration on responses to infant faces and potential moderation by OXTR genotype. Psychopharmacology (Berl). 224(4):469-476 (2012).
McGilvray I et al. Hepatic cell–type specific gene expression better predicts HCV treatment outcome than IL28B genotype. Gastroenterology. 142(5):1122-1131 (2012).
McGrath LM et al. A latent modeling approach to genotype–phenotype relationships: maternal problem behavior clusters, prenatal smoking, and MAOA genotype. Arch Womens Ment Health. 15(4):269-282 (2012).
Mehrotra S et al. Genetic and functional evaluation of the role of DLL1 in susceptibility to visceral leishmaniasis in India. Infect Genet Evol. 12(6):1195-1201 (2012).
Mercer KB et al. Acute and Posttraumatic Stress Symptoms in a Prospective Gene Environment Study of a University Campus Shooting. Arch Gen Psychiatry. 69(1):89-97 (2012).
Mittal VA et al. BDNF Val66Met and spontaneous dyskinesias in non-clinical psychosis. Schizophr Res. 140(1-3):65-70 (2012).
Miyatake S et al. Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease. Neurology. 78(11):803-810 (2012).
Morales D et al. Translational spatial task and its relationship to HIV-associated neurocognitive disorders and apolipoprotein E in HIV-seropositive women. J Neurovirol. 18(6):488-502 (2012).
Moreau C et al. Vitamin K antagonists in children with heart disease: height and VKORC1 genotype are the main determinants of the warfarin dose requirement. Blood. 119(3):861-867 (2012).
Neugut AI et al. The breast cancer quality of care study (BQUAL): a multi-center study to determine causes for noncompliance with breast cancer adjuvant therapy. Breast J. 18(3):203-213 (2012).
Newcomb P et al. Acute effects of walking environment and GSTMI variants in children with asthma. Biol Res Nurs. 14(1):55-64 (2012).
Newman DP et al. Dopamine transporter genotype predicts attentional asymmetry in healthy adults. Neuropsychologia. 50(12):2823-2829 (2012).
Nicoletti P et al. Genomewide pharmacogenetics of bisphosphonate-induced osteonecrosis of the jaw: the role of RBMS3. Oncologist. 17(2):279-287 (2012).
Nikolova Y, Bogdan R and Pizzagalli DA. Perception of a naturalistic stressor interacts with 5-HTTLPR/rs25531 genotype and gender to impact reward responsiveness. Neuropsychobiology. 65(1):45-54 (2012).
Nova P et al. Modeling caffeine concentrations with the Stanford caffeine questionnaire: preliminary evidence for an interaction of chronotype with the effects of caffeine on sleep. Sleep Med. 13(4):362-367 (2012).
Nriagu J et al. E-cadherin polymorphisms and susceptibility to arsenic-related skin lesions in West Bengal, India. Sci Total Environ. 420:65-72 (2012).
Nunes AP et al. Quality of DNA extracted from saliva samples collected with the Oragene kit DNA self-collection kit. BMC Med Res Methodol. 12(1):65 (2012).
O Neill MS et al. Air pollution, inflammation and preterm birth in Mexico City: Study design and methods. Sci Total Environ. S0048-9697(12):01370-01378 (2012).
Olsen NJ et al. The Healthy Start project: a randomized, controlled intervention to prevent overweight among normal weight, preschool children at high risk of future overweight. BMC Public Health. 12:590 (2012).
Omair A et al. An Association Study of Interleukin 18 Receptor Genes (IL18R1 and IL18RAP) in Lumbar Disc Degeneration. Open Orthop J. 6:164-171 (2012).
Omair A et al. Genetic contribution of catechol-Omethyltransferase variants in treatment outcome of low back pain: a prospective genetic association study. BMC Musculoskelet Disord. 13(1):76 (2012).
Ostergaard P et al. Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy. Am J Hum Genet. 90(2):356-362 (2012).
Overödder H and Navér L. Clara cell protein 10 polymorphism is not associated with severe respiratory syncytial virus infection. Acta Paediatr. 101(1):34-37 (2012).
Parkman HP et al. Clinical response and side effects of metoclopramide: associations with clinical, demographic, and pharmacogenetic parameters. J Clin Gastroenterol. 46(6):494-503 (2012).
Parry DA et al. Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta. Am J Hum Genet. 91(3):565-571 (2012).
Patel HY et al. Screening glaucoma genes in adult glaucoma suggests a multiallelic contribution of CYP1B1 to open-angle glaucoma phenotypes. Clin Experiment Ophthalmol. 40(4):e208-217 (2012).
Paterson RL et al. Application of a high-throughput genotyping method for loci exclusion in non-consanguineous Australian pedigrees with autosomal recessive retinitis pigmentosa. Mol Vis. 18:2043-2052 (2012).
Peter B, Matsushita M and Raskind WH. Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family. Psychiatr Genet. 22(5):226-234 (2012).
Petersen IT et al. Interaction between serotonin transporter polymorphism (5-HTTLPR) and stressful life events in adolescents' trajectories of anxious/depressed symptoms. Dev Psychol. 48(5):1463-1475 (2012).
Pietola L et al. Speech recognition and communication outcomes with cochlear implantation in Usher syndrome type 3. Otol Neurotol. 33(1):38-41 (2012).
Pinel P et al. Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. J Neurosci. 32(3):817-825 (2012).
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