Scientific Publications
2011 [ view all publications ⌂ ]
Aberg E et al. The functional Val158Met polymorphism in catechol-O-methyltransferase (COMT) is associated with depression and motivation in men from a Swedish population-based study. J Affect Disorders. 129(1-3):158-166 (2011).
Adamson MM et al. Reduced hippocampal activity during encoding in cognitively normal adults carrying the APOE ɛ4 allele. Neuropsychologia. 49(9):2448-2455 (2011).
Akdi A et al. Common variants of the thyroglobulin gene are associated with differentiated thyroid cancer risk. Thyroid. 21(5):519-525 (2011).
Akers NK et al. Multiplexed, ligation-dependent probe amplification for rapid and inexpensive HLA-DQB1 allelotyping. Tissue Antigens. 78(4):275-280 (2011).
Almalte Z et al. Novel associations between activating killer-cell immunoglobulin-like receptor genes and childhood leukemia. Blood. 118(5):1323-1328 (2011).
Al-Meeri A et al. Effect of different sampling strategies for a single geographic region in Yemen on standard genetic analyses of mitochondrial DNA sequence data. Mitochondrial DNA. 22(3):66-70 (2011).
Alvarado DM et al. Pitx1 haploinsufficiency causes clubfoot in humans and a clubfoot-like phenotype in mice. Hum Mol Genet. 20(20):3943–3952 (2011).
Anderson LN et al. Vitamin D-related genetic variants, interactions with vitamin D exposure, and breast cancer risk among Caucasian women in Ontario. Cancer Epidemiol Biomarkers Prev. 20(8):1708-1717 (2011).
Armbruster D et al. Predicting cortisol stress responses in older individuals: Influence of serotonin receptor 1A gene (HTR1A) and stressful life events. Horm Behav. 60(1):105-111 (2011).
Armour CM et al. 17p13.3 microduplications are associated with split-hand/foot malformation and long-bone deficiency (SHFLD). Eur J Hum Genet. 19(11):1144-1151 (2011).
Arnett J et al. Autosomal dominant progressive sensorineural hearing loss due to a novel mutation in the KCNQ4 gene. Arch Otolaryngol Heand Neck Surg. 137(1):54-59 (2011).
Badulli C et al. A new approach to safely type for HLA the HIV infected people eligible to abacavir therapy: Saliva or buccal swab as reliable DNA sources. Clin Chim Acta. 412(21-22):1195-1998 (2011).
Baum M et al. Nucleotide sequence of the Na+/H+ exchanger-8 in patients with congenital sodium diarrhea. J Pediatr Gastroenterol Nutr. 53(5):474-477 (2011).
Baye TM et al. Differences in candidate gene association between European ancestry and African American asthmatic children. PLoS One. 6(2):e16522 (2011).
Beevers CG et al. Associations between serotonin transporter gene promoter region (5-HTTLPR) polymorphism and gaze bias for emotional information. J Abnorm Psychol. 120(1):187-197 (2011).
Bidwell LC et al. A Family Based Association Study of DRD4, DAT1, and 5HTT and Continuous Traits of Attention-Deficit Hyperactivity Disorder. Behav Genet. 41(1):165-174 (2011).
Bocklandt S et al. Epigenetic predictor of age. PLoS One. 6(6):e14821 (2011).
Bogdan R et al. Corticotropin-releasing hormone receptor type 1 (CRHR1) genetic variation and stress interact to influence reward learning. J Neurosci. 31(37):13246–13254 (2011).
Bondurant KL et al. Establishment of a southern breast cancer cohort. Breast J. 17(3):281–288 (2011).
Boyden SE et al. Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE. BMC Med Genet. 12:87 (2011).
Bradley B et al. Association between childhood maltreatment and adult emotional dysregulation in a low-income, urban, African American sample: Moderation by oxytocin receptor gene. Dev Psychopathol. 23:439-452 (2011).
Braet W et al. fMRI activation during response inhibition and error processing: The role of the DAT1 gene in typically developing adolescents and those diagnosed with ADHD. Neuropsychologia. 49(7):1641-1650 (2011).
Bralten J et al. Association of the alzheimer’s gene SORL1 with hippocampal volume in young, healthy adults. Am J Psychiatry. 168(10):1083-1089 (2011).
Brenner L et al. Novel splice mutation in microthalmia-associated transcription factor in Waardenburg Syndrome. Genet Test Mol Biomarkers. 15(7-8):252-259 (2011).
Brody GH et al. Perceived discrimination, serotonin transporter linked polymorphic region status, and the development of conduct problems. Dev Psychopathol. 23(2):617-627 (2011).
Butali A et al. Genetic studies in the Nigerian population implicate a MSX1 mutation in complex oral facial clefting disorders. Cleft Palate Craniofac J. 48(6):646–653 (2011).
Chen H et al. Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations. Br J Dermatol. 165(1):106-114 (2011).
Coenen KR et al. Genetic risk score does not correlate with body mass index of Latina women in a clinical trial. Clin Transl Sci. 4(5):323-327 (2011).
Colzato LS et al. BDNF Val66 Met polymorphism is associated with higher anticipatory cortisol stress response, anxiety, and alcohol consumption in healthy adults. Psychoneuroendocrinology. 36(10):1562-1569 (2011).
Cruciani F et al. Strong intra- and inter-continental differentiation revealed by Y chromosome SNPs M269, U106 and U152. Forensic Sci Int Genet. 5(3):e49-e52 (2011).
Dai J et al. A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia. J Hum Genet. 56(5):398-400 (2011).
David R et al. Lack of association between COMT polymorphisms and apathy in alzheimer’s disease. J Alzheimers Dis. 27(1):155-161 (2011).
de Wildt SN et al. The interactions of age, genetics, and disease severity on tacrolimus dosing requirements after pediatric kidney and liver transplantation. Eur J Clin Pharmacol. 67(12):1231–1241 (2011).
Deng X et al. SeqGene: a comprehensive software solution for mining exome- and transcriptome- sequencing data. BMC Bioinformatics. 12:267 (2011).
DeYoung CG et al. Sources of cognitive exploration: genetic variation in the prefrontal dopamine system predicts openness/intellect. J Res Pers. 45(4):364-371 (2011).
Dick DM et al. CHRM2, parental monitoring, and adolescent externalizing behavior: evidence for gene-environment interaction. Psychol Sci. 22(4):481-489 (2011).
Dmitrieva J et al. Gender-specific expression of the DRD4 gene on adolescent delinquency, anger and thrill seeking. Soc Cogn Affect Neurosci. 6(1):82-89 (2011).
Doll BB, Hutchison KE and Frank MJ. Dopaminergic genes predict individual differences in susceptibility to confirmation bias. J Neurosci. 31(16):6188-6198 (2011).
Dolmans GH et al. Wnt signaling and dupuytren’s disease. N Engl J Med. 365(4):307-317 (2011).
Donenberg T et al. A high prevalence of BRCA1 mutations among breast cancer patients from the Bahamas. Breast Cancer Res Treat. 125(2):591-596 (2011).
Duncan EL et al. Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. PLoS Genet. 7(4):e1001372 (2011).
Egan KM et al. Cancer susceptibility variants and the risk of adult glioma in a US case–control study. J Neurooncol. 104(2):535-542 (2011).
Eller AG et al. Vascular endothelial growth factor-A gene polymorphisms in women with recurrent pregnancy loss. J Reprod Immunol. 88(1):48-52 (2011).
Feigl B et al. Persons with age-related maculopathy risk genotypes and clinically normal eyes have reduced mesopic vision. Invest Ophthalmol Vis Sci. 52(2):1145-1150 (2011).
Fergusson DM et al. MAOA, abuse exposure and antisocial behaviour: 30-year longitudinal study. Br J Psychiatry. 198(6):457-463 (2011).
Filges I et al. Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism. Clin Genet. 79(1):79-85 (2011).
Fode P, Stegger M and Andersen PS. Human b-defensin 3 (DEFB103) and its influence on Staphylococcus aureus nasal carriage. Int J Infect Dis. 15(6):e388-e394 (2011).
Foley C, O’Farrelly C and Meade KG. Technical note: Comparative analyses of the quality and yield of genomic DNA from invasive and noninvasive, automated and manual extraction methods. J Dairy Sci. 94(6):3159-3165 (2011).
Froehlich TE et al. Pharmacogenetic predictors of methylphenidate dose-response in attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry. 50(11):1129-1139 (2011).
Furman DJ et al. Altered timing of amygdala activation during sad mood elaboration as a function of 5-HTTLPR. Soc Cogn Affect Neurosci. 6(3):270-276 (2011).
Furman DJ, Chen MC and Gotlib IH. Variant in oxytocin receptor gene is associated with amygdala volume. Psychoneuroendocrinology. 36(6):891-897 (2011).
Furuichi T et al. CANT1 mutation is also responsible for Desbuquois dysplasia, type 2 and Kim variant. J Med Genet. 48(1):32-37 (2011).
Gallione CJ et al. A founder mutation in the Ashkenazi Jewish population affecting messenger RNA splicing of the CCM2 gene causes cerebral cavernous malformations. Genet Med. 13(7):662-666 (2011).
Gan-Or Z et al. Homozygosity for the MTX1 c.184T>A (p.S63T) alteration modifies the age of onset in GBA-associated Parkinson's disease. Neurogenetics. 12(4):325-332 (2011).
Gao J et al. An exploratory study on CLU, CR1 and PICALM and Parkinson disease. PLoS One. 6(8):e24211 (2011).
Gao J et al. Apolipoprotein E genotypes and the risk of Parkinson disease. Neurobiol Aging. 32(11):2106.e1-2106.e6 (2011).
Garanto A et al. High transcriptional complexity of the retinitis pigmentosa CERKL gene in human and mouse. Invest Ophthalmol Vis Sci. 52(8):5202-5214 (2011).
Garcia-Donas J et al. Single nucleotide polymorphism associations with response and toxic effects in patients with advanced renal-cell carcinoma treated with first-line sunitinib: a multicentre, observational, prospective study. Lancet Oncol. 12(12):1143-1150 (2011).
Ghadirivasfi M et al. Hypomethylation of the serotonin receptor type-2A gene (HTR2A) at T102C polymorphic site in DNA derived from the saliva of patients with Schizophrenia and Bipolar Disorder. Am J Med Genet B Neuropsychiatr Genet. 156B(5):536-545 (2011).
Goel A et al. De novo constitutional MLH1 epimutations confer early-onset colorectal cancer in two new sporadic Lynch syndrome cases, with derivation of the epimutation on the paternal allele in one. Int J Cancer. 128(4):869-878 (2011).
Gruber R et al. Filaggrin genotype in ichthyosis vulgaris predicts abnormalities in epidermal structure and function. Am J Pathol. 178(5):2252-2263 (2011).
Guevara-Aguirre J et al. Growth hormone receptor deficiency is associated with a major reduction in pro-aging signaling, cancer, and diabetes in humans. Sci Transl Med. 3(70):70ra13 (2011).
Guo R et al. Canonical nuclear factor κB pathway links tumorigenesis of synchronous mantle-cell lymphoma, clear-cell renal-cell carcinoma, and GI stromal tumor. J Clin Oncol. 29(10):e257-261 (2011).
Hagleitner MM et al. Taqman genotyping assays can be used on decalcified and paraffin-embedded tissue from patients with osteosarcoma. Pediatr Blood Cancer. 56(1):35-38 (2011).
Hankin BL et al. Association between 5-HTTLPR and vorderline personality disorder traits among youth. Front Psychiatry. 2:6 (2011).
Harubz R et al. A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation. Am J Hum Genet. 88(3):351-361 (2011).
Hauser RM and Weir D. Longitudinal studies of aging in the United States. EurAmerica. 41(1):87-179 (2011).
Herlihy AS et al. The psychosocial impact of Klinefelter syndrome and factors influencing quality of life. Genet Med. 13(7):632-642 (2011).
Hoffmann TJ et al. Next generation genome-wide association tool: Design and coverage of a high-throughput European-optimized SNP array. Genomics. 98(2):79-89 (2011).
Hofstatter EW et al. PALB2 mutations in familial breast and pancreatic cancer. Fam Cancer. 10(2):225-231 (2011).
Holman EA, Lucas-Thompson RG, Lu T. Social constraints, genetic vulnerability, and mental health following collective stress. J Trauma Stress. 24(5):497-505 (2011).
International Parkinson Disease Genomics Consortium et al. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet. 377(9766):641-649 (2011).
Intusoma U et al. Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity. Eur J Paediatr Neurol. 15(5):432-438 (2011).
Jacobs RH et al. Maternal depressive history, teen 5HTTLPR genotype, and the processing of emotional faces: Exploring mechanisms of risk. Behav Res Ther. 49(1):80-84 (2011).
Jenness JL et al. Chronic family stress interacts with 5-HTTLPR to predict prospective depressive symptoms among youth. Depress Anxiety. 28(12):1074-1080 (2011).
Kennedy Q et al. The roles of COMT val158met status and aviation expertise in flight simulator performance and cognitive ability. Behav Genet. 41(5):700-708 (2011).
Khelifa MB et al. A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosis. Mol Hum Reprod. 17(12):762-768 (2011).
Kilpatrick LA et al. The HTR3A polymorphism c. -42C>T is associated with amygdala responsiveness in patients with irritable bowel syndrome. Gastroenterology. 140(7):1943–1951 (2011).
Kim HS et al. Gene–culture interaction: oxytocin receptor polymorphism (OXTR) and emotion regulation. Soc Psychol Personal Sci. 2(6):665-672 (2011).
Kogan A et al. Thin-slicing study of the oxytocin receptor (OXTR) gene and the evaluation and expression of the prosocial disposition. Proc Natl Acad Sci USA. 108(48):19189-19192 (2011).
Koni AC et al. DNA yield and quality of saliva samples and suitability for large-scale epidemiological studies in children. Int J Obes (Lond). 35(1):S113–S118 (2011).
Koster ES et al. FCER2 T2206C variant associated with chronic symptoms and exacerbations in steroid-treated asthmatic children. Allergy. 66(12):1546–1552 (2011).
Kovacic MB et al. Identification of KIF3A as a novel candidate gene for childhood asthma using RNA expression and population allelic frequencies differences. PLoS One. 6(8):e23714 (2011).
Krawetz SA et al. Establishing a biologic specimens repository for reproductive clinical trials: technical aspects. Syst Biol Reprod Med. 57(5):222–227 (2011).
Lacobucci I et al. CDKN2A/B alterations impair prognosis in adult BCR-ABL1 positive acute lymphoblastic leukemia patients. Clin Cancer Res. 17(23):7413-7423 (2011).
Landaas ET et al. No association between the serotonin transporter gene polymorphism 5-HTTLPR and cyclothymic temperament as measured by TEMPS-A. J Affect Disord. 129(1-3):308-312 (2011).
Lau K et al. Non-invasive screening of HLA-DPA1 and HLA-DPB1 alleles for persistent hepatitis B virus infection: Susceptibility for vertical transmission and toward a personalized approach for vaccination and treatment. Clin Chim Acta. 412(11-12):952-957 (2011).
Lee E et al. The association of polymorphisms in hormone metabolism pathway genes, menopausal hormone therapy, and breast cancer risk: a nested case-control study in the California Teachers Study cohort. Breast Cancer Res. 13(2):R37 (2011).
Lee SR et al. Salivary diagnostics – a new industry: perspectives from business development, government, regulatory, and payers. Adv Dent Res. 23(4):369-374 (2011).
Lehmann AS et al. Collection of human genomic DNA from neonates: a comparison between umbilical cord blood and buccal swabs. Am J Obstet Gynecol. 204(4):362.e1-362.e6 (2011).
Lemos C et al. A role for endothelin receptor type A in migraine without aura susceptibility? A study in Portuguese patients. Eur J Neurol. 18(4):649-655 (2011).
Licis AK et al. Novel genetic findings in an extended family pedigree with sleepwalking. Neurology. 76(1):49-52 (2011).
Lim CKP et al. Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children. Behav Brain Funct. 7:16 (2011).
Lindstedt F et al. Perception of thermal pain and the thermal grill illusion Is associated with polymorphisms in the serotonin transporter gene. PLoS One. 6(3):e17752 (2011).
Listman JB et al. Southeast Asian origins of five hill tribe populations and correlation of genetic to linguistic relationships inferred with genome-wide SNP data. Am J Phys Anthropol. 144(2):300-308 (2011).
Lonsdorf TB et al. 5-HTTLPR andCOMTval158met genotype gate amygdala reactivity and habituation. Biol Psychol. 87(1):106-112 (2011).
Lovden M et al. Performance-related increases in hippocampal N-acetylaspartate (NAA) induced by spatial navigation training are restricted to BDNF val homozygotes. Cereb Cortex. 21(6):1435-1442 (2011).
Lynch HT, Aldoss I and Lynch JF. The identification and management of hereditary diffuse gastric cancer in a large Jordanian family. Fam Cancer. 10(4):667-672 (2011).
Mancuso R et al. Intrafamiliar Transmission of KSHV and Seronegative Infection in Family Members of Classic Kaposi's Sarcoma Patients. J Gen Virol. 92(4):744-751 (2011).
Marsh AA et al. Serotonin transporter genotype (5-HTTLPR) predicts utilitarian moral judgments. PLoS One. 6(10):e25148 (2011).
Mata J and Gotlib IH. 5-HTTLPR moderates the relation between changes in depressive and bulimic symptoms in adolescent girls: a longitudinal study. Int J Eat Disord. 44(5):383–388 (2011).
Mata R et al. DAT1 Polymorphism Is Associated with Risk Taking in the Balloon Analogue Risk Task (BART). PLoS One. 7(6):e39135 (2011).
McDevitt JK et al. Neuronal structural protein polymorphism and concussion in college athletes. Brain Inj. 25(11):1108-1113 (2011).
Mehrotra S et al. Genetic and functional evaluation of the role of CXCR1 and CXCR2 in susceptibility to visceral leishmaniasis in north-east India. BMC Med Genet. 12(162):1-7 (2011).
Mehrotra S et al. No evidence for association between SLC11A1 and visceral leishmaniasis in India. BMC Med Genet. 12:71 (2011).
Mehta D et al. Using polymorphisms in FKBP5 to define biologically distinct subtypes of posttraumatic stress disorder: evidence from endocrine and gene expression studies. Arch Gen Psychiatry. 68(9):901-910 (2011).
Mells GF et al. Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. Nat Genet. 43(4):329-332 (2011).
Mendoza-Fandino GA et al. A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia. Clin Genet. 80(3):265-272 (2011).
Miller EK et al. Atopy history and the genomics of wheezing after influenza vaccination in children 6–59 months of age. Vaccine. 29(18):3431-3437 (2011).
Mitchell C et al. Role of mother’s genes and environment in postpartum depression. Proc Natl Acad Sci USA. 108(20):8189-8193 (2011).
Mitsouras K et al. Development of a PCR Assay to Detect Papillomavirus Infection in the Snow Leopard. BMC Vet Res. 7:1-11 (2011).
Mogil JS et al. Pain sensitivity and vasopressin analgesia are mediated by a gene-sex-environment interaction. Nat Neurosci. 14(12):1569-1573 (2011).
Mueller A et al. Interaction of serotonin transporter gene-linked polymorphic region and stressful life events predicts cortisol stress response. Neuropsychopharmacology. 36(7):1332–1339 (2011).
Narusyte J et al. Parental criticism and externalizing behavior problems in adolescents: the role of environment and genotype-environment correlation. J Abnorm Psychol. 120(2):365-376 (2011).
Nauwelaers G et al. DNA adduct formation of 4-Aminobiphenyl and heterocyclic aromatic amines in human hepatocytes. Chem Res Toxicol. 24(6):913-925 (2011).
Necker J et al. Detection of APC germ line mosaicism in patients with de novo familial adenomatous polyposis: a plea for the protein truncation test. J Med Genet. 48(8):526-529 (2011).
Nohesara S et al. DNA hypomethylation of MB-COMT promoter in the DNA derived from saliva in schizophrenia and bipolar disorder. J Psychiatr Res. 45(11):1432-1438 (2011).
Osland et al. Association study of a variable-number tandem repeat polymorphism in the clock gene PERIOD3 and chronotype in Norwegian university students. Chronobiol Int. 28(9):764-770 (2011).
Palejev D et al. An Application of the Elastic Net for an Endophenotype Analysis. Behav Genet. 41:120-124 (2011).
Pansuriya TC et al. Genome-wide analysis of Ollier disease: Is it all in the genes. Orphanet J Rare Dis. 6:2 (2011).
Parkman HP et al. Domperidone Treatment for Gastroparesis: Demographic and Pharmacogenetic Characterization of Clinical Efficacy and Side-Effects. Dig Dis Sci. 56(1):115-124 (2011).
Patel RS et al. High resolution of microRNA signatures in human whole saliva. Arch Oral Biol. 56(12):1506-1513 (2011).
Pereira AC et al. Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder. Am J Med Genet B Neuropsychiatr Genet. 156(2):177-187 (2011).
Peters BJM et al. Genetic variability within the cholesterol lowering pathway and the effectiveness of statins in reducing the risk of MI. Atherosclerosis. 217(2):458-464 (2011).
Ray LA. Stress-Induced and Cue-Induced Craving for Alcohol in Heavy Drinkers: Preliminary Evidence of Genetic Moderation by the OPRM1 and CRH-BP Genes. Alcohol Clin Exp Res. 35(1):166-174 (2011).
Rees SD et al. An FTO variant is associated with Type 2 diabetes in South Asian populations after accounting for body mass index and waist circumference. Diabet Med. 28(6):673-80 (2011).
Rees SD et al. Replication of 13 genome-wide association (GWA)-validated risk variants for type 2 diabetes in Pakistani populations. Diabetologia. 54(6):1368–1374 (2011).
Rollison DE et al. Telomere length in myelodysplastic syndromes. Leuk Lymphoma. 52(8):1528–1536 (2011).
Rossnerova A et al. Factors affecting the frequency of micronuclei in asthmatic and healthy children from Ostrava. Mutat Res. 708(1-2):44-49 (2011).
Roy-Gagnon MH et al. Genomic and genealogical investigation of the French Canadian founder population structure. Hum Genet. 129(5):521-531 (2011).
Ruiz-Contreras AE et al. Involvement of the AATn polymorphism of the CNR1 gene in the efficiency of procedural learning in humans. Neurosci Lett. 494(3):202-206 (2011).
Rye MS et al. FBXO11, a regulator of the TGFβ pathway, is associated with severe otitis media in Western Australian children. Genes Immun. 12(5):352-359 (2011).
Saad M et al. Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. Hum Mol Genet. 20(3):615-627 (2011).
Saitsu H et al. Paternal mosaicism of an STXBP1 mutation in OS. Clin Genet. 80(5):484-488 (2011).
Sakata S et al. Differential effects of organic nitrates on arterial diameter among healthy Japanese participants with different mitochondrial aldehyde dehydrogenase 2 genotypes: randomised crossover trial. BMJ Open. 1(1):e000133 (2011).
Salum GA et al. The multidimensional evaluation and treatment of anxiety in children and adolescents: rationale, design, methods and preliminary findings. Revista Brasileira de Psiquiatria. 33(2):181-195 (2011).
Saphire-Bernstein S et al. Oxytocin receptor gene (OXTR) is related to psychological resources. Proc Natl Acad Sci USA. 108(37):15118-15122 (2011).
Sapienza C et al. DNA methylation profiling identifies epigenetic differences between diabetes patients with ESRD and diabetes patients without nephropathy. Epigenetics. 6(1):20-28 (2011).
Scholes C et al. Genetic diversity and evidence for population admixture in Batak Negritos from Palawan. Am J Phys Anthropol. 146(1):62-72 (2011).
Schreiner F et al. Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults. BMC Med Genet. 12:115 (2011).
Sharma S et al. Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. Hum Mol Genet. 20(7):1456-1466 (2011).
Shete A et al. Genome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene Consortium. Cancer Res. 71(24):7568-7575 (2011).
Shook D et al. Effect of dopamine transporter genotype on caudate volume in childhood ADHD and controls. Am J Med Genet B Neuropsychiatr Genet. 156B(1):28-35 (2011).
Simon JR et al. Dopamine transporter genotype predicts implicit sequence learning. Behav Brain Res. 216(1):452-457 (2011).
Simons RL et al. Social environment, genes, and aggression: Evidence for the differential susceptibility perspective. Am Sociol Rev. 76(6):833-912 (2011).
Small BJ et al. Catechol-O-methyltransferase genotype modulates cancer treatment-related cognitive deficits in breast cancer survivors. Cancer. 117(7):1369-1376 (2011).
Southgate L et al. Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies. Am J Hum Genet. 88(5):574-585 (2011).
Suling M et al. Design and results of the pretest of the IDEFICS study. Int J Obes (Lond). 35 Suppl 1:S30–S44 (2011).
Szperl AM et al. Functional Characterization of Mutations in the Myosin Vb Gene Associated With Microvillus Inclusion Disease. J Pediatr Gastroenterol Nutr. 52(3):307-313 (2011).
Tartter MA and Ray LA. The serotonin transporter polymorphism (5-HTTLPR) and alcohol problems in heavy drinkers: moderation by depressive symptoms. Front Psychiatry. 2:49 (2011).
Thombs DL et al. 5-HTTLPR genotype and associations with intoxication and intention to drive: results from a field study of bar patrons. Addict Biol. 16(1):133-141 (2011).
Thomis MA et al. Genome-wide linkage scan for resistance to muscle fatigue. Scand J Med Sci Sports. 21(4):580-588 (2011).
Thompson RJ et al. Oxytocin receptor gene polymorphism (rs2254298) interacts with familial risk for psychopathology to predict symptoms of depression and anxiety in adolescent girls. Psychoneuroendocrinology. 36(1):144-147 (2011).
Ting TY, Wong RWK and Rabiec ABM. Analysis of genetic polymorphisms in skeletal Class I crowding. Am J Orthod Dentofacial Orthop. 140(1):e9-e15 (2011).
Tocchetto A et al. Evidence of association between Val66Met polymorphism at BDNF gene and anxiety disorders in a community sample of children and adolescents. Neurosci Lett. 502(3):197-200 (2011).
Tomson SN et al. The genetics of colored sequence synesthesia: suggestive evidence of linkage to 16q and genetic heterogeneity for the condition. Behav Brain Res. 223:48-52 (2011).
Tran PX et al. Association of retinoic acid receptor genes with meningomyelocele. Birth Defects Res A Clin Mol Teratol. 91(1):39–43 (2011).
Tremblay N et al. Familial ventricular aneurysms and septal defects map to chromosome 10p15. Eur Heart J. 32:568-573 (2011).
Tuvblad C et al. The genetic and environmental etiology of antisocial behavior from childhood to emerging adulthood. Behav Genet. 41:629-640 (2011).
van der Zwaluw CS, Kuntsche E and Engels RCME. Risky alcohol use in adolescence: the role of genetics (DRD2, SLC6A4) and coping motives. Alcohol Clin Exp Res. 35(4):756-763 (2011).
van Holstein M et al. Human cognitive flexibility depends on dopamine D2 receptor signaling. Psychopharmacology (Berl). 218(3):567-578 (2011).
Velayos-Baeza A et al. Chorea-acanthocytosis genotype in the original critchley Kentucky neuroacanthocytosis kindred. Arch Neurol. 68(10):1330-1333 (2011).
Vieira AR et al. Detection of streptococcusmutans genomic DNA in human DNA samples extracted from saliva and blood. ISRN Dent. 2011:543561 (2011).
Weymouth KS et al. Variants in genes that encode muscle contractile proteins influence risk for isolated clubfoot. Am J Med Genet A. 155:2170-2179 (2011).
Wiener M, Lohoff FW and Coslett HB. Double dissociation of dopamine genes and timing in humans. J Cogn Neurosci. 23(10):2811-2821 (2011).
Wilson ML et al. A fetal variant in the GCM1 gene is associated with pregnancy induced hypertension in a predominantly hispanic population. Int J Mol Epidemiol Genet. 2(3):196-206 (2011).
Wilson NJ et al. A large mutational study in pachyonychia congenita. J Invest Dermatol. 131(5):1018-1024 (2011).
Windelinckx A et al. Identification and prioritization of NUAK1 and PPP1CC as positional candidate loci for skeletal muscle strength phenotypes. Physiol Genomics. 43:981-992 (2011).
Wright JT et al. Amelogenesis imperfecta: genotype-phenotype studies in 71 families. Cells Tissues Organs. 194(2-4):278-283 (2011).
Yalcin O et al. An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures. Epilepsia. 52(5):975-983 (2011).
Zhang Y et al. Polymorphisms in the nitric oxide synthase 1 gene are associated with severe chronic rhinosinusitis. Am J Rhinol Allergy. 25(2):e49-e54 (2011).
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