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  • Support → Scientific Publications → 2010

    Scientific Publications

    2010 [ view all publications ⌂ ]

    Acevedo SF et al. Apolipoprotein E4 and Sex Affect Neurobehavioral Performance in Primary School Children. Pediatr Res. 67(3):293-299 (2010).

    Aldave AJ et al. Linkage of Posterior Amorphous Corneal Dystrophy to Chromosome 12q21.33 and Exclusion of Coding Region Mutations in KERA, LUM, DCN, and EPYC. Invest Ophthalmol Vis Sci. 51(8):4006-4012 (2010).

    Antypa N and Van der Does AJW. Serotonin transporter gene, childhood emotional abuse and cognitive vulnerability to depression. Genes Brain Behav. 9:615-620 (2010).

    Antypa N et al. Relationships among 5-HTT genotype, life events and gender in the recognition of facial emotions. Neuroscience. 10(42):1-11 (2010).

    Armbruster D et al. Influence of functional tryptophan hydroxylase 2 gene variation and sex on the startle response in children, young adults, and older adults. Biol Psychiatry. 83:214-221 (2010).

    Arrington CB et al. Haploinsufficiency of the LIM Domain Containing Preferred Translocation Partner in Lipoma (LPP) Gene in Patients With Tetralogy of Fallot and VACTERL Association. Am J Med Genet A. 152A:2919-2923 (2010).

    Bahlo M et al. Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies. Cancer Epidemiol Biomarkers Prev. 19(3):794-798 (2010).

    Beall CM et al. Natural selection on EPAS1 (HIF2?) associated with low hemoglobin concentration in Tibetan highlanders. Proc Natl Acad Sci USA. 107(25):11459-11464 (2010).

    Benedek G et al. Opposing effects of the HLA-DRB1*0301-DQB1*0201 haplotype on the risk for multiple sclerosis in diverse Arab populations in Israel. Genes Immun. 11:423-431 (2010).

    Benjet C, Thompson RJ and Gotlib IH. 5-HTTLPR Moderates the Effect of Relational Peer Victimization on Depressive Symptoms in Adolescent Girls. J Child Psychol Psychiatry. 51(2):173-179 (2010).

    Bernard G et al. Tremor-ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3-10q23.31. Neurogenetics. 11:457-464 (2010).

    Bismark AW et al. Polymorphisms of the HTR1a allele are linked to frontal brain electrical asymmetry. Biol Psychol. 83:153-158 (2010).

    Blanton SH et al. Ethnic Heterogeneity of IRF6 AP-2a Binding Site Promoter SNP Association With Nonsyndromic Cleft Lip and Palate. Cleft Palate Craniofac J. 47(6):574-577 (2010).

    Blanton SH et al. Family-based study shows heterogeneity of a susceptibility locus on chromosome 8q24 for nonsyndromic cleft lip and palate. Birth Defects Res A Clin Mol Teratol. 88(4):256-259 (2010).

    Brocke B et al. Stathmin, a gene regulating neural plasticity, affects fear and anxiety processing in humans. Am J Med Genet B. 153B(1):243-251 (2010).

    Bryant RA et al. Preliminary Evidence of the Short Allele of the Serotonin Transporter Gene Predicting Poor Response to Cognitive Behavior Therapy in Posttraumatic Stress Disorder. Biol Psychiatry. 67:1217-1219 (2010).

    Camilleri S, Scerri C and McDonald F. P7-Methylation status of the RUNX2 promoter in a family with ectopic maxillary canines. Bull Group Int Rech Sci Stomatol Odontol. 49:98-99 (2010).

    Carvalho FM et al. FAM5C Contributes to Aggressive Periodontitis. PLoS One. 5(4):e10053 (2010).

    Chen J et al. Optimization of Zygosity Determination by Questionnaire and DNA Genotyping in Chinese Adolescent Twins. Twin Res Hum Genet. 13(2):194-200 (2010).

    Chien W et al. Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan. Prog Neuropsychopharmacol Biol Psychiatry. 34:189-192 (2010).

    Cohn AC et al. Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutations. Eye. 25(2):208-217 (2010).

    Colzato LS et al. The flexible mind is associated with the catechol-O-methyltransferase (COMT) Val158Met polymorphism: Evidence for a role of dopamine in the control of task-switching. Neuropsychologia. 48(9):2764-2768 (2010).

    Colzato LS, Pratt J and Hommel B. Dopaminergic control of attentional flexibility: inhibition of return is associated with the dopamine transporter gene (DAT1). Front Hum Neurosci. 4:53 (2010).

    Corominas R et al. Association Study of the Serotoninergic System in Migraine in the Spanish Population. Am J Med Genet B. 153B:177-184 (2010).

    Cunningham VJ et al. Skeletal phenotype of mandibuloacral dysplasia associated with mutations in ZMPSTE24. Bone. 47(3):591-597 (2010).

    de Visser L et al. Trait anxiety affects decision-making differently in healthy men and women: Towards gender-specific endophenotypes of anxiety. Neuropsychologia. 48(6):1598-1606 (2010).

    Dillon DG et al. Variation in TREK1 Gene Linked to Depression-Resistant Phenotype is Associated with Potentiated Neural Responses to Rewards in Humans. Hum Brain Mapp. 31(2):210-221 (2010).

    Dupont WD et al. Protein Phosphatase 2A Subunit Gene Haplotypes and Proliferative Breast Disease Modify Breast Cancer Risk. Cancer. 116(1):8-19 (2010).

    Edwards AC et al. MAOA-uVNTR and early physical discipline interact to influence delinquent behavior. J Child Psychol Psychiatry. 51(6):679-687 (2010).

    Ells A et al. Severe retinopathy of prematurity associated with FZD4 mutations. Ophthalmic Genet. 31(1):37-43 (2010).

    Epstein LH, Dearing KK and Erbe RW. Parent-child concordance of Taq1 A1 allele predicts similarity of parent-child weight loss in behavioral family-based treatment programs. Appetite. 55(2):363-366 (2010).

    Fajans SS et al. Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60. Transl Res. 156(1):7-14 (2010).

    Fang F et al. Association Between Blood Lead and the Risk of Amyotrophic Lateral Sclerosis. Am J Epidemiol. 171(10):1126-1133 (2010).

    Fesenko DO et al. HLA-DQA1, AB0, and AMEL Genotyping of Biological Material with Biochips. Mol Biol. 44(3):401-406 (2010).

    Franke B et al. Genetic Variation in CACNA1C, a Gene Associated with Bipolar Disorder, Influences Brainstem Rather than Gray Matter Volume in Healthy Individuals. Biol Psychiatry. 68(6):586-588 (2010).

    Frazier-Bowers SA et al. Primary failure of eruption and PTH1R: The importance of a genetic diagnosis for orthodontic treatment planning. Am J Orthod Dentofacial Orthop. 137(2):160.e1-160.e7 (2010).

    Gale DP et al. Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis. Lancet. 376(9743):794-801 (2010).

    Girard N et al. Analysis of Genetic Variants in Never-Smokers with Lung Cancer Facilitated by an Internet-Based Blood Collection Protocol: A Preliminary Report. Clin Cancer Res. 16(2):755-763 (2010).

    Golledge J et al. A population-based study of polymorphisms in genes related to sex hormones and abdominal aortic aneurysm. Eur J Hum Genet. 19(3):363-366 (2010).

    Gra OA et al. Analysis of Genetic Predisposition to Pulmonary Tuberculosis in Native Russians. Genetika. 46(2):262-271 (2010).

    Greene CM et al. Dopaminergic genotype influences spatial bias in healthy adults. Neuropsychologia. 48(9):2458-2464 (2010).

    Gurnett CA et al. Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1. Hum Mol Gen. 19(7):1165-1173 (2010).

    Harmsze AM et al. CYP2C19*2 and CYP2C9*3 alleles are associated with stent thrombosis: a case-control study. Eur Heart J. 31(24):3046-3053 (2010).

    Heim C et al. Effect of childhood trauma on adult depression and neuroendocrine function: sex-specific moderation by CRH receptor 1 gene. Front Behav Neurosci. 3:41 (2010).

    Hennis PJ et al. The Lack of Associations Between Alleles at the Hypoxia-Inducible Factor 1A C1772T Loci and Responses to Acute Hypoxia. Wilderness Environ Med. 21(3):219-228 (2010).

    Holmes AJ, Bogdan R and Pizzagalli DA. Serotonin Transporter Genotype and Action Monitoring Dysfunction: A Possible Substrate Underlying Increased Vulnerability to Depression. Neuropsychopharmacology. 35(5):1186-1197 (2010).

    Hradsky O et al. The CTLA4 variants may interact with the IL23R- and NOD2-conferred risk in development of Crohn's disease. BMC Med Genet. 11:91 (2010).

    Johansson S et al. Common Q1 Variants in the TPH1 and TPH2 Regions Are Not Associated With Persistent ADHD in a Combined Sample of 1,636 Adult Cases and 1,923 Controls From Four European Populations. Am J Med Genet B. 153B(5):1008-1015 (2010).

    Jordan G et al. The dimensionality of color vision in carriers of anomalous trichromacy. J Vis. 10(8):12 (2010).

    Jurez-Cedillo T et al. Cost-effective analysis of genotyping using oral cells in the geriatric population. Genet Mol Res. 9(3):1886-1895 (2010).

    Katerberg H et al. The Role of the COMT Val158Met Polymorphism in the Phenotypic Expression of Obsessive-Compulsive Disorder. Am J Med Genet B. 153B(1):167-176 (2010).

    Keller KL et al. Sex Differences in the Effects of Inherited Bitter Thiourea Sensitivity on Body Weight in 4-6-Year-Old Children. Obesity (Silver Spring). 18(6):1194-1200 (2010).

    Kennerson ML et al. Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy. Am J Hum Genet. 86(3):343-352 (2010).

    Khor CC et al. Hepatocyte Growth Factor and Retinal Arteriolar Diameter in Singapore Chinese. Ophthalmology. 117(5):939-945 (2010).

    Kim HS et al. Culture, distress, and oxytocin receptor polymorphism (OXTR) interact to influence emotional support seeking. Proc Natl Acad Sci USA. 107(36):15717-15721 (2010).

    Kolassa I et al. The Risk of Posttraumatic Stress Disorder After Trauma Depends on Traumatic Load and the Catechol-O-Methyltransferase Val158Met Polymorphism. Biol Psychiatry. 67(4):304-308 (2010).

    Kripke DF et al. Genotyping Sleep Disorders Patients. Psychiatry Investig. 7(1):36-42 (2010).

    Ladouceur M et al. An Efficient Paradigm for Genetic Epidemiology Cohort Creation. PLoS One. 5(11):e14045 (2010).

    Landa I et al. Allelic variant at K79 (COT) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels. Endocr-Relat Cancer. 17:317-328 (2010).

    Landaas ET et al. An international multicenter association study of the serotonin transporter gene in persistent ADHD. Genes Brain Behav. 9:449-458 (2010).

    Lavebratt C et al. PER2 Variantion Is Associated With Depression Vulnerability. Am J Med Genet B. 153B:570-581 (2010).

    Leskela S et al. Polymorphisms in cytochromes P450 2C8 and 3A5 are associated with paclitaxel neurotoxicity. Pharmacogenomics J. 11(2):121-129 (2010).

    Li X et al. Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. J Allergy Clin Immunol. 125:328-335 (2010).

    Lopate G et al. Familial ALS with extreme phenotypic variability due to the I113T SOD1 mutation. Amyotroph Lateral Sc. 11:232-236 (2010).

    Martin IT et al. Guide for Investigators Conducting International Cancer Research Involving Developing Nations. Cancer. 116(6):1396-1399 (2010).

    Martinez ME et al. Comparative study of breast cancer in Mexican and Mexican-American women. Health. 2(9):1040-1048 (2010).

    Mata J, Thompson RJ and Gotlib IH. BDNF Genotype Moderates the Relation Between Physical Activity and Depressive Symptoms. Health Psychol. 29(2):130-133 (2010).

    Mather KA et al. No Associations Between Telomere Length and Age-Sensitive Indicators of Physical Function in Mid and Later Life. J Gerontol A Biol Sci Med Sci. 65(8):792-799 (2010).

    McElroy JA et al. Genetic Variation at a Metallothionein 2A Promoter Single-Nucleotide Polymorphism in White and Black Females in Midwestern United States. J Toxicol Env Heal A. 73(19):1283-1287 (2010).

    McGregor TL et al. Consanguinity Mapping of Congenital Heart Disease in a South Indian Population. PLoS One. 5(4):e10286 (2010).

    Metcalfe KA et al. Screening for Founder Mutations in BRCA1 and BRCA2 in Unselected Jewish Women. J Clin Oncol. 28(3):387-391 (2010).

    Morgan JE et al. Genetic Diagnosis of Familial Breast Cancer Using Clonal Sequencing. Hum Mutat. 31(4):484-491 (2010).

    Ness KK et al. Characteristics of Responders to a Request for a Buccal Cell Specimen Among Survivors of Childhood Cancer and Their Sibling. Pediatr Blood Cancer. 55:165-170 (2010).

    O'Byrne MR et al. Association of Folate Receptor (FOLR1, FOLR2, FOLR3) and Reduced Folate Carrier (SLC19A1) Genes with Meningomyelocele. Birth Defects Res A. 88:689-694 (2010).

    Ozturk A, Famili P and Vieira AR. The Antimicrobial Peptide DEFB1 Is Associated with Caries. J Dent Res. 89(6):631-636 (2010).

    Pagnamenta AT et al. Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biol Psychiatry. 68(4):320-328 (2010).

    Park J et al. Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD. Prog Neuropsychopharmacol Biol Psychiatry. 34(4):697-702 (2010).

    Peplies J et al. Quality management for the collection of biological samples in multicentre studies. Eur J Epidemiol. 25:607-617 (2010).

    Perez-Duenas B et al. Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in the FOLR1 gene. J Inherit Metab Dis. 33(6):795-802 (2010).

    Perez-Edgar K et al. Variations in the serotonin-transporter gene are associated with attention bias patterns to positive and negative emotion faces. Biol Psychol. 83:269-271 (2010).

    Peters BJM et al. Variants of ADAMTS1 modify the effectiveness of statins in reducing the risk of myocardial infarction. Pharmacogenet Genom. 20:766-774 (2010).

    Rankin JK et al. HOXA1 mutations are not a common cause of Mobius syndrome. J AAPOS. 14(1):78-80 (2010).

    Ressler KJ. Polymorphisms in CRHR1 and the Serotonin Transporter Loci: Gene X Gene X Environment Interactions on Depressive Symptoms. Am J Med Genet B. 153B:812-824 (2010).

    Rethorst CD et al. The association of 5-HTTLPR genotype and depressive symptoms is moderated by physical activity. J Psychiat Res. 45(2):189-199 (2010).

    Ribases M et al. Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study. Genes Brain Behav. 10(2):149-157 (2010).

    Robitaille JM et al. The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease. Br J Ophthalmol. 95(4):574-579 (2010).

    Rodriguez-Paris J et al. Genotyping with a 198 Mutation Arrayed Primer Extension Array for Hereditary Hearing Loss: Assessment of Its Diagnostic Value for Medical Practice. PLoS One. 5(7):e11804 (2010).

    Rojas O-L et al. HLA class II polymorphism in Latin American patients with multiple sclerosis. Autoimmun Rev. 9:407-413 (2010).

    Sagreiya H et al. Extending and evaluating a warfarin dosing algorithm that includes CYP4F2 and pooled rare variants of CYP2C9. Pharmacogenet Genom. 20(7):407-413 (2010).

    Sanchez-Mora C et al. Meta-Analysis of Brain-Derived Neurotrophic Factor p.Val66Met in Adult ADHD in Four European Populations. Am J Med Genet B. 153B:512-523 (2010).

    Santtila P et al. The Dopamine Transporter Gene (DAT1) Polymorphism is Associated with Premature Ejaculation. J Sex Med. 7:1538-1546 (2010).

    Schelleman H et al. New genetic variant that might improve warfarin dose prediction in African Americans. Br J Clin Pharmacol. 70(3):393-399 (2010).

    Schmidt S et al. Association of ALS with head injury, cigarette smoking and APOE genotypes. J Neurol Sci. 291:22-29 (2010).

    Sebastian CL et al. Effects of age and MAOA genotype on the neural processing of social rejection. Genes Brain Behav. 9(6):628-637 (2010).

    Sen S et al. A Prospective Cohort Study Investigating Factors Associated With Depression During Medical Internship. Arch Gen Psychiatry. 67(6):557-565 (2010).

    Stice E et al. Reward circuitry responsivity to food predicts future increases in body mass: Moderating effects of DRD2 and DRD4. NeuroImage. 50:1618-1625 (2010).

    Stollstorff M et al. Neural response to working memory load varies by dopamine transporter genotype in children. NeuroImage. 53:970-977 (2010).

    Teeuw ME et al. Do cosanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of a case-control study. BMC Med Genet. 11(113):1-5 (2010).

    Thomason ME et al. COMT genotype affects prefrontal white matter pathways in children and adolescents. NeuroImage. 53:926-934 (2010).

    Thomason ME et al. Neural and behavioral responses to threatening emotion faces in children as a function of the short allele of the serotonin transporter gene. Biol Psychol. 85(1):38-44 (2010).

    Tsianos GI et al. Associations of polymorphisms of eight muscle- or metabolism-related genes with performance in Mount Olympus marathon runners. J Appl Physiol. 108:567-574 (2010).

    Turner SW et al. A methodology to establish a database to study gene environment interactions for childhood asthma. BMC Med Res Methodol. 10:107 (2010).

    van der Mei IAF et al. Human Leukocyte Antigen-DR15, Low Infant Sibling Exposure and Multiple Sclerosis: Gene-Environment Interaction. Ann Neurol. 67:259-263 (2010).

    van der Zanden LFM et al. Genetics of Hypospadias: Are Single-Nucleotide Polymorphisms in SRD5A2, ESR1, ESR2, and ATF3 Really Associated with the Malformation. J Clin Endocrinol Metab. 95(5):2384-2390 (2010).

    van Wingen G et al. The brain-derived neurotrophic factor Val66Met polymorphism affects memory formation and retrieval of biologically salient stimuli. NeuroImage. 50:1212-1218 (2010).

    Viltrop T et al. Comparison of DNA extraction methods for multiplex polymerase chain reaction. Anal Biochem. 398(2):260-262 (2010).

    Voisey J et al. A polymorphism in the dysbindin gene (DTNBP1) associated with multiple psychiatric disorders including schizophrenia. Behav Brain Funct. 6(41):1-7 (2010).

    Way BM and Taylor SE. The Serotonin Transporter Promoter Polymorphism Is Associated with Cortisol Response to Psychosocial Stress. Biol Psychiatry. 67:487-492 (2010).

    Wendell S et al. Taste Genes Associated with Dental Caries. J Dent Res. 89(11):1198-1202 (2010).

    Wessel J et al. Resequencing of Nicotinic Acetylcholine Receptor Genes and Association of Common and Rare Variants with the Fagerstrom Test for Nicotine Dependence. Neuropsychopharmacology. 35:2392-2402 (2010).

    Windelinckx A et al. Comprehensive fine mapping of chr12q12-14 and follow-up replication identify activin receptor 1B (ACVR1B) as a muscle strength gene. Eur J Hum Genet. 19:208-215 (2010).

    Xiao J et al. Novel THAP1 sequence variants in primary dystonia. Neurology. 74:229-238 (2010).

    Yokoyama JS, Erdman CA and Hamilton SP. Array-Based Whole-Genome Survey of Dog Saliva DNA Yields High Quality SNP Data. PLoS One. 5(5):e10809 (2010).

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