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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).

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).

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. Epub ahead of print (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. Epub ahead of print (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).

Banducci AN et al. A 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).

Barfield RT et al. Accounting for population stratification in DNA methylation studies. Genet Epidemiol. Epub ahead of print (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).

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. 165(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. 165(1):68-76 (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).

Buhler 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. Epub ahead of print (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).

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).

Chaussain C et al. Dental caries and enamelin haplotype. J Dent Res. Epub ahead of print (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).

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. Epub ahead of print (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):201-215 (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. 1:101-106 (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. Epub ahead of print (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).

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).

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).

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).

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

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).

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).

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).

Han MR et al. Evaluating 17 breast cancer susceptibility loci in the Nashville breast health study. Breast Cancer. Epub ahead of print (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).

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

Ho-Urriola J et al. Melanocortin-4 receptor polymorphism rs17782313: association with obesity and eating in the absence of hunger in Chilean children. Nutrition. 30(2):145-149 (2014).

Kantaputra P et al. Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations. Am J Med Genet A. Epub ahead of print (2014).

Kantaputra P, Kaewgahya M and Kantaputra W. WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity. Am J Med Genet A. 164(4):360-363 (2014).

Kruijt AW, Putman P and Van der Does W. The 5-HTTLPR polymorphism, early and recent life stress, and cognitive endophenotypes of depression. Cogn Emot. Epub ahead of print (2014).

Kwok CT et al. The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotype. Eur J Hum Genet. 22(5):617-624 (2014).

Lawrance-Owen A et al. Counterphase modulation flicker photometry: phenotypic and genotypic associations. JOSA A. 31(4):A226-A231 (2014).

Li JJ and Lee SS. Negative emotionality mediates the association of 5-HTTLPR genotype and depression in children with and without ADHD. Psychiatry Res. 215(1):163-169 (2014).

Lohoff FW et al. Functional genetic variants in the vesicular monoamine transporter 1 modulate emotion processing. Mol Psychiatry. 19(1):129-139 (2014).

Lonsdorf TB et al. Attention biases and habituation of attention biases are associated with 5-HTTLPR and COMTval158met. Cogn Affect Behav Neurosci. 14(1):354-363 (2014).

Louis ED et al. Essential Tremor in a Charcot-Marie-Tooth Type 2C Kindred Does Not Segregate with the TRPV4 R269H Mutation. Case Rep Neurol. 6(1):1-6 (2014).

Maruszak A et al. Mitochondrial DNA variation is associated with elite athletic status in the Polish population. Scand J Med Sci Sports. 24(2):311-318 (2014).

Mfuna Endam L et al. Genetic variations in taste receptors are associated with chronic rhinosinusitis: a replication study. Int Forum Allergy Rhinol. 4(3):200-206 (2014).

O'Meara H et al. Electronic health records For biological sample collection: feasibility study of statin-induced myopathy using the clinical practice research datalink. Br J Clin Pharmacol. 77(5):831-883 (2014).

Palmer JR, Ambrosone CB and Olshan AF. A collaborative study of the etiology of breast cancer subtypes in African American women: the AMBER consortium. Cancer Causes Control. 25(3):309-319 (2014).

Pedneault M et al. The association between CHRN genetic variants and dizziness at first inhalation of cigarette smoke. Addict Behav. 39(1):316-320 (2014).

Perez-Edgar K et al. DRD4 and striatal modulation of the link between childhood behavioral inhibition and adolescent anxiety. Soc Cogn Affect Neurosci. 9(4):445-453 (2014).

Poulter JA et al. A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta. Hum Mol Genet. 23(8):2189-2197 (2014).

Poulter JA et al. Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta. Eur J Hum Genet. 22(1):132-135 (2014).

Qin Y et al. Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: No association with premature ovarian failure (POF) in Serbian women. Maturitas. 77(1):64-67 (2014).

Quan L et al. Cytokine and cytokine receptor genes of the adaptive immune response are differentially associated with breast cancer risk in American women of African and European ancestry. Int J Cancer. 134(6):1408-1421 (2014).

Raghavan M et al. Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans. Nature. 505(7481):87-91 (2014).

Raj SM et al. Variation at diabetes- and obesity-associated loci may mirror neutral patterns of human population diversity and diabetes prevalence in India. Ann Hum Genet. 77(5):392-408 (2014).

Rose EJ et al. Effects of a novel schizophrenia risk variant rs7914558 at CNNM2 on brain structure and attributional style. Br J Psychiatry. 204:115-121 (2014).

Ruiz-Contreras AE et al. Performance in working memory and attentional control is associated with the rs2180619 SNP in the CNR1 gene. Genes Brain Behav. 13(2):173-178 (2014).

Rye MS et al. Genetic and functional evidence for a locus controlling otitis media at chromosome 10q26.3. BMC Med Genet. Epub ahead of print (2014).

Salminen LE et al. Triallelic relationships between the serotonin transporter polymorphism and cognition among healthy older adults. Int J Neurosci. 124(5):331-338 (2014).

Sargen MR, Hoffstad O and Margolis DJ. Warm, humid, and high sun exposure climates are associated with poorly controlled eczema: PEER (Pediatric Eczema Elective Registry) Cohort, 2004-2012. J Invest Dermatol. Epub ahead of print (2014).

Schuck K et al. Initial responses to the first dose of nicotine in novel smokers: The role of exposure to environmental smoking and genetic predisposition. Psychol Health. Epub ahead of print (2014).

Stuart K et al. BDNF and COMT polymorphisms have a limited association with episodic memory performance or engagement in complex cognitive activity in healthy older adults. Neurobiol Learn Mem. Epub ahead of print (2014).

Thomas S et al. Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation. Eur J Hum Genet. 22(3):244-249 (2014).

van der Zwaluw CS et al. Different trajectories of adolescent alcohol use: testing gene-environment interactions. Alcohol Clin Exp Res. 38(3):704-712 (2014).

van Tilburg MA et al. Irritable bowel syndrome may be associated with maternal inheritance and mitochondrial DNA control region sequence variants. Dig Dis Sci. Epub ahead of print (2014).

Vogel S et al. Linking genetic variants of the mineralocorticoid receptor and negative memory bias: Interaction with prior life adversity. Psychoneuroendocrinology. 40:181-190 (2014).

Wiggins JL et al. Age-related effect of serotonin transporter genotype on amygdala and prefrontal cortex function in adolescence. Hum Brain Mapp. 35(2):646-658 (2014).

Yamaguchi T et al. Genome-wide association study of degenerative bony changes of the temporomandibular joint. Oral Dis. 20(4):409-415 (2014).

Zahid M et al. Unbalanced estrogen metabolism in ovarian cancer. Int J Cancer. 134(10):2414-23 (2014).

Abe Y et al. Association of melanogenesis genes with skin color variation among Japanese females. J Dermatol Sci. 69(2):167-172 (2013).

Ackermann S et al. The BclI polymorphism of the glucocorticoid receptor gene is associated with emotional memory performance in healthy individuals. Psychoneuroendocrinology. 38(7):1203-1207 (2013).

Addis L et al. Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci. Genes Brain Behav. Epub ahead of print (2013).

Agnafors S et al. Effect of gene, environment and maternal depressive symptoms on pre-adolescence behavior problems - a longitudinal study. Child Adolesc Psychiatry Ment Health. 7(1):1-9 (2013).

Agopian AJ et al. Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida. Birth Defects Res A Clin Mol Teratol. 97(9):597-601 (2013).

Albertsen HM et al. Genome-wide association study link novel loci to endometriosis. PLoS One. 8(3):e58257 (2013).

AlFawaz S et al. Recessive oligodontia linked to a homozygous loss-offunction mutation in the SMOC2 gene. Arch Oral Biol. 58(5):462-466 (2013).

Allen AL et al. Bitterness of the non-nutritive sweetener acesulfame potassium varies with polymorphisms in TAS2R9 and TAS2R31. Chem Senses. 38(5):379-389 (2013).

Allen AL, McGeary JE and Hayes JE. Rebaudioside A and Rebaudioside D bitterness do not covary with Acesulfame K bitterness or polymorphisms in TAS2R9 and TAS2R31. Chemosens Percept. 6(3):109–117 (2013).

Almli LM et al. ADCYAP1R1 genotype associates with post-traumatic stress symptoms in highly traumatized African-American females. Am J Med Genet Part B. 162B(3):262-272 (2013).

Alromaih S et al. CD8A gene polymorphisms predict severity factors in chronic rhinosinusitis. Int Forum Allergy Rhinol. 3(8):605-611 (2013).

Alvarado DM et al. Copy number analysis of 413 isolated talipes equinovarus patients suggests role for transcriptional regulators of early limb development. Eur J Hum Genet. 21(4):373-380 (2013).

Amankwah EK et al. SWI/SNF gene variants and glioma risk and outcome. Cancer Epidemiol. 37(2):162-165 (2013).

Andersson E et al. Genetic polymorphisms in monoamine systems and outcome of cognitive behavior therapy for social anxiety disorder. PLoS One. 8(11):e79015 (2013).

Andreassen KE et al. Genetic variation in AKT1, PTEN and the 8q24 locus, and the risk of testicular germ cell tumor. Hum Reprod. 28(7):1995-2002 (2013).

Angstadt AY et al. The effect of copy number variation in the phase II detoxification genes UGT2B17 and UGT2B28 on colorectal cancer risk. Cancer. 119(13):2477-2485 (2013).

Anic GM et al. Toenail iron, genetic determinants of iron status, and the risk of glioma. Cancer Causes Control. 24(12):2051-2058 (2013).

Anthonappa RP, King NM and Rabie AB. Evaluation of the long-term storage stability of saliva as a source of human DNA. Clin Oral Investig. 17(7):1719-1725 (2013).

Ashmore JH et al. Association of dietary and supplemental folate intake and polymorphisms in three FOCM pathway genes with colorectal cancer in a population-based case-control study. Genes Chromosomes Cancer. 52(10):945-953 (2013).

Baggott MJ et al. Psychopharmacology of theobromine in healthy volunteers. Psychopharmacology. 228(1):109-118 (2013).

Baker TE, Stockwell T and Holroyd CB. Constraints on decision making: Implications from genetics, personality, and addiction. Cogn Affect Behav Neurosci. 13(3):417-436 (2013).

Bakhtiari P et al. Exclusion of pathogenic promoter region variants and identification of novel nonsense mutations in the zinc finger E-box binding homeobox 1 gene in posterior polymorphous corneal dystrophy. Mol Vis. 19:575-580 (2013).

Balci F et al. Epistasis effects of dopamine genes on interval timing and reward magnitude in humans. Neuropsychologia. 51(2):293-308 (2013).

Bashash M et al. Genetic polymorphisms at TIMP3 are associated with survival of adenocarcinoma of the gastroesophageal junction. PLoS One. 8(3):e59157 (2013).

Basu Mallick C et al. The light skin allele of SLC24A5 in South Asians and Europeans shares identity by descent. PLoS Genet. 9(11):e1003912 (2013).

Bayer J et al. Estrogen and the male hippocampus: Genetic variation in the aromatase gene predicting serum estrogen is associated with hippocampal gray matter volume in men. Hippocampus. 23(2):117-121 (2013).

Berryhill ME et al. COMT and ANKK1-Taq-Ia genetic polymorphisms influence visual working memory. PLoS One. 8(1):e55862 (2013).

Best LG et al. IBC CARe microarray allelic population prevalences in an American Indian population. PLoS One. 8(9):e75080 (2013).

Best LG et al. Two variants of the C-reactive protein gene are associated with risk of pre-eclampsia in an American Indian population. PLoS One. 8(8):e71231 (2013).

Bhutta MF et al. Alternative recruitment strategies influence saliva sample return rates in community-based genetic association studies. Ann Hum Genet. 77(3):244-250 (2013).

Binia A et al. A polymorphism affecting MYB binding within the promoter of the PDCD4 gene is associated with severe asthma in children. Hum Mutat. 34(8):1131-1139 (2013).

Blake K et al. Methacholine PC20 in African Americans and whites with asthma with homozygous genotypes at ADRB2 codon 16. Pulm Pharmacol Ther. 26(3):342-347 (2013).

Bortsov AV et al. Polymorphisms in the glucocorticoid receptor co-chaperone FKBP5 predict persistent musculoskeletal pain after traumatic stress exposure. Pain. 154(8):1419-1426 (2013).

Bosten JM et al. Individual differences provide psychophysical evidence for separate on- and off-pathways deriving from short-wave cones. JOSA A. 31(4):A47-A54 (2013).

Bousman CA et al. Effects of NRG1 and DAOA genetic variation on transition to psychosis in individuals at ultra-high risk for psychosis. Transl Psychiatry. 3:e251 (2013).

Bradley B et al. Family environment and adult resilience: contributions of positive parenting and the oxytocin receptor gene. Eur J Psychotraumatol. 4:21659 (2013).

Brammer WA and Lee SS. Prosociality and negative emotionality mediate the association of serotonin transporter genotype with childhood ADHD and ODD. J Clin Child Adolesc Psychol. 42(6):809-819 (2013).

Briseno-Ruiz J et al. Role of TRAV locus in low caries experience. Hum Genet. 132(9):1015-1025 (2013).

Brody GH et al. Harsh parenting and adolescent health: A longitudinal analysis with genetic moderation. Health Psychol. Epub ahead of print (2013).

Brody GH et al. Supportive Family Environments, Genes That Confer Sensitivity, and Allostatic Load Among Rural African American Emerging Adults: A Prospective Analysis. J Fam Psychol. 27(1):22-29 (2013).

Brody GH, Chen YF and Beach SRH. Differential susceptibility to prevention: GABAergic, dopaminergic, and multilocus effects. J Child Psychol Psychiatry. 54(8):863-871 (2013).

Brookes C et al. Diagnostic genetics at a distance: Von Hippel-Lindau Disease and a novel mutation. Genet Res Int. 2013:189196 (2013).

Broos S et al. Is PPARa intron 7 G/C polymorphism associated with muscle strength characteristics in nonathletic young men. Scand J Med Sci Sports. 23(4):494-500 (2013).

Bruwer Z et al. Predictive genetic testing in children: Constitutional mismatch repair deficiency cancer predisposing syndrome. J Genet Couns. Epub ahead of print (2013).

Bryant RA et al. The association between the oxytocin receptor gene (OXTR) and hypnotizability. Psychoneuroendocrinology. 38(10):1979-1984 (2013).

Caldwell W et al. The role of the Val66Met polymorphism of the brain derived neurotrophic factor gene in coping strategies relevant to depressive symptoms. PLoS One. 8(6):e65547 (2013).

Cao C et al. Stathmin genotype is associated with reexperiencing symptoms of posttraumatic stress disorder in Chinese earthquake survivors. Prog Neuropsychopharmacol Biol Psychiatry. 44:296-300 (2013).

Capredon M et al. Tracing Arab-Islamic inheritance in Madagascar: study of the Y-chromosome and mitochondrial DNA in the Antemoro. PLoS One. 8(11):e80932 (2013).

Carr DF et al. SLCO1B1 genetic variant associated With statin-induced myopathy: a proof-of-concept study using the clinical practice research datalink. Clin Pharmacol Ther. 94(6):695-701 (2013).

Carr KA et al. Two functional serotonin polymorphisms moderate the effect of food reinforcement on BMI. Behav Neurosci. 127(3):387-399 (2013).

Cerit H, Jans LAW and de Does W. The effect of tryptophan on the cortisol response to social stress is modulated by the 5-HTTLPR genotype. Psychoneuroendocrinology. 38(2):201-208 (2013).

Chang Z et al. Developmental twin study of attention problems: high heritabilities throughout development. JAMA Psychiatry. 70(3):311-318 (2013).

Chavarria-Siles I et al. Genes encoding heterotrimeric G-proteins are associated with gray matter volume variations in the medial frontal cortex. Cereb Cortex. 32(5):1025-1030 (2013).

Chen J, Li X and McGue M. The interacting effect of the BDNF Val66Met polymorphism and stressful life events on adolescent depression is not an artifact of gene–environment correlation: evidence from a longitudinal twin study. J Child Psychol Psychiatry. 54(10):1066-1073 (2013).

Chen KM et al. Human Papilloma Virus prevalence in a multiethnic screening population. Otolaryngol Head Neck Surg. 148(3):436-442 (2013).

Chen S et al. Haplotype-assisted accurate noninvasive fetal whole genome recovery through maternal plasma sequencing. Genome Med. 5(2):18 (2013).

Chenoweth MJ et al. CYP2A6 slow nicotine metabolism is associated with increased quitting by adolescent smokers. Pharmacogenet Genomics. 23(4):232-235 (2013).

Cheon BK et al. Gene x environment interaction on intergroup bias: the role of 5-HTTLPR and perceived outgroup threat. Soc Cogn Affect Neurosci. Epub ahead of print (2013).

Cheung YK et al. HLA-B alleles associated with severe cutaneous reactions to antiepileptic drugs in Han Chinese. Epilepsia. 54(7):1307-1314 (2013).

Chin ELH, da Silva C and Hegde M. Assessment of clinical analytical sensitivity and specificity of next-generation sequencing for detection of simple and complex mutations. BMC Genet. 14:6 (2013).

Cipollini M et al. TPO genetic variants and risk of differentiated thyroid carcinoma in two European populations. Int J Cancer. 133(12):2843-2851 (2013).

Colzato LS et al. Genetic marker of norepinephrine synthesis predicts individual differences in post-error slowing: A pilot study. Neuropsychologia. 51(13):2600-2604 (2013).

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. Epub ahead of print (2013).

Colzato LS, van den WIldenberg WPM and Hommel B. The genetic impact (C957T-DRD2) on inhibitory control is magnified by aging. Neuropsychologia. 51(7):1377-1381 (2013).

Colzato LS, Zmigrod S and Hommel B. Dopamine, norepinephrine, and the management of sensorimotor bindings: Individual differences in updating of stimulus-response episodes pre predicted by DAT1, but not DBH5΄-ins/del. Exp Brain Res. 228(2):213-220 (2013).

Contractor H et al. Aldehyde dehydrogenase-2 inhibition blocks remote preconditioning in experimental and human models. Basic Res Cardiol. 108(3):343 (2013).

Cortes A et al. Resequencing and fine-mapping of the chromosome 12q13-14 locus associated with multiple sclerosis refines the number of implicated genes. Hum Mol Genet. 22(11):2283-2292 (2013).

Courtney KE, Ghahremani DG and Ray LA. Fronto-striatal functional connectivity during response inhibition in alcohol dependence. Addict Biol. 18(3):593-604 (2013).

Coutton C et al. Fine characterisation of a recombination hotspot at the DPY19L2 locus and resolution of the paradoxical excess of duplications over deletions in the general population. PLoS Genetics. 9(3):e1003363 (2013).

Cugino D et al. Polymorphisms of matrix metalloproteinase gene and adiposity indices in European children: results of the IDEFICS study. Int J Obesity. 37(12):1539-1544 (2013).

Cui Y et al. Ancient DNA analysis of Mid-Holocene individuals from the Northwest Coast of North America reveals different evolutionary paths for mitogenomes. PLoS One. 8(7):e66948 (2013).

Cummins TD et al. Alpha-2A adrenergic receptor gene variants are associated with increased intra-individual variability in response time. Mol Psychiatry. Epub ahead of print (2013).

Davies RW et al. A 680 kb duplication at the FTO locus in a kindred with obesity and a distinct body fat distribution. Eur J Hum Genet. 21(12):1417-1422 (2013).

Daw J et al. Genetic sensitivity to peer behaviors: 5HTTLPR, smoking, and alcohol consumption. J Health Soc Behav. 54(1):92-108 (2013).

De Beaumont L et al. Motor system alterations in retired former athletes: the role of aging and concussion history. BMC Neurol. 13:109 (2013).

de la Salle S et al. Effects of COMT genotype on sensory gating and its modulation by nicotine: Differences in low and high P50 suppressors. Neuroscience. 241:147-156 (2013).

De Roach JN et al. Establishment and evolution of the Australian Inherited Retinal Disease Register and DNA Bank. Clin Experiment Ophthalmol. 41(5):476-483 (2013).

Decorte I et al. Effect of saliva stabilisers on detection of porcine reproductive and respiratory syndrome virus in oral fluid by quantitative reverse transcriptase real-time PCR. Vet J. 197(2):224-228 (2013).

Derenko M et al. Complete mitochondrial DNA diversity in Iranians. PLoS One. 8(11):e80673 (2013).

Descamps V et al. Saliva polymerase chain reaction assay for detection and follow-up of herpesvirus reactivation in patients with drug reaction with eosinophilia and systemic symptoms (DRESS). JAMA Dermatol. 149(5):565-569 (2013).

Draaken M et al. Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12. Birth Defects Res A Clin Mol Teratol. 97(3):133-139 (2013).

Durães C et al. Phenotype-genotype profiles in Crohn's disease predicted by genetic markers in autophagy-related genes (GOIA study II). Inflamm Bowel Dis. 19(2):230-239 (2013).

Duvesh R et al. Association study in a South Indian population supports rs1015213 as a risk factor for primary angle closure. Invest Ophthalmol Vis Sci. 54(8):5624-5628 (2013).

Dworschak GC et al. De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL-like association and analysis of EFNB2 in patients with anorectal malformations. Am J Med Genet A. 161A(12):3035-3041 (2013).

Earp MA et al. Inherited common variants in mitochondrial DNA and invasive serous epithelial ovarian cancer risk. BMC Res Notes. 6(1):425 (2013).

Edea Z et al. Genetic diversity, population structure and relationships in indigenous cattle populations of Ethiopia and Korean Hanwoo breeds using SNP markers. Front Genet. 4:35 (2013).

Edwards TL et al. BET1L and TNRC6B associate with increasing fibroid volume and fibroid type among European Americans. Hum Genet. 132(8):943-953 (2013).

Edwards TL et al. Genome-wide association study identifies possible genetic risk factors for colorectal adenomas. Cancer Epidemiol Biomarkers Prev. 22(7):1219-1226 (2013).

Edwards TL, Hartmann KE and Velez Edwards DR. Variants in BET1L and TNRC6B associate with increasing fibroid volume and fibroid type among European Americans. Hum Genet. 132(12):1-9 (2013).

El Andalousi J et al. A single-center cohort of Canadian children with VUR reveals renal phenotypes important for genetic studies. Pediatr Nephrol. 28(9):1813-1819 (2013).

Ergoz N et al. Genetic variation in Ameloblastin is associated with caries in asthmatic children. Eur Arch Paediatr Dent. Epub ahead of print (2013).

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