about
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureGenome-wide association study of Tourette's syndromeThe novel mouse Polo-like kinase 5 responds to DNA damage and localizes in the nucleolusSingle-nucleotide polymorphism in the human mu opioid receptor gene alters beta-endorphin binding and activity: possible implications for opiate addictionEmbryonic stem cells and somatic cells differ in mutation frequency and typeLinkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locusFunctional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence.Mouse embryonic stem cells, but not somatic cells, predominantly use homologous recombination to repair double-strand DNA breaksA systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom countsComparative anatomy of the human APRT gene and enzyme: nucleotide sequence divergence and conservation of a nonrandom CpG dinucleotide arrangementAssignment of the genes for malate oxidoreductase decarboxylating to chromosome 6 and peptidase B and lactate dehydrogenase B to chromosome 12 in manThe linkage of genes for the human interferon-induced antiviral protein and indophenol oxidase-B traits to chromosome G-21Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.Cloning and recombinant expression of a novel human low molecular weight Ca(2+)-dependent phospholipase A2Groups IV, V, and X phospholipases A2s in human neutrophils: role in eicosanoid production and gram-negative bacterial phospholipid hydrolysisAssociation of the kappa-opioid system with alcohol dependenceModulation of DNA end joining by nuclear proteinsRare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypesThe tumor suppressor SirT2 regulates cell cycle progression and genome stability by modulating the mitotic deposition of H4K20 methylationLow-molecular-weight, calcium-dependent phospholipase A2 genes are linked and map to homologous chromosome regions in mouse and humanHPRT-APRT-deficient mice are not a model for lesch-nyhan syndromeNovel group V phospholipase A2 involved in arachidonic acid mobilization in murine P388D1 macrophagesPositive Selection on Loci Associated with Drug and Alcohol DependenceCloning and characterization of novel rat and mouse low molecular weight Ca(2+)-dependent phospholipase A2s containing 16 cysteinesCloning, expression and partial characterization of a novel rat phospholipase A2Mlh1 mediates tissue-specific regulation of mitotic recombinationVariants located upstream of CHRNB4 on chromosome 15q25.1 are associated with age at onset of daily smoking and habitual smokingDescription of the data from the Collaborative Study on the Genetics of Alcoholism (COGA) and single-nucleotide polymorphism genotyping for Genetic Analysis Workshop 14Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6.A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinksGenome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA familiesMultiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with AutismA genome-wide association study of DSM-IV cannabis dependence.Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependenceAssociation of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event-related oscillations and alcohol dependenceThe Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methodsGenetic association of GABA-A receptor alpha-2 and mu opioid receptor with cocaine cue-reactivity: evidence for inhibitory synaptic neurotransmission involvement in cocaine dependence.2,8-Dihydroxyadenine urolithiasis in a patient with considerable residual adenine phosphoribosyltransferase activity in cell extracts but with mutations in both copies of APRT.New Jersey Center for Tourette Syndrome sharing repository: methods and sample description.A new statistic to evaluate imputation reliability
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P50
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Jay A Tischfield
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Jay A Tischfield
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Jay A. Tischfield
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