Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses. - Wikidata - awgldk - TriplyDB

Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses.

Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses.

http://www.wikidata.org/entity/Q34573373

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Evidence for X-chromosomal schizophrenia associated with microRNA alterations From Genetics to Epigenetics: New Perspectives in Tourette Syndrome Research Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.Mapping asthma-associated variants in admixed populations Slitrk5 deficiency impairs corticostriatal circuitry and leads to obsessive-compulsive-like behaviors in mice Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparities Characterization of SLITRK1 variation in obsessive-compulsive disorder Animal models of tic disorders: a translational perspective.Nogo Receptor 1 (RTN4R) as a candidate gene for schizophrenia: analysis using human and mouse genetic approaches.New Jersey Center for Tourette Syndrome sharing repository: methods and sample description.Genetic studies in pediatric ITP: outlook, feasibility, and requirements.The presence of KIR2DS5 confers protection against adult immune thrombocytopenia.Discovery of rare variants via sequencing: implications for the design of complex trait association studies.Patrocles: a database of polymorphic miRNA-mediated gene regulation in vertebrates Efficient utilization of rare variants for detection of disease-related genomic regions Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease.Genetics of obsessive-compulsive disorder and related disorders.Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data.The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals.Genome-wide association study of copy number variation identified gremlin1 as a candidate gene for lean body mass Identification of rare variants in Alzheimer's disease.Porcine SLITRK1: Molecular cloning and characterization Slitrks as emerging candidate genes involved in neuropsychiatric disorders The Inheritance of Tourette Disorder: A review A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders The genetics of Tourette disorder The genetics of Tourette syndrome: a review.Large-scale analysis reveals a functional single-nucleotide polymorphism in the 5'-flanking region of PRDM16 gene associated with lean body mass.Cosmopolitan and ethnic-specific replication of genetic risk factors for asthma in 2 Latino populations Additional support for the association of SLITRK1 var321 and Tourette syndrome Tourette Syndrome: Bridging the Gap between Genetics and Biology Rare Synaptogenesis-Impairing Mutations in SLITRK5 Are Associated with Obsessive Compulsive Disorder.Mouse models of neurodevelopmental disease of the basal ganglia and associated circuits.Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample.Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism.A sequencing-based survey of functional APAF1 alleles in a large sample of individuals with affective illness and population controls.Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology MicroRNAs in psychiatric and neurodevelopmental disorders.Imaging genetics and development: challenges and promises.Tourette syndrome: gene expression as a tool to discover drug targets.

P2860

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P2860

Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses.

http://www.wikidata.org/entity/Q34573373

description

2006 nî lūn-bûn

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2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2006 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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Overrepresentation of rare var ...... ation of association analyses.

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Overrepresentation of rare var ...... ation of association analyses.

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Overrepresentation of rare var ...... ation of association analyses.

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Overrepresentation of rare var ...... ation of association analyses.

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Overrepresentation of rare var ...... ation of association analyses.

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Overrepresentation of rare var ...... ation of association analyses.

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Overrepresentation of rare var ...... ation of association analyses.

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Overrepresentation of rare var ...... ation of association analyses.

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Overrepresentation of rare var ...... ation of association analyses.

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P1433

Human Molecular Genetics

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Overrepresentation of rare var ...... ation of association analyses.

@en

P2093

Allan Naarden

http://www.w3.org/2001/XMLSchema#string

Ann E Pulver

http://www.w3.org/2001/XMLSchema#string

Carol A Mathews

http://www.w3.org/2001/XMLSchema#string

Cathy L Budman

http://www.w3.org/2001/XMLSchema#string

Chiara Sabatti

http://www.w3.org/2001/XMLSchema#string

Dianne Keen-Kim

http://www.w3.org/2001/XMLSchema#string

Gerald Erenberg

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Luis Diego Herrera

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Nelson B Freimer

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Ruth D Bruun

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P2860

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

Assessing the impact of population stratification on genetic association studies

Mutation of MEF2A in an inherited disorder with features of coronary artery disease

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

Sequence variants in SLITRK1 are associated with Tourette's syndrome

Genomic control for association studies

Population structure, differential bias and genomic control in a large-scale, case-control association study

Lack of MEF2A mutations in coronary artery disease.

Genetics and epidemiology of Tourette syndrome.

Ancestry-environment interactions and asthma risk among Puerto Ricans.

P304

3324-3328

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scholarly article

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10.1093/HMG/DDL408

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22

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15

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2006-10-11T00:00:00Z

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6760561

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17035247

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