Are rare variants responsible for susceptibility to complex diseases? - sprookjes - yvandenbroek - TriplyDB

Are rare variants responsible for susceptibility to complex diseases?

Are rare variants responsible for susceptibility to complex diseases?

http://www.wikidata.org/entity/Q22337172

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Human genetics and genomics a decade after the release of the draft sequence of the human genome The use of racial, ethnic, and ancestral categories in human genetics research Finding the missing heritability of complex diseases Crohn's disease risk alleles on the NOD2 locus have been maintained by natural selection on standing variation Genetics of autism spectrum disorder Missense mutations in the MEFV gene are associated with fibromyalgia syndrome and correlate with elevated IL-1beta plasma levels Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism Five years of GWAS discovery Rare independent mutations in renal salt handling genes contribute to blood pressure variation Strong association of de novo copy number mutations with autism Multiple rare variants in the etiology of autism spectrum disorders The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucoma PLINK: a tool set for whole-genome association and population-based linkage analyses A genetic study of autism in Costa Rica: multiple variables affecting IQ scores observed in a preliminary sample of autistic cases Focusing on the genetics of hearing: you ain't heard nothin' yet.Complex genetic diseases: controversy over the Croesus code.Neurogenetic interactions and aberrant behavioral co-morbidity of attention deficit hyperactivity disorder (ADHD): dispelling myths.Toward precision medicine in Alzheimer's disease Severe infectious diseases of childhood as monogenic inborn errors of immunity Statistical analysis for genome-wide association study Network biomarkers reveal dysfunctional gene regulations during disease progression Molecular mechanisms of disease-causing missense mutations APOL1 kidney risk alleles: population genetics and disease associations Amish revisited: next-generation sequencing studies of psychiatric disorders among the Plain people Collective effects of common SNPs in foraging decisions in Caenorhabditis elegans and an integrative method of identification of candidate genes.Understanding rare and common diseases in the context of human evolution Genetic diagnosis and prognosis of Alzheimer's disease: challenges and opportunities Mapping asthma-associated variants in admixed populations Signatures of natural selection in the human genome Sodium channels SCN1A, SCN2A and SCN3A in familial autism No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network Interacting haplotypes at the NPAS3 locus alter risk of schizophrenia and bipolar disorder Single nucleotide polymorphisms in succinate dehydrogenase subunits and citrate synthase genes: association results for impaired spermatogenesis Mutation screening and association analysis of six candidate genes for autism on chromosome 7q Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease The role of phospholipases A2 in schizophrenia Exploring potential sources of differential vulnerability and susceptibility in risk from environmental hazards to expand the scope of risk assessment Investigation and functional characterization of rare genetic variants in the adipose triglyceride lipase in a large healthy working population Novel adiponectin variants identified in type 2 diabetic patients reveal multimerization and secretion defects

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Are rare variants responsible for susceptibility to complex diseases?

http://www.wikidata.org/entity/Q22337172

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2001 nî lūn-bûn

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2001 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2001 թվականի հունիսին հրատարակված գիտական հոդված

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Are rare variants responsible for susceptibility to complex diseases?

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Are rare variants responsible for susceptibility to complex diseases?

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Are rare variants responsible for susceptibility to complex diseases?

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Are rare variants responsible for susceptibility to complex diseases?

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Are rare variants responsible for susceptibility to complex diseases?

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Are rare variants responsible for susceptibility to complex diseases?

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Are rare variants responsible for susceptibility to complex diseases?

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Are rare variants responsible for susceptibility to complex diseases?

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Are rare variants responsible for susceptibility to complex diseases?

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Are rare variants responsible for susceptibility to complex diseases?

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Are rare variants responsible for susceptibility to complex diseases?

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American Journal of Human Genetics

P1476

Are rare variants responsible for susceptibility to complex diseases?

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Pritchard JK

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P2860

Searching for genetic determinants in the new millennium

A genomic screen of autism: evidence for a multilocus etiology.

Estimate of the mutation rate per nucleotide in humans

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

Characterization of single-nucleotide polymorphisms in coding regions of human genes

Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

When did the human population size start increasing?

Compensatory mutations, antibiotic resistance and the population genetics of adaptive evolution in bacteria

The future of genetic studies of complex human diseases

Epidemiology of neurofibromatosis type 1.

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124-137

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10.1086/321272

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