The allelic architecture of human disease genes: common disease-common variant... or not?
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The use of racial, ethnic, and ancestral categories in human genetics researchFinding the missing heritability of complex diseasesFunctional consequences of PRODH missense mutationsReplication of association between working memory and Reelin, a potential modifier gene in schizophreniaComparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effectsMultiple rare variants in the etiology of autism spectrum disordersInterpopulation linkage disequilibrium patterns of GABRA2 and GABRG1 genes at the GABA cluster locus on human chromosome 4Genetic design and statistical power of nested association mapping in maizeThe neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer diseaseIntegration of text- and data-mining using ontologies successfully selects disease gene candidatesSystematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia.An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population.Severe infectious diseases of childhood as monogenic inborn errors of immunityNew insights from monogenic diabetes for "common" type 2 diabetesInsights into blood lipids from rare variant discoveryRethinking mechanisms of autoimmune pathogenesisQuantitative magnetic resonance imaging traits as endophenotypes for genetic mapping in epilepsyUnderstanding rare and common diseases in the context of human evolutionGenetics in Parkinson disease: Mendelian versus non-Mendelian inheritanceInteracting haplotypes at the NPAS3 locus alter risk of schizophrenia and bipolar disorderStrong association of de novo copy number mutations with sporadic schizophreniaBeyond race: towards a whole-genome perspective on human populations and genetic variationThe emergence of human-evolutionary medical genomicsRealizing the promise of population biobanks: a new model for translationGenomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphismsSize matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiologyNatural selection on genes that underlie human disease susceptibilityBioProspecting: novel marker discovery obtained by mining the bibleomeMeta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33A HapMap harvest of insights into the genetics of common diseaseA novel genome-information content-based statistic for genome-wide association analysis designed for next-generation sequencing dataCandidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABATThe Power of Theory, Research Design, and Transdisciplinary Integration in Moving Psychopathology Forward.Genetic dissection of a model complex trait using the Drosophila Synthetic Population Resource.A variational Bayes discrete mixture test for rare variant associationSimulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.Effective filtering strategies to improve data quality from population-based whole exome sequencing studies.Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpointThe Int7G24A variant of transforming growth factor-beta receptor type I is a risk factor for colorectal cancer in the male Spanish population: a case-control study.Utilizing the Jaccard index to reveal population stratification in sequencing data: a simulation study and an application to the 1000 Genomes Project.
P2860
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P2860
The allelic architecture of human disease genes: common disease-common variant... or not?
description
2002 nî lūn-bûn
@nan
2002 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
The allelic architecture of human disease genes: common disease-common variant... or not?
@ast
The allelic architecture of human disease genes: common disease-common variant... or not?
@en
The allelic architecture of human disease genes: common disease-common variant... or not?
@en-gb
type
label
The allelic architecture of human disease genes: common disease-common variant... or not?
@ast
The allelic architecture of human disease genes: common disease-common variant... or not?
@en
The allelic architecture of human disease genes: common disease-common variant... or not?
@en-gb
prefLabel
The allelic architecture of human disease genes: common disease-common variant... or not?
@ast
The allelic architecture of human disease genes: common disease-common variant... or not?
@en
The allelic architecture of human disease genes: common disease-common variant... or not?
@en-gb
P3181
P356
P1476
The allelic architecture of human disease genes: common disease-common variant... or not?
@en
P2093
J. K. Pritchard
P304
P3181
P356
10.1093/HMG/11.20.2417
P577
2002-10-01T00:00:00Z