about
Of toasters and molecular ticker tapesGenome-wide associations of gene expression variation in humansInteractions among genes in the ErbB-Neuregulin signalling network are associated with increased susceptibility to schizophreniaHuman genetics and genomics a decade after the release of the draft sequence of the human genomeAssociation of toll-interacting protein gene polymorphisms with atopic dermatitisAssociation analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility.Finding the missing heritability of complex diseasesGenetics of autism spectrum disorderThe genetics of attention deficit/hyperactivity disorder in adults, a reviewThe genetics of bipolar disorderRevealing the genetic basis of multiple sclerosis: are we there yet?Methods for high-density admixture mapping of disease genesAre rare variants responsible for susceptibility to complex diseases?How many diseases does it take to map a gene with SNPs?Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic EpidemiologyPathogenesis of coronary artery disease: focus on genetic risk factors and identification of genetic variantsA genomic pathway approach to a complex disease: axon guidance and Parkinson diseaseFunction2Gene: a gene selection tool to increase the power of genetic association studies by utilizing public databases and expert knowledgeESPRESSO: taking into account assessment errors on outcome and exposures in power analysis for association studiesEstimation of significance thresholds for genomewide association scansSequence variants in SLC16A11 are a common risk factor for type 2 diabetes in MexicoUSF1 on trialGenetic implication of a novel thiamine transporter in human hypertension.Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus.Strong Amerind/white sex bias and a possible Sephardic contribution among the founders of a population in northwest ColombiaHeterogeneity and the genetics of autism.The tumor-necrosis-factor receptor-associated periodic syndrome: new mutations in TNFRSF1A, ancestral origins, genotype-phenotype studies, and evidence for further genetic heterogeneity of periodic fevers.The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditionsSupport for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locusPolysubstance abuse-vulnerability genes: genome scans for association, using 1,004 subjects and 1,494 single-nucleotide polymorphismsIdentification of four gene variants associated with myocardial infarction.A sibship test for linkage in the presence of association: the sib transmission/disequilibrium testConsistent long-range linkage disequilibrium generated by admixture in a Bantu-Semitic hybrid population.A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31Complement factor H polymorphism in age-related macular degenerationGenome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson diseaseGenetic aspects of Alzheimer diseaseInteraction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysisFive years of GWAS discovery
P2860
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P2860
description
1996 nî lūn-bûn
@nan
1996 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
The future of genetic studies of complex human diseases
@ast
The future of genetic studies of complex human diseases
@en
type
label
The future of genetic studies of complex human diseases
@ast
The future of genetic studies of complex human diseases
@en
prefLabel
The future of genetic studies of complex human diseases
@ast
The future of genetic studies of complex human diseases
@en
P3181
P1433
P1476
The future of genetic studies of complex human diseases
@en
P2093
P304
P3181
P356
10.1126/SCIENCE.273.5281.1516
P407
P577
1996-09-13T00:00:00Z