The 'common disease-common variant' hypothesis and familial risks.
about
A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasmsCandidate gene-based association study of antipsychotic-induced movement disorders in long-stay psychiatric patients: a prospective studyDatabase of genetic studies of bipolar disorderThe role of genetic variation in the causation of mental illness: an evolution-informed framework.Representation of genetic association via attributable familial relative risks in order to identify polymorphisms functionally relevant to rheumatoid arthritis.Other cancers in lung cancer families are overwhelmingly smoking-related cancers.Interpretation of association signals and identification of causal variants from genome-wide association studiesLow-penetrance susceptibility variants in familial colorectal cancer.Genetic predisposition to colorectal cancer: where we stand and future perspectivesEarly-onset colorectal cancer: a sporadic or inherited disease?Undefined familial colorectal cancer.Antipsychotic-induced movement disorders in long-stay psychiatric patients and 45 tag SNPs in 7 candidate genes: a prospective studyEpigenetic inheritance and the missing heritability problem.Rare and common variants: twenty arguments.T2DM: Why Epigenetics?Association of polymorphisms in the aldosterone-regulated sodium reabsorption pathway with blood pressure among Hispanics.Association of a genetic risk score with prevalent and incident myocardial infarction in subjects undergoing coronary angiography.Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling Pathways.Association between copy number variation losses and alcohol dependence across African American and European American ethnic groups.What is complex about complex disorders?Comparison of six statistics of genetic association regarding their ability to discriminate between causal variants and genetically linked markers.BDNF and CGRP interaction: implications in migraine susceptibility.Familial association of inflammatory bowel diseases with other autoimmune and related diseases.Psychiatric genetics gets a boost.Association study of common variants within the G protein-coupled receptor kinase 6 gene and schizophrenia susceptibility in Han Chinese.Searching for the missing heritability of complex diseases
P2860
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P2860
The 'common disease-common variant' hypothesis and familial risks.
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
The 'common disease-common variant' hypothesis and familial risks.
@ast
The 'common disease-common variant' hypothesis and familial risks.
@en
type
label
The 'common disease-common variant' hypothesis and familial risks.
@ast
The 'common disease-common variant' hypothesis and familial risks.
@en
prefLabel
The 'common disease-common variant' hypothesis and familial risks.
@ast
The 'common disease-common variant' hypothesis and familial risks.
@en
P2860
P50
P1433
P1476
The 'common disease-common variant' hypothesis and familial risks.
@en
P2860
P356
10.1371/JOURNAL.PONE.0002504
P407
P577
2008-06-18T00:00:00Z