Rare variant hypothesis for multifactorial inheritance: susceptibility to colorectal adenomas as a model.
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Messing up disorder: how do missense mutations in the tumor suppressor protein APC lead to cancer?Investigation and functional characterization of rare genetic variants in the adipose triglyceride lipase in a large healthy working populationGenome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in EuropeCommon and rare variants in multifactorial susceptibility to common diseasesAn optimized procedure for the design and evaluation of Ecotilling assays.Discovery, linkage disequilibrium and association analyses of polymorphisms of the immune complement inhibitor, decay-accelerating factor gene (DAF/CD55) in type 1 diabetesExcess congenital non-synonymous variation in leukemia-associated genes in MLL- infant leukemia: a Children's Oncology Group report.High-throughput discovery of rare insertions and deletions in large cohortsA new testing strategy to identify rare variants with either risk or protective effect on disease.Polymorphisms in the adenomatous polyposis coli (APC) gene and advanced colorectal adenoma riskThe genetic architecture of Alzheimer's disease: beyond APP, PSENs and APOE.Paraoxonase gene mutations in amyotrophic lateral sclerosis.Rare and low frequency variant stratification in the UK population: description and impact on association tests.A novel approach for the simultaneous analysis of common and rare variants in complex traitsA genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancerCharacterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms.Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disordersCancer genetics: colorectal cancer as a model.Type 2 Diabetes Genetics: Beyond GWAS.Novel CDH1 germline mutations identified in Chinese gastric cancer patients.Power analysis for case-control association studies of samples with known family histories.Disease Risk Assessment Using a Voronoi-Based Network Analysis of Genes and Variants Scores.Stabilized beta-catenin in lung epithelial cells changes cell fate and leads to tracheal and bronchial polyposisPatient and tumor characteristics may raise clinicians' awareness of familial colorectal cancer: a Norwegian population-based study.Systems genetics analysis of cancer susceptibility: from mouse models to humans.An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene.
P2860
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P2860
Rare variant hypothesis for multifactorial inheritance: susceptibility to colorectal adenomas as a model.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Rare variant hypothesis for mu ...... olorectal adenomas as a model.
@ast
Rare variant hypothesis for mu ...... olorectal adenomas as a model.
@en
type
label
Rare variant hypothesis for mu ...... olorectal adenomas as a model.
@ast
Rare variant hypothesis for mu ...... olorectal adenomas as a model.
@en
prefLabel
Rare variant hypothesis for mu ...... olorectal adenomas as a model.
@ast
Rare variant hypothesis for mu ...... olorectal adenomas as a model.
@en
P2093
P356
P1433
P1476
Rare variant hypothesis for mu ...... olorectal adenomas as a model.
@en
P2093
Bruce Winney
Nicola S Fearnhead
Walter F Bodmer
P304
P356
10.4161/CC.4.4.1591
P577
2005-04-07T00:00:00Z