Literature DB >> 15753653

Rare variant hypothesis for multifactorial inheritance: susceptibility to colorectal adenomas as a model.

Nicola S Fearnhead1, Bruce Winney, Walter F Bodmer.   

Abstract

The rare variant hypothesis postulates that genetic susceptibility to colorectal neoplasia within the general population is due to a number of low frequency variants in a variety of different genes. Each variant confers a moderate, but detectable, increase in relative risk of developing the disease. Recent evidence suggests that a quarter of patients with multiple adenomatous polyps are due to rare but functionally important variants in just five genes.

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Year:  2005        PMID: 15753653     DOI: 10.4161/cc.4.4.1591

Source DB:  PubMed          Journal:  Cell Cycle        ISSN: 1551-4005            Impact factor:   4.534


  25 in total

1.  High-throughput discovery of rare insertions and deletions in large cohorts.

Authors:  Francesco L M Vallania; Todd E Druley; Enrique Ramos; Jue Wang; Ingrid Borecki; Michael Province; Robi D Mitra
Journal:  Genome Res       Date:  2010-11-01       Impact factor: 9.043

2.  A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer.

Authors:  T Djureinovic; J Skoglund; J Vandrovcova; X-L Zhou; A Kalushkova; L Iselius; A Lindblom
Journal:  Gut       Date:  2005-09-08       Impact factor: 23.059

Review 3.  Systems genetics analysis of cancer susceptibility: from mouse models to humans.

Authors:  David Quigley; Allan Balmain
Journal:  Nat Rev Genet       Date:  2009-07-28       Impact factor: 53.242

4.  Novel CDH1 germline mutations identified in Chinese gastric cancer patients.

Authors:  Qin-Hua Chen; Wei Deng; Xiao-Wei Li; Xiu-Fang Liu; Jing-Mei Wang; Li-Feng Wang; Nong Xiao; Qiong He; Ya-Ping Wang; Yi-Mei Fan
Journal:  World J Gastroenterol       Date:  2013-02-14       Impact factor: 5.742

5.  Power analysis for case-control association studies of samples with known family histories.

Authors:  Bo Peng; Biao Li; Younghun Han; Christopher I Amos
Journal:  Hum Genet       Date:  2010-04-11       Impact factor: 4.132

6.  Paraoxonase gene mutations in amyotrophic lateral sclerosis.

Authors:  Nicola Ticozzi; Ashley Lyn LeClerc; Pamela J Keagle; Jonathan D Glass; Anne-Marie Wills; Marka van Blitterswijk; Daryl A Bosco; Ildefonso Rodriguez-Leyva; Cinzia Gellera; Antonia Ratti; Franco Taroni; Diane McKenna-Yasek; Peter C Sapp; Vincenzo Silani; Clement E Furlong; Robert H Brown; John E Landers
Journal:  Ann Neurol       Date:  2010-07       Impact factor: 10.422

Review 7.  Human genetic variation and its contribution to complex traits.

Authors:  Kelly A Frazer; Sarah S Murray; Nicholas J Schork; Eric J Topol
Journal:  Nat Rev Genet       Date:  2009-04       Impact factor: 53.242

8.  Type 2 Diabetes Genetics: Beyond GWAS.

Authors:  Dharambir K Sanghera; Piers R Blackett
Journal:  J Diabetes Metab       Date:  2012-06-23

Review 9.  Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders.

Authors:  Jonathan Sebat; Deborah L Levy; Shane E McCarthy
Journal:  Trends Genet       Date:  2009-10-31       Impact factor: 11.639

10.  Stabilized beta-catenin in lung epithelial cells changes cell fate and leads to tracheal and bronchial polyposis.

Authors:  Changgong Li; Aimin Li; Min Li; Yiming Xing; Hongyan Chen; Lingyan Hu; Caterina Tiozzo; Stewart Anderson; Makoto Mark Taketo; Parviz Minoo
Journal:  Dev Biol       Date:  2009-07-23       Impact factor: 3.582

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