Literature DB >> 12952017

Polymorphically duplicated genes: their relevance to phenotypic variation in humans.

Paul R Buckland1.   

Abstract

A number of disorders are known to be caused by duplication of genes, but these are all rare events. However, there is evidence that polymorphic gene duplication may be common and a growing number of genes are known to be duplicated in a polymorphic manner although phenotypes cannot be associated with most of these. Gene duplication occurring due to cytogenetic abnormalities such as Down syndrome predisposes the patients to a variety of complex disorders. It is possible therefore that many complex disorders and variable phenotypes are associated with duplication of genes.

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Year:  2003        PMID: 12952017     DOI: 10.1080/07853890310001276

Source DB:  PubMed          Journal:  Ann Med        ISSN: 0785-3890            Impact factor:   4.709


  28 in total

1.  Segmental duplications and copy-number variation in the human genome.

Authors:  Andrew J Sharp; Devin P Locke; Sean D McGrath; Ze Cheng; Jeffrey A Bailey; Rhea U Vallente; Lisa M Pertz; Royden A Clark; Stuart Schwartz; Rick Segraves; Vanessa V Oseroff; Donna G Albertson; Daniel Pinkel; Evan E Eichler
Journal:  Am J Hum Genet       Date:  2005-05-25       Impact factor: 11.025

2.  Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.

Authors:  Devin P Locke; Andrew J Sharp; Steven A McCarroll; Sean D McGrath; Tera L Newman; Ze Cheng; Stuart Schwartz; Donna G Albertson; Daniel Pinkel; David M Altshuler; Evan E Eichler
Journal:  Am J Hum Genet       Date:  2006-06-15       Impact factor: 11.025

3.  The fine-scale and complex architecture of human copy-number variation.

Authors:  George H Perry; Amir Ben-Dor; Anya Tsalenko; Nick Sampas; Laia Rodriguez-Revenga; Charles W Tran; Alicia Scheffer; Israel Steinfeld; Peter Tsang; N Alice Yamada; Han Soo Park; Jong-Il Kim; Jeong-Sun Seo; Zohar Yakhini; Stephen Laderman; Laurakay Bruhn; Charles Lee
Journal:  Am J Hum Genet       Date:  2008-01-24       Impact factor: 11.025

4.  Completing the map of human genetic variation.

Authors:  Evan E Eichler; Deborah A Nickerson; David Altshuler; Anne M Bowcock; Lisa D Brooks; Nigel P Carter; Deanna M Church; Adam Felsenfeld; Mark Guyer; Charles Lee; James R Lupski; James C Mullikin; Jonathan K Pritchard; Jonathan Sebat; Stephen T Sherry; Douglas Smith; David Valle; Robert H Waterston
Journal:  Nature       Date:  2007-05-10       Impact factor: 49.962

5.  A comprehensive profile of DNA copy number variations in a Korean population: identification of copy number invariant regions among Koreans.

Authors:  Jae Pil Jeon; Sung Mi Shim; Jong Sun Jung; Hye Young Nam; Hye Jin Lee; Berm Seok Oh; Kuchan Kim; Hyung Lae Kim; Bok Ghee Han
Journal:  Exp Mol Med       Date:  2009-09-30       Impact factor: 8.718

6.  Copy number variant analysis of human embryonic stem cells.

Authors:  Hao Wu; Kevin J Kim; Kshama Mehta; Salvatore Paxia; Andrew Sundstrom; Thomas Anantharaman; Ali I Kuraishy; Tri Doan; Jayati Ghosh; April D Pyle; Amander Clark; William Lowry; Guoping Fan; Tim Baxter; Bud Mishra; Yi Sun; Michael A Teitell
Journal:  Stem Cells       Date:  2008-03-27       Impact factor: 6.277

7.  Simultaneous discovery and testing of deletions for disease association in SNP genotyping studies.

Authors:  Jared R Kohler; David J Cutler
Journal:  Am J Hum Genet       Date:  2007-08-14       Impact factor: 11.025

Review 8.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

9.  Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis.

Authors:  Tie-Lin Yang; Xiang-Ding Chen; Yan Guo; Shu-Feng Lei; Jin-Tang Wang; Qi Zhou; Feng Pan; Yuan Chen; Zhi-Xin Zhang; Shan-Shan Dong; Xiang-Hong Xu; Han Yan; Xiaogang Liu; Chuan Qiu; Xue-Zhen Zhu; Teng Chen; Meng Li; Hong Zhang; Liang Zhang; Betty M Drees; James J Hamilton; Christopher J Papasian; Robert R Recker; Xiao-Ping Song; Jing Cheng; Hong-Wen Deng
Journal:  Am J Hum Genet       Date:  2008-11-06       Impact factor: 11.025

10.  Lgals6, a 2-million-year-old gene in mice: a case of positive Darwinian selection and presence/absence polymorphism.

Authors:  Denis Houzelstein; Isabelle R Gonçalves; Annie Orth; François Bonhomme; Pierre Netter
Journal:  Genetics       Date:  2008-03       Impact factor: 4.562

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