Literature DB >> 16391945

Large-scale characterization of public database SNPs causing non-synonymous changes in three ethnic groups.

James Ireland1, Victoria E H Carlton, Matthew Falkowski, Martin Moorhead, Karen Tran, Francisco Useche, Paul Hardenbol, Ayca Erbilgin, Ron Fitzgerald, Thomas D Willis, Malek Faham.   

Abstract

Single nucleotide polymorphisms (SNPs) that lead to non-synonymous changes in proteins may have functional effects and be subject to selection. Hence they are of particular interest in the study of genetic diseases. We have genotyped approximately 28,000 such SNPs in three ethnic populations (the HapMap plates) and ten primate species and analyzed these data for evidence of selection. We find SNPs predicted by PolyPhen to be damaging, have lower allele frequencies, and are particularly likely to be population-specific. We have also grouped SNPs by molecular function or biological process of the associated genes and find evidence that selection may be acting in concert on classes of genes.

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Year:  2005        PMID: 16391945     DOI: 10.1007/s00439-005-0105-x

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  39 in total

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2.  Multiplexed genotyping with sequence-tagged molecular inversion probes.

Authors:  Paul Hardenbol; Johan Banér; Maneesh Jain; Mats Nilsson; Eugeni A Namsaraev; George A Karlin-Neumann; Hossein Fakhrai-Rad; Mostafa Ronaghi; Thomas D Willis; Ulf Landegren; Ronald W Davis
Journal:  Nat Biotechnol       Date:  2003-05-05       Impact factor: 54.908

3.  Analysis of CARD15 polymorphisms in Korean patients with ankylosing spondylitis reveals absence of common variants seen in western populations.

Authors:  Tae-Hwan Kim; Proton Rahman; Jae-Bum Jun; Hye-Soon Lee; Yong-Wook Park; Ho Joon Im; Tara Snelgrove; Lynette Peddle; David Hallett; Robert D Inman
Journal:  J Rheumatol       Date:  2004-10       Impact factor: 4.666

4.  Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays.

Authors:  Malek Faham; Jianbiao Zheng; Martin Moorhead; Hossein Fakhrai-Rad; Eugeni Namsaraev; Kee Wong; Zhiyong Wang; Shu G Chow; Liana Lee; Kent Suyenaga; Jennifer Reichert; Andrew Boudreau; James Eberle; Carsten Bruckner; Maneesh Jain; George Karlin-Neumann; Hywel B Jones; Thomas D Willis; Joseph D Buxbaum; Ronald W Davis
Journal:  Proc Natl Acad Sci U S A       Date:  2005-10-03       Impact factor: 11.205

5.  Global distribution of the CCR5 gene 32-basepair deletion.

Authors:  J J Martinson; N H Chapman; D C Rees; Y T Liu; J B Clegg
Journal:  Nat Genet       Date:  1997-05       Impact factor: 38.330

6.  Complement factor H polymorphism and age-related macular degeneration.

Authors:  Albert O Edwards; Robert Ritter; Kenneth J Abel; Alisa Manning; Carolien Panhuysen; Lindsay A Farrer
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7.  CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease.

Authors:  Suzanne Lesage; Habib Zouali; Jean-Pierre Cézard; Jean-Frédéric Colombel; Jacques Belaiche; Sven Almer; Curt Tysk; Colm O'Morain; Miquel Gassull; Vibeke Binder; Yigael Finkel; Robert Modigliani; Corinne Gower-Rousseau; Jeanne Macry; Françoise Merlin; Mathias Chamaillard; Anne-Sophie Jannot; Gilles Thomas; Jean-Pierre Hugot
Journal:  Am J Hum Genet       Date:  2002-03-01       Impact factor: 11.025

Review 8.  Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease.

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Journal:  Am J Hum Genet       Date:  2004-06-18       Impact factor: 11.025

10.  Natural selection on the olfactory receptor gene family in humans and chimpanzees.

Authors:  Yoav Gilad; Carlos D Bustamante; Doron Lancet; Svante Pääbo
Journal:  Am J Hum Genet       Date:  2003-08-07       Impact factor: 11.025

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  6 in total

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Review 2.  Functional single nucleotide polymorphism-based association studies.

Authors:  Victoria E H Carlton; James S Ireland; Francisco Useche; Malek Faham
Journal:  Hum Genomics       Date:  2006-06       Impact factor: 4.639

3.  Genetic variants in major histocompatibility complex-linked genes associate with pediatric liver transplant rejection.

Authors:  Rakesh Sindhi; Brandon W Higgs; Daniel E Weeks; Chethan Ashokkumar; Ronald Jaffe; Cecilia Kim; Patrick Wilson; Nydia Chien; Joseph Glessner; Anjan Talukdar; George Mazariegos; M Michael Barmada; Edward Frackleton; Nancy Petro; Andrew Eckert; Hakon Hakonarson; Robert Ferrell
Journal:  Gastroenterology       Date:  2008-06-03       Impact factor: 22.682

4.  Replication study of SNP associations for colorectal cancer in Hong Kong Chinese.

Authors:  J W Ho; S-c Choi; Y-f Lee; T C Hui; S S Cherny; M-M Garcia-Barceló; L Carvajal-Carmona; R Liu; S-h To; T-k Yau; C C Chung; C C Yau; S M Hui; P Y Lau; C-h Yuen; Y-w Wong; S Ho; S S Fung; I P Tomlinson; R S Houlston; K K Cheng; P C Sham
Journal:  Br J Cancer       Date:  2010-12-21       Impact factor: 7.640

5.  Risk of eighteen genome-wide association study-identified genetic variants for colorectal cancer and colorectal adenoma in Han Chinese.

Authors:  Chunwen Tan; Wangxiong Hu; Yanqin Huang; Jiaojiao Zhou; Shu Zheng
Journal:  Oncotarget       Date:  2016-11-22

6.  An association-adjusted consensus deleterious scheme to classify homozygous Mis-sense mutations for personal genome interpretation.

Authors:  Thanawadee Preeprem; Greg Gibson
Journal:  BioData Min       Date:  2013-12-23       Impact factor: 2.522

  6 in total

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