Literature DB >> 17495918

Completing the map of human genetic variation.

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.   

Abstract

Entities:  

Mesh：

Year:  2007        PMID： 17495918      PMCID： PMC2685471          DOI： 10.1038/447161a

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


× No keyword cloud information.
  43 in total

1.  A haplotype map of the human genome.

Authors: 
Journal:  Nature       Date:  2005-10-27       Impact factor: 49.962

2.  Whole-genome patterns of common DNA variation in three human populations.

Authors:  David A Hinds; Laura L Stuve; Geoffrey B Nilsen; Eran Halperin; Eleazar Eskin; Dennis G Ballinger; Kelly A Frazer; David R Cox
Journal:  Science       Date:  2005-02-18       Impact factor: 47.728

3.  Fine-scale structural variation of the human genome.

Authors:  Eray Tuzun; Andrew J Sharp; Jeffrey A Bailey; Rajinder Kaul; V Anne Morrison; Lisa M Pertz; Eric Haugen; Hillary Hayden; Donna Albertson; Daniel Pinkel; Maynard V Olson; Evan E Eichler
Journal:  Nat Genet       Date:  2005-05-15       Impact factor: 38.330

4.  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

5.  A high-resolution survey of deletion polymorphism in the human genome.

Authors:  Donald F Conrad; T Daniel Andrews; Nigel P Carter; Matthew E Hurles; Jonathan K Pritchard
Journal:  Nat Genet       Date:  2005-12-04       Impact factor: 38.330

6.  Widening the spectrum of human genetic variation.

Authors:  Evan E Eichler
Journal:  Nat Genet       Date:  2006-01       Impact factor: 38.330

Review 7.  Structural variation in the human genome.

Authors:  Lars Feuk; Andrew R Carson; Stephen W Scherer
Journal:  Nat Rev Genet       Date:  2006-02       Impact factor: 53.242

8.  Common deletions and SNPs are in linkage disequilibrium in the human genome.

Authors:  David A Hinds; Andrew P Kloek; Michael Jen; Xiyin Chen; Kelly A Frazer
Journal:  Nat Genet       Date:  2005-12-04       Impact factor: 38.330

9.  The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility.

Authors:  Enrique Gonzalez; Hemant Kulkarni; Hector Bolivar; Andrea Mangano; Racquel Sanchez; Gabriel Catano; Robert J Nibbs; Barry I Freedman; Marlon P Quinones; Michael J Bamshad; Krishna K Murthy; Brad H Rovin; William Bradley; Robert A Clark; Stephanie A Anderson; Robert J O'connell; Brian K Agan; Seema S Ahuja; Rosa Bologna; Luisa Sen; Matthew J Dolan; Sunil K Ahuja
Journal:  Science       Date:  2005-01-06       Impact factor: 47.728

Review 10.  Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes.

Authors:  James R Lupski; Pawel Stankiewicz
Journal:  PLoS Genet       Date:  2005-12       Impact factor: 5.917
View more
  87 in total

Review 1.  Recent advances in understanding the role of nutrition in human genome evolution.

Authors:  Kaixiong Ye; Zhenglong Gu
Journal:  Adv Nutr       Date:  2011-11-03       Impact factor: 8.701

2.  Public data archives for genomic structural variation.

Authors:  Deanna M Church; Ilkka Lappalainen; Tam P Sneddon; Jonathan Hinton; Michael Maguire; John Lopez; John Garner; Justin Paschall; Michael DiCuccio; Eugene Yaschenko; Stephen W Scherer; Lars Feuk; Paul Flicek
Journal:  Nat Genet       Date:  2010-10       Impact factor: 38.330

3.  Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion.

Authors:  Ivon Cuscó; Roser Corominas; Mònica Bayés; Raquel Flores; Núria Rivera-Brugués; Victoria Campuzano; Luis A Pérez-Jurado
Journal:  Genome Res       Date:  2008-02-21       Impact factor: 9.043

4.  Scanning the human genome at kilobase resolution.

Authors:  Jun Chen; Yeong C Kim; Yong-Chul Jung; Zhenyu Xuan; Geoff Dworkin; Yanming Zhang; Michael Q Zhang; San Ming Wang
Journal:  Genome Res       Date:  2008-02-21       Impact factor: 9.043

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.  Extensive copy-number variation of the human olfactory receptor gene family.

Authors:  Janet M Young; Raelynn M Endicott; Sean S Parghi; Megan Walker; Jeffrey M Kidd; Barbara J Trask
Journal:  Am J Hum Genet       Date:  2008-08       Impact factor: 11.025

7.  Segmental copy number variation shapes tissue transcriptomes.

Authors:  Charlotte N Henrichsen; Nicolas Vinckenbosch; Sebastian Zöllner; Evelyne Chaignat; Sylvain Pradervand; Frédéric Schütz; Manuel Ruedi; Henrik Kaessmann; Alexandre Reymond
Journal:  Nat Genet       Date:  2009-03-08       Impact factor: 38.330

Review 8.  Mouse models in bone marrow transplantation and adoptive cellular therapy.

Authors:  Caroline Arber; Malcolm K Brenner; Pavan Reddy
Journal:  Semin Hematol       Date:  2013-06-11       Impact factor: 3.851

Review 9.  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

10.  Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes.

Authors:  Fereydoun Hormozdiari; Can Alkan; Evan E Eichler; S Cenk Sahinalp
Journal:  Genome Res       Date:  2009-05-15       Impact factor: 9.043
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.