Literature DB >> 17597779

The population genetics of structural variation.

Donald F Conrad1, Matthew E Hurles.   

Abstract

Population genetics is central to our understanding of human variation, and by linking medical and evolutionary themes, it enables us to understand the origins and impacts of our genomic differences. Despite current limitations in our knowledge of the locations, sizes and mutational origins of structural variants, our characterization of their population genetics is developing apace, bringing new insights into recent human adaptation, genome biology and disease. We summarize recent dramatic advances, describe the diverse mutational origins of chromosomal rearrangements and argue that their complexity necessitates a re-evaluation of existing population genetic methods.

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Year:  2007        PMID: 17597779      PMCID: PMC2716079          DOI: 10.1038/ng2042

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  74 in total

Review 1.  Adjusting the focus on human variation.

Authors:  M Przeworski; R R Hudson; A Di Rienzo
Journal:  Trends Genet       Date:  2000-07       Impact factor: 11.639

2.  Inference of population structure using multilocus genotype data.

Authors:  J K Pritchard; M Stephens; P Donnelly
Journal:  Genetics       Date:  2000-06       Impact factor: 4.562

3.  Are rare variants responsible for susceptibility to complex diseases?

Authors:  J K Pritchard
Journal:  Am J Hum Genet       Date:  2001-06-12       Impact factor: 11.025

Review 4.  Molecular mechanisms for constitutional chromosomal rearrangements in humans.

Authors:  L G Shaffer; J R Lupski
Journal:  Annu Rev Genet       Date:  2000       Impact factor: 16.830

5.  De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.

Authors:  D Warburton
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

6.  High frequencies of alpha-thalassaemia are the result of natural selection by malaria.

Authors:  J Flint; A V Hill; D K Bowden; S J Oppenheimer; P R Sill; S W Serjeantson; J Bana-Koiri; K Bhatia; M P Alpers; A J Boyce
Journal:  Nature       Date:  1986 Jun 19-25       Impact factor: 49.962

7.  Allele frequencies at microsatellite loci: the stepwise mutation model revisited.

Authors:  A M Valdes; M Slatkin; N B Freimer
Journal:  Genetics       Date:  1993-03       Impact factor: 4.562

8.  Unequal exchange at the Charcot-Marie-Tooth disease type 1A recombination hot-spot is not elevated above the genome average rate.

Authors:  L L Han; M P Keller; W Navidi; P F Chance; N Arnheim
Journal:  Hum Mol Genet       Date:  2000-07-22       Impact factor: 6.150

9.  High resolution of human evolutionary trees with polymorphic microsatellites.

Authors:  A M Bowcock; A Ruiz-Linares; J Tomfohrde; E Minch; J R Kidd; L L Cavalli-Sforza
Journal:  Nature       Date:  1994-03-31       Impact factor: 49.962

10.  A novel human DNA polymorphism resulting from transfer of DNA from chromosome 6 to chromosome 16.

Authors:  Z Wong; N J Royle; A J Jeffreys
Journal:  Genomics       Date:  1990-06       Impact factor: 5.736

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  93 in total

1.  Natural selection and the distribution of identity-by-descent in the human genome.

Authors:  Anders Albrechtsen; Ida Moltke; Rasmus Nielsen
Journal:  Genetics       Date:  2010-06-30       Impact factor: 4.562

Review 2.  From microscopes to microarrays: dissecting recurrent chromosomal rearrangements.

Authors:  Beverly S Emanuel; Sulagna C Saitta
Journal:  Nat Rev Genet       Date:  2007-11       Impact factor: 53.242

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.  An algorithm for inferring complex haplotypes in a region of copy-number variation.

Authors:  Mamoru Kato; Yusuke Nakamura; Tatsuhiko Tsunoda
Journal:  Am J Hum Genet       Date:  2008-07-17       Impact factor: 11.025

5.  Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history.

Authors:  Philip M Kim; Hugo Y K Lam; Alexander E Urban; Jan O Korbel; Jason Affourtit; Fabian Grubert; Xueying Chen; Sherman Weissman; Michael Snyder; Mark B Gerstein
Journal:  Genome Res       Date:  2008-10-08       Impact factor: 9.043

Review 6.  African genetic diversity: implications for human demographic history, modern human origins, and complex disease mapping.

Authors:  Michael C Campbell; Sarah A Tishkoff
Journal:  Annu Rev Genomics Hum Genet       Date:  2008       Impact factor: 8.929

7.  Lower linkage disequilibrium at CNVs is due to both recurrent mutation and transposing duplications.

Authors:  Daniel R Schrider; Matthew W Hahn
Journal:  Mol Biol Evol       Date:  2010-01       Impact factor: 16.240

Review 8.  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

9.  Microbial variome database: point mutations, adaptive or not, in bacterial core genomes.

Authors:  Sujay Chattopadhyay; Fred Taub; Sandip Paul; Scott J Weissman; Evgeni V Sokurenko
Journal:  Mol Biol Evol       Date:  2013-03-14       Impact factor: 16.240

Review 10.  Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis.

Authors:  Iuliana Ionita-Laza; Angela J Rogers; Christoph Lange; Benjamin A Raby; Charles Lee
Journal:  Genomics       Date:  2008-10-19       Impact factor: 5.736

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