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Reduced purifying selection prevails over positive selection in human copy number variant evolution

pengarang

Chris Ponting

Caleb Webber

Joris A Veltman

Rolph Pfundt

diterbitkan dalam: Genome Research

tanggal publikasi: 2008-11

bahasa: Inggris

Cites articles 81

Date

Judul

Pengarang

2008-04-25

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

Evan E. Eichler, Mary-Claire King, Anjene M. Addington, Alex S Nord, Jonathan Sebat, Tom Walsh, Sean Davis, Nitin Gogtay, Andrew Singleton, Robert L Findling, Judith L. Rapoport
2007-10

Diet and the evolution of human amylase gene copy number variation

Nathaniel Dominy, Richard Redon, Anne Stone, Katrina G Claw
2007-04-20

Strong association of de novo copy number mutations with autism

Michael Wigler, Daniel Geschwind, Terho Lehtimäki, Mary-Claire King, Jonathan Sebat, Tom Walsh, James S. Sutcliffe, Peter K. Gregersen, Dorothy Warburton, David H. Ledbetter
2007-02-28

Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysis

Adrianus Henricus Maria Geurts van Kessel, Joris A Veltman
2007-12-23

The Mouse Genome Database (MGD): mouse biology and model systems

Judith A. Blake, Carol J Bult
2007-12-02

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders
2007-12-04

A portrait of copy-number polymorphism in Drosophila melanogaster
2007-10-11

OPTIC: orthologous and paralogous transcripts in clades

Andreas Heger, Chris Ponting
2007-07-01

Mutational and selective effects on copy-number variants in the human genome

Deborah A Nickerson, Evan E. Eichler
2007-01-01

Reduced efficacy of selection in regions of the Drosophila genome that lack crossing over

Brian Charlesworth
2007-01-01

Variation of CNV distribution in five different ethnic populations.

Lisenka Vissers, Esther van de Vosse
2006-11-23

Global variation in copy number in the human genome

Xavier Estivill i Pallejà, Chris Tyler-Smith, Mònica Gratacòs, Daisuke Komura, Richard Redon, Juan R. González, Stephen W. Scherer, Armand Valsesia, Jeffrey R MacDonald, Lars Feuk, Jennifer L Freeman, Tatiana Zerjal, Hiroyuki Aburatani, Matthew Hurles, Donald F Conrad, Nigel Carter
2006-11

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

Kristel Sleegers, Christine Van Broeckhoven, Cornelia M. van Duijn, Ilse Gijselinck, Jessie Theuns, Dirk Goossens, Nathalie Brouwers
2006-09

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

Alan Pittman, Carla Rosenberg, Andrew John Lees, Helen V. Firth
2006-02-17

Bias of selection on human copy-number variants

Chris Ponting
2006-02

Structural variation in the human genome

Stephen W. Scherer, Lars Feuk
2006-01-01

The UCSC Genome Browser Database: update 2006

Angie S. Hinrichs, Terrence S. Furey, Jakob Skou Pedersen, Adam C. Siepel
2006-01-01

Ensembl 2006

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2006-12-05

A comprehensive analysis of common copy-number variations in the human genome

Carolyn J. Brown, Calum E MacAulay, Evan E. Eichler
2006-09-26

A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination

Sarah J. Lindsay, James R. Lupski
2006-09-01

Phylogenetic reconstruction of orthology, paralogy, and conserved synteny for dog and human

Chris Ponting
2006-08-05

A new perspective on isochore evolution

Adam Eyre-Walker, Laurent Duret
2006-08-13

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism

Lisenka Vissers, Samantha J.L. Knight, Frank Kooy, Corrado Romano, Marco Fichera, Erik Sistermans, Joris A Veltman, Han G. Brunner, Adrianus Henricus Maria Geurts van Kessel, Rolph Pfundt, David A Koolen, Nicole de Leeuw, Nine V. A. M. Knoers, Regina Regan, Britt-Marie Anderlid, Edwin Reyniers, Albert Schinzel, Alessandra Baumer, Jacqueline Schoumans, Bert B A de Vries
2006-08-13

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

Peggy S Eis, Evan E. Eichler
2006-01-01

Structural variation of the human genome

Evan E. Eichler
2006-04-10

A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications

Mario Ventura, Mariano Rocchi, NISC Comparative Sequencing Program, Eric D. Green, Evan E. Eichler
2006-02-01

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

Timothy Vyse, Enrico Petretto, Penny J Norsworthy, Tim Aitman, Matthew David John Hodges
2006-01-01

Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation.

Wei Chen, Vera M. Kalscheuer
2006-03-01

Identification of frequent chromosome copy-number polymorphisms by use of high-resolution single-nucleotide-polymorphism arrays

Kari Hemminki, Barbara Burwinkel, Michael Wirtenberger
2006-01-01

Common deletion polymorphisms in the human genome.

Steven A McCarroll, David Altshuler, Pardis Sabeti, Mark Joseph Daly, Stacey Gabriel, Michael C. Zody, Jeffrey C Barrett
2006-04-28

GC content evolution of the human and mouse genomes: insights from the study of processed pseudogenes in regions of different recombination rates

Laurent Duret
2006-11-01

Human genomics: in search of normality

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