R
Richard K. Wilson
Researcher at Nationwide Children's Hospital
Publications - 501
Citations - 294778
Richard K. Wilson is an academic researcher from Nationwide Children's Hospital. The author has contributed to research in topics: Genome & Gene. The author has an hindex of 173, co-authored 463 publications receiving 260000 citations. Previous affiliations of Richard K. Wilson include University of Washington & St. Jude Children's Research Hospital.
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Journal ArticleDOI
Integrated and sequence-ordered BAC- and YAC-based physical maps for the rat genome
Martin Krzywinski,John W. Wallis,Claudia Gosele,Claudia Gosele,Ian Bosdet,Readman Chiu,Tina Graves,Oliver Hummel,Dan Layman,Carrie Mathewson,Natasja Wye,Baoli Zhu,Derek Albracht,Jennifer Asano,Sarah Barber,Mabel Brown-John,Susanna Chan,Steve Chand,Alison Cloutier,Jonathon Davito,Chris Fjell,Tony Gaige,Detlev Ganten,Noreen Girn,Kurtis Guggenheimer,Heinz Himmelbauer,Thomas Kreitler,Thomas Kreitler,Stephen Leach,Darlene Lee,Hans Lehrach,Michael Mayo,Kelly Mead,Teika Olson,Pawan Pandoh,Anna Liisa Prabhu,Heesun Shin,Simone Tänzer,Jason Thompson,Miranda Tsai,Jason Walker,George S. Yang,Mandeep Sekhon,LaDeana W. Hillier,Heike Zimdahl,Heike Zimdahl,Andre Marziali,Kazutoyo Osoegawa,Shaying Zhao,Asim Sarosh Siddiqui,Pieter J. de Jong,Wes Warren,Elaine R. Mardis,John Douglas Mcpherson,Richard K. Wilson,Norbert Hubner,Steven J.M. Jones,Marco A. Marra,Jacqueline E. Schein +58 more
TL;DR: The fingerprint map is a high-resolution integrative data resource that provides genome-ordered associations among BAC, YAC, and PAC clones and the assembled sequence of the rat genome.
Book ChapterDOI
Massively Parallel Sequencing Approaches for Characterization of Structural Variation
TL;DR: Methods and software algorithms that have been developed to detect SVs and copy number changes using massively parallel sequencing data are presented and visualization and de novo assembly strategies for characterizing SV breakpoints and removing false positives are described.
Journal ArticleDOI
A transposon-based strategy for sequencing repetitive DNA in eukaryotic genomes.
TL;DR: A strategy to efficiently and accurately sequence repetitive DNA in the nematode Caenorhabditis elegans using integrated artificial transposons and automated fluorescent sequencing and a website database to track and cross-reference transposon-like repetitive elements is established.
Journal ArticleDOI
A non-human primate system for large-scale genetic studies of complex traits
Anna J. Jasinska,Michelle K. Lin,Michelle K. Lin,Oi-Wa Choi,Joseph DeYoung,Olivera Grujic,Sit-yee Kong,Yoon Jung,Mathew J. Jorgensen,Lynn A. Fairbanks,Trudy R. Turner,Rita M. Cantor,Jessica Wasserscheid,Jessica Wasserscheid,Ken Dewar,Ken Dewar,Wesley C. Warren,Richard K. Wilson,George M. Weinstock,J. David Jentsch,Nelson B. Freimer +20 more
TL;DR: The value of pedigree and population samples of the Caribbean vervet for linkage and association mapping studies of quantitative traits and the imminent whole genome sequencing of many of these vervet samples will enhance the power of such investigations by providing a comprehensive catalog of genetic variation.
Journal ArticleDOI
The Contribution of GWAS Loci in Familial Dyslipidemias.
Pietari Ripatti,Joel T. Rämö,Joel T. Rämö,Joel T. Rämö,Sanni Söderlund,Ida Surakka,Niina Matikainen,Matti Pirinen,Päivi Pajukanta,Antti-Pekka Sarin,Antti-Pekka Sarin,Pirkka-Pekka Laurila,Pirkka-Pekka Laurila,Christian Ehnholm,Veikko Salomaa,Richard K. Wilson,Aarno Palotie,Nelson B. Freimer,Marja-Riitta Taskinen,Samuli Ripatti,Samuli Ripatti +20 more
TL;DR: Familial combined hyperlipidemia is highly polygenic, supporting the hypothesis that variants across the whole allele frequency spectrum contribute to this complex familial trait.