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
Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome
Majesta O'Bleness,Veronica B. Searles,C. Michael Dickens,David P. Astling,Derek Albracht,Angel C.Y. Mak,Yvonne Y. Y. Lai,Chin Lin,Catherine Chu,Tina Graves,Pui-Yan Kwok,Richard K. Wilson,James M. Sikela +12 more
TL;DR: The corrected sequence identified a recent segmental duplication that added 20 additional DUF1220 copies to the human genome, and may have facilitated the chromosome 1 pericentric inversion that is among the most notable human-specific genomic landmarks.
Journal ArticleDOI
Detailed analysis of a contiguous 22-Mb region of the maize genome.
Fusheng Wei,Joshua C. Stein,Chengzhi Liang,Jianwei Zhang,Robert S. Fulton,Regina S. Baucom,Emanuele De Paoli,Shiguo Zhou,Lixing Yang,Yujun Han,Shiran Pasternak,Apurva Narechania,Lifang Zhang,Cheng Ting Yeh,Kai Ying,Dawn H. Nagel,Kristi Collura,David Kudrna,Jennifer Currie,Jinke Lin,Hyeran Kim,Angelina Angelova,Gabriel Scara,Marina Wissotski,Wolfgang Golser,Laura Courtney,Scott Kruchowski,Tina Graves,Susan M. Rock,Stephanie Adams,Lucinda Fulton,Catrina Fronick,William Courtney,Melissa Kramer,Lori Spiegel,Lydia Nascimento,Ananth Kalyanaraman,Cristian Chaparro,Jean-Marc Deragon,Phillip San Miguel,Ning Jiang,Susan R. Wessler,Pamela J. Green,Yeisoo Yu,David C. Schwartz,Blake C. Meyers,Jeffrey L. Bennetzen,Robert A. Martienssen,W. Richard McCombie,Srinivas Aluru,Sandra W. Clifton,Patrick S. Schnable,Doreen Ware,Richard K. Wilson,Rod A. Wing +54 more
TL;DR: The results demonstrate the feasibility of refining the B73 RefGen_v1 genome assembly by incorporating optical map, high-resolution genetic map, and comparative genomic data sets and improvements in gene and repeat annotation will serve to promote future functional genomic and phylogenomic research in maize and other grasses.
Journal ArticleDOI
Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits
Yu S. Huang,Yu S. Huang,Vasily Ramensky,Anna J. Jasinska,Anna J. Jasinska,Yoon Jung,Oi Wa Choi,Rita M. Cantor,Nikoleta Juretic,Jessica Wasserscheid,Jay R. Kaplan,Matthew J. Jorgensen,Thomas D. Dyer,Ken Dewar,John Blangero,Richard K. Wilson,Wesley C. Warren,George M. Weinstock,Nelson B. Freimer +18 more
TL;DR: The first genome-wide high-resolution polymorphism resource for non-human primate association and linkage studies, constructed for the Caribbean-origin vervet monkey, or African green monkey, is reported.
Journal ArticleDOI
A dominant mutation in hexokinase 1 (HK1) causes retinitis pigmentosa.
Lori S. Sullivan,Daniel C. Koboldt,Sara J. Bowne,Steven Lang,Susan H. Blanton,Elizabeth Cadena,Cheryl E. Avery,Richard A. Lewis,Kaylie Webb-Jones,Dianna K H Wheaton,David G. Birch,Razck Coussa,Huanan Ren,Irma Lopez,Christina Chakarova,Robert K. Koenekoop,Charles A. Garcia,Robert S. Fulton,Richard K. Wilson,George M. Weinstock,Stephen P. Daiger +20 more
TL;DR: It is hypothesized that the effect of this mutation is limited to the retina, as no systemic abnormalities in glycolysis were detected and the whole-exome next-generation sequencing identified an HK1 mutation in five adRP families.
Journal ArticleDOI
Somatic Mutations of PIK3R1 Promote Gliomagenesis
Steven N. Quayle,Jennifer Y. Lee,Lydia W.T. Cheung,Li Ding,Ruprecht Wiedemeyer,Robert W. Dewan,Emmet Huang-Hobbs,Li Zhuang,Richard K. Wilson,Keith L. Ligon,Gordon B. Mills,Lewis C. Cantley,Lynda Chin +12 more
TL;DR: Introducing a subset of the mutations identified in human GBM, in the nSH2 and iSH2 domains, increases signaling through the PI3K pathway and promotes tumorigenesis of primary normal human astrocytes in an orthotopic xenograft model, suggesting that GBM patients whose tumors carry mutant PIK3R1 alleles may benefit from treatment with inhibitors of AKT.