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Robert S. Fulton
Researcher at Washington University in St. Louis
Publications - 254
Citations - 167513
Robert S. Fulton is an academic researcher from Washington University in St. Louis. The author has contributed to research in topics: Genome & Gene. The author has an hindex of 109, co-authored 230 publications receiving 143530 citations. Previous affiliations of Robert S. Fulton include University of Washington & Brown University.
Papers
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Journal ArticleDOI
Corrigendum: Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators
Daniel W. Bellott,Jennifer F. Hughes,Helen Skaletsky,Laura G. Brown,Tatyana Pyntikova,Ting-Jan Cho,Natalia Koutseva,Sara Zaghlul,Tina Graves,Susie Rock,Colin Kremitzki,Robert S. Fulton,Shannon Dugan,Yan Ding,Donna Morton,Ziad Khan,Lora Lewis,Christian J. Buhay,Qiaoyan Wang,Jennifer Watt,Michael Holder,Sandy Lee,Lynne V. Nazareth,Jessica Alföldi,Steve Rozen,Donna M. Muzny,Wesley C. Warren,Richard A. Gibbs,Rick K. Wilson,David C. Page +29 more
TL;DR: This corrects the article to show that the method used to derive the H2O2 “spatially aggregating force” is based on a two-step process, not a single step, like in the previous version of this paper.
Posted ContentDOI
A domestic cat whole exome sequencing resource for trait discovery
Alana R. Rodney,Reuben M. Buckley,Robert S. Fulton,Catrina Fronick,Todd Richmond,Christopher R Helps,Peter Pantke,Dianne J. Trent,Leslie A. Lyons,Wesley C. Warren +9 more
TL;DR: The results show the discovery potential of deep exome sequencing to validate existing disease gene models and identify novel gene candidate alleles for many common and rare diseases in cats.
Journal ArticleDOI
Precise breakpoint detection in a patient with 9p- syndrome.
Jeffrey K. Ng,Eleanor I Sams,Dustin Baldridge,Milinn Kremitzki,Daniel J. Wegner,Tina A. Graves Lindsay,Robert S. Fulton,F. Sessions Cole,Tychele N. Turner +8 more
TL;DR: The results indicate that clinical genomic assessment of individuals with complex karyotypes can be refined to a single-base-pair resolution when utilizing Bionano and 10× Genomics sequencing.
Journal ArticleDOI
Clonal Evolution Revealed by Whole Genome Sequencing in a Case of Primary Myelofibrosis Transformed to Secondary Acute Myeloid Leukemia
Daniel A.C. Fisher,Christopher A. Miller,Michael D. McLellan,Robert S. Fulton,Katherine L. Martin,Charu Kaiwar,Deborah M. Moore,Timothy J. Ley,Stephen T. Oh +8 more
TL;DR: The findings suggest that transformation to sAML in this patient was largely driven by the combination of mutations in ASXL1, IDH1, and RUNX1, with possible contribution from a small number of additional mutations.
Journal ArticleDOI
No evidence that G6PD deficiency affects the efficacy or safety of daunorubicin in acute lymphoblastic leukemia induction therapy.
Katherine M. Robinson,Wenjian Yang,Seth E. Karol,Nancy Kornegay,Dennis W. Jay,Cheng Cheng,John K. Choi,Dario Campana,Ching-Hon Pui,Brent L. Wood,Michael J. Borowitz,Julie M. Gastier-Foster,Eric C. Larsen,Naomi J. Winick,William L. Carroll,Mignon L. Loh,Elizabeth A. Raetz,Stephen P. Hunger,Meenakshi Devidas,Elaine R. Mardis,Robert S. Fulton,Mary V. Relling,Sima Jeha +22 more
TL;DR: Anthracyclines are used in induction therapy of pediatric acute lymphoblastic leukemia and are known to generate oxidative stress; whether this translates into enhanced antileukemic activity or hemolytic effects in patients with glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is unknown.