R
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.
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Journal ArticleDOI
Evolution of symbiotic bacteria in the distal human intestine.
Jian Xu,Michael A. Mahowald,Ruth E. Ley,Catherine A. Lozupone,Micah Hamady,Eric C. Martens,Bernard Henrissat,Bernard Henrissat,Pedro M. Coutinho,Pedro M. Coutinho,Patrick Minx,P. Latreille,Holland S. Cordum,Andrew Van Brunt,Kyung-Ae Kim,Robert S. Fulton,Lucinda Fulton,Sandra W. Clifton,Richard K. Wilson,Robin D. Knight,Jeffrey I. Gordon +20 more
TL;DR: In this article, the authors examined how the intestinal environment affects microbial genome evolution and found that lateral gene transfer, mobile elements, and gene amplification have played important roles in affecting the ability of gut-dwelling Bacteroidetes to vary their cell surface, sense their environment, and harvest nutrient resources present in the distal intestine.
Journal ArticleDOI
Comparative and demographic analysis of orang-utan genomes.
Devin P. Locke,LaDeana W. Hillier,Wesley C. Warren,Kim C. Worley,Lynne V. Nazareth,Donna M. Muzny,Shiaw-Pyng Yang,Zhengyuan Wang,Asif T. Chinwalla,Patrick Minx,Makedonka Mitreva,Lisa Cook,Kim D. Delehaunty,Catrina Fronick,Heather Schmidt,Lucinda Fulton,Robert S. Fulton,Joanne O. Nelson,Vincent Magrini,Craig Pohl,Tina Graves,Chris Markovic,Andy Cree,Huyen Dinh,Jennifer Hume,Christie Kovar,Gerald R. Fowler,Gerton Lunter,Gerton Lunter,Stephen Meader,Andreas Heger,Chris P. Ponting,Tomas Marques-Bonet,Tomas Marques-Bonet,Can Alkan,Lin Chen,Ze Cheng,Jeffrey M. Kidd,Evan E. Eichler,Evan E. Eichler,Simon D. M. White,Stephen M. J. Searle,Albert J. Vilella,Yuan Chen,Paul Flicek,Jian Ma,Jian Ma,Brian J. Raney,Bernard B. Suh,Richard Burhans,Javier Herrero,David Haussler,Rui Faria,Rui Faria,Olga Fernando,Olga Fernando,Fleur Darré,Domènec Farré,Elodie Gazave,Meritxell Oliva,Arcadi Navarro,Roberta Roberto,Oronzo Capozzi,Nicoletta Archidiacono,Giuliano Della Valle,Stefania Purgato,Mariano Rocchi,Miriam K. Konkel,Jerilyn A. Walker,Brygg Ullmer,Mark A. Batzer,Arian F.A. Smit,Robert Hubley,Claudio Casola,Daniel R. Schrider,Matthew W. Hahn,Víctor Quesada,Xose S. Puente,Gonzalo R. Ordóñez,Carlos López-Otín,Tomas Vinar,Brona Brejova,Aakrosh Ratan,Robert S. Harris,Webb Miller,Carolin Kosiol,Heather A. Lawson,Vikas Taliwal,André L. Martins,Adam Siepel,Arindam RoyChoudhury,Xin Ma,Jeremiah D. Degenhardt,Carlos Bustamante,Ryan N. Gutenkunst,Thomas Mailund,Julien Y. Dutheil,Asger Hobolth,Mikkel H. Schierup,Oliver A. Ryder,Yuko Yoshinaga,Pieter J. de Jong,George M. Weinstock,Jeffrey Rogers,Elaine R. Mardis,Richard A. Gibbs,Richard K. Wilson +106 more
TL;DR: The orang-utan species, Pongo abelii and Pongo pygmaeus, are the most phylogenetically distant great apes from humans, thereby providing an informative perspective on hominid evolution and a primate polymorphic neocentromere, found in both Pongo species are described.
Journal ArticleDOI
Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes
Timothy A. Graubert,Dong Shen,Li Ding,Theresa Okeyo-Owuor,Cara L Lunn,Jin Shao,Kilannin Krysiak,Chris Harris,Daniel C. Koboldt,David E. Larson,Michael D. McLellan,David J. Dooling,Rachel Abbott,Robert S. Fulton,Heather Schmidt,Joelle Kalicki-Veizer,Michelle O'Laughlin,Marcus Grillot,Jack Baty,Sharon Heath,John L. Frater,Talat Nasim,Talat Nasim,Daniel C. Link,Michael H. Tomasson,Peter Westervelt,John F. DiPersio,Elaine R. Mardis,Timothy J. Ley,Richard K. Wilson,Matthew J. Walter +30 more
TL;DR: A missense mutation affecting the serine at codon 34 (Ser34) in U2AF1 was recurrently present in 13 out of 150 subjects with de novo MDS, and suggestive evidence of an increased risk of progression to sAML associated with this mutation is found.
Journal ArticleDOI
Recurrent DNMT3A mutations in patients with myelodysplastic syndromes
Matthew J. Walter,Li Ding,Dong Shen,Jin Shao,Marcus Grillot,Michael D. McLellan,Robert S. Fulton,Heather Schmidt,Joelle Kalicki-Veizer,Michelle O'Laughlin,Cyriac Kandoth,Jack Baty,Peter Westervelt,John F. DiPersio,Elaine R. Mardis,Richard K. Wilson,Timothy J. Ley,Timothy A. Graubert +17 more
TL;DR: DNMT3A mutations were expressed in the majority of cells in all tested mutant samples regardless of myeloblast counts, suggesting that DNMT3B mutations occur early in the course of MDS, and may have prognostic value in de novo MDS.
Journal ArticleDOI
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,Richard K. Wilson,David C. Page +29 more
TL;DR: It is proposed that beyond its roles in testis determination and spermatogenesis, the Y chromosome is essential for male viability, and has unappreciated roles in Turner’s syndrome and in phenotypic differences between the sexes in health and disease.