M
Michael Snyder
Researcher at Stanford University
Publications - 938
Citations - 150929
Michael Snyder is an academic researcher from Stanford University. The author has contributed to research in topics: Gene & Genome. The author has an hindex of 169, co-authored 840 publications receiving 130225 citations. Previous affiliations of Michael Snyder include Wyss Institute for Biologically Inspired Engineering & Public Health Research Institute.
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Journal ArticleDOI
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.
Elisavet Fotiou,Silvia Martin-Almedina,Michael A. Simpson,Shin Lin,Kristiana Gordon,Glen Brice,Giles Atton,Iona Jeffery,David C. Rees,Cyril Mignot,Julie Vogt,Tessa Homfray,Michael Snyder,Stanley G. Rockson,Steve Jeffery,Peter S. Mortimer,Sahar Mansour,Pia Ostergaard +17 more
TL;DR: Findings indicate that PIEZO1 is also involved in the development of lymphatic structures, and this work reports an autosomal recessive form of GLD with a high incidence of non-immune hydrops fetalis and childhood onset of facial and four limb lymphoedema.
A comparative encyclopedia of DNA elements in the mouse genome
Feng Yue,Feng Yue,Yong Cheng,Alessandra Breschi,Jeff Vierstra,Weisheng Wu,Weisheng Wu,Tyrone Ryba,Tyrone Ryba,Richard Sandstrom,Zhihai Ma,Carrie A. Davis,Benjamin D. Pope,Yin Shen,Dmitri D. Pervouchine,Sarah Djebali,Robert E. Thurman,Rajinder Kaul,Eric Rynes,Anthony Kirilusha,Georgi K. Marinov,Brian A. Williams,Diane Trout,Henry Amrhein,Katherine I. Fisher-Aylor,Igor Antoshechkin,Gilberto DeSalvo,Lei Hoon See,Meagan Fastuca,Jorg Drenkow,Chris Zaleski,Alexander Dobin,Pablo Prieto,Julien Lagarde,Giovanni Bussotti,Andrea Tanzer,Olgert Denas,Kanwei Li,M. A. Bender,M. A. Bender,Miaohua Zhang,Rachel Byron,Mark Groudine,Mark Groudine,David McCleary,Long Pham,Zhen Ye,Samantha Kuan,Lee Edsall,Yi-Chieh Wu,Matthew D. Rasmussen,Mukul S. Bansal,Manolis Kellis,Manolis Kellis,Cheryl A. Keller,Christapher S. Morrissey,Tejaswini Mishra,Deepti Jain,Nergiz Dogan,Robert S. Harris,Philip Cayting,Trupti Kawli,Alan P. Boyle,Alan P. Boyle,Ghia Euskirchen,Anshul Kundaje,Shin Lin,Yiing Lin,Camden Jansen,Venkat S. Malladi,Melissa S. Cline,Drew T. Erickson,Vanessa M. Kirkup,Katrina Learned,Cricket A. Sloan,Kate R. Rosenbloom,Beatriz Lacerda de Sousa,Kathryn Beal,Miguel Pignatelli,Paul Flicek,Jin Lian,Tamer Kahveci,Dongwon Lee,W. James Kent,Miguel Santos,Javier Herrero,Cedric Notredame,Audra K. Johnson,Shinny Vong,Kristen Lee,Daniel Bates,Fidencio Neri,Morgan Diegel,Theresa K. Canfield,Peter J. Sabo,Matthew S. Wilken,Thomas A. Reh,Erika Giste,Anthony Shafer,Tanya Kutyavin,Eric Haugen,Douglas Dunn,Alex Reynolds,Shane Neph,Richard Humbert,R. Scott Hansen,Marella F. T. R. de Bruijn,Licia Selleri,Alexander Y. Rudensky,Steven Z. Josefowicz,Robert M. Samstein,Evan E. Eichler,Stuart H. Orkin,Dana N. Levasseur,Thalia Papayannopoulou,Kai Hsin Chang,Arthur I. Skoultchi,Srikanta Gosh,Christine M. Disteche,Piper M. Treuting,Yanli Wang,Mitchell J. Weiss,Gerd A. Blobel,Xiaoyi Cao,Sheng Zhong,Ting Wang,Peter J. Good,Rebecca F. Lowdon,Rebecca F. Lowdon,Leslie B. Adams,Leslie B. Adams,Xiao Qiao Zhou,Michael J. Pazin,Elise A. Feingold,Barbara J. Wold,James Taylor,Ali Mortazavi,Sherman M. Weissman,John A. Stamatoyannopoulos,Michael Snyder,Roderic Guigó,Thomas R. Gingeras,David M. Gilbert,Ross C. Hardison,Michael A. Beer,Bing Ren +145 more
TL;DR: By comparing with the human genome, this work not only confirms substantial conservation in the newly annotated potential functional sequences, but also finds a large degree of divergence of sequences involved in transcriptional regulation, chromatin state and higher order chromatin organization.
Journal ArticleDOI
Genomic analysis of mycosis fungoides and Sézary syndrome identifies recurrent alterations in TNFR2
Alexander Ungewickell,Aparna Bhaduri,Eon J. Rios,Jason A. Reuter,Carolyn S. Lee,Angela Mah,Ashley M. Zehnder,Robert S. Ohgami,Shashikant Kulkarni,Randall Armstrong,Wen-Kai Weng,Dita Gratzinger,Mahkam Tavallaee,Alain H. Rook,Michael Snyder,Youn H. Kim,Paul A. Khavari,Paul A. Khavari +17 more
TL;DR: Recurrent point mutations and genomic gains of TNFRSF1B, encoding the tumor necrosis factor receptor TNFR2, are reported in 18% of patients with mycosis fungoides and Sézary syndrome, finding a recurrent CTLA4-CD28 fusion, as well as mutations in downstream signaling mediators of these receptors.
Journal ArticleDOI
Sequencing Y Chromosomes Resolves Discrepancy in Time to Common Ancestor of Males Versus Females
G. David Poznik,Brenna M. Henn,Brenna M. Henn,Muh Ching Yee,Elzbieta Sliwerska,Ghia Euskirchen,Alice A. Lin,Michael Snyder,Lluis Quintana-Murci,Lluis Quintana-Murci,Jeffrey M. Kidd,Jeffrey M. Kidd,Peter A. Underhill,Carlos Bustamante +13 more
TL;DR: The findings suggest that, contrary to previous claims, male lineages do not coalesce significantly more recently than female lineages.
Journal ArticleDOI
Mapping accessible chromatin regions using Sono-Seq
Raymond K. Auerbach,Ghia Euskirchen,Joel Rozowsky,Nathan Lamarre-Vincent,Zarmik Moqtaderi,Philippe Lefrançois,Kevin Struhl,Mark Gerstein,Michael Snyder +8 more
TL;DR: The results demonstrate that Sono-Seq can be a useful and simple method by which to map many local alterations in chromatin structure and provide insights into the mapping of binding sites by using ChIP–Seq experiments and the value of reference samples that should be used in such experiments.