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
Multiple Long-Read Sequencing Survey of Herpes Simplex Virus Dynamic Transcriptome.
Dóra Tombácz,Norbert Moldován,Zsolt Balázs,Gábor Gulyás,Zsolt Csabai,Miklós Boldogkői,Michael Snyder,Zsolt Boldogkői +7 more
TL;DR: Overall, the results demonstrated that the HSV-1 transcripts form an extremely complex pattern of overlaps, and that entire viral genome is transcriptionally active.
Posted ContentDOI
Deep learning-based detection of COVID-19 using wearables data
Gireesh K. Bogu,Michael Snyder +1 more
TL;DR: In this article, a deep learning approach based on a Long Short-Term Memory Networks-based autoencoder, called LAAD, was developed to predict COVID-19 infection by detecting abnormal resting heart rate in test data relative to the user baseline.
Journal ArticleDOI
Statins Are Associated With Increased Insulin Resistance and Secretion.
Fahim Abbasi,Cindy Lamendola,Cindy Lamendola,Chelsea S. Harris,Chelsea S. Harris,Vander Harris,Vander Harris,Ming-Shian Tsai,Ming-Shian Tsai,Pragya Tripathi,Pragya Tripathi,Fakhar Abbas,Fakhar Abbas,Gerald M. Reaven,Gerald M. Reaven,Peter D. Reaven,Michael Snyder,Michael Snyder,Sun H. Kim,Joshua W. Knowles +19 more
TL;DR: In this paper, the authors conducted an open-label clinical trial of atorvastatin 40 mg daily in adults without known atherosclerotic cardiovascular disease or type 2 diabetes at baseline.
Journal ArticleDOI
Large-scale mutagenesis: yeast genetics in the genome era.
Susana Vidan,Michael Snyder +1 more
TL;DR: The completion of the DNA sequence of the budding yeast Saccharomyces cerevisiae resulted in the identification of a large number of genes, but the function of most of these genes is not known.
Journal ArticleDOI
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss
Rajini R Haraksingh,Fereshteh Jahanbani,Juan Rodriguez-Paris,Joel Gelernter,Kari C. Nadeau,John S. Oghalai,Iris Schrijver,Michael Snyder +7 more
TL;DR: It is concluded that many known as well as novel loci and distinct types of mutations not typically tested in clinical settings can contribute to the etiology of hearing loss.