Michael P. Snyder

Department of Genetics, Stanford University

Research Area

Biography

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 7	2015

Other Publications

Article	Year
Microtubule capture by the cleavage apparatus is required for proper spindle positioning in yeast. Genes & development\| PubMed ID: 12101122	2002
Landscape of next-generation sequencing technologies. Analytical chemistry\| PubMed ID: 21612267	2011
A comprehensive map of mobile element insertion polymorphisms in humans. PLoS genetics\| PubMed ID: 21876680	2011
A core erythroid transcriptional network is repressed by a master regulator of myelo-lymphoid differentiation. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 22357756	2012
Correlation of Global MicroRNA Expression With Basal Cell Carcinoma Subtype. G3 (Bethesda, Md.)\| PubMed ID: 22384406	2012
Tcf7 is an important regulator of the switch of self-renewal and differentiation in a multipotential hematopoietic cell line. PLoS genetics\| PubMed ID: 22412390	2012
Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy. Science translational medicine\| PubMed ID: 22517884	2012
Extensive genetic variation in somatic human tissues. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 23043118	2012
SeqFold: genome-scale reconstruction of RNA secondary structure integrating high-throughput sequencing data. Genome research\| PubMed ID: 23064747	2013
Copy Number Variation detection from 1000 Genomes Project exon capture sequencing data. BMC bioinformatics\| PubMed ID: 23157288	2012
The variable somatic genome. Cell cycle (Georgetown, Tex.)\| PubMed ID: 23255102	2013
Two methods for full-length RNA sequencing for low quantities of cells and single cells. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 23267071	2013
High-throughput sequencing for biology and medicine. Molecular systems biology\| PubMed ID: 23340846	2013
Overview of high throughput sequencing technologies to elucidate molecular pathways in cardiovascular diseases. Circulation research\| PubMed ID: 23743227	2013
Functional genomic screen of human stem cell differentiation reveals pathways involved in neurodevelopment and neurodegeneration. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 23836664	2013
Impacts of variation in the human genome on gene regulation. Journal of molecular biology\| PubMed ID: 23871684	2013
Haplotype structure and positive selection at TLR1. European journal of human genetics : EJHG\| PubMed ID: 24002163	2014
Defective sphingosine 1-phosphate receptor 1 (S1P1) phosphorylation exacerbates TH17-mediated autoimmune neuroinflammation. Nature immunology\| PubMed ID: 24076635	2013
Specific plasma autoantibody reactivity in myelodysplastic syndromes. Scientific reports\| PubMed ID: 24264604	2013
Landscape and variation of RNA secondary structure across the human transcriptome. Nature\| PubMed ID: 24476892	2014
Divergence in a master variator generates distinct phenotypes and transcriptional responses. Genes & development\| PubMed ID: 24532717	2014
Extended lifespan and reduced adiposity in mice lacking the FAT10 gene. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 24706839	2014
Quantitative analysis of RNA-protein interactions on a massively parallel array reveals biophysical and evolutionary landscapes. Nature biotechnology\| PubMed ID: 24727714	2014
Defining functional DNA elements in the human genome. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 24753594	2014
Sushi.R: flexible, quantitative and integrative genomic visualizations for publication-quality multi-panel figures. Bioinformatics (Oxford, England)\| PubMed ID: 24903420	2014
Defining a personal, allele-specific, and single-molecule long-read transcriptome. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 24961374	2014
H3K4me3 breadth is linked to cell identity and transcriptional consistency. Cell\| PubMed ID: 25083876	2014
Genomic analysis of fibrolamellar hepatocellular carcinoma. Human molecular genetics\| PubMed ID: 25122662	2015
Shared functions of plant and mammalian StAR-related lipid transfer (START) domains in modulating transcription factor activity. BMC biology\| PubMed ID: 25159688	2014
Genome-wide map of regulatory interactions in the human genome. Genome research\| PubMed ID: 25228660	2014
Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 25275169	2014
Widespread contribution of transposable elements to the innovation of gene regulatory networks. Genome research\| PubMed ID: 25319995	2014
A comparative encyclopedia of DNA elements in the mouse genome. Nature\| PubMed ID: 25409824	2014
Principles of regulatory information conservation between mouse and human. Nature\| PubMed ID: 25409826	2014
Topologically associating domains are stable units of replication-timing regulation. Nature\| PubMed ID: 25409831	2014
Comparison of the transcriptional landscapes between human and mouse tissues. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 25413365	2014
Personalized sequencing and the future of medicine: discovery, diagnosis and defeat of disease. Pharmacogenomics\| PubMed ID: 25493570	2014
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss. BMC genomics\| PubMed ID: 25528277	2014
Comprehensive transcriptome analysis using synthetic long-read sequencing reveals molecular co-association of distant splicing events. Nature biotechnology\| PubMed ID: 25985263	2015
High-throughput sequencing technologies. Molecular cell\| PubMed ID: 26000844	2015
Transcriptome Signature and Regulation in Human Somatic Cell Reprogramming. Stem cell reports\| PubMed ID: 26004630	2015
Mango: a bias-correcting ChIA-PET analysis pipeline. Bioinformatics (Oxford, England)\| PubMed ID: 26034063	2015
Single-cell chromatin accessibility reveals principles of regulatory variation. Nature\| PubMed ID: 26083756	2015