Risultati della ricerca - Evan A. Boyle
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An Expanded View of Complex Traits: From Polygenic to Omnigenic di Evan A. Boyle, Yang Li, Jonathan K. Pritchard
Pubblicazione 2017Revisão -
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High‐resolution mapping of cancer cell networks using co‐functional interactions di Evan A. Boyle, Jonathan K. Pritchard, William J. Greenleaf
Pubblicazione 2018Artigo -
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Saturation editing of genomic regions by multiplex homology-directed repair di Gregory M. Findlay, Evan A. Boyle, Ronald J. Hause, Jason C. Klein, Jay Shendure
Pubblicazione 2014Artigo -
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Reduced signal for polygenic adaptation of height in UK Biobank di Jeremy J. Berg, Arbel Harpak, Nasa Sinnott-Armstrong, Anja Moltke Jørgensen, Hakhamanesh Mostafavi, Yair Field, Evan A. Boyle, Xinjun Zhang, Fernando Racimo, Jonathan K. Pritchard, Graham Coop
Pubblicazione 2018Pré-impressão -
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Recurrent de novo mutations implicate novel genes underlying simplex autism risk di Brian J. O’Roak, Holly A.F. Stessman, Evan A. Boyle, Kali Witherspoon, Beth Martin, C. Lee, Laura Vives, Carl Baker, Joseph B. Hiatt, D. A. Nickerson, Raphael Bernier, Jay Shendure, Evan E. Eichler
Pubblicazione 2014Artigo -
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Large-scale evaluation of the ability of RNA-binding proteins to activate exon inclusion di Jonathan C. Schmok, Manya Jain, Lena Annika Street, Alex T. Tankka, Danielle Schafer, Hsuan-Lin Her, Sara Elmsaouri, Maya L. Gosztyla, Evan A. Boyle, Pratibha Jagannatha, En‐Ching Luo, Ester J. Kwon, Marko Jovanović, G Yeo
Pubblicazione 2024Artigo -
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Genome-scale measurement of off-target activity using Cas9 toxicity in high-throughput screens di David W. Morgens, Michael Wainberg, Evan A. Boyle, Oana Ursu, Carlos L. Araya, C. Kimberly Tsui, Michael S. Haney, Gaelen T. Hess, Kyuho Han, Edwin E. Jeng, Amy Li, M Snyder, William J. Greenleaf, Anshul Kundaje, Michael C. Bassik
Pubblicazione 2017Artigo -
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Expanded palette of RNA base editors for comprehensive RBP-RNA interactome studies di Hugo C. Medina-Muñoz, Eric Kofman, Pratibha Jagannatha, Evan A. Boyle, Tao Yu, Krysten L. Jones, Jasmine R. Mueller, Grace D. Lykins, Andrew T. Doudna, Samuel S. Park, Steven M. Blue, Brodie L. Ranzau, Rahul M. Kohli, Alexis C. Komor, G Yeo
Pubblicazione 2024Artigo -
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Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia di Alissa M. D’Gama, Ying Geng, Javier Couto, Beth Martin, Evan A. Boyle, Christopher M. LaCoursiere, Amer A. Hossain, Nicole E. Hatem, Brenda J. Barry, David J. Kwiatkowski, Harry V. Vinters, A. James Barkovich, Jay Shendure, Gary W. Mathern, Christopher A. Walsh, Annapurna Poduri
Pubblicazione 2015Artigo -
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Deep sequencing of multiple regions of glial tumors reveals spatial heterogeneity for mutations in clinically relevant genes di Akash Kumar, Evan A. Boyle, Mari Tokita, Andrei M. Mikheev, Michelle C Sanger, Emily J. Girard, John R. Silber, Luis F. Gonzalez‐Cuyar, Joseph B. Hiatt, Andrew Adey, Choli Lee, Jacob O. Kitzman, Donald E. Born, Daniel L. Silbergeld, James M. Olson, Robert Rostomily, Jay Shendure
Pubblicazione 2014Artigo -
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Caspase-8, association with Alzheimer’s Disease and functional analysis of rare variants di Jan Rehker, Johanna Rodhe, Ryan Nesbitt, Evan A. Boyle, Beth Martin, Jenny Lord, Ilker Karaca, Adam C. Naj, Frank Jessen, Seppo Helisalmi, Hilkka Soininen, Mikko Hiltunen, Alfredo Ramı́rez, Martin Scherer, Lindsay A. Farrer, Jonathan L. Haines, Margaret A. Pericak‐Vance, Wendy H. Raskind, Carlos Cruchaga, Gerard D. Schellenberg, Bertrand Joseph, Zoran Brkanac
Pubblicazione 2017Artigo -
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Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study di Ghayda Mirzaa, Valerio Conti, Andrew E. Timms, Christopher D. Smyser, Sarah Ahmed, Melissa Carter, Sarah Barnett, Robert B. Hufnagel, Amy Goldstein, Yoko Narumi‐Kishimoto, Carissa Olds, Sarah Collins, Kathreen Johnston, Jean‐François Deleuze, Patrick Nitschké, Kathryn Friend, Catharine Harris, Allison L. Goetsch, Beth Martin, Evan A. Boyle, Elena Parrini, Davide Mei, Lorenzo Tattini, Anne Slavotinek, Ed Blair, Christopher Barnett, Jay Shendure, Jamel Chelly, William B. Dobyns, Renzo Guerrini
Pubblicazione 2015Artigo -
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Identification of phagocytosis regulators using magnetic genome-wide CRISPR screens di Michael S. Haney, Christopher J. Bohlen, David W. Morgens, James Ousey, Amira Barkal, C. Kimberly Tsui, Braeden K. Ego, Roni Levin, Roarke A. Kamber, Hannah Y. Collins, Andrew F. Tucker, Amy Li, Daan Vorselen, Ramon Lorenzo D. Labitigan, Emily Crane, Evan A. Boyle, Lihua Jiang, Joanne Chan, Esther Rincón, William J. Greenleaf, Billy Li, M Snyder, Irving L. Weissman, Julie A. Theriot, Sean R. Collins, Ben A. Barres, Michael C. Bassik
Pubblicazione 2018Artigo
Strumenti per la ricerca:
Soggetti correlati
Biology
Genetics
Gene
Computational biology
Computer science
Mutation
Neuroscience
Genome
Medicine
Phenotype
Cell biology
Evolutionary biology
Exome sequencing
Programming language
Adaptation (eye)
CRISPR
DNA
Epilepsy
RNA
Signal transduction
Amplicon
Artificial intelligence
Biobank
Bioinformatics
Cas9
Chemistry
Cortical dysplasia
DNA sequencing
Deep sequencing
Dysplasia