檢索結果 - Matthew DeFelice
- Showing 1 - 11 results of 11
-
1
DGAT1 mutation is linked to a congenital diarrheal disorder 由 Joel T. Haas, Harland S. Winter, Elaine T. Lim, Andrew Kirby, Brendan Blumenstiel, Matthew DeFelice, Stacey Gabriel, Chaim Jalas, David Branski, Carrie A. Grueter, Mauro Sérgio Toporovski, Tobias C. Walther, Mark J. Daly, Robert V. Farese
出版 2012Artigo -
2
High-Throughput Detection of Actionable Genomic Alterations in Clinical Tumor Samples by Targeted, Massively Parallel Sequencing 由 Nikhil Wagle, Michael F. Berger, Matthew J. Davis, Brendan Blumenstiel, Matthew DeFelice, Panisa Pochanard, Matthew D. Ducar, Paul Van Hummelen, Laura E. MacConaill, William C. Hahn, Matthew Meyerson, Stacey Gabriel, Levi A. Garraway
出版 2011Artigo -
3
The Structure of Haplotype Blocks in the Human Genome 由 Stacey Gabriel, S. F. Schaffner, Huy Nguyen, Jamie Moore, Jessica Roy, Brendan Blumenstiel, John M. Higgins, Matthew DeFelice, Amy L. Lochner, Maura Faggart, Shau Neen Liu-Cordero, Charles N. Rotimi, Adebowale Adeyemo, Stephen S. Rich, Ryk Ward, Eric S. Lander, Mark J. Daly, David Altshuler
出版 2002Artigo -
4
The Genomic Landscape of Pediatric Ewing Sarcoma 由 Brian D. Crompton, Chip Stewart, Amaro Taylor‐Weiner, Gabriela Alexe, Kyle C. Kurek, Monica L. Calicchio, Adam Kieżun, Scott L. Carter, Sachet A. Shukla, Swapnil Mehta, Aaron R. Thorner, Carmen de Torres, Cinzia Lavarino, Mariona Suñol, Aaron McKenna, Andrey Sivachenko, Kristian Cibulskis, Michael S. Lawrence, Petar Stojanov, Mara Rosenberg, Lauren Ambrogio, Daniel Auclair, Sara Seepo, Brendan Blumenstiel, Matthew DeFelice, Iván Imaz-Rosshandler, Angela Schwarz‐Cruz y Celis, Miguel N. Rivera, Carlos Rodríguez‐Galindo, Mark D. Fleming, Todd R. Golub, Gad Getz, Jaume Mora, Kimberly Stegmaier
出版 2014Artigo -
5
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing 由 Andrew Kirby, Andreas Gnirke, David B. Jaffe, Veronika Barešová, Nathalie Pochet, Brendan Blumenstiel, Chun Ye, Daniel Aird, Christine Stevens, James Robinson, Moran N. Cabili, Irit Gat‐Viks, Edward Kelliher, Riza M. Daza, Matthew DeFelice, Helena Hůlková, Jana Sovová, Petr Vyleťal, Corinne Antignac, Mitchell Guttman, Robert E. Handsaker, Danielle Perrin, Scott Steelman, Snævar Sigurðsson, Steven J. Scheinman, Carrie Sougnez, Kristian Cibulskis, Melissa Parkin, Todd J. Green, Elizabeth J. Rossin, Michael C. Zody, Ramnik J. Xavier, Martin R. Pollak, Seth L. Alper, Kerstin Lindblad‐Toh, Stacey B. Gabriel, P. Suzanne Hart, Aviv Regev, Chad Nusbaum, Stanislav Kmoch, Anthony J. Bleyer, Eric S. Lander, Mark J. Daly
出版 2013Artigo -
6
Whole-genome association study of bipolar disorder 由 Pamela Sklar, Jordan W. Smoller, Jinbo Fan, Manuel A. R. Ferreira, Roy H. Perlis, Kim Chambert, Vishwajit L. Nimgaonkar, Matthew B. McQueen, Stephen V. Faraone, Andrew Kirby, Paul I. W. de Bakker, Matthew N. Ogdie, Michael E. Thase, Gary S. Sachs, Katherine EO Todd-Brown, Stacey B. Gabriel, Carrie Sougnez, Camille Gates, Brendan Blumenstiel, Matthew DeFelice, Kristin Ardlie, Jennifer Franklin, W.J. Muir, Kevin A. McGhee, Donald J. MacIntyre, Alan McLean, MP D VanBeck, Andrew McQuillin, Nicholas Bass, Mark W. Robinson, Jacob Lawrence, Adebayo Anjorin, David Curtis, Edward M. Scolnick, Mark J. Daly, Douglas Blackwood, Hugh Gurling, Shaun Purcell
出版 2008Artigo -
7
Sensitive Detection of Minimal Residual Disease in Patients Treated for Early-Stage Breast Cancer 由 Heather A. Parsons, Justin Rhoades, Sarah C. Reed, Gregory Gydush, Priyanka Ram, Pedro Exman, Kan Xiong, Christopher Lo, Tianyu Li, Mark Fleharty, Gregory J. Kirkner, Denisse Rotem, Ofir Cohen, Fangyan Yu, Mariana Fitarelli-Kiehl, Wai Yie Leong, Melissa E. Hughes, Shoshana M. Rosenberg, Laura C. Collins, Kathy D. Miller, Brendan Blumenstiel, Lorenzo Trippa, Carrie Cibulskis, Donna Neuberg, Matthew DeFelice, Samuel S. Freeman, Niall J. Lennon, Nikhil Wagle, Gavin Ha, Daniel G. Stover, Atish D. Choudhury, Gad Getz, Eric P. Winer, Matthew Meyerson, Nancy U. Lin, Ian E. Krop, J. Christopher Love, G. Mike Makrigiorgos, Ann H. Partridge, Erica L. Mayer, Todd R. Golub, Viktor A. Adalsteinsson
出版 2020Artigo -
8
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder 由 Manuel A. R. Ferreira, Michael O’Donovan, Yan Meng, Ian Jones, Douglas M. Ruderfer, Lisa Jones, Jinbo Fan, George Kirov, Roy H. Perlis, Elaine Green, Jordan W. Smoller, Detelina Grozeva, Jennifer Stone, Ivan Nikolov, Kimberly Chambert, Marian L. Hamshere, Vishwajit L. Nimgaonkar, Valentina Moskvina, Michael E. Thase, Sian Caesar, Gary S. Sachs, Jennifer Franklin, Katherine Gordon‐Smith, Kristin G. Ardlie, Stacey Gabriel, Christine Fraser, Brendan Blumenstiel, Matthew DeFelice, Gerome Breen, Michael Gill, Derek W. Morris, Amanda Elkin, Walter Muir, Kevin A. McGhee, Richard Williamson, Donald J. MacIntyre, Alan Maclean, David St Clair, Michelle Robinson, M. Van Beck, Ana Carla Pereira, Radhika Kandaswamy, Andrew McQuillin, David Collier, Nicholas Bass, Allan H. Young, Jacob Lawrence, I. Nicol Ferrier, Adebayo Anjorin, Anne Farmer, David Curtis, Edward M. Scolnick, Peter McGuffin, Mark J. Daly, Aiden Corvin, Peter Holmans, Douglas Blackwood, Hugh Gurling, Michael J. Owen, Shaun Purcell, Pamela Sklar, Nick Craddock
出版 2008Artigo -
9
Transmission from vaccinated individuals in a large SARS-CoV-2 Delta variant outbreak 由 Katherine J. Siddle, Lydia A. Krasilnikova, Gage K. Moreno, S. F. Schaffner, Johanna Vostok, Nicholas FitzGerald, Jacob E. Lemieux, Nikolaos Barkas, Christine Loreth, Ivan Specht, Christopher H. Tomkins-Tinch, Jillian S. Paull, Beau Schaeffer, Bradford P. Taylor, Bryn C. Loftness, Hillary Johnson, Petra Schubert, Hanna Shephard, Matthew Doucette, Timelia Fink, Andrew S. Lang, Stephanie Baez, John Beauchamp, Scott Hennigan, Erika Buzby, Stephanie Ash, Jessica Brown, Selina Clancy, Seana Cofsky, Luc Gagne, Joshua C. Hall, Rachel Harrington, Gabrielle Gionet, Katherine C. DeRuff, Megan E. Vodzak, Gordon Adams, Sabrina T. Dobbins, Sarah D. Slack, Steven K. Reilly, Lisa M. Anderson, Michelle Cipicchio, Matthew DeFelice, Jonna Grimsby, Scott E. Anderson, Brendan Blumenstiel, James C. Meldrim, Heather M. Rooke, Gina Vicente, Natasha L. Smith, Katelyn S. Messer, Faye L. Reagan, Zoe M. Mandese, Matthew Lee, Marianne C. Ray, Marissa Fisher, Maesha A. Ulcena, Corey M. Nolet, Sean English, Katie Larkin, Kyle Vernest, Sushma Chaluvadi, Deirdre Arvidson, Maurice Melchiono, Theresa Covell, Vaira Harik, Taylor Brock-Fisher, Molly Dunn, Amanda Kearns, William P. Hanage, C. Bernard, Anthony Philippakis, Niall J. Lennon, Stacey Gabriel, Glen R. Gallagher, Sandra Smole, Lawrence C. Madoff, Catherine Brown, Daniel J. Park, Bronwyn MacInnis, Pardis C. Sabeti
出版 2021Artigo -
10
A second generation human haplotype map of over 3.1 million SNPs 由 Kelly A. Frazer, Dennis G. Ballinger, David R. Cox, David A. Hinds, Laura L. Stuvé, Richard A. Gibbs, John W. Belmont, Andrew Boudreau, Paul Hardenbol, Suzanne M. Leal, Shiran Pasternak, David A. Wheeler, T. D. Willis, Fuli Yu, Huanming Yang, Changqing Zeng, Yang Gao, Haoran Hu, Weitao Hu, Chaohua Li, Wei Lin, Siqi Liu, Hao Pan, Xiaoli Tang, Jian Wang, Wei Wang, Jun Yu, Bo Zhang, Qingrun Zhang, Hongbin Zhao, Hui Zhao, Jun Zhou, Stacey Gabriel, Rachel Barry, Brendan Blumenstiel, Amy L. Camargo, Matthew DeFelice, Maura Faggart, Mary Goyette, Supriya Gupta, Jamie Moore, Huy Nguyen, Robert C. Onofrio, Melissa Parkin, Jessica Roy, Erich Stahl, Ellen Winchester, Liuda Ziaugra, David Altshuler, Yan Shen, Zhijian Yao, Wei Huang, Xun Chu, Yungang He, Jin Li, Yangfan Liu, Yayun Shen, Weiwei Sun, Haifeng Wang, Yi Wang, Ying Wang, Xiaoyan Xiong, Liang Xu, Mary Miu Yee Waye, Stephen Kwok‐Wing Tsui, Hong Xue, J. Tze‐Fei Wong, Luana Galver, Jian-Bing Fan, Kevin L. Gunderson, Sarah S. Murray, Arnold Oliphant, Mark S. Chee, Alexandre Montpetit, Fanny Chagnon, Vincent Ferretti, Martin Leboeuf, Jean François Olivier, Michael Phillips, Stéphanie Roumy, Clémentine Sallée, Andrei Verner, Thomas J. Hudson, Pui‐Yan Kwok, Dongmei Cai, Daniel C. Koboldt, Raymond D. Miller, Ludmila Pawlikowska, Patricia Taillon‐Miller, Ming Xiao, Lap Chee Tsui, William Mak, You‐Qiang Song, Paul Kwong Hang Tam, Yusuke Nakamura, Takahisa Kawaguchi, Takuya Kitamoto, Takashi Morizono, Atsushi Nagashima, Yozo Ohnishi
出版 2007Artigo -
11
Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA 由 Rebecca Earnest, Rockib Uddin, Nicholas Matluk, Nicholas Renzette, Sarah E. Turbett, Katherine J. Siddle, Christine Loreth, Gordon Adams, Christopher H. Tomkins-Tinch, Mary E. Petrone, Jessica E. Rothman, Mallery I. Breban, Robert T. Koch, Kendall Billig, Joseph R. Fauver, Chantal B.F. Vogels, Kaya Bilgüvar, Bony De Kumar, Marie L. Landry, David R. Peaper, Kevin Kelly, Greg Omerza, Heather Grieser, Sim Meak, John Martha, Hannah B. Dewey, Susan Kales, Daniel Berenzy, Kristin Carpenter‐Azevedo, Ewa King, Richard C. Huard, Vlad Novitsky, Mark Howison, J. Kebbeh Darpolor, Akarsh Manne, Rami Kantor, Sandra Smole, Catherine Brown, Timelia Fink, Andrew S. Lang, Glen R. Gallagher, Virginia E. Pitzer, Pardis C. Sabeti, Stacey Gabriel, Bronwyn MacInnis, Ryan Tewhey, Mark D. Adams, Daniel J. Park, Jacob E. Lemieux, Nathan D. Grubaugh, Ahmad Altajar, Alexandra DeJesus, Anderson F. Brito, Anne E. Watkins, Anthony Muyombwe, Brendan Blumenstiel, Caleb Neal, Chaney C. Kalinich, Chen Liu, Christine Loreth, Christopher Castaldi, Claire Pearson, C. Bernard, Corey M. Nolet, David Ferguson, Erika Buzby, Éva László, Faye L. Reagan, Gina Vicente, Heather M. Rooke, Heidi Munger, Hillary Johnson, Irina R. Tikhonova, Isabel M. Ott, Jafar Razeq, James C. Meldrim, Jessica Brown, Jianhui Wang, Johanna Vostok, John Beauchamp, Jonna Grimsby, Joshua C. Hall, Katelyn S. Messer, Katie Larkin, Kyle Vernest, Lawrence C. Madoff, Lisa M. Green, Lori Webber, Luc Gagne, Maesha A. Ulcena, Marianne C. Ray, Marissa Fisher, Mary Barter, Matthew Lee, Matthew DeFelice, Michelle Cipicchio, Natasha L. Smith, Niall J. Lennon, Nicholas FitzGerald, Nicholas Kerantzas
出版 2022Artigo
相關主題
Biology
Gene
Genetics
Medicine
Allele
Genetic association
Genotype
Single-nucleotide polymorphism
Disease
Haplotype
Internal medicine
Mutation
Pathology
2019-20 coronavirus outbreak
Bipolar disorder
Cancer
Coronavirus disease 2019 (COVID-19)
DNA sequencing
Engineering
Evolutionary biology
Exome sequencing
Genome
Genome-wide association study
Genotyping
Infectious disease (medical specialty)
Massive parallel sequencing
Outbreak
SNP
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
Tag SNP