Resultados de Procura por Autor :: APM

1

Recognition of Handwriting from Electromyography por Michael D. Linderman, Mikhail Lebedev, Joseph S. Erlichman

Publicado 2009

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2

Personal Genome Sequencing in Ostensibly Healthy Individuals and the PeopleSeq Consortium por Michael D. Linderman, Daiva E. Nielsen, Robert C. Green

Publicado 2016

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3

Computational solutions to large-scale data management and analysis por Eric E. Schadt, Michael D. Linderman, Jon M. Sorenson, L. Lee, Garry P. Nolan

Publicado 2010

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4

Cloud and heterogeneous computing solutions exist today for the emerging big data problems in biology por Eric E. Schadt, Michael D. Linderman, Jon M. Sorenson, L. Lee, Garry P. Nolan

Publicado 2011

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5

HermesB: A Continuous Neural Recording System for Freely Behaving Primates por Gopal Santhanam, Michael D. Linderman, Vikash Gilja, Afsheen Afshar, Stephen I. Ryu, Teresa H. Meng, Krishna V. Shenoy

Publicado 2007

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6

Analytical validation of whole exome and whole genome sequencing for clinical applications por Michael D. Linderman, Tracy Brandt, Lisa Edelmann, Omar Jabado, Yumi Kasai, Ruth Kornreich, Milind Mahajan, Hardik Shah, Andrew Kasarskis, Eric E. Schadt

Publicado 2014

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7

Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project por Saskia C. Sanderson, Michael D. Linderman, Sabrina A. Suckiel, Randi E. Zinberg, Melissa Wasserstein, Andrew Kasarskis, George A. Díaz, Eric E. Schadt

Publicado 2017

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8

Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project por Saskia C. Sanderson, Michael D. Linderman, Sabrina A. Suckiel, George A. Díaz, Randi E. Zinberg, Kadija Ferryman, Melissa Wasserstein, Andrew Kasarskis, Eric E. Schadt

Publicado 2015

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9

Extracting a cellular hierarchy from high-dimensional cytometry data with SPADE por Peng Qiu, Erin F. Simonds, Sean C. Bendall, Kenneth D. Gibbs, Robert V. Bruggner, Michael D. Linderman, Karen Sachs, Garry P. Nolan, Sylvia K. Plevritis

Publicado 2011

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10

Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium por Emilie S. Zoltick, Michael D. Linderman, Molly A. McGinniss, Erica Ramos, Mad Price Ball, George M. Church, Debra G. B. Leonard, Stacey Pereira, Amy L. McGuire, C. Thomas Caskey, Saskia C. Sanderson, Eric E. Schadt, Daiva E. Nielsen, Scott Crawford, Robert C. Green

Publicado 2019

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11

Genetic identification of a common collagen disease in Puerto Ricans via identity-by-descent mapping in a health system por Gillian M. Belbin, Jacqueline A. Odgis, Elena P. Sorokin, Muh-Ching Yee, Sumita Kohli, Benjamin S. Glicksberg, Christopher R. Gignoux, Genevieve L. Wojcik, Tielman Van Vleck, Janina M. Jeff, Michael D. Linderman, Claudia Schurmann, Douglas M. Ruderfer, Xiaoqiang Cai, Amanda Merkelson, Anne E. Justice, Kristin L. Young, Misa Graff, Kari E. North, Ulrike Peters, Regina James, Lucia A. Hindorff, Ruth Kornreich, Lisa Edelmann, Omri Gottesman, Eli Stahl, Judy H. Cho, Ruth J. F. Loos, Erwin P. Böttinger, Girish N. Nadkarni, Noura S. Abul‐Husn, Eimear E. Kenny

Publicado 2017

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12

Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis por Supinda Bunyavanich, Eric E. Schadt, Blanca E. Himes, Jessica Lasky‐Su, Weiliang Qiu, Ross Lazarus, John Ziniti, Ariella Cohain, Michael D. Linderman, Dara G. Torgerson, Celeste Eng, María Pino-Yanes, Badri Padhukasahasram, James J. Yang, Rasika A. Mathias, Terri H. Beaty, Xingnan Li, Penelope E. Graves, Isabelle Romieu, Blanca del Río Navarro, Muhammad T. Salam, Hita Vora, Dan L. Nicolae, Carole Ober, Fernando D. Martínez, Eugene R. Bleecker, Deborah A. Meyers, W. James Gauderman, Frank D. Gilliland, Esteban G. Burchard, Kathleen C. Barnes, L. Keoki Williams, Stephanie J. London, Bin Zhang, Benjamin A. Raby, Scott T. Weiss

Publicado 2014

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13

Development and clinical application of an integrative genomic approach to personalized cancer therapy por Andrew Uzilov, Wei Ding, Marc Y. Fink, Yevgeniy Antipin, Andrew S. Brohl, Claire Davis, Chun Yee Lau, Chetanya Pandya, Hardik Shah, Yumi Kasai, James Powell, Mark Micchelli, Rafael Castellanos, Zhongyang Zhang, Michael D. Linderman, Yayoi Kinoshita, Micol Zweig, Katie Raustad, Kakit Cheung, Diane Castillo, Melissa Wooten, Imane Bourzgui, Leah Newman, Gintaras Deikus, Bino Mathew, Jun Zhu, Benjamin S. Glicksberg, Aye S. Moe, Jun Liao, Lisa Edelmann, Joel T. Dudley, Robert G. Maki, Andrew Kasarskis, Randall F. Holcombe, Milind Mahajan, Ke Hao, Boris Reva, Janina A. Longtine, Daniela Starcevic, Robert Sebra, Michael Donovan, Shuyu Li, Eric E. Schadt, Rong Chen

Publicado 2016

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14

Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network por Zhao Chen, Hua Tang, Rehan Qayyum, Ursula M. Schick, Michael A. Nalls, Robert E. Handsaker, Jin Li, Yingchang Lu, Lisa R. Yanek, Brendan J. Keating, Yan Meng, Frank J.A. van Rooij, Yukinori Okada, Michiaki Kubo, Laura J. Rasmussen‐Torvik, Margaux F. Keller, Leslie A. Lange, Michele K. Evans, Erwin P. Böttinger, Michael D. Linderman, Douglas M. Ruderfer, Hákon Hákonarson, George Papanicolaou, Alan B. Zonderman, Omri Gottesman, Cynthia A. Thomson, Elad Ziv, Andrew B. Singleton, Ruth J. F. Loos, Patrick Sleiman, Santhi K. Ganesh, Steven A. McCarroll, Diane M. Becker, James G. Wilson, Guillaume Lettre, Alexander P. Reiner

Publicado 2013

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15

Toward clinical genomics in everyday medicine: perspectives and recommendations por Susan Delaney, Michael Hultner, Howard J. Jacob, David H. Ledbetter, Jeanette McCarthy, M.A. Ball, Kenneth B. Beckman, John W. Belmont, Cinnamon S. Bloss, Michael F. Christman, Andy Cosgrove, Stephen A. Damiani, Timothy Danis, Massimo Delledonne, Michael J. Dougherty, Joel T. Dudley, W. Andrew Faucett, Jennifer Friedman, David H. Haase, T S Hays, Stu Heilsberg, Jeff Huber, Leah Kaminsky, Nikki Ledbetter, Warren H. Lee, Elissa Levin, Ondrej Libiger, Michael D. Linderman, Richard L. Love, David Magnus, AnneMarie Martland, Susan L. McClure, Scott E. Megill, Helen Messier, Robert L. Nussbaum, Latha Palaniappan, Bradley Patay, Bradley W. Popovich, John Quackenbush, Mark J. Savant, Michael M. Su, Sharon F. Terry, Steven Tucker, William T Wong, Robert C. Green

Publicado 2016

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16

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci por Kyle J. Gaulton, Teresa Ferreira, Yeji Lee, Anne Raimondo, Reedik Mägi, Michael E. Reschen, Anubha Mahajan, Adam E. Locke, Nigel W. Rayner, Neil Robertson, Robert A. Scott, Inga Prokopenko, Laura J. Scott, Todd Green, Thomas Sparsø, Dorothée Thuillier, Loïc Yengo, Harald Grallert, Simone Wahl, Mattias Frånberg, Rona J. Strawbridge, Hans A. Kestler, Himanshu Chheda, Lewin Eisele, Stefan Gustafsson, Valgerður Steinthórsdóttir, Guðmar Þorleifsson, Lu Qi, Lennart C. Karssen, Jin‐Moo Lee, Sara M. Willems, Man Li, Han Chen, Christian Fuchsberger, Phoenix Kwan, Clement Ma, Michael D. Linderman, Yingchang Lu, Soren K. Thomsen, Jana K. Rundle, Nicola L. Beer, Martijn van de Bunt, Anil Chalisey, Hyun Min Kang, Benjamin F. Voight, Gonçalo R. Abecasis, Peter Almgren, Damiano Baldassarre, Beverley Balkau, Rafn Benediktsson, Matthias Blüher, Heiner Boeing, Lori L. Bonnycastle, Erwin P. Böttinger, Noël P. Burtt, Jason Carey, G. Charpentier, Peter S. Chines, Marilyn C. Cornelis, David Couper, Andrew Crenshaw, Rob M. van Dam, Alex S. F. Doney, Mozhgan Dorkhan, Sarah Edkins, Johan G. Eriksson, Tõnu Esko, Elodie Eury, João Fadista, Jason Flannick, Pierre Fontanillas, Caroline S. Fox, Paul W. Franks, Karl Gertow, Christian Gieger, Bruna Gigante, Omri Gottesman, George Grant, Niels Grarup, Christopher J. Groves, Maija Hassinen, Henri Theil, Christian Herder, Oddgeir L. Holmen, Ástráður B. Hreiðarsson, Steve E. Humphries, Sarah Hunt, Anne Jackson, Anna Jonsson, Marit E. Jørgensen, Torben Jørgensen, Wen‐Hong L. Kao, Nicola D. Kerrison, Leena Kinnunen, Norman Klopp, Augustine Kong, Péter Kovács, Peter Kraft, Jasmina Kravić, Cordelia Langford

Publicado 2015

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