Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Dina N Paltoo"'
Autor:
Stephanie O M Dyke, Anthony A Philippakis, Jordi Rambla De Argila, Dina N Paltoo, Erin S Luetkemeier, Bartha M Knoppers, Anthony J Brookes, J Dylan Spalding, Mark Thompson, Marco Roos, Kym M Boycott, Michael Brudno, Matthew Hurles, Heidi L Rehm, Andreas Matern, Marc Fiume, Stephen T Sherry
Publikováno v:
PLoS Genetics, Vol 12, Iss 1, p e1005772 (2016)
A systematic way of recording data use conditions that are based on consent permissions as found in the datasets of the main public genome archives (NCBI dbGaP and EMBL-EBI/CRG EGA).
Externí odkaz:
https://doaj.org/article/dba8b7865e8c40ae9da832cc978bc9f9
Autor:
J Gustav Smith, Jared W Magnani, Cameron Palmer, Yan A Meng, Elsayed Z Soliman, Solomon K Musani, Kathleen F Kerr, Renate B Schnabel, Steven A Lubitz, Nona Sotoodehnia, Susan Redline, Arne Pfeufer, Martina Müller, Daniel S Evans, Michael A Nalls, Yongmei Liu, Anne B Newman, Alan B Zonderman, Michele K Evans, Rajat Deo, Patrick T Ellinor, Dina N Paltoo, Christopher Newton-Cheh, Emelia J Benjamin, Reena Mehra, Alvaro Alonso, Susan R Heckbert, Ervin R Fox, Candidate-gene Association Resource (CARe) Consortium
Publikováno v:
PLoS Genetics, Vol 7, Iss 2, p e1001304 (2011)
The PR interval on the electrocardiogram reflects atrial and atrioventricular nodal conduction time. The PR interval is heritable, provides important information about arrhythmia risk, and has been suggested to differ among human races. Genome-wide a
Externí odkaz:
https://doaj.org/article/916dd9b034a04cfab045fdad07271c1b
Autor:
Guillaume Lettre, Cameron D Palmer, Taylor Young, Kenechi G Ejebe, Hooman Allayee, Emelia J Benjamin, Franklyn Bennett, Donald W Bowden, Aravinda Chakravarti, Al Dreisbach, Deborah N Farlow, Aaron R Folsom, Myriam Fornage, Terrence Forrester, Ervin Fox, Christopher A Haiman, Jaana Hartiala, Tamara B Harris, Stanley L Hazen, Susan R Heckbert, Brian E Henderson, Joel N Hirschhorn, Brendan J Keating, Stephen B Kritchevsky, Emma Larkin, Mingyao Li, Megan E Rudock, Colin A McKenzie, James B Meigs, Yang A Meng, Tom H Mosley, Anne B Newman, Christopher H Newton-Cheh, Dina N Paltoo, George J Papanicolaou, Nick Patterson, Wendy S Post, Bruce M Psaty, Atif N Qasim, Liming Qu, Daniel J Rader, Susan Redline, Muredach P Reilly, Alexander P Reiner, Stephen S Rich, Jerome I Rotter, Yongmei Liu, Peter Shrader, David S Siscovick, W H Wilson Tang, Herman A Taylor, Russell P Tracy, Ramachandran S Vasan, Kevin M Waters, Rainford Wilks, James G Wilson, Richard R Fabsitz, Stacey B Gabriel, Sekar Kathiresan, Eric Boerwinkle
Publikováno v:
PLoS Genetics, Vol 7, Iss 2, p e1001300 (2011)
Coronary heart disease (CHD) is the leading cause of mortality in African Americans. To identify common genetic polymorphisms associated with CHD and its risk factors (LDL- and HDL-cholesterol (LDL-C and HDL-C), hypertension, smoking, and type-2 diab
Externí odkaz:
https://doaj.org/article/d9f44e2061144ffba888d0850b646b15
Autor:
Kevin R. King, MD, PhD, Luanda P. Grazette, MD, MPH, Dina N. Paltoo, PhD, MPH, John T. McDevitt, PhD, Samuel K. Sia, PhD, Paddy M. Barrett, MD, Fred S. Apple, PhD, Paul A. Gurbel, MD, Ralph Weissleder, MD, PhD, Hilary Leeds, JD, Erin J. Iturriaga, MSN, Anupama K. Rao, MD, Bishow Adhikari, PhD, Patrice Desvigne-Nickens, MD, Zorina S. Galis, PhD, Peter Libby, MD
Publikováno v:
JACC: Basic to Translational Science, Vol 1, Iss 1, Pp 73-86 (2016)
Point-of-care technologies (POC or POCT) are enabling innovative cardiovascular diagnostics that promise to improve patient care across diverse clinical settings. The National Heart, Lung, and Blood Institute convened a working group to discuss POCT
Externí odkaz:
https://doaj.org/article/fcda88bebd8443269c273e929b4780cd
Autor:
Tamar B. Rubinstein, Melissa A. Haendel, Jonathan Pevsner, Christoffer Nellåker, Paul Avillach, Domenica Taruscio, Stephen C. Groft, Rebecca M. Goodwin, Dina N. Paltoo, Nomi L. Harris, Peter N. Robinson, Vojtech Huser, Marco Roos, Julie A. McMurry, Mats G. Hansson, Matthew Might, Barend Mons, Yaffa R. Rubinstein, Helene Cederroth, Alison P Rockett-Frase, Gareth Baynam, William A. Gahl, Deborah Mascalzoni, Esther van Enckevort, Manuel Posada
Publikováno v:
JAMIA Open
Repisalud
Instituto de Salud Carlos III (ISCIII)
Repisalud
Instituto de Salud Carlos III (ISCIII)
The premise of Open Science is that research and medical management will progress faster if data and knowledge are openly shared. The value of Open Science is nowhere more important and appreciated than in the rare disease (RD) community. Research in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be23627405e1f832a3596a4894cb3fd4
https://europepmc.org/articles/PMC7660964/
https://europepmc.org/articles/PMC7660964/
Autor:
Hilary S. Leeds, Samuel K. Sia, Anupama K. Rao, Luanda Grazette, Bishow B. Adhikari, Ralph Weissleder, Paddy M. Barrett, Patrice Desvigne-Nickens, Fred S. Apple, Peter Libby, Kevin R. King, Erin Iturriaga, Paul A. Gurbel, Zorina S. Galis, John T. McDevitt, Dina N. Paltoo
Publikováno v:
JACC: Basic to Translational Science, Vol 1, Iss 1, Pp 73-86 (2016)
Point-of-care technologies (POC or POCT) are enabling innovative cardiovascular diagnostics that promise to improve patient care across diverse clinical settings. The National Heart, Lung, and Blood Institute convened a working group to discuss POCT
Autor:
Carolyn M. Hutter, Ryan D. Hernandez, Leah E. Mechanic, Chun Li, Gabriel Rosenfeld, Bo Peng, John S. Witte, George J. Papanicolaou, Jason H. Moore, Dina N. Paltoo, Elizabeth R. Hauser, Kimberly A. McAllister, Eric J. Feuer, David A. Liberles, Vineet Bafna, Elizabeth M. Gillanders, Huann-Sheng Chen, Marylyn D. Ritchie, Christopher I. Amos
Publikováno v:
Genetic Epidemiology. 39:11-19
Genetic simulation programs are used to model data under specified assumptions to facilitate the understanding and study of complex genetic systems. Standardized data sets generated using genetic simulation are essential for the development and appli
Autor:
Christopher Newton-Cheh, Sathanur R. Srinivasan, Jerome I. Rotter, Luigi Ferrucci, Alvaro Alonso, Yongmei Liu, Renate B. Schnabel, Tandaw E. Samdarshi, Margaux F. Keller, Marian C. Limacher, Takaaki Tanaka, J. C. Bis, Ervin R. Fox, Omer T. Njajou, Dina N. Paltoo, Gerardo Heiss, Patrick T. Ellinor, Zhu Ming Zhang, AB Singleton, Christy L. Avery, Gang Li, Michele K. Evans, Dan E. Arking, Jennifer G. Robinson, Kari E. North, Mike A. Nalls, Anne M. Butler, Sarah G. Buxbaum, Gregory M. Marcus, A.B. Newman, Ermeg L. Akylbekova, Maurizio Trevisan, Alan B. Zonderman, David S. Siscovick, P. Miguel Quibrera, Wei Chen, Herman A. Taylor, Eric A. Whitsel, Jared W. Magnani, Nona Sotoodehnia, Alexander P. Reiner, Sarah S. Murray, Rajat Deo, Steven A. Lubitz, Bruce M. Psaty, Emelia J. Benjamin, Kathleen F. Kerr, Susan R. Heckbert, J. G. Smith, Lin Y. Chen, Reena Mehra, Susan Redline, Daniel S. Evans, Nicholas J. Schork, Steve Cummings, Wen-Chi Hsueh, Gerald S. Berenson, Elsayed Z. Soliman, Erin N. Smith
Publikováno v:
Heart rhythm, vol 10, iss 3
Background Genome-wide association studies have identified several genetic loci associated with variation in resting heart rate in European and Asian populations. No study has evaluated genetic variants associated with heart rate in African Americans
Autor:
Dina N. Paltoo, Bartha Maria Knoppers, J. Dylan Spalding, Stephanie O.M. Dyke, Stephen T. Sherry, Erin S. Luetkemeier, Michael Brudno, Jordi Rambla De Argila, Andreas Matern, Kym M. Boycott, Marco Roos, Mark Thompson, Heidi L. Rehm, Matthew E. Hurles, Marc Fiume, Anthony A. Philippakis, Anthony J. Brookes
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 12, Iss 1, p e1005772 (2016)
PLoS Genetics, 12(1)
PLoS Genetics, Vol 12, Iss 1, p e1005772 (2016)
PLoS Genetics, 12(1)
A systematic way of recording data use conditions that are based on consent permissions as found in the datasets of the main public genome archives (NCBI dbGaP and EMBL-EBI/CRG EGA). SOMD is supported by the Canadian Institutes of Health Research (gr
Autor:
Isaac S. Kohane, Gail P. Jarvik, Mark A. Hoffman, Howard P. Levy, George J. Papanicolaou, Dina N. Paltoo, Daniel R. Masys, Nicholas R. Anderson, Neil F. Abernethy
Publikováno v:
Journal of Biomedical Informatics. 45(3):419-422
Graphical abstractDisplay Omitted Highlights? Molecular sequence data will be an important component of EHRs. ? The volume and complexity of the data are key features. ? Desiderata for representing this data in EHRs are presented. ? A technical appro