Zoekresultaten - James R. Priest
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1
Maternal Obesity and Diabetes Mellitus as Risk Factors for Congenital Heart Disease in the Offspring door Emmi Helle, James R. Priest
Gepubliceerd in 2020Revisão -
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Phenome-wide Burden of Copy-Number Variation in the UK Biobank door Matthew Aguirre, Manuel A. Rivas, James R. Priest
Gepubliceerd in 2019Artigo -
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Birthweight, Type 2 Diabetes Mellitus, and Cardiovascular Disease door Daniela Zanetti, Emmi Tikkanen, Stefan Gustafsson, James R. Priest, Stephen Burgess, Erik Ingelsson
Gepubliceerd in 2018Artigo -
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Exome-Based Case-Control Analysis Highlights the Pathogenic Role of Ciliary Genes in Transposition of the Great Arteries door Xuanyu Liu, Wen Chen, Wenke Li, James R. Priest, Yuanyuan Fu, Kunjing Pang, Baihui Ma, Bianmei Han, Xuewen Liu, Shengshou Hu, Zhou Zhou
Gepubliceerd in 2020Artigo -
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Genomic Sequencing of Pleistocene Cave Bears door James P. Noonan, Michael Hofreiter, Doug Smith, James R. Priest, Nadin Rohland, Gernot Rabeder, Johannes Krause, John C. Detter, Svante Pääbo, Edward M. Rubin
Gepubliceerd in 2005Artigo -
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Transcriptomic Profiling Maps Anatomically Patterned Subpopulations among Single Embryonic Cardiac Cells door Guang Li, Adele Xu, Sopheak Sim, James R. Priest, Xueying Tian, Tooba Khan, Thomas Quertermous, Bin Zhou, Philip S. Tsao, Stephen R. Quake, Sean M. Wu
Gepubliceerd in 2016Artigo -
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Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing door James R. Priest, Scott R. Ceresnak, Frederick E. Dewey, Lindsey Malloy-Walton, Kyla Dunn, Megan E. Grove, Marco Pérez, Katsuhide Maeda, Anne M. Dubin, Euan A. Ashley
Gepubliceerd in 2014Artigo -
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Weakly supervised classification of aortic valve malformations using unlabeled cardiac MRI sequences door Jason Fries, Paroma Varma, Vincent S. Chen, Ke Xiao, Heliodoro Tejeda, Priyanka Saha, Jared Dunnmon, Henry Chubb, Shiraz A. Maskatia, Madalina Fiterau, Scott L. Delp, Euan A. Ashley, Christopher Ré, James R. Priest
Gepubliceerd in 2019Artigo -
13
Substantial Cardiovascular Morbidity in Adults With Lower-Complexity Congenital Heart Disease door Priyanka Saha, Praneetha Potiny, Joseph Rigdon, Melissa L. Morello, Catherine Tcheandjieu, Anitra Romfh, Susan M. Fernandes, Doff B. McElhinney, Daniel Bernstein, George K. Lui, Gary M. Shaw, Erik Ingelsson, James R. Priest
Gepubliceerd in 2019Artigo -
14
Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association door Mary Ella Pierpont, Martina Brueckner, Wendy K. Chung, Vidu Garg, Ronald V. Lacro, Amy L. McGuire, Seema Mital, James R. Priest, William T. Pu, Amy E. Roberts, Stephanie M. Ware, Bruce D. Gelb, Mark W. Russell
Gepubliceerd in 2018Revisão -
15
Targeting HDAC6 to treat heart failure with preserved ejection fraction in mice door Sara Ranjbarvaziri, Aliya Zeng, Iris Wu, Amara Greer-Short, Farshad Farshidfar, Ana Budan, Emma Xu, Reva Shenwai, Matthew Kozubov, Cindy Li, Melissa Van Pell, Francis Grafton, Charles Mackay, Xiaomei Song, James R. Priest, Gretchen Argast, Mohammad A. Mandegar, Timothy Hoey, Jin Yang
Gepubliceerd in 2024Artigo -
16
Epistasis regulates genetic control of cardiac hypertrophy door Qianru Wang, Tiffany M. Tang, Michelle Youlton, Chad S. Weldy, Ana Kenney, Omer Ronen, J. Weston Hughes, Elizabeth T. Chin, Shirley Sutton, Abhineet Agarwal, Xiao Li, Merle Behr, Karl Kumbier, Christine S. Moravec, W.H. Wilson Tang, Kenneth B. Margulies, Thomas P. Cappola, Atul J. Butte, Rima Arnaout, James B. Brown, James R. Priest, Victoria N. Parikh, Bin Yu, Euan A. Ashley
Gepubliceerd in 2025Artigo -
17
Clonally expanding smooth muscle cells promote atherosclerosis by escaping efferocytosis and activating the complement cascade door Ying Wang, Vivek Nanda, Daniel DiRenzo, Jianqin Ye, Sophia Xiao, Yoko Kojima, Kathryn L. Howe, Kai-Uwe Jarr, Alyssa M. Flores, Pavlos Tsantilas, Noah L. Tsao, Abhiram Rao, Alexandra Newman, Anne V. Eberhard, James R. Priest, Arno Ruusalepp, Gerard Pasterkamp, Lars Mäegdefessel, Clint L. Miller, Lars Lind, Simon Koplev, Johan Björkegren, Gary K. Owens, Erik Ingelsson, Irving L. Weissman, Nicholas J. Leeper
Gepubliceerd in 2020Artigo -
18
Congenital heart disease risk loci identified by genome-wide association study in European patients door Harald Lahm, Meiwen Jia, Martina Dreßen, Felix Wirth, Nazan Puluca, Ralf Gilsbach, Bernard Keavney, Julie Cleuziou, Nicole Beck, Olga Bondareva, Elda Dzilic, Melchior Burri, Karl Christian König, Johannes A. Ziegelmüller, Claudia Abou‐Ajram, Irina Neb, Zhong Zhang, S. Doppler, Elisa Mastantuono, Peter Lichtner, Gertrud Eckstein, Jürgen Hörer, Peter Ewert, James R. Priest, Lutz Hein, Rüdiger Lange, Thomas Meitinger, Heather J. Cordell, Bertram Müller‐Myhsok, Markus Krane
Gepubliceerd in 2020Artigo -
19
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects door James R. Priest, Kazutoyo Osoegawa, Nebil Mohammed, Vivek Nanda, Ramendra Kundu, Kathleen Schultz, Edward J. Lammer, Santhosh Girirajan, Todd E. Scheetz, Daryl Waggott, François Haddad, Sushma Reddy, Daniel Bernstein, Trudy L. Burns, Jeffrey D. Steimle, Xinan Yang, Ivan P. Moskowitz, Matthew E. Hurles, Richard P. Lifton, Debbie A. Nickerson, Michael J. Bamshad, Evan E. Eichler, Seema Mital, Val C. Sheffield, Thomas Quertermous, Bruce D. Gelb, Michael A. Portman, Euan A. Ashley
Gepubliceerd in 2016Artigo -
20
Early somatic mosaicism is a rare cause of long-QT syndrome door James R. Priest, Charles Gawad, Kristopher M. Kahlig, Joseph Kwong‐Leung Yu, Tom O’Hara, Patrick M. Boyle, Sridharan Rajamani, Michael J. Clark, Sarah Garcia, Scott R. Ceresnak, Jason Harris, Seán Boyle, Frederick E. Dewey, Lindsey Malloy-Walton, Kyla Dunn, Megan E. Grove, Marco Pérez, Norma Neff, Richard Chen, Katsuhide Maeda, Anne M. Dubin, Luiz Belardinelli, John West, Christian Antolik, Daniela Macaya, Thomas Quertermous, Natalia A. Trayanova, Stephen R. Quake, Euan A. Ashley
Gepubliceerd in 2016Artigo
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Biology
Genetics
Gene
Medicine
Internal medicine
Cardiology
Phenotype
Endocrinology
Genome
Heart disease
Bioinformatics
Computational biology
Diabetes mellitus
Disease
Genotype
Pathology
Population
Environmental health
Mutation
Single-nucleotide polymorphism
Cell
Cell biology
Computer science
Evolutionary biology
Exome sequencing
Genetic association
Heart failure
Obstetrics
Offspring
Pregnancy