Rezultati - Jeffery Haessler
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1
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease od Derek Klarin, Emma Busenkell, Renae Judy, Julie A. Lynch, Michael G. Levin, Jeffery Haessler, Krishna G. Aragam, Mark Chaffin, Mary E. Haas, Sara Lindström, Themistocles L. Assimes, Jie Huang, Kyung Min Lee, Qing Shao, Jennifer E. Huffman, Christopher Kabrhel, Yunfeng Huang, Yan V. Sun, Marijana Vujković, Danish Saleheen, Donald R. Miller, Peter D. Reaven, Scott L. DuVall, William E. Boden, Saiju Pyarajan, Alex P. Reiner, David‐Alexandre Trégouët, Peter K. Henke, Charles Kooperberg, J. Michael Gaziano, John Concato, Daniel J. Rader, Kelly Cho, Kyong–Mi Chang, Peter W.F. Wilson, Nicholas L. Smith, Christopher J. O’Donnell, Philip S. Tsao, Sekar Kathiresan, T. Andrea, Scott M. Damrauer, Pradeep Natarajan
Izdano 2019Artigo -
2
Association of exome sequences with plasma C-reactive protein levels in >9000 participants od Ursula M. Schick, Paul L. Auer, Joshua C. Bis, Honghuang Lin, Peng Wei, Nathan Pankratz, Leslie A. Lange, Jennifer A. Brody, Nathan O. Stitziel, Daniel S. Kim, Christopher S. Carlson, Myriam Fornage, Jeffery Haessler, Li Hsu, Rebecca D. Jackson, Charles Kooperberg, Suzanne M. Leal, Bruce M. Psaty, Eric Boerwinkle, Russell P. Tracy, Diego Ardissino, Svati H. Shah, Cristen J. Willer, Ruth J. F. Loos, Olle Melander, Ruth McPherson, Kees Hovingh, Muredach P. Reilly, Hugh Watkins, Domenico Girelli, Pierre Fontanillas, Daniel I. Chasman, Stacey Gabriel, Richard A. Gibbs, Deborah A. Nickerson, Sekar Kathiresan, Ulrike Peters, Josée Dupuis, James G. Wilson, Stephen S. Rich, Alanna C. Morrison, Emelia J. Benjamin, Myron D. Gross, Alex P. Reiner
Izdano 2014Artigo -
3
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors od Florian Thibord, Derek Klarin, Jennifer A. Brody, Ming‐Huei Chen, Michael G. Levin, Daniel I. Chasman, Ellen L. Goode, Kristian Hveem, Maris Teder‐Laving, Ángel Martínez-Pérez, Dylan Aïssi, Delphine Daian-Bacq, Kaoru Ito, Pradeep Natarajan, Pamela L. Lutsey, Girish N. Nadkarni, Paul S. de Vries, Gabriel Cuéllar-Partida, Brooke N. Wolford, Jack Pattee, Charles Kooperberg, Sigrid K. Brækkan, Ruifang Li‐Gao, Noémie Saut, Corriene Sept, Marine Germain, Renae Judy, Kerri L. Wiggins, Darae Ko, Christopher J. O’Donnell, Kent D. Taylor, Franco Giulianini, Mariza de Andrade, Therese Haugdahl Nøst, Anne Boland, Jean‐Philippe Empana, Satoshi Koyama, Thomas Gilliland, Ron Do, Jennifer E. Huffman, Xin Wang, Wei Zhou, José Manuel Soria, Juan Carlos Souto, Nathan Pankratz, Jeffery Haessler, Kristian Hindberg, Frits R. Rosendaal, Constance Turman, Robert Olaso, Rachel L. Kember, Traci M. Bartz, Julie A. Lynch, Susan R. Heckbert, Sebastian M. Armasu, Ben Brumpton, David M. Smadja, Xavier Jouven, Issei Komuro, Katharine Clapham, Ruth J. F. Loos, Cristen J. Willer, Maria Sabater‐Lleal, James S. Pankow, Alexander P. Reiner, Vânia M. Morelli, Paul M. Ridker, Astrid van Hylckama Vlieg, Jean-François Deleuze, Peter Kraft, Daniel J. Rader, Kyung Min Lee, Bruce M. Psaty, Anne Heidi Skogholt, Joseph Emmerich, Pierre Suchon, Stephen S. Rich, Ha My T. Vy, Weihong Tang, Rebecca D. Jackson, John‐Bjarne Hansen, Pierre‐Emmanuel Morange, Christopher Kabrhel, David‐Alexandre Trégouët, Scott M. Damrauer, Andrew D. Johnson, Nicholas L. Smith
Izdano 2022Artigo
Iskalna orodja:
Sorodne teme
Biology
Gene
Genetic association
Genetics
Genome-wide association study
Genotype
Medicine
Single-nucleotide polymorphism
Bioinformatics
Candidate gene
Allele
Allele frequency
Biobank
Disease
Environmental health
Exome
Exome sequencing
Factor V Leiden
Genetic variants
HNF1A
Internal medicine
Locus (genetics)
Mathematics
Mendelian randomization
Minor allele frequency
Multiple comparisons problem
Phenotype
Population
Prothrombin G20210A
Statistics