Sekar Kathiresan
}} Sekar Kathiresan is chief executive officer and co-founder of Verve Therapeutics. Verve is pioneering a new approach to the care of cardiovascular disease by developing single-course gene-editing therapies that safely and durably lower plasma LDL cholesterol in order to treat atherosclerotic cardiovascular disease.Kathiresan is a cardiologist and a geneticist who has helped define the inherited basis for heart attack risk and made groundbreaking discoveries of genetic mutations which confer resistance to cardiovascular disease. Prior to joining Verve in July 2019, he served as director of the Massachusetts General Hospital Center for Genomic Medicine and was the Ofer and Shelly Nemirovsky MGH Research Scholar. He also served as director of the Cardiovascular Disease Initiative at the Broad Institute and was a Professor of Medicine at Harvard Medical School.
Kathiresan’s research laboratory focused on understanding the inherited basis for blood lipids and myocardial infarction and using these insights to improve preventive cardiac care. Among his scientific contributions, Kathiresan has helped highlight new biological mechanisms underlying heart attack, discovered mutations that protect against heart attack risk, highlighted triglyceride-rich lipoproteins as a therapeutic target, and developed a framework to interpret the genome for heart attack risk which includes monogenic, somatic, and polygenic drivers of disease risk. He has over 152,000 citations and a h-index of 138 according to Google Scholar.
For his research contributions, he has been honored with a Distinguished Scientist Award from the American Heart Association and the 2018 Curt Stern Award from the American Society of Human Genetics. His clinical focus is the prevention of myocardial infarction in individuals with a family history of heart attack. Provided by Wikipedia
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Genetic determinants of plasma triglycerides by Christopher T. Johansen, Sekar Kathiresan, Robert A. Hegele
Published 2011-02-01
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Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population by Ilaria Guella, Rosanna Asselta, Diego Ardissino, Pier Angelica Merlini, Flora Peyvandi, Sekar Kathiresan, Pier Mannuccio Mannucci, Marco Tubaro, Stefano Duga
Published 2010-11-01
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Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study. by Rahul C Deo, David Reich, Arti Tandon, Ermeg Akylbekova, Nick Patterson, Alicja Waliszewska, Sekar Kathiresan, Daniel Sarpong, Herman A Taylor, James G Wilson
Published 2009-01-01
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The mouse QTL map helps interpret human genome-wide association studies for HDL cholesterol[S] by Magalie S. Leduc, Malcolm Lyons, Katayoon Darvishi, Kenneth Walsh, Susan Sheehan, Sarah Amend, Allison Cox, Marju Orho-Melander, Sekar Kathiresan, Beverly Paigen, Ron Korstanje
Published 2011-06-01
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Polymorphisms at newly identified lipid-associated loci are associated with blood lipids and cardiovascular disease in an Asian Malay population[S] by E. Shyong Tai, Xue Ling Sim, Twee Hee Ong, Tien Yin Wong, Seang Mei Saw, Tin Aung, Sekar Kathiresan, Marju Orho-Melander, Jose M. Ordovas, Jonathan T. Tan, Mark Seielstad
Published 2009-03-01
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EDEM3 Modulates Plasma Triglyceride Level through Its Regulation of LRP1 Expression by Yu-Xin Xu, Gina M. Peloso, Taylor H. Nagai, Taiji Mizoguchi, Amy Deik, Kevin Bullock, Honghuang Lin, Kiran Musunuru, Qiong Yang, Ramachandran S. Vasan, Robert E. Gerszten, Clary B. Clish, Daniel Rader, Sekar Kathiresan
Published 2020-04-01
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Neurocognitive trajectory and proteomic signature of inherited risk for Alzheimer's disease. by Manish D Paranjpe, Mark Chaffin, Sohail Zahid, Scott Ritchie, Jerome I Rotter, Stephen S Rich, Robert Gerszten, Xiuqing Guo, Susan Heckbert, Russ Tracy, John Danesh, Eric S Lander, Michael Inouye, Sekar Kathiresan, Adam S Butterworth, Amit V Khera
Published 2022-09-01
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Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis. by Daniel I Chasman, Guillaume Paré, Samia Mora, Jemma C Hopewell, Gina Peloso, Robert Clarke, L Adrienne Cupples, Anders Hamsten, Sekar Kathiresan, Anders Mälarstig, José M Ordovas, Samuli Ripatti, Alex N Parker, Joseph P Miletich, Paul M Ridker
Published 2009-11-01
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Mining the LIPG allelic spectrum reveals the contribution of rare and common regulatory variants to HDL cholesterol. by Sumeet A Khetarpal, Andrew C Edmondson, Avanthi Raghavan, Hemanth Neeli, Weijun Jin, Karen O Badellino, Serkalem Demissie, Alisa K Manning, Stephanie L DerOhannessian, Megan L Wolfe, L Adrienne Cupples, Mingyao Li, Sekar Kathiresan, Daniel J Rader
Published 2011-12-01
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Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction. by Aenne S Thormaehlen, Christian Schuberth, Hong-Hee Won, Peter Blattmann, Brigitte Joggerst-Thomalla, Susanne Theiss, Rosanna Asselta, Stefano Duga, Pier Angelica Merlini, Diego Ardissino, Eric S Lander, Stacey Gabriel, Daniel J Rader, Gina M Peloso, Rainer Pepperkok, Sekar Kathiresan, Heiko Runz
Published 2015-02-01
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Polygenic Risk Score Identifies Patients at Increased Risk for Abdominal Aortic Aneurysm and May Benefit from Ultrasound Screening by Derek Klarin, Ozan Dikilitas, Brooke Wolford, Michael Levin, Ishan Paranjpe, Renae Judy, Julie Lynch, Themistocles L. Assimes, Yan Sun, Daniel Rader, Peter W. Wilson, Salvatore Scali, Scott Berceli, Sekar Kathiresan, Pradeep Natarajan, Girish Nadkarni, Cristen Willer, Iftikhar Kullo, Scott M. Damrauer, Philip Tsao
Published 2020-01-01
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GalNAc-Lipid nanoparticles enable non-LDLR dependent hepatic delivery of a CRISPR base editing therapy by Lisa N. Kasiewicz, Souvik Biswas, Aaron Beach, Huilan Ren, Chaitali Dutta, Anne Marie Mazzola, Ellen Rohde, Alexandra Chadwick, Christopher Cheng, Sara P. Garcia, Sowmya Iyer, Yuri Matsumoto, Amit V. Khera, Kiran Musunuru, Sekar Kathiresan, Padma Malyala, Kallanthottathil G. Rajeev, Andrew M. Bellinger
Published 2023-05-01
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Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions by Akl C. Fahed, Minxian Wang, Julian R. Homburger, Aniruddh P. Patel, Alexander G. Bick, Cynthia L. Neben, Carmen Lai, Deanna Brockman, Anthony Philippakis, Patrick T. Ellinor, Christopher A. Cassa, Matthew Lebo, Kenney Ng, Eric S. Lander, Alicia Y. Zhou, Sekar Kathiresan, Amit V. Khera
Published 2020-08-01
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Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy by James P. Pirruccello, Alexander Bick, Minxian Wang, Mark Chaffin, Samuel Friedman, Jie Yao, Xiuqing Guo, Bharath Ambale Venkatesh, Kent D. Taylor, Wendy S. Post, Stephen Rich, Joao A. C. Lima, Jerome I. Rotter, Anthony Philippakis, Steven A. Lubitz, Patrick T. Ellinor, Amit V. Khera, Sekar Kathiresan, Krishna G. Aragam
Published 2020-05-01
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Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction. by Gavin Lucas, Carla Lluís-Ganella, Isaac Subirana, Muntaser D Musameh, Juan Ramon Gonzalez, Christopher P Nelson, Mariano Sentí, Myocardial Infarction Genetics Consortium, Wellcome Trust Case Control Consortium, Stephen M Schwartz, David Siscovick, Christopher J O'Donnell, Olle Melander, Veikko Salomaa, Shaun Purcell, David Altshuler, Nilesh J Samani, Sekar Kathiresan, Roberto Elosua
Published 2012-01-01
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RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies. by Christian Herder, Wouter Peeters, Thomas Illig, Jens Baumert, Dominique P V de Kleijn, Frans L Moll, Ulrike Poschen, Norman Klopp, Martina Müller-Nurasyid, Michael Roden, Michael Preuss, CARDIoGRAM Consortium, Mahir Karakas, Christa Meisinger, Barbara Thorand, Gerard Pasterkamp, Wolfgang Koenig, Themistocles L Assimes, Panos Deloukas, Jeanette Erdmann, Hilma Holm, Sekar Kathiresan, Inke R König, Ruth McPherson, Muredach P Reilly, Robert Roberts, Nilesh J Samani, Heribert Schunkert, Alexandre F R Stewart
Published 2011-01-01
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Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium. by Megan L Grove, Bing Yu, Barbara J Cochran, Talin Haritunians, Joshua C Bis, Kent D Taylor, Mark Hansen, Ingrid B Borecki, L Adrienne Cupples, Myriam Fornage, Vilmundur Gudnason, Tamara B Harris, Sekar Kathiresan, Robert Kraaij, Lenore J Launer, Daniel Levy, Yongmei Liu, Thomas Mosley, Gina M Peloso, Bruce M Psaty, Stephen S Rich, Fernando Rivadeneira, David S Siscovick, Albert V Smith, Andre Uitterlinden, Cornelia M van Duijn, James G Wilson, Christopher J O'Donnell, Jerome I Rotter, Eric Boerwinkle
Published 2013-01-01
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