Dawood Darbar

Active 1994–2025

104
Papers
31,359
Citations
71
h-index
101
i10-index

Citations

Citations per year for Dawood Darbar1951: 1 citations1987: 1 citations1995: 1 citations1996: 7 citations1997: 6 citations1998: 15 citations1999: 8 citations2000: 7 citations2001: 13 citations2002: 8 citations2003: 7 citations2004: 19 citations2005: 16 citations2006: 19 citations2007: 12 citations2008: 28 citations2009: 44 citations2010: 103 citations2011: 124 citations2012: 139 citations2013: 162 citations2014: 170 citations2015: 151 citations2016: 145 citations2017: 168 citations2018: 145 citations2019: 455 citations2020: 1,033 citations2021: 1,534 citations2022: 1,473 citations2023: 1,090 citations2024: 1,800 citations2025: 892 citations2026: 52 citations1952–1986: no citations, so these years are not shown1988–1994: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,493 citing papers, 22.4% of this breakdownUnited Kingdom: 1,751 citing papers, 8.7% of this breakdownGermany: 1,210 citing papers, 6% of this breakdownCanada: 960 citing papers, 4.8% of this breakdownNetherlands: 904 citing papers, 4.5% of this breakdownChina: 897 citing papers, 4.5% of this breakdownItaly: 743 citing papers, 3.7% of this breakdownAustralia: 719 citing papers, 3.6% of this breakdownFrance: 714 citing papers, 3.6% of this breakdownSpain: 597 citing papers, 3% of this breakdownDenmark: 470 citing papers, 2.3% of this breakdownSweden: 468 citing papers, 2.3% of this breakdown
0%22.4%Other 30.6%

Fields

  • Medicine45.9%
  • Biochemistry, Genetics and Molecular Biology45.1%
  • Neuroscience3.3%
  • Immunology and Microbiology2.2%
  • Computer Science0.7%
  • Pharmacology, Toxicology and Pharmaceutics0.6%
  • Other2.2%

Topics

  • Genomics and Rare Diseases5.7%
  • Genetic Associations and Epidemiology5.6%
  • Atrial Fibrillation Management and Outcomes4%
  • Cardiac electrophysiology and arrhythmias3.8%
  • Cancer Genomics and Diagnostics2.2%
  • Cardiac Arrhythmias and Treatments2.1%
  • Other76.6%

Coauthors

All papers

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  1. The mutational constraint spectrum quantified from variation in 141,456 humans

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Zachary Zappala, Anne O’Donnell‐Luria, Eric Vallabh Minikel, Ben Weisburd, Monkol Lek, James S. Ware, Christopher Vittal, Irina M. Armean, Louis Bergelson, Kristian Cibulskis, Kristen M. Connolly, Miguel Covarrubias, Stacey Donnelly, Steven Ferriera, Stacey Gabriel, Jeff Gentry, Namrata Gupta, Thibault Jeandet, Diane Kaplan, Christopher Llanwarne, Ruchi Munshi, Sam Novod, Nikelle Petrillo, David Roazen, Valentín Ruano-Rubio, Andrea Saltzman, Molly Schleicher, José Soto, Kathleen Tibbetts, Charlotte Tolonen, Gordon Wade, Michael E. Talkowski, Carlos A. Aguilar‐Salinas, Tariq Ahmad, Christine M. Albert, Diego Ardissino, Gil Atzmon, John Barnard, Laurent Beaugerie, Emelia J. Benjamin, Michael Boehnke, Lori L. Bonnycastle, Erwin P. Böttinger, Donald W. Bowden, Matthew J. Bown, John C. Chambers, Juliana C.N. Chan, Daniel I. Chasman, Judy H. Cho, Mina K. Chung, Bruce M. Cohen, Adolfo Correa, Dana Dabelea, Mark J. Daly, Dawood Darbar, Ravindranath Duggirala, Josée Dupuis, Patrick T. Ellinor, Roberto Elosúa, Jeanette Erdmann, Tõnu Esko, Martti Färkkilâ, José C. Florez, André Franke, Gad Getz, Benjamin Gläser, Stephen J. Glatt, David Goldstein, Clicerio González, Leif Groop and 77 more - Nature 2020 cited by 10,328

  2. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Dan E. Arking, Stella Aslibekyan, Paul L. Auer, John Barnard, R. Graham Barr, Lucas Barwick, Lewis C. Becker, Rebecca Beer, Emelia J. Benjamin, Lawrence F. Bielak, John Blangero, Michael Boehnke, Donald W. Bowden, Jennifer A. Brody, Esteban G. Burchard, Brian E. Cade, James F. Casella, Brandon Chalazan, Daniel I. Chasman, Yii‐Der Ida Chen, Michael H. Cho, Seung Hoan Choi, Mina K. Chung, Clary B. Clish, Adolfo Correa, Joanne E. Curran, Brian Custer, Dawood Darbar, Michelle Daya, Mariza de Andrade, Dawn L. DeMeo, Susan K. Dutcher, Patrick T. Ellinor, Leslie S. Emery, Celeste Eng, Diane Fatkin, Tasha E. Fingerlin, Lukas Forer, Myriam Fornage, Nora Franceschini, Christian Fuchsberger, Stephanie M. Fullerton, Søren Germer, Mark T. Gladwin, Daniel J. Gottlieb, Xiuqing Guo, Michael E. Hall, Jiang He, Nancy L. Heard‐Costa, Susan R. Heckbert, Marguerite R. Irvin, Jill M. Johnsen, Andrew D. Johnson, Robert C. Kaplan, Sharon L. R. Kardia, Tanika N. Kelly, Shannon Kelly, Eimear E. Kenny, Douglas P. Kiel, Robert Klemmer, Barbara A. Konkle, Charles Kooperberg, Anna Köttgen, Leslie A. Lange, Jessica Lasky‐Su, Daniel Levy, Xihong Lin, Keng‐Han Lin, Chunyu Liu, Ruth J. F. Loos and 325 more - Nature 2021 cited by 2,355

  3. A genomic mutational constraint map using variation in 76,156 human genomes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nikelle Petrillo, Gordon Wade, Thibault Jeandet, Ruchi Munshi, Kathleen Tibbetts, María T. Abreu, Carlos A. Aguilar‐Salinas, Tariq Ahmad, Christine M. Albert, Diego Ardissino, Irina M. Armean, Elizabeth G. Atkinson, Gil Atzmon, John Barnard, Samantha Baxter, Laurent Beaugerie, Emelia J. Benjamin, David Benjamin, Michael Boehnke, Lori L. Bonnycastle, Erwin P. Böttinger, Donald W. Bowden, Matthew J. Bown, Harrison Brand, Steven R. Brant, Ted Brookings, Sam Bryant, Sarah E. Calvo, Hannia Campos, John C. Chambers, Juliana C.N. Chan, Katherine R. Chao, Sinéad B. Chapman, Daniel I. Chasman, Rex L. Chisholm, Judy H. Cho, Rajiv Chowdhury, Mina K. Chung, Wendy K. Chung, Kristian Cibulskis, Bruce M. Cohen, Kristen M. Connolly, Adolfo Correa, Beryl B. Cummings, Dana Dabelea, John Danesh, Dawood Darbar, Phil Darnowsky, Joshua C. Denny, Ravindranath Duggirala, Josée Dupuis, Patrick T. Ellinor, Roberto Elosúa, James Emery, Eleina England, Jeanette Erdmann, Tõnu Esko, Emily Evangelista, Diane Fatkin, José C. Florez, André Franke, Jack Fu, Martti Färkkilâ, Kiran Garimella, Jeff Gentry, Gad Getz, David C. Glahn, Benjamin Gläser, Stephen J. Glatt, David B. Goldstein and 138 more - Nature 2023 cited by 1,411

  4. Inherited causes of clonal haematopoiesis in 97,691 whole genomes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sharon L. R. Kardia, Jiang He, Robert C. Kaplan, Nicholas L. Smith, Donna K. Arnett, David A. Schwartz, Adolfo Correa, Mariza de Andrade, Xiuqing Guo, Barbara A. Konkle, Brian Custer, Juan M. Peralta, Hongsheng Gui, Deborah A. Meyers, Stephen T. McGarvey, Ida Yii-Der Chen, M. Benjamin Shoemaker, Patricia A. Peyser, Jai Broome, Stephanie M. Gogarten, Fei Fei Wang, Quenna Wong, May E. Montasser, Michelle Daya, Eimear E. Kenny, Kari E. North, Lenore J. Launer, Brian E. Cade, Joshua C. Bis, Michael H. Cho, Jessica Lasky‐Su, Donald W. Bowden, L. Adrienne Cupples, Angel C. Y. Mak, Lewis C. Becker, Jennifer A. Smith, Tanika N. Kelly, Stella Aslibekyan, Susan R. Heckbert, Hemant K. Tiwari, Ivana V. Yang, John A. Heit, Steven A. Lubitz, Jill M. Johnsen, Joanne E. Curran, Sally E. Wenzel, Daniel E. Weeks, D. C. Rao, Dawood Darbar, Jee‐Young Moon, Russell P. Tracy, Erin Buth, Nicholas Rafaels, Ruth J. F. Loos, Peter Durda, Yongmei Liu, Lifang Hou, Jiwon Lee, Priyadarshini Kachroo, Barry I. Freedman, Daniel Levy, Lawrence F. Bielak, James E. Hixson, James S. Floyd, Eric A. Whitsel, Patrick T. Ellinor, Marguerite R. Irvin, Tasha E. Fingerlin, Laura M. Raffield, Sebastian M. Armasu and 314 more - Nature 2020 cited by 757

  5. Multi-ethnic genome-wide association study for atrial fibrillation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mina K. Chung, John W. Cole, David Conen, James P. Cook, Harry J. Crijns, Michael J. Cutler, Scott M. Damrauer, Brian R. Daniels, Dawood Darbar, Graciela Delgado, Joshua C. Denny, Martin Dichgans, Marcus Dörr, Elton Dudink, Samuel C. Dudley, Nada Esa, Tõnu Esko, Markku Eskola, Diane Fatkin, Stephan B. Felix, Ian Ford, Oscar H. Franco, Bastiaan Geelhoed, Raji P. Grewal, Vilmundur Guðnason, Xiuqing Guo, Namrata Gupta, Stefan Gustafsson, Rebecca Gutmann, Anders Hamsten, Tamara B. Harris, Caroline Hayward, Susan R. Heckbert, Jussi Hernesniemi, Lynne J. Hocking, Albert Hofman, Andréa R. V. R. Horimoto, Jie Huang, Paul L. Huang, Jennifer E. Huffman, Erik Ingelsson, Esra Gücük İpek, Kaoru Ito, Jordi Jiménez‐Conde, Renée Johnson, J. Wouter Jukema, Stefan Kääb, Mika Kähönen, Yoichiro Kamatani, John P. Kane, Adnan Kastrati, Sekar Kathiresan, Petra Katschnig‐Winter, Maryam Kavousi, Thorsten Kessler, Bas Kietselaer, Paulus Kirchhof, Marcus E. Kleber, Stacey Knight, José Eduardo Krieger, Michiaki Kubo, Lenore J. Launer, Jari Laurikka, Terho Lehtimäki, Kirsten Leineweber, Rozenn N. Lemaître, Man Li, Hong Euy Lim, Henry J. Lin, Honghuang Lin and 118 more - Nature Genetics 2018 cited by 810

  6. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lewis C. Becker, Rebecca Beer, Emelia J. Benjamin, Lawrence F. Bielak, John Blangero, Michael Boehnke, Donald W. Bowden, Jennifer A. Brody, Esteban G. Burchard, Brian E. Cade, James F. Casella, Brandon Chalazan, Yii‐Der Ida Chen, Michael H. Cho, Seung Hoan Choi, Mina K. Chung, Clary B. Clish, Adolfo Correa, Joanne E. Curran, Brian Custer, Dawood Darbar, Michelle Daya, Mariza de Andrade, Dawn L. DeMeo, Susan K. Dutcher, Patrick T. Ellinor, Leslie S. Emery, Diane Fatkin, Lukas Forer, Myriam Fornage, Nora Franceschini, Christian Fuchsberger, Stephanie M. Fullerton, Søren Germer, Mark T. Gladwin, Daniel J. Gottlieb, Xiuqing Guo, Michael E. Hall, Jiang He, Nancy L. Heard‐Costa, Susan R. Heckbert, Marguerite R. Irvin, Jill M. Johnsen, Andrew D. Johnson, Sharon L. R. Kardia, Tanika N. Kelly, Shannon Kelly, Eimear E. Kenny, Douglas P. Kiel, Robert Klemmer, Barbara A. Konkle, Charles Kooperberg, Anna Köttgen, Leslie A. Lange, Jessica Lasky‐Su, Daniel Levy, Xihong Lin, Keng‐Han Lin, Chunyu Liu, Ruth J. F. Loos, Lori Garman, Robert E. Gerszten, Steven A. Lubitz, Kathryn L. Lunetta, Angel C. Y. Mak, Ani Manichaikul, Alisa K. Manning, Rasika A. Mathias, David D. McManus, Stephen T. McGarvey and 78 more - 2019 cited by 423

  7. Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes

    Authors: , , , , , , , , , , , , , , , , , - JAMA Cardiology 2021 cited by 172

  8. Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Brandon K. Fornwalt, Diane T. Smelser, Aris Baras, Frederick E. Dewey, Cashell E. Jaquish, George Papanicolaou, Nona Sotoodehnia, David R. Van Wagoner, Bruce M. Psaty, Sekar Kathiresan, Dawood Darbar, Álvaro Alonso, Susan R. Heckbert, Mina K. Chung, Dan M. Roden, Emelia J. Benjamin, Michael F. Murray, Kathryn L. Lunetta, Steven A. Lubitz, Patrick T. Ellinor - JAMA 2018 cited by 233

  9. Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lifang Hou, Donald M. Lloyd‐Jones, Susan Redline, Brian E. Cade, Bruce M. Psaty, Joshua C. Bis, Jennifer A. Brody, Edwin K. Silverman, Jeong H. Yun, Dandi Qiao, Nicholette D. Palmer, Barry I. Freedman, Donald W. Bowden, Michael H. Cho, Dawn L. DeMeo, Ramachandran S. Vasan, Lisa R. Yanek, Lewis C. Becker, Sharon L. R. Kardia, Patricia A. Peyser, Jiang He, Michiel Rienstra, Pim van der Harst, Robert C. Kaplan, Susan R. Heckbert, Nicholas L. Smith, Kerri L. Wiggins, Donna K. Arnett, Marguerite R. Irvin, Hemant K. Tiwari, Michael J. Cutler, Stacey Knight, J. Brent Muhlestein, Adolfo Correa, Laura M. Raffield, Yan Gao, Mariza de Andrade, Jerome I. Rotter, Stephen S. Rich, Russell P. Tracy, Barbara A. Konkle, Jill M. Johnsen, Marsha M. Wheeler, J. G. Smith, Olle Melander, Peter M. Nilsson, Brian Custer, Ravindranath Duggirala, Joanne E. Curran, John Blangero, Stephen T. McGarvey, L. Keoki Williams, Shujie Xiao, Mao Yang, C. Charles Gu, Yii‐Der Ida Chen, Wen‐Jane Lee, Gregory M. Marcus, John P. Kane, Clive R. Pullinger, M. Benjamin Shoemaker, Dawood Darbar, Dan M. Roden, Christine M. Albert, Charles Kooperberg, Ying Zhou, JoAnn E. Manson, Pinkal Desai, Andrew D. Johnson, Rasika A. Mathias and 418 more - Nature 2023 cited by 106

  10. Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thibault Jeandet, Diane Kaplan, Kristen M. Laricchia, Christopher Llanwarne, Eric Vallabh Minikel, Ruchi Munshi, Benjamin M. Neale, Sam Novod, Nikelle Petrillo, Timothy Poterba, David Roazen, Valentín Ruano-Rubio, Andrea Saltzman, Kaitlin E. Samocha, Molly Schleicher, Cotton Seed, Matthew Solomonson, José Soto, Grace Tiao, Kathleen Tibbetts, Charlotte Tolonen, Christopher Vittal, Gordon Wade, Arcturus Wang, Qingbo S. Wang, Nicholas A. Watts, Ben Weisburd, Carlos A. Aguilar‐Salinas, Tariq Ahmad, Christine M. Albert, Diego Ardissino, Gil Atzmon, John Barnard, Laurent Beaugerie, Emelia J. Benjamin, Michael Boehnke, Lori L. Bonnycastle, Erwin P. Böttinger, Donald W. Bowden, Matthew J. Bown, John C. Chambers, Juliana C.N. Chan, Daniel I. Chasman, Judy H. Cho, Mina K. Chung, Bruce M. Cohen, Adolfo Correa, Dana Dabelea, Mark J. Daly, Dawood Darbar, Ravindranath Duggirala, Josée Dupuis, Patrick T. Ellinor, Roberto Elosúa, Jeanette Erdmann, Tõnu Esko, Martti Färkkilâ, José C. Florez, André Franke, Gad Getz, Benjamin Gläser, Stephen J. Glatt, David Goldstein, Clicerio González, Leif Groop, Christopher Haiman, Craig L. Hanis, Matthew B. Harms, Mikko Hiltunen, Matti Holi and 71 more - Nature Communications 2020 cited by 191

  11. Evaluating drug targets through human loss-of-function genetic variation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Diane Kaplan, Konrad J. Karczewski, Kristen M. Laricchia, Christopher Llanwarne, Eric V. Minikel, Ruchi Munshi, Benjamin M. Neale, Sam Novod, Anne H. O’Donnell-Luria, Nikelle Petrillo, Timothy Poterba, David Roazen, Valentin Ruano-Rubio, Andrea Saltzman, Kaitlin E. Samocha, Molly Schleicher, Cotton Seed, Matthew Solomonson, Jose Soto, Grace Tiao, Kathleen Tibbetts, Charlotte Tolonen, Christopher Vittal, Gordon Wade, Arcturus Wang, Qingbo Wang, James S. Ware, Nicholas A. Watts, Ben Weisburd, Nicola Whiffin, Carlos A. Aguilar Salinas, Tariq Ahmad, Christine M. Albert, Diego Ardissino, Gil Atzmon, John Barnard, Laurent Beaugerie, Emelia J. Benjamin, Michael Boehnke, Lori L. Bonnycastle, Erwin P. Bottinger, Donald W. Bowden, Matthew J. Bown, John C. Chambers, Juliana C. Chan, Daniel Chasman, Judy Cho, Mina K. Chung, Bruce Cohen, Adolfo Correa, Dana Dabelea, Mark J. Daly, Dawood Darbar, Ravindranath Duggirala, Josée Dupuis, Patrick T. Ellinor, Roberto Elosua, Jeanette Erdmann, Tõnu Esko, Martti Färkkilä, Jose Florez, Andre Franke, Gad Getz, Benjamin Glaser, Stephen J. Glatt, David Goldstein, Clicerio Gonzalez, Leif Groop, Christopher Haiman, Craig Hanis and 74 more - Nature 2020 cited by 181

  12. Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia Genes

    Authors: , , , , , , , , , , , , , , , , , , , , , - JAMA Cardiology 2022 cited by 52

  13. Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Meher Preethi Boorgula, Wei Zhao, Lisa R. Yanek, Kerri L. Wiggins, James E. Hixson, C. Charles Gu, Gina M. Peloso, Dan M. Roden, Muagututi‘a Sefuiva Reupena, Chii‐Min Hwu, Dawn L. DeMeo, Kari E. North, Shannon Kelly, Solomon K. Musani, Joshua C. Bis, Donald M. Lloyd‐Jones, Jill M. Johnsen, Michael Preuß, Russell P. Tracy, Patricia A. Peyser, Dandi Qiao, Pinkal Desai, Joanne E. Curran, Barry I. Freedman, Hemant K. Tiwari, Sameer Chavan, Jennifer A. Smith, Nicholas L. Smith, Tanika N. Kelly, Bertha Hidalgo, L. Adrienne Cupples, Daniel E. Weeks, Nicola L. Hawley, Ryan L. Minster, The Samoan Obesity, Lifestyle and Genetic Adaptations Study (OLaGA) Group, Ranjan Deka, Take Naseri, Lisa de las Fuentes, Laura M. Raffield, Alanna C. Morrison, Paul S. de Vries, Christie M. Ballantyne, Eimear E. Kenny, Stephen S. Rich, Eric A. Whitsel, Michael H. Cho, M. Benjamin Shoemaker, Betty S. Pace, John Blangero, Nicholette D. Palmer, Braxton D. Mitchell, Alan R. Shuldiner, Kathleen C. Barnes, Susan Redline, Sharon L.R. Kardia, Gonçalo R. Abecasis, Lewis C. Becker, Susan R. Heckbert, Jiang He, Wendy S. Post, Donna K. Arnett, Ramachandran S. Vasan, Dawood Darbar, Scott T. Weiss, Stephen T. McGarvey, Mariza de Andrade, Yii‐Der Ida Chen, Robert C. Kaplan, Deborah A. Meyers, Brian Custer and 21 more - Science Advances 2022 cited by 94

  14. Meta-analysis identifies six new susceptibility loci for atrial fibrillation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lenore J. Launer, R. W. Davies, Matthew Borkovich, Tamara B. Harris, Honghuang Lin, Uwe Völker, Henry Völzke, David J. Milan, Albert Hofman, Eric Boerwinkle, Lin Y. Chen, Elsayed Z. Soliman, Benjamin F. Voight, Li Guo, Aravinda Chakravarti, Michiaki Kubo, Usha B. Tedrow, Lynda M. Rose, Paul M. Ridker, David Conen, Tatsuhiko Tsunoda, Tetsushi Furukawa, Nona Sotoodehnia, Siyan Xu, Naoyuki Kamatani, Daniel Levy, Yusuke Nakamura, Babar Parvez, Saagar Mahida, Karen L. Furie, Jonathan Rosand, Raafia Muhammad, Bruce M. Psaty, Thomas Meitinger, Siegfried Perz, H‐Erich Wichmann, Jacqueline C.M. Witteman, W.H. Linda Kao, Sekar Kathiresan, Dan M. Roden, André G. Uitterlinden, Fernando Rivadeneira, Barbara McKnight, Marketa Sjögren, Anne B. Newman, Yongmei Liu, Michael H. Gollob, Olle Melander, Toshihiro Tanaka, Bruno H. Stricker, Stephan B. Felix, Álvaro Alonso, Dawood Darbar, John Barnard, Daniel I. Chasman, Susan R. Heckbert, Emelia J. Benjamin, Vilmundur Guðnason, Stefan Kääb - Nature Genetics 2012 cited by 609

  15. Transcript expression-aware annotation improves rare variant interpretation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laura D. Gauthier, Jeff Gentry, Namrata Gupta, Thibault Jeandet, Diane Kaplan, Konrad J. Karczewski, Kristen M. Laricchia, Christopher Llanwarne, Eric Vallabh Minikel, Ruchi Munshi, Benjamin M. Neale, Sam Novod, Anne O’Donnell‐Luria, Nikelle Petrillo, Timothy Poterba, David Roazen, Valentín Ruano-Rubio, Andrea Saltzman, Kaitlin E. Samocha, Molly Schleicher, Cotton Seed, Matthew Solomonson, José Soto, Grace Tiao, Kathleen Tibbetts, Charlotte Tolonen, Christopher Vittal, Gordon Wade, Arcturus Wang, Qingbo S. Wang, James S. Ware, Nicholas A. Watts, Ben Weisburd, Nicola Whiffin, Carlos A. Aguilar‐Salinas, Tariq Ahmad, Christine M. Albert, Diego Ardissino, Gil Atzmon, John Barnard, Laurent Beaugerie, Emelia J. Benjamin, Michael Boehnke, Lori L. Bonnycastle, Erwin P. Böttinger, Donald W. Bowden, Matthew J. Bown, John C. Chambers, Juliana C.N. Chan, Daniel I. Chasman, Judy H. Cho, Mina K. Chung, Bruce M. Cohen, Adolfo Correa, Dana Dabelea, Mark J. Daly, Dawood Darbar, Ravindranath Duggirala, Josée Dupuis, Patrick T. Ellinor, Roberto Elosúa, Jeanette Erdmann, Tõnu Esko, Martti Färkkilâ, José C. Florez, André Franke, Gad Getz, Benjamin Gläser, Stephen J. Glatt, David Goldstein and 78 more - Nature 2020 cited by 202

  16. Common variants in KCNN3 are associated with lone atrial fibrillation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David J. Milan, Siegfried Perz, Tōnu Esko, Anna Köttgen, Susanne Moebus, Christopher Newton‐Cheh, Man Li, Stefan Möhlenkamp, Thomas J. Wang, W.H. Linda Kao, Ramachandran S. Vasan, Markus M. Nöthen, Calum A. MacRae, Bruno H. Stricker, Albert Hofman, André G. Uitterlinden, Daniel Levy, Eric Boerwinkle, Andres Metspalu, Eric J. Topol, Aravinda Chakravarti, Vilmundur Guðnason, Bruce M. Psaty, Dan M. Roden, Thomas Meitinger, H-Erich Wichmann, Jacqueline C.M. Witteman, John Barnard, Dan E. Arking, Emelia J. Benjamin, Susan R. Heckbert, Stefan Kääb - Nature Genetics 2010 cited by 486

  17. The APPLE score: a novel and simple score for the prediction of rhythm outcomes after catheter ablation of atrial fibrillation

    Authors: , , , , , , , , , , , , , - Clinical Research in Cardiology 2015 cited by 226

  18. 2012 ACCF/AHA/HRS Focused Update Incorporated Into the ACCF/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael J. Silka, Lynne W. Stevenson, William G. Stevenson, Paul D. Varosy, Jeffrey L. Anderson, Alice K. Jacobs, Jonathan L. Halperin, Nancy M. Albert, Mark A. Creager, David L. DeMets, Steven M. Ettinger, Robert A. Guyton, Judith S. Hochman, Frederick G. Kushner, E. Magnus Ohman, William G. Stevenson, Clyde W. Yancy - Circulation 2012 cited by 1,492

  19. Ion Channel and Structural Remodeling in Obesity-Mediated Atrial Fibrillation

    Authors: , , , , , , , , , , , - Circulation Arrhythmia and Electrophysiology 2020 cited by 101

  20. Cardiac Sodium Channel ( SCN5A ) Variants Associated with Atrial Fibrillation

    Authors: , , , , , , , - Circulation 2008 cited by 341

  21. Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nikelle Petrillo, Gordon Wade, Thibault Jeandet, Ruchi Munshi, Kathleen Tibbetts, María T. Abreu, Carlos A. Aguilar‐Salinas, Tariq Ahmad, Christine M. Albert, Diego Ardissino, Irina M. Armean, Elizabeth G. Atkinson, Gil Atzmon, John Barnard, Samantha Baxter, Laurent Beaugerie, Emelia J. Benjamin, David Benjamin, Michael Boehnke, Lori L. Bonnycastle, Erwin P. Böttinger, Donald W. Bowden, Matthew J. Bown, Harrison Brand, Steven R. Brant, Ted Brookings, Sam Bryant, Sarah E. Calvo, Hannia Campos, John C. Chambers, Juliana C.N. Chan, Katherine R. Chao, Sinéad B. Chapman, Daniel I. Chasman, Rex L. Chisholm, Judy H. Cho, Rajiv Chowdhury, Mina K. Chung, Wendy K. Chung, Kristian Cibulskis, Bruce M. Cohen, Kristen M. Connolly, Adolfo Correa, Beryl B. Cummings, Dana Dabelea, John Danesh, Dawood Darbar, Phil Darnowsky, Joshua C. Denny, Ravindranath Duggirala, Josée Dupuis, Patrick T. Ellinor, Roberto Elosúa, James Emery, Eleina England, Jeanette Erdmann, Tõnu Esko, Emily Evangelista, Diane Fatkin, José C. Florez, André Franke, Jack Fu, Martti Färkkilâ, Kiran Garimella, Jeff Gentry, Gad Getz, David C. Glahn, Benjamin Gläser, Stephen J. Glatt, David B. Goldstein and 138 more - Nature 2024 cited by 184

  22. The effect of LRRK2 loss-of-function variants in humans

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