Colm O’Dushlaine

Active 2005–2025

Also published as
Colm O'Dushlaine · Colm Ó'Dúshláine
51
Papers
18,917
Citations
40
h-index
43
i10-index

Citations

Citations per year for Colm O’Dushlaine1991: 1 citations1999: 3 citations2002: 2 citations2003: 1 citations2004: 1 citations2006: 3 citations2007: 7 citations2008: 24 citations2009: 89 citations2010: 85 citations2011: 83 citations2012: 114 citations2013: 152 citations2014: 326 citations2015: 306 citations2016: 277 citations2017: 343 citations2018: 324 citations2019: 868 citations2020: 843 citations2021: 886 citations2022: 664 citations2023: 435 citations2024: 585 citations2025: 278 citations2026: 16 citations1992–1998: no citations, so these years are not shown2000–2001: no citations, so these years are not shown2005: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,262 citing papers, 23.7% of this breakdownUnited Kingdom: 1,379 citing papers, 10% of this breakdownChina: 738 citing papers, 5.4% of this breakdownGermany: 719 citing papers, 5.2% of this breakdownNetherlands: 584 citing papers, 4.3% of this breakdownCanada: 573 citing papers, 4.2% of this breakdownAustralia: 551 citing papers, 4% of this breakdownSweden: 513 citing papers, 3.7% of this breakdownItaly: 465 citing papers, 3.4% of this breakdownDenmark: 391 citing papers, 2.8% of this breakdownFrance: 339 citing papers, 2.5% of this breakdownSpain: 308 citing papers, 2.2% of this breakdown
0%23.7%Other 28.6%

Fields

  • Biochemistry, Genetics and Molecular Biology47.1%
  • Medicine35.6%
  • Neuroscience10.2%
  • Psychology3.4%
  • Immunology and Microbiology1.1%
  • Computer Science0.5%
  • Other2.1%

Topics

  • Genetic Associations and Epidemiology10.6%
  • Genomics and Rare Diseases4.4%
  • Genomic variations and chromosomal abnormalities3.5%
  • Genetics and Neurodevelopmental Disorders3.4%
  • Liver Disease Diagnosis and Treatment2.9%
  • Lipid metabolism and disorders2.3%
  • Other72.9%

Coauthors

All papers

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  1. Biobank-driven genomic discovery yields new insight into atrial fibrillation biology

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Whitney Hornsby, Frederick E. Dewey, Michael Boehnke, Sachin Kheterpal, Bhramar Mukherjee, Seunggeun Lee, Hyun Min Kang, Hilma Hólm, Jacob O. Kitzman, Jordan A. Shavit, José Jalife, Chad M. Brummett, Tanya M. Teslovich, David J. Carey, Daníel F. Guðbjartsson, Kāri Stefánsson, Gonçalo R. Abecasis, Kristian Hveem, Cristen J. Willer - Nature Genetics 2018 cited by 936

  2. A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Scott M. Damrauer, Daniel J. Rader, Brian Zambrowicz, William C. Olson, Andrew Murphy, Ingrid B. Borecki, Alan R. Shuldiner, Jeffrey G. Reid, John D. Overton, George D. Yancopoulos, Helen H. Hobbs, Jonathan C. Cohen, Omri Gottesman, Tanya M. Teslovich, Aris Baras, Tooraj Mirshahi, Jesper Gromada, Frederick E. Dewey - New England Journal of Medicine 2018 cited by 805

  3. Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kae‐Woei Liang, Xiuqing Guo, Jerome I. Rotter, Yii‐Der I. Chen, William E. Kraus, Svati H. Shah, Scott M. Damrauer, Aeron Small, Daniel J. Rader, Anders Berg Wulff, Børge G. Nordestgaard, Anne Tybjærg‐Hansen, Anita M. van den Hoek, Hans M.G. Princen, David H. Ledbetter, David J. Carey, John D. Overton, Jeffrey G. Reid, William J. Sasiela, Poulabi Banerjee, Alan R. Shuldiner, Ingrid B. Borecki, Tanya M. Teslovich, George D. Yancopoulos, Scott Mellis, Jesper Gromada, Aris Baras - New England Journal of Medicine 2017 cited by 875

  4. Exome sequencing and characterization of 49,960 individuals in the UK Biobank

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Cristen J. Willer, Kristian Hveem, Joseph B. Leader, David J. Carey, David H. Ledbetter, Lon R. Cardon, George D. Yancopoulos, Aris N. Economides, Giovanni Coppola, Alan R. Shuldiner, Suganthi Balasubramanian, Michael Cantor, Matthew R. Nelson, John C. Whittaker, Jeffrey G. Reid, Jonathan Marchini, John D. Overton, Robert A. Scott, Gonçalo R. Abecasis, Laura M. Yerges-Armstrong, Aris Baras - Nature 2020 cited by 636

  5. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter A Holmans, Ian Jones, George K Kirov, Sarah E. Bergen, Ivan Nikolov, Michael J Owen, Peter Holmans, Stanley Zammit, Katherine Gordon‐Smith, Nicholas Craddock, Lyudmila Georgieva, John S Witte, Detelina Grozeva, Ian D. Jones, Marian L. Hamshere, Ole A Andreassen, Srdjan Djurovic, Morten Mattingsdal, Michael O‘Donovan, Michael J. Owen, Anita Thapar, Robert C Thompson, Stanley J Watson, Nicholas Craddock, Lyudmila Georgieva, Nicholas Bass, Ian D. Jones, Hugh Gurling, Radhika Kandaswamy, Michael O‘Donovan, Michael J. Owen, Anita Thapar, Michael E. Goddard, Michael E. Goddard, Richard Anney, Devin Absher, Richard M. Myers, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ole A. Andreassen, Ingrid Melle, Ingrid Agartz, Robert C. Thompson, Stanley J. Watson, Huda Akil, Fan Meng, Farooq Amin, Ole A. Andreassen, Ingrid Melle, Robert Krasucki, Adebayo Anjorin, Khalid Choudhury, Jacob Lawrence, Hugh Gurling, Jonathan Pimm, Nicholas Bass, Radhika Kandaswamy, Andrew McQuillin, Vinay Puri, Elaine Kenny, Aiden Corvin, Paul Cormican, Derek W. Morris, Richard Anney, Emma M. Quinn, Gary Donohoe, Michael Gill, Louise Gallagher, Dan E. Arking and 270 more - Nature Genetics 2013 cited by 2,353

  6. Computationally efficient whole genome regression for quantitative and binary traits

    Authors: , , , , , , , , , , , , , , , , - Nature Genetics 2020 cited by 1,551

  7. Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2016 cited by 510

  8. Genetic identification of familial hypercholesterolemia within a single U.S. health care system

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Science 2016 cited by 428

  9. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David Collier, Bryan J Mowry, Peter McGuffin, Anne Farmer, Jonna Kuntsi, Ian W. Craig, Stephen Newhouse, Stephen Newhouse, Katherine Gordon-Smith, Detelina Grozeva, Douglas M. Ruderfer, George K Kirov, Valentina Moskvina, Daniëlle Posthuma, Michael J Owen, Nigel Williams, Enda M. Byrne, Sang Lee, Nicholas Craddock, Naomi R. Wray, Pamela Sklar, Michael E Goddard, John S Witte, Tatiana Foroud, Daniel L Koller, Devin Absher, Richard M Myers, Anita Thapar, Ole A Andreassen, Ian Jones, Nigel Williams, Detelina Grozeva, Huda Akil, Peter Holmans, Michael J. Owen, Stanley J Watson, Farooq Amin, Adebayo Anjorin, Nicholas Bass, Khalid Choudhury, Hugh Gurling, Anita Thapar, Ian Jones, Nigel Williams, Pamela Sklar, Michael J. Owen, Vinay Puri, Richard Anney, Paul Cormican, Aiden Corvin, Gary J Donohoe, Louise Gallagher, John S. Witte, Daniel L. Koller, Tatiana Foroud, Richard M. Myers, Devin Absher, Srdjan Djurovic, Morten Mattingsdal, Maria H Azevedo, Ingrid Agartz, Lena Backlund, Ingrid Agartz, Huda Akil, Stanley J. Watson, Fan Meng, Robert C. Thompson, Farooq Amin, Tobias Banaschewski, Jack D Barchas and 275 more - Nature Neuroscience 2015 cited by 798

  10. Genome-wide association analysis identifies 13 new risk loci for schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kenneth S. Kendler, Kuang Lin, Derek W. Morris, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, F. Anthony O’Neill, Michael J. Owen, Milica Pejovic Milovancevic, Daniëlle Posthuma, John Powell, Alexander Richards, Brien P. Riley, Douglas M. Ruderfer, Dan Rujescu, Engilbert Sigurðsson, Teimuraz Silagadze, August B. Smit, Hreinn Stefánsson, Stacy Steinberg, Jaana Suvisaari, Sarah Tosato, Matthijs Verhage, James Walters, Elvira Bramon, Aiden Corvin, Michael O‘Donovan, Kari Stefansson, Edward M. Scolnick, Shaun Purcell, Steven A. McCarroll, Pamela Sklar, Christina M. Hultman, Patrick F. Sullivan - Nature Genetics 2013 cited by 1,565

  11. Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Anthony Marcketta, Matthew S. Lebo, Christina Austin‐Tse, Heather Mason‐Suares, Shannon Bruse, Scott Mellis, Robert S. Phillips, Neil Stahl, Andrew Murphy, Aris N. Economides, Kimberly A. Skelding, Christopher D. Still, James R. Elmore, Ingrid B. Borecki, George D. Yancopoulos, F. Daniel Davis, W. Andrew Faucett, Omri Gottesman, Marylyn D. Ritchie, Alan R. Shuldiner, Jeffrey G. Reid, David H. Ledbetter, Aris Baras, David J. Carey - Science 2016 cited by 607

  12. Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lawrence M. Dolan, Kimberly L. Drews, Amanda Elliott, James S. Floyd, Stacey Gabriel, María Eugenia Garay-Sevilla, Humberto Garcia‐Ortíz, Myron Gross, Sohee Han, Nancy L. Heard‐Costa, Anne Jackson, Marit E. Jørgensen, Hyun Min Kang, Megan M. Kelsey, Bong-Jo Kim, Heikki A. Koistinen, Johanna Kuusisto, Joseph B. Leader, Allan Linneberg, Ching‐Ti Liu, Jianjun Liu, Valeriya Lyssenko, Alisa K. Manning, Anthony Marcketta, Juan Manuel Malacara-Hernández, Angélica Martínez‐Hernández, Karen Matsuo, Elizabeth J. Mayer‐Davis, Elvia Mendoza‐Caamal, Karen L. Mohlke, Alanna C. Morrison, Anne Ndungu, Maggie Ng, Colm O’Dushlaine, A. J. Payne, Catherine Pihoker, Wendy S. Post, Michael Preuß, Bruce M. Psaty, Ramachandran S. Vasan, N. William Rayner, Alexander P. Reiner, M. Revilla, Neil R. Robertson, Nicola Santoro, Claudia Schurmann, Wing Yee So, Xavier Soberón, Heather M. Stringham, Tim M. Strom, Claudia H. T. Tam, Farook Thameem, Brian Tomlinson, Jason Torres, Russell P. Tracy, Rob M. van Dam, Marijana Vujković, Shuai Wang, Ryan Welch, Daniel R. Witte, Tien Yin Wong, Gil Atzmon, Nir Barzilai, John Blangero, Lori L. Bonnycastle, Donald W. Bowden, John C. Chambers, Edmund Chan, Ching‐Yu Cheng, Yoon Shin Cho and 73 more - Nature 2019 cited by 338

  13. Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Roberto Elosúa, Ruth McPherson, Martin Farrall, Hugh Watkins, Eric S. Lander, Daniel J. Rader, John Danesh, Diego Ardissino, Stacey Gabriel, Cristen J. Willer, Gonçalo R. Abecasis, Danish Saleheen, Frederick E. Dewey, Sekar Kathiresan - JAMA 2017 cited by 204

  14. A polygenic burden of rare disruptive mutations in schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven A. McCarroll, Pamela Sklar - Nature 2014 cited by 1,461

  15. Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kyoko Watanabe, Lauren Gurski, Shane McCarthy, Hyun Min Kang, Lee Dobbyn, Eli A. Stahl, Anurag Verma, Giorgio Sirugo, RGC Management and Leadership Team, Gonçalo R. Abecasis, Michael Cantor, Giovanni Coppola, Andrew Deubler, Aris N. Economides, Katia Karalis, Luca A. Lotta, Alan R. Shuldiner, Sequencing and Lab Operations, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Maria Sotiropoulos Padilla, Manasi Pradhan, Kia Manoochehri, Thomas D. Schleicher, Louis Widom, Sarah E. Wolf, Ricardo H. Ulloa, Amelia Averitt, Dadong Li, Sameer Malhotra, Jeffrey Staples, Genome Informatics, Suying Bao, Boris Boutkov, Siying Chen, Gisu Eom, Alicia Hawes, Shareef Khalid, Olga Krasheninina, Rouel Lanche, Evan K. Maxwell, George Mitra, Mona Nafde, Sean O’Keeffe, Max Orelus, Razvan Panea, Tommy Polanco, Ayesha Rasool, Jeffrey G. Reid, William Salerno, Jeffrey Staples, Kathie Sun, Jiwen Xin, Analytical Genomics and Data Science, Joshua Backman, Manuel Allen Revez Ferreira, Arkopravo Ghosh, Christopher E. Gillies, Eric Jorgenson, Hyun Min Kang, Michael D. Kessler, Alexander Li, Nan Lin, Daren Liu, Adam E. Locke, Arden Moscati and 68 more - Nature Genetics 2022 cited by 179

  16. Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Cassandra M. Hartle, Lukas Habegger, Samantha N. Fetterolf, Teresa Tusié‐Luna, Andrew P. Morris, Hilma Hólm, Valgerður Steinthórsdóttir, Patrick Sulem, Unnur Thorsteinsdottir, Jerome I. Rotter, Lee‐Ming Chuang, Scott M. Damrauer, David Birtwell, Chad M. Brummett, Amit V. Khera, Pradeep Natarajan, Marju Orho‐Melander, Jason Flannick, Luca A. Lotta, Cristen J. Willer, Oddgeir L. Holmen, Marylyn D. Ritchie, David H. Ledbetter, Andrew Murphy, Ingrid B. Borecki, Jeffrey G. Reid, John D. Overton, Ola Hansson, Leif Groop, Svati H. Shah, William E. Kraus, Daniel J. Rader, Yii‐Der Ida Chen, Kristian Hveem, Nicholas J. Wareham, Sekar Kathiresan, Olle Melander, Kāri Stefánsson, Børge G. Nordestgaard, Anne Tybjærg‐Hansen, Gonçalo R. Abecasis, David Altshuler, José C. Florez, Michael Boehnke, Mark I. McCarthy, George D. Yancopoulos, David J. Carey, Alan R. Shuldiner, Aris Baras, Frederick E. Dewey, Jesper Gromada - Nature Communications 2018 cited by 153

  17. Promoting the genomic revolution in Africa through the Nigerian 100K Genome Project

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Chiemela Njoku, Bari J. Ballew, Cameron D. Palmer, Abdullahi Musa, Abdulrasheed M. Mujtaba, Abiodun Popoola, Abubakar M. Bello, Anthony Anyanwu, Ashiru Yusuf, G. E. Bozimo, Goddy Bassey, Hadiza Bala, Istifanus Bala Bosan, Jemimah Edah, Mutiu Jimoh, Kenneth Nwankwo, Olalekan Ojo, Marcus Inyama, Maryam Apanpa, M. Mustapha, Musa Ali-Gombe, Olubukola Ojo, Oludare Adeyemi, Samuel Ajayi, Sanusi Bala, Temitope Ojo, Usman Malami Aliyu, Yemi Raheem Raji, Zainab Tanko, Amina Mohammed, David Oladele, Muhammed Hamzat, Emmanuel I. Agaba, Emeka Nwankwo, Ifeoma Ulasi, Jonah Musa, Umeora Odidika, Omolola Salako, Oyekanmi Nashiru, Babatunde Lawal Salako, Colm O’Dushlaine, Abasi Ene–Obong - Nature Genetics 2022 cited by 63

  18. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nicholas J. Schork, Cinnamon S. Bloss, Tatiana Foroud, Daniel L. Koller, Elliot S. Gershon, Chunyu Liu, Judith A. Badner, William A. Scheftner, William Lawson, Evaristus Nwulia, Maria Hipolito, William Coryell, John Rice, William Byerley, Francis J. McMahon, Thomas G. Schulze, Wade H. Berrettini, Falk W. Lohoff, James B. Potash, Pamela B. Mahon, Melvin G. McInnis, Sebastian Zöllner, Peng Zhang, David W. Craig, Szabocls Szelinger, Thomas B. Barrett, René Breuer, Sandra Meier, Jana Strohmaier, Stephanie H. Witt, Federica Tozzi, Anne Farmer, Peter McGuffin, John S. Strauss, Wei Xu, James L Kennedy, John B. Vincent, K. Matthews, Richard Day, Manuel A. R. Ferreira, Colm Ó'Dúshláine, Roy H. Perlis, Soumya Raychaudhuri, Douglas M. Ruderfer, Phil H Lee, Jordan W. Smoller, Jun Li, Devin Absher, William E. Bunney, Jack D. Barchas, Alan F. Schatzberg, Edward G. Jones, Fan Meng, Robert C. Thompson, Stanley J. Watson, Richard M. Myers, Huda Akil, Michael Boehnke, Kim Chambert, Jennifer L. Moran, Ed Scolnick, Srdjan Djurovic, Ingrid Melle, Gunnar Morken, Michael Gill, Derek W. Morris, Emma M. Quinn, Thomas W. Mühleisen, Franziska Degenhardt, Manuel Mattheisen and 72 more - Nature Genetics 2011 cited by 1,412

  19. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mantosh Dewan, James Nemesh, Diana O. Perkins, Shaun Purcell, Jeffrey J. Rakofsky, Edward M. Scolnick, Brooke M. Sklar, Pamela Sklar, Jordan W. Smoller, Patrick F. Sullivan, Fabìo Macciardi, Stephen R. Marder, Ruben C. Gur, Raquel E. Gur, David Braff, Monica E. Calkins, Robert R. Freedman, Michael F. Green, Tiffany A. Greenwood, Laura C. Lazzeroni, Gregory A. Light, Keith H. Nuechterlein, Allen D. Radant, Larry J. Seidman, Larry J. Siever, Jeremy M. Silverman, William S. Stone, Catherine A. Sugar, Neal R. Swerdlow, Debby W. Tsuang, Ming T. Tsuang, Bruce I. Turetsky, Humberto Nicolini, Michael Escamilla, Marquis P. Vawter, Janet L. Sobell, Dolores Malaspina, Douglas S. Lehrer, P.F. Buckley, Mark Hyman Rapaport, James A. Knowles, Ayman H. Fanous, Michele T. Pato, Steven A. McCarroll, Carlos N. Pato - Molecular Psychiatry 2019 cited by 141

  20. Rare chromosomal deletions and duplications increase risk of schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Robert Krasucki, Jacob Lawrence, N J Bass, Douglas H. R. Blackwood, Walter J. Muir, Kevin A. McGhee, Ben Pickard, P. Malloy, AB MacLean, M. Van Beck, Aiden Corvin, M Gill, Derek W. Morris, Colm Ó'Dúshláine, Elaine Kenny, C M Hultman, Paul Lichtenstein, Emma F. Thelander, Carlos N. Pato, Michele T. Pato, Helena Medeiros, Celia Carvalho, A H Fanous, David Conti, James A. Knowles, David St Clair, Soh Leh Kwan, P F Sullivan, P F Sullivan, Stuart MacGregor, Peter M. Visscher, Draga Toncheva, Vihra Milanova, Waddington Jl, Srinivasa Thirumalai, Digby Quested, David Curtis, Caroline Crombie, Gillian Fraser, Nicholas Walker, Frank Middleton, Christopher Morley, Carlos Paz Ferreira, Antonio Macedo, M. Helena Azevedo - Nature 2008 cited by 1,512

  21. Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation

    Authors: , , , , , , , , , , , , - Cell stem cell 2022 cited by 60

  22. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Phil Lee, Mark J. Daly, Benjamin M. Neale, Richard A. Belliveau, Sarah E. Bergen, Elizabeth Bevilacqua, Kimberley D. Chambert, Colm Ó'Dúshláine, Edward M. Scolnick, Jordan W. Smoller, Jennifer L. Moran, Aarno Palotie, Tracey L. Petryshen, Wenting Wu, Douglas S. Greer, Danny Antaki, Aniket Shetty, Madhusudan Gujral, William M. Brandler, Dheeraj Malhotra, Karin V. Fuentes Fajarado, Michelle S. Maile, Peter Holmans, Noa Carrera, Nick Craddock, Valentina Escott‐Price, Lyudmila Georgieva, Marian L. Hamshere, David Kavanagh, Sophie E. Legge, Andrew Pocklington, Alexander Richards, Douglas M. Ruderfer, Nigel Williams, George Kirov, Michael J. Owen, Dalila Pinto, Guiqing Cai, Kenneth L. Davis, Elodie Drapeau, Joseph I. Friedman, Vahram Haroutunian, Elena Parkhomenko, Abraham Reichenberg, Jeremy M. Silverman, Joseph D. Buxbaum, Enrico Domenici, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Ole A. Andreassen, Erik G. Jönsson, Erik Söderman, Margot Albus, Madeline Alexander, Claudine Laurent, Douglas F. Levinson, Farooq Amin, Joshua Atkins, Murray J. Cairns, Rodney J. Scott, Paul A. Tooney, Jing Wu, Silviu‐Alin Bacanu, Tim B. Bigdeli, Mark A. Reimers, Bradley T. Webb, Aaron R. Wolen, Brandon K. Wormley and 268 more - Cell Genomics 2023 cited by 43

  23. Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Omri Gottesman, Anthony Marcketta, Colm O’Dushlaine, Marylyn D. Ritchie, Tom Wilsgaard, Ruth J. F. Loos, Timothy M. Frayling, Michael Boehnke, Erik Ingelsson, David J. Carey, Frederick E. Dewey, Hyun Min Kang, Gonçalo R. Abecasis, Kristian Hveem, Cristen J. Willer - The American Journal of Human Genetics 2017 cited by 118

  24. An allelic-series rare-variant association test for candidate-gene discovery

    Authors: , , , , , , , , - The American Journal of Human Genetics 2023 cited by 28