Kenneth Rice

Active 1993–2026

113
Papers
28,257
Citations
85
h-index
111
i10-index

Citations

Citations per year for Kenneth Rice1972: 1 citations1988: 2 citations1991: 1 citations1994: 4 citations1995: 4 citations1996: 1 citations1997: 1 citations1998: 6 citations1999: 9 citations2000: 15 citations2001: 12 citations2002: 11 citations2003: 11 citations2004: 12 citations2005: 14 citations2006: 17 citations2007: 27 citations2008: 28 citations2009: 50 citations2010: 197 citations2011: 288 citations2012: 337 citations2013: 350 citations2014: 347 citations2015: 329 citations2016: 354 citations2017: 364 citations2018: 397 citations2019: 1,237 citations2020: 1,174 citations2021: 1,202 citations2022: 857 citations2023: 591 citations2024: 776 citations2025: 314 citations2026: 21 citations1973–1987: no citations, so these years are not shown1989–1990: no citations, so these years are not shown1992–1993: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,950 citing papers, 20.4% of this breakdownUnited Kingdom: 1,845 citing papers, 9.5% of this breakdownChina: 1,210 citing papers, 6.3% of this breakdownGermany: 1,066 citing papers, 5.5% of this breakdownNetherlands: 934 citing papers, 4.8% of this breakdownCanada: 780 citing papers, 4% of this breakdownAustralia: 717 citing papers, 3.7% of this breakdownSweden: 705 citing papers, 3.6% of this breakdownFrance: 617 citing papers, 3.2% of this breakdownItaly: 603 citing papers, 3.1% of this breakdownDenmark: 497 citing papers, 2.6% of this breakdownSpain: 479 citing papers, 2.5% of this breakdown
0%20.4%Other 30.8%

Fields

  • Medicine45.9%
  • Biochemistry, Genetics and Molecular Biology38.9%
  • Neuroscience5.3%
  • Psychology2.4%
  • Nursing2.1%
  • Immunology and Microbiology1.5%
  • Other3.9%

Topics

  • Genetic Associations and Epidemiology10.1%
  • Vitamin D Research Studies1.8%
  • Bioinformatics and Genomic Networks1.6%
  • Genetic Mapping and Diversity in Plants and Animals1.6%
  • Epigenetics and DNA Methylation1.6%
  • Genomics and Rare Diseases1.4%
  • Other81.9%

Coauthors

All papers

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  1. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Carlos Cruchaga, John Danesh, Paul I. W. de Bakker, Anita L. DeStefano, Marcel den Hoed, Qing Duan, Stefan T. Engelter, Guido J. Falcone, Rebecca F. Gottesman, Raji P. Grewal, Vilmundur Guðnason, Stefan Gustafsson, Jeffrey Haessler, Tamara B. Harris, Ahamad Hassan, Aki S. Havulinna, Susan R. Heckbert, Elizabeth G. Holliday, George Howard, Fang‐Chi Hsu, Hyacinth I. Hyacinth, M. Arfan Ikram, Erik Ingelsson, Marguerite R. Irvin, Xueqiu Jian, Jordi Jiménez‐Conde, Julie A. Johnson, J. Wouter Jukema, Masahiro Kanai, Keith L. Keene, Brett Kissela, Dawn Kleindorfer, Charles Kooperberg, Michiaki Kubo, Leslie A. Lange, Carl D. Langefeld, Claudia Langenberg, Lenore J. Launer, Jin‐Moo Lee, Robin Lemmens, Didier Leys, Cathryn M. Lewis, Wei‐Yu Lin, Arne G. Lindgren, Erik Lorentzen, Patrik K. E. Magnusson, Jane Maguire, Ani Manichaikul, Patrick F. McArdle, James F. Meschia, Braxton D. Mitchell, Thomas H. Mosley, Michael A. Nalls, Toshiharu Ninomiya, Martin O’Donnell, Bruce M. Psaty, Sara L. Pulit, Kristiina Rannikmäe, Alex P. Reiner, Kathryn M. Rexrode, Kenneth Rice, Stephen S. Rich, Paul M. Ridker, Natalia S. Rost, Peter M. Rothwell, Jerome I. Rotter, Tatjana Rundek, Ralph L. Sacco, Saori Sakaue, Michèle M. Sale and 328 more - Nature Genetics 2018 cited by 1,726

  2. Analysis of shared heritability in common disorders of the brain

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , M. Ilyas Kamboh, Eric B. Larson, Ekaterina Rogaeva, Peter St George‐Hyslop, Håkon Håkonarson, Walter A. Kukull, Lindsay A. Farrer, Lisa L. Barnes, Thomas G. Beach, F. Yesim Demirci, Elizabeth Head, Christine M. Hulette, Gregory A. Jicha, John S.K. Kauwe, Jeffrey A. Kaye, James B. Leverenz, Allan I. Levey, Andrew P. Lieberman, V. Shane Pankratz, Wayne W. Poon, Joseph F. Quinn, Andrew J. Saykin, Lon S. Schneider, Amanda Smith, Joshua A. Sonnen, Robert A. Stern, Vivianna M. Van Deerlin, Linda J. Van Eldik, Denise Harold, Giancarlo Russo, David C. Rubinsztein, Anthony Bayer, Magda Tsolaki, Petra Proitsi, Nick C. Fox, Harald Hampel, Michael J. Owen, Simon Mead, Peter Passmore, Kevin Morgan, Markus M. Nöthen, Jonathan M. Schott, Martin N. Rossor, Michelle K. Lupton, Per Hoffmann, Johannes Kornhuber, Brian Lawlor, Andrew McQuillin, Ammar Al‐Chalabi, Joshua C Bis, Agustı́n Ruiz, Merçé Boada, Sudha Seshadri, Alexa Beiser, Kenneth Rice, Sven J. van der Lee, Philip L. De Jager, Daniel H. Geschwind, Matthias Riemenschneider, Steffi G. Riedel‐Heller, Jerome I. Rotter, Gerhard Ransmayr, Bradley T. Hyman, Carlos Cruchaga, Montserrat Alegret, Bendik S. Winsvold, Priit Palta, Kai-How Farh, Ester Cuenca-León, Nicholas A. Furlotte and 477 more - Science 2018 cited by 2,050

  3. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thor Aspelund, Albert V. Smith, Vilmundur Guðnason, Thor Aspelund, Albert Hofman, María Soler Artigas, Nick Shrine, Louise V. Wain, Martin D. Tobin, André G. Uitterlinden, Najaf Amin, Yurii S. Aulchenko, Cornelia M. van Duijn, M. Arfan Ikram, Eric J.G. Sijbrands, John C. Chambers, Cornelia M. van Duijn, Peter Würtz, Ayşe Demirkan, Albert Hofman, Aaron Isaacs, Gonçalo R. Abecasis, Germaine C. Verwoert, André G. Uitterlinden, Eric J.G. Sijbrands, Joshua C. Bis, Bruce M. Psaty, Lenore Launer, Germaine C. Verwoert, Tamara B. Harris, M. Arfan Ikram, Jian’an Luan, Germaine C. Verwoert, André G. Uitterlinden, Simon Heath, Daniel Levy, Péter Vollenweider, Peter Würtz, Elin Org, Gudrun Veldre, John C. Chambers, Paul Elliott, Weihua Zhang, Gonçalo R. Abecasis, Jennifer L. Bragg‐Gresham, Uwe Völker, Alexander Teumer, Joshua C. Bis, Nicole L. Glazer, Bruce M. Psaty, Tamara B. Harris, Melissa N. Garcia, Lenore J. Launer, Nicole Soranzo, Jing Zhao, Ruth J. F. Loos, Nicholas J. Wareham, Mark Lathrop, Diana Zélénika, Simon Heath, Siim Sõber, Maris Laan, Gudrun Veldre, Elin Org, Halit Ongen, Anuj Goel, Afshin Parsa, Nanette Steinle, Alan R. Shuldiner, Yuri Milaneschi and 246 more - Nature 2011 cited by 2,083

  4. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael C. Mahaney, Ani Manichaikul, Lisa W. Martin, Rasika A. Mathias, Stephen T. McGarvey, Braxton D. Mitchell, May E. Montasser, Jill E. Moore, Alanna C. Morrison, Jeffrey R. O’Connell, Nicholette D. Palmer, Akhil Pampana, Juan M. Peralta, Patricia A. Peyser, Bruce M. Psaty, Susan Redline, Kenneth Rice, Stephen S. Rich, Jennifer A. Smith, Hemant K. Tiwari, Michael Y. Tsai, Ramachandran S. Vasan, Fei Fei Wang, Daniel E. Weeks, Zhiping Weng, James G. Wilson, Lisa R. Yanek, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan Arking, Donna K. Arnett, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Lawrence F. Bielak, Joshua C. Bis, Thomas W. Blackwell, John Blangero, Eric Boerwinkle, Donald W. Bowden, Russell P. Bowler, Jennifer Brody, Ulrich Broeckel, Jai Broome, Karen Bunting and 459 more - Nature Genetics 2020 cited by 290

  5. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marcus E. Kleber, Yuri Milaneschi, Christian Mueller, Mahmudul Huq, Efthymia Vlachopoulou, Leo-Pekka Lyytikäinen, Christopher Oldmeadow, Joris Deelen, Markus Perola, Jing Hua Zhao, Bjarke Feenstra, Behrooz Z. Alizadeh, H. Marike Boezen, Lude Franke, Pim van der Harst, Gerjan Navis, Marianne G. Rots, Harold Snieder, Morris Swertz, Bruce H. R. Wolffenbuttel, Cisca Wijmenga, Marzyeh Amini, Emelia J. Benjamin, Daniel I. Chasman, Abbas Dehghan, Tarunveer S. Ahluwalia, James B. Meigs, Russell P. Tracy, Behrooz Z. Alizadeh, Symen Ligthart, Josh Bis, Gudny Eiriksdottir, Nathan Pankratz, Myron Gross, Alex Rainer, Harold Snieder, James Wilson, Bruce M. Psaty, Josée Dupuis, Bram P. Prins, Urmo Vaso, Maria G. Stathopoulou, Lude Franke, Terho Lehtimäki, Wolfgang Köenig, Yalda Jamshidi, Sophie Siest, Ali Abbasi, André G. Uitterlinden, Mohammadreza Abdollahi, Renate B. Schnabel, Ursula M. Schick, Ilja M. Nolte, Aldi T. Kraja, Yi‐Hsiang Hsu, Daniel S. Tylee, Alyson Zwicker, Rudolf Uher, George Davey-Smith, Alanna C. Morrison, Andrew A. Hicks, Cornelia M. van Duijn, Cavin Ward‐Caviness, Eric Boerwinkle, Jerome I. Rotter, Kenneth Rice, Leslie A. Lange, Markus Perola, Eco J. C. de Geus, Andrew P. Morris and 249 more - The American Journal of Human Genetics 2018 cited by 453

  6. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lorenz Risch, Ulf Gyllensten, Olle Melander, Harriëtte Riese, James F. Wilson, Harry Campbell, Stephen S. Rich, Bruce M. Psaty, Yingchang Lu, Jerome I. Rotter, Xiuqing Guo, Kenneth Rice, Péter Vollenweider, Johan Sundström, Claudia Langenberg, Martin D. Tobin, Vilmantas Giedraitis, Jian’an Luan, Jaakko Tuomilehto, Zoltán Kutalik, Samuli Ripatti, Veikko Salomaa, Giorgia Girotto, Stella Trompet, J. Wouter Jukema, Pim van der Harst, Paul M. Ridker, Franco Giulianini, Véronique Vitart, Anuj Goel, Hugh Watkins, Sarah E. Harris, Ian J. Deary, Peter J. van der Most, Albertine J. Oldehinkel, Bernard Keavney, Caroline Hayward, Archie Campbell, Michael Boehnke, Laura J. Scott, Thibaud Boutin, Chrysovalanto Mamasoula, Marjo‐Riitta Järvelin, Annette Peters, Christian Gieger, Edward G. Lakatta, Francesco Cucca, Jennie Hui, Paul Knekt, Stefan Enroth, Martin H. de Borst, Ozren Polašek, Maria Pina Concas, Eulalia Catamo, Massimiliano Cocca, Ruifang Li-Gao, Edith Hofer, Helena Schmidt, Beatrice Spedicati, Melanie Waldenberger, David P. Strachan, Maris Laan, Alexander Teumer, Marcus Dörr, Vilmundur Guðnason, James P. Cook, Daniela Ruggiero, Ivana Kolčić, Eric Boerwinkle, Michela Traglia and 98 more - Nature Genetics 2024 cited by 182

  7. Detectable clonal mosaicism from birth to old age and its relationship to cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , William J. Blot, Lisa B. Signorello, Sue A. Ingles, Stephen J. Chanock, Sonja I. Berndt, Loı̈c Le Marchand, Brian E. Henderson, Kristine R. Monroe, John A. Heit, Mariza de Andrade, Sebastian M. Armasu, C Régnier, William L. Lowe, M. Geoffrey Hayes, Mary L. Marazita, Eleanor Feingold, Jeffrey C. Murray, Mads Melbye, Bjarke Feenstra, Jae H. Kang, Janey L. Wiggs, Gail P. Jarvik, Andrew McDavid, Venkatraman Seshan, Daniel B. Mirel, Andrew Crenshaw, Nataliya Sharopova, Anastasia L. Wise, Jess Shen, David R. Crosslin, David Levine, Xiuwen Zheng, Jenna Udren, Siiri Bennett, Sarah C. Nelson, Stephanie M. Gogarten, Matthew P. Conomos, Patrick J. Heagerty, Teri A. Manolio, Louis R. Pasquale, Christopher A. Haiman, Neil E. Caporaso, Bruce S. Weir - Nature Genetics 2012 cited by 599

  8. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Xiuqing Guo, Rita R. Kalyani, Charles Kooperberg, Brian G. Kral, Leslie A. Lange, Bridget M. Lin, Ani Manichaikul, Alisa K. Manning, Lisa W. Martin, Rasika A. Mathias, James B. Meigs, Braxton D. Mitchell, May E. Montasser, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Nicholette D. Palmer, Patricia A. Peyser, Bruce M. Psaty, Laura M. Raffield, Susan Redline, Alex P. Reiner, Muagututi‘a Sefuiva Reupena, Kenneth Rice, Stephen S. Rich, Jennifer A. Smith, Kent D. Taylor, Margaret A. Taub, Ramachandran S. Vasan, Daniel E. Weeks, James G. Wilson, Lisa R. Yanek, Wei Zhao, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Nathan R. Blue, Russell P. Bowler, Ulrich Broeckel, Jai Broome, Deborah Brown and 413 more - Nature Methods 2022 cited by 109

  9. Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models

    Authors: , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2016 cited by 478

  10. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Megan L. Grove, Albert V. Smith, Shih‐Jen Hwang, Han Chen, Tianxiao Huan, Gülüm Kosova, Nathan O. Stitziel, Sekar Kathiresan, Nilesh J. Samani, Heribert Schunkert, Panos Deloukas, Man Li, Christian Fuchsberger, Cristian Pattaro, Mathias Gorski, Charles Kooperberg, George Papanicolaou, Jacques E. Rossouw, Jessica D. Faul, Sharon L. R. Kardia, Claude Bouchard, Leslie J. Raffel, André G. Uitterlinden, Oscar H. Franco, Ramachandran S. Vasan, Christopher J. O’Donnell, Kent D. Taylor, Kiang Liu, Erwin P. Böttinger, Omri Gottesman, E. Warwick Daw, Franco Giulianini, Santhi K. Ganesh, Elias Salfati, Tamara B. Harris, Lenore J. Launer, Marcus Dörr, Stephan B. Felix, Rainer Rettig, Henry Völzke, Eric H. Kim, Wen‐Jane Lee, I‐Te Lee, Wayne H-H Sheu, Krystal S. Tsosie, Digna R. Velez Edwards, Ching‐Ti Liu, Adolfo Correa, David R. Weir, Uwe Völker, Paul M. Ridker, Eric Boerwinkle, Vilmundur Guðnason, Alex P. Reiner, Cornelia M. van Duijn, Ingrid B. Borecki, Todd L. Edwards, Aravinda Chakravarti, Jerome I. Rotter, Bruce M. Psaty, Ruth J. F. Loos, Myriam Fornage, Georg Ehret, Christopher Newton‐Cheh, Daniel Levy, Daniel I. Chasman - Nature Genetics 2016 cited by 273

  11. Quality control and quality assurance in genotypic data for genome‐wide association studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Genetic Epidemiology 2010 cited by 498

  12. A Re-Evaluation of Fixed Effect(s) Meta-Analysis

    Authors: , , - Journal of the Royal Statistical Society Series A (Statistics in Society) 2017 cited by 294

  13. 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

  14. Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , George Papanicolaou, Thomas Lumley, Adam A. Szpiro, Kari E. North, Kenneth Rice, Timothy A. Thornton, Cathy C. Laurie - The American Journal of Human Genetics 2016 cited by 370

  15. Genome-wide association study of blood pressure and hypertension

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jerome I. Rotter, Josef Coresh, Emelia J. Benjamin, André G. Uitterlinden, Gerardo Heiss, Caroline S. Fox, Jacqueline C.M. Witteman, Eric Boerwinkle, Thomas J. Wang, Vilmundur Guðnason, Martin G. Larson, Aravinda Chakravarti, Bruce M. Psaty, Cornelia M. van Duijn - Nature Genetics 2009 cited by 1,383

  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. Common genetic determinants of vitamin D insufficiency: a genome-wide association study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Myles Wolf, Kenneth Rice, David Goltzman, Nick Hidiroglou, Martin Ladouceur, Nicholas J. Wareham, Lynne J. Hocking, Deborah Hart, Nigel Arden, Cyrus Cooper, Suneil Malik, William D. Fraser, Anna-Liisa Hartikainen, Guangju Zhai, Helen M. Macdonald, Nita G. Forouhi, Ruth J. F. Loos, David M. Reid, Alan J. Hakim, Elaine Dennison, Ching‐Ti Liu, Chris Power, Helen E. Stevens, Laitinen Jaana, Ramachandran S. Vasan, Nicole Soranzo, Jörg Bojunga, Bruce M. Psaty, Mattias Lorentzon, Tatiana Foroud, Tamara B. Harris, Albert Hofman, John-Olov Jansson, Jane A. Cauley, André G. Uitterlinden, Quince Gibson, Marjo‐Riitta Järvelin, David Karasik, David S. Siscovick, Michael J. Econs, Stephen B. Kritchevsky, José C. Florez, John A. Todd, Josée Dupuis, Elina Hyppönen, Timothy D. Spector - The Lancet 2010 cited by 1,542

  18. Genetic Loci Associated with Plasma Phospholipid n-3 Fatty Acids: A Meta-Analysis of Genome-Wide Association Studies from the CHARGE Consortium

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Luigi Ferrucci, Myriam Fornage, Michael Y. Tsai, Dariush Mozaffarian, Lyn M. Steffen - PLoS Genetics 2011 cited by 429

  19. Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Anna Köttgen, Olivier Le Bacquer, François Pattou, Jalal Taneera, Valgerður Steinthórsdóttir, Denis Rybin, Kristin Ardlie, Michael Sampson, Lu Qi, Mandy van Hoek, Michael N. Weedon, Yurii S. Aulchenko, Benjamin F. Voight, Harald Grallert, Beverley Balkau, Richard N. Bergman, Suzette J. Bielinski, Amélie Bonnefond, Lori L. Bonnycastle, Knut Borch‐Johnsen, Yvonne Böttcher, Eric J. Brunner, Thomas A. Buchanan, Suzannah J. Bumpstead, Christine Cavalcanti-Proença, G. Charpentier, Yii-Der Ida Chen, Peter S. Chines, Francis S. Collins, Marilyn C. Cornelis, Gabriel Crawford, Jérôme Delplanque, Alex S. F. Doney, Josephine M. Egan, Michael R. Erdos, Mathieu Firmann, Nita G. Forouhi, Caroline S. Fox, Mark O. Goodarzi, Jürgen Graessler, Aroon D. Hingorani, Bo Isomaa, Torben Jørgensen, Mika Kivimäki, Péter Kovács, Knut Krohn, Meena Kumari, Torsten Lauritzen, Claire Lévy‐Marchal, Vladimir Mayor, Jarred B. McAteer, Stephen Eyre, Braxton D. Mitchell, Karen L. Mohlke, Mario A. Morken, Narisu Narisu, Colin N A Palmer, Ruth Pakyz, Laura Pascoe, Felicity Payne, Daniel S. Pearson, Wolfgang Rathmann, Annelli Sandbæk, Avan Aihie Sayer, Laura J. Scott, Stephen J. Sharp, Eric J.G. Sijbrands, Andrew B. Singleton, David S. Siscovick, Nicholas L. Smith and 13 more - Nature Genetics 2010 cited by 636

  20. Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jennifer G. Robinson, David S. Siscovick, Pamela J. Schreiner, Josyf C. Mychaleckyj, James S. Pankow, Albert Hofman, André G. Uitterlinden, Tamara B. Harris, Kent D. Taylor, Jeanette M. Stafford, Lindsay M. Reynolds, Riccardo E. Marioni, Abbas Dehghan, Oscar H. Franco, Aniruddh P. Patel, Yingchang Lu, George Hindy, Omri Gottesman, Erwin P. Böttinger, Olle Melander, Marju Orho‐Melander, Ruth J. F. Loos, Stefano Duga, Piera Angelica Merlini, Martin Farrall, Anuj Goel, Rosanna Asselta, Domenico Girelli, Nicola Martinelli, Svati H. Shah, William E. Kraus, Mingyao Li, Daniel J. Rader, Muredach P. Reilly, Ruth McPherson, Hugh Watkins, Diego Ardissino, Qunyuan Zhang, Judy Wang, Michael Y. Tsai, Herman A. Taylor, Adolfo Correa, Michael Griswold, Leslie A. Lange, John M. Starr, Igor Rudan, Guðný Eiríksdóttir, Lenore J. Launer, José M. Ordovás, Daniel Levy, Yu Chen, Alex P. Reiner, Caroline Hayward, Ozren Polašek, Ian J. Deary, Ingrid B. Borecki, Ching‐Ti Liu, Vilmundur Guðnason, James G. Wilson, Cornelia M. van Duijn, Charles Kooperberg, Stephen S. Rich, Bruce M. Psaty, Jerome I. Rotter, Christopher J. O’Donnell, Kenneth Rice, Eric Boerwinkle, Sekar Kathiresan, L. Adrienne Cupples - The American Journal of Human Genetics 2014 cited by 348

  21. GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alan B. Zonderman, Albert Hofman, Alexander Teumer, Amanda J. Cox, André G. Uitterlinden, Andrew Wong, Andries J. Smit, Anne B. Newman, Annie Britton, Arno Ruusalepp, Bengt Sennblad, Bo Hedblad, Bogdan Paşaniuc, Brenda W.J.H. Penninx, Carl D. Langefeld, Christina L. Wassel, Christophe Tzourio, Cristiano Fava, Damiano Baldassarre, Daniel H. O’Leary, Daniel Teupser, Diana Kuh, Elena Tremoli, Elmo Mannarino, Enzo Grossi, E BOERWINKLE, Eric E. Schadt, Erik Ingelsson, Fabrizio Veglia, Fernando Rivadeneira, Frank Beutner, Ganesh Chauhan, Gerardo Heiss, Harold Snieder, Harry Campbell, Henry Völzke, Hugh S. Markus, Ian J. Deary, J. Wouter Jukema, Jacqueline de Graaf, Jacqueline Price, Janne Pott, Jemma C. Hopewell, Jingjing Liang, Joachim Thiery, Jorgen Engmann, Karl Gertow, Kenneth Rice, Kent D. Taylor, Klodian Dhana, Lambertus A. Kiemeney, Lars Lind, Laura M. Raffield, Lenore J. Launer, Lesca M. Holdt, Marcus Dörr, Martin Dichgans, Matthew Traylor, Matthias Sitzer, Meena Kumari, Mika Kivimäki, Mike A. Nalls, Olle Melander, Olli T. Raitakari, Oscar H. Franco, Oscar L. Rueda‐Ochoa, Panos Roussos, Peter H. Whincup, Philippe Amouyel, Philippe Giral and 203 more - Nature Communications 2018 cited by 178

  22. Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2022 cited by 57

  23. Survival is affected by mutation type and molecular mechanism in vascular Ehlers–Danlos syndrome (EDS type IV)

    Authors: , , , , , - Genetics in Medicine 2014 cited by 300

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