Alanna C. Morrison

2001–2025 年に発表

134
論文数
18,074
被引用数
69
h 指数
123
i10 指数

被引用数

Alanna C. Morrison の年別被引用数1972 年: 被引用 1 件1988 年: 被引用 1 件1991 年: 被引用 2 件1996 年: 被引用 2 件1998 年: 被引用 1 件2002 年: 被引用 4 件2003 年: 被引用 5 件2004 年: 被引用 2 件2005 年: 被引用 3 件2006 年: 被引用 4 件2007 年: 被引用 10 件2008 年: 被引用 10 件2009 年: 被引用 23 件2010 年: 被引用 59 件2011 年: 被引用 98 件2012 年: 被引用 64 件2013 年: 被引用 96 件2014 年: 被引用 92 件2015 年: 被引用 115 件2016 年: 被引用 158 件2017 年: 被引用 226 件2018 年: 被引用 233 件2019 年: 被引用 617 件2020 年: 被引用 694 件2021 年: 被引用 791 件2022 年: 被引用 784 件2023 年: 被引用 656 件2024 年: 被引用 1,023 件2025 年: 被引用 502 件2026 年: 被引用 53 件1973〜1987 年は被引用が無いため表示していません1989〜1990 年は被引用が無いため表示していません1992〜1995 年は被引用が無いため表示していません1997 年は被引用が無いため表示していません1999〜2001 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 2,769 件、この内訳の 21.4%イギリス: 引用元論文 1,216 件、この内訳の 9.4%中国: 引用元論文 1,000 件、この内訳の 7.7%ドイツ: 引用元論文 688 件、この内訳の 5.3%オランダ: 引用元論文 611 件、この内訳の 4.7%カナダ: 引用元論文 489 件、この内訳の 3.8%オーストラリア: 引用元論文 431 件、この内訳の 3.3%スウェーデン: 引用元論文 426 件、この内訳の 3.3%イタリア: 引用元論文 420 件、この内訳の 3.2%フランス: 引用元論文 334 件、この内訳の 2.6%フィンランド: 引用元論文 297 件、この内訳の 2.3%デンマーク: 引用元論文 291 件、この内訳の 2.3%
0%21.4%その他 30.7%

分野

  • Biochemistry, Genetics and Molecular Biology45.7%
  • Medicine43.8%
  • Immunology and Microbiology3.1%
  • Neuroscience2.5%
  • Nursing1%
  • Psychology0.7%
  • その他3.2%

トピック

  • Genetic Associations and Epidemiology12%
  • Epigenetics and DNA Methylation2.7%
  • Lipoproteins and Cardiovascular Health2.5%
  • Diabetes, Cardiovascular Risks, and Lipoproteins1.9%
  • Bioinformatics and Genomic Networks1.9%
  • Genomics and Rare Diseases1.8%
  • その他77.2%

共著者

全論文

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  1. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Adnan Kastrati, Thorsten Kessler, Theodosios Kyriakou, Tomasz Konopka, Ling Li, Lijiang Ma, Thomas Meitinger, Sören Mucha, Matthias Munz, Federico Murgia, Jonas B. Nielsen, Markus M. Nöthen, Shichao Pang, Tobias Reinberger, Gavin R. Schnitzler, Damian Smedley, Guðmar Þorleifsson, Moritz von Scheidt, Jacob C. Ulirsch, Biobank Japan, EPIC-CVD, John Danesh, Davíð O. Arnar, Noël P. Burtt, Maria C. Costanzo, Jason Flannick, Kaoru Ito, Dongkeun Jang, Yoichiro Kamatani, Amit V. Khera, Issei Komuro, Iftikhar J. Kullo, Luca A. Lotta, Christopher P. Nelson, Robert Roberts, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Tom R. Webb, Aris Baras, Johan Björkegren, Eric Boerwinkle, George Dedoussis, Hilma Hólm, Kristian Hveem, Olle Melander, Alanna C. Morrison, Marju Orho‐Melander, Lοukianos S. Rallidis, Arno Ruusalepp, Marc S. Sabatine, Kāri Stefánsson, Pierre Zalloua, Patrick T. Ellinor, Martin Farrall, John Danesh, Christian T. Ruff, Hilary K. Finucane, Jemma C. Hopewell, Robert Clarke, Rajat M. Gupta, Jeanette Erdmann, Nilesh J. Samani, Heribert Schunkert, Hugh Watkins, Cristen J. Willer, Panos Deloukas, Sekar Kathiresan, Adam S. Butterworth, Paul S. de Vries, Moritz von Scheidt - Nature Genetics 2022 被引用: 706

  2. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Graciela E. Delgado, Spiros Denaxas, Alex S. F. Doney, Marcus Dörr, Samuel C. Dudley, Michael E. Dunn, Gunnar Engström, Tõnu Esko, Stephan B. Felix, Chris Finan, Ian Ford, Mohsen Ghanbari, Sahar Ghasemi, Vilmantas Giedraitis, Franco Giulianini, John S. Gottdiener, Stefan Groß, Daníel F. Guðbjartsson, Rebecca Gutmann, Christopher M. Haggerty, Pim van der Harst, Craig Hyde, Erik Ingelsson, J. Wouter Jukema, Maryam Kavousi, Kay‐Tee Khaw, Marcus E. Kleber, Lars Køber, Andrea Koekemoer, Claudia Langenberg, Lars Lind, Cecilia M. Lindgren, Barry London, Luca A. Lotta, Ruth C. Lovering, Jian’an Luan, Patrik K. E. Magnusson, Anubha Mahajan, Kenneth B. Margulies, Winfried März, Olle Melander, Ify Mordi, Thomas M. Morgan, Andrew D. Morris, Andrew P. Morris, Alanna C. Morrison, Michael W. Nagle, Christopher P. Nelson, Alexander Niessner, Teemu Niiranen, Michelle L. O’Donoghue, Anjali Owens, Colin N. A. Palmer, Helen Parry, Markus Perola, Eliana Portilla-Fernández, Bruce M. Psaty, Goncalo Abecasis, Joshua Backman, Xiaodong Bai, Suganthi Balasubramanian, Nilanjana Banerjee, Aris Baras, Leland Barnard, Christina Beechert, Andrew Blumenfeld, Michael Cantor, Yating Chai, Jonathan Chung, Giovanni Coppola ほか 103 名 - Nature Communications 2020 被引用: 929

  3. ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies

    著者: , , , , , - The American Journal of Human Genetics 2019 被引用: 500

  4. Association of Clonal Hematopoiesis With Incident Heart Failure

    著者: , , , , , , , , , , , , , , , , , , , , , , , , - Journal of the American College of Cardiology 2021 被引用: 215

  5. Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Piera Angelica Merlini, Diego Ardissino, Danish Saleheen, Stacey Gabriel, Sekar Kathiresan - Journal of the American College of Cardiology 2016 被引用: 939

  6. Clonal Hematopoiesis Is Associated With Higher Risk of Stroke

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , NHLBI Trans-Omics for Precision Medicine Program, Pradeep Natarajan, Alexander P. Reiner - Stroke 2021 被引用: 206

  7. CD163+ macrophages promote angiogenesis and vascular permeability accompanied by inflammation in atherosclerosis

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Dan E. Arking, Eric Boerwinkle, Alanna C. Morrison, Jeanette Erdmann, Nona Sotoodehnia, Renu Virmani, Aloke V. Finn - Journal of Clinical Investigation 2018 被引用: 327

  8. American Heart Association’s Life’s Simple 7: Lifestyle Recommendations, Polygenic Risk, and Lifetime Risk of Coronary Heart Disease

    著者: , , , , , , , , , , - Circulation 2022 被引用: 196

  9. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alan F. Wright, Alan R. Shuldiner, Alanna C. Morrison, Albert Hofman, Albert V. Smith, Albert W. Dreisbach, André Franke, André G. Uitterlinden, Andres Metspalu, Anke Tönjes, Antonio Lupo, Antonietta Robino, Åsa Johansson, Ayşe Demirkan, Barbara Kollerits, Barry I. Freedman, Belén Ponte, Ben A. Oostra, Bernhard Paulweber, Bernhard K. Krämer, Braxton D. Mitchell, Brendan M. Buckley, Carmen A. Peralta, Caroline Hayward, Catherine Helmer, Charles N. Rotimi, Christian M. Shaffer, Christian Müller, Cinzia Sala, Cornelia M. van Duijn, Aude Saint-Pierre, Daniel Ackermann, Daniel Shriner, Daniela Ruggiero, Daniela Toniolo, Yingchang Lu, Daniele Cusi, Darina Czamara, David Ellinghaus, David S. Siscovick, Douglas M. Ruderfer, Christian Gieger, Harald Grallert, Elena Rochtchina, Elizabeth J. Atkinson, Elizabeth G. Holliday, Eric Boerwinkle, Erika Salvi, Erwin P. Böttinger, Federico Murgia, Fernando Rivadeneira, Florian Ernst, Florian Kronenberg, Frank B. Hu, Gerjan Navis, Gary C. Curhan, G. Ehret, Georg Homuth, Stefan Coassin, Gian Andri Thun, Giorgio Pistis, Giovanni Gambaro, Giovanni Malerba, Grant W. Montgomery, Guðný Eiríksdóttir, Gunnar Jacobs, Li Guo, H-Erich Wichmann, Harry Campbell, Helena Schmidt ほか 600 名 - Nature Communications 2016 被引用: 536

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 459 名 - Nature Genetics 2020 被引用: 290

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 249 名 - The American Journal of Human Genetics 2018 被引用: 453

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 98 名 - Nature Genetics 2024 被引用: 182

  13. Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populations

    著者: , , , , , , , , , , , , , , , , , , , , , , - Communications Biology 2022 被引用: 107

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 73 名 - Nature 2019 被引用: 338

  15. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Santhi K. Ganesh, Misa Graff, Namrata Gupta, Jiang He, Susan R. Heckbert, Bertha Hidalgo, Chani J. Hodonsky, Marguerite R. Irvin, Andrew D. Johnson, Eric Jorgenson, Robert C. Kaplan, Sharon L. R. Kardia, Tanika N. Kelly, Charles Kooperberg, Jessica Lasky‐Su, Ruth J. F. Loos, Steven A. Lubitz, Rasika A. Mathias, Caitlin McHugh, Courtney G. Montgomery, Jee‐Young Moon, Alanna C. Morrison, Nicholette D. Palmer, Nathan Pankratz, George Papanicolaou, Juan M. Peralta, Patricia A. Peyser, Stephen S. Rich, Jerome I. Rotter, Edwin K. Silverman, Jennifer A. Smith, Nicholas L. Smith, Kent D. Taylor, Timothy A. Thornton, Hemant K. Tiwari, Russell P. Tracy, Tao Wang, Scott T. Weiss, Lu‐Chen Weng, Kerri L. Wiggins, James G. Wilson, Lisa R. Yanek, Sebastian Zöllner, Kari E. North, Paul L. Auer, TOPMed Hematology & Hemostasis Working Group, Laura M. Raffield, Alex P. Reiner, Yun Li - PLoS Genetics 2019 被引用: 322

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 413 名 - Nature Methods 2022 被引用: 109

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 273

  18. Prospective Study of Epigenetic Age Acceleration and Incidence of Cardiovascular Disease Outcomes in the ARIC Study (Atherosclerosis Risk in Communities)

    著者: , , , , - Circulation Genomic and Precision Medicine 2018 被引用: 198

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 21 名 - Science Advances 2022 被引用: 94

  20. Whole genome sequence analysis of blood lipid levels in >66,000 individuals

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael Preuß, May E. Montasser, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Nicholette D. Palmer, Patricia A. Peyser, Muagututi‘a Sefuiva Reupena, Jennifer A. Smith, Xiao Sun, Kent D. Taylor, Russell P. Tracy, Michael Y. Tsai, Zhe Wang, Yuxuan Wang, Wei Bao, John T. Wilkins, Lisa R. Yanek, Wei Zhao, Donna K. Arnett, John Blangero, Eric Boerwinkle, Donald W. Bowden, Yii‐Der Ida Chen, Adolfo Correa, L. Adrienne Cupples, Susan K. Dutcher, Patrick T. Ellinor, Myriam Fornage, Stacey Gabriel, Søren Germer, Richard A. Gibbs, Jiang He, Robert C. Kaplan, Sharon L. R. Kardia, Ryan Kim, Charles Kooperberg, Ruth J. F. Loos, Karine A. Viaud‐Martinez, Rasika A. Mathias, Stephen T. McGarvey, Braxton D. Mitchell, Deborah A. Nickerson, Kari E. North, Bruce M. Psaty, Susan Redline, Alex P. Reiner, Ramachandran S. Vasan, Stephen S. Rich, Cristen J. Willer, Jerome I. Rotter, Daniel J. Rader, Xihong Lin, 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, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas ほか 338 名 - Nature Communications 2022 被引用: 74

  21. Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Petra Vissink, Jie Yao, Wei Zhao, Eric Boerwinkle, Mark O. Goodarzi, Vilmundur Guðnason, J. Wouter Jukema, Sharon L. R. Kardia, Ruth J. F. Loos, Ching‐Ti Liu, Alisa K. Manning, Dennis O. Mook‐Kanamori, James S. Pankow, H. Susan J. Picavet, Naveed Sattar, Eleanor M. Simonsick, W. M. Monique Verschuren, Ko Willems van Dijk, José C. Florez, Jerome I. Rotter, James B. Meigs, Josée Dupuis, Miriam S. Udler - Diabetes Care 2022 被引用: 68

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 1,383

  23. A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

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