Marylyn D. Ritchie
1991–2026 年に発表
- 別表記
- Marylyn D Ritchie
- 306
- 論文数
- 36,322
- 被引用数
- 95
- h 指数
- 245
- i10 指数
被引用数
引用元
国・地域
機関
分野
- Biochemistry, Genetics and Molecular Biology43.4%
- Medicine33.3%
- Computer Science6.7%
- Pharmacology, Toxicology and Pharmaceutics3.9%
- Neuroscience3.1%
- Immunology and Microbiology1.6%
- その他8%
トピック
- Genetic Associations and Epidemiology9.2%
- Bioinformatics and Genomic Networks4.2%
- Genomics and Rare Diseases3%
- Gene expression and cancer classification2.4%
- Genetic Mapping and Diversity in Plants and Animals1.7%
- Pharmacogenetics and Drug Metabolism1.6%
- その他77.9%
共著者
- Jason H. Moore44
- Shefali S. Verma42
- Scott M. Dudek37
- Sarah A. Pendergrass35
- Anurag Verma32
- Gail P. Jarvik31
- Dana C. Crawford30
- Dan M. Roden28
- Joshua C. Denny28
- Daniel J. Rader24
- Iftikhar J. Kullo24
- Yuki Bradford24
- David R. Crosslin21
- Anastasia Lucas20
- Renae Judy20
- Eric B. Larson19
- Dokyoon Kim18
- Li Shen18
- Michael G. Levin17
- Catherine A. McCarty16
- Scott M. Damrauer15
- William S. Bush15
- Håkon Håkonarson14
- Rongling Li14
全論文
- Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
著者: James J. Lee, Robbee Wedow, Aysu Okbay, Edward Kong, Omeed Maghzian, Meghan Zacher, Tuan Anh Nguyen-Viet, Peter N. Bowers, Julia Sidorenko, Richard Karlsson Linnér, Mark Alan Fontana, Tushar Kundu, Chan Wook Lee, Hui Li, Ruoxi Li, Rebecca Royer, Pascal Timshel, Raymond K. Walters, Emily A. Willoughby, Loïc Yengo, Maris Alver, Yanchun Bao, David W. Clark, Felix R. Day, Nicholas A. Furlotte, Peter K. Joshi, Kathryn E. Kemper, Aaron Kleinman, Claudia Langenberg, Reedik Mägi, Joey W. Trampush, Shefali S. Verma, Yang Wu, Max Lam, Jing Hua Zhao, Zhili Zheng, Jason D. Boardman, Harry Campbell, Jeremy Freese, Kathleen Mullan Harris, Caroline Hayward, Pamela Herd, Meena Kumari, Todd Lencz, Jian’an Luan, Anil K. Malhotra, Andres Metspalu, Lili Milani, Ken K. Ong, John R. B. Perry, David J. Porteous, Marylyn D. Ritchie, Melissa Smart, Blair H. Smith, Joyce Y. Tung, Nicholas J. Wareham, James F. Wilson, Jonathan Beauchamp, Dalton Conley, Tõnu Esko, Steven F. Lehrer, Patrik K. E. Magnusson, Sven Oskarsson, Tune H. Pers, Matthew R. Robinson, Kevin Thom, Chelsea Watson, Christopher F. Chabris, Michelle N. Meyer, David Laibson, Jian Yang, Magnus Johannesson, Philipp Koellinger, Patrick Turley, Peter M. Visscher, Daniel J. Benjamin, David Cesarini - Nature Genetics 2018 被引用: 2,846
- Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
著者: Catherine Tcheandjieu, Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni, Shining Ma, Kyung Min Lee, Huaying Fang, Fei Chen, Yingchang Lu, Noah L. Tsao, Sridharan Raghavan, Satoshi Koyama, Bryan R. Gorman, Marijana Vujković, Derek Klarin, Michael G. Levin, Nasa Sinnott-Armstrong, Genevieve L. Wojcik, Mary E. Plomondon, Thomas M. Maddox, Stephen W. Waldo, Alexander G. Bick, Saiju Pyarajan, Jie Huang, Rebecca J. Song, Yuk‐Lam Ho, Steven Buyske, Charles Kooperberg, Jeffrey Haessler, Ruth J. F. Loos, Ron Do, Marie Verbanck, Kumardeep Chaudhary, Kari E. North, Christy L. Avery, Mariaelisa Graff, Christopher A. Haiman, Loı̈c Le Marchand, Lynne R. Wilkens, Joshua C. Bis, Hampton L. Leonard, Botong Shen, Leslie A. Lange, Ayush Giri, Ozan Dikilitas, Iftikhar J. Kullo, Ian B. Stanaway, Gail P. Jarvik, Allan Gordon, Scott J. Hebbring, Bahram Namjou, Kenneth M. Kaufman, Kaoru Ito, Kazuyoshi Ishigaki, Yoichiro Kamatani, Shefali S. Verma, Marylyn D. Ritchie, Rachel L. Kember, Aris Baras, Luca A. Lotta, Biobank Japan, Million Veteran Program, Sekar Kathiresan, Elizabeth R. Hauser, Donald R. Miller, Jennifer S. Lee, Danish Saleheen, Peter D. Reaven, Kelly Cho, J. Michael Gaziano, Pradeep Natarajan, Jennifer E. Huffman, Benjamin F. Voight, Daniel J. Rader, Kyong‐Mi Chang, Julie A. Lynch, Scott M. Damrauer, Peter W.F. Wilson, Hua Tang, Yan V. Sun, Philip S. Tsao, Christopher J. O’Donnell, Themistocles L. Assimes - Nature Medicine 2022 被引用: 353
- Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease
著者: Frederick E. Dewey, Viktoria Gusarova, Richard L. Dunbar, Colm O’Dushlaine, Claudia Schurmann, Omri Gottesman, Shane McCarthy, Cristopher V. Van Hout, Shannon Bruse, Hayes M. Dansky, Joseph B. Leader, Michael F. Murray, Marylyn D. Ritchie, H. Lester Kirchner, Lukas Habegger, Alex Lopez, John S. Penn, An Sha Zhao, Weiping Shao, Neil Stahl, Andrew Murphy, Sara Hamon, Aurelie Bouzelmat, Rick Zhang, Brad Shumel, Robert Pordy, Daniel A. Gipe, Gary Herman, Wayne Huey‐Herng Sheu, I‐Te Lee, 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 被引用: 875
- PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations
著者: Joshua C. Denny, Marylyn D. Ritchie, Melissa A. Basford, Jill M. Pulley, Lisa Bastarache, Kristin Brown-Gentry, Deede Wang, Daniel R. Masys, Dan M. Roden, Dana C. Crawford - Bioinformatics, Bioinform. 2010 被引用: 1,339
- Methods of integrating data to uncover genotype–phenotype interactions
著者: Marylyn D. Ritchie, Emily Holzinger, Ruowang Li, Sarah A. Pendergrass, Dokyoon Kim - Nature Reviews Genetics 2015 被引用: 1,087
- Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
著者: Joshua C. Denny, Lisa Bastarache, Marylyn D. Ritchie, Robert J. Carroll, Raquel Zink, Jonathan D. Mosley, Julie R Field, Jill M. Pulley, Andrea H. Ramirez, Erica Bowton, Melissa Basford, David Carrell, Peggy Peissig, Abel Kho, Jennifer A. Pacheco, Luke V. Rasmussen, David R. Crosslin, Paul K. Crane, Jyotishman Pathak, Suzette J. Bielinski, Sarah A. Pendergrass, Hua Xu, Lucia A. Hindorff, Rongling Li, Teri A. Manolio, Christopher G. Chute, Rex L. Chisholm, Eric B. Larson, Gail P. Jarvik, Murray H. Brilliant, Catherine A. McCarty, Iftikhar J. Kullo, Jonathan L. Haines, Dana C. Crawford, Daniel R. Masys, Dan M. Roden - Nature Biotechnology 2013 被引用: 1,126
- Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease
著者: Hongbo Liu, Tomohito Doke, Dong Guo, Xin Sheng, Ziyuan Ma, Joseph Park, Ha My T. Vy, Girish N. Nadkarni, Amin Abedini, Zhen Miao, Matthew Palmer, Benjamin F. Voight, Hongzhe Li, Christopher D. Brown, Marylyn D. Ritchie, Yan Shu, Katalin Suszták - Nature Genetics 2022 被引用: 214
- The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future
著者: Omri Gottesman, Helena Kuivaniemi, Gerard Tromp, W. Andrew Faucett, Rongling Li, Teri A. Manolio, Saskia C. Sanderson, Joseph Kannry, Randi E. Zinberg, Melissa Basford, Murray H. Brilliant, David J. Carey, Rex L. Chisholm, Christopher G. Chute, John J. Connolly, David R. Crosslin, Joshua C. Denny, Carlos J. Gallego, Jonathan L. Haines, Håkon Håkonarson, John B. Harley, Gail P. Jarvik, Isaac S. Kohane, Iftikhar J. Kullo, Eric B. Larson, Catherine A. McCarty, Marylyn D. Ritchie, Dan M. Roden, Maureen E. Smith, Erwin P. Böttinger, Marc S. Williams - Genetics in Medicine 2013 被引用: 739
- Characterizing Heterogeneity in Neuroimaging, Cognition, Clinical Symptoms, and Genetics Among Patients With Late-Life Depression
著者: Junhao Wen, Cynthia H.Y. Fu, Duygu Tosun, Yogasudha Veturi, Zhijian Yang, Ahmed Abdulkadir, Elizabeth Mamourian, Dhivya Srinivasan, Ioanna Skampardoni, Ashish Singh, Hema Nawani, Jingxuan Bao, Güray Erus, Haochang Shou, Mohamad Habes, Jimit Doshi, Erdem Varol, R. Scott Mackin, Aristeidis Sotiras, Yong Fan, Andrew J. Saykin, Yvette I. Sheline, Li Shen, Marylyn D. Ritchie, David A. Wolk, Marilyn Albert, Susan M. Resnick, Christos Davatzikos, Michael W. Weiner, Paul Aisen, Ronald Petersen, Clifford R. Jack, William J. Jagust, John Q. Trojanowki, Arthur W. Toga, Laurel Beckett, Robert C. Green, Andrew J. Saykin, John C. Morris, Leslie M. Shaw, Enchi Liu, Tom Montine, Ronald G. Thomas, Michael Donohue, Sarah Walter, Devon Gessert, Tamie Sather, Gus Jiminez, Danielle Harvey, Matt A. Bernstein, Nick C. Fox, Paul M. Thompson, Norbert Schuff, Charles DeCarli, Bret Borowski, Jeff Gunter, Matthew L. Senjem, Prashanthi Vemuri, David T. Jones, Kejal Kantarci, Chad Ward, Robert A. Koeppe, Norm Foster, Eric M. Reiman, Kewei Chen, Chet Mathis, Susan Landau, Nigel J. Cairns, Lisa Taylor Reinwald, Virginia Lee, Magdalena Korecka, Michal Figurski, Karen Crawford, Scott Neu, Tatiana Foroud, Steven Potkin, Li Shen, Kelley Faber, Sungeun Kim, Kwangsik Nho, Zaven Kachaturian, Richard Frank, Peter J. Snyder, Susan Molchan, Jeffrey Kaye, Joseph F. Quinn, Betty Lind, Raina Carter, Sara Dolen, Lon S. Schneider, Sonia Pawluczyk, Mauricio Beccera, Liberty Teodoro, Bryan M. Spann, James B. Brewer, Helen Vanderswag, Adam Fleisher, Judith L. Heidebrink, Joanne Lord, Sara S. Mason ほか 214 名 - JAMA Psychiatry 2022 被引用: 147
- Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease
著者: Frederick E. Dewey, Viktoria Gusarova, Colm O’Dushlaine, Omri Gottesman, Jesus Trejos, Charleen Hunt, Cristopher V. Van Hout, Lukas Habegger, David G. Buckler, Ka-Man V. Lai, Joseph B. Leader, Michael F. Murray, Marylyn D. Ritchie, H. Lester Kirchner, David H. Ledbetter, John S. Penn, Alexander Lopez, Ingrid B. Borecki, John D. Overton, Jeffrey G. Reid, David J. Carey, Andrew Murphy, George D. Yancopoulos, Aris Baras, Jesper Gromada, Alan R. Shuldiner - New England Journal of Medicine 2016 被引用: 510
- Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
著者: Michael G. Levin, Noah L. Tsao, Pankhuri Singhal, Chang Liu, Ha My T. Vy, Ishan Paranjpe, Joshua Backman, Tiffany R. Bellomo, William P. Bone, Kiran J. Biddinger, Qin Hui, Ozan Dikilitas, Benjamin A. Satterfield, Yifan Yang, Michael P. Morley, Yuki Bradford, Megan F. Burke, Nosheen Reza, Brian Charest, Renae Judy, Megan J. Puckelwartz, Håkon Håkonarson, Atlas Khan, Leah C. Kottyan, Iftikhar J. Kullo, Yuan Luo, Elizabeth M. McNally, Laura J. Rasmussen‐Torvik, Sharlene M. Day, Ron Do, Lawrence S. Phillips, Patrick T. Ellinor, Girish N. Nadkarni, Marylyn D. Ritchie, Zoltàn Arany, Thomas P. Cappola, Kenneth B. Margulies, Krishna G. Aragam, Christopher M. Haggerty, Jacob Joseph, Yan V. Sun, Benjamin F. Voight, Scott M. Damrauer - Nature Communications 2022 被引用: 146
- Whole-genome sequencing reveals host factors underlying critical COVID-19
著者: Athanasios Kousathanas, Erola Pairo‐Castineira, Konrad Rawlik, A. Stuckey, Christopher A. Odhams, Susan Walker, Clark D Russell, Tomas Malinauskas, Yang Wu, Jonathan Millar, Xia Shen, Katherine S. Elliott, Fiona Griffiths, Wilna Oosthuyzen, Kirstie Morrice, Seán Keating, Bo Wang, Daniel R. Rhodes, Lucija Klarić, Marie Zechner, Nick Parkinson, Afshan Siddiq, Peter Goddard, Sally Donovan, David M. Maslove, Alistair Nichol, Malcolm G. Semple, Tala Zainy, F. Maleady-Crowe, Linda Todd, Shahla Salehi, Julian C. Knight, Greg Elgar, G. C. Chan, Prabhu Arumugam, Christine Patch, Augusto Rendon, David Bentley, Clare Kingsley, Jack A. Kosmicki, Julie Horowitz, Aris Baras, Gonçalo R. Abecasis, Manuel A. R. Ferreira, Anne E. Justice, Tooraj Mirshahi, Matthew T. Oetjens, Daniel J. Rader, Marylyn D. Ritchie, Anurag Verma, Tom Fowler, Manu Shankar‐Hari, Charlotte Summers, Charles Hinds, Peter Horby, Lowell Ling, Daniel F. McAuley, Hugh Montgomery, Peter Openshaw, Paul Elliott, Timothy Walsh, Albert Tenesa, GenOMICC investigators, GenOMICC co-investigators, J. Kenneth Baillie, Colin B. Begg, Sara Clohisey, Charles Hinds, Peter Horby, Julian Knight, Lowell Ling, David M. Maslove, Danny McAuley, Johnny Millar, Hugh Montgomery, Alistair Nichol, Peter J. M. Openshaw, Alexandre C. Pereira, Chris P. Ponting, Kathy Rowan, Malcolm G. Semple, Manu Shankar‐Hari, Charlotte Summers, Timothy Walsh, Latha Aravindan, Ruth Armstrong, Heather Biggs, Ceilia Boz, Adam Brown, Richard Clark, Audrey Coutts, J. Terrence Coyle, Louise Cullum, Sukamal Das, Nicky Day, Lorna Donnelly, Esther Duncan, Angie Fawkes, Paul Finernan, Max Head Fourman ほか 2,299 名 - Nature 2022 被引用: 347
- The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse Population
著者: Anurag Verma, Scott M. Damrauer, Nawar Naseer, JoEllen Weaver, Colleen Morse Kripke, Lindsay Guare, Giorgio Sirugo, Rachel L. Kember, Theodore G. Drivas, Scott Dudek, Yuki Bradford, Anastasia Lucas, Renae Judy, Shefali S. Verma, Emma A. Meagher, Katherine L. Nathanson, Michael D. Feldman, Marylyn D. Ritchie, Daniel J. Rader, For The Penn Medicine BioBank - Journal of Personalized Medicine 2022 被引用: 147
- Why Is the Electronic Health Record So Challenging for Research and Clinical Care?
著者: John H. Holmes, James Beinlich, Mary Regina Boland, Kathryn H. Bowles, Yong Chen, Tessa S. Cook, George Demiris, Michael Draugelis, Laura Fluharty, Peter Gabriel, Robert W. Grundmeier, C. William Hanson, Daniel S. Herman, Blanca E. Himes, Rebecca A. Hubbard, Charles E. Kahn, Dokyoon Kim, Ross Koppel, Qi Long, Nebojša Mirković, Jeffrey S. Morris, Danielle L. Mowery, Marylyn D. Ritchie, Ryan J. Urbanowicz, Jason H. Moore - Methods of Information in Medicine 2021 被引用: 114
- Prior vaccination promotes early activation of memory T cells and enhances immune responses during SARS-CoV-2 breakthrough infection
著者: Mark M. Painter, Timothy S. Johnston, Kendall A. Lundgreen, Jefferson Santos, Juliana S. Qin, Rishi R. Goel, Sokratis A. Apostolidis, Divij Mathew, Bria Fulmer, Justine C. Williams, Michelle L. McKeague, Ajinkya Pattekar, Ahmad Goode, Sean Nasta, Amy E. Baxter, Josephine R. Giles, Ashwin N. Skelly, Laura E Felley, M. A. McLaughlin, JoEllen Weaver, Penn Medicine BioBank, Marylyn D. Ritchie, Michael D. Feldman, JoEllen Weaver, Nawar Naseer, Afiya Poindexter, Ashlei Brock, Khadijah Hu-Sain, Yi-An Ko, Meghan Livingstone, Fred Vadivieso, Ashley Kloter, Stephanie DerOhannessian, Teo Tran, Linda Morrel, Ned Haubein, Joseph Dunn, Anurag Verma, Colleen Morse, Marjorie Risman, Renae Judy, Shefali S. Verma, Yuki Bradford, Scott Dudek, Theodore Drivas, Oliva Kuthuru, Jeanette Dougherty, Sharon Adamski, Sherea Long, Macy Kee, Cynthia Clendenin, Ricardo da Silva Antunes, Alba Grifoni, Daniela Weiskopf, Alessandro Sette, Alexander C. Huang, Daniel J. Rader, Scott E. Hensley, Paul Bates, Allison R. Greenplate, E. John Wherry - Nature Immunology 2023 被引用: 107
- From GWAS to Gene: Transcriptome-Wide Association Studies and Other Methods to Functionally Understand GWAS Discoveries
著者: Binglan Li, Marylyn D. Ritchie - Frontiers in Genetics 2021 被引用: 156
- Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target
著者: Tanmoy Roychowdhury, Derek Klarin, Michael G. Levin, Joshua M. Spin, Yae Hyun Rhee, Alicia Deng, Colwyn A. Headley, Noah L. Tsao, Corry Gellatly, Verena Zuber, Fred Shen, Whitney Hornsby, Ina Holst Laursen, Shefali S. Verma, Adam E. Locke, Guðmundur Einarsson, Guðmar Þorleifsson, Sarah E. Graham, Ozan Dikilitas, Jack Pattee, Renae Judy, Ferran Paüls-Vergés, Jonas B. Nielsen, Brooke N. Wolford, Ben Brumpton, Jaume Dilmé, Olga Peypoch, Laura Calsina Juscafresa, Todd L. Edwards, Dadong Li, Karina Banasik, Søren Brunak, Rikke Louise Jacobsen, Minerva T. Garcia-Barrio, Jifeng Zhang, Lars Melholt Rasmussen, Regent Lee, Ashok Handa, Anders Wanhainen, Kevin Mani, Jes S. Lindholt, Lasse M. Obel, Ewa Strauss, Grzegorz Oszkinis, Christopher P. Nelson, Katie Saxby, Joost A. van Herwaarden, Sander W. van der Laan, Jessica van Setten, Mercedes Camacho, Frank M. Davis, Rachael Wasikowski, Lam C. Tsoi, Jóhann E. Guðjónsson, Jonathan L. Eliason, Dawn M. Coleman, Peter K. Henke, Santhi K. Ganesh, Y. Eugene Chen, Weihua Guan, James S. Pankow, Nathan Pankratz, Ole Birger Pedersen, Christian Erikstrup, Weihong Tang, Kristian Hveem, Daníel F. Guðbjartsson, Sólveig Grétarsdóttir, Unnur Þorsteinsdóttir, Hilma Hólm, Kāri Stefánsson, Manuel A. R. Ferreira, Aris Baras, Iftikhar J. Kullo, Marylyn D. Ritchie, Alex Hørby Christensen, Kasper Iversen, Nikolaj Eldrup, Henrik Sillesen, Sisse Rye Ostrowski, Henning Bundgaard, Henrik Ullum, Stephen Burgess, Dipender Gill, Katherine Gallagher, Maria Sabater‐Lleal, DiscovEHR, UK Aneurysm Growth Study, Frank Dudbridge, Nilesh J. Samani, VA Million Veteran Program, Ida Surakka, Gregory T. Jones, Matthew J. Bown, Philip S. Tsao, Cristen J. Willer, Scott M. Damrauer - Nature Genetics 2023 被引用: 94
- Genetic identification of familial hypercholesterolemia within a single U.S. health care system
著者: Noura S. Abul‐Husn, Kandamurugu Manickam, Laney K. Jones, Eric A. Wright, Dustin N. Hartzel, Claudia Gonzaga‐Jauregui, Colm O’Dushlaine, Joseph B. Leader, H. Lester Kirchner, D’Andra M. Lindbuchler, Marci L Barr, Monica A. Giovanni, Marylyn D. Ritchie, John D. Overton, Jeffrey G. Reid, Raghu Metpally, Amr H. Wardeh, Ingrid B. Borecki, George D. Yancopoulos, Aris Baras, Alan R. Shuldiner, Omri Gottesman, David H. Ledbetter, David J. Carey, Frederick E. Dewey, Michael F. Murray - Science 2016 被引用: 428
- Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries
著者: Abdul Rouf Banday, Megan L. Stanifer, Oscar Flórez-Vargas, Olusegun O. Onabajo, Brenen W. Papenberg, Muhammad Atif Zahoor, Lisa Mirabello, Timothy J. Ring, Chia‐Han Lee, Paul S. Albert, Evangelos Andreakos, Evgeny Arons, Gregory S. Barsh, Leslie G. Biesecker, David L. Boyle, Mark Brahier, Andrea N. Burnett‐Hartman, Mary Carrington, Euijin Chang, Pyoeng Gyun Choe, Rex L. Chisholm, Leandro M. Colli, Clifton L. Dalgard, Carolynn M. Dude, Jeff Edberg, Nathan Erdmann, Heather Spencer Feigelson, Benedito Antônio Lopes da Fonseca, Gary S. Firestein, Adam J. Gehring, Cuncai Guo, Michelle Ho, Steven M. Holland, Amy Hutchinson, Hogune Im, Les’Shon S. Irby, Michael G. Ison, Naima T. Joseph, Hong Bin Kim, Robert J. Kreitman, Bruce R. Korf, Steven M. Lipkin, Siham Mahgoub, Iman Mohammed, Г. Пасчоалини, Jennifer A. Pacheco, Michael J. Peluso, Daniel J. Rader, David T. Redden, Marylyn D. Ritchie, Brooke Rosenblum, M. Elizabeth Ross, Hanaísa P. Sant Anna, Sharon A. Savage, Sudha Sharma, Eleni Siouti, Alicia K. Smith, Vasiliki Triantafyllia, Joselin M. Vargas, Jose D. Vargas, Anurag Verma, Vibha Vij, Duane R. Wesemann, Meredith Yeager, Xu G. Yu, Yu Zhang, Steeve Boulant, Stephen J. Chanock, Jordan J. Feld, Ludmila Prokunina‐Olsson - Nature Genetics 2022 被引用: 138
- Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
著者: Frederick E. Dewey, Michael F. Murray, John D. Overton, Lukas Habegger, Joseph B. Leader, Samantha N. Fetterolf, Colm O’Dushlaine, Cristopher V. Van Hout, Jeffrey Staples, Claudia Gonzaga‐Jauregui, Raghu Metpally, Sarah A. Pendergrass, Monica A. Giovanni, H. Lester Kirchner, Suganthi Balasubramanian, Noura S. Abul‐Husn, Dustin N. Hartzel, Daniel R. Lavage, Korey A. Kost, Jonathan S. Packer, Alexander Lopez, John S. Penn, Semanti Mukherjee, Nehal Gosalia, Manoj Kanagaraj, Alexander Li, Lyndon J. Mitnaul, Lance J. Adams, Thomas N. Person, Kavita Praveen, 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 被引用: 607
- Genetics of height and risk of atrial fibrillation: A Mendelian randomization study
著者: Michael G. Levin, Renae Judy, Dipender Gill, Marijana Vujković, Shefali S. Verma, Yuki Bradford, Marylyn D. Ritchie, Matthew C. Hyman, Saman Nazarian, Daniel J. Rader, Benjamin F. Voight, Scott M. Damrauer - PLoS Medicine 2020 被引用: 197
- The genetic architecture of multimodal human brain age
著者: Junhao Wen, Bingxin Zhao, Zhijian Yang, Güray Erus, Ioanna Skampardoni, Elizabeth Mamourian, Yuhan Cui, Gyujoon Hwang, Jingxuan Bao, Aleix Boquet-Pujadas, Zhen Zhou, Yogasudha Veturi, Marylyn D. Ritchie, Haochang Shou, Paul M. Thompson, Li Shen, Arthur W. Toga, Christos Davatzikos - Nature Communications 2024 被引用: 63
- Biocomputing '97 - Proceedings of the Pacific Symposium
著者: Russ B. Altman, A. Keith Dunker, Lawrence Hunter, Tiffany Murray, Teri E. Klein, Marylyn D. Ritchie - 1996 被引用: 162
- Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants
著者: Christopher M. Haggerty, Scott M. Damrauer, Michael G. Levin, David Birtwell, David J. Carey, Alicia Golden, Dustin N. Hartzel, Yirui Hu, Renae Judy, Melissa Kelly, Rachel L. Kember, H. Lester Kirchner, Joseph B. Leader, Lusha W. Liang, Chris McDermott‐Roe, Apoorva Babu, Michael P. Morley, Zachariah Nealy, Thomas N. Person, Arichanah Pulenthiran, Aeron Small, Diane T. Smelser, Richard C. Stahl, Amy C. Sturm, Heather Williams, Aris Baras, Kenneth B. Margulies, Thomas P. Cappola, Frederick E. Dewey, Anurag Verma, Xinyuan Zhang, Adolfo Correa, Michael E. Hall, James Wilson, Marylyn D. Ritchie, Daniel J. Rader, Michael F. Murray, Brandon K. Fornwalt, Zoltàn Arany, On behalf of the DiscovEHR and Penn Medicine Biobank Studies - Circulation 2019 被引用: 160
