Marylyn DeRiggi Ritchie (Marylyn Ritchie, Marylyn D Ritchie)

ORCID

Publication Activity (10 Years)

Years Active: 2014-2024
Publications (10 Years): 65

Top Venues

Nature communications

Nature genetics

medRxiv : the preprint server for health sciences

Journal of medical Internet research

This page only lists publications with an associated author ORCID identifier.

Publications

Joseph D Romano, Van Q Truong, Rachit Kumar, Mythreye Venkatesan, Britney E Graham, Yun Hao, Nicholas Matsumoto, Xi Li, Zhiping Wang, Marylyn DeRiggi Ritchie, Li Shen, Jason H Moore
The Alzheimer's Knowledge Base: A Knowledge Graph for Alzheimer Disease Research. Journal of medical Internet research 26 (2024)
Joseph D Romano, Van Q Truong, Rachit Kumar, Mythreye Venkatesan, Britney E Graham, Yun Hao, Nicholas Matsumoto, Xi Li, Zhiping Wang, Marylyn DeRiggi Ritchie, Li Shen, Jason H Moore
The Alzheimer's Knowledge Base: A Knowledge Graph for Alzheimer Disease Research. Journal of medical Internet research 26 (2024)
Junhao Wen, Bingxin Zhao, Zhijian Yang, Guray Erus, Ioanna Skampardoni, Elizabeth Mamourian, Yuhan Cui, Gyujoon Hwang, Jingxuan Bao, Aleix Boquet-Pujadas, Zhen Zhou, Yogasudha Veturi, Marylyn DeRiggi Ritchie, Haochang Shou, Paul M Thompson, Li Shen, Arthur W Toga, Christos Davatzikos
The genetic architecture of multimodal human brain age. Nature communications 15 (1) (2024)
Allison Chae, Michael S Yao, Hersh Sagreiya, Ari D Goldberg, Neil Chatterjee, Matthew T MacLean, Jeffrey T Duda, Ameena Elahi, Arijitt Borthakur, Marylyn DeRiggi Ritchie, Daniel James Rader, Charles E Kahn, Walter R Witschey, James C Gee
Strategies for Implementing Machine Learning Algorithms in the Clinical Practice of Radiology. Radiology 310 (1) (2024)
Junhao Wen, Bingxin Zhao, Zhijian Yang, Guray Erus, Ioanna Skampardoni, Elizabeth Mamourian, Yuhan Cui, Gyujoon Hwang, Jingxuan Bao, Aleix Boquet-Pujadas, Zhen Zhou, Yogasudha Veturi, Marylyn DeRiggi Ritchie, Haochang Shou, Paul M Thompson, Li Shen, Arthur W Toga, Christos Davatzikos
The genetic architecture of multimodal human brain age. Nature communications 15 (1) (2024)
Allison Chae, Michael S Yao, Hersh Sagreiya, Ari D Goldberg, Neil Chatterjee, Matthew T MacLean, Jeffrey T Duda, Ameena Elahi, Arijitt Borthakur, Marylyn DeRiggi Ritchie, Daniel James Rader, Charles E Kahn, Walter R Witschey, James C Gee
Strategies for Implementing Machine Learning Algorithms in the Clinical Practice of Radiology. Radiology 310 (1) (2024)
Jack A Kosmicki, Anthony Marcketta, Deepika Sharma, Silvio Alessandro Di Gioia, Samantha Batista, Xiao-Man Yang, Gannie Tzoneva, Hector Martinez, Carlo Sidore, Michael D Kessler, Julie E Horowitz, Genevieve H L Roberts, Anne E Justice, Nilanjana Banerjee, Marie V Coignet, Joseph B Leader, Danny S Park, Rouel Lanche, Evan Maxwell, Spencer C Knight, Xiaodong Bai, Harendra Guturu, Asher Baltzell, Ahna R Girshick, Shannon R McCurdy, Raghavendran Partha, Adam J Mansfield, David A Turissini, Miao Zhang, Joelle Mbatchou, Kyoko Watanabe, Anurag Verma, Giorgio Sirugo, null null, null null, null null, null null, Marylyn DeRiggi Ritchie, William J Salerno, Alan R Shuldiner, Daniel James Rader, Tooraj Mirshahi, Jonathan Marchini, John D Overton, David J Carey, Lukas Habegger, Jeffrey G Reid, Aris N Economides, Christos A Kyratsous, Katia Karalis, Alina Baum, Michael N Cantor, Kristin A Rand, Eurie L Hong, Catherine A Ball, Katherine Siminovitch, Aris Baras, Gonçalo R Abecasis, Manuel A R Ferreira
Genetic risk factors for COVID-19 and influenza are largely distinct. Nature genetics (2024)
Joseph D Romano, Van Q Truong, Rachit Kumar, Mythreye Venkatesan, Britney E Graham, Yun Hao, Nicholas Matsumoto, Xi Li, Zhiping Wang, Marylyn DeRiggi Ritchie, Li Shen, Jason H Moore
The Alzheimer's Knowledge Base: A Knowledge Graph for Alzheimer Disease Research. Journal of medical Internet research 26 (2024)
Jack A Kosmicki, Anthony Marcketta, Deepika Sharma, Silvio Alessandro Di Gioia, Samantha Batista, Xiao-Man Yang, Gannie Tzoneva, Hector Martinez, Carlo Sidore, Michael D Kessler, Julie E Horowitz, Genevieve H L Roberts, Anne E Justice, Nilanjana Banerjee, Marie V Coignet, Joseph B Leader, Danny S Park, Rouel Lanche, Evan Maxwell, Spencer C Knight, Xiaodong Bai, Harendra Guturu, Asher Baltzell, Ahna R Girshick, Shannon R McCurdy, Raghavendran Partha, Adam J Mansfield, David A Turissini, Miao Zhang, Joelle Mbatchou, Kyoko Watanabe, Anurag Verma, Giorgio Sirugo, null null, null null, null null, null null, Marylyn DeRiggi Ritchie, William J Salerno, Alan R Shuldiner, Daniel James Rader, Tooraj Mirshahi, Jonathan Marchini, John D Overton, David J Carey, Lukas Habegger, Jeffrey G Reid, Aris N Economides, Christos A Kyratsous, Katia Karalis, Alina Baum, Michael N Cantor, Kristin A Rand, Eurie L Hong, Catherine A Ball, Katherine Siminovitch, Aris Baras, Gonçalo R Abecasis, Manuel A R Ferreira
Genetic risk factors for COVID-19 and influenza are largely distinct. Nature genetics 56 (8) (2024)
Junhao Wen, Bingxin Zhao, Zhijian Yang, Guray Erus, Ioanna Skampardoni, Elizabeth Mamourian, Yuhan Cui, Gyujoon Hwang, Jingxuan Bao, Aleix Boquet-Pujadas, Zhen Zhou, Yogasudha Veturi, Marylyn DeRiggi Ritchie, Haochang Shou, Paul M Thompson, Li Shen, Arthur W Toga, Christos Davatzikos
The genetic architecture of multimodal human brain age. Nature communications 15 (1) (2024)
Jack A Kosmicki, Anthony Marcketta, Deepika Sharma, Silvio Alessandro Di Gioia, Samantha Batista, Xiao-Man Yang, Gannie Tzoneva, Hector Martinez, Carlo Sidore, Michael D Kessler, Julie E Horowitz, Genevieve H L Roberts, Anne E Justice, Nilanjana Banerjee, Marie V Coignet, Joseph B Leader, Danny S Park, Rouel Lanche, Evan Maxwell, Spencer C Knight, Xiaodong Bai, Harendra Guturu, Asher Baltzell, Ahna R Girshick, Shannon R McCurdy, Raghavendran Partha, Adam J Mansfield, David A Turissini, Miao Zhang, Joelle Mbatchou, Kyoko Watanabe, Anurag Verma, Giorgio Sirugo, null null, null null, null null, null null, Marylyn DeRiggi Ritchie, William J Salerno, Alan R Shuldiner, Daniel James Rader, Tooraj Mirshahi, Jonathan Marchini, John D Overton, David J Carey, Lukas Habegger, Jeffrey G Reid, Aris N Economides, Christos A Kyratsous, Katia Karalis, Alina Baum, Michael N Cantor, Kristin A Rand, Eurie L Hong, Catherine A Ball, Katherine Siminovitch, Aris Baras, Gonçalo R Abecasis, Manuel A R Ferreira
Genetic risk factors for COVID-19 and influenza are largely distinct. Nature genetics 56 (8) (2024)
Allison Chae, Michael S Yao, Hersh Sagreiya, Ari D Goldberg, Neil Chatterjee, Matthew T MacLean, Jeffrey T Duda, Ameena Elahi, Arijitt Borthakur, Marylyn DeRiggi Ritchie, Daniel James Rader, Charles E Kahn, Walter R Witschey, James C Gee
Strategies for Implementing Machine Learning Algorithms in the Clinical Practice of Radiology. Radiology 310 (1) (2024)
Daniel Hui, Scott Dudek, Krzysztof Kiryluk, Theresa L Walunas, Iftikhar J Kullo, Wei-Qi Wei, Hemant K Tiwari, Josh F Peterson, Wendy K Chung, Brittney Davis, Atlas Khan, Leah C Kottyan, Nita A Limdi, QiPing Feng, Megan J Puckelwartz, Chunhua Weng, Johanna L Smith, Elizabeth W Karlson, null null, Gail P Jarvik, Marylyn DeRiggi Ritchie
Risk factors affecting polygenic score performance across diverse cohorts. medRxiv : the preprint server for health sciences (2024)
Junhao Wen, Bingxin Zhao, Zhijian Yang, Guray Erus, Ioanna Skampardoni, Elizabeth Mamourian, Yuhan Cui, Gyujoon Hwang, Jingxuan Bao, Aleix Boquet-Pujadas, Zhen Zhou, Yogasudha Veturi, Marylyn DeRiggi Ritchie, Haochang Shou, Paul M Thompson, Li Shen, Arthur W Toga, Christos Davatzikos
The genetic architecture of multimodal human brain age. Nature communications 15 (1) (2024)
Daniel Hui, Scott Dudek, Krzysztof Kiryluk, Theresa L Walunas, Iftikhar J Kullo, Wei-Qi Wei, Hemant K Tiwari, Josh F Peterson, Wendy K Chung, Brittney Davis, Atlas Khan, Leah C Kottyan, Nita A Limdi, QiPing Feng, Megan J Puckelwartz, Chunhua Weng, Johanna L Smith, Elizabeth W Karlson, null null, Gail P Jarvik, Marylyn DeRiggi Ritchie
Risk factors affecting polygenic score performance across diverse cohorts. medRxiv : the preprint server for health sciences (2024)
Allison Chae, Michael S Yao, Hersh Sagreiya, Ari D Goldberg, Neil Chatterjee, Matthew T MacLean, Jeffrey T Duda, Ameena Elahi, Arijitt Borthakur, Marylyn DeRiggi Ritchie, Daniel James Rader, Charles E Kahn, Walter R Witschey, James C Gee
Strategies for Implementing Machine Learning Algorithms in the Clinical Practice of Radiology. Radiology 310 (1) (2024)
Junhao Wen, Bingxin Zhao, Zhijian Yang, Guray Erus, Ioanna Skampardoni, Elizabeth Mamourian, Yuhan Cui, Gyujoon Hwang, Jingxuan Bao, Aleix Boquet-Pujadas, Zhen Zhou, Yogasudha Veturi, Marylyn DeRiggi Ritchie, Haochang Shou, Paul M Thompson, Li Shen, Arthur W Toga, Christos Davatzikos
The genetic architecture of multimodal human brain age. Nature communications 15 (1) (2024)
Daniel Hui, Scott Dudek, Krzysztof Kiryluk, Theresa L Walunas, Iftikhar J Kullo, Wei-Qi Wei, Hemant K Tiwari, Josh F Peterson, Wendy K Chung, Brittney Davis, Atlas Khan, Leah C Kottyan, Nita A Limdi, QiPing Feng, Megan J Puckelwartz, Chunhua Weng, Johanna L Smith, Elizabeth W Karlson, Regeneron Genetics Center, Gail P Jarvik, Marylyn DeRiggi Ritchie
Risk factors affecting polygenic score performance across diverse cohorts. medRxiv : the preprint server for health sciences (2024)
Joseph D Romano, Van Q Truong, Rachit Kumar, Mythreye Venkatesan, Britney E Graham, Yun Hao, Nicholas Matsumoto, Xi Li, Zhiping Wang, Marylyn DeRiggi Ritchie, Li Shen, Jason H Moore
The Alzheimer's Knowledge Base: A Knowledge Graph for Alzheimer Disease Research. Journal of medical Internet research 26 (2024)
Jack A Kosmicki, Anthony Marcketta, Deepika Sharma, Silvio Alessandro Di Gioia, Samantha Batista, Xiao-Man Yang, Gannie Tzoneva, Hector Martinez, Carlo Sidore, Michael D Kessler, Julie E Horowitz, Genevieve H L Roberts, Anne E Justice, Nilanjana Banerjee, Marie V Coignet, Joseph B Leader, Danny S Park, Rouel Lanche, Evan Maxwell, Spencer C Knight, Xiaodong Bai, Harendra Guturu, Asher Baltzell, Ahna R Girshick, Shannon R McCurdy, Raghavendran Partha, Adam J Mansfield, David A Turissini, Miao Zhang, Joelle Mbatchou, Kyoko Watanabe, Anurag Verma, Giorgio Sirugo, null null, null null, null null, null null, Marylyn DeRiggi Ritchie, William J Salerno, Alan R Shuldiner, Daniel James Rader, Tooraj Mirshahi, Jonathan Marchini, John D Overton, David J Carey, Lukas Habegger, Jeffrey G Reid, Aris N Economides, Christos A Kyratsous, Katia Karalis, Alina Baum, Michael N Cantor, Kristin A Rand, Eurie L Hong, Catherine A Ball, Katherine Siminovitch, Aris Baras, Gonçalo R Abecasis, Manuel A R Ferreira
Genetic risk factors for COVID-19 and influenza are largely distinct. Nature genetics 56 (8) (2024)
Junhao Wen, Bingxin Zhao, Zhijian Yang, Guray Erus, Ioanna Skampardoni, Elizabeth Mamourian, Yuhan Cui, Gyujoon Hwang, Jingxuan Bao, Aleix Boquet-Pujadas, Zhen Zhou, Yogasudha Veturi, Marylyn DeRiggi Ritchie, Haochang Shou, Paul M Thompson, Li Shen, Arthur W Toga, Christos Davatzikos
The genetic architecture of multimodal human brain age. Nature communications 15 (1) (2024)
Junhao Wen, Bingxin Zhao, Zhijian Yang, Guray Erus, Ioanna Skampardoni, Elizabeth Mamourian, Yuhan Cui, Gyujoon Hwang, Jingxuan Bao, Aleix Boquet-Pujadas, Zhen Zhou, Yogasudha Veturi, Marylyn DeRiggi Ritchie, Haochang Shou, Paul M Thompson, Li Shen, Arthur W Toga, Christos Davatzikos
The genetic architecture of multimodal human brain age. Nature communications 15 (1) (2024)
Nosheen Reza, Michael G Levin, Mahesh K Vidula, Paco E Bravo, Scott M Damrauer, Marylyn DeRiggi Ritchie, null null, Choudhary Anwar A Chahal, Anjali Tiku Owens
Prevalence of Pathogenic Variants in Dilated Cardiomyopathy-Associated Genes in Patients Evaluated for Cardiac Sarcoidosis. Circulation. Genomic and precision medicine (2023)
Aeron M Small, Gina M Peloso, Jason Linefsky, Jayashri Aragam, Ashley Galloway, Vidisha Tanukonda, Lu-Chen Wang, Zhi Yu, Margaret Sunitha Selvaraj, Eric H Farber-Eger, Michael T Baker, Shefali Setia Verma, Simon S K Lee, Michael H Preuss, Marylyn DeRiggi Ritchie, Scott M Damrauer, Daniel James Rader, Quinn S Wells, Ruth J F Loos, Steven A Lubitz, George Thanassoulis, Kelly Cho, Peter W F Wilson, null null, Pradeep Natarajan, Christopher J O'Donnell
Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program. Circulation 147 (12) (2023)
Aeron M Small, Gina M Peloso, Jason Linefsky, Jayashri Aragam, Ashley Galloway, Vidisha Tanukonda, Lu-Chen Wang, Zhi Yu, Margaret Sunitha Selvaraj, Eric H Farber-Eger, Michael T Baker, Shefali Setia Verma, Simon S K Lee, Michael H Preuss, Marylyn DeRiggi Ritchie, Scott M Damrauer, Daniel James Rader, Quinn S Wells, Ruth J F Loos, Steven A Lubitz, George Thanassoulis, Kelly Cho, Peter W F Wilson, null null, Pradeep Natarajan, Christopher J O'Donnell
Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program. Circulation (2023)
Dominic B Dwyer, Ganesh B Chand, Alessandro Pigoni, Adyasha Khuntia, Junhao Wen, Mathilde Antoniades, Gyujoon Hwang, Guray Erus, Jimit Doshi, Dhivya Srinivasan, Erdem Varol, Rene S Kahn, Hugo G Schnack, Eva Meisenzahl, Stephen J Wood, Chuanjun Zhuo, Aristeidis Sotiras, Russell T Shinohara, Haochang Shou, Yong Fan, Maristela Schaulfelberger, Pedro Rosa, Paris Alexandros Lalousis, Rachel Upthegrove, Antonia N Kaczkurkin, Tyler Maxwell Moore, Barnaby Nelson, Raquel E Gur, Ruben C Gur, Marylyn DeRiggi Ritchie, Theodore D Satterthwaite, Robin M Murray, Marta Di Forti, Simone Ciufolini, Marcus V Zanetti, Daniel H Wolf, Christos Pantelis, Benedicto Crespo-Facorro, Geraldo F Busatto, Christos Davatzikos, Nikolaos Koutsouleris, Paola Dazzan
Psychosis brain subtypes validated in first-episode cohorts and related to illness remission: results from the PHENOM consortium. Molecular psychiatry (2023)
Tanmoy Roychowdhury, Derek M 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 E Hornsby, Ina Holst Laursen, Shefali Setia Verma, Adam E Locke, Gudmundur Einarsson, Gudmar Thorleifsson, Sarah E Graham, Ozan Dikilitas, Jack W Pattee, Renae L Judy, Ferran Pauls-Verges, Jonas B Nielsen, Brooke N Wolford, Ben Michael Brumpton, Jaime Dilme, Olga Peypoch, Laura Calsina Juscafresa, Todd L Edwards, Dadong Li, Karina Banasik, Soren Brunak, Rikke Louise Jacobsen, Minerva T Garcia-Barrio, Jifeng Zhang, Lars M Rasmussen, Regent Lee, Ashok Handa, Anders Wanhainen, Kevin Mani, Jes S Lindholt, Lasse Mollegaard Obel, Ewa Strauss, Grzegorz Oszkinis, Christopher P Nelson, Katie L Saxby, Joost A Van Herwaarden, Sander W van der Laan, Jessica van Setten, Mercedes Camacho, Frank M Davis, Rachael Wasikowski, Lam C Tsoi, Johann E Gudjonsson, Jonathan L Eliason, Dawn M Coleman, Peter K Henke, Santhi K Ganesh, Y Eugene Chen, Weihua Guan, James S Pankow, Nathan D Pankratz, Ole Birger Vesterager Pedersen, Christian Erikstrup, Weihong Tang, Kristian Hveem, Daníel F Guðbjartsson, Solveig Gretarsdottir, Unnur Thorsteinsdottir, Hilma Hólm, Kári Stefánsson, Manuel A R Ferreira, Aris Baras, Iftikhar J Kullo, Marylyn DeRiggi Ritchie, Alex H Christensen, Kasper K Iversen, Nikolaj Eldrup, Henrik Sillesen, Sisse Rye Ostrowski, Henning Bundgaard, Henrik Ullum, Stephen Burgess, Dipender Gill, Katherine Gallagher, Maria Sabater-Lleal, null null, null null, null null, null null, null null, Ida Surakka, Gregory T Jones, Matthew J Bown, Philip S Tsao, Cristen J Willer, Scott M Damrauer
Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target. Nature genetics (2023)
Guang Yang, Pablo González, Mariangeli Moneró, Kelvin Carrasquillo, Jessicca Y Renta, Dagmar F Hernandez-Suarez, Mariana R Botton, Kyle R Melin, Stuart A Scott, Gualberto Ruaño, Abiel Roche-Lima, Cristina Alarcon, Marylyn DeRiggi Ritchie, Minoli A Perera, Jorge Duconge
Discovery of Ancestry-specific Variants Associated with Clopidogrel Response among Caribbean Hispanics. medRxiv : the preprint server for health sciences (2023)
Derek M Klarin, Poornima Devineni, Anoop K Sendamarai, Anthony R Angueira, Sarah E Graham, Ying H Shen, Michael G Levin, James Paul Pirruccello, Ida Surakka, Purushotham R Karnam, Tanmoy Roychowdhury, Yanming Li, Minxian Wang, Krishna G Aragam, Kaavya Paruchuri, Verena Zuber, Gabrielle E Shakt, Noah L Tsao, Renae L Judy, Ha My T Vy, Shefali Setia Verma, Daniel James Rader, Ron Do, Joseph E Bavaria, Girish Nitin Nadkarni, Marylyn DeRiggi Ritchie, null null, Stephen Burgess, Dong-Chuan Guo, Patrick T Ellinor, Scott A LeMaire, Dianna M Milewicz, Cristen J Willer, Pradeep Natarajan, Philip S Tsao, Saiju Pyarajan, Scott M Damrauer
Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program. Nature genetics (2023)
Brenda Xiao, Digna R Velez Edwards, Anastasia Lucas, Theodore G Drivas, Kathryn J Gray Guseh, Brendan Keating, Chunhua Weng, David L Veenstra, Hakon H Hakonarson, Leah C Kottyan, Noemie Elhadad, Wei-Qi Wei, Yuan Luo, Dokyoon Kim, Marylyn DeRiggi Ritchie, Shefali Setia Verma, null null
Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions. Journal of the American Heart Association 12 (5) (2023)
Aeron M Small, Gina M Peloso, Jason Linefsky, Jayashri Aragam, Ashley Galloway, Vidisha Tanukonda, Lu-Chen Wang, Zhi Yu, Margaret Sunitha Selvaraj, Eric H Farber-Eger, Michael T Baker, Shefali Setia Verma, Simon S K Lee, Michael H Preuss, Marylyn DeRiggi Ritchie, Scott M Damrauer, Daniel James Rader, Quinn S Wells, Ruth J F Loos, Steven A Lubitz, George Thanassoulis, Kelly Cho, Peter W F Wilson, null null, Pradeep Natarajan, Christopher J O'Donnell
Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program. Circulation 147 (12) (2023)
Michael G Levin, Jennifer E Huffman, Anurag Verma, Kyle A Sullivan, Alexis A Rodriguez, David Kainer, Michael R Garvin, Matthew J Lane, Mikaela Cashman, J Izaak Miller, Hyejung Won, Binglan Li, Yuan Luo, David L Veenstra, Hakon Hakonarson, Elizabeth A Jasper, Alexander G Bick, Philip S Tsao, Marylyn DeRiggi Ritchie, Daniel A Jacobson, Ravi K Madduri, Scott M Damrauer
Genetics of varicose veins reveals polygenic architecture and genetic overlap with arterial and venous disease. Nature cardiovascular research 2 (1) (2023)
Brenda Xiao, Digna R Velez Edwards, Anastasia Lucas, Theodore G Drivas, Kathryn J Gray Guseh, Brendan Keating, Chunhua Weng, David L Veenstra, Hakon H Hakonarson, Leah C Kottyan, Noemie Elhadad, Wei-Qi Wei, Yuan Luo, Dokyoon Kim, Marylyn DeRiggi Ritchie, Shefali Setia Verma, null null
Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions. Journal of the American Heart Association (2023)
Milton Pividori, Sumei Lu, Binglan Li, Chun Su, Matthew E Johnson, Wei-Qi Wei, QiPing Feng, Bahram Namjou, Krzysztof Kiryluk, Iftikhar J Kullo, Yuan Luo, Blair D Sullivan, Benjamin F Voight, Carsten Skarke, Marylyn DeRiggi Ritchie, Struan F A Grant, null null, Casey S Greene
Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms. Nature communications 14 (1) (2023)
Brenda Xiao, Digna R Velez Edwards, Anastasia Lucas, Theodore G Drivas, Kathryn J Gray Guseh, Brendan Keating, Chunhua Weng, David L Veenstra, Hakon H Hakonarson, Leah C Kottyan, Noemie Elhadad, Wei-Qi Wei, Yuan Luo, Dokyoon Kim, Marylyn DeRiggi Ritchie, Shefali Setia Verma, null null
Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions. Journal of the American Heart Association 12 (5) (2023)
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 Vujkovic, Derek M Klarin, Michael G Levin, Nicholas A Sinnott-Armstrong, Genevieve L Wojcik, Mary E Plomondon, Thomas M Maddox, Stephen W Waldo, Alexander G Bick, Saiju Pyarajan, Jie Huang, Rebecca Song, Yuk-Lam Anne 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, Loïc Le Marchand, Lynne R Wilkens, Joshua C Bis, Hampton Leonard, Botong Shen, Leslie A Lange, Ayush Giri, Ozan Dikilitas, Iftikhar J Kullo, Ian B Stanaway, Gail P Jarvik, Adam S Gordon, Scott Hebbring, Bahram Namjou, Kenneth M Kaufman, Kaoru Ito, Kazuyoshi Ishigaki, Yoichiro Kamatani, Shefali S Verma, Marylyn DeRiggi Ritchie, Rachel L Kember, Aris Baras, Luca A Lotta, null null, null null, null null, null null, 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 James 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
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations. Nature medicine 28 (8) (2022)
Michael G Levin, Noah L Tsao, Pankhuri Singhal, Chang Liu, Ha My T Vy, Ishan Paranjpe, Joshua D 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 Burke, Nosheen Reza, Brian Charest, null null, Renae L Judy, Megan J Puckelwartz, Hakon Hakonarson, 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 Nitin Nadkarni, Marylyn DeRiggi Ritchie, Zoltan Arany, Thomas P Cappola, Kenneth B Margulies, Krishna G Aragam, Christopher M Haggerty, Jacob Joseph, Yan V Sun, Benjamin F Voight, Scott M Damrauer
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure. Nature communications 13 (1) (2022)
A Rouf Banday, Megan L Stanifer, Oscar Florez-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, Barbara B Biesecker, David L Boyle, Mark S Brahier, Andrea Burnett-Hartman, Mary N Carrington, Euijin Chang, Pyeong Gyun Choe, Rex L Chisholm, Leandro Machado Colli, Cliffton 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 Holland, Amy A Hutchinson, Hogune Im, Les'Shon Irby, Michael G Ison, Naima T Joseph, Hong Bin Kim, Robert J Kreitman, Bruce R Korf, Steven M Lipkin, Siham M Mahgoub, Iman Mohammed, Guilherme L Paschoalini, Jennifer Allen Pacheco, Michael J Peluso, Daniel James Rader, David T Redden, Marylyn DeRiggi Ritchie, Brooke Rosenblum, Margaret Elizabeth Ross, Hanaisa 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 Yu, Yu Zhang, Steeve Boulant, Stephen J Chanock, Jordan J Feld, Ludmila Prokunina-Olsson
Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries. Nature genetics 54 (8) (2022)
Julie E Horowitz, Jack A Kosmicki, Amy Damask, Deepika Sharma, Genevieve H L Roberts, Anne E Justice, Nilanjana Banerjee, Marie V Coignet, Ashish Yadav, Joseph B Leader, Anthony Marcketta, Danny S Park, Rouel Lanche, Evan Maxwell, Spencer C Knight, Xiaodong Bai, Harendra Guturu, Dylan Sun, Asher Baltzell, Fabricio S P Kury, Joshua D Backman, Ahna R Girshick, Colm O'Dushlaine, Shannon R McCurdy, Raghavendran Partha, Adam J Mansfield, David A Turissini, Alexander H Li, Miao Zhang, Joelle Mbatchou, Kyoko Watanabe, Lauren Gurski, Shane E McCarthy, Hyun M Kang, Lee Dobbyn, Eli Stahl, Anurag Verma, Giorgio Sirugo, null null, Marylyn DeRiggi Ritchie, Marcus Jones, Suganthi Balasubramanian, Katherine Siminovitch, William J Salerno, Alan R Shuldiner, Daniel James Rader, Tooraj Mirshahi, Adam E Locke, Jonathan Marchini, John D Overton, David J Carey, Lukas Habegger, Michael N Cantor, Kristin A Rand, Eurie L Hong, Jeffrey G Reid, Catherine A Ball, Aris Baras, Gonçalo R Abecasis, Manuel A R Ferreira
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease. Nature genetics 54 (4) (2022)
Binglan Li, Katrin Sangkuhl, Karl Keat, Ryan M Whaley, Mark Woon, Shefali Setia Verma, Scott Dudek, Sony Tuteja, Anurag Verma, Michelle Whirl-Carrillo, Marylyn DeRiggi Ritchie, Teri E Klein
How to Run the Pharmacogenomics Clinical Annotation Tool (PharmCAT). Clinical pharmacology and therapeutics (2022)
Anurag Verma, Noah L Tsao, Lauren O Thomann, Yuk-Lam Anne Ho, Sudha K Iyengar, Shiuh-Wen Luoh, Rotonya M Carr, Dana C Crawford, Jimmy T Efird, Jennifer E Huffman, Adriana M Hung, Kerry L Ivey, Michael G Levin, Julie A Lynch, Pradeep Natarajan, Saiju Pyarajan, Alexander G Bick, Lauren Costa, Giulio Genovese, Richard L Hauger, Ravi K Madduri, Gita A Pathak, Renato Polimanti, Benjamin Voight, Marijana Vujkovic, Seyedeh Maryam Zekavat, Hongyu Zhao, Marylyn DeRiggi Ritchie, null null, Kyong-Mi Chang, Kelly Cho, Juan P Casas, Philip S Tsao, John Michael Gaziano, Christopher J O'Donnell, Scott M Damrauer, Katherine P Liao
A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program. PLoS genetics 18 (4) (2022)
Catherine Tcheandjieu, Ke Xiao, Helio Tejeda, Julie A Lynch, Sanni E Ruotsalainen, Tiffany Bellomo, Madhuri Palnati, Renae Judy, Derek M Klarin, Rachel L Kember, Shefali Verma, null null, null null, null null, Aarno Palotie, Mark Daly, Marylyn DeRiggi Ritchie, Daniel James Rader, Manuel A Rivas, Themistocles L Assimes, Philip Tsao, Scott Damrauer, James R Priest
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease. Nature genetics 54 (6) (2022)
Xinyuan Zhang, Anastasia M Lucas, Yogasudha Veturi, Theodore G Drivas, William P Bone, Anurag Verma, Wendy K Chung, David Crosslin, Joshua C Denny, Scott Hebbring, Gail P Jarvik, Iftikhar J Kullo, Eric B Larson, Laura J Rasmussen-Torvik, Daniel J Schaid, Jordan W Smoller, Ian B Stanaway, Wei-Qi Wei, Chunhua Weng, Marylyn DeRiggi Ritchie
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders. Nature communications 13 (1) (2022)
Hongbo Liu, Tomohito Doke, Dong Guo, Xin Sheng, Ziyuan Ma, Joseph Park, Ha My T Vy, Girish Nitin Nadkarni, Amin Abedini, Zhen Miao, Matthew Palmer, Benjamin F Voight, Hongzhe Li, Christopher D Brown, Marylyn DeRiggi Ritchie, Yan Shu, Katalin Suszták
Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease. Nature genetics 54 (7) (2022)
Athanasios Kousathanas, Erola Pairo-Castineira, Konrad Rawlik, Alex 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, Sean Keating, Bo Wang, Daniel Rhodes, Lucija Klarić, Marie Zechner, Nicholas J Parkinson, Afshan Siddiq, Peter Goddard, Sally Donovan, David Maslove, Alistair Nichol, Malcolm Gracie Semple, Tala Zainy, Fiona Maleady-Crowe, Linda Todd, Shahla Salehi, Julian C Knight, Greg Elgar, Georgia Chan, Prabhu Arumugam, Christine Patch, Augusto Rendon, David Bentley, Clare Kingsley, Jack A Kosmicki, Julie E Horowitz, Aris Baras, Gonçalo R Abecasis, Manuel A R Ferreira, Anne Justice, Tooraj Mirshahi, Matthew Oetjens, Daniel James Rader, Marylyn DeRiggi Ritchie, Anurag Verma, Tom A Fowler, Manu Shankar-Hari, Charlotte Summers, Charles J Hinds, Peter Horby, Lowell Ling, Daniel Francis McAuley, Hugh E Montgomery, Peter J M Openshaw, Paul Elliott, Timothy Walsh, Albert Tenesa, null null, null null, null null, Angie Fawkes, Lee Murphy, Kathryn M Rowan, Chris Paul Ponting, Veronique Vitart, James F Wilson, Jian Yang, Andrew D Bretherick, Richard H Scott, Sara Clohisey Hendry, Loukas Moutsianas, Andrew Law, Mark J Caulfield, John Kenneth Baillie
Whole-genome sequencing reveals host factors underlying critical COVID-19. Nature 607 (7917) (2022)
Yogasudha Veturi, Anastasia Lucas, Yuki Bradford, Daniel Hui, Scott Dudek, Elizabeth Theusch, Anurag Verma, Jason E Miller, Iftikhar J Kullo, Hakon H Hakonarson, Patrick Sleiman, Daniel Schaid, Charles M Stein, Digna R Velez Edwards, QiPing Feng, Wei-Qi Wei, Marisa W Medina, Ronald M Krauss, Thomas J Hoffmann, Neil Risch, Benjamin F Voight, Daniel J Rader, Marylyn DeRiggi Ritchie
A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. Nature genetics 53 (7) (2021)
Ning Shang, Atlas Khan, Fernanda Polubriaginof, Francesca Zanoni, Karla Mehl, David A Fasel, Paul E Drawz, Robert J Carrol, Joshua C Denny, Matthew A Hathcock, Adelaide M Arruda-Olson, Peggy L Peissig, Richard A Dart, Murray H Brilliant, Eric B Larson, David S Carrell, Sarah Pendergrass, Shefali Setia Verma, Marylyn DeRiggi Ritchie, Barbara Benoit, Vivian S Gainer, Elizabeth W Karlson, Adam S Gordon, Gail P Jarvik, Ian B Stanaway, David R Crosslin, Sumit Mohan, Iuliana Ionita-Laza, Nicholas P Tatonetti, Ali G Gharavi, George Hripcsak, Chunhua Weng, Krzysztof Kiryluk
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies. NPJ digital medicine 4 (1) (2021)
Joseph Park, Anastasia M Lucas, Xinyuan Zhang, Kumardeep Chaudhary, Judy H Cho, Girish Nadkarni, Amanda Dobbyn, Geetha Chittoor, Navya Shilpa Josyula, Nathan Katz, Joseph H Breeyear, Shadi Ahmadmehrabi, Theodore G Drivas, Venkata R M Chavali, Maria Fasolino, Hisashi Sawada (澤田悠), Alan Daugherty, Yanming Li, Chen Zhang, Yuki Bradford, JoEllen Weaver, Anurag Verma, Renae L Judy, Rachel L Kember, John D Overton, Jeffrey G Reid, Manuel A R Ferreira, Alexander H Li, Aris Baras, Scott A LeMaire, Ying H Shen, Ali Naji, Klaus H Kaestner, Golnaz Vahedi, Todd L Edwards, Jinbo Chen, Scott M Damrauer, Anne E Justice, Ron Do, Marylyn DeRiggi Ritchie, Daniel James Rader
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations. Nature medicine 27 (1) (2021)
David S M Lee, Joseph Park, Andrew Kromer, Aris Baras, Daniel James Rader, Marylyn DeRiggi Ritchie, Louis R Ghanem, Yoseph Barash
Disrupting upstream translation in mRNAs is associated with human disease. Nature communications 12 (1) (2021)
Lova L Sun, Sanjna Surya, Noah G Goodman, Anh N Le, Gregory Kelly, Olutosin Owoyemi, Heena Desai, Cathy Zheng, Shannon DeLuca, Madeline L Good, Jasmin Hussain, Seth D Jeffries, Yolanda R Kry, Emily M Kugler, Maikel Mansour, John Ndicu, AnnaClaire Osei-Akoto, Timothy Prior, Stacy L Pundock, Lisa A Varughese, JoEllen Weaver, Abigail Doucette, Scott Dudek, Shefali Setia Verma, Sigrid Gouma, Madison E Weirick, Christopher M McAllister, Erin M Bange, Peter E Gabriel, Marylyn DeRiggi Ritchie, Daniel James Rader, Robert H Vonderheide, Lynn M Schuchter, Anurag Verma, Ivan P Maillard, Ronac Mamtani, Scott E Hensley, Robert Gross, E Paul Wileyto, Alexander C Huang, Kara N Maxwell, Angela M DeMichele
SARS-CoV-2 Seropositivity and Seroconversion in Patients Undergoing Active Cancer-Directed Therapy. JCO oncology practice 17 (12) (2021)
Xiangchen Gu, Hongliu Yang, Xin Sheng, Yi-An Ko, Chengxiang Qiu, Jiwhan Park, Shizheng Huang, Rachel L Kember, Renae L Judy, Joseph Park, Scott M Damrauer, Girish Nadkarni, Ruth J F Loos, Ha My Thi Vy, Kumardeep Chaudhary, Erwin P Böttinger, Ishan Paranjpe, Aparna Saha, Christopher D Brown, Shreeram Akilesh, Adriana M Hung, Matthew Palmer, Aris Baras, John D Overton, Jeffrey G Reid, Marylyn DeRiggi Ritchie, Daniel J Rader, Katalin Suszták
Kidney disease genetic risk variants alter lysosomal beta-mannosidase (MANBA) expression and disease severity. Science translational medicine 13 (576) (2021)
Ruowang Li, Rui Duan, Xinyuan Zhang, Thomas Lumley, Sarah Pendergrass, Christopher R Bauer, Hakon H Hakonarson, David S Carrell, Jordan W Smoller, Wei-Qi Wei, Robert Carroll, Digna R Velez Edwards, Georgia Wiesner, Patrick Sleiman, Josh C Denny, Jonathan D Mosley, Marylyn DeRiggi Ritchie, Yong Chen, Jason H Moore
Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics. Nature communications 12 (1) (2021)
Emily E Hartwell, Alison K Merikangas, Shefali Setia Verma, Marylyn DeRiggi Ritchie, null null, Henry R Kranzler, Rachel L Kember
Genetic liability for substance use associated with medical comorbidities in electronic health records of African- and European-ancestry individuals. Addiction biology (2021)
Michael G Levin, Renae Judy, Dipender Gill, Marijana Vujkovic, Shefali Setia Verma, Yuki Bradford, null null, Marylyn DeRiggi Ritchie, Matthew C Hyman, Saman Nazarian, Daniel James Rader, Benjamin F Voight, Scott M Damrauer
Genetics of height and risk of atrial fibrillation: A Mendelian randomization study. PLoS medicine 17 (10) (2020)
Jason E Miller, Yogasudha Veturi, Marylyn DeRiggi Ritchie
Innovative strategies for annotating the "relationSNP" between variants and molecular phenotypes. BioData mining 12 (2019)
Elisabetta Manduchi, Patryk R Orzechowski, Marylyn DeRiggi Ritchie, Jason H Moore
Exploration of a diversity of computational and statistical measures of association for genome-wide genetic studies. BioData mining 12 (2019)
Casey S Greene, Lana X Garmire, Jack A Gilbert, Marylyn DeRiggi Ritchie, Lawrence E Hunter
Celebrating parasites. Nature genetics 49 (4) (2019)
Viktoria Gusarova, Colm O'Dushlaine, Tanya M Teslovich, Peter N Benotti, Tooraj Mirshahi, Omri Gottesman, Cristopher V Van Hout, Michael F Murray, Anubha Mahajan, Jonas Bille Nielsen, Lars G Fritsche, Anders Berg Wulff, Daníel F Guðbjartsson, Marketa Sjögren, Connor A Emdin, Robert A Scott, Wen-Jane Lee, Aeron Small, Lydia C Kwee, Om Prakash Dwivedi, Rashmi B Prasad, Shannon E Bruse, Alexander E Lopez, John Penn, Anthony Marcketta, Joseph B Leader, Christopher D Still, H Lester Kirchner, Uyenlinh L Mirshahi, Amr H Wardeh, Cassandra M Hartle, Lukas Habegger, Samantha N Fetterolf, Teresa Tusie-Luna, Andrew P Morris, Hilma Holm, Valgerdur Steinthorsdottir, Patrick Sulem, Unnur Thorsteinsdottir, Jerome I Rotter, Lee-Ming Chuang, Scott 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 DeRiggi Ritchie, David H Ledbetter, Andrew J Murphy, Ingrid B Borecki, Jeffrey G Reid, John D Overton, Ola Hansson, Leif C Groop, Svati H Shah, William E Kraus, Daniel J Rader, Yii-Der I Chen, Kristian Hveem, Nicholas J Wareham, Sekar Kathiresan, Olle Melander, Kari Stefansson, Børge Grønne Nordestgaard, Anne Tybjærg-Hansen, Goncalo R Abecasis, David Altshuler, Jose C Florez, Michael Boehnke, Mark I McCarthy, George D Yancopoulos, David J Carey, Alan R Shuldiner, Aris Baras, Frederick E Dewey, Jesper Gromada
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes. Nature communications 9 (1) (2018)
Jessica van Setten, Jennifer A Brody, Yalda Jamshidi, Brenton R Swenson, Anne M Butler, Harry Campbell, Fabiola M Del Greco, Daniel S Evans, Quince Gibson, Daniel F Gudbjartsson, Kathleen F Kerr, Bouwe P Krijthe, Leo-Pekka Lyytikainen, Christian Müller, Martina Müller-Nuraysid, Ilja Maria Nolte, Sandosh Padmanabhan, Marylyn DeRiggi Ritchie, Antonietta Robino, Albert Vernon Smith, Maristella Steri, Toshiko Tanaka, Alexander Teumer, Stella Trompet, Sheila Ulivi, Niek Verweij, Xiaoyan Yin, David O Arnar, Folkert W. Asselbergs, Joel S Bader, John Barnard, Josh Bis, Stefan Blankenberg, Eric Boerwinkle, Yuki Bradford, Brendan M Buckley, Mina K Chung, Dana Crawford, Marcel den Hoed, Josh C Denny, Anna F Dominiczak, Georg B Ehret, Mark Eijgelsheim, Patrick T Ellinor, Stephan B Felix, Oscar H Franco, Lude H Franke, Tamara B Harris, Hilma Holm, Gandin Ilaria, Annamaria Iorio, Mika Kähönen, Ivana Kolcic, Jan A Kors, Edward G Lakatta, Lenore J Launer, Honghuang Lin, Henry J Lin, Ruth J F Loos, Steven A Lubitz, Peter W Macfarlane, Jared W Magnani, Irene Mateo Leach, Thomas Meitinger, Braxton D Mitchell, Thomas Munzel, George J Papanicolaou, Annette Peters, Arne Pfeufer, Peter P Pramstaller, Olli T Raitakari, Jerome I Rotter, Igor Rudan, Nilesh J Samani, David Schlessinger, Claudia T Silva Aldana, Moritz F Sinner, Jonathan D Smith, Harold Snieder, Elsayed Z Soliman, Timothy D Spector, David J Stott, Konstantin Strauch, Kirill V Tarasov, Unnur Thorsteinsdottir, Andre G Uitterlinden, David R Van Wagoner, Uwe Völker, Henry Völzke, Melanie Waldenberger, Harm-Jan Westra, Philipp S Wild, Tanja Zeller, Alvaro Alonso, Christy L Avery, Stefania Bandinelli, Emelia J Benjamin, Francesco Cucca, Marcus Dörr, Luigi Ferrucci, Paolo Gasparini, Vilmundur Gudnason, Caroline Hayward, Susan R Heckbert, Andrew A Hicks, Johan Wouter Jukema, Stefan Kääb, Terho Lehtimäki, Yongmei Liu, Patricia B Munroe, Afshin Parsa, Ozren Polasek, Bruce M Psaty, Dan M Roden, Renate B Schnabel, Gianfranco Sinagra, Kari Stefansson, Bruno H Stricker, Pim van der Harst, Cornelia M van Duijn, James F Wilson, Sina A Gharib, Paul I W de Bakker, Aaron Isaacs, Dan E Arking, Nona Sotoodehnia
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity. Nature communications 9 (1) (2018)
James J Lee, Robbee Wedow, Aysu Okbay, Edward Kong, Omeed Maghzian, Meghan Zacher, Tuan Anh Nguyen-Viet, Peter Bowers, Julia Sidorenko, Richard Karlsson Linnér, Mark Alan Fontana, Tushar Kundu, Chanwook Lee, Hui Li, Ruoxi Li, Rebecca Royer, Pascal N Timshel, Raymond K Walters, Emily A Willoughby, Loïc Yengo, null null, null null, null null, 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 Setia 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 A Milani, Ken K Ong, John R B Perry, David J Porteous, Marylyn DeRiggi Ritchie, Melissa C Smart, Blair Hamilton Smith, Joyce Y Tung, Nicholas J Wareham, James F Wilson, Jonathan P Beauchamp, Dalton C 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 I Laibson, Jian Yang, Magnus Johannesson, Philipp D Koellinger, Patrick Turley, Peter M Visscher, Daniel J Benjamin, David Cesarini
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Nature genetics 50 (8) (2018)
Jonathan D Mosley, QiPing Feng, Quinn S Wells, Sara L Van Driest, Christian M Shaffer, Todd L Edwards, Lisa Bastarache, Wei-Qi Wei, Lea K Davis, Catherine A McCarty, Will Thompson, Christopher G Chute, Gail P Jarvik, Adam S Gordon, Melody R Palmer, David R Crosslin, Eric B Larson, David S Carrell, Iftikhar J Kullo, Jennifer Allen Pacheco, Peggy L Peissig, Murray H Brilliant, James G Linneman, Bahram Namjou, Marc S Williams, Marylyn DeRiggi Ritchie, Kenneth M Borthwick, Shefali S Verma, Jason H Karnes, Scott T Weiss, Thomas J Wang, C Michael Stein, Josh C Denny, Dan M Roden
A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers. Nature communications 9 (1) (2018)
Anna Okula Basile, Marylyn DeRiggi Ritchie
Informatics and machine learning to define the phenotype. Expert review of molecular diagnostics 18 (3) (2018)
Ruowang Li, Dokyoon Kim, Heather E Wheeler, Scott M Dudek, Mary Eileen Dolan, Marylyn DeRiggi Ritchie
Integration of genetic and functional genomics data to uncover chemotherapeutic induced cytotoxicity. The pharmacogenomics journal 19 (2) (2018)
Molly A Hall, John Wallace, Anastasia Lucas, Dokyoon Kim, Anna O Basile, Shefali S Verma, Cathy A McCarty, Murray H Brilliant, Peggy L Peissig, Terrie E Kitchner, Anurag Verma, Sarah A Pendergrass, Scott M Dudek, Jason H Moore, Marylyn DeRiggi Ritchie
PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies. Nature communications 8 (1) (2017)
Jessica N Cooke Bailey, Stephanie J Loomis, Jae Hee Kang, R Rand Allingham, Puya Gharahkhani, Chiea Chuen Khor, Kathryn P Burdon, Hugues Aschard, Daniel I Chasman, Robert P Igo, Pirro G Hysi, Craig A Glastonbury, Allison Ashley-Koch, Murray Brilliant, Andrew A Brown, Donald L Budenz, Alfonso Buil, Ching-Yu Cheng, Hyon Choi, William G Christen, Gary Curhan, Immaculata De Vivo, John H Fingert, Paul J Foster, Charles Fuchs, Douglas Gaasterland, Terry Gaasterland, Alex W Hewitt, Frank Hu, David J Hunter, Anthony P Khawaja, Richard K Lee, Zheng Li, Paul R Lichter, David A Mackey, Peter McGuffin, Paul Mitchell, Sayoko E Moroi, Shamira A Perera, Keating W Pepper, Qibin Qi, Tony Realini, Julia E Richards, Paul M Ridker, Eric Rimm, Robert Ritch, Marylyn DeRiggi Ritchie, Joel S Schuman, William K Scott, Kuldev Singh, Arthur J Sit, Yeunjoo E Song, Rulla M Tamimi, Fotis Topouzis, Ananth C Viswanathan, Shefali Setia Verma, Douglas Vollrath, Jie Jin Wang, Nicole Weisschuh, Bernd Wissinger, Gadi Wollstein, Tien Y Wong, Brian L Yaspan, Donald J Zack, Kang Zhang, Epic-Norfolk Eye Study, null null, Robert N Weinreb, Margaret A Pericak-Vance, Kerrin Small, Christopher J Hammond, Tin Aung, Yutao Liu, Eranga N Vithana, Stuart MacGregor, Jamie E Craig, Peter Kraft, Gareth Howell, Michael A Hauser, Louis R Pasquale, Jonathan L Haines, Janey L Wiggs
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Nature genetics 48 (2) (2016)
Dan E Arking, Sara L Pulit, Lia Crotti, Pim van der Harst, Patricia B Munroe, Tamara T Koopmann, Nona Sotoodehnia, Elizabeth J Rossin, Michael Morley, Xinchen Wang, Andrew D Johnson, Alicia Lundby, Daníel F Gudbjartsson, Peter A Noseworthy, Mark Eijgelsheim, Yuki Bradford, Kirill V Tarasov, Marcus Dörr, Martina Müller-Nurasyid, Annukka M Lahtinen, Ilja M Nolte, Albert Vernon Smith, Joshua C Bis, Aaron Isaacs, Stephen J Newhouse, Daniel S Evans, Wendy S Post, Daryl Waggott, Leo-Pekka Lyytikäinen, Andrew A Hicks, Lewin Eisele, David Ellinghaus, Caroline Hayward, Pau Navarro, Sheila Ulivi, Toshiko Tanaka, David J Tester, Stéphanie Chatel, Stefan Gustafsson, Meena Kumari, Richard W Morris, Åsa T Naluai, Sandosh Padmanabhan, Alexander Kluttig, Bernhard Strohmer, Andrie G Panayiotou, Maria Torres, Michael Knoflach, Jaroslav A Hubacek, Kamil Slowikowski, Soumya Raychaudhuri, Runjun D Kumar, Tamara B Harris, Lenore J Launer, Alan R Shuldiner, Alvaro Alonso, Joel S Bader, Georg Ehret, Hailiang Huang, W H Linda Kao, James B Strait, Peter W Macfarlane, Morris Brown, Mark J Caulfield, Nilesh J Samani, Florian Kronenberg, Johann Willeit, null null, null null, J Gustav Smith, Karin H Greiser, Henriette Meyer Zu Schwabedissen, Karl Werdan, Massimo Carella, Leopoldo Zelante, Susan R Heckbert, Bruce M Psaty, Jerome I Rotter, Ivana Kolcic, Ozren Polašek, Alan F Wright, Maura Griffin, Mark J Daly, null null, David O Arnar, Hilma Hólm, Unnur Thorsteinsdottir, null null, Joshua C Denny, Dan M Roden, Rebecca L Zuvich, Valur Emilsson, Andrew S Plump, Martin G Larson, Christopher J O'Donnell, Xiaoyan Yin, Marco Bobbo, Adamo P D'Adamo, Annamaria Iorio, Gianfranco Sinagra, Angel Carracedo, Steven R Cummings, Michael A Nalls, Antti Jula, Kimmo K Kontula, Annukka Marjamaa, Lasse Oikarinen, Markus Perola, Kimmo Porthan, Raimund Erbel, Per Hoffmann, Karl-Heinz Jöckel, Hagen Kälsch, Markus M Nöthen, null null, Marcel den Hoed, Ruth J F Loos, Dag S Thelle, Christian Gieger, Thomas Meitinger, Siegfried Perz, Annette Peters, Hanna Prucha, Moritz F Sinner, Melanie Waldenberger, Rudolf A de Boer, Lude Franke, Pieter A van der Vleuten, Britt Maria Beckmann, Eimo Martens, Abdennasser Bardai, Nynke Hofman, Arthur A M Wilde, Elijah R Behr, Chrysoula Dalageorgou, John R Giudicessi, Argelia Medeiros-Domingo, Julien Barc, Florence Kyndt, Vincent Probst, Alice Ghidoni, Roberto Insolia, Robert M Hamilton, Stephen W Scherer, Jeffrey Brandimarto, Kenneth Margulies, Christine E Moravec, Fabiola del Greco M, Christian Fuchsberger, Jeffrey R O'Connell, Wai K Lee, Graham C M Watt, Harry Campbell, Sarah H Wild, Nour E El Mokhtari, Norbert Frey, Folkert W Asselbergs, Irene Mateo Leach, Gerjan Navis, Maarten P van den Berg, Dirk J van Veldhuisen, Manolis Kellis, Bouwe P Krijthe, Oscar H Franco, Albert Hofman, Jan A Kors, André G Uitterlinden, Jacqueline C M Witteman, Lyudmyla Kedenko, Claudia Lamina, Ben A Oostra, Gonçalo R Abecasis, Edward G Lakatta, Antonella Mulas, Marco Orrú, David Schlessinger, Manuela Uda, Marcello R P Markus, Uwe Völker, Harold Snieder, Timothy D Spector, Johan Ärnlöv, Lars Lind, Johan Sundström, Ann-Christine Syvänen, Mika Kivimaki, Mika Kähönen, Nina Mononen, Olli T Raitakari, Jorma S Viikari, Vera Adamkova, Stefan Kiechl, Maria Brion, Andrew N Nicolaides, Bernhard Paulweber, Johannes Haerting, Anna F Dominiczak, Fredrik Nyberg, Peter H Whincup, Aroon D Hingorani, Jean-Jacques Schott, Connie R Bezzina, Erik Ingelsson, Luigi Ferrucci, Paolo Gasparini, James F Wilson, Igor Rudan, Andre Franke, Thomas W Mühleisen, Peter P Pramstaller, Terho J Lehtimäki, Andrew D Paterson, Afshin Parsa, Yongmei Liu, Cornelia M van Duijn, David S Siscovick, Vilmundur Gudnason, Yalda Jamshidi, Veikko Salomaa, Stephan B Felix, Serena Sanna, Marylyn DeRiggi Ritchie, Bruno H Stricker, Kari Stefansson, Laurie A Boyer, Thomas P Cappola, Jesper V Olsen, Kasper Lage, Peter J Schwartz, Stefan Kääb, Aravinda Chakravarti, Michael J Ackerman, Arne Pfeufer, Paul I W de Bakker, Christopher Newton-Cheh
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nature genetics 46 (8) (2014)

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Marylyn DeRiggi Ritchie (Marylyn Ritchie, Marylyn D Ritchie)