Iftikhar J. Kullo
Active 1988–2026
- Also published as
- Iftikhar J Kullo
- 186
- Papers
- 19,840
- Citations
- 83
- h-index
- 163
- i10-index
Citations
Citation sources
Countries
Institutions
Fields
- Medicine44.7%
- Biochemistry, Genetics and Molecular Biology33.7%
- Computer Science6.7%
- Health Professions3.2%
- Pharmacology, Toxicology and Pharmaceutics2.9%
- Immunology and Microbiology1.9%
- Other6.9%
Topics
- Genetic Associations and Epidemiology7.2%
- Genomics and Rare Diseases3.4%
- Machine Learning in Healthcare3.1%
- Biomedical Text Mining and Ontologies2.3%
- BRCA gene mutations in cancer2.3%
- Lipoproteins and Cardiovascular Health2.1%
- Other79.6%
Coauthors
- Gail P. Jarvik41
- Ozan Dikilitas32
- Eric B. Larson28
- David R. Crosslin26
- Joshua C. Denny26
- Marylyn D. Ritchie23
- Christopher G. Chute22
- Håkon Håkonarson21
- Jennifer A. Pacheco20
- Luke V. Rasmussen20
- Marc S. Williams18
- Wei‐Qi Wei18
- David Carrell17
- Kent R. Bailey16
- Daniel J. Schaid15
- Dan M. Roden14
- Jyotishman Pathak14
- Suzette J. Bielinski14
- Catherine A. McCarty13
- Rongling Li13
- Wendy K. Chung13
- Laura J. Rasmussen‐Torvik12
- Ning Shang12
- Peggy Peissig12
All papers
- Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Authors: Krishna G. Aragam, Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Deepak Atri, E. Weeks, Minxian Wang, George Hindy, Wei Zhou, Christopher Grace, Carolina Roselli, Nicholas Marston, Frederick Kamanu, Ida Surakka, Loreto Muñoz Venegas, Paul Sherliker, Satoshi Koyama, Kazuyoshi Ishigaki, Bjørn Olav Åsvold, Michael R. Brown, Ben Brumpton, Paul S. de Vries, Olga Giannakopoulou, Tota Giardoglou, Daníel F. Guðbjartsson, Ulrich Güldener, Syed M. Ijlal Haider, Anna Helgadóttir, M Ibrahim, 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 cited by 706
- Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Authors: 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 cited by 353
- Principles and methods for transferring polygenic risk scores across global populations
Authors: Linda Kachuri, Nilanjan Chatterjee, Jibril Hirbo, Daniel J. Schaid, Iman K. Martin, Iftikhar J. Kullo, Eimear E. Kenny, Bogdan Paşaniuc, Paul L. Auer, Matthew P. Conomos, David V. Conti, Yi Ding, Ying Wang, Haoyu Zhang, Yuji Zhang, John S. Witte, Tian Ge - Nature Reviews Genetics 2023 cited by 313
- Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
Authors: 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 cited by 1,126
- Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations
Authors: Niall J. Lennon, Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin, Jennifer E. Below, Sonja I. Berndt, Wendy K. Chung, James J. Cimino, Ellen Wright Clayton, John J. Connolly, David R. Crosslin, Ozan Dikilitas, Digna R. Velez Edwards, QiPing Feng, Marissa Fisher, Robert R. Freimuth, Tian Ge, Sonja Berndt, Joel N. Hirschhorn, Ruth J. F. Loos, Joseph Glessner, Allan Gordon, Candace Patterson, Håkon Håkonarson, Maegan Harden, Margaret Harr, Joel N. Hirschhorn, Clive Hoggart, Li Hsu, Marguerite R. Irvin, Gail P. Jarvik, Elizabeth W. Karlson, Atlas Khan, Amit V. Khera, Krzysztof Kiryluk, Iftikhar J. Kullo, Katie Larkin, Nita A. Limdi, Jodell E. Linder, Ruth J. F. Loos, Yuan Luo, Edyta Małolepsza, Teri A. Manolio, Lisa J. Martin, L.R. McCarthy, Elizabeth M. McNally, James B. Meigs, Tesfaye B. Mersha, Jonathan D. Mosley, Anjene Musick, Bahram Namjou, Nihal Pai, Lorenzo L. Pesce, Ulrike Peters, Josh F. Peterson, Cynthia A. Prows, Megan J. Puckelwartz, Heidi L. Rehm, Dan M. Roden, Elisabeth A. Rosenthal, Robb Rowley, Konrad Teodor Sawicki, Daniel J. Schaid, Roelof A. J. Smit, Johanna L. Smith, Jordan W. Smoller, Minta Thomas, Hemant K. Tiwari, Diana M. Toledo, Nataraja Sarma Vaitinadin, David L. Veenstra, Theresa L. Walunas, Zhe Wang, Wei‐Qi Wei, Chunhua Weng, Georgia L. Wiesner, Xianyong Yin, Eimear E. Kenny - Nature Medicine 2024 cited by 189
- Genome-wide polygenic score to predict chronic kidney disease across ancestries
Authors: Atlas Khan, Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru, Alana Jones, Edyta Małolepsza, Ozan Dikilitas, Iftikhar J. Kullo, Daniel J. Schaid, Elizabeth W. Karlson, Tian Ge, James B. Meigs, Jordan W. Smoller, Christoph Lange, David R. Crosslin, Gail P. Jarvik, Pavan K. Bhatraju, Jacklyn N. Hellwege, Paulette D. Chandler, Laura Rasmussen Torvik, Alex Fedotov, Cong Liu, Christopher Kachulis, Niall J. Lennon, Noura S. Abul‐Husn, Judy H. Cho, Iuliana Ionita‐Laza, Ali G. Gharavi, Wendy K. Chung, George Hripcsak, Chunhua Weng, Girish N. Nadkarni, Marguerite R. Irvin, Hemant K. Tiwari, Eimear E. Kenny, Nita A. Limdi, Krzysztof Kiryluk - Nature Medicine 2022 cited by 162
- The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future
Authors: 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 cited by 739
- Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Authors: 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 cited by 146
- Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations
Authors: Tian Ge, Marguerite R. Irvin, Amit Patki, Vinodh Srinivasasainagendra, Kuang Lin, Hemant K. Tiwari, Nicole D. Armstrong, Barbara Benoit, Chia‐Yen Chen, Karmel W. Choi, James J. Cimino, Brittney H. Davis, Ozan Dikilitas, Bethany Etheridge, Yen‐Chen Anne Feng, Vivian S. Gainer, Hailiang Huang, Gail P. Jarvik, Christopher Kachulis, Eimear E. Kenny, Atlas Khan, Krzysztof Kiryluk, Leah C. Kottyan, Iftikhar J. Kullo, Christoph Lange, Niall J. Lennon, Aaron Leong, Edyta Małolepsza, Ayme D. Miles, Shawn N. Murphy, Bahram Namjou, Renuka Narayan, Mark J. O’Connor, Jennifer A. Pacheco, Emma Perez, Laura J. Rasmussen‐Torvik, Elisabeth A. Rosenthal, Daniel J. Schaid, Maria Stamou, Miriam S. Udler, Wei‐Qi Wei, Scott T. Weiss, Maggie C. Y. Ng, Jordan W. Smoller, Matthew S. Lebo, James B. Meigs, Nita A. Limdi, Elizabeth W. Karlson - Genome Medicine 2022 cited by 173
- Polygenic scores in biomedical research
Authors: Iftikhar J. Kullo, Cathryn M. Lewis, Michael Inouye, Alicia R. Martin, Samuli Ripatti, Nilanjan Chatterjee - Nature Reviews Genetics 2022 cited by 186
- Returning integrated genomic risk and clinical recommendations: The eMERGE study
Authors: Jodell E. Linder, Aimee Allworth, Harris T. Bland, Pedro J. Caraballo, Rex L. Chisholm, Ellen Wright Clayton, David R. Crosslin, Ozan Dikilitas, Alanna DiVietro, Edward D. Esplin, Sophie Forman, Robert R Freimuth, Adam S Gordon, Richard Green, Maegan Harden, Ingrid A. Holm, Gail P. Jarvik, Elizabeth W. Karlson, Sofia Labrecque, Niall J. Lennon, Nita A. Limdi, Kathleen F. Mittendorf, Shawn N. Murphy, Lori A. Orlando, Cynthia A. Prows, Luke V. Rasmussen, Laura J. Rasmussen‐Torvik, Robb Rowley, Konrad Teodor Sawicki, Tara Schmidlen, Shannon Terek, David L. Veenstra, Digna R. Velez Edwards, Devin Absher, Noura S. Abul‐Husn, Jorge Alsip, Hana Bangash, Mark Beasley, Jennifer E. Below, Eta S. Berner, James Booth, Wendy K. Chung, James J. Cimino, John J. Connolly, Patrick Davis, Beth Devine, Stephanie M. Fullerton, Candace Guiducci, Melissa L. Habrat, Heather S. Hain, Håkon Håkonarson, Margaret Harr, Eden Haverfield, Valentina Hernandez, Christin Hoell, Martha Horike‐Pyne, George Hripcsak, Marguerite R. Irvin, Christopher Kachulis, Dean Karavite, Eimear E. Kenny, Atlas Khan, Krzysztof Kiryluk, Bruce R. Korf, Leah C. Kottyan, Iftikhar J. Kullo, Katie Larkin, Cong Liu, Edyta Małolepsza, Teri A. Manolio, Thomas May, Elizabeth M. McNally, Frank Mentch, Alexandra Miller, Sean D Mooney, Priyanka Murali, Brenda Mutai, Naveen Muthu, Bahram Namjou, Emma Perez, Megan J. Puckelwartz, Tejinder Rakhra-Burris, Dan M. Roden, Elisabeth A. Rosenthal, Seyedmohammad Saadatagah, Maya Sabatello, Dan Schaid, Baergen I. Schultz, Lynn Seabolt, Gabriel Q. Shaibi, Richard R. Sharp, Brian Shirts, Maureen E. Smith, Jordan W. Smoller, Rene Sterling, Sabrina A. Suckiel, Jeritt G. Thayer, Hemant K. Tiwari, Susan Brown Trinidad, Theresa L. Walunas and 317 more - Genetics in Medicine 2023 cited by 118
- Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target
Authors: 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 cited by 94
- Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates
Authors: Iftikhar J. Kullo, Hayan Jouni, Erin Austin, Sherry‐Ann Brown, Teresa Kruisselbrink, Iyad Isseh, Raad A. Haddad, Tariq S. Marroush, Khader Shameer, Janet E. Olson, Ulrich Broeckel, Robert C. Green, Daniel J. Schaid, Víctor M. Montori, Kent R. Bailey - Circulation 2016 cited by 270
- Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Authors: Derek Klarin, Shefali S. Verma, Renae Judy, Ozan Dikilitas, Brooke N. Wolford, Ishan Paranjpe, Michael G. Levin, Cuiping Pan, Catherine Tcheandjieu, Joshua M. Spin, Julie A. Lynch, Themistocles L. Assimes, Linn Åldstedt Nyrønning, Erney Mattsson, Todd L. Edwards, Joshua C. Denny, Eric B. Larson, Ming Ta Michael Lee, David Carrell, Yanfei Zhang, Gail P. Jarvik, Ali G. Gharavi, John B. Harley, Frank Mentch, Jennifer A. Pacheco, Håkon Håkonarson, Anne Heidi Skogholt, Laurent F. Thomas, Maiken E. Gabrielsen, Kristian Hveem, Jonas B. Nielsen, Wei Zhou, Lars G. Fritsche, Jie Huang, Pradeep Natarajan, Yan V. Sun, Scott L. DuVall, Daniel J. Rader, Kelly Cho, Kyong‐Mi Chang, Peter W.F. Wilson, Christopher J. O’Donnell, Sekar Kathiresan, Salvatore T. Scali, Scott A. Berceli, Cristen J. Willer, Gregory T. Jones, Matthew J. Bown, Girish N. Nadkarni, Iftikhar J. Kullo, Marylyn D. Ritchie, Scott M. Damrauer, Philip S. Tsao, J. Michael Gaziano, Rachel Ramoni, Jean C. Beckham, Jim Breeling, Kyong‐Mi Chang, Grant D. Huang, Sumitra Muralidhar, Christopher J. O’Donnell, Jonathan Romero, Philip S. Tsao, Sumitra Muralidhar, Jennifer Moser, Stacey B. Whitbourne, Jessica V. Brewer, John Concato, Stuart Warren, Dean P. Argyres, Philip S. Tsao, J. Michael Gaziano, Brady Stephens, Mary T. Brophy, Donald E. Humphries, Nhan Do, Shahpoor Shayan, Xuan‐Mai T. Nguyen, Christopher J. O’Donnell, Saiju Pyarajan, Philip S. Tsao, Kelly Cho, Saiju Pyarajan, Elizabeth R. Hauser, Yan V. Sun, Hongyu Zhao, Peter W.F. Wilson, Rachel McArdle, Louis J. Dell’Italia, John B. Harley, Clement J. Zablocki, Jeff Whittle, Jean Beckham, John A. Wells, Salvador Gutierrez, Gretchen Gibson, Laurence S. Kaminsky, Gerardo Villareal, Scott Kinlay, Junzhe Xu and 47 more - Circulation 2020 cited by 145
- The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies
Authors: the eMERGE Team, Catherine A. McCarty, Rex L. Chisholm, Christopher G. Chute, Iftikhar J. Kullo, Gail P. Jarvik, Eric B. Larson, Rongling Li, Daniel R. Masys, Marylyn D. Ritchie, Dan M. Roden, Jeffery P. Struewing, Wendy A. Wolf - BMC Medical Genomics 2011 cited by 729
- Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network
Authors: Katherine M. Newton, Peggy Peissig, A. N. Kho, Suzette J. Bielinski, Richard L. Berg, Vijaya Choudhary, Melissa Basford, Christopher G. Chute, Iftikhar J. Kullo, R. Li, Jennifer A. Pacheco, Luke V. Rasmussen, Leslie Spangler, Joshua C. Denny - Journal of the American Medical Informatics Association 2013 cited by 426
- GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network
Authors: The eMERGE Network, Bahram Namjou, Todd Lingren, Yongbo Huang, Sreeja Parameswaran, Beth L. Cobb, Ian B. Stanaway, John J. Connolly, Frank Mentch, Barbara Benoit, Xinnan Niu, Wei‐Qi Wei, Robert J. Carroll, Jennifer A. Pacheco, Isaac T. W. Harley, Senad Divanovic, David Carrell, Eric B. Larson, David J. Carey, Shefali S. Verma, Marylyn D. Ritchie, Ali G. Gharavi, Shawn N. Murphy, Marc S. Williams, David R. Crosslin, Gail P. Jarvik, Iftikhar J. Kullo, Håkon Håkonarson, Rongling Li, Stavra A. Xanthakos, John B. Harley - BMC Medicine 2019 cited by 205
- Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Authors: Yask Gupta, David J. Friedman, Michelle T. McNulty, Atlas Khan, Brandon M. Lane, Chen Wang, Juntao Ke, Gina Jin, Benjamin Wooden, Andrea L. Knob, Tze Yin Lim, Gerald B. Appel, Kinsie Huggins, Lili Liu, Adele Mitrotti, Megan C. Stangl, Andrew S. Bomback, Rik Westland, Monica Bodria, Maddalena Marasà, Ning Shang, David J. Cohen, Russell J. Crew, William Morello, Pietro A. Canetta, Jai Radhakrishnan, Jeremiah Martino, Qingxue Liu, Wendy K. Chung, Angelica Espinoza, Yuan Luo, Wei‐Qi Wei, QiPing Feng, Chunhua Weng, Yilu Fang, Iftikhar J. Kullo, Mohammadreza Naderian, Nita A. Limdi, Marguerite R. Irvin, Hemant K. Tiwari, Sumit Mohan, Maya K. Rao, Geoffrey K. Dube, Ninad S. Chaudhary, Orlando M. Gutiérrez, Suzanne E. Judd, Mary Cushman, Leslie A. Lange, Ethan M. Lange, Daniel L. Bivona, Miguel Verbitsky, Cheryl A. Winkler, Jeffrey B. Kopp, Dominick Santoriello, Ibrahim Batal, Sérgio Veloso Brant Pinheiro, Eduardo A. Oliveira, Ana Cristina Simões e Silva, Isabella Pisani, Enrico Fiaccadori, Fangming Lin, Loreto Gesualdo, Antonio Amoroso, Gian Marco Ghiggeri, Vivette D. D’Agati, Riccardo Magistroni, Eimear E. Kenny, Ruth J. F. Loos, Giovanni Montini, Friedhelm Hildebrandt, Dirk S. Paul, Slavé Petrovski, David B. Goldstein, Matthias Kretzler, Rasheed Gbadegesin, Ali G. Gharavi, Krzysztof Kiryluk, Matthew G. Sampson, Martin R. Pollak, Simone Sanna‐Cherchi - Nature Communications 2023 cited by 68
- Quality Control Procedures for Genome‐Wide Association Studies
Authors: Stephen Turner, Loren L. Armstrong, Yuki Bradford, Christopher S. Carlson, Dana C. Crawford, Andrew Crenshaw, Mariza de Andrade, Kimberly F. Doheny, Jonathan L. Haines, Geoffrey Hayes, Gail P. Jarvik, Lan Jiang, Iftikhar J. Kullo, Rongling Li, Hua Ling, Teri A. Manolio, Martha Matsumoto, Catherine A. McCarty, Andrew McDavid, Daniel B. Mirel, Justin Paschall, Elizabeth Pugh, Luke V. Rasmussen, Russell A. Wilke, Rebecca L. Zuvich, Marylyn D. Ritchie - Current Protocols in Human Genetics 2011 cited by 378
- Genome-Wide Association Study of Peripheral Artery Disease
Authors: Natalie R. van Zuydam, Alexander Stiby, Moustafa Abdalla, Erin Austin, Emma H. Dahlström, Stela McLachlan, Efthymia Vlachopoulou, Emma Ahlqvist, Chen Di Liao, Niina Sandholm, Carol Forsblom, Anubha Mahajan, Neil R. Robertson, Nigel W. Rayner, Eero Lindholm, Juha Sinisalo, Markus Perola, Milla Kallio, Emily Weiss, Jackie F. Price, Andrew D. Paterson, Barbara E.K. Klein, Veikko Salomaa, Colin N.A. Palmer, Per‐Henrik Groop, Leif Groop, Mark I. McCarthy, Mariza de Andrade, Andrew P. Morris, Jemma C. Hopewell, Helen M. Colhoun, Iftikhar J. Kullo, Sólveig Grétarsdóttir, Guðmar Þorleifsson, Unnur Þorsteinsdóttir, Kāri Stefánsson, Mark Michael, Timo Kanninen, Barbara Thorand, Giuseppe Remuzzi, David B. Dunger, Angela C. Shore, Ulf Smith, Seppo Ylä‐Herttuala, Claudio Cobelli, Riccardo Bellazzi, Ele Ferrannini, Carlo Patrono, Pirjo Nuutila, Paul McKeague, Birgit Steckel-Hamann, Li‐Ming Gan, Everson Nogoceke, Piero Tortoli, Bernd Jablonka, Mary-Julia Brosnan - Circulation Genomic and Precision Medicine 2021 cited by 86
- Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups
Authors: Ozan Dikilitas, Daniel J. Schaid, Matthew Kosel, Robert J. Carroll, Christopher G. Chute, Joshua C. Denny, Alex Fedotov, QiPing Feng, Håkon Håkonarson, Gail P. Jarvik, Ming Ta Michael Lee, Jennifer A. Pacheco, Robb Rowley, Patrick Sleiman, Christoph Stein, Amy C. Sturm, Wei‐Qi Wei, Georgia L. Wiesner, Marc S. Williams, Yanfei Zhang, Teri A. Manolio, Iftikhar J. Kullo - The American Journal of Human Genetics 2020 cited by 173
- Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
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