Aris Baras

Active 2015–2025

109
Papers
20,209
Citations
60
h-index
108
i10-index

Citations

Citations per year for Aris Baras1991: 1 citations1994: 1 citations1996: 1 citations2004: 2 citations2007: 2 citations2011: 2 citations2012: 1 citations2016: 18 citations2017: 53 citations2018: 104 citations2019: 464 citations2020: 749 citations2021: 1,029 citations2022: 1,327 citations2023: 1,100 citations2024: 1,773 citations2025: 899 citations2026: 49 citations1992–1993: no citations, so these years are not shown1995: no citations, so this year is not shown1997–2003: no citations, so these years are not shown2005–2006: no citations, so these years are not shown2008–2010: no citations, so these years are not shown2013–2015: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,125 citing papers, 22.7% of this breakdownUnited Kingdom: 1,322 citing papers, 9.6% of this breakdownChina: 1,106 citing papers, 8.1% of this breakdownGermany: 707 citing papers, 5.1% of this breakdownNetherlands: 567 citing papers, 4.1% of this breakdownCanada: 556 citing papers, 4.1% of this breakdownItaly: 493 citing papers, 3.6% of this breakdownAustralia: 469 citing papers, 3.4% of this breakdownSweden: 444 citing papers, 3.2% of this breakdownFrance: 394 citing papers, 2.9% of this breakdownDenmark: 365 citing papers, 2.7% of this breakdownSpain: 301 citing papers, 2.2% of this breakdown
0%22.7%Other 28.3%

Fields

  • Medicine51.5%
  • Biochemistry, Genetics and Molecular Biology39.5%
  • Immunology and Microbiology2.9%
  • Neuroscience1.6%
  • Nursing0.8%
  • Psychology0.8%
  • Other2.9%

Topics

  • Genetic Associations and Epidemiology9.8%
  • Liver Disease Diagnosis and Treatment3.7%
  • Genomics and Rare Diseases3.3%
  • Diabetes, Cardiovascular Risks, and Lipoproteins2.8%
  • Lipoproteins and Cardiovascular Health2.6%
  • Lipid metabolism and disorders2.4%
  • Other75.4%

Coauthors

All papers

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  1. Exome sequencing and analysis of 454,787 UK Biobank participants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , William Salerno, Alan R. Shuldiner, Luca A. Lotta, John D. Overton, Michael Cantor, Jeffrey G. Reid, George D. Yancopoulos, Hyun Min Kang, Jonathan Marchini, Aris Baras, Gonçalo R. Abecasis, Manuel A. R. Ferreira - Nature 2021 cited by 1,077

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 and 103 more - Nature Communications 2020 cited by 929

  4. Biobank-driven genomic discovery yields new insight into atrial fibrillation biology

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Whitney Hornsby, Frederick E. Dewey, Michael Boehnke, Sachin Kheterpal, Bhramar Mukherjee, Seunggeun Lee, Hyun Min Kang, Hilma Hólm, Jacob O. Kitzman, Jordan A. Shavit, José Jalife, Chad M. Brummett, Tanya M. Teslovich, David J. Carey, Daníel F. Guðbjartsson, Kāri Stefánsson, Gonçalo R. Abecasis, Kristian Hveem, Cristen J. Willer - Nature Genetics 2018 cited by 936

  5. Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Yan V. Sun, Scott L. DuVall, Kelly Cho, Jennifer S. Lee, J. Michael Gaziano, Lawrence S. Phillips, James B. Meigs, Peter D. Reaven, Peter W.F. Wilson, Todd L. Edwards, Daniel J. Rader, Scott M. Damrauer, Christopher J. O’Donnell, Philip S. Tsao, Mark A. Atkinson, Al C. Powers, Ali Naji, Klaus H. Kaestner, Gonçalo R. Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Karina Toledo, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Xiaodong Bai, Suganthi Balasubramanian, Leland Barnard, Andrew Blumenfeld, Gisu Eom, Lukas Habegger, Alicia Hawes, Shareef Khalid, Evan K. Maxwell, William Salerno, Jeffrey Staples, Ashish Yadav, Marcus B. Jones, Lyndon J. Mitnaul, VA Million Veteran Program, Samuel M. Aguayo, Sunil K. Ahuja, Zuhair K. Ballas, Sujata Bhushan, Edward J. Boyko, David Cohen, John Concato, Joseph I. Constans, Louis J. Dell’Italia, Joseph Fayad, Ronald Fernando, Hermes Flórez, Melinda A. Gaddy, Saib Gappy and 82 more - Nature Genetics 2020 cited by 801

  6. A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Scott M. Damrauer, Daniel J. Rader, Brian Zambrowicz, William C. Olson, Andrew Murphy, Ingrid B. Borecki, Alan R. Shuldiner, Jeffrey G. Reid, John D. Overton, George D. Yancopoulos, Helen H. Hobbs, Jonathan C. Cohen, Omri Gottesman, Tanya M. Teslovich, Aris Baras, Tooraj Mirshahi, Jesper Gromada, Frederick E. Dewey - New England Journal of Medicine 2018 cited by 805

  7. Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laurent F. Thomas, Margo Tuerlings, John Loughlin, Nigel Arden, Fraser Birrell, Andrew Carr, Panos Deloukas, Michael Doherty, Andrew W. McCaskie, William Ollier, Ashok Rai, Stuart H. Ralston, Tim D. Spector, Gillian A. Wallis, Amy E. Martinsen, Cristen J. Willer, Egil A. Fors, Ingunn Mundal, Knut Hagen, Kristian Bernhard Nilsen, Marie Udnesseter Lie, Sigrid Børte, Ben Brumpton, Jonas B. Nielsen, Lars G. Fritsche, Wei Zhou, Ingrid Heuch, Kjersti Storheim, Evangelos Tyrpenou, A. Koukakis, Dimitrios Chytas, Dimitrios Stergios Evangelopoulos, Chronopoulos Efstathios, Spiros G. Pneumaticos, Vasileios S. Nikolaou, Κonstantinos Ν. Malizos, Lydia Anastasopoulou, Gonçalo R. Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Andrew Deubler, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Katia Karalis, Katherine Siminovitch, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Xiaodong Bai, Suganthi Balasubramanian, Boris Boutkov, Gisu Eom, Lukas Habegger, Alicia Hawes, Olga Krasheninina, Rouel Lanche, Adam J. Mansfield and 55 more - Cell 2021 cited by 467

  8. Common and rare variant associations with clonal haematopoiesis phenotypes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Raquel P. Deering, Charles Paulding, Alan R. Shuldiner, Gavin Thurston, Adolfo A. Ferrando, Will Salerno, Jeffrey G. Reid, John D. Overton, Jonathan Marchini, Hyun Min Kang, Aris Baras, Gonçalo R. Abecasis, Eric Jorgenson - Nature 2022 cited by 304

  9. Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  10. Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 875

  11. Mucus sialylation determines intestinal host-commensal homeostasis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thomas Oellerich, Stacy A. Malaker, Lixin Zheng, Carolyn R. Bertozzi, Yu Zhang, Helen Matthews, Will Montgomery, Han‐Yu Shih, Jiansheng Jiang, Marcus B. Jones, Aris Baras, Alan R. Shuldiner, Claudia Gonzaga‐Jauregui, Scott B. Snapper, Aleixo M. Muise, Dror S. Shouval, Ahmet Özen, Kuan‐Ting Pan, Chuan Wu, Michael J. Lenardo - Cell 2022 cited by 243

  12. Exome sequencing and characterization of 49,960 individuals in the UK Biobank

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Cristen J. Willer, Kristian Hveem, Joseph B. Leader, David J. Carey, David H. Ledbetter, Lon R. Cardon, George D. Yancopoulos, Aris N. Economides, Giovanni Coppola, Alan R. Shuldiner, Suganthi Balasubramanian, Michael Cantor, Matthew R. Nelson, John C. Whittaker, Jeffrey G. Reid, Jonathan Marchini, John D. Overton, Robert A. Scott, Gonçalo R. Abecasis, Laura M. Yerges-Armstrong, Aris Baras - Nature 2020 cited by 636

  13. Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm, Deepika Dokuru, Luke M. Evans, Eco J. C. de Geus, Sudheer Giddaluru, Scott D. Gordon, K. Paige Harden, W. David Hill, Amanda Hughes, Shona M. Kerr, Yongkang Kim, Hyeokmoon Kweon, Antti Latvala, Debbie A. Lawlor, Liming Li, Kuang Lin, Per Magnus, Patrik K. E. Magnusson, Travis T. Mallard, Pekka Martikainen, Melinda C. Mills, Pål R. Njølstad, John D. Overton, Nancy L. Pedersen, David J. Porteous, Jeffrey G. Reid, Karri Silventoinen, Melissa C. Southey, Camilla Stoltenberg, Elliot M. Tucker–Drob, Margaret J. Wright, Hyeokmoon Kweon, Philipp Koellinger, Daniel J. Benjamin, Patrick Turley, Laurence J. Howe, Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho, Geetha Chittoor, Rafael Ahlskog, Penelope A. Lind, Teemu Palviainen, Matthijs D. van der Zee, Rosa Cheesman, Massimo Mangino, Yunzhang Wang, Shuai Li, Lucija Klaric, Scott M. Ratliff, Lawrence F. Bielak, Marianne Nygaard, Alexandros Giannelis, Emily A. Willoughby, Chandra A. Reynolds, Jared V. Balbona, Ole A. Andreassen, Helga Ask, Dorret I. Boomsma, Archie Campbell, Harry Campbell, Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm and 96 more - Nature Genetics 2022 cited by 393

  14. Safety and efficacy of itepekimab in patients with moderate-to-severe COPD: a genetic association study and randomised, double-blind, phase 2a trial

    Authors: , , , , , , , , , , , , , , , - The Lancet Respiratory Medicine 2021 cited by 206

  15. Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Pablo Kuri‐Morales, Jesús Alegre-Díaz, Jason Torres, Jonathan Emberson, Rory Collins, Suganthi Balasubramanian, Alicia Hawes, Marcus Herbert Jones, Brian Zambrowicz, Andrew Murphy, Charles Paulding, Giovanni Coppola, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Michael Cantor, Hyun Min Kang, Gonçalo R. Abecasis, Katia Karalis, Aris N. Economides, Jonathan Marchini, George D. Yancopoulos, Mark W. Sleeman, Judith Y. Altarejos, Giusy Della Gatta, Roberto Tapia-Conyer, Michal L. Schwartzman, Aris Baras, Manuel A. R. Ferreira, Luca A. Lotta - Science 2021 cited by 276

  16. Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Slavé Petrovski, Melissa Miller, Aris Baras, Lyndon J. Mitnaul, Jeffrey G. Reid, Oleg Moiseyenko, Carlos Garcia Rios, Saurabh Saha, Gonçalo R. Abecasis, Nilanjana Banerjee, Christina Beechert, Boris Boutkov, Michael Cantor, Giovanni Coppola, Aris N. Economides, Gisu Eom, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Lukas Habegger, Marcus B. Jones, Rouel Lanche, Michael Lattari, Michelle G. LeBlanc, Dadong Li, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Thomas D. Schleicher, Deepika Sharma, Alan R. Shuldiner, Jeffrey Staples, Cristopher V. Van Hout, Louis Widom, Sarah E. Wolf, Sally John, Chia‐Yen Chen, David Sexton, Varant Kupelian, Eric Marshall, T. Swan, Susan Eaton, Jimmy Z. Liu, Stephanie Loomis, Megan E. Jensen, Saranya Duraisamy, Jason Tetrault, David Merberg, Sunita Badola, Mark Reppell, Jason Grundstad, Xiuwen Zheng, Aimée M. Deaton, Margaret M. Parker, Lucas D. Ward, Alexander O. Flynn-Carroll, Caroline A. Austin, Ruth March, Menelas N. Pangalos, Adam Platt and 11 more - Nature Genetics 2021 cited by 427

  17. A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nicholas J. Hand, Ching‐Ti Liu, Michelle T. Long, Jie Yao, Matthew J. Budoff, Jingyi Tan, Xiaohui Li, Henry J. Lin, Yii‐Der Ida Chen, Kent D. Taylor, Ruey‐Kang R. Chang, Ronald M. Krauss, Sílvia Vilarinho, Joseph Brancale, Jonas B. Nielsen, Adam E. Locke, Marcus B. Jones, Niek Verweij, Aris Baras, K. Rajender Reddy, Brent A. Neuschwander‐Tetri, Jeffrey B. Schwimmer, Arun J. Sanyal, Naga Chalasani, Kathleen A. Ryan, Braxton D. Mitchell, Dipender Gill, Andrew D. Wells, Elisabetta Manduchi, Yedidya Saiman, Nadim Mahmud, Donald R. Miller, Peter D. Reaven, Lawrence S. Phillips, Sumitra Muralidhar, Scott L. DuVall, Jennifer Lee, Themistocles L. Assimes, Saiju Pyarajan, Kelly Cho, Todd L. Edwards, Scott M. Damrauer, Peter W.F. Wilson, J. Michael Gaziano, Christopher J. O’Donnell, Amit V. Khera, Struan F.A. Grant, Christopher D. Brown, Philip S. Tsao, Danish Saleheen, Luca A. Lotta, Lisa Bastarache, Quentin M. Anstee, Ann K. Daly, James B. Meigs, Jerome I. Rotter, Julie A. Lynch, VA Million Veteran Program, Daniel J. Rader, Benjamin F. Voight, Kyong‐Mi Chang - Nature Genetics 2022 cited by 194

  18. Computationally efficient whole genome regression for quantitative and binary traits

    Authors: , , , , , , , , , , , , , , , , - Nature Genetics 2020 cited by 1,551

  19. Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laura Fachal, Martti Färkkilâ, William A. Faubion, Manuel A. R. Ferreira, Denis Franchimont, Stacey Gabriel, Tian Ge, Michel Georges, Kyle Gettler, Mamta Giri, Benjamin Gläser, Siegfried Goerg, Philippe Goyette, Daniel B. Graham, Eija Hämäläinen, Talin Haritunians, Graham Heap, Mikko Hiltunen, Marc P. Hoeppner, Julie Horowitz, Peter M. Irving, Vivek Iyer, Chaim Jalas, Judith R. Kelsen, Hamed Khalili, Barbara S. Kirschner, Kimmo Kontula, Jukka Koskela, Subra Kugathasan, Juozas Kupčinskas, Christopher A Lamb, Matthias Laudes, Chloé Lévesque, Adam P. Levine, James D. Lewis, Claire Liefferinckx, Britt-Sabina Loescher, Édouard Louis, John Mansfield, Sandra May, Jacob L. McCauley, Emebet Mengesha, Myriam Mni, Paul Moayyedi, Christopher J. Moran, Rodney D. Newberry, Sirimon O’Charoen, David T. Okou, Bas Oldenburg, Harry Ostrer, Aarno Palotie, Jean Paquette, Joel Pekow, Inga Peter, Marieke Pierik, Cyriel Y. Ponsioen, Nikolas Pontikos, Natalie J. Prescott, Ann E. Pulver, Souad Rahmouni, Daniel L Rice, Päivi Saavalainen, Bruce E. Sands, R. Balfour Sartor, Elena Schiff, Stefan Schreiber, L. Philip Schumm, Anthony W. Segal, Philippe Seksik, Rasha Shawky and 33 more - Nature Genetics 2022 cited by 189

  20. Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations

    Authors: , , , , , , , , , , , , , , , , , , , - Nature Communications 2019 cited by 535

  21. Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alicia Hawes, Marcus B. Jones, Katia Karalis, Shareef Khalid, Olga Krasheninina, Rouel Lanche, Michael Lattari, Dadong Li, Alexander Lopez, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Lyndon J. Mitnaul, Mona Nafde, Jonas B. Nielsen, Sean O’Keeffe, Max Orelus, John D. Overton, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Jeffrey G. Reid, William Salerno, Thomas D. Schleicher, Alan R. Shuldiner, Katherine Siminovitch, Jeffrey Staples, Ricardo H. Ulloa, Niek Verweij, Louis Widom, Sarah E. Wolf, Krishna G. Aragam, Kathryn L. Lunetta, Christopher M. Haggerty, Steven A. Lubitz, Patrick T. Ellinor - Nature Genetics 2022 cited by 173

  22. Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2016 cited by 510

  23. Genetics of blood lipids among 300,000 multi-ethnic participants of the Million Veteran Program

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Aliya Naheed, Amit V. Khera, John Danesh, Kyong‐Mi Chang, Gonçalo R. Abecasis, Cristen J. Willer, Frederick E. Dewey, David J. Carey, John Concato, J. Michael Gaziano, Christopher J. O’Donnell, Philip S. Tsao, Sekar Kathiresan, Daniel J. Rader, Peter W.F. Wilson, Themistocles L. Assimes - Nature Genetics 2018 cited by 709

  24. Germline Mutations in CIDEB and Protection against Liver Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael Cantor, Brian Zambrowicz, Andrew Murphy, Gonçalo R. Abecasis, Manuel A. R. Ferreira, Ēriks Šmagris, Viktoria Gusarova, Mark W. Sleeman, George D. Yancopoulos, Jonathan Marchini, Hyun Min Kang, Katia Karalis, Alan R. Shuldiner, Giusy Della Gatta, Adam E. Locke, Aris Baras, Luca A. Lotta - New England Journal of Medicine 2022 cited by 121