Aris Baras
Active 2015–2025
- 109
- Papers
- 20,209
- Citations
- 60
- h-index
- 108
- i10-index
Citations
Citation sources
Countries
Institutions
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
- John D. Overton41
- Jeffrey G. Reid34
- Luca A. Lotta25
- Gonçalo R. Abecasis17
- Xiaodong Bai17
- Alan R. Shuldiner16
- Colm O’Dushlaine15
- Jack A. Kosmicki15
- Joshua Backman15
- Michael Cantor15
- Alexander Lopez14
- David J. Carey14
- Evan K. Maxwell14
- Giovanni Coppola14
- Manuel A. R. Ferreira14
- Anthony Marcketta13
- Lukas Habegger13
- Marcus B. Jones13
- Suganthi Balasubramanian13
- Aris N. Economides12
- Cristopher V. Van Hout12
- Frederick E. Dewey12
- Joelle Mbatchou12
- Joseph B. Leader12
All papers
- Exome sequencing and analysis of 454,787 UK Biobank participants
Authors: Joshua Backman, Alexander Li, Anthony Marcketta, Dylan Sun, Joelle Mbatchou, Michael D. Kessler, Christian Benner, Daren Liu, Adam E. Locke, Suganthi Balasubramanian, Ashish Yadav, Nilanjana Banerjee, Christopher E. Gillies, Amy Damask, Simon Liu, Xiaodong Bai, Alicia Hawes, Evan K. Maxwell, Lauren Gurski, Kyoko Watanabe, Jack A. Kosmicki, Veera M. Rajagopal, Jason Mighty, DiscovEHR, Marcus B. Jones, Lyndon J. Mitnaul, Eli A. Stahl, Giovanni Coppola, Eric Jorgenson, Lukas Habegger, 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
- 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
- Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Authors: Sonia Shah, Albert Henry, Carolina Roselli, Honghuang Lin, Garðar Sveinbjörnsson, Ghazaleh Fatemifar, Åsa K. Hedman, Jemma B. Wilk, Michael P. Morley, Mark Chaffin, Anna Helgadóttir, Niek Verweij, Abbas Dehghan, Peter Almgren, Charlotte Andersson, Krishna G. Aragam, Johan Ärnlöv, Joshua Backman, Mary L. Biggs, Heather L. Bloom, Jeffrey Brandimarto, Michael R. Brown, Leonard Buckbinder, David J. Carey, Daniel I. Chasman, Xing Chen, Xu Chen, Jonathan Chung, William A. Chutkow, James P. Cook, 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
- Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
Authors: Jonas B. Nielsen, Rósa B. Þórólfsdóttir, Lars G. Fritsche, Wei Zhou, Morten W. Skov, Sarah E. Graham, Todd J. Herron, Shane McCarthy, Ellen M. Schmidt, Garðar Sveinbjörnsson, Ida Surakka, Michael R. Mathis, Masatoshi Yamazaki, Ryan Crawford, Maiken E. Gabrielsen, Anne Heidi Skogholt, Oddgeir L. Holmen, Maoxuan Lin, Brooke N. Wolford, Rounak Dey, Håvard Dalen, Patrick Sulem, Jonathan H. Chung, Joshua Backman, Davíð O. Arnar, Unnur Þorsteinsdóttir, Aris Baras, Colm O’Dushlaine, Anders G. Holst, Xiaoquan Wen, 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
- 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: Marijana Vujković, Jacob M. Keaton, Julie A. Lynch, Donald R. Miller, Jin Zhou, Catherine Tcheandjieu, Jennifer E. Huffman, Themistocles L. Assimes, Kimberly Lorenz, Xiang Zhu, Austin T. Hilliard, Renae Judy, Jie Huang, Kyung Min Lee, Derek Klarin, Saiju Pyarajan, John Danesh, Olle Melander, Asif Rasheed, Nadeem Hayat Mallick, Shahid Hameed, Irshad Hussain Qureshi, Muhammad Afzal, Uzma Malik, Anjum Jalal, Shahid Abbas, Xin Sheng, Long Gao, Klaus H. Kaestner, Katalin Suszták, 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
- A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease
Authors: Noura S. Abul‐Husn, Xiping Cheng, Alexander Li, Yurong Xin, Claudia Schurmann, Panayiotis E. Stevis, Yashu Liu, Julia Kozlitina, Stefan Stender, G. Craig Wood, Ann Stepanchick, Matthew Still, Shane McCarthy, Colm O’Dushlaine, Jonathan S. Packer, Suganthi Balasubramanian, Nehal Gosalia, David Esopi, Sun Y. Kim, Semanti Mukherjee, Alexander Lopez, Erin D. Fuller, John S. Penn, Xin Chu, Jonathan Z. Luo, Uyenlinh L. Mirshahi, David J. Carey, Christopher D. Still, Michael D. Feldman, Aeron Small, 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
- Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
Authors: Cindy G. Boer, Konstantinos Hatzikotoulas, Lorraine Southam, Lilja Stefánsdóttir, Yanfei Zhang, Rodrigo Coutinho de Almeida, Tian Wu, Jie Zheng, April Hartley, Maris Teder‐Laving, Anne Heidi Skogholt, Chikashi Terao, Eleni Zengini, George Alexiadis, Andrei Barysenka, Gyða Björnsdóttir, Maiken E. Gabrielsen, Arthur Gilly, Þorvaldur Ingvarsson, Marianne Bakke Johnsen, Helgi Jónsson, M. Kloppenburg, Almut Luetge, Sigrún H. Lund, Reedik Mägi, Massimo Mangino, Rob G. H. H. Nelissen, Manu Shivakumar, Julia Steinberg, Hiroshi Takuwa, 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
- Common and rare variant associations with clonal haematopoiesis phenotypes
Authors: Michael D. Kessler, Amy Damask, Sean O’Keeffe, Nilanjana Banerjee, Dadong Li, Kyoko Watanabe, Anthony Marketta, Michael Van Meter, Stefan Semrau, Julie Horowitz, Jing Tang, Jack A. Kosmicki, Veera M. Rajagopal, Yuxin Zou, Yariv Houvras, Arkopravo Ghosh, Christopher E. Gillies, Joelle Mbatchou, Ryan R. White, Niek Verweij, Jonas Bovijn, Neelroop Parikshak, Michelle G. LeBlanc, Marcus B. Jones, David J. Glass, Luca A. Lotta, Michael Cantor, Gurinder S. Atwal, Adam E. Locke, Manuel A. R. Ferreira, 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
- 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
- Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease
Authors: 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 cited by 875
- Mucus sialylation determines intestinal host-commensal homeostasis
Authors: Yikun Yao, Girak Kim, Samantha Shafer, Zuojia Chen, Satoshi Kubo, Yanlong Ji, Jialie Luo, Weiming Yang, Sebastian P. Perner, Chrysi Kanellopoulou, Ann Y. Park, Ping Jiang, Jian Li, Safa Barış, Elif Karakoç-Aydıner, Deniz Ertem, Daniel J. Mulder, Neil Warner, Anne M. Griffiths, Chani Topf‐Olivestone, Michal Kori, Lael Werner, Jodie Ouahed, Michael Field, Chengyu Liu, Benjamin Schwarz, Catharine M. Bosio, Sundar Ganesan, Jian Song, Henning Urlaub, 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
- Exome sequencing and characterization of 49,960 individuals in the UK Biobank
Authors: Cristopher V. Van Hout, Ioanna Tachmazidou, Joshua Backman, Joshua Hoffman, Daren Liu, Ashutosh Kumar Pandey, Claudia Gonzaga‐Jauregui, Shareef Khalid, Bin Ye, Nilanjana Banerjee, Alexander Li, Colm O’Dushlaine, Anthony Marcketta, Jeffrey Staples, Claudia Schurmann, Alicia Hawes, Evan K. Maxwell, Leland Barnard, Alexander Lopez, John S. Penn, Lukas Habegger, Andrew Blumenfeld, Xiaodong Bai, Sean O’Keeffe, Ashish Yadav, Kavita Praveen, Marcus B. Jones, William Salerno, Wendy K. Chung, Ida Surakka, 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
- Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects
Authors: 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, Aris Baras, Christopher R. Bauer, Dorret I. Boomsma, Archie Campbell, Harry Campbell, 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
- Safety and efficacy of itepekimab in patients with moderate-to-severe COPD: a genetic association study and randomised, double-blind, phase 2a trial
Authors: Klaus F. Rabe, Bartolomé R. Celli, Michael E. Wechsler, Raolat M. Abdulai, Xiaodong Luo, Maarten M. Boomsma, Heribert Staudinger, Julie Horowitz, Aris Baras, Manuel A. R. Ferreira, Marcella Ruddy, Michael C. Nivens, Nikhil Amin, David M. Weinreich, George D. Yancopoulos, Hélène Goulaouic - The Lancet Respiratory Medicine 2021 cited by 206
- Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity
Authors: Parsa Akbari, Ankit Gilani, Olukayode Sosina, Jack A. Kosmicki, Lori Khrimian, Yi‐Ya Fang, Trikaldarshi Persaud, Víctor Garcia, Dylan Sun, Alexander Li, Joelle Mbatchou, Adam E. Locke, Christian Benner, Niek Verweij, Nan Lin, Sakib Hossain, Kevin Agostinucci, Jonathan V. Pascale, Ercument Dirice, Michael E. Dunn, William E. Kraus, Svati H. Shah, Yii‐Der I. Chen, Jerome I. Rotter, Daniel J. Rader, Olle Melander, Christopher D. Still, Tooraj Mirshahi, David J. Carey, Jaime Berúmen, 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
- Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank
Authors: Joseph D. Szustakowski, Suganthi Balasubramanian, Erika Kvikstad, Shareef Khalid, Paola G. Bronson, Ariella Sasson, Emily Wong, Daren Liu, J. Wade Davis, Carolina Haefliger, A. Katrina Loomis, Rajesh Mikkilineni, Hyun Ji Noh, Samir Wadhawan, Xiaodong Bai, Alicia Hawes, Olga Krasheninina, Ricardo H. Ulloa, Alex E. Lopez, Erin N. Smith, Jeffrey F. Waring, Christopher D. Whelan, Ellen Tsai, John D. Overton, William Salerno, Howard J. Jacob, Sándor Szalma, Heiko Runz, Gregory Hinkle, Paul Nioi, 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
- A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
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