Aris Baras

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 49

Top Venues

Nature genetics

Nature

Nature communications

Nature medicine

Regeneron Pharmaceuticals Inc

Duke University School of Medicine (PHD)

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

Affiliation History

Regeneron Pharmaceuticals Inc

United States

Vice President and Head :: Regeneron Genetics Center

Education History

Duke University School of Medicine

United States

PHD

Duke University

United States

BSC

Publications

Alice Giontella, Mikael Åkerlund, Kevin Bronton, Cristiano Fava, Luca A Lotta, Aris Baras, John D Overton, Marcus Jones, Andreas Bergmann, Paul Kaufmann, Yulia Ilina, Olle Melander
Deficiency of Peptidylglycine-alpha-amidating Monooxygenase, a Cause of Sarcopenic Diabetes Mellitus. The Journal of clinical endocrinology and metabolism (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)
Kathie Y Sun, Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor, Joshua D Backman, Tyler Joseph, Evan Maxwell, George Mitra, Alexander Gorovits, Adam Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, Anthony Marcketta, Adam E Locke, Liron Ganel, Alicia Hawes, Michael D Kessler, Deepika Sharma, Jeffrey Staples, Jonas Bovijn, Sahar Gelfman, Alessandro Di Gioia, Veera Manikandan Rajagopal, Alexander Lopez, Jennifer Rico Varela, Jesus Alegre, Jaime Berumen-Campos, Roberto Tapia-Conyer, Pablo Kuri-Morales, Jason M Torres, Jonathan R Emberson, Rory Collins, null null, null null, Michael N Cantor, Timothy A Thornton, Hyun Min Kang, John D Overton, Alan R Shuldiner, M Laura Cremona, Mona Nafde, Aris Baras, Gonçalo R Abecasis, Jonathan Marchini, Jeffrey G Reid, William J Salerno, Suganthi Balasubramanian
A deep catalogue of protein-coding variation in 983,578 individuals. Nature 631 (8021) (2024)
Kathie Y Sun, Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor, Joshua D Backman, Tyler Joseph, Evan Maxwell, George Mitra, Alexander Gorovits, Adam Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, Anthony Marcketta, Adam E Locke, Liron Ganel, Alicia Hawes, Michael D Kessler, Deepika Sharma, Jeffrey Staples, Jonas Bovijn, Sahar Gelfman, Alessandro Di Gioia, Veera Manikandan Rajagopal, Alexander Lopez, Jennifer Rico Varela, Jesus Alegre, Jaime Berumen-Campos, Roberto Tapia-Conyer, Pablo Kuri-Morales, Jason M Torres, Jonathan R Emberson, Rory Collins, null null, null null, Michael N Cantor, Timothy A Thornton, Hyun Min Kang, John D Overton, Alan R Shuldiner, M Laura Cremona, Mona Nafde, Aris Baras, Gonçalo R Abecasis, Jonathan Marchini, Jeffrey G Reid, William J Salerno, Suganthi Balasubramanian
A deep catalogue of protein-coding variation in 983,578 individuals. Nature (2024)
Juan Lorenzo Rodriguez-Flores, Shareef Khalid, Neelroop N Parikshak, Asif Rasheed, Bin Ye, Manav Kapoor, Joshua D Backman, Farshid Sepehrband, Silvio Alessandro Di Gioia, Sahar Gelfman, Tanima De, Nilanjana Banerjee, Deepika Sharma, Hector Martinez, Sofia Castaneda, David D'Ambrosio, Xingmin A Zhang, Pengcheng Xun, Ellen Tsai, I-Chun Tsai, null null, Maleeha Zaman Khan, Muhammad Jahanzaib, Muhammad Rehan Mian, Muhammad Bilal Liaqat, Khalid Mahmood, Tanvir Us Salam, Muhammad Hussain, Javed Iqbal, Faizan Aslam, Michael N Cantor, Gannie Tzoneva, John Overton, Jonathan Marchini, Jeffrey G Reid, Aris Baras, Niek Verweij, Luca A Lotta, Giovanni Coppola, Katia Karalis, Aris N Economides, Sergio Fazio, Wolfgang B Liedtke, John Danesh, Ayeesha Kamal, Philippe Frossard, Thomas Coleman, Alan R Shuldiner, Danish Saleheen
NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke. 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)
Andrey Ziyatdinov, Jason M Torres, Jesus Alegre, Joshua D Backman, Joelle Mbatchou, Michael Turner, Sheila M Gaynor, Tyler Joseph, Yuxin Zou, Daren Liu, Rachel Wade, Jeffrey Staples, Razvan Panea, Alex Popov, Xiaodong Bai, Suganthi Balasubramanian, Lukas Habegger, Rouel Lanche, Alex Lopez, Evan Maxwell, Marcus Jones, Humberto Garcia-Ortiz, Raúl Ramírez-Reyes, Rogelio Santacruz-Benítez, Abhishek Nag, Katherine R Smith, Amy Damask, Nan Lin, Charles Paulding, Mark Reppell, Sebastian Zöllner, Eric Jorgensen, William Salerno, Slavé Petrovski, John Overton, Jeffrey G Reid, Timothy A Thornton, Gonçalo R Abecasis, Jaime Berumen-Campos, Lorena Orozco-Orozco, Rory Collins, null null, null null, Aris Baras, Michael R Hill, Jonathan R Emberson, Jonathan Marchini, Pablo Kuri-Morales, Roberto Tapia-Conyer
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City. Nature (2024)
Kathie Y Sun, Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor, Joshua D Backman, Tyler Joseph, Evan Maxwell, George Mitra, Alexander Gorovits, Adam Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, Anthony Marcketta, Adam E Locke, Liron Ganel, Alicia Hawes, Michael D Kessler, Deepika Sharma, Jeffrey Staples, Jonas Bovijn, Sahar Gelfman, Alessandro Di Gioia, Veera Manikandan Rajagopal, Alexander Lopez, Jennifer Rico Varela, Jesus Alegre, Jaime Berumen-Campos, Roberto Tapia-Conyer, Pablo Kuri-Morales, Jason M Torres, Jonathan R Emberson, Rory Collins, null null, null null, Michael N Cantor, Timothy A Thornton, Hyun Min Kang, John D Overton, Alan R Shuldiner, M Laura Cremona, Mona Nafde, Aris Baras, Gonçalo R Abecasis, Jonathan Marchini, Jeffrey G Reid, William J Salerno, Suganthi Balasubramanian
A deep catalogue of protein-coding variation in 983,578 individuals. Nature (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)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (2024)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics (2024)
Kathie Y Sun, Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor, Joshua D Backman, Tyler Joseph, Evan Maxwell, George Mitra, Alexander Gorovits, Adam Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, Anthony Marcketta, Adam E Locke, Liron Ganel, Alicia Hawes, Michael D Kessler, Deepika Sharma, Jeffrey Staples, Jonas Bovijn, Sahar Gelfman, Alessandro Di Gioia, Veera Manikandan Rajagopal, Alexander Lopez, Jennifer Rico Varela, Jesus Alegre, Jaime Berumen-Campos, Roberto Tapia-Conyer, Pablo Kuri-Morales, Jason M Torres, Jonathan R Emberson, Rory Collins, null null, null null, Michael N Cantor, Timothy A Thornton, Hyun Min Kang, John D Overton, Alan R Shuldiner, M Laura Cremona, Mona Nafde, Aris Baras, Gonçalo R Abecasis, Jonathan Marchini, Jeffrey G Reid, William J Salerno, Suganthi Balasubramanian
A deep catalogue of protein-coding variation in 983,578 individuals. Nature 631 (8021) (2024)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (2024)
Michael E Dunn, Aaron Kithcart, Jee Hae Kim, Andre Jo-Hao Ho, Matthew C Franklin, Annabel Romero Hernandez, Jan de Hoon, Wouter Botermans, Jonathan Meyer, Ximei Jin, Dongqin Zhang, Justin Torello, Daniel Jasewicz, Vishal Kamat, Elena Garnova, Nina Liu, Michael Rosconi, Hao Pan, Satyajit Karnik, Michael E Burczynski, Wenjun Zheng, Ashique Rafique, Jonas B Nielsen, Tanima De, Niek Verweij, Anita Pandit, Adam E Locke, Naga Chalasani, Olle Melander, Tae-Hwi Schwantes-An, null null, Aris Baras, Luca A Lotta, Bret J Musser, Jason Mastaitis, Kishor B Devalaraja-Narashimha, Andrew J Rankin, Tammy Huang, Gary Herman, William Olson, Andrew J Murphy, George D Yancopoulos, Benjamin A Olenchock, Lori Morton
Agonist antibody to guanylate cyclase receptor NPR1 regulates vascular tone. Nature (2024)
Kathie Y Sun, Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor, Joshua D Backman, Tyler Joseph, Evan Maxwell, George Mitra, Alexander Gorovits, Adam Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, Anthony Marcketta, Adam E Locke, Liron Ganel, Alicia Hawes, Michael D Kessler, Deepika Sharma, Jeffrey Staples, Jonas Bovijn, Sahar Gelfman, Alessandro Di Gioia, Veera Manikandan Rajagopal, Alexander Lopez, Jennifer Rico Varela, Jesus Alegre, Jaime Berumen-Campos, Roberto Tapia-Conyer, Pablo Kuri-Morales, Jason M Torres, Jonathan R Emberson, Rory Collins, null null, null null, Michael N Cantor, Timothy A Thornton, Hyun Min Kang, John D Overton, Alan R Shuldiner, M Laura Cremona, Mona Nafde, Aris Baras, Gonçalo R Abecasis, Jonathan Marchini, Jeffrey G Reid, William J Salerno, Suganthi Balasubramanian
A deep catalogue of protein-coding variation in 983,578 individuals. Nature 631 (8021) (2024)
Kathie Y Sun, Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor, Joshua D Backman, Tyler Joseph, Evan Maxwell, George Mitra, Alexander Gorovits, Adam Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, Anthony Marcketta, Adam E Locke, Liron Ganel, Alicia Hawes, Michael D Kessler, Deepika Sharma, Jeffrey Staples, Jonas Bovijn, Sahar Gelfman, Alessandro Di Gioia, Veera Manikandan Rajagopal, Alexander Lopez, Jennifer Rico Varela, Jesus Alegre, Jaime Berumen-Campos, Roberto Tapia-Conyer, Pablo Kuri-Morales, Jason M Torres, Jonathan R Emberson, Rory Collins, null null, null null, Michael N Cantor, Timothy A Thornton, Hyun Min Kang, John D Overton, Alan R Shuldiner, M Laura Cremona, Mona Nafde, Aris Baras, Gonçalo R Abecasis, Jonathan Marchini, Jeffrey G Reid, William J Salerno, Suganthi Balasubramanian
A deep catalogue of protein-coding variation in 983,578 individuals. Nature 631 (8021) (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)
Kathie Y Sun, Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor, Joshua D Backman, Tyler Joseph, Evan Maxwell, George Mitra, Alexander Gorovits, Adam Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, Anthony Marcketta, Adam E Locke, Liron Ganel, Alicia Hawes, Michael D Kessler, Deepika Sharma, Jeffrey Staples, Jonas Bovijn, Sahar Gelfman, Alessandro Di Gioia, Veera Manikandan Rajagopal, Alexander Lopez, Jennifer Rico Varela, Jesus Alegre, Jaime Berumen-Campos, Roberto Tapia-Conyer, Pablo Kuri-Morales, Jason M Torres, Jonathan R Emberson, Rory Collins, null null, null null, Michael N Cantor, Timothy A Thornton, Hyun Min Kang, John D Overton, Alan R Shuldiner, M Laura Cremona, Mona Nafde, Aris Baras, Gonçalo R Abecasis, Jonathan Marchini, Jeffrey G Reid, William J Salerno, Suganthi Balasubramanian
A deep catalogue of protein-coding variation in 983,578 individuals. Nature (2024)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (2024)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (2024)
Kathie Y Sun, Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor, Joshua D Backman, Tyler Joseph, Evan Maxwell, George Mitra, Alexander Gorovits, Adam Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, Anthony Marcketta, Adam E Locke, Liron Ganel, Alicia Hawes, Michael D Kessler, Deepika Sharma, Jeffrey Staples, Jonas Bovijn, Sahar Gelfman, Alessandro Di Gioia, Veera Manikandan Rajagopal, Alexander Lopez, Jennifer Rico Varela, Jesus Alegre, Jaime Berumen-Campos, Roberto Tapia-Conyer, Pablo Kuri-Morales, Jason M Torres, Jonathan R Emberson, Rory Collins, null null, null null, Michael N Cantor, Timothy A Thornton, Hyun Min Kang, John D Overton, Alan R Shuldiner, M Laura Cremona, Mona Nafde, Aris Baras, Gonçalo R Abecasis, Jonathan Marchini, Jeffrey G Reid, William J Salerno, Suganthi Balasubramanian
A deep catalogue of protein-coding variation in 983,578 individuals. Nature 631 (8021) (2024)
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 Gillies, Joelle Mbatchou, Ryan R White, Niek Verweij, Jonas Bovijn, Neelroop N Parikshak, Michelle G LeBlanc, Marcus Jones, null null, null null, David J Glass, Luca A Lotta, Michael N Cantor, Gurinder S Atwal, Adam E Locke, Manuel A R Ferreira, Raquel Deering, Charles Paulding, Alan R Shuldiner, Gavin Thurston, Adolfo A Ferrando, Will Salerno, Jeffrey G Reid, John D Overton, Jonathan Marchini, Hyun M Kang, Aris Baras, Gonçalo R Abecasis, Eric Jorgensen
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes. Nature (2023)
Sahar Gelfman, Arden Moscati, Santiago Mendez Huergo, Rujin Wang, Veera Rajagopal, Neelroop N Parikshak, Vijay Kumar Pounraja, Esteban Chen, Michelle Leblanc, Ralph Hazlewood, Jan Freudenberg, Blerta Cooper, Ann J Ligocki, Charles G Miller, Tavé Van Zyl, Jonathan Weyne, Carmelo Romano, Botir Sagdullaev, Olle Melander, Aris Baras, null null, Eli A Stahl, Giovanni Coppola
A large meta-analysis identifies genes associated with anterior uveitis. Nature communications 14 (1) (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)
Veera M Rajagopal, Kyoko Watanabe, Joelle Mbatchou, Ariane Ayer, Peter Quon, Deepika Sharma, Michael D Kessler, Kavita Praveen, Sahar Gelfman, Neelroop N Parikshak, Jacqueline M Otto, Suying Bao, Shek Man Chim, Elias Pavlopoulos, Andreja Avbersek, Manav Kapoor, Esteban Chen, Marcus B Jones, Michelle Leblanc, Jonathan R Emberson, Rory Collins, Jason M Torres, Pablo Kuri Morales, Roberto Tapia-Conyer, Jesus Alegre, Jaime Berumen-Campos, null null, null null, Alan R Shuldiner, Suganthi Balasubramanian, Gonçalo R Abecasis, Hyun M Kang, Jonathan Marchini, Eli A Stahl, Eric Jorgensen, Robert Sanchez, Wolfgang Liedtke, Matthew Anderson, Michael N Cantor, David Lederer, Aris Baras, Giovanni Coppola
Rare coding variants in CHRNB2 reduce the likelihood of smoking. Nature genetics (2023)
Sirui Zhou, Olukayode A Sosina, Jonas Bovijn, Laetitia Laurent, Vasundhara Sharma, Parsa Akbari, Vincenzo Forgetta, Lai Jiang, Jack A Kosmicki, Nilanjana Banerjee, John A Morris, Erin Oerton, Marcus Jones, Michelle G LeBlanc, null null, Vincent Idone, John D Overton, Jeffrey G Reid, Michael N Cantor, Gonçalo R Abecasis, David Goltzman, Celia M T Greenwood, Claudia Langenberg, Aris Baras, Aris N Economides, Manuel A R Ferreira, Sarah Hatsell, Claes Ohlsson, John Brent Richards, Luca A Lotta
Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis. Nature genetics 55 (8) (2023)
Andrey Ziyatdinov, Jason M Torres, Jesus Alegre, Joshua D Backman, Joelle Mbatchou, Michael Turner, Sheila M Gaynor, Tyler Joseph, Yuxin Zou, Daren Liu, Rachel Wade, Jeffrey Staples, Razvan Panea, Alex Popov, Xiaodong Bai, Suganthi Balasubramanian, Lukas Habegger, Rouel Lanche, Alex Lopez, Evan Maxwell, Marcus Jones, Humberto Garcia-Ortiz, Raúl Ramírez-Reyes, Rogelio Santacruz-Benítez, Abhishek Nag, Katherine R Smith, Amy Damask, Nan Lin, Charles Paulding, Mark Reppell, Sebastian Zöllner, Eric Jorgensen, William Salerno, Slavé Petrovski, John Overton, Jeffrey G Reid, Timothy A Thornton, Gonçalo R Abecasis, Jaime Berumen-Campos, Lorena Orozco-Orozco, Rory Collins, null null, null null, Aris Baras, Michael R Hill, Jonathan R Emberson, Jonathan Marchini, Pablo Kuri-Morales, Roberto Tapia-Conyer
Genotyping, sequencing and analysis of 140,000 adults from Mexico City. Nature (2023)
Kavita Praveen, Lee Dobbyn, Lauren Gurski, Ariane H Ayer, Jeffrey Staples, Shawn Mishra, Yu Bai, Alexandra Kaufman, Arden Moscati, Christian Benner, Esteban Chen, Siying Chen, Alexander Popov, Janell Smith, null null, null null, null null, Olle Melander, Marcus B Jones, Jonathan Marchini, Suganthi Balasubramanian, Brian Zambrowicz, Meghan C Drummond, Aris Baras, Gonçalo R Abecasis, Manuel A R Ferreira, Eli A Stahl, Giovanni Coppola
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults. Communications biology 5 (1) (2022)
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)
Marijana Vujkovic, Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J Cordell, Jing He, Yevgeniy Gindin, Chuhan Chung, Robert P Myers, Carolin V Schneider, Joseph Park, Kyung Min Lee, Marina Serper, Rotonya M Carr, David E Kaplan, Mary E Haas, Matthew T MacLean, Walter R Witschey, Xiang Zhu, Catherine Tcheandjieu, Rachel L Kember, Henry R Kranzler, Anurag Verma, Ayush Giri, Derek M Klarin, Yan V Sun, Jie Huang, Jennifer E Huffman, Kate Townsend Creasy, 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 Chang, Ronald M Krauss, Silvia 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 S Lee, Themistocles L Assimes, Saiju Pyarajan, Kelly Cho, Todd L Edwards, Scott M Damrauer, Peter W 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, null null, null null, null null, null null, Daniel James Rader, Benjamin F Voight, Kyong-Mi Chang
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. Nature genetics 54 (6) (2022)
Nan Lin, Amy Damask, Anita Boyapati, Jennifer D Hamilton, Sara Hamon, Nils Ternes, Michael C Nivens, John Penn, Alexander Lopez, Jeffrey G Reid, John Overton, Alan R Shuldiner, Gonçalo R Abecasis, Aris Baras, Charles Paulding
UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab. The pharmacogenomics journal 22 (3) (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)
Eric D Carruth, Maria Qureshi, Amro Alsaid, Melissa A Kelly, Hugh Calkins, Brittney Murray, Crystal Tichnell, Amy C Sturm, null null, Aris Baras, H Lester Kirchner, Brandon K Fornwalt, Cynthia A James, Christopher M Haggerty
Loss-of-Function FLNC Variants Are Associated With Arrhythmogenic Cardiomyopathy Phenotypes When Identified Through Exome Sequencing of a General Clinical Population. Circulation. Genomic and precision medicine 15 (4) (2022)
Alice Giontella, Luca A Lotta, Aris Baras, Pietro Minuz, Dipender Gill, Olle Melander, Cristiano Fava
Calcium, Its Regulatory Hormones, and Their Causal Role on Blood Pressure: A Two-Sample Mendelian Randomization Study. The Journal of clinical endocrinology and metabolism 107 (11) (2022)
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 Gillies, Joelle Mbatchou, Ryan R White, Niek Verweij, Jonas Bovijn, Neelroop N Parikshak, Michelle G LeBlanc, Marcus Jones, null null, null null, David J Glass, Luca A Lotta, Michael N Cantor, Gurinder S Atwal, Adam E Locke, Manuel A R Ferreira, Raquel Deering, Charles Paulding, Alan R Shuldiner, Gavin Thurston, Adolfo A Ferrando, Will Salerno, Jeffrey G Reid, John D Overton, Jonathan Marchini, Hyun M Kang, Aris Baras, Gonçalo R Abecasis, Eric Jorgensen
Common and rare variant associations with clonal haematopoiesis phenotypes. Nature 612 (7939) (2022)
Laurence J Howe, Michel G Nivard, Tim T Morris, Ailin F 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 Klarić, Scott M Ratliff, Lawrence F Bielak, Marianne Nygaard, Alexandros Giannelis, Emily A Willoughby, Chandra A Reynolds, Jared V Balbona, Ole Andreas Andreassen, Helga Ask, Aris Baras, Christopher R Bauer, Dorret I Boomsma, Archie I Campbell, Harry Campbell, Zhengming Chen, Paraskevi Christofidou, Elizabeth C Corfield, Christina C Dahm, Deepika R Dokuru, Luke M Evans, Eco J C de Geus, Sudheer Giddaluru, Scott D Gordon, Kathryn Paige Harden, W David Hill, Amanda M Hughes, Shona M Kerr, Yongkang Kim, Hyeokmoon Kweon, Antti Latvala, Deborah A Lawlor, Liming Li, Kuang Lin, Per Magnus, Patrik K E Magnusson, Travis T Mallard, Pekka T Martikainen, Melinda C Mills, Pal Rasmus Njolstad, 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, null null, null null, John K Hewitt, Matthew C Keller, Michael C Stallings, James J Lee, Kaare Christensen, Sharon L R Kardia, Patricia A Peyser, Jennifer A Smith, James F Wilson, John L Hopper, Sara Hägg, Timothy D Spector, Jean-Baptiste Pingault, Robert Plomin, Karoline Alexandra Havdahl, Meike Bartels, Nicholas G Martin, Sven Oskarsson, Anne E Justice, Iona Y Millwood, Kristian Hveem, Øyvind Naess, Cristen J Willer, Bjørn Olav Åsvold, Philipp D Koellinger, Jaakko A Kaprio, Sarah E Medland, Robin G Walters, Daniel J Benjamin, Patrick Turley, David M Evans, George Davey Smith, Caroline Hayward, Ben Michael Brumpton, Gibran Hemani, Neil Martin Davies
Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Nature genetics 54 (5) (2022)
Parsa Akbari, Olukayode A Sosina, Jonas Bovijn, Karl Landheer, Jonas B Nielsen, Minhee Kim, Senem Aykul, Tanima De, Mary E Haas, George Hindy, Nan Lin, Ian R Dinsmore, Jonathan Z Luo, Stefanie Hectors, Benjamin Geraghty, Mary Germino, Lampros Panagis, Prodromos Parasoglou, Johnathon R Walls, Gabor Halasz, Gurinder S Atwal, null null, null null, Marcus Jones, Michelle G LeBlanc, Christopher D Still, David J Carey, Alice Giontella, Marju Orho-Melander, Jaime Berumen-Campos, Pablo Kuri-Morales, Jesus Alegre, Jason M Torres, Jonathan R Emberson, Rory Collins, Daniel James Rader, Brian Zambrowicz, Andrew J Murphy, Suganthi Balasubramanian, John D Overton, Jeffrey G Reid, Alan R Shuldiner, Michael Cantor, Gonçalo R Abecasis, Manuel A R Ferreira, Mark W Sleeman, Viktoria Gusarova, Judith Altarejos, Charles Harris, Aris N Economides, Vincent Idone, Katia Karalis, Giusy Della Gatta, Tooraj Mirshahi, George D Yancopoulos, Olle Melander, Jonathan Marchini, Roberto Tapia-Conyer, Adam E Locke, Aris Baras, Niek Verweij, Luca A Lotta
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes. Nature communications 13 (1) (2022)
Kavita Praveen, Gaurang C Patel, Lauren Gurski, Ariane H Ayer, Trikaladarshi Persaud, Matthew D Still, Lawrence Miloscio, Tavé Van Zyl, Silvio Alessandro Di Gioia, Ben Michael Brumpton, Kristi Krebs, Bjørn Olav Åsvold, Esteban Chen, Venkata R M Chavali, Wen Fury, Harini V Gudiseva, Sarah Hyde, Eric Jorgensen, Stephanie Lefebvre, Dadong Li, Alexander Li, James Mclninch, Brijeshkumar Patel, Jeremy S Rabinowitz, Rebecca Salowe, Claudia Schurmann, Anne-Sofie Seidelin, Eli A Stahl, Dylan Sun, Tanya M Teslovich, Anne Tybjærg-Hansen, Cristen J Willer, Scott Waldron, Sabrina Walley, Hua Yang, Sarthak Zaveri, null null, null null, null null, Ying Hu, Kristian Hveem, Olle Melander, Lili A Milani, Stefan Stender, Joan M O'Brien, Marcus B Jones, Gonçalo R Abecasis, Michael N Cantor, Jonathan Weyne, Katia Karalis, Aris N Economides, Giusy Della Gatta, Manuel A R Ferreira, George D Yancopoulos, Aris Baras, Carmelo Romano, Giovanni Coppola
ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma. Communications biology 5 (1) (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)
Krishna G Aragam, Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N Wolford, Deepak S Atri, Elle M Weeks, Minxian Wang, George Hindy, Wei Zhou, Christopher Grace, Carolina Roselli, Nicholas A Marston, Frederick K Kamanu, Ida Surakka, Loreto Muñoz Venegas, Paul Sherliker, Satoshi Koyama, Kazuyoshi Ishigaki, Bjørn Olav Åsvold, Michael R Brown, Ben Michael Brumpton, Paul S de Vries, Olga Giannakopoulou, Panagiota Giardoglou, Daníel F Guðbjartsson, Ulrich Güldener, Syed M Ijlal Haider, Anna Helgadottir, Maysson 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 Schnitzler, Damian Smedley, Gudmar Thorleifsson, Moritz von Scheidt, Jacob C Ulirsch, null null, null null, David O Arnar, Noël P Burtt, Maria C Costanzo, Jason Flannick, Shefali S Verma, Dong-Keun Jang, Yoichiro Kamatani, Amit V Khera, Issei Komuro, Iftikhar J Kullo, Luca A Lotta, Christopher P Nelson, Robert Roberts, Gudmundur Thorgeirsson, Unnur Thorsteinsdottir, Thomas R Webb, Aris Baras, Johan L M Bjorkegren, Eric Boerwinkle, George Dedoussis, Hilma Hólm, Kristian Hveem, Olle Melander, Alanna C Morrison, Marju Orho-Melander, Loukianos S Rallidis, Arno Ruusalepp, Marc S Sabatine, Kári Stefánsson, Pierre Zalloua, Patrick T Ellinor, Martin Farrall, John Danesh, Christian T Ruff, Hilary K Finucane, Jemma C Hopewell, Robert J Clarke, Rajat M Gupta, Jeanette Erdmann, Nilesh J Samani, Heribert Schunkert, Hugh C Watkins, Cristen J Willer, Panos Deloukas, Sekar Kathiresan, Adam S Butterworth, null null
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants. Nature genetics 54 (12) (2022)
Joshua D Backman, Alexander H 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 Maxwell, Lauren Gurski, Kyoko Watanabe, Jack A Kosmicki, Veera Rajagopal, Jason Mighty, null null, null null, Marcus Jones, Lyndon Mitnaul, Eli Stahl, Giovanni Coppola, Eric Jorgensen, Lukas Habegger, William J Salerno, Alan R Shuldiner, Luca A Lotta, John D Overton, Michael N Cantor, Jeffrey G Reid, George Yancopoulos, Hyun M Kang, Jonathan Marchini, Aris Baras, Gonçalo R Abecasis, Manuel A R Ferreira
Exome sequencing and analysis of 454,787 UK Biobank participants. Nature 599 (7886) (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)
Lucas D Ward, Ho-Chou Tu, Chelsea B Quenneville, Shira Tsour, Alexander O Flynn-Carroll, Margaret M Parker, Aimee M Deaton, Patrick A J Haslett, Luca A Lotta, Niek Verweij, Manuel A R Ferreira, null null, null null, Aris Baras, Gregory Hinkle, Paul Nioi
GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms. Nature communications 12 (1) (2021)
Joseph D Szustakowski, Suganthi Balasubramanian, Erika M Kvikstad, Shareef Khalid, Paola G Bronson, Ariella Sasson, Emily Wong, Daren Liu, Justin Wade Davis, Carolina Haefliger, A Katrina Loomis, Rajesh Mikkilineni, Hyun Ji Noh, Samir Wadhawan, Xiaodong Bai, Alicia Hawes, Olga Krasheninina, Ricardo Ulloa, Alex E Lopez, Erin N Smith, Jeffrey F Waring, Christopher D Whelan, Ellen A Tsai, John D Overton, William J Salerno, Howard Jacob, Sandor Szalma, Heiko Runz, Gregory Hinkle, Paul Nioi, Slavé Petrovski, Melissa R Miller, Aris Baras, Lyndon J Mitnaul, Jeffrey G Reid, null null
Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank. Nature genetics 53 (7) (2021)
Joelle Mbatchou, Leland Barnard, Joshua Backman, Anthony Marcketta, Jack A Kosmicki, Andrey Ziyatdinov, Christian Benner, Colm O'Dushlaine, Mathew Barber, Boris Boutkov, Lukas Habegger, Manuel Ferreira, Aris Baras, Jeffrey G Reid, Goncalo Abecasis, Evan Maxwell, Jonathan Marchini
Computationally efficient whole-genome regression for quantitative and binary traits. Nature genetics 53 (7) (2021)
Ida Surakka, Lars G Fritsche, Wei Zhou, Joshua Backman, Jack A Kosmicki, Haocheng Lu, Ben Brumpton, Jonas Bille Nielsen, Maiken E Gabrielsen, Anne Heidi Skogholt, Brooke N Wolford, Sarah E Graham, Y Eugene Chen, Seunggeun Lee, Hyun Min Kang, Arnulf Langhammer, Siri Forsmo, Bjørn Olav Åsvold, Unnur Styrkársdóttir, Hilma Hólm, Daníel F Guðbjartsson, Kari Stefansson, Aris Baras, null null, Goncalo R Abecasis, Kristian Hveem, Cristen J Willer
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk. Nature communications 11 (1) (2020)
Cristopher V Van Hout, Ioanna Tachmazidou, Joshua D Backman, Joshua D Hoffman, Daren Liu, Ashutosh K Pandey, Claudia Gonzaga-Jauregui, Shareef Khalid, Bin Ye, Nilanjana Banerjee, Alexander H Li, Colm O'Dushlaine, Anthony Marcketta, Jeffrey Staples, Claudia Schurmann, Alicia Hawes, Evan Maxwell, Leland Barnard, Alexander Lopez, John Penn, Lukas Habegger, Andrew L Blumenfeld, Xiaodong Bai, Sean O'Keeffe, Ashish Yadav, Kavita Praveen, Marcus Jones, William J Salerno, Wendy K Chung, Ida Surakka, Cristen J Willer, Kristian Hveem, Joseph B Leader, David J Carey, David H Ledbetter, null null, Lon Cardon, George D Yancopoulos, Aris N Economides, Giovanni Coppola, Alan R Shuldiner, Suganthi Balasubramanian, Michael Cantor, null null, Matthew R Nelson, John Whittaker, Jeffrey G Reid, Jonathan Marchini, John D Overton, Robert A Scott, Gonçalo R Abecasis, Laura M Yerges-Armstrong, Aris Baras
Exome sequencing and characterization of 49,960 individuals in the UK Biobank. Nature 586 (7831) (2020)
Om Prakash Dwivedi, Mikko Lehtovirta, Benoit Hastoy, Vikash Chandra, Nicole A J Krentz, Sandra Kleiner, Deepak Jain, Ann-Marie Richard, Fernando Abaitua, Nicola L Beer, Antje K Grotz, Rashmi B Prasad, Ola Hansson, Emma Ahlqvist, Ulrika Krus, Isabella Artner, Anu Suoranta, Daniel Gomez, Aris Baras, Benoite Champon, Anthony J Payne, Daniella Moralli, Soren K Thomsen, Philipp Kramer, Ioannis I Spiliotis, Reshma Ramracheya, Pauline Chabosseau, Andria Theodoulou, Rebecca Cheung, Martijn van de Bunt, Jason Flannick, Maddalena Trombetta, Enzo Bonora, Claes B Wolheim, Leena Sarelin, Riccardo C Bonadonna, Patrik Rorsman, Benjamin Davies, Julia Brosnan, Mark I McCarthy, Timo Otonkoski, Jens O Lagerstedt, Guy A Rutter, Jesper Gromada, Anna L Gloyn, Tiinamaija Tuomi, Leif C Groop
Loss of ZnT8 function protects against diabetes by enhanced insulin secretion. Nature genetics 51 (11) (2019)

Aris Baras.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Aris Baras