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Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
Author(s) -
Guillaume ButlerLaporte,
Gundula Povysil,
Jack A. Kosmicki,
Elizabeth T. Cirulli,
Theodore G. Drivas,
Simone Furini,
Chadi Saad,
Axel Schmidt,
Pawel Olszewski,
Urszula Korotko,
Mathieu Quinodoz,
Elifnaz Çelik,
Kousik Kundu,
Klaudia Walter,
Junghyun Jung,
Amy Stockwell,
Laura Sloofman,
Daniel M. Jordan,
Ryan Thompson,
Diane Del Valle,
Nicole W. Simons,
Esther Cheng,
Robert Sebra,
Eric E. Schadt,
Seunghee KimSchulze,
Sacha Gnjatic,
Miriam Mérad,
Joseph D. Buxbaum,
Noam D. Beckmann,
Alexander Charney,
Bartlomiej Przychodzen,
Timothy S. Chang,
Tess D. Pottinger,
Ning Shang,
Fabian Brand,
Francesca Fava,
Francesca Mari,
Karolina Chwiałkowska,
Magdaleiemira,
Szymon Puła,
J Kenneth Baillie,
Alexander Stuckey,
Antonio Salas,
Xabier Bello,
Jacobo Pardo-Seco,
Alberto Gómez-Carballa,
Irene RiveroCalle,
Federico MartinónTorres,
Andrea Ganna,
Konrad J. Karczewski,
Kumar Veerapen,
Mathieu Bourgey,
Guillaume Bourque,
Robert Eveleigh,
Vincenzo Forgetta,
David R. Morrison,
David Langlais,
Mark Lathrop,
Vincent Mooser,
Teruyuki Nakanishi,
Robert Frithiof,
Michael Hultström,
Miklós Lipcsey,
Yanara Marincevic-Zuniga,
Jessica Nordlund,
Kelly Schiabor Barrett,
William Lee,
Alexandre Bolze,
Simon White,
Stephen Riffle,
Francisco Tanudjaja,
Efren Sandoval,
Iva Neveux,
Shaun Dabe,
Nicolas Casadei,
Susanne Motameny,
Manal Alaamery,
Salam Massadeh,
Nora Aljawini,
Mansour S Almutairi,
Yaseen M. Arabi,
Saleh Alqahtani,
Fawz S. Al Harthi,
Amal Almutairi,
Fatima Alqubaishi,
Sarah Alotaibi,
Albandari Binowayn,
Ebtehal A. Alsolm,
Hadeel El Bardisy,
Mohammad Fawzy,
Fang Cai,
Nicole Soranzo,
Adam S. Butterworth,
Daniel H. Geschwind,
Stephanie Arteaga,
Alexis Stephens,
Manish J. Butte,
Paul C. Boutros,
Takafumi N. Yamaguchi,
Tao Shu,
Stefan Eng,
Timothy Sanders,
Paul Tung,
Michael E. Broudy,
Yu Pan,
Alfredo González,
Nikhil Chavan,
Ruth Johnson,
Bogdan Paşaniuc,
Brian L. Yaspan,
Sandra Smieszek,
Carlo Rivolta,
Stéphanie Bibert,
Pierre–Yves Bochud,
Maciej Dąbrowski,
Paweł Zawadzki,
Mateusz Sypniewski,
Elżbieta Kaja,
Pajaree Chariyavilaskul,
Voraphoj Nilaratanakul,
Nattiya Hirankarn,
Vorasuk Shotelersuk,
Monnat Pongpanich,
Chureerat Phokaew,
Wanna Chetruengchai,
Katsushi Tokunaga,
Masaya Sugiyama,
Yosuke Kawai,
Takanori Hasegawa,
Tatsuhiko Naito,
Ho Namkoong,
Ryuya Edahiro,
Akinori Kimura,
Seishi Ogawa,
Takanori Kanai,
Koichi Fukunaga,
Yukinori Okada,
Seiya Imoto,
Satoru Miyano,
Serghei Mangul,
Malak Abedalthagafi,
Hugo Zeberg,
Joseph J. Grzymski,
Nicole Washington,
Stephan Ossowski,
Kerstin U. Ludwig,
Eva C. Schulte,
Olaf Rieß,
Marcin Moniuszko,
Mirosław Kwaśniewski,
Hamdi Mbarek,
Said I. Ismail,
Anurag Verma,
David Goldstein,
Krzysztof Kiryluk,
Alessandra Renieri,
Manuel Ferreira,
J. Brent Richards
Publication year - 2022
Publication title -
plos genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.587
H-Index - 233
eISSN - 1553-7404
pISSN - 1553-7390
DOI - 10.1371/journal.pgen.1010367
Subject(s) - biology , genome wide association study , exome , exome sequencing , genetics , genetic association , disease , human genetics , genotype , single nucleotide polymorphism , gene , mutation , medicine , pathology