Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

Trpchevska, Natalia; Freidin, Maxim B.; Broer, Linda; Oosterloo, Berthe C.; Yao, Shuyang; Zhou, Yitian; Vona, Barbara; Bishop, Charles; Bizaki-Vallaskangas, Argyro; Canlon, Barbara; Castellana, Fabio; Chasman, Daniel I.; Cherny, Stacey; Christensen, Kaare; Concas, Maria Pina; Correa, Adolfo; Elkon, Ran; Mengel-From, Jonas; Gao, Yan; Giersch, Anne B. S.; Girotto, Giorgia; Gudjonsson, Alexander; Gudnason, Vilmundur; Heard-Costa, Nancy L.; Hertzano, Ronna; v.B. Hjelmborg, Jacob; Hjerling-Leffler, Jens; Hoffman, Howard J.; Kaprio, Jaakko; Kettunen, Johannes; Krebs, Kristi; Kahler, Anna K.; Lallemend, Francois; Launer, Lenore J.; Lee, I-Min; Leonard, Hampton; Li, Chuan-Ming; Lowenheim, Hubert; Magnusson, Patrik K. E.; van Meurs, Joyce; Milani, Lili; Morton, Cynthia C.; Makitie, Antti; Nalls, Mike A.; Nardone, Giuseppe Giovanni; Nygaard, Marianne; Palviainen, Teemu; Pratt, Sheila; Quaranta, Nicola; Ramo, Joel; Saarentaus, Elmo; Sardone, Rodolfo; Satizabal, Claudia L.; Schweinfurth, John M.; Seshadri, Sudha; Shiroma, Eric; Shulman, Eldad; Simonsick, Eleanor; Spankovich, Christopher; Tropitzsch, Anke; Lauschke, Volker M.; Sullivan, Patrick F.; Goedegebure, Andre; Cederroth, Christopher R.; Williams, Frances M. K.; Nagtegaal, Andries Paul

Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

Autor(en):

Trpchevska, Natalia; Freidin, Maxim B.; Broer, Linda; Oosterloo, Berthe C.; Yao, Shuyang; Zhou, Yitian; Vona, Barbara; Bishop, Charles; Bizaki-Vallaskangas, Argyro; Canlon, Barbara; Castellana, Fabio; Chasman, Daniel I.; Cherny, Stacey; Christensen, Kaare; Concas, Maria Pina; Correa, Adolfo; Elkon, Ran; Mengel-From, Jonas; Gao, Yan; Giersch, Anne B. S.; Girotto, Giorgia; Gudjonsson, Alexander; Gudnason, Vilmundur; Heard-Costa, Nancy L.; Hertzano, Ronna; v.B. Hjelmborg, Jacob; Hjerling-Leffler, Jens; Hoffman, Howard J.; Kaprio, Jaakko; Kettunen, Johannes; Krebs, Kristi; Kahler, Anna K.; Lallemend, Francois; Launer, Lenore J.; Lee, I-Min; Leonard, Hampton; Li, Chuan-Ming; Lowenheim, Hubert; Magnusson, Patrik K. E.; van Meurs, Joyce; Milani, Lili; Morton, Cynthia C.; Makitie, Antti; Nalls, Mike A.; Nardone, Giuseppe Giovanni; Nygaard, Marianne; Palviainen, Teemu; Pratt, Sheila; Quaranta, Nicola; Ramo, Joel; Saarentaus, Elmo; Sardone, Rodolfo; Satizabal, Claudia L.; Schweinfurth, John M.; Seshadri, Sudha; Shiroma, Eric; Shulman, Eldad; Simonsick, Eleanor; Spankovich, Christopher; Tropitzsch, Anke; Lauschke, Volker M.; Sullivan, Patrick F.; Goedegebure, Andre; Cederroth, Christopher R.; Williams, Frances M. K.; Nagtegaal, Andries Paul

Tübinger Autor(en):

Vona, Barbara
Löwenheim, Hubert Martin
Tropitzsch, Anke

Erschienen in:

American Journal of Human Genetics (2022), Bd. 109, H. 6, S. 1077-1091

Verlagsangabe:

Cell Press

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1016/j.ajhg.2022.04.010

ISSN:

0002-9297