Number of items: 2.
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Trpchevska, Natalia, Freidin, Maxim B, Broer, Linda, Oosterloo, Berthe C, Yao, Shuyang, Zhou, Yitian, Vona, Barbara, Bishop, Charles, Bizaki-Vallaskangas, Argyro, Canlon, Barbara et al (show 56 more authors) , Castellana, Fabio, Chasman, Daniel I, Cherny, Stacey, Christensen, Kaare, Concas, Maria Pina, Correa, Adolfo, Elkon, Ran, Mengel-From, Jonas, Gao, Yan, Giersch, Anne BS, 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 KE, 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
ORCID: 0000-0003-1383-1850, 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 MK and Nagtegaal, Andries Paul
(2022)
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss.
AMERICAN JOURNAL OF HUMAN GENETICS, 109 (6).
pp. 1077-1091.
Collapse authors list.
van der Lee, Sven J
ORCID: 0000-0003-1606-8643, Conway, Olivia J, Jansen, Iris, Carrasquillo, Minerva M, Kleineidam, Luca
ORCID: 0009-0006-3309-6856, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R, Stringa, Najada, Chen, Jason A et al (show 98 more authors) , Zettergren, Anna, Andlauer, Till FM
ORCID: 0000-0002-2917-5889, Diez-Fairen, Monica
ORCID: 0000-0003-1882-0309, Simon-Sanchez, Javier, Lleó, Alberto, Zetterberg, Henrik, Nygaard, Marianne
ORCID: 0000-0003-0703-2665, Blauwendraat, Cornelis, Savage, Jeanne E, Mengel-From, Jonas
ORCID: 0000-0003-1573-8908, Moreno-Grau, Sonia, Wagner, Michael
ORCID: 0000-0003-2589-6440, Fortea, Juan
ORCID: 0000-0002-1340-638X, Keogh, Michael J, Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A
ORCID: 0000-0001-6380-2420, Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar
ORCID: 0000-0002-2148-381X, Riedel-Heller, Steffi
ORCID: 0000-0003-4321-6090, Illán-Gala, Ignacio
ORCID: 0000-0002-5418-2052, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo
ORCID: 0000-0002-1413-5091, Morris, Christopher M
ORCID: 0000-0002-3749-0993, Indakoetxea, Begoña, Collij, Lyduine E, Scherer, Martin, Morenas-Rodríguez, Estrella, Ironside, James W
ORCID: 0000-0001-5869-2108, van Berckel, Bart NM, Alcolea, Daniel
ORCID: 0000-0002-3819-3245, Wiendl, Heinz, Strickland, Samantha L, Pastor, Pau
ORCID: 0000-0002-7493-8777, Rodríguez Rodríguez, Eloy
ORCID: 0000-0001-7742-677X, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer, , EADB (Alzheimer Disease European DNA biobank), , IFGC (International FTD-Genomics Consortium), IPDGC (The Interna, , IPDGC (The International Parkinson Disease Genomics Consortium), , RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementi, , Netherlands Brain Bank (NBB), , Boeve, Bradley F, Petersen, Ronald C, Ferman, Tanis J, van Gerpen, Jay A, Reinders, Marcel JT, Uitti, Ryan J, Tárraga, Lluís, Maier, Wolfgang, Dols-Icardo, Oriol
ORCID: 0000-0003-2656-8748, Kawalia, Amit, Dalmasso, Maria Carolina
ORCID: 0000-0002-4901-9955, Boada, Mercè
ORCID: 0000-0003-2617-3009, Zettl, Uwe K, van Schoor, Natasja M
ORCID: 0000-0002-0870-0795, Beekman, Marian
ORCID: 0000-0003-0585-6206, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo López, Pantelyat, Alexander
ORCID: 0000-0002-6427-7485, Wszolek, Zbigniew K, Ross, Owen A
ORCID: 0000-0003-4813-756X, Dickson, Dennis W, Graff-Radford, Neill R, Knopman, David, Rademakers, Rosa, Lemstra, Afina W
ORCID: 0000-0002-8933-3260, Pijnenburg, Yolande AL
ORCID: 0000-0003-2464-1905, Scheltens, Philip
ORCID: 0000-0002-1046-6408, Gasser, Thomas
ORCID: 0000-0002-1069-1146, Chinnery, Patrick F
ORCID: 0000-0002-7065-6617, Hemmer, Bernhard, Huisman, Martijn A
ORCID: 0000-0002-9285-6759, Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A
ORCID: 0000-0001-7039-1105, Sørensen, Thorkild IA, Heutink, Peter
ORCID: 0000-0001-5218-1737, Sánchez-Juan, Pascual, Posthuma, Danielle
ORCID: 0000-0001-7582-2365, GIFT (Genetic Investigation in Frontotemporal Dementia and Alzhe, , Clarimón, Jordi, Christensen, Kaare, Ertekin-Taner, Nilüfer, Scholz, Sonja W
ORCID: 0000-0002-6623-0429, Ramirez, Alfredo
ORCID: 0000-0003-4991-763X, Ruiz, Agustín
ORCID: 0000-0003-2633-2495, Slagboom, Eline, van der Flier, Wiesje M and Holstege, Henne
ORCID: 0000-0002-7688-3087
(2019)
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
Acta neuropathologica, 138 (2).
pp. 237-250.
This list was generated on Sat May 18 05:26:12 2024 BST.