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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.

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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.