Number of items: 2.
Collapse authors list.
Feng, YCA, Howrigan, DP, Abbott, LE, Tashman, K, Cerrato, F, Singh, T, Heyne, H, Byrnes, A, Churchhouse, C, Watts, N et al (show 90 more authors) , Solomonson, M, Lal, D, Heinzen, EL, Dhindsa, RS, Stanley, KE, Cavalleri, GL, Hakonarson, H, Helbig, I, Krause, R, May, P, Weckhuysen, S, Petrovski, S, Kamalakaran, S, Sisodiya, SM, Cossette, P, Cotsapas, C, De Jonghe, P, Dixon-Salazar, T, Guerrini, R, Kwan, P, Marson, AG ORCID: 0000-0002-6861-8806, Stewart, R, Depondt, C, Dlugos, DJ, Scheffer, IE, Striano, P, Freyer, C, McKenna, K, Regan, BM, Bellows, ST, Leu, C, Bennett, CA, Johns, EMC, Macdonald, A, Shilling, H, Burgess, R, Weckhuysen, D, Bahlo, M, O'Brien, TJ, Todaro, M, Stamberger, H, Andrade, DM, Sadoway, TR, Mo, K, Krestel, H, Gallati, S, Papacostas, SS, Kousiappa, I, Tanteles, GA, Štěrbová, K, Vlčková, M, Sedláčková, L, Laššuthová, P, Klein, KM, Rosenow, F, Reif, PS, Knake, S, Kunz, WS, Zsurka, G, Elger, CE, Bauer, J, Rademacher, M, Pendziwiat, M, Muhle, H, Rademacher, A, van Baalen, A, von Spiczak, S, Stephani, U, Afawi, Z, Korczyn, AD, Kanaan, M, Canavati, C, Kurlemann, G, Müller-Schlüter, K, Kluger, G, Häusler, M, Blatt, I, Lemke, JR, Krey, I, Weber, YG, Wolking, S, Becker, F, Hengsbach, C, Rau, S, Maisch, AF, Steinhoff, BJ, Schulze-Bonhage, A, Schubert-Bast, S, Schreiber, H and Borggräfe, I
(2019)
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals.
American Journal of Human Genetics, 105 (2).
pp. 267-282.
Collapse authors list.
Kosmicki, JA, Horowitz, JE, Banerjee, N, Lanche, R, Marcketta, A, Maxwell, E, Bai, X, Sun, D, Backman, JD, Sharma, D et al (show 70 more authors) , Kang, HM, O’Dushlaine, C, Yadav, A, Mansfield, AJ, Li, AH, Watanabe, K, Gurski, L, McCarthy, SE, Locke, AE, Khalid, S, O’Keeffe, S, Mbatchou, J, Chazara, O, Huang, Y, Kvikstad, E, O’Neill, A, Nioi, P, Parker, MM, Petrovski, S, Runz, H, Szustakowski, JD, Wang, Q, Wong, E, Cordova-Palomera, A, Smith, EN, Szalma, S, Zheng, X, Esmaeeli, S, Davis, JW, Lai, Y-P, Chen, X, Justice, AE ORCID: 0000-0002-8903-8712, Leader, JB, Mirshahi, T, Carey, DJ, Verma, A, Sirugo, G, Ritchie, MD, Rader, DJ, Povysil, G, Goldstein, DB, Kiryluk, K, Pairo-Castineira, E, Rawlik, K, Pasko, D, Walker, S, Meynert, A, Kousathanas, A, Moutsianas, L, Tenesa, A, Caulfield, M, Scott, R, Wilson, JF, Baillie, JK ORCID: 0000-0001-5258-793X, Butler-Laporte, G, Nakanishi, T, Lathrop, M, Richards, JB, Jones, M, Balasubramanian, S, Salerno, W ORCID: 0000-0003-2975-4108, Shuldiner, AR, Marchini, J, Overton, JD, Habegger, L, Cantor, MN, Reid, JG ORCID: 0000-0001-8645-4713, Baras, A, Abecasis, GR and Ferreira, MA
(2020)
A catalog of associations between rare coding variants and COVID-19 outcomes.
[Preprint]
This list was generated on Sun Jan 7 23:08:27 2024 GMT.