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Genetic inactivation of zinc transporter SLC39A5 improves liver function and hyperglycemia in obesogenic settings by Shek Man Chim, Kristen Howell, John Dronzek, Weizhen Wu, Cristopher Van Hout, Manuel AR Ferreira, Bin Ye, Alexander Li, Susannah Brydges, Vinayagam Arunachalam, Anthony Marcketta, Adam E Locke, Jonas Bovijn, Niek Verweij, Tanima De, Luca Lotta, Lyndon Mitnaul, Michelle LeBlanc, Regeneron Genetics Center, David J Carey, Olle Melander, Alan Shuldiner, Katia Karalis, Aris N Economides, Harikiran Nistala, DiscovEHR collaboration, Regeneron Genetics Center

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ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma by Kavita Praveen, Gaurang C. Patel, Lauren Gurski, Ariane H. Ayer, Trikaladarshi Persaud, Matthew D. Still, Lawrence Miloscio, Tavé Van Zyl, Silvio Alessandro Di Gioia, Ben Brumpton, Kristi Krebs, Bjørn Olav Åsvold, Esteban Chen, Venkata R. M. Chavali, Wen Fury, Harini V. Gudiseva, Sarah Hyde, Eric Jorgenson, Stephanie Lefebvre, Dadong Li, Alexander Li, James Mclninch, Brijeshkumar Patel, Jeremy S. Rabinowitz, Rebecca Salowe, Claudia Schurmann, Anne-Sofie Seidelin, Eli Stahl, Dylan Sun, Tanya M. Teslovich, Anne Tybjærg-Hansen, Cristen Willer, Scott Waldron, Sabrina Walley, Hua Yang, Sarthak Zaveri, Regeneron Genetics Center, GHS-RGC DiscovEHR Collaboration, Estonian Biobank Research Team, Ying Hu, Kristian Hveem, Olle Melander, Lili Milani, Stefan Stender, Joan M. O’Brien, Marcus B. Jones, Gonçalo R. Abecasis, Michael N. Cantor, Jonathan Weyne, Katia Karalis, Aris Economides, Giusy Della Gatta, Manuel A. Ferreira, George D. Yancopoulos, Aris Baras, Carmelo Romano, Giovanni Coppola

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Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes by Parsa Akbari, Olukayode A. Sosina, Jonas Bovijn, Karl Landheer, Jonas B. Nielsen, Minhee Kim, Senem Aykul, Tanima De, Mary E. Haas, George Hindy, Nan Lin, Ian R. Dinsmore, Jonathan Z. Luo, Stefanie Hectors, Benjamin Geraghty, Mary Germino, Lampros Panagis, Prodromos Parasoglou, Johnathon R. Walls, Gabor Halasz, Gurinder S. Atwal, Regeneron Genetics Center, DiscovEHR Collaboration, Marcus Jones, Michelle G. LeBlanc, Christopher D. Still, David J. Carey, Alice Giontella, Marju Orho-Melander, Jaime Berumen, Pablo Kuri-Morales, Jesus Alegre-Díaz, Jason M. Torres, Jonathan R. Emberson, Rory Collins, Daniel J. Rader, Brian Zambrowicz, Andrew J. Murphy, Suganthi Balasubramanian, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Michael Cantor, Goncalo R. Abecasis, Manuel A. R. Ferreira, Mark W. Sleeman, Viktoria Gusarova, Judith Altarejos, Charles Harris, Aris N. Economides, Vincent Idone, Katia Karalis, Giusy Della Gatta, Tooraj Mirshahi, George D. Yancopoulos, Olle Melander, Jonathan Marchini, Roberto Tapia-Conyer, Adam E. Locke, Aris Baras, Niek Verweij, Luca A. Lotta

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Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets by Wain, L, Shrine, N, Artigas, M, Erzurumluoglu, A, Noyvert, B, Bossini-Castillo, L, Obeidat, M, Henry, A, Portelli, M, Hall, R, Billington, C, Rimington, T, Fenech, A, John, C, Blake, T, Jackson, V, Allen, R, Prins, B, Understanding Society Scientific Group, Campbell, A, Porteous, D, Jarvelin, M, Wielscher, M, James, A, Hui, J, Wareham, N, Zhao, J, Wilson, J, Joshi, P, Stubbe, B, Rawal, R, Schulz, H, Imboden, M, Probst-Hensch, N, Karrasch, S, Gieger, C, Deary, I, Harris, S, Marten, J, Rudan, I, Enroth, S, Gyllensten, U, Kerr, S, Polasek, O, Kähönen, M, Surakka, I, Vitart, V, Hayward, C, Lehtimäki, T, Raitakari, O, Evans, D, Henderson, A, Pennell, C, Wang, C, Sly, P, Wan, E, Busch, R, Hobbs, B, Litonjua, A, Sparrow, D, Gulsvik, A, Bakke, P, Crapo, J, Beaty, T, Hansel, N, Mathias, R, Ruczinski, I, Barnes, K, Bossé, Y, Joubert, P, van den Berge, M, Brandsma, C, Paré, P, Sin, D, Nickle, D, Hao, K, Gottesman, O, Dewey, F, Bruse, S, Carey, D, Kirchner, H, Geisinger-Regeneron DiscovEHR Collaboration, Jonsson, S, Thorleifsson, G, Jonsdottir, I, Gislason, T, Stefansson, K, Schurmann, C, Nadkarni, G, Bottinger, E, Loos, R, Walters, R, Chen, Z, Millwood, I, Vaucher, J, Kurmi, O, Li, L, Hansell, A, Brightling, C, Zeggini, E, Cho, M, Silverman, E, Sayers, I, Trynka, G, Morris, A, Strachan, D, Hall, I, Tobin, M

Rare coding variants in CHRNB2 reduce the likelihood of smoking by Rajagopal, VM, Watanabe, K, Mbatchou, J, Emberson, J, Collins, R, Torres, J

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