Browsing by Author Cooper-Knock, Johnathan

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Issue DateTitleAuthor(s)
2021Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyRheenen, Wouter van; Spek, Rick A.A. van der; Bakker, Mark K.; Vugt, Joke J.F.A. van; Hop, Paul J.; Zwamborn, Ramona A. J.; Klein, Niek de; Westra, Harm-Jan; Bakker, Olivier B.; Deelen, Patrick; Shireby, Gemma; Hannon, Eilis; Moisse, Matthieu; Baird, Denis; Restuadi, Restuadi; Dolzhenko, Egor; Dekker, Annelot M.; Gawor, Klara; Westeneng, Henk-Jan; Tazelaar, Gijs H.P.; Eijk, Kristel R. van; Kooyman, Maarten; Byrne, Ross P.; Doherty, Mark; Heverin, Mark; Khleifat, Ahmad Al; Iacoangeli, Alfredo; Shatunov, Aleksey; Ticozzi, Nicola; Cooper-Knock, Johnathan; Smith, Bradley N.; Gromicho, Marta; Chandran, Siddharthan; Pal, Suvankar; Morrison, Karen E.; Shaw, Pamela J.; Hardy, John; Orrell, Richard W.; Sendtner, Michael; Meyer, Thomas; Başak, Nazli; Kooi, Anneke J. van der; Ratti, Antonia; Fogh, Isabella; Gellera, Cinzia; Lauria, Giuseppe; Corti, Stefania; Cereda, Cristina; Sproviero, Daisy; D’Alfonso, Sandra; Sorarù, Gianni; Siciliano, Gabriele; Filosto, Massimiliano; Padovani, Alessandro; Chiò, Adriano; Calvo, Andrea; Moglia, Cristina; Brunetti, Maura; Canosa, Antonio; Grassano, Maurizio; Beghi, Ettore; Pupillo, Elisabetta; Logroscino, Giancarlo; Nefussy, Beatrice; Osmanovic, Alma; Nordin, Angelica; Lerner, Yossef; Zabari, Michal; Gotkine, Marc; Baloh, Robert H.; Bell, Shaughn; Vourc’h, Patrick; Corcia, Philippe; Couratier, Philippe; Millecamps, Stéphanie; Meininger, Vincent; Salachas, François; Mora Pardina, Jesus S.; Assialioui, Abdelilah; Rojas-García, Ricardo; Dion, Patrick A.; Ross, Jay P.; Ludolph, Albert C.; Weishaupt, Jochen H.; Brenner, David; Freischmidt, Axel; Bensimon, Gilbert; Brice, Alexis; Durr, Alexandra; Payan, Christine A.M.; Saker-Delye, Safa; Wood, Nicholas W.; Topp, Simon; Rademakers, Rosa; Tittmann, Lukas; Lieb, Wolfgang; Franke, Andre; Ripke, Stephan; Braun, Alice; Kraft, Julia; Whiteman, David C.; Olsen, Catherine M.; Uitterlinden, Andre G.; Hofman, Albert; Rietschel, Marcella; Cichon, Sven; Nöthen, Markus M.; Amouyel, Philippe; Traynor, Bryan J.; Singleton, Andrew B.; Mitne Neto, Miguel; Cauchi, Ruben J.; Ophoff, Roel A.; Wiedau-Pazos, Martina; Lomen-Hoerth, Catherine; Deerlin, Vivianna M. van; Grosskreutz, Julian; Roediger, Annekathrin; Gaur, Nayana; Jörk, Alexander; Barthel, Tabea; Theele, Erik; Ilse, Benjamin; Stubendorff, Beatrice; Witte, Otto W.; Steinbach, Robert; Hübner, Christian A.; Graff, Caroline; Brylev, Lev; Fominykh, Vera; Demeshonok, Vera; Ataulina, Anastasia; Rogelj, Boris; Koritnik, Blaž; Zidar, Janez; Ravnik-Glavač, Metka; Glavač, Damjan; Stević, Zorica; Drory, Vivian; Povedano, Monica; Blair, Ian P.; Kiernan, Matthew C.; Benyamin, Beben; Henderson, Robert D.; Furlong, Sarah; Mathers, Susan; McCombe, Pamela A.; Needham, Merrilee; Ngo, Shyuan T.; Nicholson, Garth A.; Pamphlett, Roger; Rowe, Dominic B.; Steyn, Frederik J.; Williams, Kelly L.; Mather, Karen A.; Sachdev, Perminder S.; Henders, Anjali K.; Wallace, Leanne; Carvalho, Mamede de; Pinto, Susana; Petri, Susanne; Weber, Markus; Rouleau, Guy A.; Silani, Vincenzo; Curtis, Charles J.; Breen, Gerome; Glass, Jonathan D.; Brown Jr., Robert H.; Landers, John E.; Shaw, Christopher E.; Andersen, Peter M.; Groen, Ewout J.N.; Es, Michael A. van; Jeroen Pasterkamp, R.; Fan, Dongsheng; Garton, Fleur C.; McRae, Allan F.; Davey Smith, George; Gaunt, Tom R.; Eberle, Michael A.; Mill, Jonathan; McLaughlin, Russell L.; Hardiman, Orla; Kenna, Kevin P.; Wray, Naomi R.; Tsai, Ellen; Runz, Heiko; Franke, Lude; Al-Chalabi, Ammar; Damme, Philip Van; Berg, Leonard H. van den; Veldink, Jan H.; SLALOM Consortium; PARALS Consortium; SLAGEN Consortium; SLAP Consortium
2022Genome-wide identification of the genetic basis of amyotrophic lateral sclerosisZhang, Sai; Cooper-Knock, Johnathan; Weimer, Annika K.; Shi, Minyi; Moll, Tobias; Marshall, Jack N.G.; Harvey, Calum; Ghahremani Nezhad, Helia; Franklin, John; Santos Souza, Cleide dos; Ning, Ke; Wang, Cheng; Li, Jingjing; Dilliott, Allison A.; Farhan, Sali; Elhaik, Eran; Pasniceanu, Iris; Livesey, Matthew R.; Eitan, Chen; Hornstein, Eran; Kenna, Kevin P.; Veldink, Jan H.; Ferraiuolo, Laura; Shaw, Pamela J.; Snyder, Michael P.; Cauchi, Ruben J.; Project MinE ALS Sequencing Consortium
2020Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk geneCooper-Knock, Johnathan; Zhang, Sai; Kenna, Kevin P.; Moll, Tobias; Franklin, John P.; Allen, Samantha; Ghahremani Nezhad, Helia; Iacoangeli, Alfredo; Yacovzada, Nancy Y.; Eitan, Chen; Hornstein, Eran; Elhaik, Eran; Celadova, Petra; Bose, Daniel; Farhan, Sali; Fishilevich, Simon; Lancet, Doron; Morrison, Karen E.; Shaw, Christopher E.; Al-Chalabi, Ammar; Veldink, Jan H.; Kirby, Janine; Snyder, Michael P.; Shaw, Pamela J.; Cauchi, Ruben J.; Project MinE ALS Sequencing Consortium
2021Value of systematic genetic screening of patients with amyotrophic lateral sclerosisShepheard, Stephanie R.; Parker, Matthew D.; Cooper-Knock, Johnathan; Verber, Nick S.; Tuddenham, Lee; Heath, Paul; Beauchamp, Nick; Place, Elsie; Sollars, Elizabeth S.A.; Turner, Martin R.; Malaspina, Andrea; Fratta, Pietro; Hewamadduma, Channa; Jenkins, Thomas M.; McDermott, Christopher J.; Wang, Dennis; Kirby, Janine; Cauchi, Ruben J.; Project MINE Consortium