Human Genome Epidemiology Literature Finder
Rare Diseases
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Records 1 - 5 (of 5 Records) |
| Query Trace: Creutzfeldt-jakob Disease[original query] |
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Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
The Lancet. Neurology 2009 Jan 8 (1): 57-66. Mead Simon, Poulter Mark, Uphill James, Beck John, Whitfield Jerome, Webb Thomas E F, Campbell Tracy, Adamson Gary, Deriziotis Pelagia, Tabrizi Sarah J, Hummerich Holger, Verzilli Claudio, Alpers Michael P, Whittaker John C, Collinge Jo |
| Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.
Neurobiology of aging 2012 Jul 33 (7): 1487.e21-8. Sanchez-Juan Pascual, Bishop Matthew T, Aulchenko Yurii S, Brandel Jean-Philippe, Rivadeneira Fernando, Struchalin Maksim, Lambert Jean-Charles, Amouyel Philippe, Combarros Onofre, Sainz Jesus, Carracedo Angel, Uitterlinden Andre G, Hofman Albert, Zerr Inga, Kretzschmar Hans A, Laplanche Jean-Louis, Knight Richard S G, Will Robert G, van Duijn Cornelia |
| Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Human molecular genetics 2012 Apr 21 (8): 1897-906. Mead Simon, Uphill James, Beck John, Poulter Mark, Campbell Tracy, Lowe Jessica, Adamson Gary, Hummerich Holger, Klopp Norman, Rückert Ina-Maria, Wichmann H-Erich, Azazi Dhoyazan, Plagnol Vincent, Pako Wandagi H, Whitfield Jerome, Alpers Michael P, Whittaker John, Balding David J, Zerr Inga, Kretzschmar Hans, Collinge Jo |
| A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk.
PloS one 2014 10 (4): e0123654. Sanchez-Juan Pascual, Bishop Matthew T, Kovacs Gabor G, Calero Miguel, Aulchenko Yurii S, Ladogana Anna, Boyd Alison, Lewis Victoria, Ponto Claudia, Calero Olga, Poleggi Anna, Carracedo Ángel, van der Lee Sven J, Ströbel Thomas, Rivadeneira Fernando, Hofman Albert, Haïk Stéphane, Combarros Onofre, Berciano José, Uitterlinden Andre G, Collins Steven J, Budka Herbert, Brandel Jean-Philippe, Laplanche Jean Louis, Pocchiari Maurizio, Zerr Inga, Knight Richard S G, Will Robert G, van Duijn Cornelia |
| Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study.
The Lancet. Neurology 2020 10 19 (10): 840-848. Jones Emma, Hummerich Holger, Viré Emmanuelle, Uphill James, Dimitriadis Athanasios, Speedy Helen, Campbell Tracy, Norsworthy Penny, Quinn Liam, Whitfield Jerome, Linehan Jacqueline, Jaunmuktane Zane, Brandner Sebastian, Jat Parmjit, Nihat Akin, How Mok Tze, Ahmed Parvin, Collins Steven, Stehmann Christiane, Sarros Shannon, Kovacs Gabor G, Geschwind Michael D, Golubjatnikov Aili, Frontzek Karl, Budka Herbert, Aguzzi Adriano, Karamuji?-?omi? Hata, van der Lee Sven J, Ibrahim-Verbaas Carla A, van Duijn Cornelia M, Sikorska Beata, Golanska Ewa, Liberski Pawel P, Calero Miguel, Calero Olga, Sanchez-Juan Pascual, Salas Antonio, Martinón-Torres Federico, Bouaziz-Amar Elodie, Haïk Stéphane, Laplanche Jean-Louis, Brandel Jean-Phillipe, Amouyel Phillipe, Lambert Jean-Charles, Parchi Piero, Bartoletti-Stella Anna, Capellari Sabina, Poleggi Anna, Ladogana Anna, Pocchiari Maurizio, Aneli Serena, Matullo Giuseppe, Knight Richard, Zafar Saima, Zerr Inga, Booth Stephanie, Coulthart Michael B, Jansen Gerard H, Glisic Katie, Blevins Janis, Gambetti Pierluigi, Safar Jiri, Appleby Brian, Collinge John, Mead Sim |
- Page last reviewed:Feb 1, 2024
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