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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Disease and ATP8B4[original query]
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. GWAS Catalog
Archives of neurology 2008 Jan 65 (1): 45-53.
Li Hao, Wetten Sally, Li Li, St Jean Pamela L, Upmanyu Ruchi, Surh Linda, Hosford David, Barnes Michael R, Briley James David, Borrie Michael, Coletta Natalie, Delisle Richard, Dhalla Daniella, Ehm Margaret G, Feldman Howard H, Fornazzari Luis, Gauthier Serge, Goodgame Neil, Guzman Danilo, Hammond Sandra, Hollingworth Paul, Hsiung Ging-Yuek, Johnson Joan, Kelly Devon D, Keren Ron, Kertesz Andrew, King Karen S, Lovestone Simon, Loy-English Inge, Matthews Paul M, Owen Michael J, Plumpton Mary, Pryse-Phillips William, Prinjha Rab K, Richardson Jill C, Saunders Ann, Slater Andrew J, St George-Hyslop Peter H, Stinnett Sandra W, Swartz Jina E, Taylor Rachel L, Wherrett John, Williams Julie, Yarnall David P, Gibson Rachel A, Irizarry Michael C, Middleton Lefkos T, Roses Allen
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease.
Nature genetics 2022 11 54 (12): 1786-1794.
Holstege Henne, Hulsman Marc, Charbonnier Camille, Grenier-Boley Benjamin, Quenez Olivier, Grozeva Detelina, van Rooij Jeroen G J, Sims Rebecca, Ahmad Shahzad, Amin Najaf, Norsworthy Penny J, Dols-Icardo Oriol, Hummerich Holger, Kawalia Amit, Amouyel Philippe, Beecham Gary W, Berr Claudine, Bis Joshua C, Boland Anne, Bossù Paola, Bouwman Femke, Bras Jose, Campion Dominique, Cochran J Nicholas, Daniele Antonio, Dartigues Jean-François, Debette Stéphanie, Deleuze Jean-François, Denning Nicola, DeStefano Anita L, Farrer Lindsay A, Fernández Maria Victoria, Fox Nick C, Galimberti Daniela, Genin Emmanuelle, Gille Johan J P, Le Guen Yann, Guerreiro Rita, Haines Jonathan L, Holmes Clive, Ikram M Arfan, Ikram M Kamran, Jansen Iris E, Kraaij Robert, Lathrop Marc, Lemstra Afina W, Lleó Alberto, Luckcuck Lauren, Mannens Marcel M A M, Marshall Rachel, Martin Eden R, Masullo Carlo, Mayeux Richard, Mecocci Patrizia, Meggy Alun, Mol Merel O, Morgan Kevin, Myers Richard M, Nacmias Benedetta, Naj Adam C, Napolioni Valerio, Pasquier Florence, Pastor Pau, Pericak-Vance Margaret A, Raybould Rachel, Redon Richard, Reinders Marcel J T, Richard Anne-Claire, Riedel-Heller Steffi G, Rivadeneira Fernando, Rousseau Stéphane, Ryan Natalie S, Saad Salha, Sanchez-Juan Pascual, Schellenberg Gerard D, Scheltens Philip, Schott Jonathan M, Seripa Davide, Seshadri Sudha, Sie Daoud, Sistermans Erik A, Sorbi Sandro, van Spaendonk Resie, Spalletta Gianfranco, Tesi Niccolo', Tijms Betty, Uitterlinden André G, van der Lee Sven J, Visser Pieter Jelle, Wagner Michael, Wallon David, Wang Li-San, Zarea Aline, Clarimon Jordi, van Swieten John C, Greicius Michael D, Yokoyama Jennifer S, Cruchaga Carlos, Hardy John, Ramirez Alfredo, Mead Simon, van der Flier Wiesje M, van Duijn Cornelia M, Williams Julie, Nicolas Gaël, Bellenguez Céline, Lambert Jean-Charl
Input of exome sequencing in early-onset cerebral amyloid angiopathy.
Alzheimer's & dementia (Amsterdam, Netherlands) 2024 11 16 (4): e70027.
Lou Grangeon, Camille Charbonnier, Stéphane Rousseau, Anne Claire Richard, Olivier Quenez, Aline Zarea, Anne Boland, Robert Olaso, Jean-François Deleuze, , Elisabeth Tournier-Lasserve, Gael Nicolas, David Wall
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