Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: MAP1A[original query] |
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Association analysis of ATF4 and ATF5, genes for interacting-proteins of DISC1, in bipolar disorder. Neuroscience letters 2007 May 417 (3): 316-21. Kakiuchi Chihiro, Ishiwata Mizuho, Nanko Shinichiro, Kunugi Hiroshi, Minabe Yoshio, Nakamura Kazuhiko, Mori Norio, Fujii Kumiko, Yamada Kazuo, Yoshikawa Takeo, Kato Tadafu |
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals. American journal of human genetics 2016 Jun . Eicher John D, Chami Nathalie, Kacprowski Tim, Nomura Akihiro, Chen Ming-Huei, Yanek Lisa R, Tajuddin Salman M, Schick Ursula M, Slater Andrew J, Pankratz Nathan, Polfus Linda, Schurmann Claudia, Giri Ayush, Brody Jennifer A, Lange Leslie A, Manichaikul Ani, Hill W David, Pazoki Raha, Elliot Paul, Evangelou Evangelos, Tzoulaki Ioanna, Gao He, Vergnaud Anne-Claire, Mathias Rasika A, Becker Diane M, Becker Lewis C, Burt Amber, Crosslin David R, Lyytikäinen Leo-Pekka, Nikus Kjell, Hernesniemi Jussi, Kähönen Mika, Raitoharju Emma, Mononen Nina, Raitakari Olli T, Lehtimäki Terho, Cushman Mary, Zakai Neil A, Nickerson Deborah A, Raffield Laura M, Quarells Rakale, Willer Cristen J, Peloso Gina M, Abecasis Goncalo R, Liu Dajiang J, , Deloukas Panos, Samani Nilesh J, Schunkert Heribert, Erdmann Jeanette, , , Fornage Myriam, Richard Melissa, Tardif Jean-Claude, Rioux John D, Dube Marie-Pierre, de Denus Simon, Lu Yingchang, Bottinger Erwin P, Loos Ruth J F, Smith Albert Vernon, Harris Tamara B, Launer Lenore J, Gudnason Vilmundur, Velez Edwards Digna R, Torstenson Eric S, Liu Yongmei, Tracy Russell P, Rotter Jerome I, Rich Stephen S, Highland Heather M, Boerwinkle Eric, Li Jin, Lange Ethan, Wilson James G, Mihailov Evelin, Mägi Reedik, Hirschhorn Joel, Metspalu Andres, Esko Tõnu, Vacchi-Suzzi Caterina, Nalls Mike A, Zonderman Alan B, Evans Michele K, Engström Gunnar, Orho-Melander Marju, Melander Olle, O'Donoghue Michelle L, Waterworth Dawn M, Wallentin Lars, White Harvey D, Floyd James S, Bartz Traci M, Rice Kenneth M, Psaty Bruce M, Starr J M, Liewald David C M, Hayward Caroline, Deary Ian J, Greinacher Andreas, Völker Uwe, Thiele Thomas, Völzke Henry, van Rooij Frank J A, Uitterlinden André G, Franco Oscar H, Dehghan Abbas, Edwards Todd L, Ganesh Santhi K, Kathiresan Sekar, Faraday Nauder, Auer Paul L, Reiner Alex P, Lettre Guillaume, Johnson Andrew |
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits. American journal of human genetics 2016 Jun . Chami Nathalie, Chen Ming-Huei, Slater Andrew J, Eicher John D, Evangelou Evangelos, Tajuddin Salman M, Love-Gregory Latisha, Kacprowski Tim, Schick Ursula M, Nomura Akihiro, Giri Ayush, Lessard Samuel, Brody Jennifer A, Schurmann Claudia, Pankratz Nathan, Yanek Lisa R, Manichaikul Ani, Pazoki Raha, Mihailov Evelin, Hill W David, Raffield Laura M, Burt Amber, Bartz Traci M, Becker Diane M, Becker Lewis C, Boerwinkle Eric, Bork-Jensen Jette, Bottinger Erwin P, O'Donoghue Michelle L, Crosslin David R, de Denus Simon, Dubé Marie-Pierre, Elliott Paul, Engström Gunnar, Evans Michele K, Floyd James S, Fornage Myriam, Gao He, Greinacher Andreas, Gudnason Vilmundur, Hansen Torben, Harris Tamara B, Hayward Caroline, Hernesniemi Jussi, Highland Heather M, Hirschhorn Joel N, Hofman Albert, Irvin Marguerite R, Kähönen Mika, Lange Ethan, Launer Lenore J, Lehtimäki Terho, Li Jin, Liewald David C M, Linneberg Allan, Liu Yongmei, Lu Yingchang, Lyytikäinen Leo-Pekka, Mägi Reedik, Mathias Rasika A, Melander Olle, Metspalu Andres, Mononen Nina, Nalls Mike A, Nickerson Deborah A, Nikus Kjell, O'Donnell Chris J, Orho-Melander Marju, Pedersen Oluf, Petersmann Astrid, Polfus Linda, Psaty Bruce M, Raitakari Olli T, Raitoharju Emma, Richard Melissa, Rice Kenneth M, Rivadeneira Fernando, Rotter Jerome I, Schmidt Frank, Smith Albert Vernon, Starr John M, Taylor Kent D, Teumer Alexander, Thuesen Betina H, Torstenson Eric S, Tracy Russell P, Tzoulaki Ioanna, Zakai Neil A, Vacchi-Suzzi Caterina, van Duijn Cornelia M, van Rooij Frank J A, Cushman Mary, Deary Ian J, Velez Edwards Digna R, Vergnaud Anne-Claire, Wallentin Lars, Waterworth Dawn M, White Harvey D, Wilson James G, Zonderman Alan B, Kathiresan Sekar, Grarup Niels, Esko Tõnu, Loos Ruth J F, Lange Leslie A, Faraday Nauder, Abumrad Nada A, Edwards Todd L, Ganesh Santhi K, Auer Paul L, Johnson Andrew D, Reiner Alexander P, Lettre Guillau |
Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness. Molecular neuropsychiatry 2015 Oct 1 (3): 175-190. Johnstone Mandy, Maclean Alan, Heyrman Lien, Lenaerts An-Sofie, Nordin Annelie, Nilsson Lars-Göran, De Rijk Peter, Goossens Dirk, Adolfsson Rolf, St Clair David M, Hall Jeremy, Lawrie Stephen M, McIntosh Andrew M, Del-Favero Jurgen, Blackwood Douglas H R, Pickard Benjamin |
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants. Nature neuroscience 2019 11 22 (12): 1961-1965. Satterstrom F Kyle, Walters Raymond K, Singh Tarjinder, Wigdor Emilie M, Lescai Francesco, Demontis Ditte, Kosmicki Jack A, Grove Jakob, Stevens Christine, Bybjerg-Grauholm Jonas, Bækvad-Hansen Marie, Palmer Duncan S, Maller Julian B, , Nordentoft Merete, Mors Ole, Robinson Elise B, Hougaard David M, Werge Thomas M, Bo Mortensen Preben, Neale Benjamin M, Børglum Anders D, Daly Mark |
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