Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Disease and MIR2113[original query] |
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Genome-wide association study reveals two new risk loci for bipolar disorder.
Nature communications 2014 5 3339. Mühleisen Thomas W, Leber Markus, Schulze Thomas G, Strohmaier Jana, Degenhardt Franziska, Treutlein Jens, Mattheisen Manuel, Forstner Andreas J, Schumacher Johannes, Breuer René, Meier Sandra, Herms Stefan, Hoffmann Per, Lacour André, Witt Stephanie H, Reif Andreas, Müller-Myhsok Bertram, Lucae Susanne, Maier Wolfgang, Schwarz Markus, Vedder Helmut, Kammerer-Ciernioch Jutta, Pfennig Andrea, Bauer Michael, Hautzinger Martin, Moebus Susanne, Priebe Lutz, Czerski Piotr M, Hauser Joanna, Lissowska Jolanta, Szeszenia-Dabrowska Neonila, Brennan Paul, McKay James D, Wright Adam, Mitchell Philip B, Fullerton Janice M, Schofield Peter R, Montgomery Grant W, Medland Sarah E, Gordon Scott D, Martin Nicholas G, Krasnow Valery, Chuchalin Alexander, Babadjanova Gulja, Pantelejeva Galina, Abramova Lilia I, Tiganov Alexander S, Polonikov Alexey, Khusnutdinova Elza, Alda Martin, Grof Paul, Rouleau Guy A, Turecki Gustavo, Laprise Catherine, Rivas Fabio, Mayoral Fermin, Kogevinas Manolis, Grigoroiu-Serbanescu Maria, Propping Peter, Becker Tim, Rietschel Marcella, Nöthen Markus M, Cichon Sv |
| Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).
Molecular psychiatry 2015 Feb 20 (2): 183-92. Davies G, Armstrong N, Bis J C, Bressler J, Chouraki V, Giddaluru S, Hofer E, Ibrahim-Verbaas C A, Kirin M, Lahti J, van der Lee S J, Le Hellard S, Liu T, Marioni R E, Oldmeadow C, Postmus I, Smith A V, Smith J A, Thalamuthu A, Thomson R, Vitart V, Wang J, Yu L, Zgaga L, Zhao W, Boxall R, Harris S E, Hill W D, Liewald D C, Luciano M, Adams H, Ames D, Amin N, Amouyel P, Assareh A A, Au R, Becker J T, Beiser A, Berr C, Bertram L, Boerwinkle E, Buckley B M, Campbell H, Corley J, De Jager P L, Dufouil C, Eriksson J G, Espeseth T, Faul J D, Ford I, , Gottesman R F, Griswold M E, Gudnason V, Harris T B, Heiss G, Hofman A, Holliday E G, Huffman J, Kardia S L R, Kochan N, Knopman D S, Kwok J B, Lambert J-C, Lee T, Li G, Li S-C, Loitfelder M, Lopez O L, Lundervold A J, Lundqvist A, Mather K A, Mirza S S, Nyberg L, Oostra B A, Palotie A, Papenberg G, Pattie A, Petrovic K, Polasek O, Psaty B M, Redmond P, Reppermund S, Rotter J I, Schmidt H, Schuur M, Schofield P W, Scott R J, Steen V M, Stott D J, van Swieten J C, Taylor K D, Trollor J, Trompet S, Uitterlinden A G, Weinstein G, Widen E, Windham B G, Jukema J W, Wright A F, Wright M J, Yang Q, Amieva H, Attia J R, Bennett D A, Brodaty H, de Craen A J M, Hayward C, Ikram M A, Lindenberger U, Nilsson L-G, Porteous D J, Räikkönen K, Reinvang I, Rudan I, Sachdev P S, Schmidt R, Schofield P R, Srikanth V, Starr J M, Turner S T, Weir D R, Wilson J F, van Duijn C, Launer L, Fitzpatrick A L, Seshadri S, Mosley T H, Deary I |
| Genetic variants in MIR2113 and MIR129-LEP are associated with the susceptibility of COPD in the Chinese Han population. Pulmonary pharmacology & therapeutics 2020 Sep 101945. Jing Jing, Xu Dan, Li Zheng, Jiang Min, Wang Jing, Zhang Ji |
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