Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: FRMD4A[original query] |
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Large-scale genome-wide association study of Asian population reveals genetic factors in FRMD4A and other loci influencing smoking initiation and nicotine dependence.
Human genetics 2012 Jun 131 (6): 1009-21. Yoon Dankyu, Kim Young-Jin, Cui Wen-Yan, Van der Vaart Andrew, Cho Yoon Shin, Lee Jong-Young, Ma Jennie Z, Payne Thomas J, Li Ming D, Park Taesu |
Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease.
Molecular psychiatry 2013 Apr 18 (4): 461-70. Lambert J-C, Grenier-Boley B, Harold D, Zelenika D, Chouraki V, Kamatani Y, Sleegers K, Ikram M A, Hiltunen M, Reitz C, Mateo I, Feulner T, Bullido M, Galimberti D, Concari L, Alvarez V, Sims R, Gerrish A, Chapman J, Deniz-Naranjo C, Solfrizzi V, Sorbi S, Arosio B, Spalletta G, Siciliano G, Epelbaum J, Hannequin D, Dartigues J-F, Tzourio C, Berr C, Schrijvers E M C, Rogers R, Tosto G, Pasquier F, Bettens K, Van Cauwenberghe C, Fratiglioni L, Graff C, Delepine M, Ferri R, Reynolds C A, Lannfelt L, Ingelsson M, Prince J A, Chillotti C, Pilotto A, Seripa D, Boland A, Mancuso M, Bossù P, Annoni G, Nacmias B, Bosco P, Panza F, Sanchez-Garcia F, Del Zompo M, Coto E, Owen M, O'Donovan M, Valdivieso F, Caffarra P, Caffara P, Scarpini E, Combarros O, Buée L, Campion D, Soininen H, Breteler M, Riemenschneider M, Van Broeckhoven C, Alpérovitch A, Lathrop M, Trégouët D-A, Williams J, Amouyel |
A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4A. European journal of human genetics : EJHG 2014 Nov . Fine Dina, Flusser Hagit, Markus Barak, Shorer Zamir, Gradstein Libe, Khateeb Shareef, Langer Yshia, Narkis Ginat, Birk Ruth, Galil Aharon, Shelef Ilan, Birk Ohad |
DNA methylation profiling in human lung tissue identifies genes associated with COPD. Epigenetics 2016 Aug 0. Morrow Jarrett D, Cho Michael H, Hersh Craig P, Pinto-Plata Victor, Celli Bartolome, Marchetti Nathaniel, Criner Gerard, Bueno Raphael, Washko George, Glass Kimberly, Choi Augustine M K, Quackenbush John, Silverman Edwin K, DeMeo Dawn |
Association of genetic risk factors with cognitive decline: the PATH through life project. Neurobiology of aging 2016 May 41 150-8. Andrews Shea J, Das Debjani, Cherbuin Nicolas, Anstey Kaarin J, Easteal Sim |
Alzheimer's Disease-Related Polymorphisms in Shunt-Responsive Idiopathic Normal Pressure Hydrocephalus. Journal of Alzheimer's disease : JAD 2017 60 (3): 1077-1085. Huovinen Joel, Helisalmi Seppo, Paananen Jussi, Laiterä Tiina, Kojoukhova Maria, Sutela Anna, Vanninen Ritva, Laitinen Marjo, Rauramaa Tuomas, Koivisto Anne M, Remes Anne M, Soininen Hilkka, Kurki Mitja, Haapasalo Annakaisa, Jääskeläinen Juha E, Hiltunen Mikko, Leinonen Vil |
Polymorphisms in the FRMD4A Gene Are Associated With Chronic Obstructive Pulmonary Disease Susceptibility in a Latin American Population. Archivos de bronconeumologia 2022 3 58 (5): 454-456. Díaz-Peña Roberto, Julià Raül F, Montes Juan F, Silva Rafael S, Olloquequi Jor |
[Translated article] Polymorphisms in the FRMD4A Gene Are Associated With Chronic Obstructive Pulmonary Disease Susceptibility in a Latin American Population. Archivos de bronconeumologia 2022 May 58 (5): T454-T456. Díaz-Peña Roberto, Julià Raül F, Montes Juan F, Silva Rafael S, Olloquequi Jor |
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- Page last updated:Apr 16, 2024
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