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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 - 5 (of 5 Records)

Query Trace: Disease and CYFIP1[original query]
Confirmed rare copy number variants implicate novel genes in schizophrenia.
Biochemical Society transactions 2010 Apr 38 (2): 445-51.
Tam Gloria W C, van de Lagemaat Louie N, Redon Richard, Strathdee Karen E, Croning Mike D R, Malloy Mary P, Muir Walter J, Pickard Ben S, Deary Ian J, Blackwood Douglas H R, Carter Nigel P, Grant Seth G
Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics.
G3 (Bethesda, Md.) 2012 Jan 2 (1): 71-8.
Ghani Mahdi, Pinto Dalila, Lee Joseph H, Grinberg Yakov, Sato Christine, Moreno Danielle, Scherer Stephen W, Mayeux Richard, St George-Hyslop Peter, Rogaeva Ekateri
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
Circulation research 2014 Oct 115 (10): 884-96.
Glessner Joseph T, Bick Alexander G, Ito Kaoru, Homsy Jason G, Rodriguez-Murillo Laura, Fromer Menachem, Mazaika Erica, Vardarajan Badri, Italia Michael, Leipzig Jeremy, DePalma Steven R, Golhar Ryan, Sanders Stephan J, Yamrom Boris, Ronemus Michael, Iossifov Ivan, Willsey A Jeremy, State Matthew W, Kaltman Jonathan R, White Peter S, Shen Yufeng, Warburton Dorothy, Brueckner Martina, Seidman Christine, Goldmuntz Elizabeth, Gelb Bruce D, Lifton Richard, Seidman Jonathan, Hakonarson Hakon, Chung Wendy
A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus.
PloS one 2016 11 (6): e0158036.
Woo Young Jae, Wang Tao, Guadalupe Tulio, Nebel Rebecca A, Vino Arianna, Del Bene Victor A, Molholm Sophie, Ross Lars A, Zwiers Marcel P, Fisher Simon E, Foxe John J, Abrahams Brett
Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects.
Circulation. Genomic and precision medicine 2022 Oct 101161CIRCGEN121003510.
Saacks Nicole A, Eales James, Spracklen Timothy F, Aldersley Thomas, Human Paul, Verryn Mark, Lawrenson John, Cupido Blanche, Comitis George, De Decker Rik, Fourie Barend, Swanson Lenise, Joachim Alexia, Brooks Andre, Ramesar Raj, Shaboodien Gasnat, Keavney Bernard D, Zühlke Liesl
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