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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 - 6 (of 6 Records)

Query Trace: Disease and GBE1[original query]
Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients.
Human genetics 2003 Dec 114 (1): 87-98.
McCarthy Jeanette J, Meyer Joanne, Moliterno David J, Newby L Kristin, Rogers William J, Topol Eric J,
The adult polyglucosan body disease mutation GBE1 c.1076A>C occurs at high frequency in persons of Ashkenazi Jewish background.
Biochemical and biophysical research communications 2012 Sep 426 (2): 286-8.
Hussain Abrar, Armistead Joy, Gushulak Lara, Kruck Christa, Pind Steven, Triggs-Raine Barbara, Natowicz Marvin
Genome-environmental risk assessment of cocaine dependence.
Frontiers in genetics 2012 3 83.
Wei Changshuai, Anthony James C, Lu Qi
Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort.
Frontiers in molecular neuroscience 2016 9 92.
Krüger Stefanie, Battke Florian, Sprecher Andrea, Munz Marita, Synofzik Matthis, Schöls Ludger, Gasser Thomas, Grehl Torsten, Prudlo Johannes, Biskup Sask
Exome sequencing and analysis of 454,787 UK Biobank participants. GWAS Catalog
Nature 2021 10 599 (7886): 628-634.
Backman Joshua D, Li Alexander H, Marcketta Anthony, Sun Dylan, Mbatchou Joelle, Kessler Michael D, Benner Christian, Liu Daren, Locke Adam E, Balasubramanian Suganthi, Yadav Ashish, Banerjee Nilanjana, Gillies Christopher E, Damask Amy, Liu Simon, Bai Xiaodong, Hawes Alicia, Maxwell Evan, Gurski Lauren, Watanabe Kyoko, Kosmicki Jack A, Rajagopal Veera, Mighty Jason, , , Jones Marcus, Mitnaul Lyndon, Stahl Eli, Coppola Giovanni, Jorgenson Eric, Habegger Lukas, Salerno William J, Shuldiner Alan R, Lotta Luca A, Overton John D, Cantor Michael N, Reid Jeffrey G, Yancopoulos George, Kang Hyun M, Marchini Jonathan, Baras Aris, Abecasis Gonçalo R, Ferreira Manuel A
Whole-exome sequencing reveals a role of HTRA1 and EGFL8 in brain white matter hyperintensities. GWAS Catalog
Brain : a journal of neurology 2021 10 144 (9): 2670-2682.
Malik Rainer, Beaufort Nathalie, Frerich Simon, Gesierich Benno, Georgakis Marios K, Rannikmäe Kristiina, Ferguson Amy C, Haffner Christof, Traylor Matthew, Ehrmann Michael, Sudlow Cathie L M, Dichgans Mart
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