Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: GBE1[original query] |
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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 |
Identification of eight candidate target genes of the recurrent 3p12-p14 loss in cervical cancer by integrative genomic profiling. The Journal of pathology 2013 May 230 (1): 59-69. Lando Malin, Wilting Saskia M, Snipstad Kristin, Clancy Trevor, Bierkens Mariska, Aarnes Eva-Katrine, Holden Marit, Stokke Trond, Sundfør Kolbein, Holm Ruth, Kristensen Gunnar B, Steenbergen Renske D M, Lyng Hei |
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 |
Risk prediction of pulmonary tuberculosis using genetic and conventional risk factors in adult Korean population.
PloS one 2017 12 (3): e0174642. Hong Eun Pyo, Go Min Jin, Kim Hyung-Lae, Park Ji W |
Novel variants in Turkish patients with glycogen storage disease. Pediatrics international : official journal of the Japan Pediatric Society 2020 5 62 (10): 1145-1150. Çakar Nafiye Emel, Gezdirici Alper, Topuz Han?m ?eyma, Önal Has |
Polygenic Profile of Elite Strength Athletes. Journal of strength and conditioning research 2020 Dec . Moreland Ethan, Borisov Oleg V, Semenova Ekaterina A, Larin Andrey K, Andryushchenko Oleg N, Andryushchenko Liliya B, Generozov Edward V, Williams Alun G, Ahmetov Ildus |
Exome sequencing and analysis of 454,787 UK Biobank participants.
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 |
A family study implicates GBE1 in the etiology of autism spectrum disorder. Human mutation 2021 10 43 (1): 16-29. Fanjul-Fernández Miriam, Brown Natasha J, Hickey Peter, Diakumis Peter, Rafehi Haloom, Bozaoglu Kiymet, Green Cherie C, Rattray Audrey, Young Savannah, Alhuzaimi Dana, Mountford Hayley S, Gillies Greta, Lukic Vesna, Vick Tanya, Finlay Keri, Coe Bradley P, Eichler Evan E, Delatycki Martin B, Wilson Sarah J, Bahlo Melanie, Scheffer Ingrid E, Lockhart Paul |
Whole-exome sequencing reveals a role of HTRA1 and EGFL8 in brain white matter hyperintensities.
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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- Page last updated:Apr 16, 2024
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