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Medrxiv : the Preprint Server for Health Sciences|July 17, 2026
Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndromeAlex Lipov, Manon Baudic, Pierre Lindenbaum, et al.
Nature Genetics|September 10, 2013
Systematic identification of trans eQTLs as putative drivers of known disease associationsHarm-Jan Westra, Marjolein J Peters, Tõnu Esko, et al.
Ebiomedicine|November 17, 2018
Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adultsPriyanka Parmar, Estelle Lowry, Giovanni Cugliari, et al.
Nature Genetics|September 8, 2009
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosisMichael A van Es, Jan H Veldink, Christiaan G J Saris, et al.
Human Molecular Genetics|November 22, 2013
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosisIsabella Fogh, Antonia Ratti, Cinzia Gellera, et al.
Annals of Neurology|December 23, 2011
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosisMichael A van Es, Helenius J Schelhaas, Paul W J van Vught, et al.
Nature Communications|September 22, 2017
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosisBeben Benyamin, Ji He, Qiongyi Zhao, et al.
Nature Genetics|December 6, 2016
Disease variants alter transcription factor levels and methylation of their binding sitesMarc Jan Bonder, René Luijk, Daria V Zhernakova, et al.
Neurobiology of Aging|September 11, 2012
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1Kreshnik B Ahmeti, Senda Ajroud-Driss, Ammar Al-Chalabi, et al.
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