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BMC Medical Genetics|October 4, 2006
Generation Scotland: the Scottish Family Health Study; a new resource for researching genes and heritabilityBlair H Smith, Harry Campbell, Douglas Blackwood, et al.
Nature Genetics|July 3, 2007
Common variants in WFS1 confer risk of type 2 diabetesManjinder S Sandhu, Michael N Weedon, Katherine A Fawcett, et al.
Wellcome Open Research|February 16, 2019
DOLORisk: study protocol for a multi-centre observational study to understand the risk factors and determinants of neuropathic painMathilde M V Pascal, Andreas C Themistocleous, Ralf Baron, et al.
Medrxiv : the Preprint Server for Health Sciences|December 18, 2025
Sex-Specific Genetic Architecture and Comorbidities of Alcohol Use BehaviorsLaura Vilar-Ribó, Mariela V Jennings, Aisha Sallah, et al.
Clinical Pharmacology and Therapeutics|June 5, 2020
Exome Sequencing Reveals Common and Rare Variants in F5 Associated With ACE Inhibitor and Angiotensin Receptor Blocker-Induced AngioedemaCyrielle Maroteau, Moneeza Kalhan Siddiqui, Abirami Veluchamy, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
The dynamic impact of location and resection on the glioma CSF proteomeCecile Riviere-Cazaux, Christopher J Graser, Arthur E Warrington, et al.
The Journal of Allergy and Clinical Immunology|March 8, 2011
Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergySara J Brown, Yuka Asai, Heather J Cordell, et al.
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