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Journal of Affective Disorders|November 21, 2012
Seasonality of mood and behavior in the Old Order AmishUttam K Raheja, Sarah H Stephens, Braxton D Mitchell, et al.
International Journal of Environmental Research and Public Health|October 19, 2019
<i>Toxoplasma gondii</i> Serointensity and Seropositivity: Heritability and Household-Related Associations in the Old Order AmishAllyson R Duffy, Jeffrey R O'Connell, Mary Pavlovich, et al.
The New England Journal of Medicine|May 23, 2014
Null mutation in hormone-sensitive lipase gene and risk of type 2 diabetesJessica S Albert, Laura M Yerges-Armstrong, Richard B Horenstein, et al.
Metabolism: Clinical and Experimental|August 11, 2015
Genome-wide association study of triglyceride response to a high-fat meal among participants of the NHLBI Genetics of Lipid Lowering Drugs and Diet Network (GOLDN)Mary K Wojczynski, Laurence D Parnell, Toni I Pollin, et al.
Diabetes Care|November 14, 2025
Novel Phenotypic Clusters of Youth-Onset Type 2 Diabetes Offer No Added Prognostic Value to Simple Clinical MeasuresRaymond J Kreienkamp, Kirk Smith, Thinley Yidzin Wangden, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2017
Developing a common framework for evaluating the implementation of genomic medicine interventions in clinical care: the IGNITE Network's Common Measures Working GroupLori A Orlando, Nina R Sperber, Corrine Voils, et al.
International Journal of Molecular Sciences|January 10, 2026
Functional Characterization of Glucokinase Variants to Aid Clinical Interpretation of Monogenic DiabetesVarsha Rajesh, Dora Evelyn Ibarra, Jing Yang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 29, 2020
Correction: Developing a common framework for evaluating the implementation of genomic medicine interventions in clinical care: the IGNITE Network's Common Measures Working GroupLori A Orlando, Nina R Sperber, Corrine Voils, et al.
Medrxiv : the Preprint Server for Health Sciences|October 9, 2023
Rare variant association analysis in 51,256 type 2 diabetes cases and 370,487 controls informs the spectrum of pathogenicity of monogenic diabetes genesPhilip Schroeder, Ravi Mandla, Alicia Huerta-Chagoya, et al.
European Journal of Neurology|December 22, 2021
Biallelic truncating variants in the muscular A-type lamin-interacting protein (MLIP) gene cause myopathy with hyperCKemiaLiat Salzer-Sheelo, Avi Fellner, Naama Orenstein, et al.
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