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Diabetes Care|April 22, 2021
Genetic Risk Factors for CVD in Type 1 Diabetes: The DCCT/EDIC StudyIonut Bebu, Sareh Keshavarzi, Xiaoyu Gao, et al.Kidney Medicine|April 14, 2021
Type IV Collagen Variants in CKD: Performance of Computational Predictions for Identifying Pathogenic VariantsCole Shulman, Emerald Liang, Misato Kamura, et al.Rheumatology (Oxford, England)|June 26, 2019
Association of systemic lupus erythematosus (SLE) genetic susceptibility loci with lupus nephritis in childhood-onset and adult-onset SLEDeclan Webber, Jingjing Cao, Daniela Dominguez, et al.Proceedings of the National Academy of Sciences of the United States of America|May 11, 2016
Epigenomic profiling reveals an association between persistence of DNA methylation and metabolic memory in the DCCT/EDIC type 1 diabetes cohortZhuo Chen, Feng Miao, Andrew D Paterson, et al.Molecular Psychiatry|November 26, 2014
The phenotypic manifestations of rare genic CNVs in autism spectrum disorderA K Merikangas, R Segurado, E A Heron, et al.Journal of Neurology|July 26, 2002
A large Calabrian kindred segregating frontotemporal dementiaS A M Curcio, T Kawarai, A D Paterson, et al.Journal of the American Society of Nephrology : JASN|October 11, 2015
Refining Genotype-Phenotype Correlation in Autosomal Dominant Polycystic Kidney DiseaseYoung-Hwan Hwang, John Conklin, Winnie Chan, et al.Clinical Chemistry and Laboratory Medicine|March 16, 2013
An enzyme linked immunosorbent assay (ELISA) for the determination of the human haptoglobin phenotypeNina S Levy, Moshe Vardi, Shany Blum, et al.Diabetes Care|February 26, 2021
Risk Factors for Longitudinal Resting Heart Rate and Its Associations With Cardiovascular Outcomes in the DCCT/EDIC StudySareh Keshavarzi, Barbara H Braffett, Rodica Pop-Busui, et al.Journal of Neurodevelopmental Disorders|June 13, 2018
A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigreesMarc Woodbury-Smith, Andrew D Paterson, Irene O'Connor, et al.Pageof 44