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Circulation|April 3, 2020
Reduced Apolipoprotein M and Adverse Outcomes Across the Spectrum of Human Heart FailureJulio A Chirinos, Lei Zhao, Yi Jia, et al.Circulation. Genomic and Precision Medicine|September 1, 2020
Heterozygous ABCG5 Gene Deficiency and Risk of Coronary Artery DiseaseAkihiro Nomura, Connor A Emdin, Hong Hee Won, et al.American Journal of Epidemiology|July 16, 2009
Underlying genetic models of inheritance in established type 2 diabetes associationsGeorgia Salanti, Lorraine Southam, David Altshuler, et al.Medrxiv : the Preprint Server for Health Sciences|July 29, 2024
Multi-omics characterization of type 2 diabetes associated genetic variationRavi Mandla, Kim Lorenz, Xianyong Yin, et al.Diabetes Care|December 18, 2019
Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHCRajashree Mishra, Mikael Åkerlund, Diana L Cousminer, et al.Nature Genetics|April 9, 2008
Identification of ten loci associated with height highlights new biological pathways in human growthGuillaume Lettre, Anne U Jackson, Christian Gieger, et al.Cell Reports|October 19, 2022
SARS-CoV-2 infections elicit higher levels of original antigenic sin antibodies compared with SARS-CoV-2 mRNA vaccinationsElizabeth M Anderson, Shuk Hang Li, Moses Awofolaju, et al.American Journal of Human Genetics|June 18, 2019
Genetic and Epigenetic Fine Mapping of Complex Trait Associated Loci in the Human LiverMinal Çalışkan, Elisabetta Manduchi, H Shanker Rao, et al.Cell Stem Cell|February 2, 2021
Pathogenic LMNA variants disrupt cardiac lamina-chromatin interactions and de-repress alternative fate genesParisha P Shah, Wenjian Lv, Joshua H Rhoades, et al.Circulation. Cardiovascular Genetics|March 26, 2016
Treatment Gaps in Adults With Heterozygous Familial Hypercholesterolemia in the United States: Data From the CASCADE-FH RegistryEmil M deGoma, Zahid S Ahmad, Emily C O'Brien, et al.Pageof 89