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Journal of Viral Hepatitis|March 27, 2007
The European Sero-Epidemiology Network 2: standardization of assay results for hepatitis B virusG Kafatos, C Anastassopoulou, A Nardone, et al.Nature Communications|September 28, 2016
Loss of RNA expression and allele-specific expression associated with congenital heart diseaseDavid M McKean, Jason Homsy, Hiroko Wakimoto, et al.Circulation. Genomic and Precision Medicine|February 7, 2022
Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or ObesitySarah U Morton, Alexandre C Pereira, Daniel Quiat, et al.Epidemiology and Infection|August 13, 2008
The European Sero-Epidemiology Network 2 (ESEN2): standardization of assay results for hepatitis A virus (HAV) to enable comparisons of seroprevalence data across 15 countriesC G Anastassopoulou, G Kafatos, A Nardone, et al.Nature Genetics|February 20, 2024
Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart diseaseFeng Xiao, Xiaoran Zhang, Sarah U Morton, et al.Biorxiv : the Preprint Server for Biology|February 6, 2026
Dysregulated TGFβ-ERK Signaling Drives Aberrant Extracellular Matrix Production in Noonan Syndrome-Associated Pulmonary Valve StenosisClifford Z Liu, Shrey Patel, Simone Sidoli, et al.Genetic Epidemiology|May 23, 2025
Genome-Wide Association Studies of Down Syndrome Associated Congenital Heart Defects Suggests a Genetically Heterogeneous Risk for CHD in DSElizabeth R Feldman, Yunqi Li, David J Cutler, et al.Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approachArchana Rai, Jonathan Klonowski, Bo Yuan, et al.Nature Communications|October 19, 2019
De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapesW Scott Watkins, E Javier Hernandez, Sergiusz Wesolowski, et al.American Journal of Human Genetics|June 21, 2025
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approachArchana Rai, Jonathan Klonowski, Bo Yuan, et al.Pageof 39