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Andrew C Edmondson

Showing results (11-20 of 73) with videos related to

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Biostatistics (Oxford, England)|September 22, 2011
A Gaussian copula approach for the analysis of secondary phenotypes in case-control genetic association studiesJing He, Hongzhe Li, Andrew C Edmondson, et al.
Molecular Genetics and Metabolism|July 30, 2025
Incidence and prevalence of phosphomannomutase 2-congenital disorder of glycosylation: Past, present, and futureAndrew C Edmondson, Tomáš Honzík, Christina Lam, et al.
Molecular Genetics and Metabolism|October 15, 2025
Corrigendum to "Incidence and prevalence of phosphomannomutase 2-congenital disorder of glycosylation: Past, present, and future [Molecular Genetics and Metabolism 146 (2025) 109188]"Andrew C Edmondson, Tomas Honzik, Christina Lam, et al.
BMC Medical Genomics|October 22, 2025
Expanding the phenotype of CARS1 variants to include congenital hyperinsulinismVictoria R Sanders, Andrew C Edmondson, Albert C Yan, et al.
American Journal of Medical Genetics. Part A|August 30, 2016
Kabuki syndrome as a cause of non-immune fetal hydrops/ascitesAshleigh Long, Elena S Sinkovskaya, Andrew C Edmondson, et al.
American Journal of Medical Genetics. Part A|March 17, 2023
Long-term outcomes in ALG13-Congenital Disorder of GlycosylationRameen Shah, Christin Johnsen, Beth A Pletcher, et al.
European Journal of Human Genetics : EJHG|October 7, 2010
Gene-based interaction analysis by incorporating external linkage disequilibrium informationJing He, Kai Wang, Andrew C Edmondson, et al.
American Journal of Medical Genetics. Part A|June 6, 2022
A rare cause of infantile achalasia: GMPPA-congenital disorder of glycosylation with two novel compound heterozygous variantsIrina Geiculescu, Jason Dranove, Graham Cosper, et al.
Molecular Genetics and Metabolism|August 19, 2023
Combined PMM2-CDG and hereditary fructose intolerance in a patient with mild clinical presentationXinying Hong, Andrew C Edmondson, Alanna Strong, et al.
Molecular Genetics and Metabolism|July 5, 2024
Coagulation abnormalities and vascular complications are common in PGM1-CDGSilvia Radenkovic, Sofie Bleukx, Nicole Engelhardt, et al.
Pageof 8

Showing results (11-20 of 73) with videos related to

Sort By:
Pageof 8
Biostatistics (Oxford, England)|September 22, 2011
A Gaussian copula approach for the analysis of secondary phenotypes in case-control genetic association studiesJing He, Hongzhe Li, Andrew C Edmondson, et al.
Molecular Genetics and Metabolism|July 30, 2025
Incidence and prevalence of phosphomannomutase 2-congenital disorder of glycosylation: Past, present, and futureAndrew C Edmondson, Tomáš Honzík, Christina Lam, et al.
Molecular Genetics and Metabolism|October 15, 2025
Corrigendum to "Incidence and prevalence of phosphomannomutase 2-congenital disorder of glycosylation: Past, present, and future [Molecular Genetics and Metabolism 146 (2025) 109188]"Andrew C Edmondson, Tomas Honzik, Christina Lam, et al.
BMC Medical Genomics|October 22, 2025
Expanding the phenotype of CARS1 variants to include congenital hyperinsulinismVictoria R Sanders, Andrew C Edmondson, Albert C Yan, et al.
American Journal of Medical Genetics. Part A|August 30, 2016
Kabuki syndrome as a cause of non-immune fetal hydrops/ascitesAshleigh Long, Elena S Sinkovskaya, Andrew C Edmondson, et al.
American Journal of Medical Genetics. Part A|March 17, 2023
Long-term outcomes in ALG13-Congenital Disorder of GlycosylationRameen Shah, Christin Johnsen, Beth A Pletcher, et al.
European Journal of Human Genetics : EJHG|October 7, 2010
Gene-based interaction analysis by incorporating external linkage disequilibrium informationJing He, Kai Wang, Andrew C Edmondson, et al.
American Journal of Medical Genetics. Part A|June 6, 2022
A rare cause of infantile achalasia: GMPPA-congenital disorder of glycosylation with two novel compound heterozygous variantsIrina Geiculescu, Jason Dranove, Graham Cosper, et al.
Molecular Genetics and Metabolism|August 19, 2023
Combined PMM2-CDG and hereditary fructose intolerance in a patient with mild clinical presentationXinying Hong, Andrew C Edmondson, Alanna Strong, et al.
Molecular Genetics and Metabolism|July 5, 2024
Coagulation abnormalities and vascular complications are common in PGM1-CDGSilvia Radenkovic, Sofie Bleukx, Nicole Engelhardt, et al.
Pageof 8