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D Webb

Showing results (801-810 of 812) with videos related to

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Brain Communications|October 3, 2025
Clinical and molecular characterization of SLC31A1-related developmental and epileptic encephalopathy: insights from 13 new casesNatalia Juliá-Palacios, Gerard Muñoz-Pujol, Reza Maroofian, et al.
Brain : a Journal of Neurology|August 8, 2020
Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorderPauline E Schneeberger, Fanny Kortüm, Georg Christoph Korenke, et al.
Social Science & Medicine (1982)|March 14, 2022
The path towards herd immunity: Predicting COVID-19 vaccination uptake through results from a stated choice study across six continentsStephane Hess, Emily Lancsar, Petr Mariel, et al.
Clinical and Translational Science|January 25, 2014
The CTSA Consortium's Catalog of Assets for Translational and Clinical Health Research (CATCHR)Jana Shirey-Rice, Brandy Mapes, Melissa Basford, et al.
Genetics in Medicine Open|July 15, 2025
Systematic phenotype and genotype characterization of Moebius syndromeBryn D Webb, Julie A Jurgens, Narisu Narisu, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Nature Genetics|June 29, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresisAlan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, et al.
Nature Aging|May 16, 2025
Large-scale network analysis of the cerebrospinal fluid proteome identifies molecular signatures of frontotemporal lobar degenerationRowan Saloner, Adam M Staffaroni, Eric B Dammer, et al.
Nature Aging|July 7, 2025
Author Correction: Large-scale network analysis of the cerebrospinal fluid proteome identifies molecular signatures of frontotemporal lobar degenerationRowan Saloner, Adam M Staffaroni, Eric B Dammer, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 28, 2026
AI-assisted teams outperform AI-led teams but not human-only teams in assessing research reproducibility in quantitative social scienceAbel Brodeur, David Valenta, Alexandru Marcoci, et al.
Pageof 82

Showing results (801-810 of 812) with videos related to

Sort By:
Pageof 82
Brain Communications|October 3, 2025
Clinical and molecular characterization of SLC31A1-related developmental and epileptic encephalopathy: insights from 13 new casesNatalia Juliá-Palacios, Gerard Muñoz-Pujol, Reza Maroofian, et al.
Brain : a Journal of Neurology|August 8, 2020
Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorderPauline E Schneeberger, Fanny Kortüm, Georg Christoph Korenke, et al.
Social Science & Medicine (1982)|March 14, 2022
The path towards herd immunity: Predicting COVID-19 vaccination uptake through results from a stated choice study across six continentsStephane Hess, Emily Lancsar, Petr Mariel, et al.
Clinical and Translational Science|January 25, 2014
The CTSA Consortium's Catalog of Assets for Translational and Clinical Health Research (CATCHR)Jana Shirey-Rice, Brandy Mapes, Melissa Basford, et al.
Genetics in Medicine Open|July 15, 2025
Systematic phenotype and genotype characterization of Moebius syndromeBryn D Webb, Julie A Jurgens, Narisu Narisu, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Nature Genetics|June 29, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresisAlan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, et al.
Nature Aging|May 16, 2025
Large-scale network analysis of the cerebrospinal fluid proteome identifies molecular signatures of frontotemporal lobar degenerationRowan Saloner, Adam M Staffaroni, Eric B Dammer, et al.
Nature Aging|July 7, 2025
Author Correction: Large-scale network analysis of the cerebrospinal fluid proteome identifies molecular signatures of frontotemporal lobar degenerationRowan Saloner, Adam M Staffaroni, Eric B Dammer, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 28, 2026
AI-assisted teams outperform AI-led teams but not human-only teams in assessing research reproducibility in quantitative social scienceAbel Brodeur, David Valenta, Alexandru Marcoci, et al.
Pageof 82