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Edwin C Oh

Showing results (51-60 of 57) with videos related to

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American Journal of Human Genetics|May 5, 2015
A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 PathologyEugenia Migliavacca, Christelle Golzio, Katrin Männik, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 18, 2013
Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease geneKoji M Nishiguchi, Richard G Tearle, Yangfan P Liu, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 13, 2026
Advancing biomarker development for chronic traumatic encephalopathy: Summary and recommendations from the 2025 Leon Thal SummitCharles Bernick, Brooke Conway Kleven, Michael L Alosco, et al.
The Science of the Total Environment|February 9, 2023
Identification and genome sequencing of an influenza H3N2 variant in wastewater from elementary schools during a surge of influenza A cases in Las Vegas, NevadaVan Vo, Anthony Harrington, Ching-Lan Chang, et al.
Nature|March 26, 2015
Loss of δ-catenin function in severe autismTychele N Turner, Kamal Sharma, Edwin C Oh, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 14, 2010
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC)Benjamin M Neale, Jesen Fagerness, Robyn Reynolds, et al.
Nature Neuroscience|September 27, 2016
Gene expression elucidates functional impact of polygenic risk for schizophreniaMenachem Fromer, Panos Roussos, Solveig K Sieberts, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
American Journal of Human Genetics|May 5, 2015
A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 PathologyEugenia Migliavacca, Christelle Golzio, Katrin Männik, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 18, 2013
Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease geneKoji M Nishiguchi, Richard G Tearle, Yangfan P Liu, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 13, 2026
Advancing biomarker development for chronic traumatic encephalopathy: Summary and recommendations from the 2025 Leon Thal SummitCharles Bernick, Brooke Conway Kleven, Michael L Alosco, et al.
The Science of the Total Environment|February 9, 2023
Identification and genome sequencing of an influenza H3N2 variant in wastewater from elementary schools during a surge of influenza A cases in Las Vegas, NevadaVan Vo, Anthony Harrington, Ching-Lan Chang, et al.
Nature|March 26, 2015
Loss of δ-catenin function in severe autismTychele N Turner, Kamal Sharma, Edwin C Oh, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 14, 2010
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC)Benjamin M Neale, Jesen Fagerness, Robyn Reynolds, et al.
Nature Neuroscience|September 27, 2016
Gene expression elucidates functional impact of polygenic risk for schizophreniaMenachem Fromer, Panos Roussos, Solveig K Sieberts, et al.
Pageof 6