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Jonathan Klonowski

Showing results (1-10 of 5) with videos related to

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Bioinformatics (Oxford, England)|September 9, 2023
aenmd: annotating escape from nonsense-mediated decay for transcripts with protein-truncating variantsJonathan Klonowski, Qianqian Liang, Zeynep Coban-Akdemir, et al.
Biorxiv : the Preprint Server for Biology|March 30, 2023
aenmd: Annotating escape from nonsense-mediated decay for transcripts with protein-truncating variantsJonathan Klonowski, Qianqian Liang, Zeynep Coban-Akdemir, 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.
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.
HGG Advances|December 10, 2021
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart diseasePolakit Teekakirikul, Wenjuan Zhu, George C Gabriel, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Bioinformatics (Oxford, England)|September 9, 2023
aenmd: annotating escape from nonsense-mediated decay for transcripts with protein-truncating variantsJonathan Klonowski, Qianqian Liang, Zeynep Coban-Akdemir, et al.
Biorxiv : the Preprint Server for Biology|March 30, 2023
aenmd: Annotating escape from nonsense-mediated decay for transcripts with protein-truncating variantsJonathan Klonowski, Qianqian Liang, Zeynep Coban-Akdemir, 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.
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.
HGG Advances|December 10, 2021
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart diseasePolakit Teekakirikul, Wenjuan Zhu, George C Gabriel, et al.
Pageof 1