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Jonah Einson

Showing results (1-10 of 9) with videos related to

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Plos One|March 13, 2024
The impact of genetically controlled splicing on exon inclusion and protein structureJonah Einson, Mariia Minaeva, Faiza Rafi, et al.
Biorxiv : the Preprint Server for Biology|June 25, 2024
Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation DatabaseSanna Gudmundsson, Moriel Singer-Berk, Sarah L Stenton, et al.
Nature Communications|November 1, 2025
Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation DatabaseSanna Gudmundsson, Moriel Singer-Berk, Sarah L Stenton, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 10, 2021
Prediagnostic White Blood Cell DNA Methylation and Risk of Breast Cancer in the Prostate Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO) CohortSusan R Sturgeon, David A Sela, Eva P Browne, et al.
Science (New York, N.Y.)|October 12, 2019
Genetic regulatory variation in populations informs transcriptome analysis in rare diseasePejman Mohammadi, Stephane E Castel, Beryl B Cummings, et al.
Cell Reports|April 20, 2022
Oncogenic Vav1-Myo1f induces therapeutically targetable macrophage-rich tumor microenvironment in peripheral T cell lymphomaJose R Cortes, Ioan Filip, Robert Albero, et al.
Genetics|June 22, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Science (New York, N.Y.)|September 11, 2020
Transcriptomic signatures across human tissues identify functional rare genetic variationNicole M Ferraro, Benjamin J Strober, Jonah Einson, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Plos One|March 13, 2024
The impact of genetically controlled splicing on exon inclusion and protein structureJonah Einson, Mariia Minaeva, Faiza Rafi, et al.
Biorxiv : the Preprint Server for Biology|June 25, 2024
Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation DatabaseSanna Gudmundsson, Moriel Singer-Berk, Sarah L Stenton, et al.
Nature Communications|November 1, 2025
Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation DatabaseSanna Gudmundsson, Moriel Singer-Berk, Sarah L Stenton, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 10, 2021
Prediagnostic White Blood Cell DNA Methylation and Risk of Breast Cancer in the Prostate Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO) CohortSusan R Sturgeon, David A Sela, Eva P Browne, et al.
Science (New York, N.Y.)|October 12, 2019
Genetic regulatory variation in populations informs transcriptome analysis in rare diseasePejman Mohammadi, Stephane E Castel, Beryl B Cummings, et al.
Cell Reports|April 20, 2022
Oncogenic Vav1-Myo1f induces therapeutically targetable macrophage-rich tumor microenvironment in peripheral T cell lymphomaJose R Cortes, Ioan Filip, Robert Albero, et al.
Genetics|June 22, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Science (New York, N.Y.)|September 11, 2020
Transcriptomic signatures across human tissues identify functional rare genetic variationNicole M Ferraro, Benjamin J Strober, Jonah Einson, et al.
Pageof 1