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Christopher A Cassa

Showing results (31-40 of 50) with videos related to

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Nature|July 1, 2015
Identification of cis-suppression of human disease mutations by comparative genomicsDaniel M Jordan, Stephan G Frangakis, Christelle Golzio, et al.
Nature|February 16, 2019
Author Correction: Predictable and precise template-free CRISPR editing of pathogenic variantsMax W Shen, Mandana Arbab, Jonathan Y Hsu, et al.
Nature|November 9, 2018
Predictable and precise template-free CRISPR editing of pathogenic variantsMax W Shen, Mandana Arbab, Jonathan Y Hsu, et al.
Nature Genetics|November 28, 2018
Reply to 'Selective effects of heterozygous protein-truncating variants'Christopher A Cassa, Donate Weghorn, Daniel J Balick, et al.
Nature Genetics|April 4, 2017
Estimating the selective effects of heterozygous protein-truncating variants from human exome dataChristopher A Cassa, Donate Weghorn, Daniel J Balick, et al.
Rheumatology (Oxford, England)|October 24, 2015
An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhoodChristopher A Cassa, Stacy E Smith, William Docken, et al.
Medrxiv : the Preprint Server for Health Sciences|September 21, 2023
Joint genotypic and phenotypic outcome modeling improves base editing variant effect quantificationJayoung Ryu, Sam Barkal, Tian Yu, et al.
Molecular Genetics & Genomic Medicine|October 6, 2015
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative diseaseSameer S Chopra, Ignaty Leshchiner, Hatice Duzkale, et al.
Biorxiv : the Preprint Server for Biology|December 31, 2025
LDLR variant classification through activity-normalized prime editing screeningPhillip J Zhou, Minja Velimirovic, Tian Yu, et al.
Nature Genetics|April 24, 2024
Joint genotypic and phenotypic outcome modeling improves base editing variant effect quantificationJayoung Ryu, Sam Barkal, Tian Yu, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Nature|July 1, 2015
Identification of cis-suppression of human disease mutations by comparative genomicsDaniel M Jordan, Stephan G Frangakis, Christelle Golzio, et al.
Nature|February 16, 2019
Author Correction: Predictable and precise template-free CRISPR editing of pathogenic variantsMax W Shen, Mandana Arbab, Jonathan Y Hsu, et al.
Nature|November 9, 2018
Predictable and precise template-free CRISPR editing of pathogenic variantsMax W Shen, Mandana Arbab, Jonathan Y Hsu, et al.
Nature Genetics|November 28, 2018
Reply to 'Selective effects of heterozygous protein-truncating variants'Christopher A Cassa, Donate Weghorn, Daniel J Balick, et al.
Nature Genetics|April 4, 2017
Estimating the selective effects of heterozygous protein-truncating variants from human exome dataChristopher A Cassa, Donate Weghorn, Daniel J Balick, et al.
Rheumatology (Oxford, England)|October 24, 2015
An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhoodChristopher A Cassa, Stacy E Smith, William Docken, et al.
Medrxiv : the Preprint Server for Health Sciences|September 21, 2023
Joint genotypic and phenotypic outcome modeling improves base editing variant effect quantificationJayoung Ryu, Sam Barkal, Tian Yu, et al.
Molecular Genetics & Genomic Medicine|October 6, 2015
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative diseaseSameer S Chopra, Ignaty Leshchiner, Hatice Duzkale, et al.
Biorxiv : the Preprint Server for Biology|December 31, 2025
LDLR variant classification through activity-normalized prime editing screeningPhillip J Zhou, Minja Velimirovic, Tian Yu, et al.
Nature Genetics|April 24, 2024
Joint genotypic and phenotypic outcome modeling improves base editing variant effect quantificationJayoung Ryu, Sam Barkal, Tian Yu, et al.
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