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Zachary Zappala

Showing results (1-10 of 17) with videos related to

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Human Heredity|January 12, 2017
Non-Coding Loss-of-Function Variation in Human GenomesZachary Zappala, Stephen B Montgomery
Nucleic Acids Research|November 30, 2007
GRSDB2 and GRS_UTRdb: databases of quadruplex forming G-rich sequences in pre-mRNAs and mRNAsOleg Kikin, Zachary Zappala, Lawrence D'Antonio, et al.
The New England Journal of Medicine|April 24, 2024
Specificity of CRISPR-Cas9 Editing in Exagamglogene AutotemcelAngela Yen, Zachary Zappala, Rebecca S Fine, et al.
The New England Journal of Medicine|October 8, 2025
Specificity of CRISPR-Cas9 Editing in Exagamglogene Autotemcel - UpdateAngela Yen, Tony Boitano, Zachary Zappala, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 4, 2013
PATH-SCAN: a reporting tool for identifying clinically actionable variantsRoxana Daneshjou, Zachary Zappala, Kim Kukurba, et al.
Human Mutation|March 3, 2017
Whole-transcriptome sequencing in blood provides a diagnosis of spinal muscular atrophy with progressive myoclonic epilepsyKristin D Kernohan, Laure Frésard, Zachary Zappala, et al.
Nature|October 13, 2017
The impact of rare variation on gene expression across tissuesXin Li, Yungil Kim, Emily K Tsang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
Long-read genome sequencing identifies causal structural variation in a Mendelian diseaseJason D Merker, Aaron M Wenger, Tam Sneddon, et al.
Genome Research|May 20, 2016
Impact of the X Chromosome and sex on regulatory variationKimberly R Kukurba, Princy Parsana, Brunilda Balliu, et al.
American Journal of Respiratory and Critical Care Medicine|July 11, 2022
Colocalization of Gene Expression and DNA Methylation with Genetic Risk Variants Supports Functional Roles of <i>MUC5B</i> and <i>DSP</i> in Idiopathic Pulmonary FibrosisRaphael Borie, Jonathan Cardwell, Iain R Konigsberg, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Human Heredity|January 12, 2017
Non-Coding Loss-of-Function Variation in Human GenomesZachary Zappala, Stephen B Montgomery
Nucleic Acids Research|November 30, 2007
GRSDB2 and GRS_UTRdb: databases of quadruplex forming G-rich sequences in pre-mRNAs and mRNAsOleg Kikin, Zachary Zappala, Lawrence D'Antonio, et al.
The New England Journal of Medicine|April 24, 2024
Specificity of CRISPR-Cas9 Editing in Exagamglogene AutotemcelAngela Yen, Zachary Zappala, Rebecca S Fine, et al.
The New England Journal of Medicine|October 8, 2025
Specificity of CRISPR-Cas9 Editing in Exagamglogene Autotemcel - UpdateAngela Yen, Tony Boitano, Zachary Zappala, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 4, 2013
PATH-SCAN: a reporting tool for identifying clinically actionable variantsRoxana Daneshjou, Zachary Zappala, Kim Kukurba, et al.
Human Mutation|March 3, 2017
Whole-transcriptome sequencing in blood provides a diagnosis of spinal muscular atrophy with progressive myoclonic epilepsyKristin D Kernohan, Laure Frésard, Zachary Zappala, et al.
Nature|October 13, 2017
The impact of rare variation on gene expression across tissuesXin Li, Yungil Kim, Emily K Tsang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
Long-read genome sequencing identifies causal structural variation in a Mendelian diseaseJason D Merker, Aaron M Wenger, Tam Sneddon, et al.
Genome Research|May 20, 2016
Impact of the X Chromosome and sex on regulatory variationKimberly R Kukurba, Princy Parsana, Brunilda Balliu, et al.
American Journal of Respiratory and Critical Care Medicine|July 11, 2022
Colocalization of Gene Expression and DNA Methylation with Genetic Risk Variants Supports Functional Roles of <i>MUC5B</i> and <i>DSP</i> in Idiopathic Pulmonary FibrosisRaphael Borie, Jonathan Cardwell, Iain R Konigsberg, et al.
Pageof 2