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Phoebe C R Parrish

Showing results (1-10 of 7) with videos related to

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Molecular Cell|February 19, 2021
CRISPR base editor screens identify variant function at scalePhoebe C R Parrish, Alice H Berger
Molecular Genetics & Genomic Medicine|July 16, 2018
Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behaviorNathan D Kopp, Phoebe C R Parrish, Michael Lugo, et al.
Arxiv|July 3, 2023
pgMAP: a pipeline to enable guide RNA read mapping from dual-targeting CRISPR screensPhoebe C R Parrish, Daniel J Groso, James D Thomas, et al.
Cell Reports|September 1, 2021
Discovery of synthetic lethal and tumor suppressor paralog pairs in the human genomePhoebe C R Parrish, James D Thomas, Austin M Gabel, et al.
Human Molecular Genetics|May 16, 2020
Whole exome sequencing in patients with Williams-Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis riskPhoebe C R Parrish, Delong Liu, Russell H Knutsen, et al.
American Journal of Medical Genetics. Part A|February 21, 2020
Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams-Beuren syndromeMichael Lugo, Zoë C Wong, Charles J Billington, et al.
Nature Communications|August 10, 2021
Integrative oncogene-dependency mapping identifies RIT1 vulnerabilities and synergies in lung cancerAthea Vichas, Amanda K Riley, Naomi T Nkinsi, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Molecular Cell|February 19, 2021
CRISPR base editor screens identify variant function at scalePhoebe C R Parrish, Alice H Berger
Molecular Genetics & Genomic Medicine|July 16, 2018
Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behaviorNathan D Kopp, Phoebe C R Parrish, Michael Lugo, et al.
Arxiv|July 3, 2023
pgMAP: a pipeline to enable guide RNA read mapping from dual-targeting CRISPR screensPhoebe C R Parrish, Daniel J Groso, James D Thomas, et al.
Cell Reports|September 1, 2021
Discovery of synthetic lethal and tumor suppressor paralog pairs in the human genomePhoebe C R Parrish, James D Thomas, Austin M Gabel, et al.
Human Molecular Genetics|May 16, 2020
Whole exome sequencing in patients with Williams-Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis riskPhoebe C R Parrish, Delong Liu, Russell H Knutsen, et al.
American Journal of Medical Genetics. Part A|February 21, 2020
Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams-Beuren syndromeMichael Lugo, Zoë C Wong, Charles J Billington, et al.
Nature Communications|August 10, 2021
Integrative oncogene-dependency mapping identifies RIT1 vulnerabilities and synergies in lung cancerAthea Vichas, Amanda K Riley, Naomi T Nkinsi, et al.
Pageof 1