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John M Greally

Showing results (181-190 of 198) with videos related to

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Human Molecular Genetics|August 18, 2022
Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disordersStacey R McGee, Shivakumar Rajamanickam, Sandeep Adhikari, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patientsNoura S Abul-Husn, Priya N Marathe, Nicole R Kelly, et al.
Public Health Genomics|January 19, 2025
Investigating the Impact of Screen-Sharing Visual Aids during Genomic Results Disclosure via Telehealth in Diverse Families in the TeleKidSeq Pilot StudyJacqueline A Odgis, Nicole R Kelly, Monisha Sebastin, et al.
American Journal of Human Genetics|October 27, 2020
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research StudiesLaura M Amendola, Kathleen Muenzen, Leslie G Biesecker, et al.
Clinical Genetics|June 19, 2023
Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq programKatherine E Bonini, Amanda Thomas-Wilson, Priya N Marathe, et al.
HGG Advances|June 26, 2024
Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual populationPriya N Marathe, Sabrina A Suckiel, Katherine E Bonini, et al.
Cell|March 10, 2010
Distinct factors control histone variant H3.3 localization at specific genomic regionsAaron D Goldberg, Laura A Banaszynski, Kyung-Min Noh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 3, 2021
GUÍA: a digital platform to facilitate result disclosure in genetic counselingSabrina A Suckiel, Jaqueline A Odgis, Katie M Gallagher, et al.
Blood Cancer Discovery|December 27, 2023
Acute Lymphoblastic Leukemia with Myeloid Mutations Is a High-Risk Disease Associated with Clonal HematopoiesisCaner Saygin, Pu Zhang, Jacob Stauber, et al.
Cancer Research|July 8, 2017
Epigenetically Aberrant Stroma in MDS Propagates Disease via Wnt/β-Catenin ActivationTushar D Bhagat, Si Chen, Matthias Bartenstein, et al.
Pageof 20

Showing results (181-190 of 198) with videos related to

Sort By:
Pageof 20
Human Molecular Genetics|August 18, 2022
Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disordersStacey R McGee, Shivakumar Rajamanickam, Sandeep Adhikari, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patientsNoura S Abul-Husn, Priya N Marathe, Nicole R Kelly, et al.
Public Health Genomics|January 19, 2025
Investigating the Impact of Screen-Sharing Visual Aids during Genomic Results Disclosure via Telehealth in Diverse Families in the TeleKidSeq Pilot StudyJacqueline A Odgis, Nicole R Kelly, Monisha Sebastin, et al.
American Journal of Human Genetics|October 27, 2020
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research StudiesLaura M Amendola, Kathleen Muenzen, Leslie G Biesecker, et al.
Clinical Genetics|June 19, 2023
Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq programKatherine E Bonini, Amanda Thomas-Wilson, Priya N Marathe, et al.
HGG Advances|June 26, 2024
Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual populationPriya N Marathe, Sabrina A Suckiel, Katherine E Bonini, et al.
Cell|March 10, 2010
Distinct factors control histone variant H3.3 localization at specific genomic regionsAaron D Goldberg, Laura A Banaszynski, Kyung-Min Noh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 3, 2021
GUÍA: a digital platform to facilitate result disclosure in genetic counselingSabrina A Suckiel, Jaqueline A Odgis, Katie M Gallagher, et al.
Blood Cancer Discovery|December 27, 2023
Acute Lymphoblastic Leukemia with Myeloid Mutations Is a High-Risk Disease Associated with Clonal HematopoiesisCaner Saygin, Pu Zhang, Jacob Stauber, et al.
Cancer Research|July 8, 2017
Epigenetically Aberrant Stroma in MDS Propagates Disease via Wnt/β-Catenin ActivationTushar D Bhagat, Si Chen, Matthias Bartenstein, et al.
Pageof 20