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Showing results (211-220 of 234) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse familiesSabrina A Suckiel, Nicole R Kelly, Jacqueline A Odgis, et al.
American Journal of Human Genetics|November 25, 2023
The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse familiesSabrina A Suckiel, Nicole R Kelly, Jacqueline A Odgis, et al.
JCI Insight|July 27, 2018
The RUNX1/IL-34/CSF-1R axis is an autocrinally regulated modulator of resistance to BRAF-V600E inhibition in melanomaOrsi Giricz, Yongkai Mo, Kimberly B Dahlman, et al.
Genome Medicine|July 19, 2022
Recommendations for clinical interpretation of variants found in non-coding regions of the genomeJamie M Ellingford, Joo Wook Ahn, Richard D Bagnall, et al.
Plos Genetics|May 31, 2014
Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorderEsther R Berko, Masako Suzuki, Faygel Beren, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 9, 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.
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.
Pageof 24

Showing results (211-220 of 234) with videos related to

Sort By:
Pageof 24
Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse familiesSabrina A Suckiel, Nicole R Kelly, Jacqueline A Odgis, et al.
American Journal of Human Genetics|November 25, 2023
The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse familiesSabrina A Suckiel, Nicole R Kelly, Jacqueline A Odgis, et al.
JCI Insight|July 27, 2018
The RUNX1/IL-34/CSF-1R axis is an autocrinally regulated modulator of resistance to BRAF-V600E inhibition in melanomaOrsi Giricz, Yongkai Mo, Kimberly B Dahlman, et al.
Genome Medicine|July 19, 2022
Recommendations for clinical interpretation of variants found in non-coding regions of the genomeJamie M Ellingford, Joo Wook Ahn, Richard D Bagnall, et al.
Plos Genetics|May 31, 2014
Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorderEsther R Berko, Masako Suzuki, Faygel Beren, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 9, 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.
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.
Pageof 24