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Candice R Finnila

Showing results (1-10 of 23) with videos related to

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Ethics & Human Research|September 22, 2019
Participant Engagement in Translational Genomics Research: Respect for Persons-and Then SomeJanet E Childerhose, Candice R Finnila, Joon-Ho Yu, et al.
Journal of Community Genetics|May 6, 2026
How parents and community care professionals use a genetic diagnosis to inform care: expanding the concept of utilityAmy A Lemke, Katelyn C McNamara, R Jean Cadigan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 29, 2024
Errors in genome sequencing result disclosures: A randomized controlled trial comparing neonatology non-genetics healthcare professionals and genetic counselorsTanner F Coleman, Jada Pugh, Whitley V Kelley, et al.
Journal of Personalized Medicine|March 25, 2022
Education and Training of Non-Genetics Providers on the Return of Genome Sequencing Results in a NICU SettingKelly M East, Meagan E Cochran, Whitley V Kelley, et al.
Clinical and Translational Science|December 8, 2023
The motivation and process for developing a consortium-wide time and motion study to estimate resource implications of innovations in the use of genome sequencing to inform patient careHannah G Hoban, Tiffany A Yip, Joanna C Chau, et al.
Genetics in Medicine Open|August 1, 2025
When families bridge the research-clinical divide: An exploration of values regarding cascade screening in genomic researchKatherine E Bonini, Lauren R Desrosiers-Battu, Ann Katherine M Foreman, et al.
AJOB Empirical Bioethics|April 12, 2021
The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child's Best Possible LifeJanet Elizabeth Childerhose, Carla Rich, Kelly M East, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testingStephanie A Felker, James Mj Lawlor, Susan M Hiatt, et al.
Genome Research|September 19, 2024
Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disordersSusan M Hiatt, James M J Lawlor, Lori H Handley, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disordersSusan M Hiatt, James M J Lawlor, Lori H Handley, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Ethics & Human Research|September 22, 2019
Participant Engagement in Translational Genomics Research: Respect for Persons-and Then SomeJanet E Childerhose, Candice R Finnila, Joon-Ho Yu, et al.
Journal of Community Genetics|May 6, 2026
How parents and community care professionals use a genetic diagnosis to inform care: expanding the concept of utilityAmy A Lemke, Katelyn C McNamara, R Jean Cadigan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 29, 2024
Errors in genome sequencing result disclosures: A randomized controlled trial comparing neonatology non-genetics healthcare professionals and genetic counselorsTanner F Coleman, Jada Pugh, Whitley V Kelley, et al.
Journal of Personalized Medicine|March 25, 2022
Education and Training of Non-Genetics Providers on the Return of Genome Sequencing Results in a NICU SettingKelly M East, Meagan E Cochran, Whitley V Kelley, et al.
Clinical and Translational Science|December 8, 2023
The motivation and process for developing a consortium-wide time and motion study to estimate resource implications of innovations in the use of genome sequencing to inform patient careHannah G Hoban, Tiffany A Yip, Joanna C Chau, et al.
Genetics in Medicine Open|August 1, 2025
When families bridge the research-clinical divide: An exploration of values regarding cascade screening in genomic researchKatherine E Bonini, Lauren R Desrosiers-Battu, Ann Katherine M Foreman, et al.
AJOB Empirical Bioethics|April 12, 2021
The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child's Best Possible LifeJanet Elizabeth Childerhose, Carla Rich, Kelly M East, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testingStephanie A Felker, James Mj Lawlor, Susan M Hiatt, et al.
Genome Research|September 19, 2024
Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disordersSusan M Hiatt, James M J Lawlor, Lori H Handley, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disordersSusan M Hiatt, James M J Lawlor, Lori H Handley, et al.
Pageof 3