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Stephanie M Fullerton

Showing results (111-120 of 118) with videos related to

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American Journal of Human Genetics|September 8, 2018
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved PopulationsLaura M Amendola, Jonathan S Berg, Carol R Horowitz, et al.
Nature Genetics|April 29, 2024
Advancing genomics to improve health equityEbony B Madden, Lucia A Hindorff, Vence L Bonham, et al.
Human Genomics|April 29, 2024
Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes projectSarah L Stenton, Melanie C O'Leary, Gabrielle Lemire, et al.
American Journal of Human Genetics|May 17, 2016
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic MedicineRobert C Green, Katrina A B Goddard, Gail P Jarvik, et al.
Medrxiv : the Preprint Server for Health Sciences|August 14, 2023
Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes ProjectSarah L Stenton, Melanie O'Leary, Gabrielle Lemire, et al.
Genome Research|February 1, 2015
Actionable exomic incidental findings in 6503 participants: challenges of variant classificationLaura M Amendola, Michael O Dorschner, Peggy D Robertson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2023
Returning integrated genomic risk and clinical recommendations: The eMERGE studyJodell E Linder, Aimee Allworth, Harris T Bland, et al.
Nature|February 11, 2021
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed ProgramDaniel Taliun, Daniel N Harris, Michael D Kessler, et al.
Pageof 12

Showing results (111-120 of 118) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 118 results.
American Journal of Human Genetics|September 8, 2018
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved PopulationsLaura M Amendola, Jonathan S Berg, Carol R Horowitz, et al.
Nature Genetics|April 29, 2024
Advancing genomics to improve health equityEbony B Madden, Lucia A Hindorff, Vence L Bonham, et al.
Human Genomics|April 29, 2024
Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes projectSarah L Stenton, Melanie C O'Leary, Gabrielle Lemire, et al.
American Journal of Human Genetics|May 17, 2016
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic MedicineRobert C Green, Katrina A B Goddard, Gail P Jarvik, et al.
Medrxiv : the Preprint Server for Health Sciences|August 14, 2023
Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes ProjectSarah L Stenton, Melanie O'Leary, Gabrielle Lemire, et al.
Genome Research|February 1, 2015
Actionable exomic incidental findings in 6503 participants: challenges of variant classificationLaura M Amendola, Michael O Dorschner, Peggy D Robertson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2023
Returning integrated genomic risk and clinical recommendations: The eMERGE studyJodell E Linder, Aimee Allworth, Harris T Bland, et al.
Nature|February 11, 2021
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed ProgramDaniel Taliun, Daniel N Harris, Michael D Kessler, et al.
Pageof 12