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Chris M Kunard

Showing results (1-10 of 6) with videos related to

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The New England Journal of Medicine|June 2, 2021
Rapid Sequencing-Based Diagnosis of Thiamine Metabolism Dysfunction SyndromeMallory J Owen, Anna-Kaisa Niemi, David P Dimmock, et al.
American Journal of Human Genetics|December 6, 2024
Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trialStephen F Kingsmore, Meredith Wright, Lauren Olsen, et al.
American Journal of Human Genetics|December 6, 2024
Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselectionStephen F Kingsmore, Meredith Wright, Laurie D Smith, et al.
American Journal of Human Genetics|August 25, 2022
A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseasesStephen F Kingsmore, Laurie D Smith, Chris M Kunard, et al.
American Journal of Human Genetics|June 2, 2023
Response to Grosse et alStephen F Kingsmore, Laurie D Smith, Chris M Kunard, et al.
Nature Communications|July 26, 2022
An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseasesMallory J Owen, Sebastien Lefebvre, Christian Hansen, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
The New England Journal of Medicine|June 2, 2021
Rapid Sequencing-Based Diagnosis of Thiamine Metabolism Dysfunction SyndromeMallory J Owen, Anna-Kaisa Niemi, David P Dimmock, et al.
American Journal of Human Genetics|December 6, 2024
Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trialStephen F Kingsmore, Meredith Wright, Lauren Olsen, et al.
American Journal of Human Genetics|December 6, 2024
Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselectionStephen F Kingsmore, Meredith Wright, Laurie D Smith, et al.
American Journal of Human Genetics|August 25, 2022
A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseasesStephen F Kingsmore, Laurie D Smith, Chris M Kunard, et al.
American Journal of Human Genetics|June 2, 2023
Response to Grosse et alStephen F Kingsmore, Laurie D Smith, Chris M Kunard, et al.
Nature Communications|July 26, 2022
An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseasesMallory J Owen, Sebastien Lefebvre, Christian Hansen, et al.
Pageof 1