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Erwin Frise

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Medrxiv : the Preprint Server for Health Sciences|December 8, 2025
Genome x Environment analysis of Sudden Unexpected Infant Death unveils etiologic heterogeneity and strong cannabis and genetic disease risksStephen F Kingsmore, Gretchen Bandoli, Daniel C Helbling, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Genome Sequencing is Critical for Forecasting Outcomes Following Congenital Cardiac SurgeryW Scott Watkins, E Javier Hernandez, Thomas Miller, et al.
Genome Medicine|October 14, 2021
Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseasesFrancisco M De La Vega, Shimul Chowdhury, Barry Moore, et al.
Nature Communications|July 10, 2025
Genome sequencing is critical for forecasting outcomes following congenital cardiac surgeryW Scott Watkins, Edgar J Hernandez, Thomas A Miller, et al.
Genome Biology|January 23, 2003
Finishing a whole-genome shotgun: release 3 of the Drosophila melanogaster euchromatic genome sequenceSusan E Celniker, David A Wheeler, Brent Kronmiller, et al.
Nature|March 28, 2014
Diversity and dynamics of the Drosophila transcriptomeJames B Brown, Nathan Boley, Robert Eisman, 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|June 2, 2023
Response to Grosse et alStephen F Kingsmore, Laurie D Smith, Chris M Kunard, 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.
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 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Medrxiv : the Preprint Server for Health Sciences|December 8, 2025
Genome x Environment analysis of Sudden Unexpected Infant Death unveils etiologic heterogeneity and strong cannabis and genetic disease risksStephen F Kingsmore, Gretchen Bandoli, Daniel C Helbling, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Genome Sequencing is Critical for Forecasting Outcomes Following Congenital Cardiac SurgeryW Scott Watkins, E Javier Hernandez, Thomas Miller, et al.
Genome Medicine|October 14, 2021
Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseasesFrancisco M De La Vega, Shimul Chowdhury, Barry Moore, et al.
Nature Communications|July 10, 2025
Genome sequencing is critical for forecasting outcomes following congenital cardiac surgeryW Scott Watkins, Edgar J Hernandez, Thomas A Miller, et al.
Genome Biology|January 23, 2003
Finishing a whole-genome shotgun: release 3 of the Drosophila melanogaster euchromatic genome sequenceSusan E Celniker, David A Wheeler, Brent Kronmiller, et al.
Nature|March 28, 2014
Diversity and dynamics of the Drosophila transcriptomeJames B Brown, Nathan Boley, Robert Eisman, 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|June 2, 2023
Response to Grosse et alStephen F Kingsmore, Laurie D Smith, Chris M Kunard, 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.
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 2