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Erica Sanford Kobayashi

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

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Frontiers in Pediatrics|March 31, 2023
Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary systemErika T Allred, Elliot A Perens, Nicole G Coufal, et al.
Orphanet Journal of Rare Diseases|December 17, 2022
NGLY1 deficiency: estimated incidence, clinical features, and genotypic spectrum from the NGLY1 RegistryCaroline R Stanclift, Selina S Dwight, Kevin Lee, et al.
Scientific Reports|October 9, 2022
Approaches to long-read sequencing in a clinical setting to improve diagnostic rateErica Sanford Kobayashi, Serge Batalov, Aaron M Wenger, et al.
The Journal of Pediatrics|July 7, 2024
Biallelic Loss of Function Variants in SENP7 Cause Immunodeficiency with Neurologic and Muscular PhenotypesErica Sanford Kobayashi, Nava Shaul Lotan, Yael Dinur Schejter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 10, 2025
Long-term follow-up of children who received rapid genomic sequencingErica Sanford Kobayashi, Laura E Tobin, Madison Arenchild, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|April 26, 2024
Rapid Whole-Genome Sequencing and Clinical Management in the PICU: A Multicenter Cohort, 2016-2023Katherine M Rodriguez, Jordan Vaught, Lisa Salz, et al.
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.
NPJ Digital Medicine|January 30, 2025
A machine learning decision support tool optimizes WGS utilization in a neonatal intensive care unitEdwin F Juarez, Bennet Peterson, Erica Sanford Kobayashi, et al.
Frontiers in Pediatrics|February 10, 2022
Cost Efficacy of Rapid Whole Genome Sequencing in the Pediatric Intensive Care UnitErica Sanford Kobayashi, Bryce Waldman, Branden M Engorn, et al.
JAMA Pediatrics|September 9, 2024
Early Newborn Metabolic Patterning and Sudden Infant Death SyndromeScott P Oltman, Elizabeth E Rogers, Rebecca J Baer, et al.
Pageof 1

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

Sort By:
Pageof 1
Frontiers in Pediatrics|March 31, 2023
Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary systemErika T Allred, Elliot A Perens, Nicole G Coufal, et al.
Orphanet Journal of Rare Diseases|December 17, 2022
NGLY1 deficiency: estimated incidence, clinical features, and genotypic spectrum from the NGLY1 RegistryCaroline R Stanclift, Selina S Dwight, Kevin Lee, et al.
Scientific Reports|October 9, 2022
Approaches to long-read sequencing in a clinical setting to improve diagnostic rateErica Sanford Kobayashi, Serge Batalov, Aaron M Wenger, et al.
The Journal of Pediatrics|July 7, 2024
Biallelic Loss of Function Variants in SENP7 Cause Immunodeficiency with Neurologic and Muscular PhenotypesErica Sanford Kobayashi, Nava Shaul Lotan, Yael Dinur Schejter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 10, 2025
Long-term follow-up of children who received rapid genomic sequencingErica Sanford Kobayashi, Laura E Tobin, Madison Arenchild, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|April 26, 2024
Rapid Whole-Genome Sequencing and Clinical Management in the PICU: A Multicenter Cohort, 2016-2023Katherine M Rodriguez, Jordan Vaught, Lisa Salz, et al.
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.
NPJ Digital Medicine|January 30, 2025
A machine learning decision support tool optimizes WGS utilization in a neonatal intensive care unitEdwin F Juarez, Bennet Peterson, Erica Sanford Kobayashi, et al.
Frontiers in Pediatrics|February 10, 2022
Cost Efficacy of Rapid Whole Genome Sequencing in the Pediatric Intensive Care UnitErica Sanford Kobayashi, Bryce Waldman, Branden M Engorn, et al.
JAMA Pediatrics|September 9, 2024
Early Newborn Metabolic Patterning and Sudden Infant Death SyndromeScott P Oltman, Elizabeth E Rogers, Rebecca J Baer, et al.
Pageof 1