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Edgar Javier Hernandez

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

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BMC Medicine|February 7, 2026
Quantifying lifetime risk for 1,401 infectious diseases across the diabetes spectrum using a Bayesian approachBoomer B Olsen, Martin Tristani-Firouzi, Karen Eilbeck, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium|May 26, 2025
Probabilistic Graphical Models for Evaluating the Utility of Data-Driven ICD Code Categories in Pediatric SepsisLourdes A Valdez, Edgar Javier Hernandez, O'Connor Matthews, et al.
Plos One|February 24, 2015
Quantitative differences in nourishment affect caste-related physiology and development in the paper wasp Polistes metricusTimothy M Judd, Peter E A Teal, Edgar Javier Hernandez, et al.
Plos One|February 21, 2024
An artificial intelligence approach for investigating multifactorial pain-related features of endometriosisAmber C Kiser, Karen C Schliep, Edgar Javier Hernandez, et al.
BMC Bioinformatics|February 22, 2018
The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization toolSteven Flygare, Edgar Javier Hernandez, Lon Phan, et al.
Genome Medicine|March 17, 2023
Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learningBennet Peterson, Edgar Javier Hernandez, Charlotte Hobbs, et al.
NPJ Genomic Medicine|June 12, 2025
MPSE identifies newborns for whole genome sequencing within 48 h of NICU admissionBennet Peterson, Edwin F Juarez, Barry Moore, et al.
Frontiers in Oncology|October 3, 2022
Genomic landscape of advanced prostate cancer patients with <i>BRCA1</i> versus <i>BRCA2</i> mutations as detected by comprehensive genomic profiling of cell-free DNAUmang Swami, Raquel Mae Zimmerman, Roberto H Nussenzveig, et al.
NPJ Genomic Medicine|July 22, 2022
A dominant negative ADIPOQ mutation in a diabetic family with renal disease, hypoadiponectinemia, and hyperceramidemiaChristopher A Simeone, Joseph L Wilkerson, Annelise M Poss, 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.
Pageof 1

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

Sort By:
Pageof 1
BMC Medicine|February 7, 2026
Quantifying lifetime risk for 1,401 infectious diseases across the diabetes spectrum using a Bayesian approachBoomer B Olsen, Martin Tristani-Firouzi, Karen Eilbeck, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium|May 26, 2025
Probabilistic Graphical Models for Evaluating the Utility of Data-Driven ICD Code Categories in Pediatric SepsisLourdes A Valdez, Edgar Javier Hernandez, O'Connor Matthews, et al.
Plos One|February 24, 2015
Quantitative differences in nourishment affect caste-related physiology and development in the paper wasp Polistes metricusTimothy M Judd, Peter E A Teal, Edgar Javier Hernandez, et al.
Plos One|February 21, 2024
An artificial intelligence approach for investigating multifactorial pain-related features of endometriosisAmber C Kiser, Karen C Schliep, Edgar Javier Hernandez, et al.
BMC Bioinformatics|February 22, 2018
The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization toolSteven Flygare, Edgar Javier Hernandez, Lon Phan, et al.
Genome Medicine|March 17, 2023
Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learningBennet Peterson, Edgar Javier Hernandez, Charlotte Hobbs, et al.
NPJ Genomic Medicine|June 12, 2025
MPSE identifies newborns for whole genome sequencing within 48 h of NICU admissionBennet Peterson, Edwin F Juarez, Barry Moore, et al.
Frontiers in Oncology|October 3, 2022
Genomic landscape of advanced prostate cancer patients with <i>BRCA1</i> versus <i>BRCA2</i> mutations as detected by comprehensive genomic profiling of cell-free DNAUmang Swami, Raquel Mae Zimmerman, Roberto H Nussenzveig, et al.
NPJ Genomic Medicine|July 22, 2022
A dominant negative ADIPOQ mutation in a diabetic family with renal disease, hypoadiponectinemia, and hyperceramidemiaChristopher A Simeone, Joseph L Wilkerson, Annelise M Poss, 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.
Pageof 1