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Paul Avillach

Showing results (1-10 of 117) with videos related to

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JMIR Medical Informatics|March 14, 2021
Retracted: Diagnostic Classification and Prognostic Prediction Using Common Genetic Variants in Autism Spectrum Disorder: Genotype-Based Deep LearningHaishuai Wang, Paul Avillach
Health Care Management Science|June 28, 2008
Improving the quality of the coding of primary diagnosis in standardized discharge summariesPaul Avillach, Michel Joubert, Marius Fieschi
AMIA ... Annual Symposium Proceedings. AMIA Symposium|August 13, 2008
A model for indexing medical documents combining statistical and symbolic knowledgePaul Avillach, Michel Joubert, Marius Fieschi
JAMIA Open|February 14, 2022
Streamlining statistical reproducibility: NHLBI ORCHID clinical trial results reproductionArnaud Serret-Larmande, Jonathan R Kaltman, Paul Avillach
Pediatric Research|November 12, 2020
The urgent need for research coordination to advance knowledge on COVID-19 in childrenFlorence T Bourgeois, Paul Avillach, Mark A Turner
JAMIA Open|August 1, 2020
Experiences implementing scalable, containerized, cloud-based NLP for extracting biobank participant phenotypes at scaleTimothy A Miller, Paul Avillach, Kenneth D Mandl
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
VarPPUD: Variant post prioritization developed for undiagnosed genetic disordersRui Yin, Alba Gutierrez, , et al.
Bioinformatics (Oxford, England)|September 11, 2019
dbgap2x: an R package to explore and extract data from the database of Genotypes and Phenotypes (dbGaP)Grégoire Versmée, Laura Versmée, Mikaël Dusenne, et al.
Plos Computational Biology|September 22, 2025
VarPPUD: Pinpointing diagnostic variants from sets of prioritized, strong candidate variantsRui Yin, Alba Gutiérrez-Sacristán, , et al.
Briefings in Bioinformatics|March 11, 2014
Translational research platforms integrating clinical and omics data: a review of publicly available solutionsVincent Canuel, Bastien Rance, Paul Avillach, et al.
Pageof 12

Showing results (1-10 of 117) with videos related to

Sort By:
Pageof 12
JMIR Medical Informatics|March 14, 2021
Retracted: Diagnostic Classification and Prognostic Prediction Using Common Genetic Variants in Autism Spectrum Disorder: Genotype-Based Deep LearningHaishuai Wang, Paul Avillach
Health Care Management Science|June 28, 2008
Improving the quality of the coding of primary diagnosis in standardized discharge summariesPaul Avillach, Michel Joubert, Marius Fieschi
AMIA ... Annual Symposium Proceedings. AMIA Symposium|August 13, 2008
A model for indexing medical documents combining statistical and symbolic knowledgePaul Avillach, Michel Joubert, Marius Fieschi
JAMIA Open|February 14, 2022
Streamlining statistical reproducibility: NHLBI ORCHID clinical trial results reproductionArnaud Serret-Larmande, Jonathan R Kaltman, Paul Avillach
Pediatric Research|November 12, 2020
The urgent need for research coordination to advance knowledge on COVID-19 in childrenFlorence T Bourgeois, Paul Avillach, Mark A Turner
JAMIA Open|August 1, 2020
Experiences implementing scalable, containerized, cloud-based NLP for extracting biobank participant phenotypes at scaleTimothy A Miller, Paul Avillach, Kenneth D Mandl
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
VarPPUD: Variant post prioritization developed for undiagnosed genetic disordersRui Yin, Alba Gutierrez, , et al.
Bioinformatics (Oxford, England)|September 11, 2019
dbgap2x: an R package to explore and extract data from the database of Genotypes and Phenotypes (dbGaP)Grégoire Versmée, Laura Versmée, Mikaël Dusenne, et al.
Plos Computational Biology|September 22, 2025
VarPPUD: Pinpointing diagnostic variants from sets of prioritized, strong candidate variantsRui Yin, Alba Gutiérrez-Sacristán, , et al.
Briefings in Bioinformatics|March 11, 2014
Translational research platforms integrating clinical and omics data: a review of publicly available solutionsVincent Canuel, Bastien Rance, Paul Avillach, et al.
Pageof 12