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Jessica Tardif

Showing results (21-30 of 28) with videos related to

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Drug and Alcohol Dependence|November 24, 2023
Costing analysis of a point-of-care drug checking program in Rhode IslandJavier A Cepeda, Erin Thompson, Merci Ujeneza, et al.
Drug and Alcohol Review|September 22, 2025
Point-Of-Care Drug-Checking: Assessing the Rhode Island Drug Supply Using FTIR Spectroscopy to Detect Fentanyl, Xylazine and Other SubstancesMerci Ujeneza, Jessica Tardif, Erin Thompson, et al.
Plos Genetics|October 16, 2025
Rare diseases load through the study of a regional populationÉlisa Michel, Claudia Moreau, Laurence Gagnon, et al.
Genetics in Medicine Open|June 30, 2025
Successes of an innovative population-based carrier screening program for 4 prevalent recessive hereditary diseases in a population with a founder effect in Quebec, CanadaCarol-Ann Fortin, Mélanie Côté-Richer, Karine Truchon, et al.
Cell Reports|November 14, 2015
A Metabolic Signature of Mitochondrial Dysfunction Revealed through a Monogenic Form of Leigh SyndromeJulie Thompson Legault, Laura Strittmatter, Jessica Tardif, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2020
DOORS syndrome and a recurrent truncating ATP6V1B2 variantEliane Beauregard-Lacroix, Guillermo Pacheco-Cuellar, Norbert F Ajeawung, et al.
American Journal of Human Genetics|November 4, 2017
Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and OsteopeniaThi Tuyet Mai Nguyen, Yoshiko Murakami, Eamonn Sheridan, et al.
Neurology|June 10, 2016
TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic featuresSimona Balestrini, Mathieu Milh, Claudia Castiglioni, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Drug and Alcohol Dependence|November 24, 2023
Costing analysis of a point-of-care drug checking program in Rhode IslandJavier A Cepeda, Erin Thompson, Merci Ujeneza, et al.
Drug and Alcohol Review|September 22, 2025
Point-Of-Care Drug-Checking: Assessing the Rhode Island Drug Supply Using FTIR Spectroscopy to Detect Fentanyl, Xylazine and Other SubstancesMerci Ujeneza, Jessica Tardif, Erin Thompson, et al.
Plos Genetics|October 16, 2025
Rare diseases load through the study of a regional populationÉlisa Michel, Claudia Moreau, Laurence Gagnon, et al.
Genetics in Medicine Open|June 30, 2025
Successes of an innovative population-based carrier screening program for 4 prevalent recessive hereditary diseases in a population with a founder effect in Quebec, CanadaCarol-Ann Fortin, Mélanie Côté-Richer, Karine Truchon, et al.
Cell Reports|November 14, 2015
A Metabolic Signature of Mitochondrial Dysfunction Revealed through a Monogenic Form of Leigh SyndromeJulie Thompson Legault, Laura Strittmatter, Jessica Tardif, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2020
DOORS syndrome and a recurrent truncating ATP6V1B2 variantEliane Beauregard-Lacroix, Guillermo Pacheco-Cuellar, Norbert F Ajeawung, et al.
American Journal of Human Genetics|November 4, 2017
Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and OsteopeniaThi Tuyet Mai Nguyen, Yoshiko Murakami, Eamonn Sheridan, et al.
Neurology|June 10, 2016
TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic featuresSimona Balestrini, Mathieu Milh, Claudia Castiglioni, et al.
Pageof 3