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Philip Awadalla

Showing results (61-70 of 110) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Geography, Ancestry, Age and Sex Shape Somatic Autosomal Mosaic Chromosomal Alterations in BloodJasmine Ryu Won Kang, Yeekyung June Kim, Kimberly Skead, et al.
Neurobiology of Aging|October 24, 2015
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosisClaire S Leblond, Ziv Gan-Or, Dan Spiegelman, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique|July 9, 2024
Canada's approach to SARS-CoV-2 sero-surveillance: Lessons learned for routine surveillance and future pandemicsSheila F O'Brien, Michael Asamoah-Boaheng, Brian Grunau, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2020
Diabetes, Brain Infarcts, Cognition, and Small Vessels in the Canadian Alliance for Healthy Hearts and Minds StudyHertzel C Gerstein, Eric E Smith, Chinthanie Ramasundarahettige, et al.
CJC Open|December 11, 2020
The Canadian Alliance for Healthy Hearts and Minds: How Well Does It Reflect the Canadian Population?Ruth E Hall, Natasa Tusevljak, C Fangyun Wu, et al.
Journal of Medical Genetics|February 21, 2013
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresiaMark E Samuels, Jacek Majewski, Najmeh Alirezaie, et al.
Nature Genetics|June 14, 2011
Variation in genome-wide mutation rates within and between human familiesDonald F Conrad, Jonathan E M Keebler, Mark A DePristo, et al.
Gut|January 20, 2026
Genetic dissection of stool frequency implicates vitamin B1 metabolism and other actionable pathways in the modulation of gut motilityCristian Díaz-Muñoz, Isotta Bozzarelli, Esteban Alexander Lopera-Maya, et al.
Plos Genetics|March 9, 2011
A population genetic approach to mapping neurological disorder genes using deep resequencingRachel A Myers, Ferran Casals, Julie Gauthier, et al.
Genome Research|May 20, 2016
Impact of the X Chromosome and sex on regulatory variationKimberly R Kukurba, Princy Parsana, Brunilda Balliu, et al.
Pageof 11

Showing results (61-70 of 110) with videos related to

Sort By:
Pageof 11
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Geography, Ancestry, Age and Sex Shape Somatic Autosomal Mosaic Chromosomal Alterations in BloodJasmine Ryu Won Kang, Yeekyung June Kim, Kimberly Skead, et al.
Neurobiology of Aging|October 24, 2015
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosisClaire S Leblond, Ziv Gan-Or, Dan Spiegelman, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique|July 9, 2024
Canada's approach to SARS-CoV-2 sero-surveillance: Lessons learned for routine surveillance and future pandemicsSheila F O'Brien, Michael Asamoah-Boaheng, Brian Grunau, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2020
Diabetes, Brain Infarcts, Cognition, and Small Vessels in the Canadian Alliance for Healthy Hearts and Minds StudyHertzel C Gerstein, Eric E Smith, Chinthanie Ramasundarahettige, et al.
CJC Open|December 11, 2020
The Canadian Alliance for Healthy Hearts and Minds: How Well Does It Reflect the Canadian Population?Ruth E Hall, Natasa Tusevljak, C Fangyun Wu, et al.
Journal of Medical Genetics|February 21, 2013
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresiaMark E Samuels, Jacek Majewski, Najmeh Alirezaie, et al.
Nature Genetics|June 14, 2011
Variation in genome-wide mutation rates within and between human familiesDonald F Conrad, Jonathan E M Keebler, Mark A DePristo, et al.
Gut|January 20, 2026
Genetic dissection of stool frequency implicates vitamin B1 metabolism and other actionable pathways in the modulation of gut motilityCristian Díaz-Muñoz, Isotta Bozzarelli, Esteban Alexander Lopera-Maya, et al.
Plos Genetics|March 9, 2011
A population genetic approach to mapping neurological disorder genes using deep resequencingRachel A Myers, Ferran Casals, Julie Gauthier, et al.
Genome Research|May 20, 2016
Impact of the X Chromosome and sex on regulatory variationKimberly R Kukurba, Princy Parsana, Brunilda Balliu, et al.
Pageof 11