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Showing results (721-730 of 731) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2016
Recommendations for the integration of genomics into clinical practiceSarah Bowdin, Adel Gilbert, Emma Bedoukian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic testAnath C Lionel, Gregory Costain, Nasim Monfared, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|February 13, 2018
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participantsMiriam S Reuter, Susan Walker, Bhooma Thiruvahindrapuram, et al.
NPJ Genomic Medicine|June 2, 2017
Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric MedicineDimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, et al.
JAMA Oncology|October 7, 2021
Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition SyndromesCatherine Goudie, Leora Witkowski, Noelle Cullinan, et al.
Cell|October 24, 2017
Comprehensive Analysis of Hypermutation in Human CancerBrittany B Campbell, Nicholas Light, David Fabrizio, et al.
Nature Genetics|February 3, 2015
Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancersAdam Shlien, Brittany B Campbell, Richard de Borja, et al.
Nature Genetics|October 21, 2024
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed HackathonAngelica Maria Delgado-Vega, Helene Cederroth, Fulya Taylan, et al.
Science Advances|December 3, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patientsLaura Bryant, Dong Li, Samuel G Cox, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 28, 2023
Large-scale analysis of structural brain asymmetries in schizophrenia via the ENIGMA consortiumDick Schijven, Merel C Postema, Masaki Fukunaga, et al.
Pageof 74

Showing results (721-730 of 731) with videos related to

Sort By:
Pageof 74
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2016
Recommendations for the integration of genomics into clinical practiceSarah Bowdin, Adel Gilbert, Emma Bedoukian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic testAnath C Lionel, Gregory Costain, Nasim Monfared, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|February 13, 2018
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participantsMiriam S Reuter, Susan Walker, Bhooma Thiruvahindrapuram, et al.
NPJ Genomic Medicine|June 2, 2017
Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric MedicineDimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, et al.
JAMA Oncology|October 7, 2021
Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition SyndromesCatherine Goudie, Leora Witkowski, Noelle Cullinan, et al.
Cell|October 24, 2017
Comprehensive Analysis of Hypermutation in Human CancerBrittany B Campbell, Nicholas Light, David Fabrizio, et al.
Nature Genetics|February 3, 2015
Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancersAdam Shlien, Brittany B Campbell, Richard de Borja, et al.
Nature Genetics|October 21, 2024
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed HackathonAngelica Maria Delgado-Vega, Helene Cederroth, Fulya Taylan, et al.
Science Advances|December 3, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patientsLaura Bryant, Dong Li, Samuel G Cox, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 28, 2023
Large-scale analysis of structural brain asymmetries in schizophrenia via the ENIGMA consortiumDick Schijven, Merel C Postema, Masaki Fukunaga, et al.
Pageof 74