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Matthew Edwards

Showing results (101-110 of 130) with videos related to

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Cancer Letters|June 26, 2016
An improved CTC isolation scheme for pairing with downstream genomics: Demonstrating clinical utility in metastatic prostate, lung and pancreatic cancerGayatri Premasekharan, Elizabeth Gilbert, Ross A Okimoto, et al.
Molecular Genetics & Genomic Medicine|January 8, 2019
Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetranceKaren J Woodward, Julie Stampalia, Hannah Vanyai, et al.
American Journal of Respiratory and Critical Care Medicine|August 4, 2025
Non-Coding DNA Variants Increase the Genetic Diagnostic Yield in Primary Ciliary DyskinesiaLizi Briggs, Cátia Brandão, Andrew Fleming, et al.
International Journal of Cardiology|May 8, 2025
High incidence of malignant arrhythmias and heart failure in patients with RBM20-associated cardiomyopathy: A multicenter cohort study and review of the literatureMartijn Tukker, Wouter P Te Rijdt, Ahmad S Amin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2018
CardioClassifier: disease- and gene-specific computational decision support for clinical genome interpretationNicola Whiffin, Roddy Walsh, Risha Govind, et al.
Journal of Medical Genetics|October 16, 2020
Neurogenetic fetal akinesia and arthrogryposis: genetics, expanding genotype-phenotypes and functional genomicsGina Ravenscroft, Joshua S Clayton, Fathimath Faiz, et al.
Nature Communications|May 1, 2020
Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunctionKathryn L Post, Manuel Belmadani, Payel Ganguly, et al.
Preventive Veterinary Medicine|February 20, 2026
The use of participatory modelling to inform management of endemic foot-and-mouth disease: A case study from Nusa Tenggara Barat, IndonesiaSandra Steele, Yuni Yupiana, Indri Permatasari, et al.
European Journal of Human Genetics : EJHG|April 11, 2024
Combined approaches, including long-read sequencing, address the diagnostic challenge of HYDIN in primary ciliary dyskinesiaAndrew Fleming, Miranda Galey, Lizi Briggs, et al.
American Journal of Disaster Medicine|December 3, 2020
No human exists in isolation or as an island: The outcomes of a multidisciplinary, global, and context-specific COVID-19 consortiumGautam S Kalyatanda, Lennox K Archibald, Shraddha Patnala, et al.
Pageof 13

Showing results (101-110 of 130) with videos related to

Sort By:
Pageof 13
Cancer Letters|June 26, 2016
An improved CTC isolation scheme for pairing with downstream genomics: Demonstrating clinical utility in metastatic prostate, lung and pancreatic cancerGayatri Premasekharan, Elizabeth Gilbert, Ross A Okimoto, et al.
Molecular Genetics & Genomic Medicine|January 8, 2019
Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetranceKaren J Woodward, Julie Stampalia, Hannah Vanyai, et al.
American Journal of Respiratory and Critical Care Medicine|August 4, 2025
Non-Coding DNA Variants Increase the Genetic Diagnostic Yield in Primary Ciliary DyskinesiaLizi Briggs, Cátia Brandão, Andrew Fleming, et al.
International Journal of Cardiology|May 8, 2025
High incidence of malignant arrhythmias and heart failure in patients with RBM20-associated cardiomyopathy: A multicenter cohort study and review of the literatureMartijn Tukker, Wouter P Te Rijdt, Ahmad S Amin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2018
CardioClassifier: disease- and gene-specific computational decision support for clinical genome interpretationNicola Whiffin, Roddy Walsh, Risha Govind, et al.
Journal of Medical Genetics|October 16, 2020
Neurogenetic fetal akinesia and arthrogryposis: genetics, expanding genotype-phenotypes and functional genomicsGina Ravenscroft, Joshua S Clayton, Fathimath Faiz, et al.
Nature Communications|May 1, 2020
Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunctionKathryn L Post, Manuel Belmadani, Payel Ganguly, et al.
Preventive Veterinary Medicine|February 20, 2026
The use of participatory modelling to inform management of endemic foot-and-mouth disease: A case study from Nusa Tenggara Barat, IndonesiaSandra Steele, Yuni Yupiana, Indri Permatasari, et al.
European Journal of Human Genetics : EJHG|April 11, 2024
Combined approaches, including long-read sequencing, address the diagnostic challenge of HYDIN in primary ciliary dyskinesiaAndrew Fleming, Miranda Galey, Lizi Briggs, et al.
American Journal of Disaster Medicine|December 3, 2020
No human exists in isolation or as an island: The outcomes of a multidisciplinary, global, and context-specific COVID-19 consortiumGautam S Kalyatanda, Lennox K Archibald, Shraddha Patnala, et al.
Pageof 13