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Matthew J Ferber

Showing results (31-40 of 41) with videos related to

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Molecular Genetics & Genomic Medicine|September 26, 2017
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genesMelissa S DeRycke, Shanaka Gunawardena, Jessica R Balcom, et al.
JCO Precision Oncology|July 16, 2024
Exome Sequencing Identifies Carriers of the Autosomal Dominant Cancer Predisposition Disorders Beyond Current Practice Guideline RecommendationsN Jewel Samadder, Emily Gay, Vanda Lindpere, et al.
Circulation. Genomic and Precision Medicine|November 12, 2025
Exome Sequencing Enhances Screening for Familial Hypercholesterolemia Within a Multi-Site Healthcare SystemN Jewel Samadder, Mariah Schroeder, Molly M Voss, et al.
Mayo Clinic Proceedings|January 7, 2014
Preemptive genotyping for personalized medicine: design of the right drug, right dose, right time-using genomic data to individualize treatment protocolSuzette J Bielinski, Janet E Olson, Jyotishman Pathak, et al.
Nature Biotechnology|November 10, 2012
Assuring the quality of next-generation sequencing in clinical laboratory practiceAmy S Gargis, Lisa Kalman, Meredith W Berry, et al.
Mayo Clinic Proceedings|December 3, 2024
Mayo Clinic Tapestry Study: A Large-Scale Decentralized Whole Exome Sequencing Study for Clinical Practice, Research Discovery, and Genomic EducationLorelei A Bandel, Robert A Vierkant, Teresa M Kruisselbrink, et al.
Epilepsia|May 27, 2021
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severityMichelle E Ernst, Evan H Baugh, Amanda Thomas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2019
CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrumEnrico D H Konrad, Niels Nardini, Almuth Caliebe, et al.
American Journal of Human Genetics|October 17, 2024
MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathwayMaolei Gong, Jiayi Li, Zailong Qin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2020
Impact of integrated translational research on clinical exome sequencingEric W Klee, Margot A Cousin, Filippo Pinto E Vairo, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Molecular Genetics & Genomic Medicine|September 26, 2017
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genesMelissa S DeRycke, Shanaka Gunawardena, Jessica R Balcom, et al.
JCO Precision Oncology|July 16, 2024
Exome Sequencing Identifies Carriers of the Autosomal Dominant Cancer Predisposition Disorders Beyond Current Practice Guideline RecommendationsN Jewel Samadder, Emily Gay, Vanda Lindpere, et al.
Circulation. Genomic and Precision Medicine|November 12, 2025
Exome Sequencing Enhances Screening for Familial Hypercholesterolemia Within a Multi-Site Healthcare SystemN Jewel Samadder, Mariah Schroeder, Molly M Voss, et al.
Mayo Clinic Proceedings|January 7, 2014
Preemptive genotyping for personalized medicine: design of the right drug, right dose, right time-using genomic data to individualize treatment protocolSuzette J Bielinski, Janet E Olson, Jyotishman Pathak, et al.
Nature Biotechnology|November 10, 2012
Assuring the quality of next-generation sequencing in clinical laboratory practiceAmy S Gargis, Lisa Kalman, Meredith W Berry, et al.
Mayo Clinic Proceedings|December 3, 2024
Mayo Clinic Tapestry Study: A Large-Scale Decentralized Whole Exome Sequencing Study for Clinical Practice, Research Discovery, and Genomic EducationLorelei A Bandel, Robert A Vierkant, Teresa M Kruisselbrink, et al.
Epilepsia|May 27, 2021
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severityMichelle E Ernst, Evan H Baugh, Amanda Thomas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2019
CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrumEnrico D H Konrad, Niels Nardini, Almuth Caliebe, et al.
American Journal of Human Genetics|October 17, 2024
MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathwayMaolei Gong, Jiayi Li, Zailong Qin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2020
Impact of integrated translational research on clinical exome sequencingEric W Klee, Margot A Cousin, Filippo Pinto E Vairo, et al.
Pageof 5