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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 8, 2019
Biparental inheritance of mitochondrial DNA in humans is not a common phenomenon
Rocio Rius, Mark J Cowley, Lisa Riley, et al.
Genome Biology
|
June 13, 2025
Cancer gene identification from RNA variant allelic frequencies using RVdriver
James R M Black, Thomas P Jones, Carlos Martínez-Ruiz, et al.
Neurogenetics
|
September 30, 2016
Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing
Kishore R Kumar, G M Wali, Mahesh Kamate, et al.
Journal for Immunotherapy of Cancer
|
November 1, 2023
Quantifying the impact of immunotherapy on RNA dynamics in cancer
Ieva Usaite, Dhruva Biswas, Krijn Dijkstra, et al.
Neurology
|
May 31, 2022
Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis
Ryan L Davis, Kishore R Kumar, Clare Puttick, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 22, 2020
The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease
Lisa G Riley, Mark J Cowley, Velimir Gayevskiy, et al.
Nature Genetics
|
October 2, 2024
MHC Hammer reveals genetic and non-genetic HLA disruption in cancer evolution
Clare Puttick, Thomas P Jones, Michelle M Leung, et al.
Cold Spring Harbor Molecular Case Studies
|
April 3, 2019
Genomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases
Mark J McCabe, Mark Pinese, Chia-Ling Chan, et al.
Neurology
|
February 11, 2021
Diagnostic Yield of Whole Genome Sequencing After Nondiagnostic Exome Sequencing or Gene Panel in Developmental and Epileptic Encephalopathies
Elizabeth Emma Palmer, Rani Sachdev, Rebecca Macintosh, et al.
Scientific Reports
|
November 21, 2019
Development and validation of a targeted gene sequencing panel for application to disparate cancers
Mark J McCabe, Marie-Emilie A Gauthier, Chia-Ling Chan, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 8, 2019
Biparental inheritance of mitochondrial DNA in humans is not a common phenomenon
Rocio Rius, Mark J Cowley, Lisa Riley, et al.
Genome Biology
|
June 13, 2025
Cancer gene identification from RNA variant allelic frequencies using RVdriver
James R M Black, Thomas P Jones, Carlos Martínez-Ruiz, et al.
Neurogenetics
|
September 30, 2016
Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing
Kishore R Kumar, G M Wali, Mahesh Kamate, et al.
Journal for Immunotherapy of Cancer
|
November 1, 2023
Quantifying the impact of immunotherapy on RNA dynamics in cancer
Ieva Usaite, Dhruva Biswas, Krijn Dijkstra, et al.
Neurology
|
May 31, 2022
Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis
Ryan L Davis, Kishore R Kumar, Clare Puttick, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 22, 2020
The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease
Lisa G Riley, Mark J Cowley, Velimir Gayevskiy, et al.
Nature Genetics
|
October 2, 2024
MHC Hammer reveals genetic and non-genetic HLA disruption in cancer evolution
Clare Puttick, Thomas P Jones, Michelle M Leung, et al.
Cold Spring Harbor Molecular Case Studies
|
April 3, 2019
Genomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases
Mark J McCabe, Mark Pinese, Chia-Ling Chan, et al.
Neurology
|
February 11, 2021
Diagnostic Yield of Whole Genome Sequencing After Nondiagnostic Exome Sequencing or Gene Panel in Developmental and Epileptic Encephalopathies
Elizabeth Emma Palmer, Rani Sachdev, Rebecca Macintosh, et al.
Scientific Reports
|
November 21, 2019
Development and validation of a targeted gene sequencing panel for application to disparate cancers
Mark J McCabe, Marie-Emilie A Gauthier, Chia-Ling Chan, et al.
Page
of 3