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Matthew Might

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2014
The shifting model in clinical diagnostics: how next-generation sequencing and families are altering the way rare diseases are discovered, studied, and treatedMatthew Might, Matt Wilsey
Prenatal Diagnosis|November 26, 2016
What happens when N = 1 and you want plus 1?Matthew Might, Cristina Casanova Might
Peerj|October 28, 2021
cdev: a ground-truth based measure to evaluate RNA-seq normalization performanceDiem-Trang Tran, Matthew Might
Cell Reports. Medicine|March 4, 2022
Why rare disease needs precision medicine-and precision medicine needs rare diseaseMatthew Might, Andrew B Crouse
Bioorganic & Medicinal Chemistry Letters|May 18, 2017
Repurposing of Proton Pump Inhibitors as first identified small molecule inhibitors of endo-β-N-acetylglucosaminidase (ENGase) for the treatment of NGLY1 deficiency, a rare genetic diseaseYiling Bi, Matthew Might, Hariprasad Vankayalapati, et al.
Kidney360|March 23, 2023
A Primer in Precision Nephrology: Optimizing Outcomes in Kidney Health and Disease through Data-Driven MedicinePushkala Jayaraman, Andrew Crouse, Girish Nadkarni, et al.
The American Journal of Bioethics : AJOB|September 24, 2019
N-of-1 Precision Medicine and Research OversightAndrew Crouse, Mariko Nakano-Okuno, Matthew Might, et al.
Plos One|January 25, 2020
A graph-based algorithm for RNA-seq data normalizationDiem-Trang Tran, Aditya Bhaskara, Balagurunathan Kuberan, et al.
Human Mutation|August 8, 2015
Participant-driven matchmaking in the genomic eraKatherine F Lambertson, Stephen A Damiani, Matthew Might, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 10, 2021
Functional characterization and potential therapeutic avenues for variants in the NTRK2 gene causing developmental and epileptic encephalopathiesAshlee Long, Andrew Crouse, Robert A Kesterson, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2014
The shifting model in clinical diagnostics: how next-generation sequencing and families are altering the way rare diseases are discovered, studied, and treatedMatthew Might, Matt Wilsey
Prenatal Diagnosis|November 26, 2016
What happens when N = 1 and you want plus 1?Matthew Might, Cristina Casanova Might
Peerj|October 28, 2021
cdev: a ground-truth based measure to evaluate RNA-seq normalization performanceDiem-Trang Tran, Matthew Might
Cell Reports. Medicine|March 4, 2022
Why rare disease needs precision medicine-and precision medicine needs rare diseaseMatthew Might, Andrew B Crouse
Bioorganic & Medicinal Chemistry Letters|May 18, 2017
Repurposing of Proton Pump Inhibitors as first identified small molecule inhibitors of endo-β-N-acetylglucosaminidase (ENGase) for the treatment of NGLY1 deficiency, a rare genetic diseaseYiling Bi, Matthew Might, Hariprasad Vankayalapati, et al.
Kidney360|March 23, 2023
A Primer in Precision Nephrology: Optimizing Outcomes in Kidney Health and Disease through Data-Driven MedicinePushkala Jayaraman, Andrew Crouse, Girish Nadkarni, et al.
The American Journal of Bioethics : AJOB|September 24, 2019
N-of-1 Precision Medicine and Research OversightAndrew Crouse, Mariko Nakano-Okuno, Matthew Might, et al.
Plos One|January 25, 2020
A graph-based algorithm for RNA-seq data normalizationDiem-Trang Tran, Aditya Bhaskara, Balagurunathan Kuberan, et al.
Human Mutation|August 8, 2015
Participant-driven matchmaking in the genomic eraKatherine F Lambertson, Stephen A Damiani, Matthew Might, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 10, 2021
Functional characterization and potential therapeutic avenues for variants in the NTRK2 gene causing developmental and epileptic encephalopathiesAshlee Long, Andrew Crouse, Robert A Kesterson, et al.
Pageof 5