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Kevin P Kenna

Showing results (1-10 of 32) with videos related to

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Human Mutation|March 1, 2013
Using reference databases of genetic variation to evaluate the potential pathogenicity of candidate disease variantsKevin P Kenna, Russell L McLaughlin, Orla Hardiman, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 4, 2018
Transcription factor Pebbled/RREB1 regulates injury-induced axon degenerationJonathan E Farley, Thomas C Burdett, Romina Barria, et al.
Current Opinion in Neurology|August 3, 2021
Advances in the genetic classification of amyotrophic lateral sclerosisJohnathan Cooper-Knock, Calum Harvey, Sai Zhang, et al.
Neurobiology of Aging|December 3, 2014
Second-generation Irish genome-wide association study for amyotrophic lateral sclerosisRussell L McLaughlin, Kevin P Kenna, Alice Vajda, et al.
Genomics|January 27, 2015
Homozygosity mapping in an Irish ALS case-control cohort describes local demographic phenomena and points towards potential recessive risk lociRussell L McLaughlin, Kevin P Kenna, Alice Vajda, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 9, 2019
The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the publicRick A A van der Spek, Wouter van Rheenen, Sara L Pulit, et al.
Journal of Medical Genetics|July 25, 2013
Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencingKevin P Kenna, Russell L McLaughlin, Susan Byrne, et al.
European Journal of Human Genetics : EJHG|January 8, 2021
Genetic analysis of ALS cases in the isolated island population of MaltaRebecca Borg, Maia Farrugia Wismayer, Karl Bonavia, et al.
Brain Communications|April 20, 2022
Unbiased metabolome screen leads to personalized medicine strategy for amyotrophic lateral sclerosisSarah Boddy, Mahjabin Islam, Tobias Moll, et al.
Cell Systems|June 11, 2022
Multiomic analysis reveals cell-type-specific molecular determinants of COVID-19 severitySai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Human Mutation|March 1, 2013
Using reference databases of genetic variation to evaluate the potential pathogenicity of candidate disease variantsKevin P Kenna, Russell L McLaughlin, Orla Hardiman, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 4, 2018
Transcription factor Pebbled/RREB1 regulates injury-induced axon degenerationJonathan E Farley, Thomas C Burdett, Romina Barria, et al.
Current Opinion in Neurology|August 3, 2021
Advances in the genetic classification of amyotrophic lateral sclerosisJohnathan Cooper-Knock, Calum Harvey, Sai Zhang, et al.
Neurobiology of Aging|December 3, 2014
Second-generation Irish genome-wide association study for amyotrophic lateral sclerosisRussell L McLaughlin, Kevin P Kenna, Alice Vajda, et al.
Genomics|January 27, 2015
Homozygosity mapping in an Irish ALS case-control cohort describes local demographic phenomena and points towards potential recessive risk lociRussell L McLaughlin, Kevin P Kenna, Alice Vajda, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 9, 2019
The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the publicRick A A van der Spek, Wouter van Rheenen, Sara L Pulit, et al.
Journal of Medical Genetics|July 25, 2013
Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencingKevin P Kenna, Russell L McLaughlin, Susan Byrne, et al.
European Journal of Human Genetics : EJHG|January 8, 2021
Genetic analysis of ALS cases in the isolated island population of MaltaRebecca Borg, Maia Farrugia Wismayer, Karl Bonavia, et al.
Brain Communications|April 20, 2022
Unbiased metabolome screen leads to personalized medicine strategy for amyotrophic lateral sclerosisSarah Boddy, Mahjabin Islam, Tobias Moll, et al.
Cell Systems|June 11, 2022
Multiomic analysis reveals cell-type-specific molecular determinants of COVID-19 severitySai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.
Pageof 4