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Kevin P Kenna

Showing results (11-20 of 32) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|June 30, 2021
Common and rare variant analyses combined with single-cell multiomics reveal cell-type-specific molecular mechanisms of COVID-19 severitySai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.
Biorxiv : the Preprint Server for Biology|August 2, 2024
predicTTE: An accessible and optimal tool for time-to-event prediction in neurological diseasesMarcel Weinreich, Harry McDonough, Nancy Yacovzada, et al.
Nature Genetics|June 10, 2024
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's diseasePaul J Hop, Dongbing Lai, Pamela J Keagle, et al.
Cell Reports|December 2, 2020
Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk GeneJohnathan Cooper-Knock, Sai Zhang, Kevin P Kenna, et al.
Neuron|January 19, 2022
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosisSai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.
Medrxiv : the Preprint Server for Health Sciences|April 18, 2024
Deep learning modeling of rare noncoding genetic variants in human motor neurons defines <i>CCDC146</i> as a therapeutic target for ALSSai Zhang, Tobias Moll, Jasper Rubin-Sigler, et al.
Heliyon|February 6, 2024
Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosisCalum Harvey, Marcel Weinreich, James A K Lee, et al.
Ebiomedicine|October 11, 2025
Optimised machine learning for time-to-event prediction in healthcare applied to timing of gastrostomy in ALS: a multi-centre, retrospective model development and validation studyMarcel Weinreich, Harry McDonough, Mark Heverin, et al.
Neurobiology of Aging|July 24, 2018
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase functionMartina de Majo, Simon D Topp, Bradley N Smith, et al.
Neurobiology of Aging|October 22, 2018
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohortGijs H P Tazelaar, Annelot M Dekker, Joke J F A van Vugt, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Medrxiv : the Preprint Server for Health Sciences|June 30, 2021
Common and rare variant analyses combined with single-cell multiomics reveal cell-type-specific molecular mechanisms of COVID-19 severitySai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.
Biorxiv : the Preprint Server for Biology|August 2, 2024
predicTTE: An accessible and optimal tool for time-to-event prediction in neurological diseasesMarcel Weinreich, Harry McDonough, Nancy Yacovzada, et al.
Nature Genetics|June 10, 2024
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's diseasePaul J Hop, Dongbing Lai, Pamela J Keagle, et al.
Cell Reports|December 2, 2020
Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk GeneJohnathan Cooper-Knock, Sai Zhang, Kevin P Kenna, et al.
Neuron|January 19, 2022
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosisSai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.
Medrxiv : the Preprint Server for Health Sciences|April 18, 2024
Deep learning modeling of rare noncoding genetic variants in human motor neurons defines <i>CCDC146</i> as a therapeutic target for ALSSai Zhang, Tobias Moll, Jasper Rubin-Sigler, et al.
Heliyon|February 6, 2024
Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosisCalum Harvey, Marcel Weinreich, James A K Lee, et al.
Ebiomedicine|October 11, 2025
Optimised machine learning for time-to-event prediction in healthcare applied to timing of gastrostomy in ALS: a multi-centre, retrospective model development and validation studyMarcel Weinreich, Harry McDonough, Mark Heverin, et al.
Neurobiology of Aging|July 24, 2018
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase functionMartina de Majo, Simon D Topp, Bradley N Smith, et al.
Neurobiology of Aging|October 22, 2018
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohortGijs H P Tazelaar, Annelot M Dekker, Joke J F A van Vugt, et al.
Pageof 4