E-LIB Suche - Ergebnisse für: Kenna, Kevin P.

1

Systematic rare variant analyses identify RAB32 as a suscep..:

Hop, Paul J. ; Lai, Dongbing ; Keagle, Pamela J....
Nature Genetics. , 2024

Link: https://doi.org/10.1038/..

2

Rare and common genetic determinants of mitochondrial funct..:

Harvey, Calum ; Weinreich, Marcel ; Lee, James A.K....
Heliyon. 10 (2024) 3 - p. e24975 , 2024

Link: https://doi.org/10.1016/..

3

Genome-wide identification of the genetic basis of amyotrop..:

Zhang, Sai ; Cooper-Knock, Johnathan ; Weimer, Annika K....
Neuron. 110 (2022) 6 - p. 992-1008.e11 , 2022

Link: https://doi.org/10.1016/..

4

Unbiased metabolome screen leads to personalized medicine s..:

Boddy, Sarah ; Islam, Mahjabin ; Moll, Tobias...
Brain Communications. 4 (2022) 2 - p. , 2022

Link: https://doi.org/10.1093/..

5

Multiomic analysis reveals cell-type-specific molecular det..:

Zhang, Sai ; Cooper-Knock, Johnathan ; Weimer, Annika K....
Cell Systems. 13 (2022) 8 - p. 598-614.e6 , 2022

Link: https://doi.org/10.1016/..

6

Whole-genome sequencing reveals that variants in the Interl..:

Eitan, Chen ; Siany, Aviad ; Barkan, Elad...
Nature Neuroscience. 25 (2022) 4 - p. 433-445 , 2022

Link: https://doi.org/10.1038/..

7

Advances in the genetic classification of amyotrophic later..:

Cooper-Knock, Johnathan ; Harvey, Calum ; Zhang, Sai...
Current Opinion in Neurology. 34 (2021) 5 - p. 756-764 , 2021

Link: https://doi.org/10.1097/..

8

Rare variant burden analysis within enhancers identifies CA..:

Cooper-Knock, Johnathan ; Zhang, Sai ; Kenna, Kevin P....
Cell Reports. 34 (2021) 5 - p. 108730 , 2021

Link: https://doi.org/10.1016/..

9

Genetic analysis of ALS cases in the isolated island popula..:

Borg, Rebecca ; Farrugia Wismayer, Maia ; Bonavia, Karl...
European Journal of Human Genetics. 29 (2021) 4 - p. 604-614 , 2021

Link: https://doi.org/10.1038/..

10

Rare Variant Burden Analysis within Enhancers Identifies CA..:

Cooper-Knock, Johnathan ; Zhang, Sai ; Kenna, Kevin P....
Cell Reports. 33 (2020) 9 - p. 108456 , 2020

Link: https://doi.org/10.1016/..

11

ATXN1 repeat expansions confer risk for amyotrophic lateral..:

Tazelaar, Gijs H P ; Boeynaems, Steven ; De Decker, Mathias...
Brain Communications. 2 (2020) 2 - p. , 2020

Link: https://doi.org/10.1093/..

12

The project MinE databrowser: bringing large-scale whole-ge..:

van der Spek, Rick A.A. ; van Rheenen, Wouter ; Pulit, Sara L....
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 20 (2019) 5-6 - p. 432-440 , 2019

Link: https://doi.org/10.1080/..

13

Association of NIPA1 repeat expansions with amyotrophic lat..:

Tazelaar, Gijs H.P. ; Dekker, Annelot M. ; van Vugt, Joke J.F.A....
Neurobiology of Aging. 74 (2019) - p. 234.e9-234.e15 , 2019

Link: https://doi.org/10.1016/..

14

Transcription factor Pebbled/RREB1 regulates injury-induced..:

Farley, Jonathan E. ; Burdett, Thomas C. ; Barria, Romina...
Proceedings of the National Academy of Sciences of the United States of America. 115 (2018) 6 - p. 1358-1363 , 2018

Link: https://www.jstor.org/st..

15

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene:

Nicolas, Aude ; Kenna, Kevin P. ; Renton, Alan E....
Neuron. 97 (2018) 6 - p. 1267-1288 , 2018

Link: https://doi.org/10.1016/..