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dr. K.P. (Kevin) Kenna

dr. K.P. (Kevin) Kenna

Associate Professor
dr. K.P. (Kevin) Kenna
  • Neurology & Neurosurgery

Research Output (40)

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

Johnson Janel O, Chia Ruth, Miller Danny E, Li Rachel, Kumaran Ravindran, Abramzon Yevgeniya, Alahmady Nada, Renton Alan E, Topp Simon D, Gibbs J Raphael, Cookson Mark R, Sabir Marya S, Dalgard Clifton L, Troakes Claire, Jones Ashley R, Shatunov Aleksey, Iacoangeli Alfredo, Al Khleifat Ahmad, Ticozzi Nicola, Silani Vincenzo, Gellera Cinzia, Blair Ian P, Dobson-Stone Carol, Kwok John B, Bonkowski Emily S, Palvadeau Robin, Tienari Pentti J, Morrison Karen E, Shaw Pamela J, Al-Chalabi Ammar, Brown Robert H, Calvo Andrea, Mora Gabriele, Al-Saif Hind, Gotkine Marc, Leigh Fawn, Chang Irene J, Perlman Seth J, Glass Ian, Scott Anna I, Shaw Christopher E, Basak A Nazli, Landers John E, Chiò Adriano, Crawford Thomas O, Kenna Kevin P, McLaughlin Russell L, van Rheenen Wouter, Veldink Jan H, van den Berg Leonard H, 30 aug 2021, In: JAMA Neurology. 78 , p. 1236-1248 13 p.

Advances in the genetic classification of amyotrophic lateral sclerosis

Cooper-Knock Johnathan, Harvey Calum, Zhang Sai, Moll Tobias, Timpanaro Ilia Sarah, Kenna Kevin P, Iacoangeli Alfredo, Veldink Jan H 2 aug 2021, In: Current Opinion in Neurology. 34 , p. 756-764

Common and rare variant analyses combined with single-cell multiomics reveal cell-type-specific molecular mechanisms of COVID-19 severity

Zhang Sai, Cooper-Knock Johnathan, Weimer Annika K, Harvey Calum, Julian Thomas H, Wang Cheng, Li Jingjing, Furini Simone, Frullanti Elisa, Fava Francesca, Renieri Alessandra, Pan Cuiping, Song Jina, Billing-Ross Paul, Gao Peng, Shen Xiaotao, Timpanaro Ilia Sarah, Kenna Kevin P, Davis Mark M, Tsao Philip S, Snyder Michael P, 21 jun 2021, p. 1-82

Genetic analysis of ALS cases in the isolated island population of Malta

Borg Rebecca, Farrugia Wismayer Maia, Bonavia Karl, Farrugia Wismayer Andrew, Vella Malcolm, van Vugt Joke J F A, Kenna Brendan J, Kenna Kevin P, Vassallo Neville, Veldink Jan H, Cauchi Ruben J apr 2021, In: European Journal of Human Genetics. 29 , p. 604-614 11 p.

The Effect of SMN Gene Dosage on ALS Risk and Disease Severity

Moisse Matthieu, Zwamborn Ramona A J, van Vugt Joke, van der Spek Rick, van Rheenen Wouter, Kenna Brendan, Van Eijk Kristel, Kenna Kevin, Corcia Philippe, Couratier Philippe, Vourc'h Patrick, Hardiman Orla, McLaughin Russell, Gotkine Marc, Drory Vivian, Ticozzi Nicola, Silani Vincenzo, de Carvalho Mamede, Mora Pardina Jesús S, Povedano Monica, Andersen Peter M, Weber Markus, Başak Nazli A, Chen Xiao, Eberle Michael A, Al-Chalabi Ammar, Shaw Chris, Shaw Pamela J, Morrison Karen E, Landers John E, Glass Jonathan D, Robberecht Wim, van Es Michael, van den Berg Leonard, Veldink Jan, Van Damme Philip, apr 2021, In: Annals of Neurology. 89 , p. 686-697 12 p.

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Dewan Ramita, Chia Ruth, Ding Jinhui, Hickman Richard A, Stein Thor D, Abramzon Yevgeniya, Ahmed Sarah, Sabir Marya S, Portley Makayla K, Tucci Arianna, Ibáñez Kristina, Shankaracharya F N U, Keagle Pamela, Rossi Giacomina, Caroppo Paola, Tagliavini Fabrizio, Waldo Maria L, Johansson Per M, Nilsson Christer F, Rowe James B, Benussi Luisa, Binetti Giuliano, Ghidoni Roberta, Jabbari Edwin, Viollet Coralie, Glass Jonathan D, Singleton Andrew B, Silani Vincenzo, Ross Owen A, Ryten Mina, Torkamani Ali, Tanaka Toshiko, Ferrucci Luigi, Resnick Susan M, Pickering-Brown Stuart, Brady Christopher B, Kowal Neil, Hardy John A, Van Deerlin Vivianna, Vonsattel Jean Paul, Harms Matthew B, Morris Huw R, Ferrari Raffaele, Landers John E, Chiò Adriano, Gibbs J Raphael, Dalgard Clifton L, Scholz Sonja W, Traynor Bryan J, , , Kenna Kevin, , , , , , 3 feb 2021, In: Neuron. 109 , p. 448-460.e4

Erratum:Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene (Cell Reports (2020) 33(9), (S2211124720314455), (10.1016/j.celrep.2020.108456))

Cooper-Knock Johnathan, Zhang Sai, Kenna Kevin P, Moll Tobias, Franklin John P, Allen Samantha, Nezhad Helia Ghahremani, Iacoangeli Alfredo, Yacovzada Nancy Y, Eitan Chen, Hornstein Eran, Elhaik Eran, Celadova Petra, Bose Daniel, Farhan Sali, Fishilevich Simon, Lancet Doron, Morrison Karen E, Shaw Christopher E, Al-Chalabi Ammar, Veldink Jan H, Kirby Janine, Snyder Michael P, Shaw Pamela J, 2 feb 2021, In: Cell Reports. 34 , p. 108730

Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

Schijven Dick, Stevelink Remi, McCormack Mark, van Rheenen Wouter, Luykx Jurjen J, Koeleman Bobby P C, Veldink Jan H, , Kenna Kevin aug 2020, In: Neurobiology of Aging. 92 , p. 153.e1-153.e5

Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

Schijven Dick, Stevelink Remi, McCormack Mark, van Rheenen Wouter, Luykx Jurjen J., Koeleman Bobby P.C., Veldink Jan H., , , Kenna Kevin 1 jan 2020, In: Neurobiology of Aging. 92 , p. 153.e1-153.e5

ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization

Tazelaar Gijs H P, Boeynaems Steven, De Decker Mathias, van Vugt Joke J F A, Kool Lindy, Goedee H Stephan, McLaughlin Russell L, Sproviero William, Iacoangeli Alfredo, Moisse Matthieu, Jacquemyn Maarten, Daelemans Dirk, Dekker Annelot M, van der Spek Rick A, Westeneng Henk-Jan, Kenna Kevin P, Assialioui Abdelilah, Da Silva Nica, Povedano Mónica, Pardina Jesus S Mora, Hardiman Orla, Salachas François, Millecamps Stéphanie, Vourc'h Patrick, Corcia Philippe, Couratier Philippe, Morrison Karen E, Shaw Pamela J, Shaw Christopher E, Pasterkamp R Jeroen, Landers John E, Van Den Bosch Ludo, Robberecht Wim, Al-Chalabi Ammar, van den Berg Leonard H, Van Damme Philip, Veldink Jan H, van Es Michael A, 2020, In: Brain communications. 2 , p. 1-13

All research output

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