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dr. K.P. (Kevin) Kenna

dr. K.P. (Kevin) Kenna

Associate Professor

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Research Output (45)

CHCHD10 variants in amyotrophic lateral sclerosis:Where is the evidence?

Kenna Kevin Jul 2018, In: Annals of Neurology. 84 , p. 110-116 7 p.

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

Nicolas Aude, Kenna Kevin P., Renton Alan E., Ticozzi Nicola, Faghri Faraz, Chia Ruth, Dominov Janice A., Kenna Brendan J., Nalls Mike A., Keagle Pamela, Rivera Alberto M., van Rheenen Wouter, Murphy Natalie A., van Vugt Joke J.F.A., Geiger Joshua T., van der Spek Rick, Pliner Hannah A., Shankaracharya , Smith Bradley N., Marangi Giuseppe, Topp Simon D., Abramzon Yevgeniya, Gkazi Athina Soragia, Eicher John D., Kenna Aoife, Logullo Francesco O., Simone Isabella L., Logroscino Giancarlo, Salvi Fabrizio, Van Eijk Kristel R., Middelkoop Bas, Moisse Matthieu, McLaughlin Russell, Van Es Michael A., Dekker Annelot, Kenna Kevin P., McLaughlin Russell, Middelkoop Bas, Moisse Matthieu, Pulit Sara, Tazelaar Gijs, van den Berg Leonard, van der Spek Rick, Van Eijk Kristel R., Van Es Michael A., van Rheenen Wouter, van Vugt Joke J.F.A., Veldink Jan H., van den Berg Leonard, Veldink Jan H., , , , , , , , , 21 Mar 2018, In: Neuron. 97 , p. 1268-1283.e6

Transcription factor Pebbled/RREB1 regulates injury-induced axon degeneration

Farley Jonathan E, Burdett Thomas C, Barria Romina, Neukomm Lukas J, Kenna Kevin P, Landers John E, Freeman Marc R 6 Feb 2018, In: Proceedings of the National Academy of Sciences of the United States of America. 115 , p. 1358-1363 6 p.

Reconsidering the causality of TIA1 mutations in ALS

Van Der Spek Rick A., Van Rheenen Wouter, Pulit Sara L., Kenna Kevin P., Ticozzi Nicola, Kooyman Maarten, McLaughlin Russell L., Moisse Matthieu, Van Eijk Kristel R., Van Vugt Joke J.F.A., Andersen Jens Peter, Nazli Basak A., Blair Ian, de Carvalho Mamede, Chio Adriano, Corcia Philippe, Couratier Phillipe, Drory Vivian E, Glass Jonathan D, Hardiman Orla, Mora Jesús S., Morrison Karen E, Mitne-Neto Miguel, Robberecht Wim, Shaw Pamela J, Panadés Monica P, Van Damme Philip, Silani Vincenzo, Gotkine Marc, Weber Markus, Van Es Michael A., Landers John E, Al-Chalabi Ammar, Van Den Berg Leonard H., Veldink Jan H., 12 Dec 2017, In: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 19 , p. 1-3 3 p.

Targeted genetic screen in amyotrophic lateral sclerosis reveals novel genetic variants with synergistic effect on clinical phenotype

Cooper-Knock Johnathan, Robins Henry, Niedermoser Isabell, Wyles Matthew, Heath Paul R., Higginbottom Adrian, Walsh Theresa, Kazoka Mbombe, Al Kheifat Ahmad, Al-Chalabi Ammar, Basak Nazli, Blair Ian, Dekker Annelot, Hardiman Orla, Hide Winston, Iacoangeli Alfredo, Kenna Kevin, Landers John, McLaughlin Russel, Mill Jonathan, Middelkoop Bas, Moisse Mattieu, Pardina Jesus Mora, Morrison Karen, Newhouse Stephen, Pulit Sara, Shatunov Aleksey, Shaw Chris, Sproviero William, Tazelaar Gijs, van Damme Philip, van den Berg Leonard, van der Spek Rick, Eijk Kristelvan, van Es Michael, van Rheenen Wouter, van Vugt Joke, Veldink Jan, Kooyman Maarten, Glass Jonathan, Robberecht Wim, Gotkine Marc, Drory Vivian, Kiernan Matthew, Neto Miguel Mitne, Ztaz Mayana, Couratier Philippe, Corcia Philippe, Silani Vincenzo, Chio Adriano, 9 Nov 2017, In: Frontiers in Molecular Neuroscience. 10

The role of de novo mutations in the development of amyotrophic lateral sclerosis

van Doormaal Perry T C, Ticozzi Nicola, Weishaupt Jochen H, Kenna Kevin P, Diekstra Frank P, Verde Federico, Andersen Peter M., Dekker Annelot M, Tiloca Cinzia, Marroquin Nicolai, Overste Daniel J, Pensato Viviana, Nürnberg Peter, Pulit Sara L, Schellevis Raymond D., Calini Daniela, Altmüller Janine, Francioli Laurent C, Muller Bernard, Castellotti Barbara, Motameny Susanne, Ratti Antonia, Wolf Joachim, Gellera Cinzia, Ludolph Albert C, van den Berg Leonard H, Kubisch Christian, Landers John E, Veldink Jan H, Silani Vincenzo, Volk Alexander E 17 Jul 2017, In: Human Mutation. 38 , p. 1534-1541 8 p.

Mutations in the vesicular trafficking protein Annexin A11 are associated with amyotrophic lateral sclerosis Bradley N. Smith

Smith Bradley N, Topp Simon D, Fallini Claudia, Shibata Hideki, Chen Han-Jou, Troakes Claire, King Andrew, Ticozzi Nicola, Kenna Kevin P, Soragia-Gkazi Athina, Miller Jack W, Sato Akane, Dias Diana Marques, Jeon Maryangel, Vance Caroline, Wong Chun Hao, de Majo Martina, Kattuah Wejdan, Mitchell Jacqueline C, Scotter Emma L, Parkin Nicholas W, Sapp Peter C, Nolan Matthew, Nestor Peter J, Simpson Michael, Weale Michael, Lek Monkel, Baas Frank, Vianney de Jong J M, Ten Asbroek Anneloor L M A, Redondo Alberto Garcia, Esteban-Pérez Jesús, Tiloca Cinzia, Verde Federico, Duga Stefano, Leigh Nigel, Pall Hardev, Morrison Karen E, Al-Chalabi Ammar, Shaw Pamela J, Kirby Janine, Turner Martin R, Talbot Kevin, Hardiman Orla, Glass Jonathan D, De Belleroche Jacqueline, Maki Masatoshi, Moss Stephen E, Miller Christopher, Gellera Cinzia, 3 May 2017, In: Science translational medicine. 9

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

van Rheenen Wouter, Shatunov Aleksey, Dekker Annelot M, McLaughlin Russell L, Diekstra Frank P, Pulit Sara L, van der Spek Rick A A, Võsa Urmo, de Jong Simone, Robinson Matthew R, Yang Jian, Fogh Isabella, van Doormaal Perry Tc, Tazelaar Gijs H P, Koppers Max, Blokhuis Anna M, Sproviero William, Jones Ashley R, Kenna Kevin P, van Eijk Kristel R, Harschnitz Oliver, Schellevis Raymond D, Brands William J, Medic Jelena, Menelaou Androniki, Vajda Alice, Ticozzi Nicola, Lin Kuang, Rogelj Boris, Vrabec Katarina, Ravnik-Glavač Metka, Koritnik Blaž, Zidar Janez, Leonardis Lea, Grošelj Leja Dolenc, Millecamps Stéphanie, Salachas François, Meininger Vincent, de Carvalho Mamede, Pinto Susana, Mora Jesus S, Rojas-García Ricardo, Polak Meraida, Ophoff Roel A. , Blauw Hylke M, de Bakker Paul I W, van Es Michael A, Pasterkamp R Jeroen, van den Berg Leonard H, Veldink Jan H, Sep 2016, In: Nature Genetics. 48 , p. 1043–1048

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

Kenna Kevin P, van Doormaal Perry T C, Dekker Annelot M, Ticozzi Nicola, Kenna Brendan J, Diekstra Frank P, van Rheenen Wouter, van Eijk Kristel R, Jones Ashley R, Keagle Pamela, Shatunov Aleksey, Sproviero William, Smith Bradley N, van Es Michael A, Topp Simon D, Kenna Aoife, Miller Jack W, Fallini Claudia, Tiloca Cinzia, McLaughlin Russell L, Vance Caroline, Troakes Claire, Colombrita Claudia, Mora Gabriele, Calvo Andrea, Verde Federico, Al-Sarraj Safa, King Andrew, Calini Daniela, de Belleroche Jacqueline, Baas Frank, van der Kooi Anneke J, de Visser Marianne, Ten Asbroek Anneloor L M A, Sapp Peter C, McKenna-Yasek Diane, Polak Meraida, Asress Seneshaw, Muñoz-Blanco José Luis, Strom Tim M, Meitinger Thomas, Morrison Karen E, Lauria Giuseppe, Williams Kelly L, Leigh P Nigel, Nicholson Garth A, Blair Ian P, Leblond Claire S, van den Berg Leonard H, Veldink Jan H, 25 Jul 2016, In: Nature Genetics. 48 , p. 1037–1042

The selective anatomical vulnerability of ALS: 'disease-defining' and 'disease-defying' brain regions

Bede Peter, Iyer Parameswaran M, Schuster Christina, Elamin Marwa, Mclaughlin Russell L, Kenna Kevin, Hardiman Orla 19 Apr 2016, In: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 17 , p. 561-570 10 p.

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