Dose-dependent expression of claudin-5 is a modifying factor in schizophrenia
Greene, C, Kealy, J, Humphries, M M, Gong, Y, Hou, J, Hudson, N, Cassidy, L M, Martiniano, R, Shashi, V, Hooper, S R, Grant, G A, Kenna, P F, Norris, K, Callaghan, C K, Islam, M dN, O'Mara, S M, Najda, Z, Campbell, S G, Pachter, J S, Thomas, J, Williams, N M, Humphries, P, Murphy, K C, Campbell, M
Published in Molecular psychiatry (01.11.2018)
Published in Molecular psychiatry (01.11.2018)
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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.
Published in Proceedings of the National Academy of Sciences - PNAS (06.02.2018)
Published in Proceedings of the National Academy of Sciences - PNAS (06.02.2018)
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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
Published in European journal of human genetics : EJHG (01.04.2021)
Published in European journal of human genetics : EJHG (01.04.2021)
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Gene-based therapies for dominantly inherited retinopathies
Farrar, G J, Millington-Ward, S, Chadderton, N, Humphries, P, Kenna, P F
Published in Gene therapy (01.02.2012)
Published in Gene therapy (01.02.2012)
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Journal Article
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
Zhang, Sai, Cooper-Knock, Johnathan, Weimer, Annika K., Shi, Minyi, Moll, Tobias, Marshall, Jack N.G., Harvey, Calum, Nezhad, Helia Ghahremani, Franklin, John, Souza, Cleide dos Santos, Ning, Ke, Wang, Cheng, Li, Jingjing, Dilliott, Allison A., Farhan, Sali, Elhaik, Eran, Pasniceanu, Iris, Livesey, Matthew R., Eitan, Chen, Hornstein, Eran, Kenna, Kevin P., Blair, Ian, Wray, Naomi R., Kiernan, Matthew, Mitne Neto, Miguel, Chio, Adriano, Cauchi, Ruben, Robberecht, Wim, van Damme, Philip, Corcia, Philippe, Couratier, Philippe, Hardiman, Orla, McLaughin, Russell, Gotkine, Marc, Drory, Vivian, Ticozzi, Nicola, Silani, Vincenzo, Veldink, Jan H., van den Berg, Leonard H., de Carvalho, Mamede, Mora Pardina, Jesus S., Povedano, Monica, Andersen, Peter, Weber, Markus, Başak, Nazli A., Al-Chalabi, Ammar, Shaw, Chris, Shaw, Pamela J., Morrison, Karen E., Landers, John E., Glass, Jonathan D., Veldink, Jan H., Ferraiuolo, Laura, Shaw, Pamela J., Snyder, Michael P.
Published in Neuron (Cambridge, Mass.) (16.03.2022)
Published in Neuron (Cambridge, Mass.) (16.03.2022)
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Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis
Harvey, Calum, Weinreich, Marcel, Lee, James A.K., Shaw, Allan C., Ferraiuolo, Laura, Mortiboys, Heather, Zhang, Sai, Hop, Paul J., Zwamborn, Ramona A.J., van Eijk, Kristel, Julian, Thomas H., Moll, Tobias, Iacoangeli, Alfredo, Al Khleifat, Ahmad, Quinn, John P., Pfaff, Abigail L., Kõks, Sulev, Poulton, Joanna, Battle, Stephanie L., Arking, Dan E., Snyder, Michael P., Veldink, Jan H., Kenna, Kevin P., Shaw, Pamela J., Cooper-Knock, Johnathan
Published in Heliyon (15.02.2024)
Published in Heliyon (15.02.2024)
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Journal Article
Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene
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, Blair, Ian, Wray, Naomi, Kiernan, Matthew, Neto, Miguel Mitne, Chio, Adriano, Cauchi, Ruben, Robberecht, Wim, van Damme, Philip, Corcia, Phillippe, Couratier, Phillipe, Hardiman, Orla, McLaughlin, Russel, Gotkine, Marc, Drory, Vivan, Ticozzi, Nicola, Silani, Vincenzo, Veldink, Jan, van den Berg, Leonard, de Carvalho, Mamede, Pardina, Jesus Mora, Povedano, Monica, Andersen, Peter, Wber, Markus, Başak, Nazli, Al-Chalabi, Ammar, Shaw, Christopher, Shaw, Pamela, Morrison, Karen, Landers, John, Glass, Jonathan, Veldink, Jan H., Kirby, Janine, Snyder, Michael P., Shaw, Pamela J.
Published in Cell reports (Cambridge) (01.12.2020)
Published in Cell reports (Cambridge) (01.12.2020)
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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
Published in Current opinion in neurology (01.10.2021)
Published in Current opinion in neurology (01.10.2021)
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Journal Article
Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal dominant Retinitis pigmentosa: the Rho(-/-) mouse
Campbell, M, Humphries, M, Kennan, A, Kenna, P, Humphries, P, Brankin, B
Published in Experimental eye research (01.09.2006)
Published in Experimental eye research (01.09.2006)
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Journal Article
Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS
Smith, Bradley N., Ticozzi, Nicola, Fallini, Claudia, Gkazi, Athina Soragia, Topp, Simon, Kenna, Kevin P., Scotter, Emma L., Kost, Jason, Keagle, Pamela, Miller, Jack W., Calini, Daniela, Vance, Caroline, Danielson, Eric W., Troakes, Claire, Tiloca, Cinzia, Al-Sarraj, Safa, Lewis, Elizabeth A., King, Andrew, Colombrita, Claudia, Pensato, Viviana, Castellotti, Barbara, de Belleroche, Jacqueline, Baas, Frank, ten Asbroek, Anneloor LMA, Sapp, Peter C., McKenna-Yasek, Diane, McLaughlin, Russell L., Polak, Meraida, Asress, Seneshaw, Esteban-Pérez, Jesús, Muñoz-Blanco, José Luis, Simpson, Michael, D’Alfonso, Sandra, Mazzini, Letizia, Comi, Giacomo P., Del Bo, Roberto, Ceroni, Mauro, Gagliardi, Stella, Querin, Giorgia, Bertolin, Cinzia, van Rheenen, Wouter, Diekstra, Frank P., Lauria, Giuseppe, Duga, Stefano, Corti, Stefania, Cereda, Cristina, Corrado, Lucia, Sorarù, Gianni, Morrison, Karen E., Williams, Kelly L., Nicholson, Garth A., Blair, Ian P., Dion, Patrick A., Leblond, Claire S., Rouleau, Guy A., Hardiman, Orla, Veldink, Jan H., van den Berg, Leonard H., Al-Chalabi, Ammar, Pall, Hardev, Shaw, Pamela J., Turner, Martin R., Talbot, Kevin, Taroni, Franco, García-Redondo, Alberto, Wu, Zheyang, Glass, Jonathan D., Gellera, Cinzia, Ratti, Antonia, Brown, Robert H., Silani, Vincenzo, Shaw, Christopher E., Landers, John E.
Published in Neuron (Cambridge, Mass.) (22.10.2014)
Published in Neuron (Cambridge, Mass.) (22.10.2014)
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Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing
Kenna, Kevin P, McLaughlin, Russell L, Byrne, Susan, Elamin, Marwa, Heverin, Mark, Kenny, Elaine M, Cormican, Paul, Morris, Derek W, Donaghy, Colette G, Bradley, Daniel G, Hardiman, Orla
Published in Journal of medical genetics (01.11.2013)
Published in Journal of medical genetics (01.11.2013)
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Journal Article
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function
de Majo, Martina, Topp, Simon D., Smith, Bradley N., Nishimura, Agnes L., Chen, Han-Jou, Gkazi, Athina Soragia, Miller, Jack, Wong, Chun Hao, Vance, Caroline, Baas, Frank, ten Asbroek, Anneloor L.M.A., Kenna, Kevin P., Ticozzi, Nicola, Redondo, Alberto Garcia, Esteban-Pérez, Jesús, Tiloca, Cinzia, Verde, Federico, Duga, Stefano, Morrison, Karen E., Shaw, Pamela J., Kirby, Janine, Turner, Martin R., Talbot, Kevin, Hardiman, Orla, Glass, Jonathan D., de Belleroche, Jacqueline, Gellera, Cinzia, Ratti, Antonia, Al-Chalabi, Ammar, Brown, Robert H., Silani, Vincenzo, Landers, John E., Shaw, Christopher E.
Published in Neurobiology of aging (01.11.2018)
Published in Neurobiology of aging (01.11.2018)
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Journal Article
The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public
van der Spek, Rick A.A., van Rheenen, Wouter, Pulit, Sara L., Kenna, Kevin P., van den Berg, Leonard H., Veldink, Jan H.
Published in Amyotrophic lateral sclerosis and frontotemporal degeneration (03.07.2019)
Published in Amyotrophic lateral sclerosis and frontotemporal degeneration (03.07.2019)
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Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease
Hop, Paul J., Lai, Dongbing, Keagle, Pamela J., Baron, Desiree M., Kenna, Brendan J., Kooyman, Maarten, Shankaracharya, Halter, Cheryl, Straniero, Letizia, Asselta, Rosanna, Bonvegna, Salvatore, Soto-Beasley, Alexandra I., Wszolek, Zbigniew K., Uitti, Ryan J., Isaias, Ioannis Ugo, Pezzoli, Gianni, Ticozzi, Nicola, Ross, Owen A., Veldink, Jan H., Foroud, Tatiana M., Kenna, Kevin P., Landers, John E.
Published in Nature genetics (01.07.2024)
Published in Nature genetics (01.07.2024)
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Journal Article
Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene
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.
Published in Cell reports (Cambridge) (02.02.2021)
Published in Cell reports (Cambridge) (02.02.2021)
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Economic and sustainability benefits of the United States Golf Association's research investment in putting green construction, naturalized rough, and turfgrass breeding
Thompson, Cole, Kridel, Donald J., Kenna, Michael P.
Published in Crop, forage & turfgrass management (2022)
Published in Crop, forage & turfgrass management (2022)
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Strategems in Vitro for Gene Therapies Directed to Dominant Mutations
Millington-Ward, Sophia, O'Neill, Brian, Tuohy, Gearoid, Al-Jandal, Najma, Kiang, Anna-Sophia, Kenna, Paul F., Palfi, Arpad, Hayden, Patrick, Mansergh, Fiona, Kennan, Avril, Humphries, Peter, Farrar, G. Jane
Published in Human molecular genetics (01.09.1997)
Published in Human molecular genetics (01.09.1997)
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Multiomic analysis reveals cell-type-specific molecular determinants of COVID-19 severity
Zhang, Sai, Cooper-Knock, Johnathan, Weimer, Annika K., Shi, Minyi, Kozhaya, Lina, Unutmaz, Derya, Harvey, Calum, Julian, Thomas H., Furini, Simone, Frullanti, Elisa, Fava, Francesca, Renieri, Alessandra, Gao, Peng, Shen, Xiaotao, Timpanaro, Ilia Sarah, Kenna, Kevin P., Baillie, J. Kenneth, Davis, Mark M., Tsao, Philip S., Snyder, Michael P.
Published in Cell Systems (17.08.2022)
Published in Cell Systems (17.08.2022)
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