X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (4) 4
humans (3) 3
als (2) 2
amyotrophic lateral sclerosis (2) 2
analysis (2) 2
basic medicine (2) 2
disease (2) 2
dna-damage (2) 2
genes (2) 2
genetic aspects (2) 2
genomes (2) 2
genomics (2) 2
medical and health sciences (2) 2
medicin och hälsovetenskap (2) 2
medicinska och farmaceutiska grundvetenskaper (2) 2
mutation - genetics (2) 2
mutations (2) 2
risk factors (2) 2
06 biological sciences (1) 1
11 medical and health sciences (1) 1
1948 (1) 1
1949 (1) 1
1969-1994 (1) 1
adams, gerry (1) 1
adams, gerry, 1948 (1) 1
adenocarcinoma (1) 1
adolescent (1) 1
als; gwas; kif5a; wes; wgs; axonal transport; cargo (1) 1
alzheimers disease (1) 1
amyotrophic lateral sclerosis - epidemiology (1) 1
amyotrophic lateral sclerosis - genetics (1) 1
amyotrophic-lateral-sclerosis (1) 1
article (1) 1
association (1) 1
axonal transport (1) 1
axonal-transport (1) 1
belfast (1) 1
biography (1) 1
cancer (1) 1
cancer genes (1) 1
carcinoma, pancreatic ductal - genetics (1) 1
carcinoma, pancreatic ductal - metabolism (1) 1
cargo (1) 1
case-control studies (1) 1
cell biology (1) 1
cerebral infarction - complications (1) 1
cerebral infarction - pathology (1) 1
charcot-marie-tooth disease (1) 1
choroidal artery (1) 1
cohort studies (1) 1
consortia (1) 1
copy-number alteration (1) 1
cytoskeleton (1) 1
developmental biology (1) 1
digestive system diseases (1) 1
dna methylation (1) 1
endocrine system diseases (1) 1
epigenesis, genetic - genetics (1) 1
exome - genetics (1) 1
familial als (1) 1
gastrointestinal diseases (1) 1
gene expression profiling (1) 1
gene expression regulation, neoplastic (1) 1
genetic association studies (1) 1
genetic predisposition to disease (1) 1
genetic research (1) 1
genetic variation (1) 1
genetics & heredity (1) 1
geniculate bodies - pathology (1) 1
genome-wide association studies (1) 1
genomics - methods (1) 1
genotype imputation (1) 1
government and politics (1) 1
gwas (1) 1
health aspects (1) 1
hemianopsia - etiology (1) 1
hemianopsia - pathology (1) 1
hereditary pancreatitis (1) 1
hereditary spastic paraplegia (1) 1
heterogeneity (1) 1
hexanucleotide repeat (1) 1
history (1) 1
hnf1a-as1 regulates proliferation (1) 1
homeostasis (1) 1
identification (1) 1
identification and classification (1) 1
inflammatory bowel diseases - complications (1) 1
ireland (1) 1
irish republican army (1) 1
irish unification question (1) 1
kif5a (1) 1
kinases (1) 1
kinesin heavy-chain (1) 1
kras (1) 1
legislators (1) 1
long noncoding rna (1) 1
magnetic resonance imaging (1) 1
male (1) 1
medical genetics (1) 1
medicinsk genetik (1) 1
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Kenna, Kevin P and van Doormaal, Perry T. C and Dekker, Annelot M and Ticozzi, Nicola and Kenna, Brendan J and Diekstra, Frank P and van Rheenen, Wouter and van Eijk, Kristel R and Jones, Ashley R and Keagle, Pamela and Shatunov, Aleksey and Sproviero, William and Smith, Bradley N and van Es, Michael A and Topp, Simon D and Kenna, Aoife and Miller, Jack W and Fallini, Claudia and Tiloca, Cinzia and McLaughlin, Russell L and Vance, Caroline and Troakes, Claire and Colombrita, Claudia and Mora, Gabriele and Calvo, Anea and Verde, Federico and Al-Sarraj, Safa and King, Anew and Calini, Daniela and de Belleroche, Jacqueline and Baas, Frank and van der Kooi, Anneke J and de Visser, Marianne and ten Asbroek, Anneloor L. M. A and Sapp, Peter C and McKenna-Yasek, Diane and Polak, Meraida and Asress, Seneshaw and Muñoz-Blanco, José Luis and Strom, Tim M and Meitinger, Thomas and Morrison, Karen E and Lauria, Giuseppe and Williams, Kelly L and Leigh, P. Nigel and Nicholson, Garth A and Blair, Ian P and Leblond, Claire S and Dion, Patrick A and Rouleau, Guy A and Pall, Hardev and Shaw, Pamela J and Turner, Martin R and Talbot, Kevin and Taroni, Franco and Boylan, Kevin B and van Blitterswijk, Marka and Rademakers, Rosa and Esteban-Pérez, Jesús and García-Redondo, Alberto and van Damme, Phillip and Robberecht, Wim and Chio, Aiano and Gellera, Cinzia and pper, Carsten and Sendtner, Michael and Ratti, Antonia and Glass, Jonathan D and Mora, Jesús S and Basak, Nazli A and Hardiman, Orla and Ludolph, Albert C and Andersen, Peter M and Weishaupt, Jochen H and Brown, Robert H and Al-Chalabi, Ammar and Silani, Vincenzo and Shaw, Christopher E and van den Berg, Leonard H and Veldink, Jan H and Landers, John E and D'alfonso, Sana and Mazzini, Letizia and Comi, Giacomo P and del Bo, Roberto and Ceroni, Mauro and Gagliardi, Stella and Querin, Giorgia and Bertolin, Cinzia and Pensato, Viviana and Castellotti, Barbara and Corti, Stefania and Cereda, Cristina and Corrado, Lucia and Sorarù, Gianni and SLAGEN Consortium and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Klinisk neurovetenskap and Umeå universitet
Nature genetics, ISSN 1061-4036, 2016, Volume 48, Issue 9, pp. 1037 - 1042
Journal Article
by Nicolas, Aude and Kenna, Kevin P and Kenna, Aoife and Kenna, Kevin and Kenna, Brendan J and Renton, Alan E and Ticozzi, Nicola and Faghri, Faraz and Chia, Ruth and Dominov, Janice A and Nalls, Mike A and Keagle, Pamela and Rivera, Alberto M and van Rheenen, Wouter and Murphy, Natalie A and van Vugt, Joke and van Vugt, Joke J.F.A and Geiger, Joshua T and Van der Spek, Rick A and Pliner, Hannah A and Shankaracharya and Smith, Bradley N and Marangi, Giuseppe and Topp, Simon D and Abramzon, Yevgeniya and Gkazi, Athina Soragia and Eicher, John D and Logullo, Francesco O and Simone, Isabella and Simone, Isabella L and Logroscino, Giancarlo and Salvi, Fabrizio and Bartolomei, Ilaria and Borghero, Giuseppe and Murru, Maria Rita and Costantino, Emanuela and Pani, Carla and Puddu, Roberta and Caredda, Carla and Piras, Valeria and Tranquilli, Stefania and Cuccu, Stefania and Corongiu, Daniela and Melis, Maurizio and Milia, Antonio and Marrosu, Francesco and Marrosu, Maria Giovanna and Floris, Gianluca and Cannas, Antonino and Capasso, Margherita and Caponnetto, Claudia and Mancardi, Gianluigi and Origone, Paola and Mandich, Paola and Conforti, Francesca L and Cavallaro, Sebastiano and Mora, Gabriele and Mora, Jesús S and Marinou, Kalliopi and Sideri, Riccardo and Penco, Silvana and Mosca, Lorena and Lunetta, Christian and Pinter, Giuseppe Lauria and Corbo, Massimo and Riva, Nilo and Carrera, Paola and Volanti, Paolo and Mandrioli, Jessica and Fini, Nicola and Fasano, Antonio and Tremolizzo, Lucio and Arosio, Alessandro and Ferrarese, Carlo and Trojsi, Francesca and Tedeschi, Gioacchino and Monsurrò, Maria Rosaria and Piccirillo, Giovanni and Femiano, Cinzia and Ticca, Anna and Ortu, Enzo and La Bella, Vincenzo and Spataro, Rossella and Colletti, Tiziana and Sabatelli, Mario and Zollino, Marcella and Conte, Amelia and Luigetti, Marco and Lattante, Serena and Santarelli, Marialuisa and Petrucci, Antonio and Pugliatti, Maura and Pirisi, Angelo and Parish, Leslie D and Occhineri, Patrizia and Giannini, Fabio and Battistini, Stefania and Ricci, Claudia and Benigni, Michele and Cau, Tea B and ... and Genomic Translation ALS Care GTAC and ALS Sequencing Consortium and Clinical Res ALS Related Disorders and NYGC ALS Consortium and ITALSGEN Consortium and SLAGEN Consortium and French ALS Consortium and Project MinE ALS Sequencing Consor and Answer ALS Fdn and Project MinE ALS Sequencing Consortium and Genomic Translation for ALS Care (GTAC) Consortium and Answer ALS Foundation and Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Umeå universitet
Neuron, ISSN 0896-6273, 03/2018, Volume 97, Issue 6, pp. 1268 - 1283.e6
Journal Article
by Kenna, Kevin P and van Doormaal, Perry T C and Dekker, Annelot M and Ticozzi, Nicola and Kenna, Brendan J and Diekstra, Frank P and van Rheenen, Wouter and van Eijk, Kristel R and Jones, Ashley R and Keagle, Pamela and Shatunov, Aleksey and Sproviero, William and Smith, Bradley N and van Es, Michael A and Topp, Simon D and Kenna, Aoife and Miller, Jack W and Fallini, Claudia and Tiloca, Cinzia and McLaughlin, Russell L and Vance, Caroline and Troakes, Claire and Colombrita, Claudia and Mora, Gabriele and Calvo, Anea and Verde, Federico and Al-Sarraj, Safa and King, Anew and Calini, Daniela and de Belleroche, Jacqueline and Baas, Frank and van der Kooi, Anneke J and de Visser, Marianne and Ten Asbroek, Anneloor L M A and Sapp, Peter C and McKenna-Yasek, Diane and Polak, Meraida and Asress, Seneshaw and Muñoz-Blanco, José Luis and Strom, Tim M and Meitinger, Thomas and Morrison, Karen E and Lauria, Giuseppe and Williams, Kelly L and Leigh, P Nigel and Nicholson, Garth A and Blair, Ian P and Leblond, Claire S and Dion, Patrick A and Rouleau, Guy A and Pall, Hardev and Shaw, Pamela J and Turner, Martin R and Talbot, Kevin and Taroni, Franco and Boylan, Kevin B and Van Blitterswijk, Marka and Rademakers, Rosa and Esteban-Pérez, Jesús and García-Redondo, Alberto and Van Damme, Phillip and Robberecht, Wim and Chio, Aiano and Gellera, Cinzia and pper, Carsten and Sendtner, Michael and Ratti, Antonia and Glass, Jonathan D and Mora, Jesús S and Basak, Nazli A and Hardiman, Orla and Ludolph, Albert C and Andersen, Peter M and Weishaupt, Jochen H and Brown, Robert H and Al-Chalabi, Ammar and Silani, Vincenzo and Shaw, Christopher E and van den Berg, Leonard H and Veldink, Jan H and Landers, John E
Nature Genetics, ISSN 1061-4036, 07/2016, Volume 48, Issue 9, p. 1037–1042
To identify genetic factors contributing to amyotrophic lateral sclerosis (ALS), we conducted whole-exome analyses of 1,022 index familial ALS (FALS) cases and... 
Journal Article
by Raphael, Benjamin J and Hruban, Ralph H and Aguirre, Andrew J and Moffitt, Richard A and Yeh, Jen Jen and Stewart, Chip and Robertson, A. Gordon and Cherniack, Andrew D and Gupta, Manaswi and Getz, Gad and Gabriel, Stacey B and Meyerson, Matthew and Cibulskis, Carrie and Fei, Suzanne S and Hinoue, Toshinori and Shen, Hui and Laird, Peter W and Ling, Shiyun and Lu, Yiling and Mills, Gordon B and Akbani, Rehan and Loher, Phillipe and Londin, Eric R and Rigoutsos, Isidore and Telonis, Aristeidis G and Gibb, Ewan A and Goldenberg, Anna and Mezlini, Aziz M and Hoadley, Katherine A and Collisson, Eric and Lander, Eric and Murray, Bradley A and Hess, Julian and Rosenberg, Mara and Bergelson, Louis and Zhang, Wei and Zhang, Hailei and Zhang, Jiashan (Julia) and Zhang, Lizhi and Cho, Juok and Tiao, Grace and Kim, Seong Hoon and Kim, Hark and Kim, Jaegil and Kim, Paula and Kim, Yong Hoon and Livitz, Dimitri and Leshchiner, Ignaty and Reardon, Brendan and Van Allen, Eliezer and Kamburov, Atanas and Beroukhim, Rameen and Saksena, Gordon and Schumacher, Steven E and Noble, Michael S and Heiman, David I and Gehlenborg, Nils and Lawrence, Michael S and Adsay, Volkan and Petersen, Gloria and Klimstra, David and Bardeesy, Nabeel and Leiserson, Mark D.M and Bowlby, Reanne and Kasaian, Katayoon and Birol, Inanc and Mungall, Andrew J and Mungall, Karen L and Sadeghi, Sara and Weinstein, John N and Spellman, Paul T and Liu, Yuexin and Liu, Jia and Amundadottir, Laufey T and Tepper, Joel and Singhi, Aatur D and Dhir, Rajiv and Paul, Drwiega and Smyrk, Thomas and Bowen, Jay and Frick, Jessica and Gastier-Foster, Julie M and Gerken, Mark and Lau, Kevin and Leraas, Kristen M and Lichtenberg, Tara M and Ramirez, Nilsa C and Renkel, Jeremy and Sherman, Mark and Wise, Lisa and Yena, Peggy and Zmuda, Erik and Shih, Juliann and Ally, Adrian and Balasundaram, Miruna and Carlsen, Rebecca and Chu, Andy and Chuah, Eric and Clarke, Amanda and Dhalla, Noreen and ... and Canc Genome Atlas Res Network and Cancer Genome Atlas Research Network. Electronic address: andrew_aguirre@dfci.harvard.edu and Cancer Genome Atlas Research Network
Cancer Cell, ISSN 1535-6108, 08/2017, Volume 32, Issue 2, pp. 185 - 203.e13
Journal Article
The Irish Times (1921-Current File), 01/1983, p. 9
Newspaper Article
Philadelphia Inquirer, ISSN 0885-6613, 05/1992
Newspaper Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.