UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (140) 140
life sciences & biomedicine (132) 132
humans (101) 101
amyotrophic lateral sclerosis (100) 100
neurosciences & neurology (89) 89
female (85) 85
male (81) 81
middle aged (67) 67
clinical neurology (62) 62
neurosciences (61) 61
aged (54) 54
adult (40) 40
neurology (31) 31
risk factors (28) 28
genetic aspects (27) 27
amyotrophic lateral sclerosis - genetics (26) 26
research (25) 25
genetics & heredity (21) 21
mutation (20) 20
genetics (16) 16
psychiatry (16) 16
analysis (15) 15
genome-wide association study (15) 15
geriatrics & gerontology (15) 15
patients (15) 15
aged, 80 and over (14) 14
genomes (14) 14
italy (14) 14
phenotype (14) 14
amyotrophic lateral sclerosis - diagnosis (13) 13
amyotrophic lateral sclerosis - psychology (13) 13
case-control studies (13) 13
disease (13) 13
genes (13) 13
internal medicine (13) 13
quality of life (13) 13
settore med/26 - neurologia (13) 13
als (12) 12
care and treatment (12) 12
cohort studies (12) 12
studies (12) 12
dementia (11) 11
disease progression (11) 11
medical and health sciences (11) 11
medical research (11) 11
medicin och hälsovetenskap (11) 11
medicine & public health (11) 11
neuroradiology (11) 11
proteins (11) 11
age (10) 10
amyotrophic lateral sclerosis - complications (10) 10
amyotrophic lateral sclerosis - epidemiology (10) 10
development and progression (10) 10
frontotemporal dementia (10) 10
genetic predisposition to disease (10) 10
genotype (10) 10
polymorphism, single nucleotide (10) 10
survival (10) 10
age of onset (9) 9
amyotrophic lateral sclerosis - pathology (9) 9
biochemistry & molecular biology (9) 9
genetic association studies (9) 9
health aspects (9) 9
motor neuron disease (9) 9
mutation - genetics (9) 9
neurodegeneration (9) 9
amyotrophic lateral sclerosis - blood (8) 8
genetic predisposition to disease - genetics (8) 8
italy - epidemiology (8) 8
life sciences (8) 8
medicine, experimental (8) 8
surgery (8) 8
adolescent (7) 7
amyotrophic lateral sclerosis - physiopathology (7) 7
clinical trials (7) 7
cognitive ability (7) 7
cross-sectional studies (7) 7
dna methylation (7) 7
double-blind method (7) 7
gene expression (7) 7
genetic loci (7) 7
loci (7) 7
medical genetics (7) 7
multidisciplinary sciences (7) 7
nervous system diseases (7) 7
neurodegenerative diseases (7) 7
neuropsychological tests (7) 7
polymorphism, single nucleotide - genetics (7) 7
proteins - genetics (7) 7
psychology (7) 7
science & technology - other topics (7) 7
survival analysis (7) 7
treatment outcome (7) 7
abridged index medicus (6) 6
age factors (6) 6
alleles (6) 6
amyotrophic lateral sclerosis - therapy (6) 6
biomarkers (6) 6
body mass index (6) 6
brain - pathology (6) 6
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by van Rheenen, Wouter and Shatunov, Aleksey and Dekker, Annelot M and McLaughlin, Russell L and Diekstra, Frank P and Pulit, Sara L and van der Spek, Rick A A and Võsa, Urmo and de Jong, Simone and Robinson, Matthew R and Yang, Jian and Fogh, Isabella and van Doormaal, Perry TC and Tazelaar, Gijs H P and Koppers, Max and Blokhuis, Anna M and Sproviero, William and Jones, Ashley R and Kenna, Kevin P and van Eijk, Kristel R and Harschnitz, Oliver and Schellevis, Raymond D and Brands, William J and Medic, Jelena and Menelaou, Androniki and Vajda, Alice and Ticozzi, Nicola and Lin, Kuang and Rogelj, Boris and Vrabec, Katarina and Ravnik-Glavač, Metka and Koritnik, Blaž and Zidar, Janez and Leonardis, Lea and Grošelj, Leja Dolenc and Millecamps, Stéphanie and Salachas, François and Meininger, Vincent and de Carvalho, Mamede and Pinto, Susana and Mora, Jesus S and Rojas-García, Ricardo and Polak, Meraida and Chandran, Siddharthan and Colville, Shuna and Swingler, Robert and Morrison, Karen E and Shaw, Pamela J and Hardy, John and Orrell, Richard W and Pittman, Alan and Sidle, Katie and Fratta, Pietro and Malaspina, Andrea and Topp, Simon and Petri, Susanne and Abdulla, Susanne and Drepper, Carsten and Sendtner, Michael and Meyer, Thomas and Ophoff, Roel A and Staats, Kim A and Wiedau-Pazos, Martina and Lomen-Hoerth, Catherine and Van Deerlin, Vivianna M and Trojanowski, John Q and Elman, Lauren and McCluskey, Leo and Basak, A Nazli and Tunca, Ceren and Hamzeiy, Hamid and Parman, Yesim and Meitinger, Thomas and Lichtner, Peter and Radivojkov-Blagojevic, Milena and Andres, Christian R and Maurel, Cindy and Bensimon, Gilbert and Landwehrmeyer, Bernhard and Brice, Alexis and Payan, Christine A M and Saker-Delye, Safaa and Dürr, Alexandra and Wood, Nicholas W and Tittmann, Lukas and Lieb, Wolfgang and Franke, Andre and Rietschel, Marcella and Cichon, Sven and Nöthen, Markus M and Amouyel, Philippe and Tzourio, Christophe and Dartigues, Jean-François and Uitterlinden, Andre G and Rivadeneira, Fernando and Estrada, Karol and Hofman, Albert and Curtis, Charles and Blauw, Hylke M and van der Kooi, Anneke J and ... and PARALS Registry and FALS Sequencing Consortium and SLALOM Group and SLAGEN Consortium and NNIPPS Study Group and SLAP Registry and SLALOM Grp and NNIPPS Study Grp
Nature genetics, ISSN 1546-1718, 07/2016, Volume 48, Issue 9, pp. 1043 - 1048
Journal Article
Journal Article
by Stolk, Lisette and Perry, John R B and Chasman, Daniel I and He, Chunyan and Mangino, Massimo and Sulem, Patrick and Barbalic, Maja and Broer, Linda and Byrne, Enda M and Ernst, Florian and Esko, Tõnu and Franceschini, Nora and Gudbjartsson, Daniel F and Hottenga, Jouke-Jan and Kraft, Peter and McArdle, Patrick F and Porcu, Eleonora and Shin, So-Youn and Smith, Albert V and van Wingerden, Sophie and Zhai, Guangju and Zhuang, Wei V and Albrecht, Eva and Alizadeh, Behrooz Z and Aspelund, Thor and Bandinelli, Stefania and Lauc, Lovorka Barac and Beckmann, Jacques S and Boban, Mladen and Boerwinkle, Eric and Broekmans, Frank J and Burri, Andrea and Campbell, Harry and Chanock, Stephen J and Chen, Constance and Cornelis, Marilyn C and Corre, Tanguy and Coviello, Andrea D and d'Adamo, Pio and Davies, Gail and de Faire, Ulf and de Geus, Eco J C and Deary, Ian J and Dedoussis, George V Z and Deloukas, Panagiotis and Ebrahim, Shah and Eiriksdottir, Gudny and Emilsson, Valur and Eriksson, Johan G and Fauser, Bart C J M and Ferreli, Liana and Ferrucci, Luigi and Fischer, Krista and Folsom, Aaron R and Garcia, Melissa E and Gasparini, Paolo and Gieger, Christian and Glazer, Nicole and Grobbee, Diederick E and Hall, Per and Haller, Toomas and Hankinson, Susan E and Hass, Merli and Hayward, Caroline and Heath, Andrew C and Hofman, Albert and Ingelsson, Erik and Janssens, A Cecile J W and Johnson, Andrew D and Karasik, David and Kardia, Sharon L R and Keyzer, Jules and Kiel, Douglas P and Kolcic, Ivana and Kutalik, Zoltán and Lahti, Jari and Lai, Sandra and Laisk, Triin and Laven, Joop S E and Lawlor, Debbie A and Liu, Jianjun and Lopez, Lorna M and Louwers, Yvonne V and Magnusson, Patrik K E and Marongiu, Mara and Martin, Nicholas G and Klaric, Irena Martinovic and Masciullo, Corrado and McKnight, Barbara and Medland, Sarah E and Melzer, David and Mooser, Vincent and Navarro, Pau and Newman, Anne B and Nyholt, Dale R and Onland-Moret, N Charlotte and Palotie, Aarno and Paré, Guillaume and Parker, Alex N and Pedersen, Nancy L and ... and LifeLines Cohort Study
Nature genetics, ISSN 1546-1718, 01/2012, Volume 44, Issue 3, pp. 260 - 268
Journal Article
Journal of neurology, ISSN 1432-1459, 10/2016, Volume 264, Issue 1, pp. 54 - 63
Journal Article
Journal Article
by Christophersen, Ingrid E and Rienstra, Michiel and Roselli, Carolina and Yin, Xiaoyan and Geelhoed, Bastiaan and Barnard, John and Lin, Honghuang and Arking, Dan E and Smith, Albert V and Albert, Christine M and Chaffin, Mark and Tucker, Nathan R and Li, Molong and Klarin, Derek and Bihlmeyer, Nathan A and Low, Siew-Kee and Weeke, Peter E and Müller-Nurasyid, Martina and Smith, J Gustav and Brody, Jennifer A and Niemeijer, Maartje N and Dörr, Marcus and Trompet, Stella and Huffman, Jennifer and Gustafsson, Stefan and Schurmann, Claudia and Kleber, Marcus E and Lyytikäinen, Leo-Pekka and Seppälä, Ilkka and Malik, Rainer and Horimoto, Andrea R V R and Perez, Marco and Sinisalo, Juha and Aeschbacher, Stefanie and Thériault, Sébastien and Yao, Jie and Radmanesh, Farid and Weiss, Stefan and Teumer, Alexander and Choi, Seung Hoan and Weng, Lu-Chen and Clauss, Sebastian and Deo, Rajat and Rader, Daniel J and Shah, Svati H and Sun, Albert and Hopewell, Jemma C and Debette, Stephanie and Chauhan, Ganesh and Yang, Qiong and Worrall, Bradford B and Paré, Guillaume and Kamatani, Yoichiro and Hagemeijer, Yanick P and Verweij, Niek and Siland, Joylene E and Kubo, Michiaki and Smith, Jonathan D and Van Wagoner, David R and Bis, Joshua C and Perz, Siegfried and Psaty, Bruce M and Ridker, Paul M and Magnani, Jared W and Harris, Tamara B and Launer, Lenore J and Shoemaker, M Benjamin and Padmanabhan, Sandosh and Haessler, Jeffrey and Bartz, Traci M and Waldenberger, Melanie and Lichtner, Peter and Arendt, Marina and Krieger, Jose E and Kähönen, Mika and Risch, Lorenz and Mansur, Alfredo J and Peters, Annette and Smith, Blair H and Lind, Lars and Scott, Stuart A and Lu, Yingchang and Bottinger, Erwin B and Hernesniemi, Jussi and Lindgren, Cecilia M and Wong, Jorge A and Huang, Jie and Eskola, Markku and Morris, Andrew P and Ford, Ian and Reiner, Alex P and Delgado, Graciela and Chen, Lin Y and Chen, Yii-Der Ida and Sandhu, Roopinder K and Li, Man and Boerwinkle, Eric and Eisele, Lewin and Lannfelt, Lars and Rost, Natalia and ... and METASTROKE Consortium of the ISGC and the AFGen Consortium and Neurology Working Group of the CHARGE Consortium and Neurology Working Grp CHARGE and AFGen Consortium and METASTROKE Consortium ISGC and Science for Life Laboratory, SciLifeLab and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
Nature genetics, ISSN 1546-1718, 04/2017, Volume 49, Issue 6, pp. 946 - 952
Journal Article
Journal Article
9.