X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (8) 8
index medicus (8) 8
multiple sclerosis (8) 8
adult (6) 6
clinical neurology (6) 6
male (6) 6
middle aged (6) 6
female (5) 5
genetic predisposition to disease (5) 5
cohort studies (4) 4
neurosciences (4) 4
relapsing-remitting (4) 4
risk (4) 4
young adult (4) 4
adolescent (3) 3
aged (3) 3
association (3) 3
disease progression (3) 3
genetic risk (3) 3
genome-wide association study (3) 3
age of onset (2) 2
aged, 80 and over (2) 2
article (2) 2
autoimmune (2) 2
chromosome mapping (2) 2
confidence intervals (2) 2
diagnostic-criteria (2) 2
disease (2) 2
double-blind (2) 2
gene expression (2) 2
gene frequency (2) 2
genetic aspects (2) 2
genetic loci (2) 2
genetic variation (2) 2
genetics (2) 2
genomes (2) 2
genotype (2) 2
heritability (2) 2
interferon beta-1a (2) 2
interferon-beta - therapeutic use (2) 2
italy - epidemiology (2) 2
medical and health sciences (2) 2
medicin och hälsovetenskap (2) 2
metaanalysis (2) 2
multiple sclerosis, relapsing-remitting - drug therapy (2) 2
multivariate analysis (2) 2
neurology (2) 2
phenotype (2) 2
placebo-controlled trial (2) 2
polymorphism, single nucleotide (2) 2
prevalence (2) 2
primary-progressive (2) 2
relapsing–remitting (2) 2
settore med/26 - neurologia (2) 2
weighted genetic risk score (2) 2
1st demyelinating event (1) 1
adaptive systems (1) 1
adjuvants, immunologic - therapeutic use (1) 1
alleles (1) 1
analysis (1) 1
annotation (1) 1
annotations (1) 1
anticoagulant treatment (1) 1
anticoagulants (1) 1
architecture (1) 1
astrocytes (1) 1
atlases (1) 1
autoimmune diseases (1) 1
basic medicine (1) 1
biological response modifiers (1) 1
brain (1) 1
cell differentiation - genetics (1) 1
cells, cultured (1) 1
central nervous system (1) 1
cerebral vein thrombosis (1) 1
cerebral veins - pathology (1) 1
child (1) 1
chromosome mapping; european continental ancestry group; gene frequency; genetic loci; genetic predisposition to disease; genetic variation; genome-wide association study; genotype; humans; multiple sclerosis; polymorphism, single nucleotide; genetics (1) 1
chromosomes (1) 1
clinical medicine (1) 1
clinical outcomes (1) 1
clinical-course (1) 1
cluster analysis (1) 1
complex traits (1) 1
consortia (1) 1
copolymer 1 (1) 1
cytokines - genetics (1) 1
cytokines - immunology (1) 1
cytokines - metabolism (1) 1
data analysis (1) 1
diagnosis (1) 1
disability (1) 1
drug therapy (1) 1
efficacy (1) 1
engineering and technology (1) 1
enrichment (1) 1
european continental ancestry group (1) 1
european continental ancestry group - genetics (1) 1
evaluation (1) 1
family (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Beecham, Ashley H and Patsopoulos, Nikolaos A and Xifara, Dionysia K and Davis, Mary F and Kemppinen, Anu and Cotsapas, Chris and Shah, Tejas S and Spencer, Chris and Booth, David and Goris, An and Oturai, Annette and Saarela, Janna and Fontaine, Bertrand and Hemmer, Bernhard and Martin, Claes and Zipp, Frauke and D'Alfonso, Sandra and Martinelli-Boneschi, Filippo and Taylor, Bruce and Harbo, Hanne F and Kockum, Ingrid and Hillert, Jan and Olsson, Tomas and Ban, Maria and Oksenberg, Jorge R and Hintzen, Rogier and Barcellos, Lisa F and Agliardi, Cristina and Alfredsson, Lars and Alizadeh, Mehdi and Anderson, Carl and Andrews, Robert and Søndergaard, Helle Bach and Baker, Amie and Band, Gavin and Baranzini, Sergio E and Barizzone, Nadia and Barrett, Jeffrey and Bellenguez, Céline and Bergamaschi, Laura and Bernardinelli, Luisa and Berthele, Achim and Biberacher, Viola and Binder, Thomas M.C and Blackburn, Hannah and Bomfim, Izaura L and Brambilla, Paola and Broadley, Simon and Brochet, Bruno and Brundin, Lou and Buck, Dorothea and Butzkueven, Helmut and Caillier, Stacy J and Camu, William and Carpentier, Wassila and Cavalla, Paola and Celius, Elisabeth G and Coman, Irène and Comi, Giancarlo and Corrado, Lucia and Cosemans, Leentje and Cournu-Rebeix, Isabelle and Cree, Bruce A.C and Cusi, Daniele and Damotte, Vincent and Defer, Gilles and Delgado, Silvia R and Deloukas, Panos and Di Sapio, Alessia and Dilthey, Alexander T and Donnelly, Peter and Dubois, Bénédicte and Duddy, Martin and Edkins, Sarah and Elovaara, Irina and Esposito, Federica and Evangelou, Nikos and Fiddes, Barnaby and Field, Judith and Franke, Andre and Freeman, Colin and Frohlich, Irene Y and Galimberti, Daniela and Gieger, Christian and Gourraud, Pierre-Antoine and Graetz, Christiane and Graham, Andrew and Grummel, Verena and Guaschino, Clara and Hadjixenofontos, Athena and Hakonarson, Hakon and Halfpenny, Christopher and Hall, Gillian and Hall, Per and Hamsten, Anders and Harley, James and Harrower, Timothy and Hawkins, Clive and Hellenthal, Garrett and Hillier, Charles and ... and Wellcome Trust Case Control Consor and Int IBD Genetics Consortium IIBDGC and International Multiple Sclerosis Genetics Consortium (IMSGC) and Wellcome Trust Case Control Consortium 2 (WTCCC2) and International IBD Genetics Consortium (IIBDGC) and Institutionen för fysik, kemi och biologi and Linköpings universitet and Bioinformatik and Tekniska högskolan
Nature Genetics, ISSN 1061-4036, 2013, Volume 45, Issue 11, pp. 1353 - 1362
Journal Article
Annals of Neurology, ISSN 0364-5134, 07/2015, Volume 78, Issue 1, pp. 115 - 127
Journal Article
Journal of Neurology, ISSN 0340-5354, 05/2017, Volume 264, Issue 5, pp. 1005 - 1007
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s00415-017-8458-3 
DIAGNOSIS | CLINICAL NEUROLOGY
Journal Article
by Patsopoulos, NA and Baranzini, SE and Santaniello, A and Shoostari, P and Cotsapas, C and Wong, G and Beecham, AH and James, T and Replogle, J and Vlachos, IS and McCabe, C and Pers, TH and Brandes, A and White, C and Keenan, B and Cimpean, M and Winn, P and Panteliadis, IP and Robbins, A and Andlauer, TFM and Zarzycki, O and Dubois, B and Goris, A and Sondergaard, HB and Sellebjerg, F and Sorensen, PS and Ullum, H and Thorner, LW and Saarela, J and Cournu-Rebeix, I and Damotte, V and Fontaine, B and Guillot-Noel, L and Lathrop, M and Vukusic, S and Berthele, A and Pongratz, V and Gasperi, C and Graetz, C and Grummel, V and Hemmer, B and Hoshi, M and Knier, B and Korn, T and Lill, CM and Luessi, F and Muhlau, M and Zipp, F and Dardiotis, E and Agliardi, C and Amoroso, A and Barizzone, N and Benedetti, MD and Bernardinelli, L and Cavalla, P and Clarelli, F and Comi, G and Cusi, D and Esposito, F and Ferre, L and Galimberti, D and Guaschino, C and Leone, MA and Martinelli, V and Moiola, L and Salvetti, M and Sorosina, M and Vecchio, D and Zauli, A and Santoro, S and Mancini, N and Zuccala, M and Mescheriakova, J and van Duijn, C and Bos, SD and Celius, EG and Spurkland, A and Comabella, M and Montalban, X and Alfredsson, L and Bomfim, IL and Gomez-Cabrero, D and Hillert, J and Jagodic, M and Linden, M and Piehl, F and Jelcic, I and Martin, R and Sospedra, M and Baker, A and Ban, M and Hawkins, C and Hysi, P and Kalra, S and Karpe, F and Khadake, J and Lachance, G and Molyneux, P and Neville, M and Thorpe, J and ... and Australia New Zealand IBDGC and Int Multiple Sclerosis Genetics Co and Initiative Crohn Colitis and Belgium Genetic Consortiumt and United Kingdom IBDGC and ANZgene and WTCCC2 and IIBDGC and NIDDK IBDGCJ and Wellcome Trust Case Control Conso and International Multiple Sclerosis Genetics Consortium and Örebro universitet and Institutionen för medicinska vetenskaper
SCIENCE, ISSN 0036-8075, 09/2019, Volume 365, Issue 6460, pp. 1417 - 1417
Journal Article
Acta Neurologica Scandinavica, ISSN 0001-6314, 11/2018, Volume 138, Issue 5, pp. 447 - 453
Journal Article
Multiple Sclerosis Journal, ISSN 1352-4585, 06/2014, Volume 20, Issue 7, pp. 802 - 811
Journal Article
Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 07/2012, Volume 10, Issue 7, pp. 1297 - 1302
Journal Article
Multiple sclerosis (Houndmills, Basingstoke, England), 06/2019, p. 1352458519851428
Multiple sclerosis (MS) is a disease in which biomarker identification is fundamental to predict response to treatments and to deliver the optimal drug to... 
Journal Article
Neurology: Neuroimmunology & Neuroinflammation, ISSN 2332-7812, 08/2015, Volume 2, Issue 4, p. e129
OBJECTIVE:To investigate the role of known multiple sclerosis (MS)-associated genetic variants in MS familial aggregation, clinical expression, and accuracy of... 
Journal Article
by Beecham, Ashley H and Patsopoulos, Nikolaos A and Xifara, Dionysia K and Davis, Mary F and Kemppinen, Anu and Cotsapas, Chris and Shah, Tejas S and Spencer, Chris and Booth, David and Goris, An and Oturai, Annette and Saarela, Janna and Fontaine, Bertrand and Hemmer, Bernhard and Martin, Claes and Zipp, Frauke and D'Alfonso, Sandra and Martinelli-Boneschi, Filippo and Taylor, Bruce and Harbo, Hanne F and Kockum, Ingrid and Hillert, Jan and Olsson, Tomas and Ban, Maria and Oksenberg, Jorge R and Hintzen, Rogier and Barcellos, Lisa F and Agliardi, Cristina and Alfredsson, Lars and Alizadeh, Mehdi and Anderson, Carl and Andrews, Robert and Søndergaard, Helle Bach and Baker, Amie and Band, Gavin and Baranzini, Sergio E and Barizzone, Nadia and Barrett, Jeffrey and Bellenguez, Céline and Bergamaschi, Laura and Bernardinelli, Luisa and Berthele, Achim and Biberacher, Viola and Binder, Thomas M C and Blackburn, Hannah and Bomfim, Izaura L and Brambilla, Paola and Broadley, Simon and Brochet, Bruno and Brundin, Lou and Buck, Dorothea and Butzkueven, Helmut and Caillier, Stacy J and Camu, William and Carpentier, Wassila and Cavalla, Paola and Celius, Elisabeth G and Coman, Irène and Comi, Giancarlo and Corrado, Lucia and Cosemans, Leentje and Cournu-Rebeix, Isabelle and Cree, Bruce A C and Cusi, Daniele and Damotte, Vincent and Defer, Gilles and Delgado, Silvia R and Deloukas, Panos and di Sapio, Alessia and Dilthey, Alexander T and Donnelly, Peter and Dubois, Bénédicte and Duddy, Martin and Edkins, Sarah and Elovaara, Irina and Esposito, Federica and Evangelou, Nikos and Fiddes, Barnaby and Field, Judith and Franke, Andre and Freeman, Colin and Frohlich, Irene Y and Galimberti, Daniela and Gieger, Christian and Gourraud, Pierre-Antoine and Graetz, Christiane and Graham, Andrew and Grummel, Verena and Guaschino, Clara and Hadjixenofontos, Athena and Hakonarson, Hakon and Halfpenny, Christopher and Hall, Gillian and Hall, Per and Hamsten, Anders and Harley, James and Harrower, Timothy and Hawkins, Clive and Hellenthal, Garrett and Hillier, Charles and ... and Institutionen för neurovetenskap och fysiologi, sektionen för klinisk neurovetenskap och rehabilitering and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Institute of Neuroscience and Physiology, Department of Clinical Neuroscience and Rehabilitation and Sahlgrenska akademin
Nature genetics, ISSN 1546-1718, 2013, Volume 45, Issue 11, p. 1353
Using the ImmunoChip custom genotyping array, we analyzed 14,498 subjects with multiple sclerosis and 24,091 healthy controls for 161,311 autosomal variants... 
Neurosciences | Genetic Predisposition to Disease | Genome-Wide Association Study | Gene Frequency | Humans | European Continental Ancestry Group | Genotype | Chromosome Mapping | Genetic Loci | Single Nucleotide | Genetic Variation | Multiple Sclerosis | genetics | immunology | Neurovetenskaper | Polymorphism
Journal Article