X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (74) 74
multiple sclerosis (74) 74
index medicus (64) 64
multiple sclerosis - genetics (51) 51
female (44) 44
male (40) 40
neurosciences (36) 36
adult (35) 35
neurology (35) 35
middle aged (32) 32
genetic predisposition to disease (29) 29
genetic aspects (28) 28
genetics (28) 28
immunology (24) 24
genome-wide association study (23) 23
genotype (23) 23
polymorphism, single nucleotide (22) 22
risk factors (22) 22
case-control studies (21) 21
susceptibility (20) 20
association (19) 19
clinical neurology (19) 19
disease (19) 19
alleles (18) 18
genome-wide association (18) 18
medicine (18) 18
diagnostic-criteria (17) 17
genomes (17) 17
article (16) 16
genes (16) 16
genetics & heredity (16) 16
multidisciplinary sciences (16) 16
multiple sclerosis - immunology (15) 15
research article (15) 15
risk (15) 15
science (15) 15
young adult (15) 15
autoimmune diseases (14) 14
genomics (14) 14
linkage disequilibrium (14) 14
clinical medicine (13) 13
hospitals (13) 13
loci (13) 13
multiple sclerosis - epidemiology (13) 13
susceptibility loci (13) 13
biochemistry & molecular biology (12) 12
gene frequency (12) 12
medical research (12) 12
research (12) 12
adolescent (11) 11
analysis (11) 11
genetic research (11) 11
medicine, experimental (11) 11
polymorphism, single nucleotide - genetics (11) 11
single nucleotide polymorphisms (11) 11
allergy and immunology (10) 10
expression (10) 10
gene expression (10) 10
genetic association studies (10) 10
genetic variation (10) 10
haplotypes (10) 10
histocompatibility antigen hla (10) 10
norway (10) 10
patients (10) 10
population (10) 10
studies (10) 10
biology (9) 9
epidemiology (9) 9
genetic predisposition to disease - genetics (9) 9
hla-drb1 chains - genetics (9) 9
immune system (9) 9
lymphocytes (9) 9
lymphocytes t (9) 9
variants (9) 9
aged (8) 8
consortia (8) 8
demyelinating disorders (8) 8
disease susceptibility (8) 8
guidelines (8) 8
magnetic resonance imaging (8) 8
medicin och hälsovetenskap (8) 8
metaanalysis (8) 8
single-nucleotide polymorphism (8) 8
autoimmunity (7) 7
child (7) 7
development and progression (7) 7
drb1 protein (7) 7
genetic testing (7) 7
hla (7) 7
hla-drb1 (7) 7
interleukin-7 receptor (7) 7
multiple-sclerosis (7) 7
pathogenesis (7) 7
replication (7) 7
central nervous system (6) 6
cerebrospinal fluid (6) 6
cerebrospinal-fluid (6) 6
clinical immunology (6) 6
cohort studies (6) 6
deoxyribonucleic acid--dna (6) 6
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Therapeutic Advances in Neurological Disorders, ISSN 1756-2856, 7/2013, Volume 6, Issue 4, pp. 237 - 248
Multiple sclerosis (MS) is universally found to be more prevalent in women than men. This has led to extensive studies of differences in the immune system or... 
Multiple sclerosis | female | genes | immunology | pregnancy | sex | VITAMIN-D | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | SPINAL-CORD | SJL/J MICE | CLINICAL NEUROLOGY | GENETIC SUSCEPTIBILITY | NEUROMYELITIS-OPTICA | DISEASE-MODIFYING DRUGS | PREGNANCY OUTCOMES | POSTPARTUM RELAPSE | T-CELLS | Reviews
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 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
by Sawcer, Stephen and Hellenthal, Garrett and Pirinen, Matti and Spencer, Chris C.A and Patsopoulos, Nikolaos A and Moutsianas, Loukas and Dilthey, Alexander and Su, Zhan and Freeman, Colin and Hunt, Sarah E and Edkins, Sarah and Gray, Emma and Booth, David R and Potter, Simon C and Goris, An and Band, Gavin and Oturai, Annette Bang and Strange, Amy and Saarela, Janna and Bellenguez, Céline and Fontaine, Bertrand and Gillman, Matthew and Hemmer, Bernhard and Gwilliam, Rhian and Zipp, Frauke and Jayakumar, Alagurevathi and Martin, Roland and Leslie, Stephen and Hawkins, Stanley and Giannoulatou, Eleni and D'Alfonso, Sandra and Blackburn, Hannah and Boneschi, Filippo Martinelli and Liddle, Jennifer and Harbo, Hanne F and Perez, Marc L and Spurkland, Anne and Waller, Matthew J and Mycko, Marcin P and Ricketts, Michelle and Comabella, Manuel and Hammond, Naomi and Kockum, Ingrid and McCann, Owen T and Ban, Maria and Whittaker, Pamela and Kemppinen, Anu and Weston, Paul and Hawkins, Clive and Widaa, Sara and Zajicek, John and Dronov, Serge and Robertson, Neil and Bumpstead, Suzannah J and Barcellos, Lisa F and Ravindrarajah, Rathi and Abraham, Roby and Alfredsson, Lars and Ardlie, Kristin and Aubin, Cristin and Baker, Amie and Baker, Katharine and Baranzini, Sergio E and Bergamaschi, Laura and Bergamaschi, Roberto and Bernstein, Allan and Berthele, Achim and Boggild, Mike and Bradfield, Jonathan P and Brassat, David and Broadley, Simon A and Buck, Dorothea and Butzkueven, Helmut and Capra, Ruggero and Carroll, William M and Cavalla, Paola and Celius, Elisabeth G and Cepok, Sabine and Chiavacci, Rosetta and Clerget-Darpoux, Françoise and Clysters, Katleen and Comi, Giancarlo and Cossburn, Mark and Cournu-Rebeix, Isabelle and Cox, Mathew B and Cozen, Wendy and Cree, Bruce A.C and Cross, Anne H and Cusi, Daniele and Daly, Mark J and Davis, Emma and De Bakker, Paul I.W and Debouverie, Marc and D'Hooghe, Marie Beatrice and Dixon, Katherine and Dobosi, Rita and Dubois, Bénédicte and Ellinghaus, David and Elovaara, Irina and Esposito, Federica and ... and Wellcome Trust Case Control Consor and Int Multiple Sclerosis Genetics Co and Wellcome Trust Case Control Consortium 2 and International Multiple Sclerosis Genetics Consortium and The International Multiple Sclerosis Genetics Consortium & The Wellcome Trust Case Control Consortium 2 and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Uppsala universitet and Institutionen för medicinska vetenskaper
Nature, ISSN 0028-0836, 08/2011, Volume 476, Issue 7359, pp. 214 - 219
Journal Article
NATURE GENETICS, ISSN 1061-4036, 09/2007, Volume 39, Issue 9, pp. 1108 - 1113
Multiple sclerosis is a chronic, often disabling, disease of the central nervous system affecting more than 1 in 1,000 people in most western countries. The... 
POLYMORPHISMS | GENE | SUSCEPTIBILITY | DISEASE | GENETICS & HEREDITY | ASSOCIATION | EXPRESSION | LOCUS | TYROSINE-PHOSPHATASE | Multiple sclerosis | Genetic variation | Physiological aspects | Dosage and administration | Genetic aspects | Research | Diagnosis | Interleukin-7 | Risk factors | Body fluids | Genetics | Gene expression | Spine
Journal Article
Nature Genetics, ISSN 1061-4036, 09/2015, Volume 47, Issue 10, pp. 1107 - 1113
Journal Article
Journal Article