Følg
Hanne Flinstad Harbo
Hanne Flinstad Harbo
Department of Neurology, Oslo University Hospital and University of Oslo
Verifisert e-postadresse på medisin.uio.no
Tittel
Sitert av
Sitert av
År
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
30352011
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
International IBD Genetics Consortium (IIBDGC), C Agliardi, L Alfredsson, ...
Nature genetics 45 (11), 1353-1360, 2013
13612013
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
International Multiple Sclerosis Genetics Consortium*†, ANZgene, ...
Science 365 (6460), eaav7188, 2019
9812019
Sex and gender issues in multiple sclerosis
HF Harbo, R Gold, M Tintoré
Therapeutic advances in neurological disorders 6 (4), 237-248, 2013
6632013
Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis
F Lundmark, K Duvefelt, E Iacobaeus, I Kockum, E Wallström, M Khademi, ...
Nature genetics 39 (9), 1108-1113, 2007
6282007
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus
W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ...
PLoS genetics 6 (2), e1000841, 2010
4612010
Common brain disorders are associated with heritable patterns of apparent aging of the brain
T Kaufmann, D van der Meer, NT Doan, E Schwarz, MJ Lund, I Agartz, ...
Nature neuroscience 22 (10), 1617-1623, 2019
4272019
The genetics of multiple sclerosis: an up‐to‐date review
PA Gourraud, HF Harbo, SL Hauser, SE Baranzini
Immunological reviews 248 (1), 87-103, 2012
4162012
Class II HLA interactions modulate genetic risk for multiple sclerosis
Nature genetics 47 (10), 1107-1113, 2015
4142015
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene
E Jakkula, V Leppä, AM Sulonen, T Varilo, S Kallio, A Kemppinen, ...
The American Journal of Human Genetics 86 (2), 285-291, 2010
2942010
Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci
OA Andreassen, HF Harbo, Y Wang, WK Thompson, AJ Schork, ...
Molecular psychiatry 20 (2), 207-214, 2015
2052015
DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis
L Kular, Y Liu, S Ruhrmann, G Zheleznyakova, F Marabita, ...
Nature communications 9 (1), 2397, 2018
2032018
Altered ovarian function and cardiovascular risk factors in valproate-treated women
JIT Isojärvi, E Taubøll, AJ Pakarinen, J van Parys, J Rättyä, HF Harbo, ...
The American journal of medicine 111 (4), 290-296, 2001
1992001
Risk for myasthenia gravis maps to a 151Pro→Ala change in TNIP1 and to human leukocyte antigen‐B*08
PK Gregersen, R Kosoy, AT Lee, J Lamb, J Sussman, D McKee, ...
Annals of neurology 72 (6), 927-935, 2012
1902012
CTLA4 promoter and exon 1 dimorphisms in multiple sclerosiso
H Flinstad Harbo, E Gulowsen Celius, F Vartdal, A Spurkland
Tissue Antigens 53 (1), 106-110, 1999
1901999
Genes in the HLA class I region may contribute to the HLA class II‐associated genetic susceptibility to multiple sclerosis
HF Harbo, BA Lie, S Sawcer, EG Celius, KZ Dai, A Oturai, J Hillert, ...
Tissue antigens 63 (3), 237-247, 2004
1772004
Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls
SE Baranzini, P Khankhanian, NA Patsopoulos, M Li, J Stankovich, ...
The American Journal of Human Genetics 92 (6), 854-865, 2013
1662013
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor
M Ban, A Goris, ÅR Lorentzen, A Baker, T Mihalova, G Ingram, DR Booth, ...
European Journal of Human Genetics 17 (10), 1309-1313, 2009
1582009
Late onset myasthenia gravis is associated with HLA DRB1* 15: 01 in the Norwegian population
AH Maniaol, A Elsais, ÅR Lorentzen, JF Owe, MK Viken, H Sæther, ...
PloS one 7 (5), e36603, 2012
1512012
Low-frequency and rare-coding variation contributes to multiple sclerosis risk
M Mitrovič, NA Patsopoulos, AH Beecham, T Dankowski, A Goris, ...
Cell 175 (6), 1679-1687. e7, 2018
1442018
Systemet kan ikke utføre handlingen. Prøv på nytt senere.
Artikler 1–20