Inger‐Lise Mero

发表

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Simon C. Potter, Joseph T. Glessner, M. Pirinen, 2011, Nature.

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

M. Pirinen, P. Donnelly, C. Spencer, 2013, Nature Genetics.

Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies

P. Striano, J. Jacobs, N. Absalom, 2022, Nature Communications.

Whole‐exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways

K. Heimdal, G. Gilfillan, Elin Tønne, 2022, American journal of medical genetics. Part A.

Oligoclonal band phenotypes in MS differ in their HLA class II association, while specific KIR ligands at HLA class I show association to MS in general

B. Lie, H. Harbo, E. Celius, 2014, Journal of Neuroimmunology.

Oligoclonal Band Status in Scandinavian Multiple Sclerosis Patients Is Associated with Specific Genetic Risk Alleles

Hanne F. Harbo, Finn Sellebjerg, Jan Hillert, 2013, PloS one.

From genes to characteristics of multiple sclerosis

H. Harbo, Inger‐Lise Mero, 2012, Acta neurologica Scandinavica. Supplementum.

Alterations in KLRB1 gene expression and a Scandinavian multiple sclerosis association study of the KLRB1 SNP rs4763655

H. Harbo, E. Celius, P. Sørensen, 2011, European Journal of Human Genetics.

Association to the Glypican-5 gene in multiple sclerosis

T. Karlsen, B. Lie, H. Harbo, 2010, Journal of Neuroimmunology.

A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis

M. Ban, B. Lie, H. Harbo, 2010, European Journal of Human Genetics.

Killer immunoglobulin‐like receptor ligand HLA‐Bw4 protects against multiple sclerosis

Marita Olsson, Erik Thorsby, Hanne F Harbo, 2009, Annals of neurology.

Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.

Ludwig Kappos, Leena Peltonen, Pentti Tienari, 2010, American journal of human genetics.

IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci

C. Gieger, M. Daly, L. Peltonen, 2010, Genes and Immunity.

Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis

K. Heimdal, C. von der Lippe, Elin Tønne, 2020, European Journal of Human Genetics.

Phenotypic expansion of the BPTF‐related neurodevelopmental disorder with dysmorphic facies and distal limb anomalies

P. Stankiewicz, K. Bowling, Yaping Yang, 2021, American journal of medical genetics. Part A.

No evidence of association between mutant alleles of the CYP27B1 gene and multiple sclerosis

M. Ban, S. Sawcer, A. Compston, 2013, Annals of Neurology.

The Genetic Association of Variants in CD6, TNFRSF1A and IRF8 to Multiple Sclerosis: A Multicenter Case-Control Study

L. Peltonen, A. Goris, S. Sawcer, 2011, PloS one.

Multiple sclerosis-associated single-nucleotide polymorphisms in CLEC16A correlate with reduced SOCS1 and DEXI expression in the thymus

B. Lie, H. Harbo, A. Spurkland, 2012, Genes and Immunity.

Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus

M. Ban, S. Sawcer, A. Compston, 2011, Genes and Immunity.

Associations between APOE Genotypes and Disease Susceptibility, Joint Damage and Lipid Levels in Patients with Rheumatoid Arthritis

Inge Christoffer Olsen, B. Lie, D. M. van der Heijde, 2013, PloS one.

IL 12 A , MPHOSPH 9 / CDK 2 AP 1 and RGS 1 are novel multiple sclerosis susceptibility loci

Winkelmann, L. Peltonen, M. Pericak-Vance, 2010 .

Oligoclonal bands and age at onset correlate with genetic risk score in multiple sclerosis

H. Harbo, E. Celius, S. Hauser, 2014, Multiple sclerosis.

Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria

Bethan E. Hoskins, A. Reymond, S. Ellard, 2022, Human molecular genetics.

Polymorphisms of the BDNF gene show neither association with multiple sclerosis susceptibility nor clinical course

B. Lie, N. Landrø, H. Harbo, 2012, Journal of Neuroimmunology.

Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study

P. G. Larsson, M. D. Vigeland, Y. Sheng, 2023, Brain & spine.

Association of Genetic Markers with CSF Oligoclonal Bands in Multiple Sclerosis Patients

A. Goris, H. Harbo, E. Celius, 2013, PloS one.

Homozygous KIDINS220 loss-of-function variants in fetuses with cerebral ventriculomegaly and limb contractures

M. D. Vigeland, Y. Sheng, K. Selmer, 2017, Human molecular genetics.

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

M. Pirinen, P. Donnelly, C. Spencer, 2013, Nature Genetics.

A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility

Simon C. Potter, M. Pirinen, P. Donnelly, 2014, Genes and Immunity.

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

C. Gieger, C. Freeman, P. Deloukas, 2013, Nature Genetics.

Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.

S. Gabriel, M. Daly, L. Peltonen, 2010, American journal of human genetics.

Assessment of gene–disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA

M. Vikkula, C. Lavarino, H. Karstensen, 2024, Orphanet journal of rare diseases.

Alterations in gene expression and a Scandinavian multiple sclerosis association study of the SNP rs4763655

H. Harbo, E. Celius, I. Kockum, 2023 .