(Q37154268)

18 August 2017

Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS. (English)

1 reference

18 August 2017

0 references

Janna Saarela

22

0 references

Seppo Meri

object named as

Seppo Meri

12

0 references

Aarno Palotie

20

object named as

Aarno Palotie

1 reference

18 August 2017

18

Mark J Daly

1 reference

18 August 2017

19

David A Hafler

1 reference

18 August 2017

Leena Peltonen-Palotie

21

object named as

Leena Peltonen

1 reference

18 August 2017

17

Philip L De Jager

1 reference

18 August 2017

15

Hanne F Harbo

1 reference

18 August 2017

Suvi P Kallio

1

1 reference

18 August 2017

Eveliina Jakkula

2

1 reference

18 August 2017

Shaun Purcell

3

1 reference

18 August 2017

Minna Suvela

4

1 reference

18 August 2017

Keijo Koivisto

5

1 reference

18 August 2017

Pentti J Tienari

6

1 reference

18 August 2017

Irina Elovaara

7

1 reference

18 August 2017

Tuula Pirttilä

8

1 reference

18 August 2017

Mauri Reunanen

9

1 reference

18 August 2017

Denis Bronnikov

10

1 reference

18 August 2017

Markku Viander

11

1 reference

18 August 2017

Jan Hillert

13

1 reference

18 August 2017

Frida Lundmark

14

1 reference

18 August 2017

Aslaug R Lorentzen

16

1 reference

18 August 2017

16 February 2009

1 reference

18 August 2017

14

0 references

published in

Human Molecular Genetics

1 reference

18 August 2017

18

1 reference

18 August 2017

1670-1683

1 reference

18 August 2017

9

1 reference

PLINK: a tool set for whole-genome association and population-based linkage analyses

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Risk alleles for multiple sclerosis identified by a genomewide study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Concordance for multiple sclerosis in Danish twins: an update of a nationwide study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Multiple sclerosis genetics: leaving no stone unturned

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

LDL-receptor mutations in Europe

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Haploview: analysis and visualization of LD and haplotype maps

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Isolates and their potential use in complex gene mapping efforts

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

A comparison of bayesian methods for haplotype reconstruction from population genotype data

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Familial hypercholesterolaemia in Finland: common, rare and mild mutations of the LDL receptor and their clinical consequences. Finnish FH-group

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

A New Statistical Method for Haplotype Reconstruction from Population Data

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Heterogeneity of multiple sclerosis lesions: implications for the pathogenesis of demyelination

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Genomewide scan of multiple sclerosis in Finnish multiplex families

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Genetic epidemiology of multiple sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

The British Isles survey of multiple sclerosis in twins

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

New diagnostic criteria for multiple sclerosis: guidelines for research protocols

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Loss of self-control in the complement system and innate autoreactivity

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Extrahepatic complement biosynthesis: where, when and why?

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Intrathecal activation of the complement system and disability in multiple sclerosis.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Reactive lysis: the complement-mediated lysis of unsensitized cells. I. The characterization of the indicator factor and its identification as C7.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

HL-A antigens and multiple sclerosis.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Studies on the clustering of multiple sclerosis in Finland I: Comparison between the domiciles and places of birth in selected subpopulations

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Refining genetic associations in multiple sclerosis

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Update and analysis of the University College London low density lipoprotein receptor familial hypercholesterolemia database.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Evaluating whole genome amplification via multiply-primed rolling circle amplification for SNP genotyping of samples with low DNA yield.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Functional analysis of the classical, alternative, and MBL pathways of the complement system: standardization and validation of a simple ELISA.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Multiple sclerosis in western Finland: evidence for a founder effect.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

A genome screen for linkage disequilibrium in Turkish multiple sclerosis

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

A whole genome screen for linkage in Turkish multiple sclerosis

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Expression of complement messenger RNAs and proteins by human oligodendroglial cells.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

A population-based study of multiple sclerosis in twins: update.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Genetics of multiple sclerosis

3 September 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

20 October 2018

12 December 2020

Genomewide Study of Multiple Sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

A full genome search in multiple sclerosis

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667286

A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2

4 December 2018

1 reference

12 December 2020

No evidence for association of multiple sclerosis with the complement factors C6 and C7

1 reference

12 December 2020

Linkage and association analysis of susceptibility regions on chromosomes 5 and 6 in 106 Scandinavian sibling pair families with multiple sclerosis

1 reference

12 December 2020

1 reference

12 December 2020

Regional and temporal variation in the incidence of multiple sclerosis in Finland 1979-1993

1 reference

12 December 2020

The endothelium is an extrahepatic site of synthesis of the seventh component of the complement system

1 reference

12 December 2020

Increasing prevalence of multiple sclerosis in Finland

1 reference

12 December 2020

The Membrane Attack Complex of Complement Causes Severe Demyelination Associated with Acute Axonal Injury

1 reference

12 December 2020

Attenuation of experimental allergic encephalomyelitis in complement component 6-deficient rats is associated with reduced complement C9 deposition, P-selectin expression, and cellular infiltrate in spinal cords

1 reference

12 December 2020

Deficiency of the complement regulator CD59a enhances disease severity, demyelination and axonal injury in murine acute experimental allergic encephalomyelitis

1 reference

12 December 2020

Human polymorphonuclear leukocytes store large amounts of terminal complement components C7 and C6, which may be released on stimulation

1 reference

12 December 2020

Identification of murine loci associated with susceptibility to chronic experimental autoimmune encephalomyelitis

1 reference

12 December 2020

Distribution of multiple sclerosis in Finland, with special reference to some geological factors

1 reference

12 December 2020

The epidemiology of multiple sclerosis in Finland: increase of prevalence and stability of foci in high-risk areas

1 reference

12 December 2020

Complement expression in human brain. Biosynthesis of terminal pathway components and regulators in human glial cells and cell lines

1 reference

12 December 2020

Fine mapping of the multiple sclerosis susceptibility locus on 5p14–p12

1 reference

12 December 2020

Immunoglobulins and complement factor C4 in adult rhinosinusitis

1 reference

12 December 2020

Old suspects found guilty--the first genome profile of multiple sclerosis

1 reference

12 December 2020

IL7RA polymorphisms and susceptibility to multiple sclerosis

1 reference

12 December 2020

The expression of complement regulatory proteins by adult human oligodendrocytes

1 reference

12 December 2020

Identifiers

DOI

10.1093/HMG/DDP073

1 reference

18 August 2017

1 reference

18 August 2017

1 reference