(Q37619291)

21 August 2017

0 references

No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis (English)

1 reference

amyotrophic lateral sclerosis

21 August 2017

0 references

0 references

0 references

author

Orla Hardiman

13

1 reference

21 August 2017

2

Jessica van Setten

1 reference

21 August 2017

Nikolaos A. Patsopoulos

Nikolaos A Patsopoulos

5

0 references

Aleksey Shatunov

Aleksey Shatunov

16

0 references

Philip Van Damme

Philip Van Damme

26

0 references

An Goris

An Goris

1

0 references

Stephen Sawcer

Stephen J Sawcer

6

0 references

Christopher Shaw

Christopher E Shaw

19

0 references

Alastair Compston

27

Alastair Compston

1 reference

21 August 2017

18

Ammar Al-Chalabi

1 reference

21 August 2017

12

Vincent Meininger

1 reference

21 August 2017

Leonard H van den Berg

30

Leonard H van den Berg

1 reference

21 August 2017

28

Wim Robberecht

1 reference

21 August 2017

23

Gabriele Mora

1 reference

21 August 2017

21

Adriano Chiò

1 reference

21 August 2017

22

Gabriella Restagno

1 reference

21 August 2017

32

Jan H Veldink

1 reference

21 August 2017

10

Peter M Andersen

1 reference

21 August 2017

0 references

20

Bryan J Traynor

1 reference

21 August 2017

31

Philip L De Jager

1 reference

21 August 2017

25

Jorge R Oksenberg

1 reference

21 August 2017

4

Stephan Ripke

1 reference

21 August 2017

14

John E Landers

1 reference

21 August 2017

11

Judith Melki

1 reference

21 August 2017

3

Frank Diekstra

1 reference

21 August 2017

33

Paul I W de Bakker

1 reference

21 August 2017

24

Roel A Ophoff

1 reference

21 August 2017

29

Bénédicte Dubois

1 reference

21 August 2017

15

Robert H Brown

1 reference

21 August 2017

International Multiple Sclerosis Genetics Consortium

7

1 reference

21 August 2017

Michael van Es

8

1 reference

21 August 2017

Australia and New Zealand MS Genetics Consortium

9

1 reference

21 August 2017

Nigel Leigh

17

1 reference

21 August 2017

13 November 2013

1 reference

21 August 2017

Human Molecular Genetics

1 reference

21 August 2017

23

1 reference

21 August 2017

7

1 reference

21 August 2017

1916-1922

1 reference

Autoimmune disease preceding amyotrophic lateral sclerosis: an epidemiologic study

21 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Concurrent multiple sclerosis and amyotrophic lateral sclerosis: where inflammation and neurodegeneration meet?

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Pervasive sharing of genetic effects in autoimmune disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Extreme Evolutionary Disparities Seen in Positive Selection across Seven Complex Diseases

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Neurodegeneration in autoimmune CNS inflammation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Genetics of motor neuron disorders: new insights into pathogenic mechanisms

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Detecting shared pathogenesis from the shared genetics of immune-related diseases

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Amyotrophic lateral sclerosis with multiple sclerosis: a clinical and pathological report

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Clinical genetics of amyotrophic lateral sclerosis: what do we really know?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Neuroinflammation in amyotrophic lateral sclerosis: role of glial activation in motor neuron disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

TNFRSF1A coding variants in 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=3943520

Familial risks for amyotrophic lateral sclerosis and autoimmune diseases

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Amyotrophic lateral sclerosis and multiple sclerosis overlap: a case report

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

The concurrence of multiple sclerosis and amyotrophic lateral sclerosis

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

T helper-17 activation dominates the immunologic milieu of both amyotrophic lateral sclerosis and progressive multiple sclerosis.

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Amyotrophic lateral sclerosis is not linked to multiple sclerosis in a population based study

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Concomitant amyotrophic lateral sclerosis and paraclinical laboratory features of multiple sclerosis: coincidence or causal relationship?

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Concurrence of multiple sclerosis and amyotrophic lateral sclerosis in patients with hexanucleotide repeat expansions of C9ORF72.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

Mortality statistics for multiple sclerosis and amyotrophic lateral sclerosis in Sweden

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3943520

A genome-wide scan in forty large pedigrees with multiple sclerosis

1 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDT574

A note on a general definition of the coefficient of determination

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDT574

Familial effects on the clinical course of multiple sclerosis

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDT574

Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditions

21 January 2018

1 reference

12 December 2020

Multiple sclerosis and amyotrophic lateral sclerosis: is there a link?

1 reference

12 December 2020

Muscle atrophy associated with multiple sclerosis: a benign condition or the onset of amyotrophic lateral sclerosis?

1 reference

12 December 2020

Distribution of multiple sclerosis in Sweden based on mortality and disability compensation statistics

1 reference

12 December 2020

Identifiers

DOI

10.1093/HMG/DDT574

1 reference

21 August 2017

1 reference

21 August 2017

PubMed publication ID

24234648

1 reference