(Q37376771)

20 August 2017

Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13. (English)

1 reference

20 August 2017

restless legs syndrome

1 reference

15

1 reference

20 August 2017

Karin Stiasny-Kolster

6

Karin Stiasny-Kolster

1 reference

20 August 2017

David Kemlink

1

0 references

Juliane Winkelmann

Juliane Winkelmann

17

0 references

Soňa Nevšímalová

Sona Nevsimalova

8

0 references

Karel Šonka

Karel Sonka

9

0 references

Giuseppe Plazzi

Giuseppe Plazzi

2

0 references

Federica Provini

Federica Provini

4

0 references

Birgit Högl

10

Birgit Högl

1 reference

20 August 2017

11

Birgit Frauscher

1 reference

20 August 2017

7

Wolfgang Oertel

1 reference

20 August 2017

14

Peter Lichtner

1 reference

20 August 2017

Georgios M Hadjigeorgiou

12

Georgios M Hadjigeorgiou

1 reference

20 August 2017

18

Pasquale Montagna

1 reference

20 August 2017

13

Peter P Pramstaller

1 reference

20 August 2017

5

Olli Polo

1 reference

20 August 2017

3

Roberto Vetrugno

1 reference

20 August 2017

Bertram Müller-Myshok

16

1 reference

20 August 2017

10 January 2008

1 reference

20 August 2017

1 reference

20 August 2017

9

1 reference

20 August 2017

2

1 reference

20 August 2017

75-82

1 reference

https://scigraph.springernature.com/pub.10.1007/s10048-007-0113-1

20 August 2017

0 references

cites work

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

A genetic risk factor for periodic limb movements in sleep

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

A human phenome-interactome network of protein complexes implicated in genetic disorders

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Family-based association study of the restless legs syndrome loci 2 and 3 in a European population

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Linkage analysis identifies a novel locus for restless legs syndrome on chromosome 2q in a South Tyrolean population isolate

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

The 14q restless legs syndrome locus in the French Canadian population

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Restless legs syndrome: diagnostic criteria, special considerations, and epidemiology. A report from the restless legs syndrome diagnosis and epidemiology workshop at the National Institutes of Health

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Autosomal dominant restless legs syndrome maps on chromosome 14q.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Structure and complex transcription pattern of the mouse SK1 K(Ca) channel gene, KCNN1

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Initial sequencing and analysis of the human genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Comprehensive human genetic maps: individual and sex-specific variation in recombination

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

A questionnaire study of 138 patients with restless legs syndrome: the 'Night-Walkers' survey

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Computer-simulation methods in human linkage analysis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

An extended transmission/disequilibrium test (TDT) for multi-allele marker loci.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Pedigree disequilibrium tests for multilocus haplotypes.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Mutations in Rab3a alter circadian period and homeostatic response to sleep loss in the mouse

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patients.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

A program for the monte carlo evaluation of significance of the extended transmission/disequilibrium test.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757615

10.1007/S10048-007-0113-1

3 December 2018

Identifiers

DOI

1 reference

20 August 2017

1 reference

20 August 2017

PubMed publication ID

18193462

1 reference