(Q37225625)

19 August 2017

Replication of restless legs syndrome loci in three European populations (English)

1 reference

19 August 2017

restless legs syndrome

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15

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19 August 2017

20

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19 August 2017

D Kemlink

1

0 references

Juliane Winkelmann

object named as

J Winkelmann

21

0 references

Karel Šonka

object named as

K Sonka

9

0 references

Werner Poewe

6

object named as

W Poewe

1 reference

19 August 2017

16

H E Wichmann

1 reference

19 August 2017

10

S Nevsimalova

1 reference

19 August 2017

12

P Lichtner

1 reference

19 August 2017

3

B Frauscher

1 reference

19 August 2017

2

O Polo

1 reference

19 August 2017

V Gschliesser

4

1 reference

19 August 2017

B Högl

5

1 reference

19 August 2017

P Vodicka

7

1 reference

19 August 2017

J Vavrova

8

1 reference

19 August 2017

B Schormair

11

1 reference

19 August 2017

K Silander

13

1 reference

19 August 2017

L Peltonen

14

1 reference

19 August 2017

A Zimprich

17

1 reference

19 August 2017

D Roeske

18

1 reference

19 August 2017

B Müller-Myhsok

19

1 reference

19 August 2017

language of work or name

English

0 references

publication date

10 March 2009

1 reference

Journal of Medical Genetics

19 August 2017

1 reference

19 August 2017

46

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19 August 2017

5

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19 August 2017

315-318

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

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

A second generation human haplotype map of over 3.1 million SNPs

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

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=2695663

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=2695663

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=2695663

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=2695663

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=2695663

The UCSC Genome Browser Database: update 2006

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

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=2695663

KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

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=2695663

Corl1, a novel neuronal lineage-specific transcriptional corepressor for the homeodomain transcription factor Lbx1

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

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=2695663

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=2695663

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=2695663

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=2695663

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

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=2695663

All in the family: the BTB/POZ, KRAB, and SCAN domains

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

Expression of Meis and Pbx genes and their protein products in the developing telencephalon: implications for regional differentiation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

Paralog group 1 hox genes regulate rhombomere 5/6 expression of vhnf1, a repressor of rostral hindbrain fates, in a meis-dependent manner

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

Regulation of nuclear translocation of extracellular signal-regulated kinase 5 by active nuclear import and export mechanisms.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

Conserved regulation of proximodistal limb axis development by Meis1/Hth

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

A Genetic Risk Factor for Periodic Limb Movements in Sleep

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2695663

4 December 2018

Identifiers

DOI

10.1136/JMG.2008.062992

1 reference

19 August 2017

1 reference

19 August 2017

1 reference