(Q35796509)

10 August 2017

Additional support for the association of SLITRK1 var321 and Tourette syndrome (English)

1 reference

Xavier Estivill i Pallejà

10 August 2017

1 reference

7

1 reference

10 August 2017

P Alonso

5

0 references

author name string

B J O'Roak

1

1 reference

10 August 2017

T M Morgan

2

1 reference

10 August 2017

D O Fishman

3

1 reference

10 August 2017

E Saus

4

1 reference

10 August 2017

M Gratacòs

6

1 reference

10 August 2017

O Teltsh

8

1 reference

10 August 2017

Y Kohn

9

1 reference

10 August 2017

K K Kidd

10

1 reference

10 August 2017

J Cho

11

1 reference

10 August 2017

R P Lifton

12

1 reference

10 August 2017

M W State

13

1 reference

10 August 2017

language of work or name

English

0 references

publication date

30 March 2010

1 reference

10 August 2017

1 reference

10 August 2017

15

1 reference

10 August 2017

5

1 reference

10 August 2017

447-450

1 reference

https://scigraph.springernature.com/pub.10.1038/mp.2009.105

10 August 2017

0 references

cites work

The behavioral spectrum of Gilles de la Tourette syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292207

MicroRNA target site polymorphisms and human disease

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292207

Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292207

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292207

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292207

Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292207

LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292207

Sequence variants in SLITRK1 are associated with Tourette's syndrome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292207

Functional SLITRK1 var321, varCDfs and SLC6A4 G56A variants and susceptibility to obsessive-compulsive disorder.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292207

A genetic profile of contemporary Jewish populations

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3292207

Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20351724

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/MP.2009.105

1 reference

Dimensions Publication ID

10 August 2017

0 references

1 reference

10 August 2017

1 reference