Genetic association signal near NTN4 in Tourette syndrome (Q34076218)

30 July 2017

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Genetic association signal near NTN4 in Tourette syndrome (English)

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30 July 2017

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32

Guy A Rouleau

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Johannes Hebebrand

14

Johannes Hebebrand

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Fotis Tsetsos

Fotis Tsetsos

5

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Dongmei Yu

Dongmei Yu

2

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Péter Nagy

Peter Nagy

16

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Yulia Worbe

Yulia Worbe

21

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Peristera Paschou

Peristera Paschou

1

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Renata Rizzo

Renata Rizzo

19

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Paul Sandor

Paul Sandor

25

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Cathy L. Barr

Cathy Barr

26

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Danielle Posthuma

Danielle Posthuma

31

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Markus M Nöthen

Markus Noethen

15

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Zsanett Tarnok

Zsanett Tarnok

18

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Eric R. Gamazon

Eric Gamazon

9

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Nancy J Cox

36

Nancy J Cox

1 reference

30 July 2017

37

Carol A Mathews

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30 July 2017

17

Csaba Barta

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30 July 2017

23

Danielle C Cath

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30 July 2017

38

Jeremiah M Scharf

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30 July 2017

13

Mara Stamenkovic

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30 July 2017

20

Christel Depienne

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30 July 2017

33

Harald Aschauer

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30 July 2017

3

Gloria Gerber

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30 July 2017

Patrick Evans

4

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30 July 2017

Lea K Davis

6

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30 July 2017

Iordanis Karagiannidis

7

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30 July 2017

Jonathan Chaponis

8

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30 July 2017

Kirsten Mueller-Vahl

10

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30 July 2017

Manfred Stuhrmann

11

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30 July 2017

Monika Schloegelhofer

12

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30 July 2017

Andreas Hartmann

22

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30 July 2017

Cathy L Budman

24

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30 July 2017

Thomas Wolanczyk

27

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30 July 2017

Harvey Singer

28

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30 July 2017

I-Ching Chou

29

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30 July 2017

Marco Grados

30

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30 July 2017

Nelson B Freimer

34

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30 July 2017

David L Pauls

35

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30 July 2017

21 July 2014

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30 July 2017

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30 July 2017

76

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30 July 2017

310-315

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30 July 2017

2

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Histidine decarboxylase deficiency causes tourette syndrome: parallel findings in humans and mice

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

The genetic basis of Gilles de la Tourette Syndrome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Genetic risk factors for type 2 diabetes: a trans-regulatory genetic architecture?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Systematic localization of common disease-associated variation in regulatory DNA

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Genome-wide association study of Tourette's syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Genetic architectures of psychiatric disorders: the emerging picture and its implications

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Patterns of cis regulatory variation in diverse human populations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Netrins: versatile extracellular cues with diverse functions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Family-based genetic association study of DLGAP3 in Tourette Syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

METAL: fast and efficient meta-analysis of genomewide association scans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

L-histidine decarboxylase and Tourette's syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Netrin, Slit and Wnt receptors allow axons to choose the axis of migration.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Estimation of significance thresholds for genomewide association scans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Principal components analysis corrects for stratification in genome-wide association studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Sequence variants in SLITRK1 are associated with Tourette's syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

snRNP Sm proteins share two evolutionarily conserved sequence motifs which are involved in Sm protein-protein interactions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANA.24215

Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140987

28 October 2018

Identifiers

DOI

10.1002/ANA.24215

1 reference

30 July 2017

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30 July 2017

1 reference