(Q73978817)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10889556%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

title

Allelic distribution of CTG18.1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxia (English)

1 reference

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8 November 2019

1 reference

1 reference

6

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8 November 2019

author name string

M G McInnis

1

1 reference

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8 November 2019

T Swift-Scanlanl

2

1 reference

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8 November 2019

A T Mahoney

3

1 reference

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8 November 2019

J Vincent

4

1 reference

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8 November 2019

G Verheyen

5

1 reference

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8 November 2019

L Oruc

7

1 reference

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8 November 2019

O Riess

8

1 reference

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8 November 2019

C Van Broeckhoven

9

1 reference

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8 November 2019

H Chen

10

1 reference

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8 November 2019

J L Kennedy

11

1 reference

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8 November 2019

D F MacKinnon

12

1 reference

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8 November 2019

R L Margolis

13

1 reference

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8 November 2019

S G Simpson

14

1 reference

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8 November 2019

F J McMahon

15

1 reference

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8 November 2019

E Gershon

16

1 reference

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8 November 2019

J Nurnberger

17

1 reference

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8 November 2019

T Reich

18

1 reference

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8 November 2019

J R DePaulo

19

1 reference

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8 November 2019

C A Ross

20

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8 November 2019

publication date

1 July 2000

1 reference

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8 November 2019

number of pages

4

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inferred from page(s)

published in

Molecular Psychiatry

1 reference

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8 November 2019

volume

5

1 reference

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8 November 2019

issue

4

1 reference

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8 November 2019

page(s)

439-442

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4000747

8 November 2019

exact match

0 references

cites work

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

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7 January 2021

Genetic anticipation and imprinting in bipolar I illness.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

Anticipation in Swedish families with bipolar affective disorder.

1 reference

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7 January 2021

Anticipation in unipolar affective disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

Expanded trinucleotide CAG repeats in families with bipolar affective disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

Two commonly expanded CAG/CTG repeat loci: involvement in affective disorders?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

Detection of expanded CAG repeats in bipolar affective disorder using the repeat expansion detection (RED) method

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

Expanded CAG repeats in schizophrenia and bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

Confirmation of association between expanded CAG/CTG repeats and both schizophrenia and bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

Analysis of genome-wide CAG/CTG repeats, and at SEF2-1B and ERDA1 in schizophrenia and bipolar affective disorder.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

Molecular interpretation of expanded RED products in bipolar disorder by CAG/CTG repeats located at chromosomes 17q and 18q

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patients

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

Intergenerational CAG repeat expansion at ERDA1 in a family with childhood-onset depression, schizoaffective disorder, and recurrent major depression

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000747

7 January 2021

Genomic survey of bipolar illness in the NIMH genetics initiative pedigrees: A preliminary report

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7 January 2021

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

1 reference

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7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4000747

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10889556%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference