Confirmation of association between expanded CAG/CTG repeats and both schizophrenia and bipolar disorder (Q71806848)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8931160%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

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

1 reference

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21 October 2019

1 reference

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M C O'Donovan

1

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21 October 2019

C Guy

2

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21 October 2019

N Craddock

3

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21 October 2019

T Bowen

4

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21 October 2019

P McKeon

5

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21 October 2019

A Macedo

6

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21 October 2019

W Maier

7

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21 October 2019

D Wildenauer

8

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21 October 2019

H N Aschauer

9

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21 October 2019

S Sorbi

10

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21 October 2019

E Feldman

11

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21 October 2019

L Mynett-Johnson

12

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21 October 2019

E Claffey

13

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21 October 2019

B Nacmias

14

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21 October 2019

J Valente

15

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21 October 2019

A Dourado

16

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21 October 2019

E Grassi

17

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21 October 2019

E Lenzinger

18

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21 October 2019

A M Heiden

19

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21 October 2019

S Moorhead

20

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21 October 2019

D Harrison

21

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21 October 2019

J Williams

22

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21 October 2019

P McGuffin

23

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21 October 2019

M J Owen

24

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21 October 2019

publication date

1 November 1996

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21 October 2019

published in

Psychological Medicine

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21 October 2019

volume

26

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21 October 2019

issue

6

1 reference

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21 October 2019

page(s)

1145-1153

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cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeat

21 October 2019

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

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Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization

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CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

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Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms

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Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

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Fragile X genotype characterized by an unstable region of DNA.

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Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8931160%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference