Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes (Q24605530)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

title

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

attention deficit hyperactivity disorder

1 February 2020

main subject

0 references

1 reference

3

1 reference

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1 February 2020

Joseph Glessner

6

1 reference

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1 February 2020

Monica D'Arcy

7

1 reference

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1 February 2020

Struan F.A. Grant

16

1 reference

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1 February 2020

Marcella Devoto

18

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1 February 2020

author name string

J Elia

1

1 reference

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1 February 2020

X Gai

2

1 reference

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1 February 2020

J C Perin

4

1 reference

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1 February 2020

E Geiger

5

1 reference

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1 February 2020

E Frackelton

9

1 reference

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1 February 2020

C Kim

10

1 reference

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1 February 2020

F Lantieri

11

1 reference

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1 February 2020

B M Muganga

12

1 reference

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1 February 2020

L Wang

13

1 reference

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1 February 2020

T Takeda

14

1 reference

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1 February 2020

E F Rappaport

15

1 reference

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1 February 2020

W Berrettini

17

1 reference

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1 February 2020

T H Shaikh

19

1 reference

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1 February 2020

H Hakonarson

20

1 reference

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1 February 2020

P S White

21

1 reference

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1 February 2020

R deBerardinis

8

1 reference

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1 February 2020

language of work or name

English

0 references

publication date

23 June 2009

1 reference

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1 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

volume

15

1 reference

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1 February 2020

page(s)

637-646

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1 February 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

Large recurrent microdeletions associated with schizophrenia

1 February 2020

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Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder

7 April 2017

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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

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12 December 2020

inferred from PubMed ID database lookup

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7 January 2021

Adult-onset Alexander disease with palatal myoclonus and intraventricular tumour

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Identifiers

DOI

10.1038/MP.2009.57

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

1 February 2020

1002123833

0 references

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

2 references