A genome-wide association study of autism reveals a common novel risk locus at 5p14.1 (Q24634148)

21

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Daria Salyakina

2

Daria Salyakina

1 reference

ORCID Public Data File 2021

Holly N Cukier

Holly N Cukier

10

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Jonathan L Haines

20

Jonathan L Haines

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Gary W Beecham

13

Gary W Beecham

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Eden R Martin

16

Eden R Martin

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Michael L Cuccaro

19

Michael L Cuccaro

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Ioanna Konidari

4

Ioanna Konidari

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author name string

Deqiong Ma

1

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James M Jaworski

3

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Patrice L Whitehead

5

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Ashley N Andersen

6

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Joshua D Hoffman

7

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Susan H Slifer

8

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Dale J Hedges

9

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Anthony J Griswold

11

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Jacob L McCauley

12

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Harry H Wright

14

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Ruth K Abramson

15

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John P Hussman

17

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John R Gilbert

describes a project that uses

18

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language of work or name

English

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publication date

May 2009

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published in

Annals of Human Genetics

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volume

73

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issue

Pt 3

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page(s)

263-73

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genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

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A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

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Common genetic variants on 5p14.1 associate with autism spectrum disorders

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Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

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Crossref

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2009.00523.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1111/J.1469-1809.2009.00523.X

1 reference

2421413

2421413

1 reference

1 reference

1 reference