Both rare and common genetic variants contribute to autism in the Faroe Islands (Q61446049)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30675382%20AND%20SRC:MED&resulttype=core&format=json

20 April 2020

title

Both rare and common genetic variants contribute to autism in the Faroe Islands (English)

1 reference

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20 April 2020

1

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20 April 2020

Freddy Cliquet

2

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20 April 2020

Julien Buratti

7

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20 April 2020

author name string

Coralie Carton

3

1 reference

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20 April 2020

Guillaume Huguet

4

1 reference

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20 April 2020

Alexandre Mathieu

5

1 reference

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20 April 2020

Thomas Kergrohen

6

1 reference

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20 April 2020

Nathalie Lemière

8

1 reference

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20 April 2020

Laurence Cuisset

9

1 reference

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20 April 2020

Thierry Bienvenu

10

1 reference

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20 April 2020

Anne Boland

11

1 reference

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20 April 2020

Jean-François Deleuze

12

1 reference

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20 April 2020

Tormodur Stora

13

1 reference

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20 April 2020

Rannva Biskupstoe

14

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20 April 2020

Jónrit Halling

15

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20 April 2020

Guðrið Andorsdóttir

16

1 reference

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20 April 2020

Eva Billstedt

17

1 reference

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20 April 2020

Thomas Bourgeron

19

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20 April 2020

Christopher Gillberg

18

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20 April 2020

language of work or name

English

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publication date

21 January 2019

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20 April 2020

1 reference

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20 April 2020

volume

4

1 reference

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20 April 2020

page(s)

1

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Creative Commons Attribution 4.0 International

20 April 2020

issue

1

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copyright license

start time

21 January 2019

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

Cytoscape

1 reference

9 June 2022

https://europepmc.org/search?query=(METHODS:'Cytoscape')

inferred from PubMed Central ID database lookup

exact match

https://scigraph.springernature.com/pub.10.1038/s41525-018-0075-2

0 references

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Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

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The intellectual disability gene Kirrel3 regulates target-specific mossy fiber synapse development in the hippocampus

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Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications.

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7 January 2021

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

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7 January 2021

Spectrum of PEX1 and PEX6 variants in Heimler syndrome

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7 January 2021

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7 January 2021

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A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism

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7 January 2021

A novel founder BBS1 mutation explains a unique high prevalence of Bardet-Biedl syndrome in the Faroe Islands.

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7 January 2021

High incidence of cystic fibrosis on the Faroe Islands: a molecular and genealogical study

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7 January 2021

Molecular genetic basis and prevalence of glycogen storage disease type IIIA in the Faroe Islands

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7 January 2021

High inbreeding in the Faroe Islands does not appear to constitute a risk factor for multiple sclerosis

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7 January 2021

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Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population.

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7 January 2021

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PubMed

https://pubmed.ncbi.nlm.nih.gov/30675382

12 December 2020

inferred from PubMed ID database lookup

Autism in the Faroe Islands: diagnostic stability from childhood to early adult life.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/30675382

12 December 2020

inferred from PubMed ID database lookup

Kalirin-9 and Kalirin-12 Play Essential Roles in Dendritic Outgrowth and Branching

1 reference

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https://pubmed.ncbi.nlm.nih.gov/30675382

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/S41525-018-0075-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30675382%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

20 April 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30675382%20AND%20SRC:MED&resulttype=core&format=json

20 April 2020

1 reference