(Q33402638)

30 May 2018

title

An investigation of ribosomal protein L10 gene in autism spectrum disorders (English)

1 reference

30 May 2018

main subject

autism spectrum disorder

0 references

0 references

6

1 reference

26 July 2017

16

1 reference

Marie-Christine Mouren-Simeoni

26 July 2017

9

Henrik Anckarsäter

0 references

13

Marie-Christine Mouren-Simeoni

0 references

Marion Leboyer

Marion Leboyer

15

0 references

Richard Delorme

Richard Delorme

2

0 references

Christopher Gillberg

14

Christopher Gillberg

1 reference

30 May 2018

10

Maria Rastam

1 reference

30 May 2018

author name string

Xiaohong Gong

1

1 reference

30 May 2018

Fabien Fauchereau

3

1 reference

30 May 2018

Christelle M Durand

4

1 reference

30 May 2018

Pauline Chaste

5

1 reference

30 May 2018

Hany Goubran-Botros

7

1 reference

30 May 2018

Gudrun Nygren

8

1 reference

30 May 2018

I Carina Gillberg

11

1 reference

30 May 2018

Svenny Kopp

12

1 reference

30 May 2018

publication date

23 January 2009

1 reference

30 May 2018

published in

BMC Medical Genetics

1 reference

30 May 2018

volume

10

1 reference

30 May 2018

page(s)

7

1 reference

30 May 2018

https://scigraph.springernature.com/pub.10.1186/1471-2350-10-7

exact match

0 references

cites work

Analysis of X chromosome inactivation in autism spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645381

Association between microdeletion and microduplication at 16p11.2 and autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645381

The systematic functional characterisation of Xq28 genes prioritises candidate disease genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645381

X-inactivation profile reveals extensive variability in X-linked gene expression in females

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645381

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645381

Assembly of the QM protein onto the 60S ribosomal subunit occurs in the cytoplasm

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645381

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645381

Autism as a strongly genetic disorder: evidence from a British twin study

21 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645381

21 June 2018

https://api.crossref.org/works/10.1186%2F1471-2350-10-7

Genetics of autism: overview and new directions

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-7

Genetic linkage analysis of the X chromosome in autism, with emphasis on the fragile X region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-7

Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-7

The Asperger Syndrome (and high-functioning autism) Diagnostic Interview (ASDI): a preliminary study of a new structured clinical interview.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-7

21 January 2018

Identifiers

DOI

10.1186/1471-2350-10-7

1 reference

30 May 2018

Dimensions Publication ID

0 references

1 reference

30 May 2018

PubMed ID

19166581

1 reference

30 May 2018