(Q36901252)

17 August 2017

Analysis of X chromosome inactivation in autism spectrum disorders (English)

1 reference

17 August 2017

autism spectrum disorder

0 references

0 references

5

1 reference

17 August 2017

26

1 reference

17 August 2017

14

Henrik Anckarsäter

1 reference

Marie-Christine Mouren-Simeoni

17 August 2017

12

Marie-Christine Mouren-Simeoni

0 references

Daniel Moreno-De-Luca

18

Daniel Moreno-De-Luca

0 references

Claudio Toma

Claudio Toma

4

0 references

Marion Leboyer

Marion Leboyer

11

0 references

Richard Delorme

Richard Delorme

7

0 references

Christopher Gillberg

17

Christopher Gillberg

1 reference

17 August 2017

15

Maria Rastam

1 reference

17 August 2017

Xiaohong Gong

1

1 reference

17 August 2017

Elena Bacchelli

2

1 reference

17 August 2017

Francesca Blasi

3

1 reference

17 August 2017

Pauline Chaste

6

1 reference

17 August 2017

Christelle M Durand

8

1 reference

17 August 2017

Fabien Fauchereau

9

1 reference

17 August 2017

Hany Goubran Botros

10

1 reference

17 August 2017

Marie-Christine Mouren-Simeoni

12

1 reference

17 August 2017

Gudrun Nygren

13

1 reference

17 August 2017

I Carina Gillberg

16

1 reference

17 August 2017

Daniel Moreno-De-Luca

18

1 reference

17 August 2017

Simona Carone

19

1 reference

17 August 2017

Ilona Nummela

20

1 reference

17 August 2017

Mari Rossi

21

1 reference

17 August 2017

Agatino Battaglia

22

1 reference

17 August 2017

International Molecular Genetic Study of Autism Consortium (IMGSAC)

23

1 reference

17 August 2017

Irma Jarvela

24

1 reference

17 August 2017

Elena Maestrini

25

1 reference

17 August 2017

1 September 2008

1 reference

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

17 August 2017

1 reference

17 August 2017

147B

1 reference

17 August 2017

830-835

1 reference

17 August 2017

6

1 reference

Defining the cause of skewed X-chromosome inactivation in X-linked mental retardation by use of a mouse model

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

The genetics of autistic disorders and its clinical relevance: a review of the literature

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

X chromosome-inactivation patterns of 1,005 phenotypically unaffected females

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Identification of MeCP2 mutations in a series of females with autistic disorder

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Mutation analysis of the coding sequence of the MECP2 gene in infantile autism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Y chromosome haplogroups in autistic subjects

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

X chromosome inactivation in carriers of Barth syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Nonrandom X-inactivation patterns in normal females: lyonization ratios vary with age.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

X-chromosome inactivation in mammals

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Autism spectrum disorders associated with X chromosome markers in French-Canadian males.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Brief report: non-random X chromosome inactivation in females with autism.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867005

Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females

4 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18361425

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/AJMG.B.30688

1 reference

17 August 2017

1 reference

17 August 2017

1 reference