(Q34959586)

5 August 2017

title

Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype (English)

1 reference

5 August 2017

1 reference

Matthew W State

1

1 reference

5 August 2017

John M Greally

2

1 reference

5 August 2017

Adam Cuker

3

1 reference

5 August 2017

Peter N Bowers

4

1 reference

5 August 2017

Octavian Henegariu

5

1 reference

5 August 2017

Thomas M Morgan

6

1 reference

5 August 2017

Murat Gunel

7

1 reference

5 August 2017

Michael DiLuna

8

1 reference

5 August 2017

Robert A King

9

1 reference

5 August 2017

Carol Nelson

10

1 reference

5 August 2017

Abigail Donovan

11

1 reference

5 August 2017

George M Anderson

12

1 reference

5 August 2017

James F Leckman

13

1 reference

5 August 2017

Trevor Hawkins

14

1 reference

5 August 2017

David L Pauls

15

1 reference

5 August 2017

Richard P Lifton

16

1 reference

5 August 2017

David C Ward

17

1 reference

5 August 2017

language of work or name

English

0 references

publication date

7 April 2003

1 reference

5 August 2017

number of pages

6

1 reference

Proceedings of the National Academy of Sciences of the United States of America

inferred from page(s)

published in

1 reference

5 August 2017

volume

100

1 reference

5 August 2017

issue

8

1 reference

5 August 2017

page(s)

4684-4689

1 reference

Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome

5 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Cloning and characterization of novel CIS family genes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Family study and segregation analysis of Tourette syndrome: evidence for a mixed model of inheritance

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Allele-specific replication timing of imprinted gene regions

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Allelic inactivation regulates olfactory receptor gene expression

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Thermal asymmetric interlaced PCR: automatable amplification and sequencing of insert end fragments from P1 and YAC clones for chromosome walking

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Genetic analysis of Tourette syndrome suggesting major gene effect

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

The inheritance of Gilles de la Tourette's syndrome and associated behaviors. Evidence for autosomal dominant transmission

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Analysis of the chromosomal DNA replication pattern using the bromodeoxyuridine labeling method

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Family data support a dominant major gene for Tourette syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Efficacy of fluvoxamine in obsessive-compulsive disorder. A double-blind comparison with placebo

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

A family study of Gilles de la Tourette syndrome.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Autosomal Dominant Gene Transmission in a Large Kindred with Gilles de la Tourette Syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Relationship of birth weight to the phenotypic expression of Gilles de la Tourette's syndrome in monozygotic twins

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=153616

Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0730775100

Asynchronous replication and allelic exclusion in the immune system

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0730775100

A population-based epidemiological study of Tourette syndrome among adolescents in Israel

21 January 2018

1 reference

12 December 2020

Association of fragile X syndrome with delayed replication of the FMR1 gene

1 reference

12 December 2020

An epidemiologic study of Gilles de la Tourette's syndrome in Israel

1 reference

12 December 2020

Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region

1 reference

12 December 2020

The mouse H19 locus mediates a transition between imprinted and non-imprinted DNA replication patterns

1 reference

12 December 2020

Position effect in human genetic disease

1 reference

12 December 2020

Complex segregation analysis of families ascertained through Gilles de la Tourette syndrome

1 reference

12 December 2020

Epigenetic silencing of CD4 in T cells committed to the cytotoxic lineage

1 reference

12 December 2020

A twin study of Tourette syndrome

1 reference

12 December 2020

Gene location in Tourette syndrome

1 reference

12 December 2020

The relationship between obsessive-compulsive disorder and Tourette's syndrome: a twin study

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.0730775100

1 reference

5 August 2017

0 references

1 reference

5 August 2017

1 reference