(Q40172707)

English

Sequencing and analyzing the t(1;7) reciprocal translocation breakpoints associated with a case of childhood-onset schizophrenia/autistic disorder

scientific article published on 19 September 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Sequencing and analyzing the t(1;7) reciprocal translocation breakpoints associated with a case of childhood-onset schizophrenia/autistic disorder (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

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1 reference

based on heuristic

inferred from title

Anjene M. Addington

2

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5

object named as

Eric D Green

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Judith L. Rapoport

4

object named as

Judith L Rapoport

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Jacquelyn R Idol

1

object named as

Jacquelyn R Idol

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

author name string

Robert T Long

3

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Europe PubMed Central

PubMed publication ID

18 September 2017

language of work or name

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publication date

19 September 2007

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Journal of Autism and Developmental Disorders

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

38

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

4

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Europe PubMed Central

PubMed publication ID

18 September 2017

668-677

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

https://scigraph.springernature.com/pub.10.1007/s10803-007-0435-8

0 references

Autistic children who become schizophrenic.

1 reference

https://api.crossref.org/works/10.1007%2FS10803-007-0435-8

21 January 2018

A physical map of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strong association of de novo copy number mutations with autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Looking for childhood-onset schizophrenia: the first 71 cases screened

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparative physical mapping of targeted regions of the rat genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Childhood-onset schizophrenia: rare but worth studying

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brief report: translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The neurodevelopmental model of schizophrenia: update 2005.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Positive associations of polymorphisms in the metabotropic glutamate receptor type 3 gene (GRM3) with schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptional Regulatory Elements in the Human Genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable and nonheritable risk factors for autism spectrum disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The DNA sequence of human chromosome 7

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytogenetic survey of 11,680 newborn infants

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP)

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A complex chromosome rearrangement in a boy with autism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pervasive developmental disorder and childhood-onset schizophrenia: comorbid disorder or a phenotypic variant of a very early onset illness?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the cat eye syndrome critical region in humans and the region of conserved synteny in mice: a search for candidate genes at or near the human chromosome 22 pericentromere

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strategies for the systematic sequencing of complex genomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 1 loci in Finnish schizophrenia families

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Initial sequencing and analysis of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17879154

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10803-007-0435-8

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

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