(Q36515959)

14 August 2017

Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia (English)

1 reference

Xavier Estivill i Pallejà

14 August 2017

1 reference

7

1 reference

14 August 2017

Anna Brunet

1

1 reference

14 August 2017

Lluís Armengol

2

1 reference

14 August 2017

Trini Pelaez

3

1 reference

14 August 2017

Roser Guillamat

4

1 reference

14 August 2017

Vicenç Vallès

5

1 reference

14 August 2017

Elisabeth Gabau

6

1 reference

14 August 2017

Miriam Guitart

8

1 reference

14 August 2017

language of work or name

English

0 references

publication date

19 February 2008

1 reference

Behavioral and Brain Functions

14 August 2017

1 reference

14 August 2017

4

1 reference

14 August 2017

10

1 reference

https://scigraph.springernature.com/pub.10.1186/1744-9081-4-10

14 August 2017

0 references

cites work

Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Mouse models of 22q11 deletion syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Microduplication and triplication of 22q11.2: a highly variable syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

The molecular genetics of the 22q11-associated schizophrenia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Genetic abnormalities of chromosome 22 and the development of psychosis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

22q11 deletion syndrome: a genetic subtype of schizophrenia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

A common molecular basis for rearrangement disorders on chromosome 22q11

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Family-based association study of markers on chromosome 22 in schizophrenia using African-American, European-American, and Chinese families.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Screening for 22q11 deletions in a schizophrenia population.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Velocardiofacial syndrome in childhood-onset schizophrenia.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2278148

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

21 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18284679

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Duplication of the 22q11.2 region associated with congenital cardiac disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18284679

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The intrafamilial variability of the 22q11.2 microduplication encompasses a spectrum from minor cognitive deficits to severe congenital anomalies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18284679

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1744-9081-4-10

1 reference

Dimensions Publication ID

14 August 2017

0 references

1 reference

14 August 2017

1 reference