1q21.1 Microduplication expression in adults (Q37278755)

19 August 2017

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1q21.1 Microduplication expression in adults (English)

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19 August 2017

6

Stephen W Scherer

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19 August 2017

Alessia Dolcetti

1

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19 August 2017

Candice K Silversides

2

1 reference

19 August 2017

Christian R Marshall

3

1 reference

19 August 2017

Anath C Lionel

4

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19 August 2017

Dimitri J Stavropoulos

5

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19 August 2017

Anne S Bassett

7

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19 August 2017

language of work or name

English

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publication date

27 September 2012

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19 August 2017

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19 August 2017

15

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19 August 2017

4

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19 August 2017

282-289

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https://scigraph.springernature.com/pub.10.1038/gim.2012.129

19 August 2017

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cites work

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays

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Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways

6 September 2017

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Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

6 September 2017

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High frequencies of de novo CNVs in bipolar disorder and schizophrenia

6 September 2017

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Genome-wide association analysis of copy number variation in recurrent depressive disorder.

6 September 2017

1 reference

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Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defects.

6 September 2017

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On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease

6 September 2017

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An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.

6 September 2017

1 reference

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A copy number variation morbidity map of developmental delay

6 September 2017

1 reference

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Understanding the impact of 1q21.1 copy number variant

6 September 2017

1 reference

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Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

6 September 2017

1 reference

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Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

6 September 2017

1 reference

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Functional impact of global rare copy number variation in autism spectrum disorders

6 September 2017

1 reference

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Strong synaptic transmission impact by copy number variations in schizophrenia

6 September 2017

1 reference

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Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease

6 September 2017

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Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

6 September 2017

1 reference

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BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Large recurrent microdeletions associated with schizophrenia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Rare chromosomal deletions and duplications increase risk of schizophrenia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Global variation in copy number in the human genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Diagnostic genome profiling in mental retardation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Centiles for adult head circumference

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Germ-line DNA copy number variation frequencies in a large North American population

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

De novo copy number variants associated with intellectual disability have a paternal origin and age bias.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3817079

3 September 2018

Identifiers

DOI

10.1038/GIM.2012.129

1 reference

19 August 2017

1 reference

19 August 2017

1 reference