16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders. (Q50310657)

2 March 2018

title

16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders. (English)

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2 March 2018

main subject

risk factor

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author name string

Arivudainambi Ramalingam

1

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2 March 2018

Xin-Gang Zhou

2

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2 March 2018

Stephanie D Fiedler

3

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2 March 2018

Sarah J Brawner

4

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2 March 2018

Julie M Joyce

5

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2 March 2018

Hong-Yu Liu

6

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2 March 2018

Shihui Yu

7

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2 March 2018

publication date

26 May 2011

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2 March 2018

Journal of Human Genetics

published in

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2 March 2018

volume

56

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2 March 2018

issue

7

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2 March 2018

page(s)

541-544

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2 March 2018

https://scigraph.springernature.com/pub.10.1038/jhg.2011.42

exact match

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cites work

Primate segmental duplications: crucibles of evolution, diversity and disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Novel microdeletion syndromes detected by chromosome microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

The sequence and analysis of duplication-rich human chromosome 16

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Validation of the Agilent 244K oligonucleotide array-based comparative genomic hybridization platform for clinical cytogenetic diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Quantitative real-time polymerase chain reaction for the verification of genomic imbalances detected by microarray-based comparative genomic hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Population analysis of large copy number variants and hotspots of human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Mitotic control of kinetochore-associated dynein and spindle orientation by human Spindly

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Mitotic spindle regulation by Nde1 controls cerebral cortical size

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Lis1-Nde1-dependent neuronal fate control determines cerebral cortical size and lamination

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.42

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/JHG.2011.42

1 reference

2 March 2018

Dimensions Publication ID

1044973069

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Fatcat ID

release_63tm7n6stncknnsznpyhoepojy

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/63tm7n6stncknnsznpyhoepojy

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

21614007

1 reference

2 March 2018