Replicated linear association between DUF1220 copy number and severity of social impairment in autism (Q28258666)

3 July 2018

title

Replicated linear association between DUF1220 copy number and severity of social impairment in autism (English)

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3 July 2018

0 references

1 reference

J M Davis

1

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3 July 2018

V B Searles Quick

series ordinal

2

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3 July 2018

J M Sikela

series ordinal

3

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3 July 2018

language of work or name

English

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publication date

11 March 2015

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3 July 2018

published in

Human Genetics

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3 July 2018

volume

134

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3 July 2018

issue

6

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3 July 2018

page(s)

569-575

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3 July 2018

DUF1220 copy number is linearly associated with increased cognitive function as measured by total IQ and mathematical aptitude scores

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1 reference

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14 July 2018

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DUF1220 protein domains drive proliferation in human neural stem cells and are associated with increased cortical volume in anthropoid primates

14 July 2018

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Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome

14 July 2018

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DUF1220 dosage is linearly associated with increasing severity of the three primary symptoms of autism

14 July 2018

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Inferring polymorphism-induced regulatory gene networks active in human lymphocyte cell lines by weighted linear mixed model analysis of multiple RNA-Seq datasets

14 July 2018

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Mode of genetic inheritance modifies the association of head circumference and autism-related symptoms: a cross-sectional study

14 July 2018

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Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait

14 July 2018

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Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder

14 July 2018

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14 July 2018

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Evolutionary history and genome organization of DUF1220 protein domains

14 July 2018

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Association testing of copy number variants in schizophrenia and autism spectrum disorders

14 July 2018

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DUF1220-domain copy number implicated in human brain-size pathology and evolution

14 July 2018

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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DUF1220 domains, cognitive disease, and human brain evolution

14 July 2018

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14 July 2018

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

14 July 2018

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

14 July 2018

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Familial aggregation of quantitative autistic traits in multiplex versus simplex autism

14 July 2018

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14 July 2018

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14 July 2018

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Strong association of de novo copy number mutations with autism

14 July 2018

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Human lineage-specific amplification, selection, and neuronal expression of DUF1220 domains

14 July 2018

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Autism at the beginning: microstructural and growth abnormalities underlying the cognitive and behavioral phenotype of autism

14 July 2018

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A novel gene family NBPF: intricate structure generated by gene duplications during primate evolution

14 July 2018

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Why the frontal cortex in autism might be talking only to itself: local over-connectivity but long-distance disconnection

14 July 2018

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14 July 2018

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Genetics of austim: complex aetiology for a heterogeneous disorder

14 July 2018

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Evidence of brain overgrowth in the first year of life in autism

14 July 2018

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Neuron number and size in prefrontal cortex of children with autism

21 January 2018

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Accelerated head growth in early development of individuals with autism

21 January 2018

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Brief report: cognitive correlates of enlarged head circumference in children with autism

21 January 2018

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Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia.

21 January 2018

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21 January 2018

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Essential versus complex autism: definition of fundamental prognostic subtypes

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25758905

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetics of autism spectrum disorders

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25758905

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00439-015-1537-6

1 reference

3 July 2018

Dimensions Publication ID

0 references

1 reference

3 July 2018

PubMed publication ID

25758905

1 reference

3 July 2018