Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes (Q35095534)

6 August 2017

Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes (English)

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X-linked intellectual disability

6 August 2017

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disability affecting intellectual abilities

1 reference

Tejasvi S Niranjan

1

1 reference

6 August 2017

Cindy Skinner

2

1 reference

6 August 2017

Melanie May

3

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6 August 2017

Tychele Turner

4

1 reference

6 August 2017

Rebecca Rose

5

1 reference

6 August 2017

Roger Stevenson

6

1 reference

6 August 2017

Charles E Schwartz

7

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6 August 2017

Tao Wang

8

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6 August 2017

language of work or name

English

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publication date

13 February 2015

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6 August 2017

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6 August 2017

10

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6 August 2017

2

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6 August 2017

e0116454

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Creative Commons Attribution 4.0 International

6 August 2017

start time

13 February 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing

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Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1).

9 July 2018

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ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity

9 July 2018

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Tet proteins connect the O-linked N-acetylglucosamine transferase Ogt to chromatin in embryonic stem cells

9 July 2018

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Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes

9 July 2018

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An integrated map of genetic variation from 1,092 human genomes

9 July 2018

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A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability

9 July 2018

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Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy

9 July 2018

1 reference

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Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Mutations in PIGO, a member of the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Fragile X and X-linked intellectual disability: four decades of discovery

9 July 2018

1 reference

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Fast gapped-read alignment with Bowtie 2

9 July 2018

1 reference

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Human genome sequencing in health and disease

9 July 2018

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Mapping rare and common causal alleles for complex human diseases

9 July 2018

1 reference

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Effective detection of rare variants in pooled DNA samples using Cross-pool tailcurve analysis

9 July 2018

1 reference

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Exome sequencing as a tool for Mendelian disease gene discovery

9 July 2018

1 reference

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Unlocking Mendelian disease using exome sequencing

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

A framework for variation discovery and genotyping using next-generation DNA sequencing data

9 July 2018

1 reference

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Autism in two females with duplications involving Xp11.22-p11.23.

9 July 2018

1 reference

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Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Genetics of early onset cognitive impairment

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Integrating common and rare genetic variation in diverse human populations

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

9 July 2018

1 reference

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ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

9 July 2018

1 reference

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A method and server for predicting damaging missense mutations

9 July 2018

1 reference

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Target-enrichment strategies for next-generation sequencing

9 July 2018

1 reference

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Exome sequencing makes medical genomics a reality

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Sequencing technologies - the next generation

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Exome sequencing identifies the cause of a mendelian disorder

9 July 2018

1 reference

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Targeted capture and massively parallel sequencing of 12 human exomes

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

The genetic landscape of intellectual disability arising from chromosome X.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Ephrin-B1 regulates axon guidance by reverse signaling through a PDZ-dependent mechanism

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

PLINK: a tool set for whole-genome association and population-based linkage analyses

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Dysregulated metabotropic glutamate receptor-dependent translation of AMPA receptor and postsynaptic density-95 mRNAs at synapses in a mouse model of fragile X syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

dbSNP: the NCBI database of genetic variation

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

GRASP-1: a neuronal RasGEF associated with the AMPA receptor/GRIP complex

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Molecular cloning and mapping of human semaphorin F from the Cri-du-chat candidate interval

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Next generation sequencing in nonsyndromic intellectual disability: from a negative molecular karyotype to a possible causative mutation detection.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Exome sequencing identifies MVK mutations in disseminated superficial actinic porokeratosis.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4332666

10.1371/JOURNAL.PONE.0116454

27 September 2018

Identifiers

DOI

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6 August 2017

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6 August 2017

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