Prediction of human disease genes by human-mouse conserved coexpression analysis (Q33325895)

25 July 2017

Prediction of human disease genes by human-mouse conserved coexpression analysis (English)

1 reference

25 July 2017

Elena Grassi

3

0 references

Martin Oti

Martin Oti

6

0 references

Rosario M. Piro

Rosario Michael Piro

2

0 references

Ugo Ala

Ugo Ala

1

0 references

Ferdinando Di Cunto

Ferdinando Di Cunto

8

0 references

author name string

Christian Damasco

4

1 reference

PubMed ID

18369433

25 July 2017

Lorenzo Silengo

5

1 reference

PubMed ID

18369433

25 July 2017

Paolo Provero

7

1 reference

25 July 2017

28 March 2008

1 reference

PLOS Computational Biology

25 July 2017

1 reference

25 July 2017

4

1 reference

25 July 2017

e1000043

1 reference

25 July 2017

3

1 reference

Creative Commons Attribution 4.0 International

25 July 2017

start time

28 March 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.

1 reference

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A human phenome-interactome network of protein complexes implicated in genetic disorders

21 June 2018

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The modular nature of genetic diseases.

21 June 2018

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Entrez Gene: gene-centered information at NCBI

21 June 2018

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21 June 2018

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A Kv4.2 truncation mutation in a patient with temporal lobe epilepsy.

21 June 2018

1 reference

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Bioinformatics methods for identifying candidate disease genes

21 June 2018

1 reference

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TOM: a web-based integrated approach for identification of candidate disease genes

21 June 2018

1 reference

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Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes

21 June 2018

1 reference

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Human protein reference database--2006 update

21 June 2018

1 reference

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G2D: a tool for mining genes associated with disease

21 June 2018

1 reference

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A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Synonymous mutations in CFTR exon 12 affect splicing and are not neutral in evolution.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Speeding disease gene discovery by sequence based candidate prioritization

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

CLOE: identification of putative functional relationships among genes by comparison of expression profiles between two species

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Structure and function of Kv4-family transient potassium channels

21 June 2018

1 reference

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Genome-wide identification of genes likely to be involved in human genetic disease

21 June 2018

1 reference

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A gene atlas of the mouse and human protein-encoding transcriptomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Network biology: understanding the cell's functional organization

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Inter-species differences of co-expression of neighboring genes in eukaryotic genomes

21 June 2018

1 reference

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Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

POCUS: mining genomic sequence annotation to predict disease genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Development of human protein reference database as an initial platform for approaching systems biology in humans

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

A gene-coexpression network for global discovery of conserved genetic modules

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Pre-mRNA splicing and human disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

The Stanford Microarray Database: data access and quality assessment tools

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Evidence for large domains of similarly expressed genes in the Drosophila genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Association of genes to genetically inherited diseases using data mining

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Comparative assessment of large-scale data sets of protein-protein interactions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Molecular cloning and characterization of CALP/KChIP4, a novel EF-hand protein interacting with presenilin 2 and voltage-gated potassium channel subunit Kv4

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

21 June 2018

1 reference

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A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Cluster analysis and display of genome-wide expression patterns

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Exclusion of malignant hyperthermia susceptibility (MHS) from a putative MHS2 locus on chromosome 17q and of the alpha 1, beta 1, and gamma subunits of the dihydropyridine receptor calcium channel as candidates for the molecular defect

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Alpha2-macroglobulin deficiency in a patient with Ehlers-Danlos syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2268251

Predicting disease genes using protein-protein interactions.

21 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PCBI.1000043

Gene expression analyses reveal molecular relationships among 20 regions of the human CNS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PCBI.1000043

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PCBI.1000043

Identification of GUCY2D gene mutations in CORD5 families and evidence of incomplete penetrance

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PCBI.1000043

Study of the voltage-gated sodium channel beta 1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)

21 January 2018

1 reference

12 December 2020

Conservation and coevolution in the scale-free human gene coexpression network

1 reference

12 December 2020

Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneity

1 reference

12 December 2020

Tetraspanin CD9 is associated with very late-acting integrins in human vascular smooth muscle cells and modulates collagen matrix reorganization

1 reference

12 December 2020

Split hand malformation, hypospadias, microphthalmia, distinctive face and short stature in two brothers suggest a new syndrome

1 reference

12 December 2020

A text-mining analysis of the human phenome

1 reference

12 December 2020

10.1371/JOURNAL.PCBI.1000043

Identifiers

DOI

1 reference

journals/ploscb/AlaPGDSOPC08

25 July 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

25 July 2017

1 reference

PubMed ID

18369433