(Q36943655)

English

Array comparative genomic hybridization and computational genome annotation in constitutional cytogenetics: suggesting candidate genes for novel submicroscopic chromosomal imbalance syndromes

scientific article published on September 2007

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scholarly article

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Europe PubMed Central

17 August 2017

1 reference

Europe PubMed Central

Array comparative genomic hybridization and computational genome annotation in constitutional cytogenetics: suggesting candidate genes for novel submicroscopic chromosomal imbalance syndromes (English)

1 reference

Europe PubMed Central

17 August 2017

genome annotation

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based on heuristic

inferred from title

Steven van Vooren

object named as

Steven Van Vooren

1

0 references

4

object named as

Yves Moreau

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Europe PubMed Central

17 August 2017

Joris R Vermeesch

5

object named as

Joris R Vermeesch

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Europe PubMed Central

17 August 2017

3

object named as

Bart De Moor

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Europe PubMed Central

17 August 2017

2

object named as

Bert Coessens

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Europe PubMed Central

17 August 2017

language of work or name

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publication date

1 September 2007

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Europe PubMed Central

17 August 2017

Genetics in Medicine

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Europe PubMed Central

17 August 2017

9

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Europe PubMed Central

17 August 2017

9

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Europe PubMed Central

17 August 2017

642-649

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Europe PubMed Central

17 August 2017

https://scigraph.springernature.com/pub.10.1097/gim.0b013e318145b27b

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Medical applications of array CGH and the transformation of clinical cytogenetics

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Structural variation in the human genome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Molecular karyotyping in human constitutional cytogenetics

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Comparative genomic hybridization

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Diagnostic genome profiling in mental retardation

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Strong association of de novo copy number mutations with autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

What's new in karyotyping? The move towards array comparative genomic hybridisation (CGH).

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalities.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

A similarity-based method for genome-wide prediction of disease-relevant human genes.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

A computational system to select candidate genes for complex human traits

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

SUSPECTS: enabling fast and effective prioritization of positional candidates

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

GeneSeeker: extraction and integration of human disease-related information from web-based genetic databases

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Gene prioritization through genomic data fusion

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

G2D: a tool for mining genes associated with disease

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Integration of text- and data-mining using ontologies successfully selects disease gene candidates

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Predicting disease genes using protein-protein interactions.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

A gene network for navigating the literature

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Mapping biomedical concepts onto the human genome by mining literature on chromosomal aberrations

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

TXTGate: profiling gene groups with text-based information

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

PhenomicDB: a new cross-species genotype/phenotype resource

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Speeding disease gene discovery by sequence based candidate prioritization

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

POCUS: mining genomic sequence annotation to predict disease genes

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

TEAM: a tool for the integration of expression, and linkage and association maps

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

CGI: a new approach for prioritizing genes by combining gene expression and protein-protein interaction data

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Computational disease gene identification: a concert of methods prioritizes type 2 diabetes and obesity candidate genes.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

A strategy to search for common obesity and type 2 diabetes genes

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Are the current ontologies in biology good ontologies?

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Computational approaches to phenotyping: high-throughput phenomics.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Ontology annotation: mapping genomic regions to biological function

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Cytogenetic genotype-phenotype studies: improving genotyping, phenotyping and data storage

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

A protocol for high-throughput phenotyping, suitable for quantitative trait analysis in mice

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Mapping phenotypes to language: a proposal to organize and standardize the clinical descriptions of malformations

1 reference

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21 January 2018

Minimum information about a microarray experiment (MIAME)-toward standards for microarray data

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

MGED standards: work in progress

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

The human phenome project

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Phenotypic abnormalities: Terminology and classification

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318145B27B

21 January 2018

Identifiers

10.1097/GIM.0B013E318145B27B

1 reference

Europe PubMed Central

17 August 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

17 August 2017

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