Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

CTGA: the database for genetic disorders in Arab populations.

Nucleic acids research - 1 Jan 2006

Tadmouri Ghazi O, Al Ali Mahmoud Taleb, Al-Haj Ali Sarah, Al Khaja Najib

Abstract excerpt

The Arabs comprise a genetically heterogeneous group that resulted from the admixture of different populations throughout history. They share many common characteristics responsible for a considerable proportion of perinatal and neonatal mortalities. To this end, the Centre for Arab Genomic Studies (CAGS) launched a pilot project to construct the 'Catalogue of Transmission Genetics in Arabs' (CTGA) database for...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Arabs
Share to Databases, Genetic
Share to Genes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Diseases, Inborn

Share to Internet

Share to Phenotype

Share to User-Computer Interface

Source

Open in PubMed Open full text

Identifiers

PMID: 16381941
DOI: 10.1093/nar/gkj015
PMCID: PMC1347378

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CTGA: the database for genetic disorders in Arab populations.PMID 16381941Read ↗

Arab genetic disease database (AGDDB): a population-specific clinical and mutation database.Semantic proximity Read ↗

Spectrum of Genetic Disorders and Gene Variants in the United Arab Emirates National Population: Insights from the CTGA DatabaseSemantic proximity Read ↗

DALIA- a comprehensive resource of Disease Alleles in Arab population.Semantic proximity Read ↗

Pathogenic variation underlying rare diseases in an Arab Population: implications for screening programsSemantic proximity Read ↗

The Israeli National Genetic database: a 10-year experience.Semantic proximity Read ↗

Profile of genetic disorders prevalent in northeast region of Cairo, EgyptSemantic proximity Read ↗

AVDB: The Arab Variation and Disease Burden DatabaseSemantic proximity Read ↗

The genomic landscape of rare disorders in the Middle EastSemantic proximity Read ↗

Burden of Mendelian disorders in a large Middle Eastern biobank.Semantic proximity Read ↗

Common disease-associated gene variants in a Saudi Arabian populationSemantic proximity Read ↗

The Genomic Landscape of Rare Disorders in the Middle EastSemantic proximity Read ↗

Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variants.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.