Catalogue of Transmission Genetics in Arabs
Names
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Catalogue of Transmission Genetics in Arabs
metasource: Fairsharing.org
version: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
CTGA
metasource: Fairsharing.org
version: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
Names
More detailed information about this field from each metasource.
Catalogue of Transmission Genetics in Arabs
metasource: Fairsharing.orgversion: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
CTGA
metasource: Fairsharing.orgversion: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
Names
More detailed information about this field from each metasource.
Catalogue of Transmission Genetics in Arabs
metasource: Fairsharing.orgversion: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
CTGA
metasource: Fairsharing.orgversion: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
The Centre for Arab Genomic Studies (CAGS) initiated the ambitious project to establish the CTGA (Catalogue of Transmission Genetics in Arabs) database for genetic disorders in Arabs with the aim to enlighten the scientific community and the public on the occurrence of inherited disorders in Arabs and to suggest future investigation strategies.
Description
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The Centre for Arab Genomic Studies (CAGS) initiated the ambitious project to establish the CTGA (Catalogue of Transmission Genetics in Arabs) database for genetic disorders in Arabs with the aim to enlighten the scientific community and the public on the occurrence of inherited disorders in Arabs and to suggest future investigation strategies.
metasource: Fairsharing.orgversion: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
In the Arab World, genetic diseases represent a major public health problem. Several factors contribute to the wide prevalence of genetic disorders in the region including the high rate of consanguinity, social trend to have more children until menopause, selective factors favoring inherited disease characters, and the lack of public awareness towards the early recognition and prevention of inherited disease. Recently, the Centre for Arab Genomic Studies (CAGS) initiated the ambitious project to establish the CTGA (Catalogue of Transmission Genetics in Arabs) database for genetic disorders in Arabs with the aim to enlighten the scientific community and the public on the occurrence of inherited disorders in Arabs and to suggest future investigation strategies. The CTGA database is continuously expanding its coverage since its public release in December 2004 by collecting data from published literature (national and international), hospital records, and personal communications. CTGA currently includes more than 900 records of Mendelian disorders described in Arab populations. Many of these records contain information about rare genetic disorders, mostly autosomal recessive, for which the genetic pathologies have not been characterized yet. Genetic linkage and genotype-phenotype correlation analyses of each of these disorders will surely offer a better understanding of the functions of the human genome. In 2004, the emphasis in the CTGA database was to collect data on the occurrence of genetic disorders in the United Arab Emirates. At present, the database is enlarging its coverage to include detailed information on genetic disorders occurring in other Arab countries.
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
Webpage:
http://www.cags.org.ae/ctga/Webpage
More detailed information about this field from each metasource.
http://www.cags.org.ae/ctga/
metasource: Fairsharing.orgversion: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
http://www.cags.org.ae/
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
Publications:
Publications
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CTGA: the database for genetic disorders in Arab populations
PMID: 16381941
metasource: Fairsharing.org
version: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
Publications
More detailed information about this field from each metasource.
CTGA: the database for genetic disorders in Arab populations
PMID: 16381941
metasource: Fairsharing.org
version: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
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CTGA: the database for genetic disorders in Arab populations
PubMed citations: 26.
26 articles citing: CTGA: the database for genetic disorders in Arab populations
The QChip1 knowledgebase and microarray for precision medicine in Qatar. PMID:35046417
A Population-Specific Major Allele Reference Genome From The United Arab Emirates Population. PMID:33968136
DALIA- a comprehensive resource of Disease Alleles in Arab population. PMID:33439861
GENE2D: A NoSQL Integrated Data Repository of Genetic Disorders Data. PMID:32781728
Genomics for All: International Open Science Genomics Projects and Capacity Building in the Developing World. PMID:30828348
A Perception on Genome-Wide Genetic Analysis of Metabolic Traits in Arab Populations. PMID:30761081
Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics. PMID:30409984
Genetics and genomic medicine in Tunisia. PMID:29663716
al mena: a comprehensive resource of human genetic variants integrating genomes and exomes from Arab, Middle Eastern and North African populations. PMID:28638141
Mapping genetic research in non-communicable disease publications in selected Arab countries: first step towards a guided research agenda. PMID:27832776
The locked genomes: A perspective from Arabia. PMID:27294028
Guidelines for acute management of hyperammonemia in the Middle East region. PMID:27099506
Regional research priorities in brain and nervous system disorders. PMID:26580328
Individualized medicine enabled by genomics in Saudi Arabia. PMID:25951871
Access to orphan drugs in the Middle East: Challenge and perspective. PMID:25343087
Genome at juncture of early human migration: a systematic analysis of two whole genomes and thirteen exomes from Kuwaiti population subgroup of inferred Saudi Arabian tribe ancestry. PMID:24896259
Mutation Spectrum and Birth Prevalence of Inborn Errors of Metabolism among Emiratis: A study from Tawam Hospital Metabolic Center, United Arab Emirates. PMID:24516753
Updates of the HbVar database of human hemoglobin variants and thalassemia mutations. PMID:24137000
Genetic substructure of Kuwaiti population reveals migration history. PMID:24066156
The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility. PMID:23860041
Consanguinity, endogamy, and genetic disorders in Tunisia. PMID:23208456
Identification of mutations underlying 20 inborn errors of metabolism in the United Arab Emirates population. PMID:22106832
Diagnosis of Sex Chromosome Disorders and Prenatal Diagnosis of Down Syndrome using Interphase Fluorescent In-Situ Hyperidization Technique. PMID:21475429
Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection. PMID:21089065
Collaborative genomics for human health and cooperation in the Mediterranean region. PMID:20664644
The Molecular Biology Database Collection: 2006 update. PMID:16381871
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genetic disorder
metasource: Fairsharing.org
version: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
genome
metasource: Fairsharing.org
version: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
human genes and diseases
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
general polymorphism databases
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
Tags
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genetic disorder
metasource: Fairsharing.orgversion: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
genome
metasource: Fairsharing.orgversion: FAIRsharing.org: CTGA; Catalogue of Transmission Genetics in Arabs; DOI: https://doi.org/10.25504/FAIRsharing.etp65g; Last edited: Jan. 8, 2019, 1:16 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
human genes and diseases
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
general polymorphism databases
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
genetic disorder genome human genes and diseases polymorphism
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