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

Unraveling the propensity of various genetic disorders and syndromes in the Koraga, an aboriginal tribe from southern India.

Journal of biosciences - 1 Jan 2024

Krishna Swathy M, Prabhu Suneetha M, DAS Ranajit

Abstract excerpt

Koragas, recognized as a particularly vulnerable tribal group (PVTG) by the Government of India, are from coastal Karnataka and Kerala. They are experiencing severe socioeconomic and health-related issues and rapid depopulation. The unique genetic makeup of Koragas has been maintained by the practice of endogamy. We aimed to identify genetic factors potentially associated with the predisposition of Koragas...

Read the complete abstract on PubMed

Topics

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

Share to Deafness
Share to Genetic Diseases, Inborn
Share to Genetics, Population

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome-Wide Association Study

Share to Haplotypes

Share to Homozygote

Share to Infant

Source

Identifiers

PMID: 38920107

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Unraveling the propensity of various genetic disorders and syndromes in the Koraga, an aboriginal tribe from southern India.PMID 38920107Read ↗

Fine-scale genetic structure and population-specific clinically relevant variants in the indigenous tribal populations of IndiaSemantic proximity Read ↗

Endogamy and high prevalence of deleterious mutations in India: evidence from strong founder events.Semantic proximity Read ↗

50,000 years of evolutionary history of India: Impact on health and disease variationSemantic proximity Read ↗

Endogamy and high prevalence of deleterious mutations in India: evidence from strong founder eventsSemantic proximity Read ↗

Complex genetic origin of Indian populations and its implications.Semantic proximity Read ↗

Population and genomic lessons from genetic analysis of two Indian populations.Semantic proximity Read ↗

Mapping the Diverse Genetic Disorders and Rare Diseases Among the Syrian Population: Implications on Refugee Health and Health Services in Host CountriesSemantic proximity Read ↗

The story of the lost twins: decoding the genetic identities of the Kumhar and Kurcha populations from the Indian subcontinent.Semantic proximity Read ↗

Rare genetic diseases in India: Steps toward a nationwide mission program.Semantic proximity Read ↗

An Atlas of Indian Genetic DiversitySemantic proximity Read ↗

Genetic landscape of the people of India: a canvas for disease gene exploration.Semantic proximity Read ↗

Clinical Applications and Implications of Common and Founder Mutations in Indian SubpopulationsSemantic proximity Read ↗

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