Strong evidence for a novel schizophrenia risk locus on chromosome 1p31.1 in homogeneous pedigrees from Tamil Nadu, India.

doi:10.1176/appi.ajp.2008.08030442

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

Community

Back to search

Article

Strong evidence for a novel schizophrenia risk locus on chromosome 1p31.1 in homogeneous pedigrees from Tamil Nadu, India.

The American journal of psychiatry - 1 Feb 2009

Holliday Elizabeth G, Nyholt Dale R, Tirupati Srinivasan, John Sujit, Ramachandran Padmavati, Ramamurti Mangala, Ramadoss Ayankaran Jothi, Jeyagurunathan Anitha, Kottiswaran Sowndari, Smith Heather J, Filippich Cheryl, Nertney Deborah A, Nancarrow Derek J, Hayward Nicholas K, Watkins W Scott, Jorde Lynn B, Thara Rangaswamy, Mowry Bryan J

Abstract excerpt

OBJECTIVE: The study of ethnically homogeneous populations may help to identify schizophrenia risk loci. The authors conducted a genomewide linkage scan for schizophrenia in an Indian population. METHOD: Participants were 441 individuals (262 affected probands and siblings) who were recruited primarily from one ethnically homogeneous group, the Tamil Brahmin caste, although individuals from other geographically...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 1

Share to Consanguinity

Share to Cyclic Nucleotide Phosphodiesterases, Type 4

Share to India

Share to Lod Score

Share to Microsatellite Repeats

Share to Schizophrenia

Source

Open in PubMed

Identifiers

PMID: 18829870
DOI: 10.1176/appi.ajp.2008.08030442

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

Strong evidence for a novel schizophrenia risk locus on chromosome 1p31.1 in homogeneous pedigrees from Tamil Nadu, India.PMID 18829870Read ↗

A reanalysis of 409 European-Ancestry and African American schizophrenia pedigrees reveals significant linkage to 8p23.3 with evidence of locus heterogeneity.Semantic proximity Read ↗

Chromosomal region 1q24.1 is associated with increased risk of schizophrenia in Pakistani population.Semantic proximity Read ↗

Evidence for schizophrenia susceptibility alleles in the Indian population: An association of neurodevelopmental genes in case-control and familial samples.Semantic proximity Read ↗

Clinical features of schizophrenia and linkage to chromosomes 5q, 6p, 8p, and 10p in the Irish Study of High-Density Schizophrenia Families.Semantic proximity Read ↗

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia.Semantic proximity Read ↗

Novel linkage to chromosome 20p using latent classes of psychotic illness in 270 Irish high-density families.Semantic proximity Read ↗

Chromosome 1 loci in Finnish schizophrenia families.Semantic proximity Read ↗

Fine mapping of the schizophrenia susceptibility locus on chromosome 1q22.Semantic proximity Read ↗

Genome scan of Han Chinese schizophrenia families from Taiwan: confirmation of linkage to 10q22.3.Semantic proximity Read ↗

Genetics of schizophrenia: recent advances.Semantic proximity Read ↗

Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms.Semantic proximity Read ↗

Genome-wide scan of homogeneous subtypes of NIMH genetics initiative schizophrenia families.Semantic proximity Read ↗

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