Evidence map›Paper›PMID 12532038›Full record

ArticleJournal of genetics2002

Candidate gene polymorphisms among North Indians and their association with schizophrenia in a case-control study.

Prachi Semwal, Suman Prasad, Panchami G Varma, A M Bhagwat, S N Deshpande, B K Thelma

Abstract read
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In one paragraph

Article in Journal of genetics, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 3 pooled it
0.5field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 3 syntheses or guidelines pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Theranostic Biomarkers for Schizophrenia.International journal of molecular sciences · 2017
    Review
  5. Review
  6. Article
  7. Genetics of schizophrenia from a clinicial perspective.International review of psychiatry (Abingdon, England) · 2012
    Review
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Prachi SemwalDepartment of Genetics, University of Delhi South Campus, Benito Juarez Road, New Delhi 110 021, India.
Suman Prasad
Panchami G Varma
A M Bhagwat
S N Deshpande
B K Thelma
University of Delhi · INAtal Bihari Vajpayee Institute of Medical Sciences and Dr. Ram Manohar Lohia Hospital · INShri Vile Parle Kelavani Mandal · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Knowledge of candidate gene polymorphisms in a population is useful for a variety of gene-disease association studies, particularly for some complex traits. A number of candidate genes, a majority of them from the monoaminergic pathway in the brain, have been very popular in association studies with schizophrenia, a neuropsychiatric disorder. In this study diallelic/multiallelic polymorphisms in some dopaminergic, serotonergic and membrane-phospholipid-related genes have been evaluated in a control population recruited from North India. Association, if any, of these allelic variants with schizophrenia has been tested using a case-control approach. The case data have been taken from our published family-based association studies in schizophrenia. Of the eight genes tested in this study, association with schizophrenia was observed for only two gene polymorphisms, one in the promoter region of the serotonin 2A receptor gene and the other in the tryptophan hydroxylase gene. One new allele for the dopamine transporter gene (with eight repeats, 570-bp size), not reported in any population so far, has been identified in one individual in our sample. The data generated in this study, besides providing a normative background for various disease association studies, are a significant contribution to the population-specific genome database, a currently growing requirement.

Indexed as

Polymorphism, GeneticAdultCase-Control StudiesCatechol O-MethyltransferaseDopamineFemaleGene FrequencyHumansIndiaMalePhospholipases APhosphoric Monoester HydrolasesReceptors, SerotoninSchizophreniaTryptophan HydroxylaseCatechol O-MethyltransferaseDopamineinositol-1,4-bisphosphate 1-phosphatasePhospholipases APhosphoric Monoester HydrolasesReceptors, SerotoninTryptophan Hydroxylase

Identifiers

PMID12532038
OpenAlexW2082008174

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.