ArticleBMC research notes2026
A parent-offspring phenotype dataset from an Indian population.
Article in BMC research notes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- A parent-offspring phenotype dataset from an Indian population.BMC research notes · 2026Article
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveThe purpose of this dataset is to document familial patterns of some observable human phenotypes within an Indian population. The data are collected to support the study of inheritance mechanisms across both well-established Mendelian traits and phenotypes with uncertain or population-dependent inheritance, and to provide a pedigree-based resource for methodological and computational research. DATA DESCRIPTION: The dataset comprises phenotypic information from 250 parent-offspring triplets. Five observable traits are recorded: ABO blood group, Rhesus (Rh) factor, widow's peak, facial dimples, and facial freckles. Data are collected using a structured questionnaire administered to adult participants, who reported their own traits as well as those of their biological parents. Minimal preprocessing was applied, and no statistical imputation was performed; missing values are explicitly encoded. Data validation was conducted by comparing observed inheritance patterns and phenotype frequencies for ABO blood groups and the Rh factor against expected population values to assess biological plausibility and population representativeness. The dataset is suitable for studies of genetic inheritance, evaluation of computational inheritance models, and development or benchmarking of intelligent imputation techniques.
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