Evidence map›Paper›PMID 42152144›Full record

ArticleBMC research notes2026

A parent-offspring phenotype dataset from an Indian population.

Padavinangady Nakul Bhat, T Manoj

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

2 authors.

Padavinangady Nakul BhatManipal Institute of Technology, Manipal Academy of Higher Education, Manipal, India.
T ManojManipal Institute of Technology, Manipal Academy of Higher Education, Manipal, India. t.manoj@manipal.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

ABO Blood-Group SystemParentsPhenotypeRh-Hr Blood-Group SystemAdultFemaleHumansIndiaMalePedigreeABO Blood-Group SystemRh-Hr Blood-Group SystemABO blood groupFamilial phenotypesHuman morphogenetic traitsMendelian inheritancePhenotypic datasetRh factor

Identifiers

PMID42152144
PMCPMC13352596

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.