ArticleData in brief2026
Open dataset of femoral cross-sectional geometry across ontogeny, including high resolution CT-derived structural variables, estimated ages, and proteomic sex identification.
Article in Data in brief, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Ontogenetic changes in long bone structure provide critical insights into the interplay between growth, mechanical loading, and skeletal development, yet open-access datasets focusing on non-adult individuals remain limited. This study presents an open dataset of femoral cross-sectional geometric properties spanning infancy to adolescence, derived from high-resolution computed tomography (CT) scans of archaeological human remains from the San Pablo Convent (Burgos, Spain). The dataset includes 72 unfused femora representing a continuous developmental sequence from 2.00 to 16.18 years of age. Cross-sectional geometric variables were extracted at four standardized and biomechanically meaningful locations along the femur: distal diaphysis, midshaft, proximal diaphysis, and femoral midneck. For each section, the dataset provides measurements of cortical and medullary areas, area ratios, second moments of area, and torsional rigidity, enabling detailed assessments of structural strength and biomechanical adaptation during growth. Age at death was estimated primarily from dental development, with complementary femoral-length-based regressions when dentition was unavailable. A key feature of this dataset is the inclusion of biological sex estimation based on amelogenin peptide identification from tooth enamel using a minimally invasive proteomic approach, allowing the investigation of sexual dimorphism prior to skeletal maturity. This resource supports reproducible research in bioarchaeology, biomechanics, and developmental skeletal biology.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.