Evidence map›Paper›PMID 42007088›Full record

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.

Julia Muñoz-Guarinos, Laura Rodríguez, José Miguel Carretero, Miguel Del Nogal Sánchez, Ana María Casas-Ferreira, José Luis Pérez Pavón, Rebeca García-González

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Julia Muñoz-GuarinosLaboratorio de Evolución Humana, Universidad de Burgos. Edificio I+D+i/CIBA, Plaza Misael Bañuelos s/n, 09001 Burgos, Spain.
Laura RodríguezLaboratorio de Evolución Humana, Universidad de Burgos. Edificio I+D+i/CIBA, Plaza Misael Bañuelos s/n, 09001 Burgos, Spain.
José Miguel CarreteroLaboratorio de Evolución Humana, Universidad de Burgos. Edificio I+D+i/CIBA, Plaza Misael Bañuelos s/n, 09001 Burgos, Spain.
Miguel Del Nogal SánchezUniversidad de Salamanca, Departamento de Química Analítica, Nutrición y Bromatología, Facultad de Ciencias Químicas, Plaza de los Caídos s/n, 37008 Salamanca, Spain.
Ana María Casas-FerreiraUniversidad de Salamanca, Departamento de Química Analítica, Nutrición y Bromatología, Facultad de Ciencias Químicas, Plaza de los Caídos s/n, 37008 Salamanca, Spain.
José Luis Pérez PavónUniversidad de Salamanca, Departamento de Química Analítica, Nutrición y Bromatología, Facultad de Ciencias Químicas, Plaza de los Caídos s/n, 37008 Salamanca, Spain.
Rebeca García-GonzálezLaboratorio de Evolución Humana, Universidad de Burgos. Edificio I+D+i/CIBA, Plaza Misael Bañuelos s/n, 09001 Burgos, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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

BioarchaeologyBiomechanicsDevelopmentGrowthSexual dimorphism

Identifiers

PMID42007088
PMCPMC13091029

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.