Evidence map›Paper›PMID 26418427›Full record

ArticlePloS one2015

Possible Further Evidence of Low Genetic Diversity in the El Sidrón (Asturias, Spain) Neandertal Group: Congenital Clefts of the Atlas.

Luis Ríos, Antonio Rosas, Almudena Estalrrich, Antonio García-Tabernero, Markus Bastir, Rosa Huguet, Francisco Pastor, Juan Alberto Sanchís-Gimeno, Marco de la Rasilla

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
32.2field-weighted citation impact, top 1% 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

9 citing papers in PubMed, 32 citations in OpenAlex.

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  9. An abundance of developmental anomalies and abnormalities in Pleistocene people.Proceedings of the National Academy of Sciences of the United States of America · 2018
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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

9 authors at 5 institutions in 1 country.

Luis RíosGroup of Paleoanthropology, Department of Paleobiology, Museo Nacional de Ciencias Naturales, Madrid, Spain; Department of Physical Anthropology, Aranzadi Society of Sciences, Donostia, Basque Country, Spain.
Antonio RosasGroup of Paleoanthropology, Department of Paleobiology, Museo Nacional de Ciencias Naturales, Madrid, Spain.
Almudena EstalrrichGroup of Paleoanthropology, Department of Paleobiology, Museo Nacional de Ciencias Naturales, Madrid, Spain.
Antonio García-TaberneroGroup of Paleoanthropology, Department of Paleobiology, Museo Nacional de Ciencias Naturales, Madrid, Spain.
Markus BastirGroup of Paleoanthropology, Department of Paleobiology, Museo Nacional de Ciencias Naturales, Madrid, Spain.
Rosa HuguetInstitut Catalá de Palecologia Humana i Evolució Social IPHES, Area de Prehistoria, Universidad Rovira i Virgili, Unidad Asociada al CSIC, Tarragona, Spain.
Francisco PastorMuseo Anatómico, Department of Anatomy and Radiology, Faculty of Medicine, Universidad de Valladolid, Valladolid, Spain.
Juan Alberto Sanchís-GimenoDepartment of Anatomy and Human Embriology, Faculty of Medicine, Universidad de Valencia, Valencia, Spain.
Marco de la RasillaÁrea de Prehistoria, Department of History, Universidad de Oviedo, Oviedo, Spain.
Museo Nacional de Ciencias Naturales · ESInstitut Català de Paleoecologia Humana i Evolució Social · ESUniversidad de Oviedo · ESUniversidad de Valladolid · ESUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present here the first cases in Neandertals of congenital clefts of the arch of the atlas. Two atlases from El Sidrón, northern Spain, present respectively a defect of the posterior (frequency in extant modern human populations ranging from 0.73% to 3.84%), and anterior (frequency in extant modern human populations ranging from 0.087% to 0.1%) arch, a condition in most cases not associated with any clinical manifestation. The fact that two out of three observable atlases present a low frequency congenital condition, together with previously reported evidence of retained deciduous mandibular canine in two out of ten dentitions from El Sidrón, supports the previous observation based on genetic evidence that these Neandertals constituted a group with close genetic relations. Some have proposed for humans and other species that the presence of skeletal congenital conditions, although without clinical significance, could be used as a signal of endogamy or inbreeding. In the present case this interpretation would fit the general scenario of high incidence of rare conditions among Pleistocene humans and the specific scenariothat emerges from Neandertal paleogenetics, which points to long-term small and decreasing population size with reduced and isolated groups. Adverse environmental factors affecting early pregnancies would constitute an alternative, non-exclusive, explanation for a high incidence of congenital conditions. Further support or rejection of these interpretations will come from new genetic and skeletal evidence from Neandertal remains.

Indexed as

Genetics, PopulationGenetic VariationAnimalsCervical AtlasFossilsNeanderthalsSpain

Identifiers

PMID26418427
PMCPMC4587856
OpenAlexW2190577595

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LicenceCC BY
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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.