Evidence map›Paper›PMID 34071952›Full record

ArticleGenes2021

Prediction of Eye Colour in Scandinavians Using the EyeColour 11 (EC11) SNP Set.

Olivia Strunge Meyer, Nina Mjølsnes Salvo, Anne Kjærbye, Marianne Kjersem, Mikkel Meyer Andersen, Erik Sørensen, Henrik Ullum, Kirstin Janssen, Niels Morling, Claus Børsting and 2 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Searching for improvements in predicting human eye colour from DNA.International journal of legal medicine · 2021
    Article
  9. 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

12 authors at 5 institutions in 2 countries.

Olivia Strunge MeyerSection of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, 2100 Copenhagen, Denmark.ORCID 0000-0002-7842-5581
Nina Mjølsnes SalvoCentre for Forensic Genetics, Department of Medical Biology, UiT-The Arctic University of Norway, 9037 Tromsø, Norway.ORCID 0000-0002-3336-1019
Anne KjærbyeSection of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, 2100 Copenhagen, Denmark.
Marianne KjersemCentre for Forensic Genetics, Department of Medical Biology, UiT-The Arctic University of Norway, 9037 Tromsø, Norway.
Mikkel Meyer AndersenDepartment of Mathematical Sciences, Aalborg University, 9220 Aalborg, Denmark.
Erik SørensenDepartment of Clinical Immunology, Copenhagen University Hospital, Rigshospitalet, 2100 Copenhagen, Denmark.
Henrik UllumStatens Serum Institut, 2300 Copenhagen, Denmark.
Kirstin JanssenCentre for Forensic Genetics, Department of Medical Biology, UiT-The Arctic University of Norway, 9037 Tromsø, Norway.ORCID 0000-0002-0663-7470
Niels MorlingSection of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, 2100 Copenhagen, Denmark.ORCID 0000-0002-9463-5087
Claus BørstingSection of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, 2100 Copenhagen, Denmark.
Gunn-Hege OlsenCentre for Forensic Genetics, Department of Medical Biology, UiT-The Arctic University of Norway, 9037 Tromsø, Norway.ORCID 0000-0002-8138-3132
Jeppe Dyrberg AndersenSection of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, 2100 Copenhagen, Denmark.ORCID 0000-0002-4395-5232
University of Copenhagen · DKUiT The Arctic University of Norway · NOAalborg University · DKCopenhagen University Hospital · DKStatens Serum Institut · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Description of a perpetrator's eye colour can be an important investigative lead in a forensic case with no apparent suspects. Herein, we present 11 SNPs (Eye Colour 11-EC11) that are important for eye colour prediction and eye colour prediction models for a two-category reporting system (blue and brown) and a three-category system (blue, intermediate, and brown). The EC11 SNPs were carefully selected from 44 pigmentary variants in seven genes previously found to be associated with eye colours in 757 Europeans (Danes, Swedes, and Italians). Mathematical models using three different reporting systems: a quantitative system (PIE-score), a two-category system (blue and brown), and a three-category system (blue, intermediate, brown) were used to rank the variants. SNPs with a sufficient mean variable importance (above 0.3%) were selected for EC11. Eye colour prediction models using the EC11 SNPs were developed using leave-one-out cross-validation (LOOCV) in an independent data set of 523 Norwegian individuals. Performance of the EC11 models for the two- and three-category system was compared with models based on the IrisPlex SNPs and the most important eye colour locus, rs12913832. We also compared model performances with the IrisPlex online tool (IrisPlex Web). The EC11 eye colour prediction models performed slightly better than the IrisPlex and rs12913832 models in all reporting systems and better than the IrisPlex Web in the three-category system. Three important points to consider prior to the implementation of eye colour prediction in a forensic genetic setting are discussed: (1) the reference population, (2) the SNP set, and (3) the reporting strategy.

Indexed as

Polymorphism, Single NucleotideEye ColorForensic GeneticsGenome-Wide Association StudyHumansModels, GeneticPhenotypeScandinavian and Nordic CountriesDNA phenotypingeye colourforensic geneticspigmentationrs12913832

Identifiers

PMID34071952
PMCPMC8227851
OpenAlexW3164905588

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.