Evidence map›Paper›PMID 26286644›Full record

ArticleEuropean journal of human genetics : EJHG2016

The more the merrier? How a few SNPs predict pigmentation phenotypes in the Northern German population.

Amke Caliebe, Melanie Harder, Rebecca Schuett, Michael Krawczak, Almut Nebel, Nicole von Wurmb-Schwark

Open access · bronzeAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Amke CaliebeInstitute of Medical Informatics and Statistics, Christian-Albrechts University Kiel, Kiel, Germany.
Melanie HarderInstitute of Legal Medicine, Christian-Albrechts University Kiel, Kiel, Germany.
Rebecca SchuettInstitute of Legal Medicine, Christian-Albrechts University Kiel, Kiel, Germany.
Michael KrawczakInstitute of Medical Informatics and Statistics, Christian-Albrechts University Kiel, Kiel, Germany.
Almut NebelInstitute of Clinical Molecular Biology, Christian-Albrechts University Kiel, Kiel, Germany.
Nicole von Wurmb-SchwarkInstitute of Legal Medicine, Christian-Albrechts University Kiel, Kiel, Germany.
Kiel University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human pigmentation traits are of great interest to many research areas, from ancient DNA analysis to forensic science. We developed a gene-based predictive model for pigmentation phenotypes in a realistic target population for forensic case work from Northern Germany and compared our model with those brought forth by previous studies of genetically more heterogeneous populations. In doing so, we aimed at answering the following research questions: (1) do existing models allow good prediction of high-quality phenotypes in a genetically similar albeit more homogeneous population? (2) Would a model specifically set up for the more homogeneous population perform notably better than existing models? (3) Can the number of markers included in existing models be reduced without compromising their predictive capability in the more homogenous population? We investigated the association between eye, hair and skin colour and 12 candidate single-nucleotide polymorphisms (SNPs) from six genes. Our study comprised two samples of 300 and 100 individuals from Northern Germany. SNP rs12913832 in HERC2 was found to be strongly associated with blue eye colour (odds ratio=40.0, P<1.2 × 10(-4)) and to yield moderate predictive power (AUC: 77%; sensitivity: 90%, specificity: 63%, both at a 0.5 threshold for blue eye colour probability). SNP associations with hair and skin colour were weaker and genotypes less predictive. A comparison with two recently published sets of markers to predict eye and hair colour revealed that the consideration of additional SNPs with weak-to-moderate effect increased the predictive power for eye colour, but not for hair colour.

Indexed as

PhenotypePolymorphism, Single NucleotideAdultEye ColorFemaleGermanyGuanine Nucleotide Exchange FactorsHair ColorHumansMaleMiddle AgedSkin PigmentationUbiquitin-Protein LigasesGuanine Nucleotide Exchange FactorsHERC2 protein, humanUbiquitin-Protein Ligases

Identifiers

PMID26286644
PMCPMC4930077
OpenAlexW1803421057

What OpenQuestion holds

Textmetadata
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.