Evidence map›Paper›PMID 30573740›Full record

ArticleNature communications2018

Dissection of genetic variation and evidence for pleiotropy in male pattern baldness.

Chloe X Yap, Julia Sidorenko, Yang Wu, Kathryn E Kemper, Jian Yang, Naomi R Wray, Matthew R Robinson, Peter M Visscher

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 3 pooled it
7.1field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 3 syntheses or guidelines pooled it, 125 citations in OpenAlex.

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  12. Androgenetic alopecia.Nature reviews. Disease primers · 2025
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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

8 authors at 2 institutions in 3 countries.

Chloe X YapInstitute for Molecular Bioscience, University of Queensland, Queensland, QLD, 4072, Australia.ORCID http://orcid.org/0000-0002-1788-2842
Julia SidorenkoInstitute for Molecular Bioscience, University of Queensland, Queensland, QLD, 4072, Australia.
Yang WuInstitute for Molecular Bioscience, University of Queensland, Queensland, QLD, 4072, Australia.ORCID http://orcid.org/0000-0002-0128-7280
Kathryn E KemperInstitute for Molecular Bioscience, University of Queensland, Queensland, QLD, 4072, Australia.
Jian YangInstitute for Molecular Bioscience, University of Queensland, Queensland, QLD, 4072, Australia.ORCID http://orcid.org/0000-0003-2001-2474
Naomi R WrayInstitute for Molecular Bioscience, University of Queensland, Queensland, QLD, 4072, Australia.ORCID http://orcid.org/0000-0001-7421-3357
Matthew R RobinsonInstitute for Molecular Bioscience, University of Queensland, Queensland, QLD, 4072, Australia.
Peter M VisscherInstitute for Molecular Bioscience, University of Queensland, Queensland, QLD, 4072, Australia. peter.visscher@uq.edu.au.ORCID http://orcid.org/0000-0002-2143-8760
The University of Queensland · AUSIB Swiss Institute of Bioinformatics · CH

Funding

Medical Research Council MC_PC_17228Medical Research Council MC_QA137853
6 · The paper itself

Abstract

Male pattern baldness (MPB) is a sex-limited, age-related, complex trait. We study MPB genetics in 205,327 European males from the UK Biobank. Here we show that MPB is strongly heritable and polygenic, with pedigree-heritability of 0.62 (SE = 0.03) estimated from close relatives, and SNP-heritability of 0.39 (SE = 0.01) from conventionally-unrelated males. We detect 624 near-independent genome-wide loci, contributing SNP-heritability of 0.25 (SE = 0.01), of which 26 X-chromosome loci explain 11.6%. Autosomal genetic variance is enriched for common variants and regions of lower linkage disequilibrium. We identify plausible genetic correlations between MPB and multiple sex-limited markers of earlier puberty, increased bone mineral density (r

Indexed as

Genetic PleiotropyGenetic VariationAge FactorsAlopeciaBone DensityHumansLinkage DisequilibriumPolymorphism, Single NucleotideUnited Kingdom

Identifiers

PMID30573740
PMCPMC6302097
OpenAlexW2905138054

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.