Evidence map›Paper›PMID 25939698›Full record

SynthesisNature communications2015

Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci.

Lam C Tsoi, Sarah L Spain, Eva Ellinghaus, Philip E Stuart, Francesca Capon, Jo Knight, Trilokraj Tejasvi, Hyun M Kang, Michael H Allen, Sylviane Lambert and 23 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed, 7 pooled it
–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

111 citing papers in PubMed, 7 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Pooled it
  7. Pooled it
  8. Immune shifts in inflammatory skin diseases.JID innovations : skin science from molecules to population health · 2026
    Review
  9. Article
  10. Article
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  12. Article
  13. Observational
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. The Role of Epigenetic Factors in the Pathogenesis of Psoriasis.International journal of molecular sciences · 2024
    Review
  20. Article

51 more citing papers are in PubMed but not listed here.

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

33 authors.

Lam C TsoiDepartment of Biostatistics, Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan 48109, USA.
Sarah L SpainDivision of Genetics and Molecular Medicine, King's College London, London WC2R 2LS, UK.
Eva EllinghausInstitute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel, 24105 Kiel, Germany.ORCID http://orcid.org/0000-0003-2914-3382
Philip E StuartDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Francesca CaponDivision of Genetics and Molecular Medicine, King's College London, London WC2R 2LS, UK.
Jo KnightNeuroscience Research, Centre for Addiction and Mental Health, Toronto, Ontario, Canada M5T 1R8.
Trilokraj TejasviDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Hyun M KangDepartment of Biostatistics, Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan 48109, USA.
Michael H AllenDivision of Genetics and Molecular Medicine, King's College London, London WC2R 2LS, UK.
Sylviane LambertDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Stefan W StollDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Stephan WeidingerDepartment of Dermatology, University Hospital, Schleswig-Holstein, Christian-Albrechts-University, 24105 Kiel, Germany.
Johann E GudjonssonDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Sulev KoksDepartment of Pathophysiology, Centre of Translational Medicine and Centre for Translational Genomics, University of Tartu, 50409 Tartu, Estonia.ORCID http://orcid.org/0000-0001-6087-6643
Külli KingoDepartment of Dermatology and Venereology, University of Tartu, 50409 Tartu, Estonia.
Tonu EskoEstonian Genome Center, University of Tartu, 51010 Tartu, Estonia.
Sayantan DasDepartment of Biostatistics, Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan 48109, USA.
Andres MetspaluEstonian Genome Center, University of Tartu, 51010 Tartu, Estonia.
Michael WeichenthalDepartment of Dermatology, University Hospital, Schleswig-Holstein, Christian-Albrechts-University, 24105 Kiel, Germany.
Charlotta EnerbackDepartment of Dermatology, Linköping University, SE-581 83 Linköping, Sweden.
Gerald G KruegerDepartment of Dermatology, University of Utah, Salt Lake City, Utah 84132, USA.
John J VoorheesDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Vinod ChandranDepartment of Medicine, Division of Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, Ontario, Canada M5T 2S8.
Cheryl F RosenDepartment of Medicine, Division of Dermatology, University of Toronto, Toronto Western Hospital, Toronto, Ontario, Canada M5T 2S8.
Proton RahmanDepartment of Medicine, Memorial University, St John's, Newfoundland, Canada A1C 5B8.
Dafna D GladmanDepartment of Medicine, Division of Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, Ontario, Canada M5T 2S8.
Andre ReisInstitute of Human Genetics, University of Erlangen-Nuremberg, Erlangen 91054, Germany.ORCID http://orcid.org/0000-0002-6301-6363
Rajan P NairDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Andre FrankeInstitute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel, 24105 Kiel, Germany.
Jonathan N W N BarkerDivision of Genetics and Molecular Medicine, King's College London, London WC2R 2LS, UK.
Goncalo R AbecasisDepartment of Biostatistics, Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan 48109, USA.
Richard C TrembathBarts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AD, UK.
James T ElderDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan 48109, USA.

Funding

Linkage analysis of familial psoriasis(Supplement)R01AR042742 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD · 1994 to 2021
$10.1M
Genetic and Genomic Dissection of Psoriatic ArthritisR01AR063611 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD, GLADMAN, DAFNA D · 2012 to 2023
$6.2M
Identification of Psoriatic Arthritis Genes in the MHCR01AR050511 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD · 2004 to 2013
$4.2M
Combined Analysis of Gene Expression and DNA Variation in PsoriasisR01AR054966 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD · 2007 to 2011
$3.2M
Functional Genomics of PsoriasisR01AR065183 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD · 2013 to 2016
$1.7M
Role of the Psoriasis Associated IL23R Risk Variants on Th17 Biology and FunctionK08AR060802 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GUDJONSSON, JOHANN ELI · 2011 to 2015
$636k
Medical Research Council G0000934Medical Research Council MR/L011808/1NIAMS NIH HHS K08 AR060802NIAMS NIH HHS R01 AR042742NIAMS NIH HHS R01AR042742NIAMS NIH HHS R01 AR050511NIAMS NIH HHS R01AR050511NIAMS NIH HHS R01 AR054966NIAMS NIH HHS R01AR054966NIAMS NIH HHS R01AR062382NIAMS NIH HHS R01 AR063611NIAMS NIH HHS R01 AR065183NIAMS NIH HHS R01AR065183Wellcome TrustWellcome Trust 068545/Z/02
6 · The paper itself

Abstract

Psoriasis is a chronic autoimmune disease with complex genetic architecture. Previous genome-wide association studies (GWAS) and a recent meta-analysis using Immunochip data have uncovered 36 susceptibility loci. Here, we extend our previous meta-analysis of European ancestry by refined genotype calling and imputation and by the addition of 5,033 cases and 5,707 controls. The combined analysis, consisting of over 15,000 cases and 27,000 controls, identifies five new psoriasis susceptibility loci at genome-wide significance (P<5 × 10(-8)). The newly identified signals include two that reside in intergenic regions (1q31.1 and 5p13.1) and three residing near PLCL2 (3p24.3), NFKBIZ (3q12.3) and CAMK2G (10q22.2). We further demonstrate that NFKBIZ is a TRAF3IP2-dependent target of IL-17 signalling in human skin keratinocytes, thereby functionally linking two strong candidate genes. These results further integrate the genetics and immunology of psoriasis, suggesting new avenues for functional analysis and improved therapies.

Indexed as

Genetic LociGenetic Predisposition to DiseaseAdaptor Proteins, Signal TransducingGenome-Wide Association StudyHumansI-kappa B ProteinsInterleukin-17KeratinocytesNuclear ProteinsPsoriasisReproducibility of ResultsRNA, MessengerTumor Necrosis Factor Receptor-Associated Peptides and ProteinsAdaptor Proteins, Signal TransducingI-kappa B ProteinsInterleukin-17NFKBIZ protein, humanNuclear ProteinsRNA, MessengerTRAF3IP2 protein, humanTumor Necrosis Factor Receptor-Associated Peptides and Proteins

Identifiers

PMID25939698
PMCPMC4422106

What OpenQuestion holds

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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.