Evidence map›Paper›PMID 20807474›Full record

ReviewDiscovery medicine2010

The genetics of systemic sclerosis.

Sandeep K Agarwal

Abstract readReview
In one paragraph

Review in Discovery medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Kidney involvement in systemic sclerosis: From pathogenesis to treatment.Journal of scleroderma and related disorders · 2018
    Review
  3. Gastrointestinal Manifestations of Systemic Sclerosis.Rheumatology (Sunnyvale, Calif.) · 2018
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Genetics, Epigenetics, and Genomics of Systemic Sclerosis.Rheumatic diseases clinics of North America · 2015
    Review
  9. Article
  10. Pathogenesis of Systemic Sclerosis.Frontiers in immunology · 2015
    Review
  11. Genetics of Interstitial Lung Disease: Vol de Nuit (Night Flight).Clinical medicine insights. Circulatory, respiratory and pulmonary medicine · 2015
    Review
  12. Genetics of systemic sclerosis: an update.Current rheumatology reports · 2012
    Review
  13. Targeting STAT4 in systemic sclerosis: a promising new direction.Expert review of clinical immunology · 2011
    Article
  14. Vascular involvement in systemic sclerosis (scleroderma).Journal of inflammation research · 2011
    Article
  15. 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

1 author at 1 institution in 1 country.

Sandeep K AgarwalDivision of Rheumatology and Clinical Immunogenetics, Department of Internal Medicine, The University of Texas Health Science Center at Houston, 6431 Fannin, MSB 5.270, Houston, Texas 77030, USA. Sandeep.K.Agarwal@uth.tmc.edu
The University of Texas Health Science Center at Houston · US

Funding

Cadherin-11 Regulation of Fibroblast-like Synoviocytes in Synovial InflammationK08AR054404 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI AGARWAL, SANDEEP K · 2008 to 2012
$601k
NIAMS NIH HHS K08 AR054404
6 · The paper itself

Abstract

Systemic sclerosis (SSc, scleroderma) is an autoimmune disease clinically characterized by progressive fibrosis in the skin and internal organs. While the pathogenesis of SSc is not completely understood, familial studies and genetic studies suggest that SSc is a complex polygenic disease. In the current review, we will discuss recent studies investigating genetic susceptibility to SSc. Candidate gene studies have identified critical immunoregulatory genes and gene regions including BANK1, FAM167A-BLK, IL23R, IRF5, STAT4, TBX21, and TNFSF4 as susceptibility genes for the development of SSc. More recently a genome-wide association study has been performed and identified CD247 (CD3-zeta) as a novel genetic risk factor for the susceptibility to SSc. Together these genetic association studies have substantially advanced our understanding of SSc pathogenesis and form the foundation for future studies seeking to understand the complexities of SSc.

Indexed as

FamilyGenetic Predisposition to DiseaseGenome-Wide Association StudyHLA AntigensHumansScleroderma, SystemicHLA Antigens

Identifiers

PMID20807474
PMCPMC3803145
OpenAlexW105605248

What OpenQuestion holds

Textmetadata
LicenceTDM
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.