Evidence map›Paper›PMID 15951742›Full record

ArticleGenes and immunity2005

Genome-wide search for sarcoidosis susceptibility genes in African Americans.

M C Iannuzzi, S K Iyengar, C Gray-McGuire, R C Elston, R P Baughman, J F Donohue, K Hirst, M A Judson, M S Kavuru, M J Maliarik and 7 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06865274 (Multicenter Prospective Interventional Study to Evaluate the Frequency of FCGR3A Gene Polymorphisms in Patients With Neuromyelitis Optica Spectrum Disorders, Myelin Oligodendrocyte Glycoprotein Antibody Disease, and Multiple Sclerosis.), which is not on this map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.9field-weighted citation impact, top 4% 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.

NCT06865274 narecruitingnot on this mapstarted 2025, after this paper: background citation

Multicenter Prospective Interventional Study to Evaluate the Frequency of FCGR3A Gene Polymorphisms in Patients With Neuromyelitis Optica Spectrum Disorders, Myelin Oligodendrocyte Glycoprotein Antibody Disease, and Multiple Sclerosis.

TypeinterventionalSponsorFondazione Policlinico Universitario Agostino Gemelli IRCCSRan2025 to 2027Enrolled50ConditionsNeuromyelitis Optica Spectrum Disorders, MOGAD, Multiple SclerosisArmsBlood draw for the laboratory assessment
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 108 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Genetics of neurosarcoidosis.Journal of neuroimmunology · 2022
    Review
  5. Novel HumanFrontiers in immunology · 2022
    Article
  6. Sarcoidosis Epidemiology: Race Matters.Frontiers in immunology · 2020
    Review
  7. Article
  8. Linking Race, Cancer Outcomes, and Tissue Repair.The American journal of pathology · 2018
    Review
  9. Article
  10. [Sarcoidosis : Dermatological view of a rare multisystem disease].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2017
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Carbon Nanotubes and Chronic Granulomatous Disease.Nanomaterials (Basel, Switzerland) · 2014
    Article
  16. Article
  17. Article
  18. Article
  19. A concise review of pulmonary sarcoidosis.American journal of respiratory and critical care medicine · 2011
    Review
  20. 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

17 authors at 13 institutions in 1 country.

M C IannuzziDivision of Pulmonary, Critical Care, and Sleep Medicine, Mount Sinai School of Medicine, New York, NY 10029, USA. Michael.Iannuzzi@mssm.edu
S K Iyengar
C Gray-McGuire
R C Elston
R P Baughman
J F Donohue
K Hirst
M A Judson
M S Kavuru
M J Maliarik
D R Moller
L S Newman
D L Rabin
C S Rose
M D Rossman
A S Teirstein
B A Rybicki
Case Western Reserve University · USHenry Ford Health System · USIcahn School of Medicine at Mount Sinai · USCleveland Clinic · USGeorgetown University · USGeorge Washington University · USJohns Hopkins Medicine · USMedical University of South Carolina · USNational Jewish Health · USUniversity of Cincinnati · USUniversity of Colorado Denver · USUniversity of North Carolina at Chapel Hill · USUniversity of Pennsylvania · US

Funding

X-LINKED EXTENSION OF THE REVISED HASEMAN-ELSTON ALGORITHM FOR LINKAGE ANALYSISP41RR003655 · NCRR · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI ELSTON, ROBERT C. · 1987 to 2011
$11.5M
SARCOIDOSIS GENETIC LINKAGE CONSORTIUMU01HL060263 · NHLBI · HENRY FORD HEALTH SYSTEM · PI IANNUZZI, MICHAEL C · 1999 to 2003
$6.5M
GENETIC ANALYSIS OF MULTIFACTORIAL TRAITSR01GM028356 · NIGMS · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI ELSTON, ROBERT C. · 1985 to 1997
–
NCRR NIH HHS P41 RR003655NHLBI NIH HHS UO1 HL060263NIGMS NIH HHS R01 GM28356
6 · The paper itself

Abstract

Sarcoidosis, a systemic granulomatous disease of unknown etiology, likely results from an environmental insult in a genetically susceptible host. In the US, African Americans are more commonly affected with sarcoidosis and suffer greater morbidity than Caucasians. We searched for sarcoidosis susceptibility loci by conducting a genome-wide, sib pair multipoint linkage analysis in 229 African-American families ascertained through two or more sibs with a history of sarcoidosis. Using the Haseman-Elston regression technique, linkage peaks with P-values less than 0.05 were identified on chromosomes 1p22, 2p25, 5p15-13, 5q11, 5q35, 9q34, 11p15 and 20q13 with the most prominent peak at D5S2500 on chromosome 5q11 (P=0.0005). We found agreement for linkage with the previously reported genome scan of a German population at chromosomes 1p and 9q. Based on the multiple suggestive regions for linkage found in our study population, it is likely that more than one gene influences sarcoidosis susceptibility in African Americans. Fine mapping of the linked regions, particularly on chromosome 5q, should help to refine linkage signals and guide further sarcoidosis candidate gene investigation.

Indexed as

Genetic Predisposition to DiseaseGenetic TestingBlack or African AmericanCardiomyopathiesChromosomes, HumanGenetic LinkageGenome, HumanHumansSarcoidosis

Identifiers

PMID15951742
OpenAlexW2035971467

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.