Evidence map›Paper›PMID 9326341›Full record

ArticleAmerican journal of human genetics1997

The significance of the 187G (H63D) mutation in hemochromatosis.

E Beutler

Registry-linked trialAbstract readLetterComment
In one paragraph

Article in American journal of human genetics, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00001455 (Iron Overload in African Americans), which is not on this map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–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.

NCT00001455 completednot on this map

Iron Overload in African Americans

TypeobservationalSponsorEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)Ran1995 to 2000Enrolled500ConditionsHemochromatosis, Iron Overload
3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Hyperferritinemia-A Clinical Overview.Journal of clinical medicine · 2021
    Review
  6. Article
  7. Article
  8. The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data.Genetics in medicine : official journal of the American College of Medical Genetics · 2016
    Article
  9. Iron overload is rare in patients homozygous for the H63D mutation.Canadian journal of gastroenterology & hepatology · 2014
    Article
  10. Article
  11. Lack of association of primary iron overload and common HFE gene mutations with liver cirrhosis in adult Indian population.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2011
    Article
  12. Non-viral causes of hepatocellular carcinoma.World journal of gastroenterology · 2010
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Contribution of the H63D mutation in HFE to murine hereditary hemochromatosis.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

E Beutler

Funding

VPA 985 IN LIVER CIRRHOSIS &ASCITESM01RR000833 · NCRR · SCRIPPS RESEARCH INSTITUTE · PI BABIOR, BERNARD M · 1985 to 2004
$14.0M
THE FORMATION AND SURVIVAL OF RED BLOOD CELLSR01HL025552 · NHLBI · SCRIPPS RESEARCH INSTITUTE · PI BEUTLER, ERNEST · 1985 to 2001
$565k
THE FORMATION AND SURVIVAL OF RED BLOOD CELLSR37HL025552 · NHLBI · SCRIPPS RESEARCH INSTITUTE · PI BEUTLER, ERNEST · 1987 to 1996
–
NCRR NIH HHS RR00833NHLBI NIH HHS HL25552
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Membrane ProteinsGene FrequencyHemochromatosisHemochromatosis ProteinHeterozygoteHistocompatibility Antigens Class IHLA AntigensHomozygoteHumansPoint MutationHemochromatosis ProteinHFE protein, humanHistocompatibility Antigens Class IHLA AntigensMembrane Proteins

Identifiers

PMID9326341
PMCPMC1715965

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.