Evidence map›Paper›PMID 25044010›Full record

ArticleAmerican journal of hematology2014

Hereditary xerocytosis revisited.

Natasha M Archer, Boris E Shmukler, Immacolata Andolfo, David H Vandorpe, Radhakrishnan Gnanasambandam, John M Higgins, Alicia Rivera, Mark D Fleming, Frederick Sachs, Philip A Gottlieb and 4 more

Abstract read
In one paragraph

Article in American journal of hematology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

25 citing papers in PubMed.

  1. Enhanced PIEZO1 function contributes to the pathogenesis of sickle cell disease.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Diagnosis and clinical management of red cell membrane disorders.Hematology. American Society of Hematology. Education Program · 2021
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. A common polymorphism in the mechanosensitive ion channelProceedings of the National Academy of Sciences of the United States of America · 2020
    Observational
  12. Article
  13. Red Blood Cells: Chasing Interactions.Frontiers in physiology · 2019
    Review
  14. Frontiers in physiology · 2019
    Article
  15. Article
  16. Article
  17. Hereditary xerocytosis: Diagnostic considerations.American journal of hematology · 2018
    Article
  18. Review
  19. 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

14 authors.

Natasha M ArcherDivision of Hematology and Oncology, Boston Children's Hospital, Boston, Massachusetts; Dana-Farber Cancer Center, Boston, Massachusetts.
Boris E Shmukler
Immacolata Andolfo
David H Vandorpe
Radhakrishnan Gnanasambandam
John M Higgins
Alicia Rivera
Mark D Fleming
Frederick Sachs
Philip A Gottlieb
Achille Iolascon
Carlo Brugnara
Seth L Alper
David G Nathan

Funding

HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
PATHOPHYSIOLOGY OF HUMAN BLOOD CELLST32HL007574 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI Daniel Evan Bauer · 1985 to 2026
$18.4M
Mechanosensitive ion channels and cortical mechanicsR01HL054887 · NHLBI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SACHS, FREDERICK · 1995 to 2016
$9.6M
Systems Biology of In Vivo Human Blood Cell PopulationsDP2DK098087 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI HIGGINS, JOHN MATTHEW · 2012 to 2012
$2.6M
A Feasibility Study of Regadenoson for the Treatment of Acute Chest SyndromeR34HL108757 · NHLBI · DANA-FARBER CANCER INST · PI FIELD, JOSHUA JEFFREY, NATHAN, DAVID G. · 2011 to 2012
$682k
NCRR NIH HHS UL1 RR025758NHLBI NIH HHS R01 HL054887NHLBI NIH HHS R01HL054887NHLBI NIH HHS R34 HL108757NHLBI NIH HHS R34HL108757NHLBI NIH HHS T32 HL007574NHLBI NIH HHS T32HL007574NIDDK NIH HHS DP2 DK098087Telethon GGP09044
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MutationAdolescentAdultAdult ChildrenAnemia, Hemolytic, CongenitalErythrocytesGlucuronosyltransferaseHemochromatosis ProteinHepatocytesHeterozygoteHistocompatibility Antigens Class IHumansHydrops FetalisIon ChannelsLiverMaleGlucuronosyltransferaseHemochromatosis ProteinHFE protein, humanHistocompatibility Antigens Class IIon ChannelsMembrane ProteinsPIEZO1 protein, humanUGT1A1 Enzyme

Identifiers

PMID25044010
PMCPMC4237618

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.