Evidence map›Paper›PMID 29222283›Full record

ReviewHematology. American Society of Hematology. Education Program2017

Hereditary thrombocytopenias: a growing list of disorders.

Patrizia Noris, Alessandro Pecci

Open access · bronzeAbstract readReview
In one paragraph

Review in Hematology. American Society of Hematology. Education Program, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
9.3field-weighted citation impact, top 1% 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

44 citing papers in PubMed, 128 citations in OpenAlex.

  1. Trial
  2. Application of High-Throughput Sequencing in the Diagnosis of Inherited Thrombocytopenia.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis · 2018
    Trial
  3. Review
  4. Review
  5. Article
  6. Review
  7. Hematology reports · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 3q26.2/Cancers · 2023
    Article
  20. A family case series of inherited thrombocytopenia.Proceedings (Baylor University. Medical Center) · 2023
    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

2 authors at 2 institutions in 1 country.

Patrizia NorisDepartment of Internal Medicine, IRCCS Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
Alessandro PecciDepartment of Internal Medicine, IRCCS Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
Istituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The introduction of high throughput sequencing (HTS) techniques greatly improved the knowledge of inherited thrombocytopenias (ITs) over the last few years. A total of 33 different forms caused by molecular defects affecting at least 32 genes have been identified; along with the discovery of new disease-causing genes, pathogenetic mechanisms of thrombocytopenia have been better elucidated. Although the clinical picture of ITs is heterogeneous, bleeding has been long considered the major clinical problem for patients with IT. Conversely, the current scenario indicates that patients with some of the most common ITs are at risk of developing additional disorders more dangerous than thrombocytopenia itself during life. In particular,

Indexed as

Genetic Diseases, InbornThrombocytopeniaCore Binding Factor Alpha 2 SubunitETS Translocation Variant 6 ProteinHumansIntercellular Signaling Peptides and ProteinsMDS1 and EVI1 Complex Locus ProteinMolecular Motor ProteinsMyosin Heavy ChainsNuclear ProteinsProto-Oncogene Proteins c-etsReceptors, ThrombopoietinRepressor ProteinsANKRD26 protein, humanCore Binding Factor Alpha 2 SubunitETS Translocation Variant 6 ProteinIntercellular Signaling Peptides and ProteinsMDS1 and EVI1 Complex Locus ProteinMECOM protein, humanMolecular Motor ProteinsMPL protein, humanMYH9 protein, humanMyosin Heavy ChainsNuclear ProteinsProto-Oncogene Proteins c-etsReceptors, ThrombopoietinRepressor ProteinsRUNX1 protein, human

Identifiers

PMID29222283
PMCPMC6142591
OpenAlexW2782773254

What OpenQuestion holds

Textmetadata
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.