Evidence map›Paper›PMID 35443567›Full record

ArticleHaematologica2022

Hereditary anemia caused by multilocus inheritance of

Barbara Eleni Rosato, Seth L Alper, Giovanna Tomaiuolo, Roberta Russo, Achille Iolascon, Immacolata Andolfo

Abstract read
In one paragraph

Article in Haematologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. 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

6 authors.

Barbara Eleni RosatoDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli 'Federico II', Napoli, Italy; CEINGE Biotecnologie Avanzate, Napoli.
Seth L AlperRenal Division and Vascular Biology Research Center, Beth Israel Deaconess Medical Center; and Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Giovanna TomaiuoloCEINGE Biotecnologie Avanzate, Napoli, Italy; Dipartimento di Ingegneria Chimica, dei Materiali e della Produzione Industriale, University of Naples Federico, 80125 Naples.
Roberta RussoDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli 'Federico II', Napoli, Italy; CEINGE Biotecnologie Avanzate, Napoli. roberta.russo@unina.it.
Achille IolasconDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli 'Federico II', Napoli, Italy; CEINGE Biotecnologie Avanzate, Napoli.
Immacolata AndolfoDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli 'Federico II', Napoli, Italy; CEINGE Biotecnologie Avanzate, Napoli. immacolata.andolfo@unina.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Anemia, Hemolytic, CongenitalAnion Exchange Protein 1, ErythrocyteATP-Binding Cassette TransportersFemaleHumansHydrops FetalisIon ChannelsMutationABCB6 protein, humanAnion Exchange Protein 1, ErythrocyteATP-Binding Cassette TransportersIon ChannelsPIEZO1 protein, humanSLC4A1 protein, human

Identifiers

PMID35443567
PMCPMC9425304

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.