Evidence map›Paper›PMID 34357004›Full record

ArticleMedicina (Kaunas, Lithuania)2021

Molecular Analysis of Prothrombotic Gene Variants in Patients with Acute Ischemic Stroke and with Transient Ischemic Attack.

Gustavo Cernera, Marika Comegna, Monica Gelzo, Marcella Savoia, Dario Bruzzese, Mauro Mormile, Federica Zarrilli, Felice Amato, Pierpaolo Di Micco, Giuseppe Castaldo

Open access · goldAbstract read
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2021. 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
1.7field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Multiple sclerosis and genetic polymorphisms in fibrinogen-mediated hemostatic pathways: a case-control study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Article
  4. Article
  5. Review
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

10 authors at 2 institutions in 1 country.

Gustavo CerneraDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, 80131 Naples, Italy.
Marika ComegnaDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, 80131 Naples, Italy.
Monica GelzoDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, 80131 Naples, Italy.ORCID 0000-0002-1500-0746
Marcella SavoiaDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, 80131 Naples, Italy.
Dario BruzzeseDipartimento di Sanità Pubblica, Università di Napoli Federico II, 80131 Naples, Italy.ORCID 0000-0001-9911-4646
Mauro MormileDipartimento di Medicina Clinica e Chirurgica, Università di Napoli Federico II, 80131 Naples, Italy.
Federica ZarrilliDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, 80131 Naples, Italy.ORCID 0000-0003-1614-6816
Felice AmatoDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, 80131 Naples, Italy.ORCID 0000-0002-0596-2933
Pierpaolo Di MiccoDipartimento di Medicina Interna, Ospedale Fatebenefratelli, 80131 Naples, Italy.
Giuseppe CastaldoDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, 80131 Naples, Italy.
Ceinge Biotecnologie Avanzate (Italy) · ITUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Brain IschemiaIschemic Attack, TransientIschemic StrokeMethylenetetrahydrofolate Reductase (NADPH2)StrokeChildFactor XIIIGenetic Predisposition to DiseaseHumansPolymorphism, GeneticRisk FactorsFactor XIIIMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humangene environmental interactionsgenetic medicinegene variantsinherited thrombophiliaischemic stroke

Identifiers

PMID34357004
PMCPMC8306646
OpenAlexW3184923543

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.