Evidence map›Paper›PMID 35330428›Full record

ArticleJournal of personalized medicine2022

Genetic Polymorphisms in a Familial Hypercholesterolemia Population from North-Eastern Europe.

Alexandra Maștaleru, Sabina Alexandra Cojocariu, Andra Oancea, Maria Magdalena Leon Constantin, Mihai Roca, Ioana Mădălina Zota, Irina Abdulan, Cristina Rusu, Roxana Popescu, Lucian Mihai Antoci and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

14 authors at 2 institutions in 1 country.

Alexandra MaștaleruDepartment of Medical Specialties I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.ORCID 0000-0002-0008-9696
Sabina Alexandra CojocariuDepartment of Medical Specialties I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.ORCID 0000-0002-9964-8741
Andra OanceaDepartment of Medical Specialties I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.ORCID 0000-0003-1356-9581
Maria Magdalena Leon ConstantinDepartment of Medical Specialties I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.ORCID 0000-0002-5836-1322
Mihai RocaDepartment of Medical Specialties I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.
Ioana Mădălina ZotaDepartment of Medical Specialties I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.ORCID 0000-0003-4053-4130
Irina AbdulanDepartment of Medical Specialties I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.
Cristina RusuDepartment of Medical Genetics, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.
Roxana PopescuDepartment of Medical Genetics, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.ORCID 0000-0002-2183-0690
Lucian Mihai AntociDepartment of Medical Genetics, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.
Cristian Gabriel CiobanuDepartment of Medical Genetics, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.
Alexandru Dan CostacheDepartment of Medical Specialties I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.ORCID 0000-0001-8544-9904
Elena CojocaruDepartment of Morphofunctional Sciences I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.ORCID 0000-0001-7859-840X
Florin MituDepartment of Medical Specialties I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iaşi, Romania.ORCID 0000-0003-1801-9327
Grigore T. Popa University of Medicine and Pharmacy · ROClinical Emergency Hospital Bucharest · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(1) Background: Familial hypercholesterolemia (FH) is one of the most prevalent inherited metabolic disorders. The purpose of the study was to investigate the role in cardiovascular disease (CVD) of

Indexed as

ACEApoB R3500Qatherosclerosismetabolic syndromeMTHFR A1298CMTHFR C677TPAI-1 4G/5G

Identifiers

PMID35330428
PMCPMC8949493
OpenAlexW4220928226

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.