Evidence map›Paper›PMID 33133164›Full record

ReviewFrontiers in genetics2020

Genetics of Familial Hypercholesterolemia: New Insights.

Michal Vrablik, Lukas Tichý, Tomas Freiberger, Vladimir Blaha, Martin Satny, Jaroslav A Hubacek

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
10.6field-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

62 citing papers in PubMed, 1 synthesis or guideline pooled it, 106 citations in OpenAlex.

  1. Pooled it
  2. Review
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  11. International journal of molecular sciences · 2025
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  18. Genetic Spectrum of Lithuanian Familial Hypercholesterolemia Patients.Journal of cardiovascular development and disease · 2025
    Article
  19. Review
  20. Review

2 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 1 country.

Michal Vrablik3rd Department of Internal Medicine, 1st Faculty of Medicine, Charles University, Prague, Czechia.
Lukas TichýCentre of Molecular Biology and Gene Therapy, University Hospital, Brno, Czechia.
Tomas FreibergerCentre for Cardiovascular Surgery and Transplantation, Brno, and Faculty of Medicine, Masaryk University, Brno, Czechia.
Vladimir BlahaInternal Gerontometabolic Department, Charles University and University Hospital Hradec Kralove, Hradec Kralove, Czechia.
Martin Satny3rd Department of Internal Medicine, 1st Faculty of Medicine, Charles University, Prague, Czechia.
Jaroslav A Hubacek3rd Department of Internal Medicine, 1st Faculty of Medicine, Charles University, Prague, Czechia.
Charles University · CZMasaryk University · CZUniversity Hospital Brno · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial hypercholesterolemia (FH) is one of the most common monogenic diseases, leading to an increased risk of premature atherosclerosis and its cardiovascular complications due to its effect on plasma cholesterol levels. Variants of three genes (

Indexed as

epidemiologyfamilial hypercholesterolemiagene scorepolygenic FHvariants

Identifiers

PMID33133164
PMCPMC7575810
OpenAlexW3092331570

What Socratic 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 Socratic graph.