Evidence map›Paper›PMID 32093271›Full record

ArticleInternational journal of molecular sciences2020

A Rare Mutation in The

Joanna Musialik, Anna Boguszewska-Chachulska, Dorota Pojda-Wilczek, Agnieszka Gorzkowska, Robert Szymańczak, Magdalena Kania, Agata Kujawa-Szewieczek, Małgorzata Wojcieszyn, Marek Hartleb, Andrzej Więcek

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Current Diagnosis and Management of Familial Hypobetalipoproteinemia 1.Journal of atherosclerosis and thrombosis · 2024
    Review
  4. Review
  5. Identification and Functional Analysis ofInternational journal of molecular sciences · 2023
    Article
  6. Article
  7. Article
  8. 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

10 authors at 3 institutions in 1 country.

Joanna MusialikDepartment of Nephrology, Transplantation and Internal Medicine, Medical University of Silesia in Katowice, 40-055 Katowice, Poland.
Anna Boguszewska-ChachulskaGenomed SA, 02-971 Warsaw, Poland.
Dorota Pojda-WilczekDepartment of Ophthalmology, Medical University of Silesia in Katowice, 40-055 Katowice, Poland.
Agnieszka GorzkowskaDepartment of Neurology, Department of Neurorehabilitation, Medical University of Silesia in Katowice, 40-055 Katowice, Poland.
Robert SzymańczakGenomed SA, 02-971 Warsaw, Poland.
Magdalena KaniaGenomed SA, 02-971 Warsaw, Poland.
Agata Kujawa-SzewieczekDepartment of Nephrology, Transplantation and Internal Medicine, Medical University of Silesia in Katowice, 40-055 Katowice, Poland.
Małgorzata WojcieszynDepartment of Gastroenterology, II John Paul Pediatric Center, 41-200 Sosnowiec, Poland.
Marek HartlebDepartment of Gastroenterology and Hepatology, Medical University of Silesia in Katowice, 40-055 Katowice, Poland.
Andrzej WięcekDepartment of Nephrology, Transplantation and Internal Medicine, Medical University of Silesia in Katowice, 40-055 Katowice, Poland.
Medical University of Silesia · PLGenomed (Poland) · PLJohn Paul II Hospital · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinical phenotypes of familial hypobetalipoproteinemia (FHBL) are related to a number of defective apolipoprotein B (

Indexed as

Apolipoprotein B-100Hypobetalipoproteinemia, Familial, Apolipoprotein BMutation, MissenseNervous System DiseasesRNA SplicingAdultAgedAmino Acid SubstitutionFemaleHigh-Throughput Nucleotide SequencingHumansMaleAPOB protein, humanApolipoprotein B-100APOB mutationfamilial hypobetalipoproteinemialiver steatosisnonalcoholic fatty liver disease

Identifiers

PMID32093271
PMCPMC7073066
OpenAlexW3007234589

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.