Evidence map›Paper›PMID 35047021›Full record

ArticleFrontiers in genetics2021

Low Detection Rates of Genetic FH in Cohort of Patients With Severe Hypercholesterolemia in the United Arabic Emirates.

Antoine Rimbert, Hinda Daggag, Peter Lansberg, Adam Buckley, Martijn Viel, Roan Kanninga, Lennart Johansson, Robin P F Dullaart, Richard Sinke, Alia Al Tikriti and 2 more

Registry-linked trialAbstract read
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In one paragraph

Article in Frontiers in genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06535542 (A Randomized Trial of Integrating Whole Genome Sequencing and Digital Twins Into the Management of Hypercholesterolemia in Emiratis), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT06535542 narecruitingnot on this mapstarted 2024, after this paper: background citation

A Randomized Trial of Integrating Whole Genome Sequencing and Digital Twins Into the Management of Hypercholesterolemia in Emiratis

TypeinterventionalSponsorAbu Dhabi Health Services CompanyRan2024 to 2026Enrolled40ConditionsHypercholesterolemia, Autosomal Dominant, Hypercholesterolemia, Autosomal Recessive, Familial Combined HypercholesterolemiaArmsWhole Genome Sequencing
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Antoine RimbertDepartment of Paediatrics, Section Molecular Genetics, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
Hinda DaggagImperial College London Diabetes Centre, Abu Dhabi, United Arab Emirates.
Peter LansbergDepartment of Paediatrics, Section Molecular Genetics, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
Adam BuckleyImperial College London Diabetes Centre, Abu Dhabi, United Arab Emirates.
Martijn VielDepartment of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
Roan KanningaDepartment of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
Lennart JohanssonDepartment of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
Robin P F DullaartDepartment of Endocrinology, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
Richard SinkeDepartment of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
Alia Al TikritiImperial College London Diabetes Centre, Abu Dhabi, United Arab Emirates.
Jan Albert KuivenhovenDepartment of Paediatrics, Section Molecular Genetics, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
Maha Taysir BarakatImperial College London Diabetes Centre, Abu Dhabi, United Arab Emirates.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

familial hypercholestelemiageneticsprevalencescreeningUnited Arab Emirates (UAE)

Identifiers

PMID35047021
PMCPMC8762259

What OpenQuestion holds

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Registered trials

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.