Evidence map›Paper›PMID 35741735›Full record

ArticleGenes2022

Potential Composite Digenic Contribution of

Bilal Azab, Omar Rabab'h, Dunia Aburizeg, Hashim Mohammad, Zain Dardas, Lina Mustafa, Ruba A Khasawneh, Heyam Awad, Ma'mon M Hatmal, Eyad Altamimi

Open access · goldAbstract readCase Reports
In one paragraph

Article in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Genes · 2022
    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 5 institutions in 2 countries.

Bilal AzabDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.ORCID 0000-0003-0293-6489
Omar Rabab'hDepartment of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, IA 52242, USA.
Dunia AburizegDepartment of Pathology and Microbiology and Forensic Medicine, School of Medicine, The University of Jordan, Amman 11942, Jordan.
Hashim MohammadDepartment of Pathology and Microbiology and Forensic Medicine, School of Medicine, The University of Jordan, Amman 11942, Jordan.
Zain DardasDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Lina MustafaDepartment of Pathology and Microbiology and Forensic Medicine, School of Medicine, The University of Jordan, Amman 11942, Jordan.
Ruba A KhasawnehDepartment of Diagnostic Radiology and Nuclear Medicine, Faculty of Medicine King Abdullah University Hospital, Jordan University of Science and Technology, Irbid 22110, Jordan.
Heyam AwadDepartment of Pathology and Microbiology and Forensic Medicine, School of Medicine, The University of Jordan, Amman 11942, Jordan.ORCID 0000-0003-3050-136X
Ma'mon M HatmalDepartment of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, The Hashemite University, Zarqa 13133, Jordan.ORCID 0000-0003-1745-8985
Eyad AltamimiPediatric Department, Faculty of Medicine, Jordan University of Science and Technology, Irbid 22110, Jordan.ORCID 0000-0003-0325-1553
University of Jordan · JOJordan University of Science and Technology · JOBaylor College of Medicine · USHashemite University · JOUniversity of Iowa · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Niemann-Pick disease type C (NPC) is an autosomal recessive neurovisceral disease characterized by progressive neurodegeneration with variable involvement of multisystemic abnormalities. Crohn's disease (CD) is an inflammatory bowel disease (IBD) with a multifactorial etiology influenced by variants in

Indexed as

Crohn DiseaseNiemann-Pick C1 ProteinNiemann-Pick Disease, Type CNod2 Signaling Adaptor ProteinFemaleGenetic Association StudiesGenetic TestingHumansNiemann-Pick C1 ProteinNOD2 protein, humanNod2 Signaling Adaptor ProteinNPC1 protein, humanCrohn’sdigenicgenotype–phenotype associationNOD2NPCNPC1

Identifiers

PMID35741735
PMCPMC9223108
OpenAlexW4281657103

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.