Evidence map›Paper›PMID 38192829›Full record

ArticleHeliyon2024

Brachyolmia, dental anomalies and short stature (DASS): Phenotype and genotype analyses of Egyptian and Pakistani patients.

Hamed Nawaz, Asia Parveen, Sher Alam Khan, Abul Khair Zalan, Muhammad Adnan Khan, Noor Muhammad, Nehal F Hassib, Mostafa I Mostafa, Rasha M Elhossini, Nehal Nabil Roshdy and 5 more

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

Article in Heliyon, 2024. 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
0.9field-weighted citation impact, top 19% 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. IsMedComm · 2025
    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

15 authors at 7 institutions in 5 countries.

Hamed NawazDepartment of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Pakistan.
Asia ParveenDepartment of Biochemistry, Faculty of Life Sciences, Gulab Devi Educational Complex, Gulab Devi Hospital, 54000, Lahore, Pakistan.
Sher Alam KhanDepartment of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Pakistan.
Abul Khair ZalanBDS, MDS Registrar Pediatric Dentistry, Department of Pediatric Dentistry, School of Dentistry, PIMS, Islamabad, Pakistan.
Muhammad Adnan KhanDental Material, Institute of Basic Medical Sciences, Khyber Medical University Peshawar, Peshawar, Pakistan.
Noor MuhammadDepartment of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Pakistan.
Nehal F HassibOrodental Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, 12622, Egypt.
Mostafa I MostafaOrodental Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, 12622, Egypt.
Rasha M ElhossiniClinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, 12622, Egypt.
Nehal Nabil RoshdyEndodontics, Faculty of Dentistry, Cairo University, Cairo, 11553, Egypt.
Asmat UllahDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Amina ArifFaculty of Science and Technology, University of Central Punjab (UCP), Lahore, Pakistan.
Saadullah KhanDepartment of Biotechnology and Genetic Engineering, Kohat University of Science and Technology (KUST), Kohat, Pakistan.
Ole AmmerpohlInstitute of Human Genetics, Ulm University and Ulm University Medical Center, 89081, Ulm, Germany.
Naveed WasifInstitute of Human Genetics, Ulm University and Ulm University Medical Center, 89081, Ulm, Germany.
Kohat University of Science and Technology · PKAgricultural Genetic Engineering Research Institute · EGBroad Institute · USUniversität Ulm · DECairo University · EGKhyber Medical University · PKUniversity of Central Punjab · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brachyolmia is a heterogeneous group of developmental disorders characterized by a short trunk, short stature, scoliosis, and generalized platyspondyly without significant deformities in the long bones. DASS (Dental Abnormalities and Short Stature), caused by alterations in the

Indexed as

Amelogenesis imperfectaBrachyolmiaExome sequencingFrameshift variantsHearing impairmentHomozygous splice acceptor siteLTBP3

Identifiers

PMID38192829
PMCPMC10772639
OpenAlexW4389763562

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.