ReviewThe application of clinical genetics2019
Review in The application of clinical genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.
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.
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.
Who cites it
24 citing papers in PubMed.
- Closely Monitored Successful Full-Term Delivery in a Woman With Spondyloepiphyseal Dysplasia Congenita: A Case Report and Literature Review.The journal of obstetrics and gynaecology research · 2026Review
- Multiple Ossification Centers of the Pubic Bone as a Supportive Radiographic Feature forDiagnostics (Basel, Switzerland) · 2026Article
- Multilevel congenital lumbar facet joint aplasia presenting with L5-S1 spondylolisthesis in a patient with connective tissue disease.Surgical neurology international · 2026Article
- Diagnostic Challenge of Phenotypic Variability inJournal of clinical research in pediatric endocrinology · 2025Article
- Functional performance and symptomatology of adults with skeletal dysplasia across self-care, mobility, and cognition-a cross-sectional study.JBMR plus · 2025Article
- Challenges in the diagnosis of fibrodysplasia ossificans progressiva with the ACVR1 mutation (c.774G > C, p.R258S): a case report and review of literature.Orphanet journal of rare diseases · 2024Review
- PdmIRD: missense variants pathogenicity prediction for inherited retinal diseases in a disease-specific manner.Human genetics · 2024Article
- Myogenic Differentiation and Immunomodulatory Properties of Rat Adipose-Derived Mesenchymal Stem/Stromal Cells.Biology · 2024Article
- Identification and functional characteristics of a novel splicing heterozygote variant ofFrontiers in genetics · 2024Article
- Surgical treatment of atlantoaxial dysplasia and scoliosis in spondyloepiphyseal dysplasia congenita: A case report.World journal of orthopedics · 2023Article
- Whole exome sequencing improves genetic diagnosis of fetal clubfoot.Human genetics · 2023Article
- Rgp1 contributes to craniofacial cartilage development and Rab8a-mediated collagen II secretion.Frontiers in endocrinology · 2023Article
- What the pediatric endocrinologist needs to know about skeletal dysplasia, a primer.Frontiers in pediatrics · 2023Review
- Case report: Whole exome sequencing and genome-wide methylation profiling of Czech dysplasia in a Chinese pedigree.Frontiers in medicine · 2023Article
- Multiple disc herniation in spondyloepiphyseal dysplasia tarda: A rare case report and review of the literature.BMC musculoskeletal disorders · 2022Review
- Familial Aggregation of a Novel Missense Variant ofChildren (Basel, Switzerland) · 2022Article
- A Computational Data Mining Strategy to Identify the Common Genetic Markers of Temporomandibular Joint Disorders and Osteoarthritis.Global medical genetics · 2022Article
- Review
- Article
- A novel homozygous variant of COL2A1 in a Chinese male with type II collagenopathy: a case report.BMC medical genomics · 2021Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The
Indexed as
Identifiers
What OpenQuestion holds
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.