ReviewJournal of developmental biology2020
Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex.
Review in Journal of developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
What it found
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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.
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Who cites it
11 citing papers in PubMed.
- Very rare combination of Pierre Robin sequence with patent ductus arteriosus, severe persistent pulmonary hypertension, and sepsis in an Afghan neonate: a case report and literature review.Oxford medical case reports · 2025Article
- Application of four-section approach for prenatal diagnosis of Pierre robin sequence.Journal of medical ultrasonics (2001) · 2025Article
- Article
- Epigenetic regulation of craniofacial development and disease.Birth defects research · 2024Review
- The Impact of Mandibular Distraction Osteogenesis on Cephalometric Measurements in Infants with Pierre Robin Sequence.The Kobe journal of medical sciences · 2023Article
- Deficiency ofInternational journal of molecular sciences · 2023Article
- Precise modulation of transcription factor levels identifies features underlying dosage sensitivity.Nature genetics · 2023Article
- Cleft Palate in Apert Syndrome.Journal of developmental biology · 2022Review
- Advances in Understanding the Pathogenesis of Craniofacial Birth Defects.Journal of developmental biology · 2022Article
- Augmented BMP4 signal impairs tongue myogenesis.Journal of molecular histology · 2021Article
- Characterization of upper airway airflow dynamics in young adults with isolated Robin sequence: An exploratory investigation.Journal of oral biology and craniofacial researchArticle
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
The phenotype currently accepted as Pierre Robin syndrome/sequence/anomalad/complex (PR) is characterized by mandibular dysmorphology, glossoptosis, respiratory obstruction, and in some cases, cleft palate. A causative sequence of developmental events is hypothesized for PR, but few clear causal relationships between discovered genetic variants, dysregulated gene expression, precise cellular processes, pathogenesis, and PR-associated anomalies are documented. This review presents the current understanding of PR phenotypes, the proposed pathogenetic processes underlying them, select genes associated with PR, and available animal models that could be used to better understand the genetic basis and phenotypic variation of PR.
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Registered trials
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