ArticleChild neurology open
Clinical Phenotype of De Novo
Article in Child neurology open. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 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
16 citing papers in PubMed, 29 citations in OpenAlex.
- Decoding GNAO1 mutations usingFrontiers in cellular neuroscience · 2025Review
- Article
- GNAO1-related neurodevelopmental disorder: Literature review and caregiver survey.Epilepsy & behavior reports · 2023Article
- Genetic modeling of GNAO1 disorder delineates mechanisms of Gαo dysfunction.Human molecular genetics · 2022Article
- Cognitive Assessment inJournal of clinical medicine · 2021Article
- Spectrum of movement disorders in GNAO1 encephalopathy: in-depth phenotyping and case-by-case analysis.Orphanet journal of rare diseases · 2020Article
- Humanization ofBiomedicines · 2020Article
- Deletion of the α subunit of the heterotrimeric Go protein impairs cerebellar cortical development in mice.Molecular brain · 2019Article
- Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region.Epilepsia · 2019Article
- Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms.Journal of inherited metabolic disease · 2018Review
- Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing.Genetics in medicine : official journal of the American College of Medical Genetics · 2018Article
- [Recurrent convulsion and pulmonary infection complicated by psychomotor retardation in an infant].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2018Article
- Movement disorder inNeurology · 2017Article
- Article
- Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies.Molecular syndromology · 2016Article
- GNAO1 encephalopathy: further delineation of a severe neurodevelopmental syndrome affecting females.Orphanet journal of rare diseases · 2016Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Mutations in the guanine nucleotide-binding protein (G protein), α activating activity polypeptide O (
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.