ArticleAmerican journal of human genetics1996
The FRAXE Syndrome: is it time for routine screening?
Article in American journal of human genetics, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 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
15 citing papers in PubMed.
- Exploring the Potential of Small Molecule-Based Therapeutic Approaches for Targeting Trinucleotide Repeat Disorders.Molecular neurobiology · 2020Review
- Autism spectrum disorder: FRAXE mutation, a rare etiology.Journal of autism and developmental disorders · 2015Article
- Dampened dopamine-mediated neuromodulation in prefrontal cortex of fragile X mice.The Journal of physiology · 2013Article
- Cytogenetic analysis of obsessive-compulsive disorder (OCD): identification of a FRAXE fragile site.American journal of medical genetics. Part A · 2003Article
- Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002Article
- Synaptic regulation of protein synthesis and the fragile X protein.Proceedings of the National Academy of Sciences of the United States of America · 2001Review
- Chromosomal fragility and human genetic disorders.Indian journal of clinical biochemistry : IJCB · 2000Article
- FRAXA and FRAXE: the results of a five year survey.Journal of medical genetics · 2000Article
- Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population.American journal of human genetics · 1999Article
- Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation.Proceedings of the National Academy of Sciences of the United States of America · 1997Article
- Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits.Proceedings of the National Academy of Sciences of the United States of America · 1997Article
- Fragile X syndrome. Molecular and clinical insights and treatment issues.The Western journal of medicine · 1997Review
- FRAXE testing.American journal of human genetics · 1996Article
- Coverage of new genetic technologies: what matters to insurers?American journal of human genetics · 1996Article
- microRNAs: tiny regulators of synapse function in development and disease.Journal of cellular and molecular medicineReview
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
8651273PMC1914605What 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.