ArticleEuropean journal of human genetics : EJHG2011
The causality of de novo copy number variants is overestimated.
Article in European journal of human genetics : EJHG, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 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.
The trial behind it
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Who cites it
19 citing papers in PubMed.
- Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.Journal of neurodevelopmental disorders · 2019Article
- Array comparative genomic hybridization and genomic sequencing in the diagnostics of the causes of congenital anomalies.Journal of applied genetics · 2017Review
- New insights into the generation and role of de novo mutations in health and disease.Genome biology · 2016Review
- CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens.Scientific reports · 2016Article
- The clustering of functionally related genes contributes to CNV-mediated disease.Genome research · 2015Article
- Parental expression is overvalued in the interpretation of rare inherited variants.European journal of human genetics : EJHG · 2015Article
- De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features.Meta gene · 2014Article
- The clinical significance of small copy number variants in neurodevelopmental disorders.Journal of medical genetics · 2014Article
- OTX2 duplication is implicated in hemifacial microsomia.PloS one · 2014Article
- The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.American journal of medical genetics. Part A · 2013Article
- Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years' clinical application for over 8,700 patients.Molecular cytogenetics · 2013Article
- Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease.Nature genetics · 2013Article
- The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants.Molecular psychiatry · 2013Review
- Atypical face shape and genomic structural variants in epilepsy.Brain : a journal of neurology · 2012Article
- 5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual Disability.Molecular syndromology · 2012Article
- De novo mutations in human genetic disease.Nature reviews. Genetics · 2012Review
- Submicroscopic chromosomal copy number variations identified in children with hypoplastic left heart syndrome.Pediatric cardiology · 2012Article
- Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnostics.European journal of human genetics : EJHG · 2012Article
- Copy number variants in a sample of patients with psychotic disorders: is standard screening relevant for actual clinical practice?Neuropsychiatric disease and treatment · 2012Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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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.