ArticleCell2010
Retrotransposition and structural variation in the human genome.
Article in Cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 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
26 citing papers in PubMed, 44 citations in OpenAlex.
- Structural polymorphism and diversity of human segmental duplications.Nature genetics · 2025Article
- Structural polymorphism and diversity of human segmental duplications.bioRxiv : the preprint server for biology · 2024Article
- LINE- and Alu-containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPV.Human mutation · 2018Article
- Article
- Detection and validation of structural variations in bovine whole-genome sequence data.Genetics, selection, evolution : GSE · 2017Article
- Activation of individual L1 retrotransposon instances is restricted to cell-type dependent permissive loci.eLife · 2016Article
- Phosphorylation of ORF1p is required for L1 retrotransposition.Proceedings of the National Academy of Sciences of the United States of America · 2015Article
- Genome-wide analyses of LINE-LINE-mediated nonallelic homologous recombination.Nucleic acids research · 2015Article
- LINE-1 retrotransposons: from 'parasite' sequences to functional elements.Journal of applied genetics · 2015Article
- Increased leukemia-associated gene expression in benzene-exposed workers.Scientific reports · 2014Article
- Transposable elements and psychiatric disorders.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2014Review
- Article
- Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage-fusion-bridge for telomere stabilization.Human genetics · 2012Article
- Review
- In utero exposures, infant growth, and DNA methylation of repetitive elements and developmentally related genes in human placenta.Environmental health perspectives · 2012Article
- Copy number variation in the domestic dog.Mammalian genome : official journal of the International Mammalian Genome Society · 2012Review
- Human genome sequencing in health and disease.Annual review of medicine · 2012Review
- Genetic and epigenetic variations contributed by Alu retrotransposition.BMC genomics · 2011Article
- Retroviruses and retroelements in diseases and in gene therapy: 15 years later.Infectious agents and cancer · 2011Article
- Long interspersed nuclear element-1 hypomethylation in cancer: biology and clinical applications.Clinical epigenetics · 2011Article
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Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
New assays are revealing that the diploid human genome contains extensive amounts of structural variation. Genome-wide approaches described in three papers in this issue (Beck et al., 2010; Huang et al., 2010; Iskow et al., 2010) paint a dynamic portrait of our genome, revealing a prominent role for repetitive sequences in shaping its structural variation.
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.