Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure.

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

8 citing papers in PubMed.

1. BCORL1, POF1B, and USP9X copy number variation in women with idiopathic diminished ovarian reserve.Journal of assisted reproduction and genetics · 2024
   Article
2. Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency.Human reproduction (Oxford, England) · 2021
   Article
3. Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypes.European journal of human genetics : EJHG · 2019
   Article
4. High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.Human reproduction (Oxford, England) · 2019
   Article
5. Copy number gain of VCX, X-linked multi-copy gene, leads to cell proliferation and apoptosis during spermatogenesis.Oncotarget · 2016
   Article
6. Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform.Human reproduction (Oxford, England) · 2014
   Article
7. Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome.Human reproduction (Oxford, England) · 2014
   Article
8. Genetics of primary ovarian insufficiency: new developments and opportunities.Human reproduction update
   Review

Corrections and comments

• Comment on
  Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF).2010

Authors and funding

7 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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