Human aneuploidy: mechanisms and new insights into an age-old problem

By So I. Nagaoka, T. Hassold, P. Hunt. Nature reviews genetics, 2012

953 citations recorded by the source corpus.

Trisomic and monosomic (aneuploid) embryos account for at least 10% of human pregnancies and, for women nearing the end of their reproductive lifespan, the incidence may exceed 50%. The errors that lead to aneuploidy almost always occur in the oocyte but, despite intensive investigation, the underlying molecular basis has remained elusive. Recent studies of humans and model organisms have shed new light on the complexity of meiotic defects, providing evidence that the age-related increase in errors in the human female is not attributable to a single factor but to an interplay between unique features of oogenesis and a host of endogenous and exogenous factors.

Subfields: Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health

View Paper: https://www.semanticscholar.org/paper/d0b46ef7c7de617ddec83be6c96f00ff1f2ce236

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Genetics

  1. N. Hunter
  2. Dominic Grün
  3. Alexander van Oudenaarden
  4. Christina Kendziorski
  5. Rhonda L. Bacher

In Pediatrics, Perinatology and Child Health

  1. N. Hunter

In Public Health, Environmental and Occupational Health

  1. Alexander van Oudenaarden

Citations in the corpus