Prenatal Diagnosis

Prenatal Diagnosis is the official journal of ISPD. Published online 13 times per year, this peer-reviewed publication communicates the results of clinical and basic research in prenatal and preimplantation diagnosis in humans, animal and in vitro models.
 
All ISPD members receive an online subscription to Prenatal Diagnosis as part of their membership. Print subscriptions are available only to institutions. General information is available on the Journal home page on the publisher's website.

Manuscript Submission

All manuscripts should be submitted on the publisher's website. Submission instructions are on the Author Resources tab of the journal home page.

Recent Issues

The Editor's Choice articles of Prenatal Diagnosis are open access. For access to all articles, please use the member journal access.

Volume 42 | Issue 10 | September 2022

Table of Contents

Editor's Choice Article:
Bardi F, Beekhuis AM, Bakker MK, Elvan‐Taşpınar A, Bilardo CM. Timing of diagnosis of fetal structural abnormalities after the introduction of universal cell-free DNA in the absence of first-trimester anatomical screening.
DOI: 10.1002/pd.6224

Volume 42 | Issue 9 | August 2022

Table of Contents

Editor's Choice Article:
Meiman J, Zhang C, Holland B. Use of fetal tele-echo at small regional hospitals increases the rate of prenatal diagnosis of congenital heart disease.
DOI: 10.1002/pd.6196

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ISPD Abstracts | 2010-2021

See All Abstract Issues

Special Issues: Abstracts of the International Conference on Prenatal Diagnosis and Therapy

Aims & Scope

Prenatal Diagnosis welcomes submissions in all aspects of prenatal screening and diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing:

  • prenatal molecular genetics, including genome sequencing and the diagnosis of single gene disorders
  • fetal therapy
  • fetal and placental cell-free nucleic acids and cells in maternal blood and other fluids
  • fetal imaging in relation to congenital anomalies, genetic syndromes and fetal phenotyping
  • prenatal cytogenetics and cytogenomics
  • prenatal and preconceptional genetic screening and counseling 
  • fetal and placental transcriptome, proteome and metabolome studies
  • development and evaluation of laboratory services for prenatal testing
  • psychosocial, legal, ethical and economic aspects of prenatal testing and fetal treatments
  • fetal and placental development and pathology 
  • preimplantation genetic testing (PGT)
     

The overriding criteria for publication are scientific merit, originality, and interest to a multidisciplinary audience.