Prenatal Diagnosis
Title Abbreviation
Prenat Diagn
Electronic ISSN
1097-0223
Readership
Cell Biologists, Cytologists, Gynecologists, Molecular Biologists, Neonatologists, Obstetricians, Pediatricians, Perinatologists, Radiologists, Ultrasound Medicine Specialists
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.
Sponsoring Association(s)
International Society for Prenatal Diagnosis (ISPD)
Publisher Name
John Wiley & Sons Ltd. - UK
Impact Factor
JCR Categories/Rank
Submission to Acceptance
Acceptance to Online Publication
Acceptance to Print Publication
Rejection Rate
Frequency
Journal Contact
Author Submission Guidelines