3.2(top 5%)
Impact Factor
3.6(top 5%)
extended IF
109(top 3%)
H-Index
2.9K
authors
7.8K
papers
142K
citations
4.7K
citing journals
26.3K
citing authors

Most Cited Articles of Prenatal Diagnosis

TitleYearCitations
Abnormal maternal serum chorionic gonadotropin levels in pregnancies with fetal chromosome abnormalities1987411
Screening for fetal aneuploidies at 11 to 13 weeks2011394
Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses1984351
Challenges in the diagnosis of fetal non-chromosomal abnormalities at 11-13 weeks2011312
Cytogenetic results from the U.S. Collaborative Study on CVS1992301
Prediction of early, intermediate and late pre-eclampsia from maternal factors, biophysical and biochemical markers at 11-13 weeks2011291
Free fetal DNA in maternal plasma in anembryonic pregnancies: confirmation that the origin is the trophoblast2007276
Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos1995269
Gestational age and maternal weight effects on fetal cell-free DNA in maternal plasma2013263
Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data. National Institute of Child Health and Development Fetal Cell Isolation Study2002262
The impact of maternal plasma DNA fetal fraction on next generation sequencing tests for common fetal aneuploidies2013250
Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci2012236
Fetal morbidity and mortality after acute human parvovirus B19 infection in pregnancy: prospective evaluation of 1018 cases2004229
A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses1984225
Combining Ultrasound and Biochemistry in First-Trimester Screening for Down's syndrome1997223
Prenatal diagnosis of congenital cytomegalovirus infection in 189 pregnancies with known outcome2001210
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy2012209
47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling1997209
Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis2015195
United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis1984195
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies2015191
Fetal liver position and perinatal outcome for congenital diaphragmatic hernia1998182
Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis1998180
Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound2012175
Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y2013174