# | Title | Journal | Year | Citations |
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1 | Screening for fetal aneuploidies at 11 to 13 weeks | Prenatal Diagnosis | 2011 | 506 |
2 | Abnormal maternal serum chorionic gonadotropin levels in pregnancies with fetal chromosome abnormalities | Prenatal Diagnosis | 1987 | 459 |
3 | Challenges in the diagnosis of fetal non‐chromosomal abnormalities at 11–13 weeks | Prenatal Diagnosis | 2011 | 385 |
4 | Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative european study on 52 965 amniocenteses | Prenatal Diagnosis | 1984 | 384 |
5 | Prediction of early, intermediate and late pre‐eclampsia from maternal factors, biophysical and biochemical markers at 11–13 weeks | Prenatal Diagnosis | 2011 | 377 |
6 | Gestational age and maternal weight effects on fetal cell‐free DNA in maternal plasma | Prenatal Diagnosis | 2013 | 346 |
7 | Cytogenetic results from the U.S. collaborative study on CVS | Prenatal Diagnosis | 1992 | 330 |
8 | Free fetal DNA in maternal plasma in anembryonic pregnancies: confirmation that the origin is the trophoblast | Prenatal Diagnosis | 2007 | 326 |
9 | Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data | Prenatal Diagnosis | 2002 | 318 |
10 | Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos | Prenatal Diagnosis | 1995 | 310 |
11 | The impact of maternal plasma DNA fetal fraction on next generation sequencing tests for common fetal aneuploidies | Prenatal Diagnosis | 2013 | 310 |
12 | Fetal morbidity and mortality after acute human parvovirus B19 infection in pregnancy: prospective evaluation of 1018 cases | Prenatal Diagnosis | 2004 | 289 |
13 | Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci | Prenatal Diagnosis | 2012 | 284 |
14 | Prenatal diagnosis of congenital cytomegalovirus infection in 189 pregnancies with known outcome | Prenatal Diagnosis | 2001 | 266 |
15 | Promises, pitfalls and practicalities of prenatal whole exome sequencing | Prenatal Diagnosis | 2018 | 262 |
16 | Combining Ultrasound and Biochemistry in First-Trimester Screening for Down's syndrome | Prenatal Diagnosis | 1997 | 258 |
17 | A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses | Prenatal Diagnosis | 1984 | 252 |
18 | Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies | Prenatal Diagnosis | 2015 | 247 |
19 | Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis | Prenatal Diagnosis | 2015 | 243 |
20 | Selective analysis of cell‐free DNA in maternal blood for evaluation of fetal trisomy | Prenatal Diagnosis | 2012 | 238 |
21 | Preterm delivery, maternal death, and vertical transmission in a pregnant woman with COVID‐19 infection | Prenatal Diagnosis | 2020 | 230 |
22 | Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound | Prenatal Diagnosis | 2012 | 222 |
23 | Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis | Prenatal Diagnosis | 1998 | 214 |
24 | United states survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis | Prenatal Diagnosis | 1984 | 211 |
25 | Prediction of pregnancy complications by first-trimester maternal serum PAPP-A and free β-hCG and with second-trimester uterine artery Doppler | Prenatal Diagnosis | 2005 | 208 |
26 | Maternal obesity and neurodevelopmental and psychiatric disorders in offspring | Prenatal Diagnosis | 2017 | 208 |
27 | The fetal circulation | Prenatal Diagnosis | 2004 | 205 |
28 | Validation of targeted sequencing of single‐nucleotide polymorphisms for non‐invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y | Prenatal Diagnosis | 2013 | 202 |
29 | A series of 238 cytomegalovirus primary infections during pregnancy: description and outcome | Prenatal Diagnosis | 2013 | 200 |
30 | Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism | Prenatal Diagnosis | 1991 | 197 |
31 | Clinical application of massively parallel sequencing‐based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11 105 pregnancies with mixed risk factors | Prenatal Diagnosis | 2012 | 197 |
32 | Fetal blood sampling via the umbilical cord using a needle guided by ultrasound report of 66 cases | Prenatal Diagnosis | 1983 | 189 |
33 | Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities | Prenatal Diagnosis | 2015 | 189 |
34 | Prenatal diagnosis of Down syndrome: a systematic review of termination rates (1995–2011) | Prenatal Diagnosis | 2012 | 188 |
35 | Prediction of gestational diabetes mellitus by maternal factors and biomarkers at 11 to 13 weeks | Prenatal Diagnosis | 2011 | 187 |
36 | A model for a new pyramid of prenatal care based on the 11 to 13 weeks' assessment | Prenatal Diagnosis | 2011 | 186 |
37 | Chorion biopsy in early pregnancy: A method of early prenatal diagnosis for inherited disorders | Prenatal Diagnosis | 1982 | 184 |
38 | Adverse outcome in pregnancy following amniotic fluid isolation ofUreaplasma urealyticum | Prenatal Diagnosis | 1992 | 182 |
39 | Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis | Prenatal Diagnosis | 2013 | 181 |
40 | Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases | Prenatal Diagnosis | 2009 | 180 |
41 | Discordant noninvasive prenatal testing results in a patient subsequently diagnosed with metastatic disease | Prenatal Diagnosis | 2013 | 179 |
42 | Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts | Prenatal Diagnosis | 2015 | 179 |
43 | An embryogenic model to explain cytogenetic inconsistencies observed in chorionic villus versus fetal tissue | Prenatal Diagnosis | 1988 | 178 |
44 | Experience with microarray‐based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies | Prenatal Diagnosis | 2012 | 178 |
45 | Fetal DNA in maternal plasma is elevated in pregnancies with aneuploid fetuses | Prenatal Diagnosis | 2000 | 174 |
46 | Congenital diaphragmatic hernia: an evaluation of the prognostic value of the lung-to-head ratio and other prenatal parameters | Prenatal Diagnosis | 2003 | 173 |
47 | Systematic review of accuracy of fetal urine analysis to predict poor postnatal renal function in cases of congenital urinary tract obstruction | Prenatal Diagnosis | 2007 | 173 |
48 | Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell‐free DNA from maternal plasma | Prenatal Diagnosis | 2013 | 173 |
49 | Prenatal ultrasound diagnosis of vasa praevia and analysis of risk factors | Prenatal Diagnosis | 2007 | 171 |
50 | Primary prevention of neural tube defects with folic acid supplementation: Cuban experience | Prenatal Diagnosis | 1990 | 169 |