Prenatal Diagnosis

Cover image for Vol. 35 Issue 3

Editor-in-Chief: Professor Diana W. Bianchi, Boston, USA

Impact Factor: 2.514

ISI Journal Citation Reports © Ranking: 2013: 18/78 (Obstetrics & Gynecology); 88/165 (Genetics & Heredity)

Online ISSN: 1097-0223

Editors' Choice

2015 (Volume 35)

Vol. 35, No. 3 (March 2015)
F. Prefumo et al.: The natural history of monoamniotic twin pregnancies: a case series and systematic review of the literature

Vol. 35, No. 2 (February 2015)
L. Sarno et al.: Maternal body mass index influences umbilical artery Doppler velocimetry in physiologic pregnancies

Vol. 35, No. 1 (January 2015)
Hui & Wood: Perinatal outcome after maternal primary cytomegalovirus infection in the first trimester: a practical update and counseling aid

2014 (Volume 34)

Vol. 34, No. 13 (December 2014)
S-A B. Clur et al.: Early detection of fetal cardiac abnormalities: how effective is it and how should we manage these patients?

Vol. 34, No. 12 (December 2014)
A. Krishnan et al.: Outcomes of fetal echocardiographic surveillance in anti-SSA exposed fetuses at a large fetal cardiology center

Vol. 34, No. 11 (Novermber 2014)
C. Davis et al.: Screening for Down syndrome – incidental diagnosis of other aneuploidies

Vol. 34, No. 10 (October 2014)
S. Chandrasekharanet al.: Do recent US Supreme Court rulings on patenting of genes and genetic diagnostics affect the practice of genetic screening and diagnosis in prenatal and reproductive care?

Vol. 34, No. 9 (September 2014)
A. Buchanan et al.: NIPT: current utilization and implications for the future of prenatal genetic counseling

Vol. 34, No. 8 (August 2014)
J. I. Pike et al.: Early fetal echocardiography: congenital heart disease detection and diagnostic accuracy in the hands of an experienced fetal cardiology program

Vol. 34, No. 6 (June 2014)
Odibo & Ghidini: Role of the second-trimester ‘genetic sonogram’ for Down syndrome screen in the era of first-trimester screening and noninvasive prenatal testing

Vol. 34, No. 5 (May 2014)
Hern : Fetal diagnostic indications for second and third trimester outpatient pregnancy termination

Vol. 34, No. 4 (April 2014)
Hildebrand et al.: Maternal obesity and risk of Down syndrome in the offspring

Vol. 34, No. 3 (March 2014)
Ailes et al.: Prenatal diagnosis of nonsyndromic congenital heart defects

Vol. 34, No. 2 (February 2014)
Feenstra et al.: Complexity of noninvasive prenatal screening and diagnostic testing for an unbalanced translocation involving chromosomes 5 and 18

Vol. 34, No. 1 (January 2014)
Bianchi et al.: In case you missed it: the 'Prenatal Diagnosis' section editors bring you the most significant advances of 2013

2013 (Volume 33)

Vol. 33, No. 10 (October 2013)
Evans et al.: Evolution of gender options in multiple pregnancy management

Vol. 33, No. 9 (September 2013)
Lindenburget al.: Long-term neurodevelopmental and cardiovascular outcome after intrauterine transfusions for fetal anaemia: a review

Vol. 33, No. 8 (August 2013)
Picone et al.: A series of 238 cytomegalovirus primary infections during pregnancy: description and outcome

Vol. 33, No. 7 (July 2013)
Wanget al.: Gestational age and maternal weight effects on fetal cell-free DNA in maternal plasma

Vol. 33, No. 6 (June 2013)
Jacobsenet al.: Effects of self-directed stress management training and home-based exercise on quality of life in cancer patients receiving chemotherapy: a randomized controlled trial

Vol. 33, No. 5 (May 2013)
Chitty et al.: Safe, accurate, prenatal diagnosis of thanatophoric dysplasia using ultrasound and free fetal DNA

Vol. 33, No. 4 (April 2013)
Kallioniemi et al.: Vaginal fluid phIGFBP-1 in prediction of preterm delivery

Vol. 33, No. 3 (March 2013)
Rose et al.: The impact of utilization of early aneuploidy screening

Vol. 33, No. 1 (January 2013)
Yaron et al.: Current controversies in prenatal diagnosis 1: screening for fragile X syndrome

2012 (Volume 32)

Vol. 32, No. 13 (December 2012)
Dan et al.: Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test

Vol. 32, No. 12 (December 2012)
Posch et al.: Prenatal genetic counseling and consanguinity

Vol. 32, No. 11 (November 2012)
Pajkrt et al.: Prenatal management of fetal forearm anomalies

Vol. 32, No. 10 (October 2012)
L. Shaffer et al.: Microarray experience with abnormal ultrasound anomalies

Vol. 32, No. 9 (September 2012)
Deloison et al.: Fetal small circumference on untrasound examination

Vol. 32, No. 8 (August 2012)
Canick et al.: DNA test for trisomies in multiple gestations

Vol. 32, No. 7 (July 2012)
Gziri et al.: Effects of chemotherapy during pregnancy on the maternal and fetal heart

Vol. 32, No. 6 (June 2012)
Fetal varicella: diagnosis, management and outcome

Vol. 32, No. 5 (May 2012)
Nemec et al.: Male genital abnormalities in intrauterine growth restriction

Vol. 32, No. 4 (April 2012)
Wapner et al.: Prenatal microarray counseling issues

Vol. 32, No. 3 (March 2012)
Nemec et al.: MR imaging of the fetal musculoskeletal system

Vol. 32, No. 2 (February 2012)
Natoli et al.: Prenatal diagnosis of down syndrome: systematic review

Vol. 32, No. 1 (January 2012)
Sparks et al.: Analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy

2011 (Volume 31)

Vol. 31, No. 13 (15 December 2011)
Fiorentino et al.: Introducing array-CGH into routine prenatal diagnosis practice

Vol. 31, No. 12 (1 December 2011)
Papastefanou et al.: Fetal intracranial translucency and cisterna magna at 11 to 14 weeks

Vol. 31, No. 11 (November 2011)
Mayer et al.: Fetal MRI in CDH

Vol. 31, No. 10 (October 2011)
Nolin et al.: Fragile X risk estimates

Vol. 31, No. 9 (September 2011)
Bakker et al.: Increased nuchal translucency and Noonan syndrome

Vol. 31, No. 8 (August 2011)
Bombard et al.: Noninvasive fetal RhD determination in first and second trimesters

Vol. 31, No. 7 (July 2011)
Ville: Fetal therapy: practical ethical considerations

Vol. 31, No. 6 (June 2011)
Benn et al.: ISPD Position Statement 1: aneuploidy screening

Vol. 31, No. 5 (May 2011)
de Jong et al.: Parvovirus B19 infection in pregnancy: new insights and management

Vol. 31, No. 4 (Apr 2011)
Egan et al.: Demographic differences in Down syndrome births

Vol. 31, No. 3 (Mar 2011)
Bui et al.: Is conventional chromosome analysis necessary in the post-array CGH era?

Vol. 31, No. 2 (Feb 2011)
de Mooij et al.: Aberrant lymphatic development in fetuses with increased NT

Vol. 31, No. 1 (Jan 2011)
Nicolaides: Screening for fetal aneuploidies at 11 to 13 weeks

2010 (Volume 30)

Vol. 30, No. 12-13 (Dec 2010)
Srisupundit et al.: Targeted array CGH for isolated CDH

Vol. 30, No. 11 (Nov 2010)
Pu et al.: Imaging fetal ventricular longitudinal functions

Vol. 30, No. 10 (Oct 2010)
Neely Kazerouni et al.: Ancillary benefits of prenatal screening

Vol. 30, No. 9 (Sep 2010)
Cuckle & Maymon: Down syndrome risk calculation for a twin fetus

Vol. 30, No. 8 (Aug 2010)
Thayyil et al.: Minimally invasive fetal postmortem examination using MRI and CT

Vol. 30, No. 7 (Jul 2010)
Deprest et al.: The making of fetal surgery

Vol. 30, No. 6 (Jun 2010)
Hills et al.: QF-PCR as stand-alone test for prenatal samples

Vol. 30, No. 5 (May 2010)
Koster et al.: First-trimester serum markers in twin pregnancies

Vol. 30, No. 4 (Apr 2010)
Zhong et al.: First-trimester assessment of placenta function

Vol. 30, No. 3 (Mar 2010)
Poon et al.: Early screening for preeclampsia

Vol. 30, No. 2 (Feb 2010)
Bilardo et al.: Parental counseling in increased nuchal translucency

Vol. 30, No. 1 (Jan 2010)
Robinson et al.: Placental trisomy in IUGR