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2022	Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis Diagnostics Gioia Mastromoro, Daniele Guadagnolo, Nader Khaleghi Hashemian, Enrica Marchionni, Alice Traversa, Antonio Pizzuti
2018	Molecular karyotyping in early miscarriages: potential for the routine use of cytogenetic microarrays Journal of Obstetrics and Gynaecology Katarzyna Szewczyk, Miroslaw Bik-Multanowski
2018	Prenatal diagnosis: the clinical usefulness of array comparative genomic hybridization Porto Biomedical Journal Marta Freitas, Joel Pinto, Carla Ramalho, Sofia Dória
2018	Pregnant Genetic Counselors in an Era of Advanced Genomic Tests: What Do the Experts Test Prenatally? Journal of Genetic Counseling Shiri Shkedi‐Rafid, Yael Hashiloni‐Dolev
2017	Efficient and cost-effective genetic analysis of products of conception and fetal tissues using a QF-PCR/array CGH strategy; five years of data Molecular Cytogenetics Celia Donaghue, Nada Davies, Joo Wook Ahn, Helen Thomas, Caroline Mackie Ogilvie, Kathy Mann
2016	Encyclopedia of Life Sciences Sandi Dheensa, Shiri Shkedi‐Rafid, Gillian Crawford, Gabrielle Bertier, Lisa Schonstein, Anneke Lucassen
2016	Gestation related karyotype, QF-PCR and CGH-array failure rates in diagnostic amniocentesis Prenatal Diagnosis Anna Lawin O'Brien, Andrea Dall'Asta, Dagmar Tapon, Kathy Mann, Joo Wook Ahn, Richard Ellis, Caroline Ogilvie, Christoph Lees
2016	First applications of a targeted exome sequencing approach in fetuses with ultrasound abnormalities reveals an important fraction of cases with associated gene defects PeerJ Constantinos Pangalos, Birgitta Hagnefelt, Konstantinos Lilakos, Christopher Konialis
2016	Approches génomiques prénatales pour la détection des mutations géniques associées à des maladies génétiques liées à des anomalies échographiques Bulletin de l'Académie Nationale de Médecine Constantin Pangalos
2016	Advances in Clinical Chemistry
2015	Whole‐genome array as a first‐line cytogenetic test in prenatal diagnosis Ultrasound in Obstetrics & Gynecology M. I. Srebniak, D. Van Opstal, M. Joosten, K. E. M. Diderich, F. A. T. de Vries, S. Riedijk, M. F. C. M. Knapen, A. T. J. I. Go, L. C. P. Govaerts, R.‐J. H. Galjaard
2015	Benefits and Burdens of Using a SNP Array in Pregnancies at Increased Risk for the Common Aneuploidies Human Mutation Diane Van Opstal, Femke de Vries, Lutgarde Govaerts, Marjan Boter, Debora Lont, Stefanie van Veen, Marieke Joosten, Karin Diderich, Robert-Jan Galjaard, Malgorzata I. Srebniak
2014	FREE FETAL DNA AS A SCREENING TEST FOR ANEUPLOIDY – DOES IT ADD UP? Fetal and Maternal Medicine Review CAROLINE OGILVIE
2014	Defining and managing incidental findings in genetic and genomic practice Journal of Medical Genetics Shiri Shkedi-Rafid, Sandi Dheensa, Gillian Crawford, Angela Fenwick, Anneke Lucassen