A citation-based method for searching scientific literature




Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
Times Cited: 130




List of shared articles



Times cited



The role of chromosomal microarray and exome sequencing in prenatal diagnosis.
Matthew Hoi Kin Chau, Kwong Wai Choy. Curr Opin Obstet Gynecol 2021
0

Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionals.
Celine Lewis, Jennifer Hammond, Jasmijn E Klapwijk, Eleanor Harding, Stina Lou, Ida Vogel, Emma J Szepe, Lisa Hui, Charlotta Ingvoldstad-Malmgren, Maria J Soller,[...]. Prenat Diagn 2021
2

Current landscape of prenatal genetic screening and testing.
Nevena Krstić, Sarah G Običan. Birth Defects Res 2020
3


Next-generation sequencing in prenatal setting: Some examples of unexpected variant association.
Berardo Rinaldi, Valerie Race, Anniek Corveleyn, Evelien Van Hoof, Marijke Bauters, Kris Van Den Bogaert, Ellen Denayer, Thomy de Ravel, Eric Legius, Marcella Baldewijns,[...]. Eur J Med Genet 2020
2

Genetic diagnosis in the fetus.
Monica H Wojcik, Rebecca Reimers, Tabitha Poorvu, Pankaj B Agrawal. J Perinatol 2020
2

Maternity health care professionals' views and experiences of fetal genomic uncertainty: A review.
Lisa Hui, Emma Szepe, Jane Halliday, Celine Lewis. Prenat Diagn 2020
3

Right or wrong? Looking through the retrospectoscope to analyse predictions made a decade ago in prenatal diagnosis and fetal surgery.
Lyn S Chitty, Alessandro Ghidini, Jan Deprest, Tim Van Mieghem, Brynn Levy, Lisa Hui, Diana W Bianchi. Prenat Diagn 2020
3

Whole Exome Sequencing: Applications in Prenatal Genetics.
Angie C Jelin, Neeta Vora. Obstet Gynecol Clin North Am 2018
23


Whole-exome sequencing in fetuses with central nervous system abnormalities.
Adi Reches, Liran Hiersch, Sharon Simchoni, Dalit Barel, Rotem Greenberg, Liat Ben Sira, Gustavo Malinger, Yuval Yaron. J Perinatol 2018
13

Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder.
Elizabeth A Normand, Alicia Braxton, Salma Nassef, Patricia A Ward, Francesco Vetrini, Weimin He, Vipulkumar Patel, Chunjing Qu, Lauren E Westerfield, Samantha Stover,[...]. Genome Med 2018
45

Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES).
Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, Wilfred H S Wong, Mandy H Y Tsang, Mullin H C Yu, Steven L C Pei, K S Yeung, Gary T K Mok, C P Lee,[...]. BMC Med Genomics 2018
15