A citation-based method for searching scientific literature

Brynn Levy, Ronald Wapner. Fertil Steril 2018
Times Cited: 96



Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey, Rhiannon Mellis, Sarah Robart, Ian R Berry, Kate E Chandler, Deirdre Cilliers, Lara Cresswell, Sandra L Edwards, Carol Gardiner, Alex Henderson, Simon T Holden, Tessa Homfray, Tracy Lester, Rebecca A Lewis, Ruth Newbury-Ecob, Katrina Prescott, Oliver W Quarrell, Simon C Ramsden, Eileen Roberts, Dagmar Tapon, Madeleine J Tooley, Pradeep C Vasudevan, Astrid P Weber, Diana G Wellesley, Paul Westwood, Helen White, Michael Parker, Denise Williams, Lucy Jenkins, Richard H Scott, Mark D Kilby, Lyn S Chitty, Matthew E Hurles, Eamonn R Maher. Lancet 2019
Times Cited: 163




List of shared articles



Times cited

A two-year prospective study assessing the performance of fetal chromosomal microarray analysis and next-generation sequencing in high-risk pregnancies.
Konstantin Ridnõi, Kai Muru, Maria Keernik, Sander Pajusalu, Eva-Liina Ustav, Pille Tammur, Triin Mölter-Väär, Tiina Kahre, Ustina Šamarina, Karin Asser,[...]. Mol Genet Genomic Med 2021
0

Clinical application of medical exome sequencing for prenatal diagnosis of fetal structural anomalies.
Min Chen, Jingsi Chen, Chunli Wang, Fei Chen, Yinong Xie, Yufan Li, Nan Li, Jing Wang, Victor Wei Zhang, Dunjin Chen. Eur J Obstet Gynecol Reprod Biol 2020
5

Trio-Based Low-Pass Genome Sequencing Reveals Characteristics and Significance of Rare Copy Number Variants in Prenatal Diagnosis.
Matthew Hoi Kin Chau, Jicheng Qian, Zihan Chen, Ying Li, Yu Zheng, Wing Ting Tse, Yvonne K Kwok, Tak Yeung Leung, Zirui Dong, Kwong Wai Choy. Front Genet 2021
0

Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.
Teresa N Sparks, Billie R Lianoglou, Rebecca R Adami, Ilina D Pluym, Kerry Holliman, Jennifer Duffy, Sarah L Downum, Sachi Patel, Amanda Faubel, Nina M Boe,[...]. N Engl J Med 2020
23

Chances and Challenges of New Genetic Screening Technologies (NIPT) in Prenatal Medicine from a Clinical Perspective: A Narrative Review.
Ivonne Bedei, Aline Wolter, Axel Weber, Fabrizio Signore, Roland Axt-Fliedner. Genes (Basel) 2021
3

Prenatal Exome Sequencing: Background, Current Practice and Future Perspectives-A Systematic Review.
Daniele Guadagnolo, Gioia Mastromoro, Francesca Di Palma, Antonio Pizzuti, Enrica Marchionni. Diagnostics (Basel) 2021
1

The role of chromosomal microarray and exome sequencing in prenatal diagnosis.
Matthew Hoi Kin Chau, Kwong Wai Choy. Curr Opin Obstet Gynecol 2021
1

Genetic Examination for Fetuses with Increased Fetal Nuchal Translucency by Genomic Technology.
Shuya Xue, Huanchen Yan, Jingsi Chen, Nan Li, Jiayan Wang, Yu Liu, Huimin Zhang, Shaoying Li, Wei Zhang, Dunjin Chen,[...]. Cytogenet Genome Res 2020
4

Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases.
Hsu P Chong, Susan Hamilton, Fionnuala Mone, Ka Wang Cheung, Fiona S Togneri, Rachel K Morris, Elizabeth Quinlan-Jones, Denise Williams, Stephanie Allen, Dominic J McMullan,[...]. Prenat Diagn 2019
8

How genomics is changing the practice of prenatal testing.
Isabel Filges, Peter Miny, Wolfgang Holzgreve, Sevgi Tercanli. J Perinat Med 2021
1

Exome Sequencing and Its Emerging Role in Prenatal Genetic Diagnosis.
Maeve K Hopkins, Lorraine Dugoff, Jeffrey A Kuller. Obstet Gynecol Surv 2020
0