A citation-based method for searching scientific literature

Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman, Susan Klugman, Thomas Scholl, Joe Leigh Simpson, Kimberly McCall, Vimla S Aggarwal, Brian Bunke, Odelia Nahum, Ankita Patel, Allen N Lamb, Elizabeth A Thom, Arthur L Beaudet, David H Ledbetter, Lisa G Shaffer, Laird Jackson. N Engl J Med 2012
Times Cited: 643



S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2013
Times Cited: 154




List of shared articles



Times cited

Chromosomal microarray analysis in pregnancies at risk for a molecular disorder.
Dong-Zhi Li, Hai-Shen Tang. J Matern Fetal Neonatal Med 2021
0

Prenatal detection of 1p36 deletion syndrome: ultrasound findings and microarray testing results.
Xun Zhang, Ping He, Jin Han, Min Pan, Xin Yang, Li Zhen, Can Liao, Dong-Zhi Li. J Matern Fetal Neonatal Med 2021
2

Clinical Application of Easychip 8x15K Platform in 4106 Pregnancies Without Ultrasound Anomalies.
Valeria Orlando, Viola Alesi, Gianluca Di Giacomo, Michela Canestrelli, Chiara Calacci, Anna Maria Nardone, Giusy Calvieri, Maria Teresa Liambo, Ester Sallicandro, Silvia Di Tommaso,[...]. Reprod Sci 2021
0

Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing.
Liubing Lan, Lingna She, Bosen Zhang, Yanhong He, Zhiyuan Zheng. J Gene Med 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
0

Detection of copy number variation associated with ventriculomegaly in fetuses using single nucleotide polymorphism arrays.
Huili Xue, Aili Yu, Na Lin, Xuemei Chen, Min Lin, Yan Wang, Hailong Huang, Liangpu Xu. Sci Rep 2021
1

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
1


Prenatal chromosome microarray: 'The UK experience'. A survey of reporting practices in UK genetic services (2012-2019).
Jenny Patterson, Diana Wellesley, Sian Morgan, Deirdre Cilliers, Stephanie Allen, Carol A Gardiner. Prenat Diagn 2021
0

Benefit versus risk of chromosomal microarray analysis performed in pregnancies with normal and positive prenatal screening results: A retrospective study.
Rami Moshonov, Keren Hod, Bella Azaria, Ifat Abadi-Korek, Rachel Berger, Mordechai Shohat. PLoS One 2021
0

Should prenatal chromosomal microarray analysis be offered for isolated fetal growth restriction? A French multicenter study.
Isabelle Monier, Aline Receveur, Véronique Houfflin-Debarge, Valérie Goua, Vanina Castaigne, Jean-Marie Jouannic, Eve Mousty, Anne-Hélène Saliou, Hanane Bouchghoul, Thierry Rousseau,[...]. Am J Obstet Gynecol 2021
0

Chromosomal Microarray Analysis in Pregnancies With Corpus Callosum or Posterior Fossa Anomalies.
Lior Greenbaum, Idit Maya, Lena Sagi-Dain, Rivka Sukenik-Halevy, Michal Berkenstadt, Hagith Yonath, Shlomit Rienstein, Adel Shalata, Eldad Katorza, Amihood Singer. Neurol Genet 2021
0

Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical Outcomes.
Meiying Cai, Hailong Huang, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Liangpu Xu, Na Lin. Risk Manag Healthc Policy 2021
0

How genomics is changing the practice of prenatal testing.
Isabel Filges, Peter Miny, Wolfgang Holzgreve, Sevgi Tercanli. J Perinat Med 2021
0

Can cell-free DNA testing be used in pregnancies with isolated fetal omphalocele? Preliminary evidence from cytogenetic results of prenatal cases.
Li-Li Xu, Li Zhen, Ji-Wu Lou, Hai-Shen Tang, Min Pan, Jin Han, Xin Yang, Dong-Zhi Li. J Matern Fetal Neonatal Med 2021
2

The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.
Annie Sy Hui, Matthew Hoi Kin Chau, Yiu Man Chan, Ye Cao, Angel Hw Kwan, Xiaofan Zhu, Yvonne K Kwok, Zihan Chen, Terence T Lao, Kwong Wai Choy,[...]. Acta Obstet Gynecol Scand 2021
1

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

Application of chromosomal microarray in fetuses with increased nuchal translucency.
Xin-Rong Zhao, Li Gao, Yi Wu, Yan-Lin Wang. J Matern Fetal Neonatal Med 2020
3

Microarray and RASopathy-disorder testing in fetuses with increased nuchal translucency.
P Sinajon, D Chitayat, M Roifman, S Wasim, S Carmona, G Ryan, A Noor, E Kolomietz, K Chong. Ultrasound Obstet Gynecol 2020
8

Chromosomal microarray analysis in prenatal diagnosis: ethical considerations of the Belgian approach.
Joke Muys, Bettina Blaumeiser, Katrien Janssens, Patrick Loobuyck, Yves Jacquemyn. J Med Ethics 2020
7



The yield of chromosomal microarray analysis among pregnancies terminated due to fetal malformations.
Yael Pasternak, Yair Daykan, Tamar Tenne, Eyal Reinstein, Netanella Miller, Gil Shechter-Maor, Idit Maya, Tal Biron-Shental, Rivka Sukenik Halevy. J Matern Fetal Neonatal Med 2020
1

Evolution of a prenatal genetic clinic-A 10-year cohort study.
Fionnuala Mone, Clare O'Connor, Susan Hamilton, Elizabeth Quinlan-Jones, Stephanie Allen, Tamas Marton, Denise Williams, Mark D Kilby. Prenat Diagn 2020
3