A citation-based method for searching scientific literature

Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
Times Cited: 511

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: 637

List of shared articles

Times cited

Clinical utility of expanded non-invasive prenatal screening and chromosomal microarray analysis in high-risk pregnancy.
X Zhu, M Chen, H Wang, Y Guo, M H K Chau, H Yan, Y Cao, Y K Y Kwok, J Chen, A S Y Hui,[...]. Ultrasound Obstet Gynecol 2021

Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.
S Stern, N Hacohen, V Meiner, S Yagel, S Zenvirt, S Shkedi-Rafid, M Macarov, D V Valsky, S Porat, N Yanai,[...]. Ultrasound Obstet Gynecol 2021

Variants of uncertain significance in prenatal microarrays: a retrospective cohort study.
A H Mardy, A P Wiita, B V Wayman, K Drexler, T N Sparks, M E Norton. BJOG 2021

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

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

The effect of polyhydramnios degree on chromosomal microarray results: a retrospective cohort analysis of 742 singleton pregnancies.
Lena Sagi-Dain, Amihood Singer, Tzipora Falik-Zaccai, Amir Peleg, Anat Bar-Shira, Michal Feingold-Zadok, Shay Ben Shachar, Idit Maya. Arch Gynecol Obstet 2021

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.
Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, Atlas Khan, Sarah E Graham, Maddalena Marasà, Hyunwoo Kim, Tze Y Lim, Patricia L Weng, Elena Sánchez-Rodríguez,[...]. J Am Soc Nephrol 2021

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

Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platform.
Jiexia Yang, Jing Wu, Haishan Peng, Yaping Hou, Fangfang Guo, Dongmei Wang, Haoxin Ouyang, Yixia Wang, Aihua Yin. Hum Genomics 2021

Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study.
Hailong Huang, Meiying Cai, Wei Ma, Na Lin, Liangpu Xu. Risk Manag Healthc Policy 2021

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

Systematic analysis of copy-number variations associated with early pregnancy loss.
Y Wang, Y Li, Y Chen, R Zhou, Z Sang, L Meng, J Tan, F Qiao, Q Bao, D Luo,[...]. Ultrasound Obstet Gynecol 2020

State-wide utilization and performance of traditional and cell-free DNA-based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study.
A Lindquist, L Hui, A Poulton, E Kluckow, B Hutchinson, M D Pertile, L Bonacquisto, L Gugasyan, A Kulkarni, J Harraway,[...]. Ultrasound Obstet Gynecol 2020

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

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

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

Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defects.
Stela Z Berisha, Shashi Shetty, Thomas W Prior, Anna L Mitchell. Birth Defects Res 2020

Nonimmune hydrops fetalis: Genetic analysis and clinical outcome.
Qiong Deng, Fang Fu, Qiuxia Yu, Ru Li, Fucheng Li, Dan Wang, Tingying Lei, Xin Yang, Can Liao. Prenat Diagn 2020