A citation-based method for searching scientific literature

Francesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, Celine Dupont, Viola Alesi, Laetitia Gouas, Nina Horelli-Kuitunen, Kwong Wai Choy, Sandra García-Herrero, Alberto Gonzalez de la Vega, Krzysztof Piotrowski, Rita Genesio, Gloria Queipo, Barbara Malvestiti, Bérénice Hervé, Brigitte Benzacken, Antonio Novelli, Philippe Vago, Kirsi Piippo, Tak Yeung Leung, Federico Maggi, Thibault Quibel, Anne Claude Tabet, Giuseppe Simoni, François Vialard. Prenat Diagn 2015
Times Cited: 154



Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute, Jing Hu, Megan P Hall, Zachary Demko, Asim Siddiqui, Matthew Rabinowitz, Susan J Gross, Matthew Hill, Peter Benn. Am J Obstet Gynecol 2015
Times Cited: 170




List of shared articles



Times cited

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
0

Potential influence of parental copy number variations on noninvasive prenatal testing (NIPT): two case reports.
Yiming Qi, Jiexia Yang, Yaping Hou, Rong Hu, Dongmei Wang, Haishan Peng, Aihua Yin. Mol Cytogenet 2020
0



Screening for 22q11.2 deletion syndrome by two non-invasive prenatal testing methodologies: A case with discordant results.
Liang-Ming Lo, Chii-Shinn Shiau, Kuang-Chao Chen, S W S Shaw, Peter Benn. Taiwan J Obstet Gynecol 2019
1

Expanding the indications for cell-free DNA in the maternal circulation: clinical considerations and implications.
Gian Carlo Di Renzo, José Luis Bartha, Catia M Bilardo. Am J Obstet Gynecol 2019
17

Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis.
Matthew Hoi Kin Chau, Ye Cao, Yvonne Ka Yin Kwok, Samantha Chan, Yiu Man Chan, Huilin Wang, Zhenjun Yang, Hoi Kin Wong, Tak Yeung Leung, Kwong Wai Choy. Am J Obstet Gynecol 2019
12

Novel perspectives in fetal biomarker implementation for the noninvasive prenatal testing.
Jiping Shi, Runling Zhang, Jinming Li, Rui Zhang. Crit Rev Clin Lab Sci 2019
3


Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions.
K Martin, S Iyengar, A Kalyan, C Lan, A L Simon, M Stosic, K Kobara, H Ravi, T Truong, A Ryan,[...]. Clin Genet 2018
33

Prenatal Screening for 22q11.2 Deletion Using a Targeted Microarray-Based Cell-Free DNA Test.
Maximilian Schmid, Eric Wang, Patrick E Bogard, Elisa Bevilacqua, Coleen Hacker, Susie Wang, Jigna Doshi, Karen White, Jennifer Kaplan, Andrew Sparks,[...]. Fetal Diagn Ther 2018
8


A case of prenatal isolated talipes and 22q11.2 deletion syndrome-an important chromosomal disorder missed by noninvasive prenatal screening.
Ka Wang Cheung, Carman Wing Sze Lai, Christopher Chun Yu Mak, Pui Wah Hui, Brian Hon Yin Chung, Anita Sik Yau Kan. Prenat Diagn 2018
5

Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples.
Harini Ravi, Gabriel McNeill, Shruti Goel, Steven D Meltzer, Nathan Hunkapiller, Allison Ryan, Brynn Levy, Zachary P Demko. PLoS One 2018
13