A citation-based method for searching scientific literature

Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker, Julie Désir, Anne Destrée, Koenraad Devriendt, Annelies Dheedene, Annelies Fieuw, Erik Fransen, Jean-Stéphane Gatot, Philip Holmgren, Mauricette Jamar, Sandra Janssens, Kathelijn Keymolen, Damien Lederer, Björn Menten, Marije Meuwissen, Benoit Parmentier, Bruno Pichon, Sonia Rombout, Yves Sznajer, Ann Van Den Bogaert, Kris Van Den Bogaert, Olivier Vanakker, Joris Vermeesch, Katrien Janssens. Prenat Diagn 2018
Times Cited: 15



Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland, Daniel Pineda-Alvarez, Swaroop Aradhya, Christa Lese Martin. Genet Med 2020
Times Cited: 136




List of shared articles



Times cited

REDBot: Natural language process methods for clinical copy number variation reporting in prenatal and products of conception diagnosis.
Mengmeng Liu, Yunshan Zhong, Hongqian Liu, Desheng Liang, Erhong Liu, Yu Zhang, Feng Tian, Qiaowei Liang, David S Cram, Hua Wang,[...]. Mol Genet Genomic Med 2020
2

Chromosomal microarray analysis in fetuses with central nervous system anomalies: An 8-year long observational study from a tertiary care university hospital.
Maddalena Santirocco, Alberto Plaja, Carlota Rodó, Irene Valenzuela, Silvia Arévalo, Neus Castells, Anna Abuli, Eduardo Tizzano, Nerea Maiz, Elena Carreras. Prenat Diagn 2021
1

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

A study of normal copy number variations in Israeli population.
Idit Maya, Pola Smirin-Yosef, Sarit Kahana, Sne Morag, Shiri Yacobson, Ifaat Agmon-Fishman, Reut Matar, Elisheva Bitton, Mordechai Shohat, Lina Basel-Salmon,[...]. Hum Genet 2021
1

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
8