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



J Helgeson, J Wardrop, T Boomer, E Almasri, W B Paxton, J S Saldivar, N Dharajiya, T J Monroe, D H Farkas, D S Grosu, R M McCullough. Prenat Diagn 2015
Times Cited: 75




List of shared articles



Times cited

Cell-free DNA analysis of maternal blood in prenatal screening for chromosomal microdeletions and microduplications: a systematic review.
Alessandra Familiari, Simona Boito, Georgios Rembouskos, Benedetta Ischia, Veronica Accurti, Isabella Fabietti, Paolo Volpe, Nicola Persico. Prenat Diagn 2021
1

The Genetics and Epigenetics of 22q11.2 Deletion Syndrome.
Qiumei Du, M Teresa de la Morena, Nicolai S C van Oers. Front Genet 2020
18


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

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


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