A citation-based method for searching scientific literature

Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, Melissa Stosic, Karen Wou, Louise Bier, Erica Spiegel, Kelly Brennan, Nicholas Stong, Vaidehi Jobanputra, Zhong Ren, Xiaolin Zhu, Caroline Mebane, Odelia Nahum, Quanli Wang, Sitharthan Kamalakaran, Colin Malone, Kwame Anyane-Yeboa, Russell Miller, Brynn Levy, David B Goldstein, Ronald J Wapner. Lancet 2019
Times Cited: 127



Hane Lee, Joshua L Deignan, Naghmeh Dorrani, Samuel P Strom, Sibel Kantarci, Fabiola Quintero-Rivera, Kingshuk Das, Traci Toy, Bret Harry, Michael Yourshaw, Michelle Fox, Brent L Fogel, Julian A Martinez-Agosto, Derek A Wong, Vivian Y Chang, Perry B Shieh, Christina G S Palmer, Katrina M Dipple, Wayne W Grody, Eric Vilain, Stanley F Nelson. JAMA 2014
Times Cited: 570




List of shared articles



Times cited

Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations.
Mathilde Lefebvre, Ange-Line Bruel, Emilie Tisserant, Nicolas Bourgon, Yannis Duffourd, Sophie Collardeau-Frachon, Tania Attie-Bitach, Paul Kuentz, Mirna Assoum, Elise Schaefer,[...]. J Med Genet 2021
0

A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective review.
E Dempsey, A Haworth, L Ive, R Dubis, H Savage, E Serra, J Kenny, F Elmslie, E Greco, B Thilaganathan,[...]. BJOG 2021
2

The diagnostic efficacy of exome data analysis using fixed neurodevelopmental gene lists: Implications for prenatal setting.
Rivka Sukenik-Halevy, Noa Ruhrman-Shahar, Naama Orenstein, Claudia Gonzaga-Jauregui, Alan R Shuldiner, Nurit Magal, Ofir Hagari, Noy Azulay, Gabriel A Lidzbarsky, Lily Bazak,[...]. Prenat Diagn 2021
1

Diagnostic yield of clinical exome sequencing as a first-tier genetic test for the diagnosis of genetic disorders in pediatric patients: results from a referral center study.
Jean-Philippe Mergnac, Arnaud Wiedemann, Céline Chery, Jean-Marie Ravel, Farès Namour, Jean-Louis Guéant, François Feillet, Abderrahim Oussalah. Hum Genet 2021
0


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
4