A citation-based method for searching scientific literature

SlavĂ© 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



Suzanne Drury, Hywel Williams, Natalie Trump, Christopher Boustred, Nicholas Lench, Richard H Scott, Lyn S Chitty. Prenat Diagn 2015
Times Cited: 111




List of shared articles



Times cited

COngenital heart disease and the Diagnostic yield with Exome sequencing (CODE) study: prospective cohort study and systematic review.
F Mone, R Y Eberhardt, R K Morris, M E Hurles, D J McMullan, E R Maher, J Lord, L S Chitty, J L Giordano, R J Wapner,[...]. Ultrasound Obstet Gynecol 2021
7

Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect.
F Qiao, Y Wang, C Zhang, R Zhou, Y Wu, C Wang, L Meng, P Mao, Q Cheng, C Luo,[...]. Ultrasound Obstet Gynecol 2021
1

Impact of prenatal exome sequencing for fetal genetic diagnosis on maternal psychological outcomes and decisional conflict in a prospective cohort.
Asha N Talati, Kelly L Gilmore, Emily E Hardisty, Anne D Lyerly, Christine Rini, Neeta L Vora. Genet Med 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

Whole Genome Sequencing in the Evaluation of Fetal Structural Anomalies: A Parallel Test with Chromosomal Microarray Plus Whole Exome Sequencing.
Jia Zhou, Ziying Yang, Jun Sun, Lipei Liu, Xinyao Zhou, Fengxia Liu, Ya Xing, Shuge Cui, Shiyi Xiong, Xiaoyu Liu,[...]. Genes (Basel) 2021
2

Increased nuchal translucency after low-risk noninvasive prenatal testing: What should we tell prospective parents?
Joanne Kelley, George McGillivray, Simon Meagher, Lisa Hui. Prenat Diagn 2021
1

The Added Value of Whole-Exome Sequencing for Anomalous Fetuses With Detailed Prenatal Ultrasound and Postnatal Phenotype.
Miao He, Liu Du, Hongning Xie, Lihe Zhang, Yujun Gu, Ting Lei, Ju Zheng, Dan Chen. Front Genet 2021
0

Exome sequencing for perinatal phenotypes: The significance of deep phenotyping.
Shagun Aggarwal, Venugopal Satidevi Vineeth, Aneek Das Bhowmik, Ashwani Tandon, Aditya Kulkarni, Dhanya Lakshmi Narayanan, Amrita Bhattacherjee, Ashwin Dalal. Prenat Diagn 2020
4


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

Genetic diagnosis in the fetus.
Monica H Wojcik, Rebecca Reimers, Tabitha Poorvu, Pankaj B Agrawal. J Perinatol 2020
2

Prenatal diagnosis of skeletal dysplasias using whole exome sequencing in China.
Jia Tang, Chenglong Zhou, Haihong Shi, Yuying Mo, Weilan Tan, Tielan Sun, Jinling Zhu, Qing Li, Hui Li, Yuping Li,[...]. Clin Chim Acta 2020
6

Exome Sequencing and Its Emerging Role in Prenatal Genetic Diagnosis.
Maeve K Hopkins, Lorraine Dugoff, Jeffrey A Kuller. Obstet Gynecol Surv 2020
0

Clinical application of medical exome sequencing for prenatal diagnosis of fetal structural anomalies.
Min Chen, Jingsi Chen, Chunli Wang, Fei Chen, Yinong Xie, Yufan Li, Nan Li, Jing Wang, Victor Wei Zhang, Dunjin Chen. Eur J Obstet Gynecol Reprod Biol 2020
5

Application of exome sequencing for prenatal diagnosis: a rapid scoping review.
Misty Pratt, Chantelle Garritty, Micere Thuku, Leila Esmaeilisaraji, Candyce Hamel, Taila Hartley, Kathryn Millar, Becky Skidmore, Shelley Dougan, Christine M Armour. Genet Med 2020
5