A citation-based method for searching scientific literature

Sarah T South, Charles Lee, Allen N Lamb, Anne W Higgins, Hutton M Kearney. Genet Med 2013
Times Cited: 158



Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu, Matthew Hardison, Richard Person, Mir Reza Bekheirnia, Magalie S Leduc, Amelia Kirby, Peter Pham, Jennifer Scull, Min Wang, Yan Ding, Sharon E Plon, James R Lupski, Arthur L Beaudet, Richard A Gibbs, Christine M Eng. N Engl J Med 2013
Times Cited: 1156




List of shared articles



Times cited

The role of chromosomal microarray and exome sequencing in prenatal diagnosis.
Matthew Hoi Kin Chau, Kwong Wai Choy. Curr Opin Obstet Gynecol 2021
0

Clinical exome sequencing as the first-tier test for diagnosing developmental disorders covering both CNV and SNV: a Chinese cohort.
Xinran Dong, Bo Liu, Lin Yang, Huijun Wang, Bingbing Wu, Renchao Liu, Hongbo Chen, Xiang Chen, Sha Yu, Bin Chen,[...]. J Med Genet 2020
8

Nonimmune hydrops fetalis: Genetic analysis and clinical outcome.
Qiong Deng, Fang Fu, Qiuxia Yu, Ru Li, Fucheng Li, Dan Wang, Tingying Lei, Xin Yang, Can Liao. Prenat Diagn 2020
1

Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies.
Vaidehi Jobanputra, Peter Andrews, Vanessa Felice, Avinash Abhyankar, Lukasz Kozon, Dino Robinson, Ferrah London, Inessa Hakker, Kazimierz Wrzeszczynski, Michael Ronemus. J Mol Diagn 2020
0

Clinical utility of genomic sequencing.
Matthew B Neu, Kevin M Bowling, Gregory M Cooper. Curr Opin Pediatr 2019
5

Towards precision nephrology: the opportunities and challenges of genomic medicine.
Jordan G Nestor, Emily E Groopman, Ali G Gharavi. J Nephrol 2018
6

Genetic basis of human congenital anomalies of the kidney and urinary tract.
Simone Sanna-Cherchi, Rik Westland, Gian Marco Ghiggeri, Ali G Gharavi. J Clin Invest 2018
30

Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases.
Michelle M Clark, Zornitza Stark, Lauge Farnaes, Tiong Y Tan, Susan M White, David Dimmock, Stephen F Kingsmore. NPJ Genom Med 2018
137