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: 161

Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
Times Cited: 6067

List of shared articles

Times cited

Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype.
Farah Qaiser, Yue Yin, Carolyn B Mervis, Colleen A Morris, Bonita P Klein-Tasman, Elaine Tam, Lucy R Osborne, Ryan K C Yuen. Orphanet J Rare Dis 2021

Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy.
Hayley S Mountford, Dorothy V M Bishop, Paul A Thompson, Nuala H Simpson, Dianne F Newbury. Am J Med Genet C Semin Med Genet 2020

A novel splicing mutation of ARHGAP29 is associated with nonsyndromic cleft lip with or without cleft palate.
Qiuxia Yu, Qiong Deng, Fang Fu, Ru Li, Wenwen Zhang, Junhui Wan, Xin Yang, Dan Wang, Fucheng Li, Shaoqing Wu,[...]. J Matern Fetal Neonatal Med 2020