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



Rolph Pfundt, Marisol Del Rosario, Lisenka E L M Vissers, Michael P Kwint, Irene M Janssen, Nicole de Leeuw, Helger G Yntema, Marcel R Nelen, Dorien Lugtenberg, Erik-Jan Kamsteeg, Nienke Wieskamp, Alexander P A Stegmann, Servi J C Stevens, Richard J T Rodenburg, Annet Simons, Arjen R Mensenkamp, Tuula Rinne, Christian Gilissen, Hans Scheffer, Joris A Veltman, Jayne Y Hehir-Kwa. Genet Med 2017
Times Cited: 70




List of shared articles



Times cited

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

European guidelines for constitutional cytogenomic analysis.
Marisa Silva, Nicole de Leeuw, Kathy Mann, Heleen Schuring-Blom, Sian Morgan, Daniela Giardino, Katrina Rack, Ros Hastings. Eur J Hum Genet 2019
26

Familial inheritance of the 3q29 microdeletion syndrome: case report and review.
Wahab A Khan, Ninette Cohen, Stuart A Scott, Elaine M Pereira. BMC Med Genomics 2019
4

Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH.
A Vetro, D Goidin, I Lesende, I Limongelli, G N Ranzani, F Novara, M C Bonaglia, B Rinaldi, F Franchi, E Manolakos,[...]. Clin Genet 2018
9