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: 159



Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers, Janneke H Schuurs-Hoeijmakers, Alex Hoischen, Rolph Pfundt, Nik Krumm, Gemma L Carvill, Deana Li, David Amaral, Natasha Brown, Paul J Lockhart, Ingrid E Scheffer, Antonino Alberti, Marie Shaw, Rosa Pettinato, Raymond Tervo, Nicole de Leeuw, Margot R F Reijnders, Beth S Torchia, Hilde Peeters, Brian J O'Roak, Marco Fichera, Jayne Y Hehir-Kwa, Jay Shendure, Heather C Mefford, Eric Haan, Jozef G├ęcz, Bert B A de Vries, Corrado Romano, Evan E Eichler. Nat Genet 2014
Times Cited: 316




List of shared articles



Times cited


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
2

Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China.
Rongyue Wang, Tingying Lei, Fang Fu, Ru Li, Xiangyi Jing, Xin Yang, Juan Liu, Dongzhi Li, Can Liao. Pediatr Neonatol 2019
9

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
5

A novel case of global developmental delay syndrome with microdeletion at 10p14-p15.3 and microduplication at 18p11.31-p11.32.
Danyan Zhang, Yijian Zhu, Xuefei Feng, Limeng Dai, Mingfu Ma, Lianbing Li, Hong Guo, Letian Zhao, Yuping Zhang, Yun Bai. Medicine (Baltimore) 2019
0

Structural variation at the CYP2C locus: Characterization of deletion and duplication alleles.
Mariana R Botton, Xingwu Lu, Geping Zhao, Elena Repnikova, Yoshinori Seki, Andrea Gaedigk, Eric E Schadt, Lisa Edelmann, Stuart A Scott. Hum Mutat 2019
4