A citation-based method for searching scientific literature

Ron Hochstenbach, Ellen van Binsbergen, John Engelen, Aggie Nieuwint, Abeltje Polstra, Pino Poddighe, Claudia Ruivenkamp, Birgit Sikkema-Raddatz, Dominique Smeets, Martin Poot. Eur J Med Genet 2009
Times Cited: 126



Anne M Slavotinek. Hum Genet 2008
Times Cited: 146




List of shared articles



Times cited


A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability.
J R M Ceroni, R L Dutra, R S Honjo, J C Llerena, A X Acosta, P F V Medeiros, M F Galera, É A Zanardo, F B Piazzon, A T Dias,[...]. Sci Rep 2018
1

Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies.
Guillermo Lay-Son, Karena Espinoza, Cecilia Vial, Juan C Rivera, María L Guzmán, Gabriela M Repetto. J Pediatr (Rio J) 2015
6


"Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes.
Maryam Rafati, Elaheh Seyyedaboutorabi, Mohammad R Ghadirzadeh, Yaser Heshmati, Homeira Adibi, Zarrintaj Keihanidoust, Mohammad R Eshraghian, Gholam Reza Javadi, Jila Dastan, Alireza Mosavi-Jarrahi,[...]. Mol Cytogenet 2012
4

Atypical face shape and genomic structural variants in epilepsy.
Krishna Chinthapalli, Emanuele Bartolini, Jan Novy, Michael Suttie, Carla Marini, Melania Falchi, Zoe Fox, Lisa M S Clayton, Josemir W Sander, Renzo Guerrini,[...]. Brain 2012
12

A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia.
Katrin Männik, Sven Parkel, Priit Palta, Olga Zilina, Helen Puusepp, Tõnu Esko, Reedik Mägi, Margit Nõukas, Andres Veidenberg, Mari Nelis,[...]. Eur J Med Genet 2011
6