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



Lisenka E L M Vissers, Joep de Ligt, Christian Gilissen, Irene Janssen, Marloes Steehouwer, Petra de Vries, Bart van Lier, Peer Arts, Nienke Wieskamp, Marisol del Rosario, Bregje W M van Bon, Alexander Hoischen, Bert B A de Vries, Han G Brunner, Joris A Veltman. Nat Genet 2010
Times Cited: 551




List of shared articles



Times cited

Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders.
Ching Moey, Susan J Hinze, Louise Brueton, Jenny Morton, Dominic J McMullan, Benjamin Kamien, Christopher P Barnett, Nicola Brunetti-Pierri, Jillian Nicholl, Jozef Gecz,[...]. Eur J Hum Genet 2016
30

Exome sequencing and whole genome sequencing for the detection of copy number variation.
Jayne Y Hehir-Kwa, Rolph Pfundt, Joris A Veltman. Expert Rev Mol Diagn 2015
45



Genetic basis of intellectual disability.
Jay W Ellison, Jill A Rosenfeld, Lisa G Shaffer. Annu Rev Med 2013
59

Pathogenic or not? Assessing the clinical relevance of copy number variants.
J Y Hehir-Kwa, R Pfundt, J A Veltman, N de Leeuw. Clin Genet 2013
36

[Advances in the identification of the aetiology of mental retardation].
Gabriel González, Víctor Raggio, María Boidi, Alejandra Tapié, Leda Roche. Rev Neurol 2013
3

[Diagnostic investigations for an unexplained developmental disability].
A Verloes, D Héron, T Billette de Villemeur, A Afenjar, C Baumann, N Bahi-Buisson, P Charles, A Faudet, A Jacquette, C Mignot,[...]. Arch Pediatr 2012
6

Discovery of variants unmasked by hemizygous deletions.
Ron Hochstenbach, Martin Poot, Isaac J Nijman, Ivo Renkens, Karen J Duran, Ruben Van't Slot, Ellen van Binsbergen, Bert van der Zwaag, Maartje J Vogel, Paulien A Terhal,[...]. Eur J Hum Genet 2012
18

Diagnostic exome sequencing in persons with severe intellectual disability.
Joep de Ligt, Marjolein H Willemsen, Bregje W M van Bon, Tjitske Kleefstra, Helger G Yntema, Thessa Kroes, Anneke T Vulto-van Silfhout, David A Koolen, Petra de Vries, Christian Gilissen,[...]. N Engl J Med 2012
970