A citation-based method for searching scientific literature

David A Koolen, Rolph Pfundt, Nicole de Leeuw, Jayne Y Hehir-Kwa, Willy M Nillesen, Ineke Neefs, Ine Scheltinga, Erik Sistermans, Dominique Smeets, Han G Brunner, Ad Geurts van Kessel, Joris A Veltman, Bert B A de Vries. Hum Mutat 2009
Times Cited: 112



Andy Itsara, Gregory M Cooper, Carl Baker, Santhosh Girirajan, Jun Li, Devin Absher, Ronald M Krauss, Richard M Myers, Paul M Ridker, Daniel I Chasman, Heather Mefford, Phyllis Ying, Deborah A Nickerson, Evan E Eichler. Am J Hum Genet 2009
Times Cited: 419




List of shared articles



Times cited

Distal 22q11.2 Microduplication: Case Report and Review of the Literature.
Elana Pinchefsky, Laurence Laneuville, Myriam Srour. Child Neurol Open 2017
7

Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability.
Magdalena Bartnik, Beata Nowakowska, Katarzyna Derwińska, Barbara Wiśniowiecka-Kowalnik, Marta Kędzior, Joanna Bernaciak, Kamila Ziemkiewicz, Tomasz Gambin, Maciej Sykulski, Natalia Bezniakow,[...]. J Appl Genet 2014
30

Detection and interpretation of genomic structural variation in health and disease.
Geert Vandeweyer, R Frank Kooy. Expert Rev Mol Diagn 2013
9

Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.
Pasquale Striano, Antonietta Coppola, Roberta Paravidino, Michela Malacarne, Stefania Gimelli, Angela Robbiano, Monica Traverso, Marianna Pezzella, Vincenzo Belcastro, Amedeo Bianchi,[...]. Arch Neurol 2012
46

High resolution array in the clinical approach to chromosomal phenotypes.
Isabel Filges, Luzia Suda, Peter Weber, Alexandre N Datta, Dirk Fischer, Patricia Dill, Réné Glanzmann, Jörg Benzing, Lukas Hegi, Friedel Wenzel,[...]. Gene 2012
7

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

Rare variants in complex traits: novel identification strategies and the role of de novo mutations.
Loubna Jouan, Julie Gauthier, Patrick A Dion, Guy A Rouleau. Hum Hered 2012
4


Genetics of early onset cognitive impairment.
Hans Hilger Ropers. Annu Rev Genomics Hum Genet 2010
223