A citation-based method for searching scientific literature

Andrew J Sharp, Sierra Hansen, Rebecca R Selzer, Ze Cheng, Regina Regan, Jane A Hurst, Helen Stewart, Sue M Price, Edward Blair, Raoul C Hennekam, Carrie A Fitzpatrick, Rick Segraves, Todd A Richmond, Cheryl Guiver, Donna G Albertson, Daniel Pinkel, Peggy S Eis, Stuart Schwartz, Samantha J L Knight, Evan E Eichler. Nat Genet 2006
Times Cited: 429



Andrew J Sharp, Heather C Mefford, Kelly Li, Carl Baker, Cindy Skinner, Roger E Stevenson, Richard J Schroer, Francesca Novara, Manuela De Gregori, Roberto Ciccone, Adam Broomer, Iris Casuga, Yu Wang, Chunlin Xiao, Catalin Barbacioru, Giorgio Gimelli, Bernardo Dalla Bernardina, Claudia Torniero, Roberto Giorda, Regina Regan, Victoria Murday, Sahar Mansour, Marco Fichera, Lucia Castiglia, Pinella Failla, Mario Ventura, Zhaoshi Jiang, Gregory M Cooper, Samantha J L Knight, Corrado Romano, Orsetta Zuffardi, Caifu Chen, Charles E Schwartz, Evan E Eichler. Nat Genet 2008
Times Cited: 403




List of shared articles



Times cited

Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders.
Trenell J Mosley, H Richard Johnston, David J Cutler, Michael E Zwick, Jennifer G Mulle. BMC Med Genomics 2021
0

BAMSI: a multi-cloud service for scalable distributed filtering of massive genome data.
Kristiina Ausmees, Aji John, Salman Z Toor, Andreas Hellander, Carl Nettelblad. BMC Bioinformatics 2018
1

Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.
Amy B Wilfert, Arvis Sulovari, Tychele N Turner, Bradley P Coe, Evan E Eichler. Genome Med 2017
52

Modulating Neuroinflammation to Treat Neuropsychiatric Disorders.
Franziska A Radtke, Gareth Chapman, Jeremy Hall, Yasir A Syed. Biomed Res Int 2017
21

Human adaptation and evolution by segmental duplication.
Megan Y Dennis, Evan E Eichler. Curr Opin Genet Dev 2016
64

Replication analyses of four chromosomal deletions with schizophrenia via independent large-scale meta-analyses.
Hong Chang, Lingyi Li, Tao Peng, Ming Li, Lei Gao, Xiao Xiao. Am J Med Genet B Neuropsychiatr Genet 2016
3

The human clinical phenotypes of altered CHRNA7 copy number.
Madelyn A Gillentine, Christian P Schaaf. Biochem Pharmacol 2015
55

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

Ohnologs are overrepresented in pathogenic copy number mutations.
Aoife McLysaght, Takashi Makino, Hannah M Grayton, Maria Tropeano, Kevin J Mitchell, Evangelos Vassos, David A Collier. Proc Natl Acad Sci U S A 2014
35

A de novo convergence of autism genetics and molecular neuroscience.
Niklas Krumm, Brian J O'Roak, Jay Shendure, Evan E Eichler. Trends Neurosci 2014
272

The genetics of microdeletion and microduplication syndromes: an update.
Corey T Watson, Tomas Marques-Bonet, Andrew J Sharp, Heather C Mefford. Annu Rev Genomics Hum Genet 2014
78

CNVs in Epilepsy.
Heather C Mefford. Curr Genet Med Rep 2014
19

Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability.
Francesca Antonacci, Megan Y Dennis, John Huddleston, Peter H Sudmant, Karyn Meltz Steinberg, Jill A Rosenfeld, Mattia Miroballo, Tina A Graves, Laura Vives, Maika Malig,[...]. Nat Genet 2014
60

SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
Guylaine D'Amours, Mathieu Langlois, Géraldine Mathonnet, Raouf Fetni, Sonia Nizard, Myriam Srour, Frédérique Tihy, Michael S Phillips, Jacques L Michaud, Emmanuelle Lemyre. BMC Med Genomics 2014
10