A citation-based method for searching scientific literature

Blake C Ballif, Aaron Theisen, Justine Coppinger, Gordon C Gowans, Joseph H Hersh, Suneeta Madan-Khetarpal, Karen R Schmidt, Raymond Tervo, Luis F Escobar, Christopher A Friedrich, Marie McDonald, Lindsey Campbell, Jeffrey E Ming, Elaine H Zackai, Bassem A Bejjani, Lisa G Shaffer. Mol Cytogenet 2008
Times Cited: 162



Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall, Anthony Leotta, Deepa Pai, Ray Zhang, Yoon-Ha Lee, James Hicks, Sarah J Spence, Annette T Lee, Kaija Puura, Terho Lehtimäki, David Ledbetter, Peter K Gregersen, Joel Bregman, James S Sutcliffe, Vaidehi Jobanputra, Wendy Chung, Dorothy Warburton, Mary-Claire King, David Skuse, Daniel H Geschwind, T Conrad Gilliam, Kenny Ye, Michael Wigler. Science 2007
Times Cited: 1798




List of shared articles



Times cited

Genetic mechanisms of neurodevelopmental disorders.
P Y Billie Au, Alison Eaton, David A Dyment. Handb Clin Neurol 2020
1

Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.
Jordi Soler, Lourdes Fañanás, Mara Parellada, Marie-Odile Krebs, Guy A Rouleau, Mar Fatjó-Vilas. J Psychiatry Neurosci 2018
21

Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.
Jordi Soler, Lourdes Fañanás, Mara Parellada, Marie-Odile Krebs, Guy A Rouleau, Mar Fatjó-Vilas. J Psychiatry Neurosci 2018
10

Microdeletion syndromes.
Gemma L Carvill, Heather C Mefford. Curr Opin Genet Dev 2013
28

Genetic architecture of reciprocal CNVs.
Christelle Golzio, Nicholas Katsanis. Curr Opin Genet Dev 2013
32

Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?
Claire Amiet, Isabelle Gourfinkel-An, Claudine Laurent, Nicolas Bodeau, Bérengère Génin, Eric Leguern, Sylvie Tordjman, David Cohen. Mol Autism 2013
25

Microdeletion and microduplication syndromes.
Lisenka E L M Vissers, Paweł Stankiewicz. Methods Mol Biol 2012
41

Genomics, intellectual disability, and autism.
Heather C Mefford, Mark L Batshaw, Eric P Hoffman. N Engl J Med 2012
181


Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
Maarten J Van Den Bossche, Mandy Johnstone, Mojca Strazisar, Benjamin S Pickard, Dirk Goossens, An-Sofie Lenaerts, Sonia De Zutter, Annelie Nordin, Karl-Fredrik Norrback, Julien Mendlewicz,[...]. Am J Med Genet B Neuropsychiatr Genet 2012
26

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
357