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



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: 420




List of shared articles



Times cited

Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.
Rebecca M Pollak, Melissa M Murphy, Michael P Epstein, Michael E Zwick, Cheryl Klaiman, Celine A Saulnier, Jennifer G Mulle. Mol Autism 2019
10

Major influence of repetitive elements on disease-associated copy number variants (CNVs).
Ana R Cardoso, Manuela Oliveira, Antonio Amorim, Luisa Azevedo. Hum Genomics 2016
10

Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.
Paweł Stankiewicz, Shashikant Kulkarni, Avinash V Dharmadhikari, Srirangan Sampath, Samarth S Bhatt, Tamim H Shaikh, Zhilian Xia, Amber N Pursley, M Lance Cooper, Marwan Shinawi,[...]. Hum Mutat 2012
31

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

The genetic variability and commonality of neurodevelopmental disease.
Bradley P Coe, Santhosh Girirajan, Evan E Eichler. Am J Med Genet C Semin Med Genet 2012
75


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

Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes.
Jill A Rosenfeld, Lindsey E Stephens, Justine Coppinger, Blake C Ballif, Joe J Hoo, Beatrice N French, Valerie C Banks, Wendy E Smith, David Manchester, Anne Chun-Hui Tsai,[...]. Eur J Hum Genet 2011
15

A de novo deletion of CALN1 in a male with a bilateral diaphragmatic defect does not definitely cause this malformation.
Anne M Slavotinek, Jill A Rosenfeld, Ryan Chao, Dimitry Niyazov, Marthand Eswara, Patricia I Bader, David W Stockton, Pawel Stankiewicz, Margaret P Adam. Am J Med Genet A 2011
1