A citation-based method for searching scientific literature

Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
Times Cited: 1148



Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
Times Cited: 909




List of shared articles



Times cited

Large mosaic copy number variations confer autism risk.
Maxwell A Sherman, Rachel E Rodin, Giulio Genovese, Caroline Dias, Alison R Barton, Ronen E Mukamel, Bonnie Berger, Peter J Park, Christopher A Walsh, Po-Ru Loh. Nat Neurosci 2021
4

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.
Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, Atlas Khan, Sarah E Graham, Maddalena Marasà, Hyunwoo Kim, Tze Y Lim, Patricia L Weng, Elena Sánchez-Rodríguez,[...]. J Am Soc Nephrol 2021
0

Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.
Elmo Christian Saarentaus, Aki Samuli Havulinna, Nina Mars, Ari Ahola-Olli, Tuomo Tapio Johannes Kiiskinen, Juulia Partanen, Sanni Ruotsalainen, Mitja Kurki, Lea Martta Urpa, Lei Chen,[...]. Mol Psychiatry 2021
0

Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.
Chloe X Yap, Gail A Alvares, Anjali K Henders, Tian Lin, Leanne Wallace, Alaina Farrelly, Tiana McLaren, Jolene Berry, Anna A E Vinkhuyzen, Maciej Trzaskowski,[...]. Mol Autism 2021
0

Genome-wide copy number variations in a large cohort of bantu African children.
Feyza Yilmaz, Megan Null, David Astling, Hung-Chun Yu, Joanne Cole, Stephanie A Santorico, Benedikt Hallgrimsson, Mange Manyama, Richard A Spritz, Audrey E Hendricks,[...]. BMC Med Genomics 2021
0

Phenotypic signatures in clinical data enable systematic identification of patients for genetic testing.
Theodore J Morley, Lide Han, Victor M Castro, Jonathan Morra, Roy H Perlis, Nancy J Cox, Lisa Bastarache, Douglas M Ruderfer. Nat Med 2021
0

Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN Mutations.
Lamis Yehia, Marilyn Seyfi, Lisa-Marie Niestroj, Roshan Padmanabhan, Ying Ni, Thomas W Frazier, Dennis Lal, Charis Eng. JAMA Netw Open 2020
2