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



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: 415




List of shared articles



Times cited

Genome-wide detection of CNVs and their association with performance traits in broilers.
Anna Carolina Fernandes, Vinicius Henrique da Silva, Carolina Purcell Goes, Gabriel Costa Monteiro Moreira, Thaís Fernanda Godoy, Adriana Mércia Guaratini Ibelli, Jane de Oliveira Peixoto, Maurício Egídio Cantão, Mônica Corrêa Ledur, Fernanda Marcondes de Rezende,[...]. BMC Genomics 2021
0

A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa.
Lilia Romdhane, Nessrine Mezzi, Hamza Dallali, Olfa Messaoud, Jingxuan Shan, Khalid A Fakhro, Rym Kefi, Lotfi Chouchane, Sonia Abdelhak. NPJ Genom Med 2021
0

Copy number variations in Japanese children with autism spectrum disorder.
Yui Sakamoto, Shuji Shimoyama, Tomonori Furukawa, Masaki Adachi, Michio Takahashi, Tamaki Mikami, Michito Kuribayashi, Ayako Osato, Daiki Tsushima, Manabu Saito,[...]. Psychiatr Genet 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

Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents.
Dinka Smajlagić, Ksenia Lavrichenko, Siren Berland, Øyvind Helgeland, Gun Peggy Knudsen, Marc Vaudel, Jan Haavik, Per Morten Knappskog, Pål Rasmus Njølstad, Gunnar Houge,[...]. Eur J Hum Genet 2021
3

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.
Yun Rose Li, Joseph T Glessner, Bradley P Coe, Jin Li, Maede Mohebnasab, Xiao Chang, John Connolly, Charlly Kao, Zhi Wei, Jonathan Bradfield,[...]. Nat Commun 2020
7

Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases.
Maria Yamasaki, Takashi Makino, Seik-Soon Khor, Hiromi Toyoda, Taku Miyagawa, Xiaoxi Liu, Hitoshi Kuwabara, Yukiko Kano, Takafumi Shimada, Toshiro Sugiyama,[...]. BMC Med Genomics 2020
2