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



Lars Feuk, Andrew R Carson, Stephen W Scherer. Nat Rev Genet 2006
Times Cited: 1139




List of shared articles



Times cited


A 44-kb deleted-type copy number variation is associated with decreasing complement component activity and calf mortality in Japanese Black cattle.
Shinji Sasaki, Youko Miki, Takayuki Ibi, Hiroyuki Wakaguri, Yuichi Yoshida, Yoshikazu Sugimoto, Yutaka Suzuki. BMC Genomics 2021
0

Genome-wide detection of CNV regions and their potential association with growth and fatness traits in Duroc pigs.
Yibin Qiu, Rongrong Ding, Zhanwei Zhuang, Jie Wu, Ming Yang, Shenping Zhou, Yong Ye, Qian Geng, Zheng Xu, Sixiu Huang,[...]. BMC Genomics 2021
0

Functional characterization of Copy Number Variations regions in Djallonké sheep.
Félix Goyache, Iván Fernández, Arnaud Stephan R Tapsoba, Amadou Traoré, Nuria A Menéndez-Arias, Isabel Álvarez. J Anim Breed Genet 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

SeeCiTe: a method to assess CNV calls from SNP arrays using trio data.
Ksenia Lavrichenko, Øyvind Helgeland, Pål R Njølstad, Inge Jonassen, Stefan Johansson. Bioinformatics 2021
0

A super scalable algorithm for short segment detection.
Ning Hao, Yue Selena Niu, Feifei Xiao, Heping Zhang. Stat Biosci 2021
0

Critical evaluation of copy number variant calling methods using DNA methylation.
Varun Kilaru, Anna K Knight, Seyma Katrinli, Dawayland Cobb, Adriana Lori, Charles F Gillespie, Adam X Maihofer, Caroline M Nievergelt, Anne L Dunlop, Karen N Conneely,[...]. Genet Epidemiol 2020
0


High confidence copy number variants identified in Holstein dairy cattle from whole genome sequence and genotype array data.
Adrien M Butty, Tatiane C S Chud, Filippo Miglior, Flavio S Schenkel, Arun Kommadath, Kirill Krivushin, Jason R Grant, Irene M Häfliger, Cord Drögemüller, Angela Cánovas,[...]. Sci Rep 2020
3