A citation-based method for searching scientific literature

Brett Trost, Susan Walker, Zhuozhi Wang, Bhooma Thiruvahindrapuram, Jeffrey R MacDonald, Wilson W L Sung, Sergio L Pereira, Joe Whitney, Ada J S Chan, Giovanna Pellecchia, Miriam S Reuter, Si Lok, Ryan K C Yuen, Christian R Marshall, Daniele Merico, Stephen W Scherer. Am J Hum Genet 2018
Times Cited: 74



Ryan E Mills, Klaudia Walter, Chip Stewart, Robert E Handsaker, Ken Chen, Can Alkan, Alexej Abyzov, Seungtai Chris Yoon, Kai Ye, R Keira Cheetham, Asif Chinwalla, Donald F Conrad, Yutao Fu, Fabian Grubert, Iman Hajirasouliha, Fereydoun Hormozdiari, Lilia M Iakoucheva, Zamin Iqbal, Shuli Kang, Jeffrey M Kidd, Miriam K Konkel, Joshua Korn, Ekta Khurana, Deniz Kural, Hugo Y K Lam, Jing Leng, Ruiqiang Li, Yingrui Li, Chang-Yun Lin, Ruibang Luo, Xinmeng Jasmine Mu, James Nemesh, Heather E Peckham, Tobias Rausch, Aylwyn Scally, Xinghua Shi, Michael P Stromberg, Adrian M Stütz, Alexander Eckehart Urban, Jerilyn A Walker, Jiantao Wu, Yujun Zhang, Zhengdong D Zhang, Mark A Batzer, Li Ding, Gabor T Marth, Gil McVean, Jonathan Sebat, Michael Snyder, Jun Wang, Kenny Ye, Evan E Eichler, Mark B Gerstein, Matthew E Hurles, Charles Lee, Steven A McCarroll, Jan O Korbel. Nature 2011
Times Cited: 707




List of shared articles



Times cited

ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data.
Andre E Minoche, Ben Lundie, Greg B Peters, Thomas Ohnesorg, Mark Pinese, David M Thomas, Andreas Zankl, Tony Roscioli, Nicole Schonrock, Sarah Kummerfeld,[...]. Genome Med 2021
5

Copy-number variation in goat genome sequence: A comparative analysis of the different litter size trait groups.
Rui-Qian Zhang, Jun-Jie Wang, Teng Zhang, Hong-Li Zhai, Wei Shen. Gene 2019
9

Identification of Copy Number Variation in Domestic Chicken Using Whole-Genome Sequencing Reveals Evidence of Selection in the Genome.
Donghyeok Seol, Byung June Ko, Bongsang Kim, Han-Ha Chai, Dajeong Lim, Heebal Kim. Animals (Basel) 2019
1

From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability.
Anna Lindstrand, Jesper Eisfeldt, Maria Pettersson, Claudia M B Carvalho, Malin Kvarnung, Giedre Grigelioniene, Britt-Marie Anderlid, Olof Bjerin, Peter Gustavsson, Anna Hammarsjö,[...]. Genome Med 2019
34