A citation-based method for searching scientific literature

Andy W Pang, Jeffrey R MacDonald, Dalila Pinto, John Wei, Muhammad A Rafiq, Donald F Conrad, Hansoo Park, Matthew E Hurles, Charles Lee, J Craig Venter, Ewen F Kirkness, Samuel Levy, Lars Feuk, Stephen W Scherer. Genome Biol 2010
Times Cited: 182



Robert E Handsaker, Joshua M Korn, James Nemesh, Steven A McCarroll. Nat Genet 2011
Times Cited: 213




List of shared articles



Times cited

Structural variation in the sequencing era.
Steve S Ho, Alexander E Urban, Ryan E Mills. Nat Rev Genet 2020
67

Comprehensive evaluation of structural variation detection algorithms for whole genome sequencing.
Shunichi Kosugi, Yukihide Momozawa, Xiaoxi Liu, Chikashi Terao, Michiaki Kubo, Yoichiro Kamatani. Genome Biol 2019
99

A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data.
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,[...]. Am J Hum Genet 2018
74

Deep whole-genome sequencing of 90 Han Chinese genomes.
Tianming Lan, Haoxiang Lin, Wenjuan Zhu, Tellier Christian Asker Melchior Laurent, Mengcheng Yang, Xin Liu, Jun Wang, Jian Wang, Huanming Yang, Xun Xu,[...]. Gigascience 2017
18

Characteristics of de novo structural changes in the human genome.
Wigard P Kloosterman, Laurent C Francioli, Fereydoun Hormozdiari, Tobias Marschall, Jayne Y Hehir-Kwa, Abdel Abdellaoui, Eric-Wubbo Lameijer, Matthijs H Moed, Vyacheslav Koval, Ivo Renkens,[...]. Genome Res 2015
67

Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms.
Alexej Abyzov, Shantao Li, Daniel Rhee Kim, Marghoob Mohiyuddin, Adrian M St├╝tz, Nicholas F Parrish, Xinmeng Jasmine Mu, Wyatt Clark, Ken Chen, Matthew Hurles,[...]. Nat Commun 2015
54

Detection of Genomic Structural Variants from Next-Generation Sequencing Data.
Lorenzo Tattini, Romina D'Aurizio, Alberto Magi. Front Bioeng Biotechnol 2015
132

Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts.
John J Connolly, Joseph T Glessner, Berta Almoguera, David R Crosslin, Gail P Jarvik, Patrick M Sleiman, Hakon Hakonarson. Front Genet 2014
8