A citation-based method for searching scientific literature

Laura Winchester, Christopher Yau, Jiannis Ragoussis. Brief Funct Genomic Proteomic 2009
Times Cited: 137



Steven A McCarroll, Finny G Kuruvilla, Joshua M Korn, Simon Cawley, James Nemesh, Alec Wysoker, Michael H Shapero, Paul I W de Bakker, Julian B Maller, Andrew Kirby, Amanda L Elliott, Melissa Parkin, Earl Hubbell, Teresa Webster, Rui Mei, James Veitch, Patrick J Collins, Robert Handsaker, Steve Lincoln, Marcia Nizzari, John Blume, Keith W Jones, Rich Rava, Mark J Daly, Stacey B Gabriel, David Altshuler. Nat Genet 2008
Times Cited: 688




List of shared articles



Times cited

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

Association Analysis to Copy Number Variation (CNV) of Opn4 Gene with Growth Traits of Goats.
LiJuan Li, Peng Yang, ShuYue Shi, ZiJing Zhang, QiaoTing Shi, JiaWei Xu, Hua He, ChuZhao Lei, ErYao Wang, Hong Chen,[...]. Animals (Basel) 2020
0

Genome-wide detection of copy number variation in Chinese indigenous sheep using an ovine high-density 600 K SNP array.
Qing Ma, Xuexue Liu, Jianfei Pan, Lina Ma, Yuehui Ma, Xiaohong He, Qianjun Zhao, Yabin Pu, Yingkang Li, Lin Jiang. Sci Rep 2017
19

Copy number variants in the sheep genome detected using multiple approaches.
Gemma M Jenkins, Michael E Goddard, Michael A Black, Rudiger Brauning, Benoit Auvray, Ken G Dodds, James W Kijas, Noelle Cockett, John C McEwan. BMC Genomics 2016
14

Genome-wide characteristics of copy number variation in Polish Holstein and Polish Red cattle using SNP genotyping assay.
A Gurgul, I Jasielczuk, T Szmatoła, K Pawlina, T Ząbek, K Żukowski, M Bugno-Poniewierska. Genetica 2015
8

Haplotype phasing and inheritance of copy number variants in nuclear families.
Priit Palta, Lauris Kaplinski, Liina Nagirnaja, Andres Veidenberg, Märt Möls, Mari Nelis, Tõnu Esko, Andres Metspalu, Maris Laan, Maido Remm. PLoS One 2015
5

Family-Based Benchmarking of Copy Number Variation Detection Software.
Marcel Elie Nutsua, Annegret Fischer, Almut Nebel, Sylvia Hofmann, Stefan Schreiber, Michael Krawczak, Michael Nothnagel. PLoS One 2015
5

A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer.
C Fernandez-Rozadilla, J B Cazier, I Tomlinson, A Brea-Fernández, M J Lamas, M Baiget, L A López-Fernández, J Clofent, L Bujanda, D Gonzalez,[...]. Hum Genet 2014
17

Copy number variations among silkworms.
Qian Zhao, Min-Jin Han, Wei Sun, Ze Zhang. BMC Genomics 2014
8

Structural genomic variation as risk factor for idiopathic recurrent miscarriage.
Liina Nagirnaja, Priit Palta, Laura Kasak, Kristiina Rull, Ole B Christiansen, Henriette S Nielsen, Rudi Steffensen, Tõnu Esko, Maido Remm, Maris Laan. Hum Mutat 2014
17

Increased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sample.
Guia Guffanti, Federica Torri, Jerod Rasmussen, Andrew P Clark, Anita Lakatos, Jessica A Turner, James H Fallon, Andrew J Saykin, Michael Weiner, Marquis P Vawter,[...]. Genomics 2013
20

The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation.
Armand Valsesia, Aurélien Macé, Sébastien Jacquemont, Jacques S Beckmann, Zoltán Kutalik. Front Genet 2013
36

A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation.
Nasrine Bendjilali, Helen Kim, Shantel Weinsheimer, Diana E Guo, Pui-Yan Kwok, Jonathan G Zaroff, Stephen Sidney, Michael T Lawton, Charles E McCulloch, Bobby P C Koeleman,[...]. PLoS One 2013
6

Copy number variation at 6q13 is associated with lung cancer risk in a Han Chinese population.
Xiao-Yun Hu, Xu-Ming Bai, Xue Qiao, Ya-Qun Zhu. Exp Lung Res 2013
5

Comparative Analysis of CNV Calling Algorithms: Literature Survey and a Case Study Using Bovine High-Density SNP Data.
Lingyang Xu, Yali Hou, Derek M Bickhart, Jiuzhou Song, George E Liu. Microarrays (Basel) 2013
25


Copy number variation of individual cattle genomes using next-generation sequencing.
Derek M Bickhart, Yali Hou, Steven G Schroeder, Can Alkan, Maria Francesca Cardone, Lakshmi K Matukumalli, Jiuzhou Song, Robert D Schnabel, Mario Ventura, Jeremy F Taylor,[...]. Genome Res 2012
175

Copy number variation in patients with cervical artery dissection.
Caspar Grond-Ginsbach, Bowang Chen, Rastislav Pjontek, Tina Wiest, Yanxiang Jiang, Barbara Burwinkel, Sandrine Tchatchou, Michael Krawczak, Stefan Schreiber, Tobias Brandt,[...]. Eur J Hum Genet 2012
21

Hybridization and amplification rate correction for affymetrix SNP arrays.
Quan Wang, Peichao Peng, Minping Qian, Lin Wan, Minghua Deng. BMC Med Genomics 2012
3