A citation-based method for searching scientific literature

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



Joshua M Korn, Finny G Kuruvilla, Steven A McCarroll, Alec Wysoker, James Nemesh, Simon Cawley, Earl Hubbell, Jim Veitch, Patrick J Collins, Katayoon Darvishi, Charles Lee, Marcia M Nizzari, Stacey B Gabriel, Shaun Purcell, Mark J Daly, David Altshuler. Nat Genet 2008
Times Cited: 590




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

DeepCNV: a deep learning approach for authenticating copy number variations.
Joseph T Glessner, Xiurui Hou, Cheng Zhong, Jie Zhang, Munir Khan, Fabian Brand, Peter Krawitz, Patrick M A Sleiman, Hakon Hakonarson, Zhi Wei. Brief Bioinform 2021
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

Benefits and limitations of genome-wide association studies.
Vivian Tam, Nikunj Patel, Michelle Turcotte, Yohan Bossé, Guillaume Paré, David Meyre. Nat Rev Genet 2019
295

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

A decade of structural variants: description, history and methods to detect structural variation.
Geòrgia Escaramís, Elisa Docampo, Raquel Rabionet. Brief Funct Genomics 2015
45

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

The Role of Constitutional Copy Number Variants in Breast Cancer.
Logan C Walker, George A R Wiggins, John F Pearson. Microarrays (Basel) 2015
6

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

Biological relevance of CNV calling methods using familial relatedness including monozygotic twins.
Christina A Castellani, Melkaye G Melka, Andrea E Wishart, M Elizabeth O Locke, Zain Awamleh, Richard L O'Reilly, Shiva M Singh. BMC Bioinformatics 2014
11

Detection of genome-wide copy number variations in two chicken lines divergently selected for abdominal fat content.
Hui Zhang, Zhi-Qiang Du, Jia-Qiang Dong, Hai-Xia Wang, Hong-Yan Shi, Ning Wang, Shou-Zhi Wang, Hui Li. BMC Genomics 2014
23


A method for calling copy number polymorphism using haplotypes.
Gun Ho Jang, Jason D Christie, Rui Feng. Front Genet 2013
2

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

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

Algorithm implementation for CNV discovery using Affymetrix and Illumina SNP array data.
Laura Winchester, Jiannis Ragoussis. Methods Mol Biol 2012
1



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

Identification of germline genomic copy number variation in familial pancreatic cancer.
Wigdan Al-Sukhni, Sarah Joe, Anath C Lionel, Nora Zwingerman, George Zogopoulos, Christian R Marshall, Ayelet Borgida, Spring Holter, Aaron Gropper, Sara Moore,[...]. Hum Genet 2012
18

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