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



Dalila Pinto, Katayoon Darvishi, Xinghua Shi, Diana Rajan, Diane Rigler, Tom Fitzgerald, Anath C Lionel, Bhooma Thiruvahindrapuram, Jeffrey R Macdonald, Ryan Mills, Aparna Prasad, Kristin Noonan, Susan Gribble, Elena Prigmore, Patricia K Donahoe, Richard S Smith, Ji Hyeon Park, Matthew E Hurles, Nigel P Carter, Charles Lee, Stephen W Scherer, Lars Feuk. Nat Biotechnol 2011
Times Cited: 293




List of shared articles



Times cited

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

Discovery of genomic variation across a generation.
Brett Trost, Livia O Loureiro, Stephen W Scherer. Hum Mol Genet 2021
1

Identification and Analysis of Genes Associated with Inherited Retinal Diseases.
Mubeen Khan, Zeinab Fadaie, St├ęphanie S Cornelis, Frans P M Cremers, Susanne Roosing. Methods Mol Biol 2019
8

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

The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
Jiaqi Liu, Yangzhong Zhou, Sen Liu, Xiaofei Song, Xin-Zhuang Yang, Yanhui Fan, Weisheng Chen, Zeynep Coban Akdemir, Zihui Yan, Yuzhi Zuo,[...]. Hum Genet 2018
21

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

A copy number variation map of the human genome.
Mehdi Zarrei, Jeffrey R MacDonald, Daniele Merico, Stephen W Scherer. Nat Rev Genet 2015
376

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

Copy number variations in the genome of the Qatari population.
Khalid A Fakhro, Noha A Yousri, Juan L Rodriguez-Flores, Amal Robay, Michelle R Staudt, Francisco Agosto-Perez, Jacqueline Salit, Joel A Malek, Karsten Suhre, Amin Jayyousi,[...]. BMC Genomics 2015
5

Copy number variation distribution in six monozygotic twin pairs discordant for schizophrenia.
Christina A Castellani, Zain Awamleh, Melkaye G Melka, Richard L O'Reilly, Shiva M Singh. Twin Res Hum Genet 2014
25

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