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



Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
Times Cited: 955




List of shared articles



Times cited

Genome sequencing data analysis for rare disease gene discovery.
Umm-Kulthum Ismail Umlai, Dhinoth Kumar Bangarusamy, Xavier Estivill, Puthen Veettil Jithesh. Brief Bioinform 2021
0

Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders.
Rolph Pfundt, Marisol Del Rosario, Lisenka E L M Vissers, Michael P Kwint, Irene M Janssen, Nicole de Leeuw, Helger G Yntema, Marcel R Nelen, Dorien Lugtenberg, Erik-Jan Kamsteeg,[...]. Genet Med 2017
75


Intellectual Disability & Rare Disorders: A Diagnostic Challenge.
Malin Kvarnung, Ann Nordgren. Adv Exp Med Biol 2017
12

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

Exome sequencing and whole genome sequencing for the detection of copy number variation.
Jayne Y Hehir-Kwa, Rolph Pfundt, Joris A Veltman. Expert Rev Mol Diagn 2015
45

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
645

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

Genomic Variation: Lessons Learned from Whole-Genome CNV Analysis.
Erin Rooney Riggs, David H Ledbetter, Christa Lese Martin. Curr Genet Med Rep 2014
11