A citation-based method for searching scientific literature

Egor Dolzhenko, Joke J F A van Vugt, Richard J Shaw, Mitchell A Bekritsky, Marka van Blitterswijk, Giuseppe Narzisi, Subramanian S Ajay, Vani Rajan, Bryan R Lajoie, Nathan H Johnson, Zoya Kingsbury, Sean J Humphray, Raymond D Schellevis, William J Brands, Matt Baker, Rosa Rademakers, Maarten Kooyman, Gijs H P Tazelaar, Michael A van Es, Russell McLaughlin, William Sproviero, Aleksey Shatunov, Ashley Jones, Ahmad Al Khleifat, Alan Pittman, Sarah Morgan, Orla Hardiman, Ammar Al-Chalabi, Chris Shaw, Bradley Smith, Edmund J Neo, Karen Morrison, Pamela J Shaw, Catherine Reeves, Lara Winterkorn, Nancy S Wexler, David E Housman, Christopher W Ng, Alina L Li, Ryan J Taft, Leonard H van den Berg, David R Bentley, Jan H Veldink, Michael A Eberle. Genome Res 2017
Times Cited: 117



Thomas Willems, Dina Zielinski, Jie Yuan, Assaf Gordon, Melissa Gymrek, Yaniv Erlich. Nat Methods 2017
Times Cited: 73




List of shared articles



Times cited

TRTools: a toolkit for genome-wide analysis of tandem repeats.
Nima Mousavi, Jonathan Margoliash, Neha Pusarla, Shubham Saini, Richard Yanicky, Melissa Gymrek. Bioinformatics 2021
4

Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing.
Abdul Rezzak Hamzeh, T Daniel Andrews, Matt A Field. Methods Mol Biol 2021
0

Pervasive cis effects of variation in copy number of large tandem repeats on local DNA methylation and gene expression.
Paras Garg, Alejandro Martin-Trujillo, Oscar L Rodriguez, Scott J Gies, Elina Hadelia, Bharati Jadhav, Miten Jain, Benedict Paten, Andrew J Sharp. Am J Hum Genet 2021
3


Systematic analysis of short tandem repeats in 38,095 exomes provides an additional diagnostic yield.
Bart P G H van der Sanden, Jordi Corominas, Michelle de Groot, Maartje Pennings, Rowdy P P Meijer, Nienke Verbeek, Bart van de Warrenburg, Meyke Schouten, Helger G Yntema, Lisenka E L M Vissers,[...]. Genet Med 2021
0

Genome-wide sequencing as a first-tier screening test for short tandem repeat expansions.
Indhu-Shree Rajan-Babu, Junran J Peng, Readman Chiu, Chenkai Li, Arezoo Mohajeri, Egor Dolzhenko, Michael A Eberle, Inanc Birol, Jan M Friedman. Genome Med 2021
2

popSTR2 enables clinical and population-scale genotyping of microsatellites.
Sn├Ždis Kristmundsdottir, Hannes P Eggertsson, Gudny A Arnadottir, Bjarni V Halldorsson. Bioinformatics 2020
3

Comparison of NGS panel and Sanger sequencing for genotyping CAG repeats in the AR gene.
Maria Santa Rocca, Margherita Ferrarini, Aichi Msaki, Cinzia Vinanzi, Marco Ghezzi, Maurizio De Rocco Ponce, Carlo Foresta, Alberto Ferlin. Mol Genet Genomic Med 2020
2


Large scale in silico characterization of repeat expansion variation in human genomes.
Sarah Fazal, Matt C Danzi, Vivian P Cintra, Dana M Bis-Brewer, Egor Dolzhenko, Michael A Eberle, Stephan Zuchner. Sci Data 2020
1

Genome-wide detection of short tandem repeat expansions by long-read sequencing.
Qian Liu, Yao Tong, Kai Wang. BMC Bioinformatics 2020
2

Profiling the genome-wide landscape of tandem repeat expansions.
Nima Mousavi, Sharona Shleizer-Burko, Richard Yanicky, Melissa Gymrek. Nucleic Acids Res 2019
34

Clinical sequencing: From raw data to diagnosis with lifetime value.
S M Caspar, N Dubacher, A M Kopps, J Meienberg, C Henggeler, G Matyas. Clin Genet 2018
40