A citation-based method for searching scientific literature

Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
Times Cited: 511



Vincent Plagnol, James Curtis, Michael Epstein, Kin Y Mok, Emma Stebbings, Sofia Grigoriadou, Nicholas W Wood, Sophie Hambleton, Siobhan O Burns, Adrian J Thrasher, Dinakantha Kumararatne, Rainer Doffinger, Sergey Nejentsev. Bioinformatics 2012
Times Cited: 288




List of shared articles



Times cited

Precise variant interpretation, phenotype ascertainment, and genotype-phenotype correlation of children in the EARLY PRO-TECT Alport trial.
Jan Boeckhaus, Julia Hoefele, Korbinian M Riedhammer, Burkhard Tönshoff, Rasmus Ehren, Lars Pape, Kay Latta, Henry Fehrenbach, Baerbel Lange-Sperandio, Matthias Kettwig,[...]. Clin Genet 2021
0


Renal and Skeletal Anomalies in a Cohort of Individuals With Clinically Presumed Hereditary Nephropathy Analyzed by Molecular Genetic Testing.
Michaela Stippel, Korbinian M Riedhammer, Bärbel Lange-Sperandio, Michaela Geßner, Matthias C Braunisch, Roman Günthner, Martin Bald, Miriam Schmidts, Peter Strotmann, Velibor Tasic,[...]. Front Genet 2021
0

High Detection Rate of Copy Number Variations Using Capture Sequencing Data: A Retrospective Study.
Yu Sun, Xiantao Ye, Yanjie Fan, Lili Wang, Xiaomei Luo, Huili Liu, Xueren Gao, Zhuwen Gong, Yu Wang, Wenjuan Qiu,[...]. Clin Chem 2020
4

Copy number variations and multiallelic variants in Korean patients with Leber congenital amaurosis.
Dongheon Surl, Saeam Shin, Seung-Tae Lee, Jong Rak Choi, Junwon Lee, Suk Ho Byeon, Sueng-Han Han, Hyun Taek Lim, Jinu Han. Mol Vis 2020
3

Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies.
Korbinian M Riedhammer, Matthias C Braunisch, Roman Günthner, Matias Wagner, Clara Hemmer, Tim M Strom, Christoph Schmaderer, Lutz Renders, Velibor Tasic, Zoran Gucev,[...]. Am J Kidney Dis 2020
8