A citation-based method for searching scientific literature

Katherine S Pollard, Melissa J Hubisz, Kate R Rosenbloom, Adam Siepel. Genome Res 2010
Times Cited: 1252



Sung Chun, Justin C Fay. Genome Res 2009
Times Cited: 653




List of shared articles



Times cited


Analysis of missense variants in the human genome reveals widespread gene-specific clustering and improves prediction of pathogenicity.
Mathieu Quinodoz, Virginie G Peter, Katarina Cisarova, Beryl Royer-Bertrand, Peter D Stenson, David N Cooper, Sheila Unger, Andrea Superti-Furga, Carlo Rivolta. Am J Hum Genet 2022
2

Machine learning methods for prediction of cancer driver genes: a survey paper.
Renan Andrades, Mariana Recamonde-Mendoza. Brief Bioinform 2022
0

Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource.
Lisa Dressler, Michele Bortolomeazzi, Mohamed Reda Keddar, Hrvoje Misetic, Giulia Sartini, Amelia Acha-Sagredo, Lucia Montorsi, Neshika Wijewardhane, Dimitra Repana, Joel Nulsen,[...]. Genome Biol 2022
2

Aggregated Genomic Data as Cohort-Specific Allelic Frequencies can Boost Variants and Genes Prioritization in Non-Solved Cases of Inherited Retinal Dystrophies.
Ionut-Florin Iancu, Irene Perea-Romero, Gonzalo Núñez-Moreno, Lorena de la Fuente, Raquel Romero, Almudena Ávila-Fernandez, María José Trujillo-Tiebas, Rosa Riveiro-Álvarez, Berta Almoguera, Inmaculada Martín-Mérida,[...]. Int J Mol Sci 2022
0

Computational Resources for the Interpretation of Variations in Cancer.
Grete Francesca Privitera, Salvatore Alaimo, Alfredo Ferro, Alfredo Pulvirenti. Adv Exp Med Biol 2022
0

Machine-learning of complex evolutionary signals improves classification of SNVs.
Sapir Labes, Doron Stupp, Naama Wagner, Idit Bloch, Michal Lotem, Ephrat L Lahad, Paz Polak, Tal Pupko, Yuval Tabach. NAR Genom Bioinform 2022
0

Genome interpretation using in silico predictors of variant impact.
Panagiotis Katsonis, Kevin Wilhelm, Amanda Williams, Olivier Lichtarge. Hum Genet 2022
0