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



Hashem A Shihab, Julian Gough, David N Cooper, Peter D Stenson, Gary L A Barker, Keith J Edwards, Ian N M Day, Tom R Gaunt. Hum Mutat 2013
Times Cited: 696




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

DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing loss.
Fengxiao Bu, Mingjun Zhong, Qinyi Chen, Yumei Wang, Xia Zhao, Qian Zhang, Xiarong Li, Kevin T Booth, Hela Azaiez, Yu Lu,[...]. Hum Genet 2022
0

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

Multiple primary malignances managed with surgical excision: a case report with next generation sequencing analysis.
Chiara Romano, Sandra Di Gregorio, Maria Stella Pennisi, Elena Tirrò, Giuseppe Broggi, Rosario Caltabiano, Livia Manzella, Martino Ruggieri, Paolo Vigneri, Antonio Di Cataldo. Mol Biol Rep 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

Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.
Cengiz Karakaya, Aylin Pelin Çil, Kaya Bilguvar, Tunahan Çakir, Mete Hakan Karalok, Recep Onur Karabacak, Ahmet Okay Caglayan. J Obstet Gynaecol Res 2022
1

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