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, Mark F Rogers, Julian Gough, Matthew Mort, David N Cooper, Ian N M Day, Tom R Gaunt, Colin Campbell. Bioinformatics 2015
Times Cited: 320




List of shared articles



Times cited

Clinical manifestations of patients with GDF2 mutations associated with hereditary hemorrhagic telangiectasia type 5.
Ahmed Farhan, Frank Yuan, Elizabeth Partan, Clifford R Weiss. Am J Med Genet A 2022
2

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

A multi-dimensional integrative scoring framework for predicting functional variants in the human genome.
Xihao Li, Godwin Yung, Hufeng Zhou, Ryan Sun, Zilin Li, Kangcheng Hou, Martin Jinye Zhang, Yaowu Liu, Theodore Arapoglou, Chen Wang,[...]. Am J Hum Genet 2022
1

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

Eph and Ephrin Variants in Malaysian Neural Tube Defect Families.
Siti Waheeda Mohd-Zin, Amelia Cheng Wei Tan, Wahib M Atroosh, Meow-Keong Thong, Abu Bakar Azizi, Nicholas D E Greene, Noraishah Mydin Abdul-Aziz. Genes (Basel) 2022
0

Non-coding regulatory elements: Potential roles in disease and the case of epilepsy.
Susanna Pagni, James D Mills, Adam Frankish, Jonathan M Mudge, Sanjay M Sisodiya. Neuropathol Appl Neurobiol 2022
1

A comparison on predicting functional impact of genomic variants.
Dong Wang, Jie Li, Yadong Wang, Edwin Wang. NAR Genom Bioinform 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

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