A citation-based method for searching scientific literature

Katherine S Pollard, Melissa J Hubisz, Kate R Rosenbloom, Adam Siepel. Genome Res 2010
Times Cited: 1263



Xiaoming Liu, Chang Li, Chengcheng Mou, Yibo Dong, Yicheng Tu. Genome Med 2020
Times Cited: 80




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
3

PHACT: Phylogeny-Aware Computing of Tolerance for Missense Mutations.
Nurdan Kuru, Onur Dereli, Emrah Akkoyun, Aylin Bircan, Oznur Tastan, Ogun Adebali. Mol Biol Evol 2022
0

X-CAP improves pathogenicity prediction of stopgain variants.
Ruchir Rastogi, Peter D Stenson, David N Cooper, Gill Bejerano. Genome Med 2022
0

VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.
Dandan Huang, Yao Zhou, Xianfu Yi, Xutong Fan, Jianhua Wang, Hongcheng Yao, Pak Chung Sham, Jihui Hao, Kexin Chen, Mulin Jun Li. Nucleic Acids Res 2022
6

Overcoming constraints on the detection of recessive selection in human genes from population frequency data.
Daniel J Balick, Daniel M Jordan, Shamil Sunyaev, Ron Do. Am J Hum Genet 2022
0

StrVCTVRE: A supervised learning method to predict the pathogenicity of human genome structural variants.
Andrew G Sharo, Zhiqiang Hu, Shamil R Sunyaev, Steven E Brenner. Am J Hum Genet 2022
7

Whole genome sequencing and inheritance-based variant filtering as a tool for unraveling missing heritability in pediatric cancer.
Charlotte Derpoorter, Ruben Van Paemel, Katrien Vandemeulebroecke, Jolien Vanhooren, Bram De Wilde, Geneviève Laureys, Tim Lammens. Pediatr Hematol Oncol 2022
0

mvPPT: A highly efficient and sensitive pathogenicity prediction tool for missense variants.
Shi-Yuan Tong, Ke Fan, Zai-Wei Zhou, Lin-Yun Liu, Shu-Qing Zhang, Yinghui Fu, Guang-Zhong Wang, Ying Zhu, Yong-Chun Yu. Genomics Proteomics Bioinformatics 2022
0

A comparison on predicting functional impact of genomic variants.
Dong Wang, Jie Li, Yadong Wang, Edwin Wang. NAR Genom Bioinform 2022
2