A citation-based method for searching scientific literature

Nilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, Sumit Middha, Shannon K McDonnell, Saurabh Baheti, Anthony Musolf, Qing Li, Emily Holzinger, Danielle Karyadi, Lisa A Cannon-Albright, Craig C Teerlink, Janet L Stanford, William B Isaacs, Jianfeng Xu, Kathleen A Cooney, Ethan M Lange, Johanna Schleutker, John D Carpten, Isaac J Powell, Olivier Cussenot, Geraldine Cancel-Tassin, Graham G Giles, Robert J MacInnis, Christiane Maier, Chih-Lin Hsieh, Fredrik Wiklund, William J Catalona, William D Foulkes, Diptasri Mandal, Rosalind A Eeles, Zsofia Kote-Jarai, Carlos D Bustamante, Daniel J Schaid, Trevor Hastie, Elaine A Ostrander, Joan E Bailey-Wilson, Predrag Radivojac, Stephen N Thibodeau, Alice S Whittemore, Weiva Sieh. Am J Hum Genet 2016
Times Cited: 518



Hannah Carter, Christopher Douville, Peter D Stenson, David N Cooper, Rachel Karchin. BMC Genomics 2013
Times Cited: 196




List of shared articles



Times cited

Whole exome sequencing in unclassified autoinflammatory diseases: more monogenic diseases in the pipeline?
Can Kosukcu, Ekim Z Taskiran, Ezgi Deniz Batu, Erdal Sag, Yelda Bilginer, Mehmet Alikasifoglu, Seza Ozen. Rheumatology (Oxford) 2021
6

Assessing performance of pathogenicity predictors using clinically relevant variant datasets.
Adam C Gunning, Verity Fryer, James Fasham, Andrew H Crosby, Sian Ellard, Emma L Baple, Caroline F Wright. J Med Genet 2021
3


Prediction of driver variants in the cancer genome via machine learning methodologies.
Mark F Rogers, Tom R Gaunt, Colin Campbell. Brief Bioinform 2021
0

OncoVar: an integrated database and analysis platform for oncogenic driver variants in cancers.
Tao Wang, Shasha Ruan, Xiaolu Zhao, Xiaohui Shi, Huajing Teng, Jianing Zhong, Mingcong You, Kun Xia, Zhongsheng Sun, Fengbiao Mao. Nucleic Acids Res 2021
9

New clinical and molecular evidence linking mutations in ARSG to Usher syndrome type IV.
Virginie G Peter, Mathieu Quinodoz, Silvia Sadio, Sebastian Held, Márcia Rodrigues, Marta Soares, Ana Berta Sousa, Luisa Coutinho Santos, Markus Damme, Carlo Rivolta. Hum Mutat 2021
4

Functional and clinical implications of genetic structure in 1686 Italian exomes.
Giovanni Birolo, Serena Aneli, Cornelia Di Gaetano, Giovanni Cugliari, Alessia Russo, Alessandra Allione, Elisabetta Casalone, Elisa Giorgio, Elvezia M Paraboschi, Diego Ardissino,[...]. Hum Mutat 2021
0

MVP predicts the pathogenicity of missense variants by deep learning.
Hongjian Qi, Haicang Zhang, Yige Zhao, Chen Chen, John J Long, Wendy K Chung, Yongtao Guan, Yufeng Shen. Nat Commun 2021
6


GPCards: An integrated database of genotype-phenotype correlations in human genetic diseases.
Bin Li, Zheng Wang, Qian Chen, Kuokuo Li, Xiaomeng Wang, Yijing Wang, Qian Zeng, Ying Han, Bin Lu, Yuwen Zhao,[...]. Comput Struct Biotechnol J 2021
0