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



Pablo Cingolani, Adrian Platts, Le Lily Wang, Melissa Coon, Tung Nguyen, Luan Wang, Susan J Land, Xiangyi Lu, Douglas M Ruden. Fly (Austin) 2012
Times Cited: 4197




List of shared articles



Times cited

Genotype-phenotype association and variant characterization in Diamond-Blackfan anemia caused by pathogenic variants in RPL35A.
Matthew D Gianferante, Marcin W Wlodarski, Evangelia Atsidaftos, Lydie Da Costa, Polyxeni Delaporta, Jason E Farrar, Frederick D Goldman, Maryam Hussain, Antonis Kattamis, Thierry Leblanc,[...]. Haematologica 2021
1

Comprehensive fundamental somatic variant calling and quality management strategies for human cancer genomes.
Xiaoyu He, Shanyu Chen, Ruilin Li, Xinyin Han, Zhipeng He, Danyang Yuan, Shuying Zhang, Xiaohong Duan, Beifang Niu. Brief Bioinform 2021
4

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

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

Exome-Wide Association Study on Alanine Aminotransferase Identifies Sequence Variants in the GPAM and APOE Associated With Fatty Liver Disease.
Oveis Jamialahmadi, Rosellina Margherita Mancina, Ester Ciociola, Federica Tavaglione, Panu K Luukkonen, Guido Baselli, Francesco Malvestiti, Dorothée Thuillier, Violeta Raverdy, Ville Männistö,[...]. Gastroenterology 2021
8

Germline and Tumor Sequencing as a Diagnostic Tool To Resolve Suspected Lynch Syndrome.
Bernard J Pope, Mark Clendenning, Christophe Rosty, Khalid Mahmood, Peter Georgeson, Jihoon E Joo, Romy Walker, Ryan A Hutchinson, Harindra Jayasekara, Sharelle Joseland,[...]. J Mol Diagn 2021
2

ATAV: a comprehensive platform for population-scale genomic analyses.
Zhong Ren, Gundula Povysil, Joseph A Hostyk, Hongzhu Cui, Nitin Bhardwaj, David B Goldstein. BMC Bioinformatics 2021
2

Candidate Markers of Olaparib Response from Genomic Data Analyses of Human Cancer Cell Lines.
Setor Amuzu, Euridice Carmona, Anne-Marie Mes-Masson, Celia M T Greenwood, Patricia N Tonin, Jiannis Ragoussis. Cancers (Basel) 2021
0

Structural analysis of new compound heterozygous variants in PEPD gene identified in a patient with Prolidase Deficiency diagnosed by exome sequencing.
Natália D Linhares, Piotr Wilk, Elżbieta Wątor, Meire A Tostes, Manfred S Weiss, Sergio D J Pena. Genet Mol Biol 2021
0