A citation-based method for searching scientific literature

Mohammad K Eldomery, Zeynep Coban-Akdemir, Tamar Harel, Jill A Rosenfeld, Tomasz Gambin, Asbjørg Stray-Pedersen, Sébastien Küry, Sandra Mercier, Davor Lessel, Jonas Denecke, Wojciech Wiszniewski, Samantha Penney, Pengfei Liu, Weimin Bi, Seema R Lalani, Christian P Schaaf, Michael F Wangler, Carlos A Bacino, Richard Alan Lewis, Lorraine Potocki, Brett H Graham, John W Belmont, Fernando Scaglia, Jordan S Orange, Shalini N Jhangiani, Theodore Chiang, Harsha Doddapaneni, Jianhong Hu, Donna M Muzny, Fan Xia, Arthur L Beaudet, Eric Boerwinkle, Christine M Eng, Sharon E Plon, V Reid Sutton, Richard A Gibbs, Jennifer E Posey, Yaping Yang, James R Lupski. Genome Med 2017
Times Cited: 111



William McLaren, Laurent Gil, Sarah E Hunt, Harpreet Singh Riat, Graham R S Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham. Genome Biol 2016
Times Cited: 1953




List of shared articles



Times cited

Current scenario of the genetic testing for rare neurological disorders exploiting next generation sequencing.
Chiara Di Resta, Giovanni Battista Pipitone, Paola Carrera, Maurizio Ferrari. Neural Regen Res 2021
2

The Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry composition.
In-Hee Lee, Jose A Negron, Carles Hernandez-Ferrer, William Jefferson Alvarez, Kenneth D Mandl, Sek Won Kong. Hum Mutat 2020
0

Prot2HG: a database of protein domains mapped to the human genome.
David Stanek, Dana M Bis-Brewer, Cima Saghira, Matt C Danzi, Pavel Seeman, Petra Lassuthova, Stephan Zuchner. Database (Oxford) 2020
2

A three-year follow-up study evaluating clinical utility of exome sequencing and diagnostic potential of reanalysis.
Jasmine L F Fung, Mullin H C Yu, Shushu Huang, Claudia C Y Chung, Marcus C Y Chan, Sander Pajusalu, Christopher C Y Mak, Vivian C C Hui, Mandy H Y Tsang, Kit San Yeung,[...]. NPJ Genom Med 2020
9

Next Generation Sequencing and Bioinformatics Analysis of Family Genetic Inheritance.
Aquillah M Kanzi, James Emmanuel San, Benjamin Chimukangara, Eduan Wilkinson, Maryam Fish, Veron Ramsuran, Tulio de Oliveira. Front Genet 2020
2

A three-year follow-up study evaluating clinical utility of exome sequencing and diagnostic potential of reanalysis.
Jasmine L F Fung, Mullin H C Yu, Shushu Huang, Claudia C Y Chung, Marcus C Y Chan, Sander Pajusalu, Christopher C Y Mak, Vivian C C Hui, Mandy H Y Tsang, Kit San Yeung,[...]. NPJ Genom Med 2020
2