A citation-based method for searching scientific literature

Ken Chen, John W Wallis, Michael D McLellan, David E Larson, Joelle M Kalicki, Craig S Pohl, Sean D McGrath, Michael C Wendl, Qunyuan Zhang, Devin P Locke, Xiaoqi Shi, Robert S Fulton, Timothy J Ley, Richard K Wilson, Li Ding, Elaine R Mardis. Nat Methods 2009
Times Cited: 931



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: 2589




List of shared articles



Times cited

Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.
Morag A Lewis, Neil J Ingham, Jing Chen, Selina Pearson, Francesca Di Domenico, Sohinder Rekhi, Rochelle Allen, Matthew Drake, Annelore Willaert, Victoria Rook,[...]. BMC Biol 2022
0

Novel PRMT7 mutation in a rare case of dysmorphism and intellectual disability.
Jessie Poquérusse, Whitney Whitford, Juliet Taylor, Salam Alburaiky, Russell G Snell, Klaus Lehnert, Jessie C Jacobsen. J Hum Genet 2022
1

DNA sequence features underlying large-scale duplications and deletions in human.
Mateusz Kołomański, Joanna Szyda, Magdalena Frąszczak, Magda Mielczarek. J Appl Genet 2022
0

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
3


Whole-Genome Sequencing Improves the Diagnosis of DFNB1 Monoallelic Patients.
Anaïs Le Nabec, Mégane Collobert, Cédric Le Maréchal, Rémi Marianowski, Claude Férec, Stéphanie Moisan. Genes (Basel) 2021
0