A citation-based method for searching scientific literature

Laura J Dumas, Majesta S O'Bleness, Jonathan M Davis, C Michael Dickens, Nathan Anderson, J G Keeney, Jay Jackson, Megan Sikela, Armin Raznahan, Jay Giedd, Judith Rapoport, Sandesh S C Nagamani, Ayelet Erez, Nicola Brunetti-Pierri, Rachel Sugalski, James R Lupski, Tasha Fingerlin, Sau Wai Cheung, James M Sikela. Am J Hum Genet 2012
Times Cited: 67



J A Bailey, A M Yavor, H F Massa, B J Trask, E E Eichler. Genome Res 2001
Times Cited: 474




List of shared articles



Times cited

Comparative Genomic Analyses of the Human NPHP1 Locus Reveal Complex Genomic Architecture and Its Regional Evolution in Primates.
Bo Yuan, Pengfei Liu, Aditya Gupta, Christine R Beck, Anusha Tejomurtula, Ian M Campbell, Tomasz Gambin, Alexandra D Simmons, Marjorie A Withers, R Alan Harris,[...]. PLoS Genet 2015
16


Modelling segmental duplications in the human genome.
Eldar T Abdullaev, Iren R Umarova, Peter F Arndt. BMC Genomics 2021
0

Human adaptation and evolution by segmental duplication.
Megan Y Dennis, Evan E Eichler. Curr Opin Genet Dev 2016
64

22q11.2 Low Copy Repeats Expanded in the Human Lineage.
Lisanne Vervoort, Nicolas Dierckxsens, Zjef Pereboom, Oronzo Capozzi, Mariano Rocchi, Tamim H Shaikh, Joris R Vermeesch. Front Genet 2021
0

iCopyDAV: Integrated platform for copy number variations-Detection, annotation and visualization.
Prashanthi Dharanipragada, Sriharsha Vogeti, Nita Parekh. PLoS One 2018
14

Coherent somatic mutation in autoimmune disease.
Kenneth Andrew Ross. PLoS One 2014
14

Disorders Associated With Diverse, Recurrent Deletions and Duplications at 1q21.1.
Hui Pang, Xiaowei Yu, Young Mi Kim, Xianfu Wang, Jeremy K Jinkins, Jianing Yin, Shibo Li, Hongcang Gu. Front Genet 2020
1