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



Jill A Rosenfeld, Ryan N Traylor, G Bradley Schaefer, Elizabeth W McPherson, Blake C Ballif, Eva Klopocki, Stefan Mundlos, Lisa G Shaffer, Arthur S Aylsworth. Eur J Hum Genet 2012
Times Cited: 61




List of shared articles



Times cited

New insights into the genetic basis of TAR (thrombocytopenia-absent radii) syndrome.
Cornelis A Albers, Ruth Newbury-Ecob, Willem H Ouwehand, Cedric Ghevaert. Curr Opin Genet Dev 2013
39

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
Ida E S√łnderby, Dennis van der Meer, Clara Moreau, Tobias Kaufmann, G Bragi Walters, Maria Ellegaard, Abdel Abdellaoui, David Ames, Katrin Amunts, Micael Andersson,[...]. Transl Psychiatry 2021
2

Focal cortical dysplasia, microcephaly and epilepsy in a boy with 1q21.1-q21.3 duplication.
Roberta Milone, Angelo Valetto, Roberta Battini, Veronica Bertini, Giulia Valvo, Giovanni Cioni, Federico Sicca. Eur J Med Genet 2016
8

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