A citation-based method for searching scientific literature

Giuseppina Marseglia, Maria Rosaria Scordo, Chiara Pescucci, Genni Nannetti, Elisabetta Biagini, Valeria Scandurra, Francesca Gerundino, Alberto Magi, Matteo Benelli, Francesca Torricelli. Eur J Med Genet 2012
Times Cited: 32



Sergey A Kornilov, Natalia Rakhlin, Roman Koposov, Maria Lee, Carolyn Yrigollen, Ahmet Okay Caglayan, James S Magnuson, Shrikant Mane, Joseph T Chang, Elena L Grigorenko. Pediatrics 2016
Times Cited: 19




List of shared articles



Times cited

Common variation within the SETBP1 gene is associated with reading-related skills and patterns of functional neural activation.
Meaghan V Perdue, Sara Mascheretti, Sergey A Kornilov, Kaja K Jasińska, Kayleigh Ryherd, W Einar Mencl, Stephen J Frost, Elena L Grigorenko, Kenneth R Pugh, Nicole Landi. Neuropsychologia 2019
7

Toward the Language Oscillogenome.
Elliot Murphy, Antonio Benítez-Burraco. Front Psychol 2018
7

Speech and language deficits are central to SETBP1 haploinsufficiency disorder.
Angela Morgan, Ruth Braden, Maggie M K Wong, Estelle Colin, David Amor, Frederique Liégeois, Siddharth Srivastava, Adam Vogel, Varoona Bizaoui, Kara Ranguin,[...]. Eur J Hum Genet 2021
0

Williams Syndrome, Human Self-Domestication, and Language Evolution.
Amy Niego, Antonio Benítez-Burraco. Front Psychol 2019
6

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.
Xiaowei Sylvia Chen, Rose H Reader, Alexander Hoischen, Joris A Veltman, Nuala H Simpson, Clyde Francks, Dianne F Newbury, Simon E Fisher. Sci Rep 2017
42

Cohesion of Cortical Language Networks During Word Processing Is Predicted by a Common Polymorphism in the SETBP1 Gene.
Natalia Rakhlin, Nicole Landi, Maria Lee, James S Magnuson, Oxana Yu Naumova, Irina V Ovchinnikova, Elena L Grigorenko. New Dir Child Adolesc Dev 2020
0