A citation-based method for searching scientific literature

Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers, Janneke H Schuurs-Hoeijmakers, Alex Hoischen, Rolph Pfundt, Nik Krumm, Gemma L Carvill, Deana Li, David Amaral, Natasha Brown, Paul J Lockhart, Ingrid E Scheffer, Antonino Alberti, Marie Shaw, Rosa Pettinato, Raymond Tervo, Nicole de Leeuw, Margot R F Reijnders, Beth S Torchia, Hilde Peeters, Brian J O'Roak, Marco Fichera, Jayne Y Hehir-Kwa, Jay Shendure, Heather C Mefford, Eric Haan, Jozef Gécz, Bert B A de Vries, Corrado Romano, Evan E Eichler. Nat Genet 2014
Times Cited: 313



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




List of shared articles



Times cited

Clinical delineation of SETBP1 haploinsufficiency disorder.
Nadieh A Jansen, Ruth O Braden, Siddharth Srivastava, Erin F Otness, Gaetan Lesca, Massimiliano Rossi, Mathilde Nizon, Raphael A Bernier, Chloé Quelin, Arie van Haeringen,[...]. Eur J Hum Genet 2021
0

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

18q12.3-q21.1 microdeletion detected in the prenatally alcohol-exposed dizygotic twin with discordant fetal alcohol syndrome phenotype.
Hanna Kahila, Heidi Marjonen, Pauliina Auvinen, Kristiina Avela, Raili Riikonen, Nina Kaminen-Ahola. Mol Genet Genomic Med 2020
3

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

Identification of SETBP1 Mutations by Gene Panel Sequencing in Individuals With Intellectual Disability or With "Developmental and Epileptic Encephalopathy".
Emanuela Leonardi, Elisa Bettella, Maria Federica Pelizza, Maria Cristina Aspromonte, Roberta Polli, Clementina Boniver, Stefano Sartori, Donatella Milani, Alessandra Murgia. Front Neurol 2020
0

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