A citation-based method for searching scientific literature

Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren, Bhooma Thiruvahindrapduram, Andreas Fiebig, Stefan Schreiber, Jan Friedman, Cees E J Ketelaars, Yvonne J Vos, Can Ficicioglu, Susan Kirkpatrick, Rob Nicolson, Leon Sloman, Anne Summers, Clare A Gibbons, Ahmad Teebi, David Chitayat, Rosanna Weksberg, Ann Thompson, Cathy Vardy, Vicki Crosbie, Sandra Luscombe, Rebecca Baatjes, Lonnie Zwaigenbaum, Wendy Roberts, Bridget Fernandez, Peter Szatmari, Stephen W Scherer. Am J Hum Genet 2008
Times Cited: 1178



Christian P Schaaf, Philip M Boone, Srirangan Sampath, Charles Williams, Patricia I Bader, Jennifer M Mueller, Oleg A Shchelochkov, Chester W Brown, Heather P Crawford, James A Phalen, Nicole R Tartaglia, Patricia Evans, William M Campbell, Anne Chun-Hui Tsai, Lea Parsley, Stephanie W Grayson, Angela Scheuerle, Carol D Luzzi, Sandra K Thomas, Patricia A Eng, Sung-Hae L Kang, Ankita Patel, Pawel Stankiewicz, Sau W Cheung. Eur J Hum Genet 2012
Times Cited: 70




List of shared articles



Times cited

Synaptic recognition molecules in development and disease.
Dhrubajyoti Chowdhury, Katherine Watters, Thomas Biederer. Curr Top Dev Biol 2021
1

Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review.
Paola Castronovo, Marco Baccarin, Arianna Ricciardello, Chiara Picinelli, Pasquale Tomaiuolo, Francesca Cucinotta, Myriam Frittoli, Carla Lintas, Roberto Sacco, Antonio M Persico. Clin Genet 2020
13

Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia.
Kanako Ishizuka, Tomoyuki Yoshida, Takeshi Kawabata, Ayako Imai, Hisashi Mori, Hiroki Kimura, Toshiya Inada, Yuko Okahisa, Jun Egawa, Masahide Usami,[...]. J Neurodev Disord 2020
0

An Overview of the Main Genetic, Epigenetic and Environmental Factors Involved in Autism Spectrum Disorder Focusing on Synaptic Activity.
Elena Masini, Eleonora Loi, Ana Florencia Vega-Benedetti, Marinella Carta, Giuseppe Doneddu, Roberta Fadda, Patrizia Zavattari. Int J Mol Sci 2020
4

Rare copy number variation in extremely impulsively violent males.
Jan Vevera, Mehdi Zarrei, Hana Hartmannová, Ivana Jedličková, Dita Mušálková, Anna Přistoupilová, Petra Oliveriusová, Helena Trešlová, Lenka Nosková, Kateřina Hodaňová,[...]. Genes Brain Behav 2019
1

Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders.
Zhonghua Hu, Xiao Xiao, Zhuohua Zhang, Ming Li. Mol Psychiatry 2019
24

Increased Ca2+ signaling in NRXN1α +/- neurons derived from ASD induced pluripotent stem cells.
Sahar Avazzadeh, Katya McDonagh, Jamie Reilly, Yanqin Wang, Stephanie D Boomkamp, Veronica McInerney, Janusz Krawczyk, Jacqueline Fitzgerald, Niamh Feerick, Matthew O'Sullivan,[...]. Mol Autism 2019
11