A citation-based method for searching scientific literature

J P Szatkiewicz, C O'Dushlaine, G Chen, K Chambert, J L Moran, B M Neale, M Fromer, D Ruderfer, S Akterin, S E Bergen, A Kähler, P K E Magnusson, Y Kim, J J Crowley, E Rees, G Kirov, M C O'Donovan, M J Owen, J Walters, E Scolnick, P Sklar, S Purcell, C M Hultman, S A McCarroll, P F Sullivan. Mol Psychiatry 2014
Times Cited: 161



Gregory Costain, Anath C Lionel, Daniele Merico, Pamela Forsythe, Kathryn Russell, Chelsea Lowther, Tracy Yuen, Janice Husted, Dimitri J Stavropoulos, Marsha Speevak, Eva W C Chow, Christian R Marshall, Stephen W Scherer, Anne S Bassett. Hum Mol Genet 2013
Times Cited: 87




List of shared articles



Times cited


Genome-wide study of copy number variation implicates multiple novel loci for schizophrenia risk in Han Chinese family trios.
Xi Wu, Cong Huai, Lu Shen, Mo Li, Chao Yang, Juan Zhang, Luan Chen, Wenli Zhu, Lingzi Fan, Wei Zhou,[...]. iScience 2021
0

Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders.
Zhonghua Hu, Xiao Xiao, Zhuohua Zhang, Ming Li. Mol Psychiatry 2019
26

A critical review of zebrafish schizophrenia models: Time for validation?
Kinga Gawel, Nancy Saana Banono, Agnieszka Michalak, Camila V Esguerra. Neurosci Biobehav Rev 2019
8

Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.
Jordi Soler, Lourdes Fañanás, Mara Parellada, Marie-Odile Krebs, Guy A Rouleau, Mar Fatjó-Vilas. J Psychiatry Neurosci 2018
21

Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.
Jordi Soler, Lourdes Fañanás, Mara Parellada, Marie-Odile Krebs, Guy A Rouleau, Mar Fatjó-Vilas. J Psychiatry Neurosci 2018
10

High-resolution copy number variation analysis of schizophrenia in Japan.
I Kushima, B Aleksic, M Nakatochi, T Shimamura, T Shiino, A Yoshimi, H Kimura, Y Takasaki, C Wang, J Xing,[...]. Mol Psychiatry 2017
58

Rare and common variants at 16p11.2 are associated with schizophrenia.
Hong Chang, Lingyi Li, Ming Li, Xiao Xiao. Schizophr Res 2017
20

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Anne S Bassett, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W C Chow, Therese van Amelsvoort, Donna McDonald-McGinn, Raquel E Gur, Ann Swillen, Marianne Van den Bree,[...]. Am J Psychiatry 2017
41