A citation-based method for searching scientific literature

Smita Yadav, Juan A Oses-Prieto, Christian J Peters, Jing Zhou, Samuel J Pleasure, Alma L Burlingame, Lily Y Jan, Yuh-Nung Jan. Neuron 2017
Times Cited: 54



S Steinberg, S de Jong, M Mattheisen, J Costas, D Demontis, S Jamain, O P H Pietiläinen, K Lin, S Papiol, J Huttenlocher, E Sigurdsson, E Vassos, I Giegling, R Breuer, G Fraser, N Walker, I Melle, S Djurovic, I Agartz, A Tuulio-Henriksson, J Suvisaari, J Lönnqvist, T Paunio, L Olsen, T Hansen, A Ingason, M Pirinen, E Strengman, D M Hougaard, T Orntoft, M Didriksen, M V Hollegaard, M Nordentoft, L Abramova, V Kaleda, M Arrojo, J Sanjuán, C Arango, B Etain, F Bellivier, A Méary, F Schürhoff, A Szoke, M Ribolsi, V Magni, A Siracusano, S Sperling, M Rossner, C Christiansen, L A Kiemeney, B Franke, L H van den Berg, J Veldink, S Curran, P Bolton, M Poot, W Staal, K Rehnstrom, H Kilpinen, C M Freitag, J Meyer, P Magnusson, E Saemundsen, I Martsenkovsky, I Bikshaieva, I Martsenkovska, O Vashchenko, M Raleva, K Paketchieva, B Stefanovski, N Durmishi, M Pejovic Milovancevic, D Lecic Tosevski, T Silagadze, N Naneishvili, N Mikeladze, S Surguladze, J B Vincent, A Farmer, P B Mitchell, A Wright, P R Schofield, J M Fullerton, G W Montgomery, N G Martin, I A Rubino, R van Winkel, G Kenis, M De Hert, J M Réthelyi, I Bitter, L Terenius, E G Jönsson, S Bakker, J van Os, A Jablensky, M Leboyer, E Bramon, J Powell, R Murray, A Corvin, M Gill, D Morris, F A O'Neill, K Kendler, B Riley, N Craddock, M J Owen, M C O'Donovan, U Thorsteinsdottir, A Kong, H Ehrenreich, A Carracedo, V Golimbet, O A Andreassen, A D Børglum, O Mors, P B Mortensen, T Werge, R A Ophoff, M M Nöthen, M Rietschel, S Cichon, M Ruggeri, S Tosato, A Palotie, D St Clair, D Rujescu, D A Collier, H Stefansson, K Stefansson. Mol Psychiatry 2014
Times Cited: 66




List of shared articles



Times cited

Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling.
Melanie Richter, Nadeem Murtaza, Robin Scharrenberg, Sean H White, Ole Johanns, Susan Walker, Ryan K C Yuen, Birgit Schwanke, Bianca Bedürftig, Melad Henis,[...]. Mol Psychiatry 2019
46

16p11.2 Copy Number Variations and Neurodevelopmental Disorders.
Benjamin Rein, Zhen Yan. Trends Neurosci 2020
4

Vascular contributions to 16p11.2 deletion autism syndrome modeled in mice.
Julie Ouellette, Xavier Toussay, Cesar H Comin, Luciano da F Costa, Mirabelle Ho, María Lacalle-Aurioles, Moises Freitas-Andrade, Qing Yan Liu, Sonia Leclerc, Youlian Pan,[...]. Nat Neurosci 2020
7

Functional Genomics Identify a Regulatory Risk Variation rs4420550 in the 16p11.2 Schizophrenia-Associated Locus.
Hong Chang, Xin Cai, Hui-Juan Li, Wei-Peng Liu, Li-Juan Zhao, Chu-Yi Zhang, Jun-Yang Wang, Jie-Wei Liu, Xiao-Lei Ma, Lu Wang,[...]. Biol Psychiatry 2021
2

Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions.
Thomas Arbogast, Parisa Razaz, Jacob Ellegood, Spencer U McKinstry, Serkan Erdin, Benjamin Currall, Tanya Aneichyk, Jason P Lerch, Lily R Qiu, Ramona M Rodriguiz,[...]. Hum Mol Genet 2019
11