A citation-based method for searching scientific literature

Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle, Heike Tost, Oliver Grimm, Solveig Kristjansdottir, Heimir Snorrason, Solveig R Davidsdottir, Larus J Gudmundsson, Gudbjorn F Jonsson, Berglind Stefansdottir, Isafold Helgadottir, Magnus Haraldsson, Birna Jonsdottir, Johan H Thygesen, Adam J Schwarz, Michael Didriksen, Tine B Stensbøl, Michael Brammer, Shitij Kapur, Jonas G Halldorsson, Stefan Hreidarsson, Evald Saemundsen, Engilbert Sigurdsson, Kari Stefansson. Nature 2014
Times Cited: 370



Shaun M Purcell, Jennifer L Moran, Menachem Fromer, Douglas Ruderfer, Nadia Solovieff, Panos Roussos, Colm O'Dushlaine, Kimberly Chambert, Sarah E Bergen, Anna Kähler, Laramie Duncan, Eli Stahl, Giulio Genovese, Esperanza Fernández, Mark O Collins, Noboru H Komiyama, Jyoti S Choudhary, Patrik K E Magnusson, Eric Banks, Khalid Shakir, Kiran Garimella, Tim Fennell, Mark DePristo, Seth G N Grant, Stephen J Haggarty, Stacey Gabriel, Edward M Scolnick, Eric S Lander, Christina M Hultman, Patrick F Sullivan, Steven A McCarroll, Pamela Sklar. Nature 2014
Times Cited: 870




List of shared articles



Times cited

Familial Psychosis Associated With a Missense Mutation at MACF1 Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the CNTN6 and CDH13 Genes.
Josep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, Aina Medina-Dols, Bàrbara Bisbal-Carrió, Víctor Asensio, Bernat Ortega-Vila, Diego Marzese, Carme Vidal, Carmen Santos,[...]. Front Genet 2021
0

Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report.
Alice Poisson, Nicolas Chatron, Audrey Labalme, Pierre Fourneret, Dorothée Ville, Marie Laure Mathieu, Damien Sanlaville, Caroline Demily, Gaëtan Lesca. BMC Med Genet 2020
0

Novel Approaches for Identifying the Molecular Background of Schizophrenia.
Arkadiy K Golov, Nikolay V Kondratyev, George P Kostyuk, And Vera E Golimbet. Cells 2020
6

Modelling Learning and Memory in Drosophila to Understand Intellectual Disabilities.
Vittoria Mariano, Tilmann Achsel, Claudia Bagni, Alexandros K Kanellopoulos. Neuroscience 2020
2

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

Investigation of de novo mutations in a schizophrenia case-parent trio by induced pluripotent stem cell-based in vitro disease modeling: convergence of schizophrenia- and autism-related cellular phenotypes.
Edit Hathy, Eszter Szabó, Nóra Varga, Zsuzsa Erdei, Csongor Tordai, Boróka Czehlár, Máté Baradits, Bálint Jezsó, Júlia Koller, László Nagy,[...]. Stem Cell Res Ther 2020
0