A citation-based method for searching scientific literature

Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp, Thomas Hansen, Klaus D Jakobsen, Pierandrea Muglia, Clyde Francks, Paul M Matthews, Arnaldur Gylfason, Bjarni V Halldorsson, Daniel Gudbjartsson, Thorgeir E Thorgeirsson, Asgeir Sigurdsson, Adalbjorg Jonasdottir, Aslaug Jonasdottir, Asgeir Bjornsson, Sigurborg Mattiasdottir, Thorarinn Blondal, Magnus Haraldsson, Brynja B Magnusdottir, Ina Giegling, Hans-Jürgen Möller, Annette Hartmann, Kevin V Shianna, Dongliang Ge, Anna C Need, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lonnqvist, Jaana Suvisaari, Annamarie Tuulio-Henriksson, Tiina Paunio, Timi Toulopoulou, Elvira Bramon, Marta Di Forti, Robin Murray, Mirella Ruggeri, Evangelos Vassos, Sarah Tosato, Muriel Walshe, Tao Li, Catalina Vasilescu, Thomas W Mühleisen, August G Wang, Henrik Ullum, Srdjan Djurovic, Ingrid Melle, Jes Olesen, Lambertus A Kiemeney, Barbara Franke, Chiara Sabatti, Nelson B Freimer, Jeffrey R Gulcher, Unnur Thorsteinsdottir, Augustine Kong, Ole A Andreassen, Roel A Ophoff, Alexander Georgi, Marcella Rietschel, Thomas Werge, Hannes Petursson, David B Goldstein, Markus M Nöthen, Leena Peltonen, David A Collier, David St Clair, Kari Stefansson. Nature 2008
Times Cited: 1221



George Kirov, Detelina Grozeva, Nadine Norton, Dobril Ivanov, Kiran K Mantripragada, Peter Holmans, Nick Craddock, Michael J Owen, Michael C O'Donovan. Hum Mol Genet 2009
Times Cited: 303




List of shared articles



Times cited

Haploinsufficiency of the schizophrenia and autism risk gene Cyfip1 causes abnormal postnatal hippocampal neurogenesis through microglial and Arp2/3 mediated actin dependent mechanisms.
Niels Haan, Laura J Westacott, Jenny Carter, Michael J Owen, William P Gray, Jeremy Hall, Lawrence S Wilkinson. Transl Psychiatry 2021
0

Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study.
Johan H Thygesen, Amelia Presman, Jasmine Harju-Seppänen, Haritz Irizar, Rebecca Jones, Karoline Kuchenbaecker, Kuang Lin, Behrooz Z Alizadeh, Isabelle Austin-Zimmerman, Agna Bartels-Velthuis,[...]. Mol Psychiatry 2020
3

Rare copy number variants in individuals at clinical high risk for psychosis: Enrichment of synaptic/brain-related functional pathways.
Vinita Jagannath, Edna Grünblatt, Anastasia Theodoridou, Beatrice Oneda, Alexander Roth, Miriam Gerstenberg, Maurizia Franscini, Nina Traber-Walker, Christoph U Correll, Karsten Heekeren,[...]. Am J Med Genet B Neuropsychiatr Genet 2020
0

Domain-Specific Cognitive Impairments in Humans and Flies With Reduced CYFIP1 Dosage.
Young Jae Woo, Alexandros K Kanellopoulos, Parisa Hemati, Jill Kirschen, Rebecca A Nebel, Tao Wang, Claudia Bagni, Brett S Abrahams. Biol Psychiatry 2019
6

Temporal dynamics of miRNAs in human DLPFC and its association with miRNA dysregulation in schizophrenia.
Zhonghua Hu, Shouguo Gao, Daniel Lindberg, Debabrata Panja, Yoshi Wakabayashi, Keshen Li, Joel E Kleinman, Jun Zhu, Zheng Li. Transl Psychiatry 2019
8

Schizophrenia and Hereditary Polyneuropathy: PMP22 Deletion as a Common Pathophysiological Link?
Dominique Endres, Simon J Maier, Christiane Ziegler, Kathrin Nickel, Anne N Riering, Benjamin Berger, Johann Lambeck, Miriam Fritz, Birgitta Gläser, Friedrich Stock,[...]. Front Psychiatry 2019
1


Double hits in schizophrenia.
Jacob A S Vorstman, Loes M Olde Loohuis, René S Kahn, Roel A Ophoff. Hum Mol Genet 2018
4