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



S Ben-Shachar, B Lanpher, J R German, M Qasaymeh, L Potocki, S C Sreenath Nagamani, L M Franco, A Malphrus, G W Bottenfield, J E Spence, S Amato, J A Rousseau, B Moghaddam, C Skinner, S A Skinner, S Bernes, N Armstrong, M Shinawi, P Stankiewicz, A Patel, S-W Cheung, J R Lupski, A L Beaudet, T Sahoo. J Med Genet 2009
Times Cited: 158




List of shared articles



Times cited

Genomic Variation, Evolvability, and the Paradox of Mental Illness.
Camillo Thomas Gualtieri. Front Psychiatry 2021
0

Human-Specific Genes, Cortical Progenitor Cells, and Microcephaly.
Michael Heide, Wieland B Huttner. Cells 2021
0


Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurodevelopmental disorders.
Ilse M van der Werf, Sandra Jansen, Petra F de Vries, Amber Gerstmans, Maartje van de Vorst, Anke Van Dijck, Bert B A de Vries, Christian Gilissen, Alexander Hoischen, Lisenka E L M Vissers,[...]. Eur J Hum Genet 2020
0

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

Common variants in FAN1, located in 15q13.3, confer risk for schizophrenia and bipolar disorder in Han Chinese.
Xuemin Jian, Jianhua Chen, Zhiqiang Li, Aamir Fahira, Weihuan Shao, Juan Zhou, Ke Wang, Yanqin Wen, Jinmai Zhang, Qiangzhen Yang,[...]. Prog Neuropsychopharmacol Biol Psychiatry 2020
1

Interactive effects between hemizygous 15q13.3 microdeletion and peripubertal stress on adult behavioral functions.
Sandra Giovanoli, Thomas M Werge, Preben B Mortensen, Michael Didriksen, Urs Meyer. Neuropsychopharmacology 2019
6

Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase Gene.
J Alexander Bodkin, Michael J Coleman, Laura J Godfrey, Claudia M B Carvalho, Charity J Morgan, Raymond F Suckow, Thea Anderson, Dost Öngür, Marc J Kaufman, Kathryn E Lewandowski,[...]. Biol Psychiatry 2019
15