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: 1220







List of shared articles



Times cited


Clinical characterization of individuals with the distal 1q21.1 microdeletion.
Stacey D Edwards, Katharina V Schulze, Jill A Rosenfeld, Lauren E Westerfield, Amanda Gerard, Bo Yuan, Elena L Grigorenko, Jennifer E Posey, Weimin Bi, Pengfei Liu. Am J Med Genet A 2021
0


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

The genetic basis of major depression.
K M Kendall, E Van Assche, T F M Andlauer, K W Choi, J J Luykx, E C Schulte, Y Lu. Psychol Med 2021
1



Dysregulation of post-transcriptional modification by copy number variable microRNAs in schizophrenia with enhanced glycation stress.
Akane Yoshikawa, Itaru Kushima, Mitsuhiro Miyashita, Kazuya Toriumi, Kazuhiro Suzuki, Yasue Horiuchi, Hideya Kawaji, Shunya Takizawa, Norio Ozaki, Masanari Itokawa,[...]. Transl Psychiatry 2021
0

A study combining whole-exome sequencing and structural neuroimaging analysis for major depressive disorder.
Kyu-Man Han, Mi-Ryung Han, Aram Kim, Wooyoung Kang, Youbin Kang, June Kang, Woo-Suk Tae, Yunjung Cho, Byung-Joo Ham. J Affect Disord 2020
0

Chromosome 15q13.3 microduplications are associated with treatment refractory major depressive disorder.
Lora McClain, Anna M Segreti, Sharon Nau, Patricia Shaw, David N Finegold, Lisa A Pan, David G Peters. Genes Brain Behav 2020
0

Regulation of NMDA glutamate receptor functions by the GluN2 subunits.
Marta Vieira, Xuan Ling Hilary Yong, Katherine W Roche, Victor Anggono. J Neurochem 2020
17

Overdispersed gene expression in schizophrenia.
Guangzao Huang, Daniel Osorio, Jinting Guan, Guoli Ji, James J Cai. NPJ Schizophr 2020
2

Do Nicotinic Receptors Modulate High-Order Cognitive Processing?
Fani Koukouli, Jean-Pierre Changeux. Trends Neurosci 2020
5

Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
Tim B Bigdeli, Giulio Genovese, Penelope Georgakopoulos, Jacquelyn L Meyers, Roseann E Peterson, Conrad O Iyegbe, Helena Medeiros, Jorge Valderrama, Eric D Achtyes, Roman Kotov,[...]. Mol Psychiatry 2020
20

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
2

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

Disorders Associated With Diverse, Recurrent Deletions and Duplications at 1q21.1.
Hui Pang, Xiaowei Yu, Young Mi Kim, Xianfu Wang, Jeremy K Jinkins, Jianing Yin, Shibo Li, Hongcang Gu. Front Genet 2020
1


Copy number variant syndromes are frequent in schizophrenia: Progressing towards a CNV-schizophrenia model.
Venuja Sriretnakumar, Clement C Zai, Syed Wasim, Brianna Barsanti-Innes, James L Kennedy, Joyce So. Schizophr Res 2019
4

Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders.
Zhonghua Hu, Xiao Xiao, Zhuohua Zhang, Ming Li. Mol Psychiatry 2019
22

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

Psychiatric genetics and the structure of psychopathology.
Jordan W Smoller, Ole A Andreassen, Howard J Edenberg, Stephen V Faraone, Stephen J Glatt, Kenneth S Kendler. Mol Psychiatry 2019
89

Whole-exome sequencing identifies variants associated with structural MRI markers in patients with bipolar disorders.
Mi-Ryung Han, Kyu-Man Han, Aram Kim, Wooyoung Kang, Youbin Kang, June Kang, Eunsoo Won, Woo-Suk Tae, Yunjung Cho, Byung-Joo Ham. J Affect Disord 2019
8

Association of Rare Copy Number Variants With Risk of Depression.
Kimberley Marie Kendall, Elliott Rees, Matthew Bracher-Smith, Sophie Legge, Lucy Riglin, Stanley Zammit, Michael Conlon O'Donovan, Michael John Owen, Ian Jones, George Kirov,[...]. JAMA Psychiatry 2019
23

Endophenotypes in Schizophrenia: Digging Deeper to Identify Genetic Mechanisms.
Tiffany A Greenwood, Andrew Shutes-David, Debby W Tsuang. J Psychiatr Brain Sci 2019
8

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
7


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

An overview of medical risk factors for childhood psychosis: Implications for research and treatment.
Marianna Giannitelli, Angèle Consoli, Marie Raffin, Renaud Jardri, Douglas F Levinson, David Cohen, Claudine Laurent-Levinson. Schizophr Res 2018
14

The integrated landscape of causal genes and pathways in schizophrenia.
Changguo Ma, Chunjie Gu, Yongxia Huo, Xiaoyan Li, Xiong-Jian Luo. Transl Psychiatry 2018
23

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