A citation-based method for searching scientific literature

Manuel A R Ferreira, Michael C O'Donovan, Yan A Meng, Ian R Jones, Douglas M Ruderfer, Lisa Jones, Jinbo Fan, George Kirov, Roy H Perlis, Elaine K Green, Jordan W Smoller, Detelina Grozeva, Jennifer Stone, Ivan Nikolov, Kimberly Chambert, Marian L Hamshere, Vishwajit L Nimgaonkar, Valentina Moskvina, Michael E Thase, Sian Caesar, Gary S Sachs, Jennifer Franklin, Katherine Gordon-Smith, Kristin G Ardlie, Stacey B Gabriel, Christine Fraser, Brendan Blumenstiel, Matthew Defelice, Gerome Breen, Michael Gill, Derek W Morris, Amanda Elkin, Walter J Muir, Kevin A McGhee, Richard Williamson, Donald J MacIntyre, Alan W MacLean, Clair David St, Michelle Robinson, Margaret Van Beck, Ana C P Pereira, Radhika Kandaswamy, Andrew McQuillin, David A Collier, Nicholas J Bass, Allan H Young, Jacob Lawrence, I Nicol Ferrier, Adebayo Anjorin, Anne Farmer, David Curtis, Edward M Scolnick, Peter McGuffin, Mark J Daly, Aiden P Corvin, Peter A Holmans, Douglas H Blackwood, Hugh M Gurling, Michael J Owen, Shaun M Purcell, Pamela Sklar, Nick Craddock. Nat Genet 2008
Times Cited: 849



Douglas M Ruderfer, Ayman H Fanous, Stephan Ripke, Andrew McQuillin, Richard L Amdur, Pablo V Gejman, Michael C O'Donovan, Ole A Andreassen, Srdjan Djurovic, Christina M Hultman, John R Kelsoe, Stephane Jamain, Mikael Landén, Marion Leboyer, Vishwajit Nimgaonkar, John Nurnberger, Jordan W Smoller, Nick Craddock, Aiden Corvin, Patrick F Sullivan, Peter Holmans, Pamela Sklar, Kenneth S Kendler. Mol Psychiatry 2014
Times Cited: 214




List of shared articles



Times cited

Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder.
Ditte Demontis, Raymond K Walters, Veera M Rajagopal, Irwin D Waldman, Jakob Grove, Thomas D Als, Søren Dalsgaard, Marta Ribasés, Jonas Bybjerg-Grauholm, Maria Bækvad-Hansen,[...]. Nat Commun 2021
2

Genetic Intersections of Language and Neuropsychiatric Conditions.
Tanner Koomar, Jacob J Michaelson. Curr Psychiatry Rep 2020
3

Replicated risk CACNA1C variants for major psychiatric disorders may serve as potential therapeutic targets for the shared depressive endophenotype.
Xiaoyun Guo, Yingmei Fu, Yong Zhang, Tong Wang, Lu Lu, Xingqun Luo, Kesheng Wang, Juncao Huang, Ting Xie, Chengchou Zheng,[...]. J Neurosci Cogn Stud 2020
0

The genetics of bipolar disorder.
Francis James A Gordovez, Francis J McMahon. Mol Psychiatry 2020
31

Gene-set Enrichment with Mathematical Biology (GEMB).
Amy L Cochran, Kenneth J Nieser, Daniel B Forger, Sebastian Zöllner, Melvin G McInnis. Gigascience 2020
1

CACNA1C risk variant affects microstructural connectivity of the amygdala.
Katharina Koch, Sophia Stegmaier, Lena Schwarz, Michael Erb, Mara Thomas, Klaus Scheffler, Dirk Wildgruber, Vanessa Nieratschker, Thomas Ethofer. Neuroimage Clin 2019
0

Associations of schizophrenia risk genes ZNF804A and CACNA1C with schizotypy and modulation of attention in healthy subjects.
Tina Meller, Simon Schmitt, Frederike Stein, Katharina Brosch, Johannes Mosebach, Dilara Yüksel, Dario Zaremba, Dominik Grotegerd, Katharina Dohm, Susanne Meinert,[...]. Schizophr Res 2019
5

Aetiology of bipolar disorder: contribution of the L-type voltage-gated calcium channels.
Xiaoyun Guo, Dengtang Liu, Tong Wang, Xingguang Luo. Gen Psychiatr 2019
3

Association of SYNE1 locus with bipolar disorder in Chinese population.
Wenqiang Li, Yongfeng Yang, Binbin Luo, Yan Zhang, Xueqin Song, Ming Li, Luxian Lv. Hereditas 2019
2

GWAS of Behavioral Traits.
Divya Mehta, Darina Czamara. Curr Top Behav Neurosci 2019
0

A decade in psychiatric GWAS research.
Tanya Horwitz, Katie Lam, Yu Chen, Yan Xia, Chunyu Liu. Mol Psychiatry 2019
29