A citation-based method for searching scientific literature


List of co-cited articles
55 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Analysis of shared heritability in common disorders of the brain.
Verneri Anttila, Brendan Bulik-Sullivan, Hilary K Finucane, Raymond K Walters, Jose Bras, Laramie Duncan, Valentina Escott-Price, Guido J Falcone, Padhraig Gormley, Rainer Malik,[...]. Science 2018
759
75

An atlas of genetic correlations across human diseases and traits.
Brendan Bulik-Sullivan, Hilary K Finucane, Verneri Anttila, Alexander Gusev, Felix R Day, Po-Ru Loh, Laramie Duncan, John R B Perry, Nick Patterson, Elise B Robinson,[...]. Nat Genet 2015
62


LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale. Nat Genet 2015
62


Genome-wide association study identifies 30 loci associated with bipolar disorder.
Eli A Stahl, Gerome Breen, Andreas J Forstner, Andrew McQuillin, Stephan Ripke, Vassily Trubetskoy, Manuel Mattheisen, Yunpeng Wang, Jonathan R I Coleman, Héléna A Gaspar,[...]. Nat Genet 2019
546
50

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
124
50

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Naomi R Wray, Stephan Ripke, Manuel Mattheisen, Maciej Trzaskowski, Enda M Byrne, Abdel Abdellaoui, Mark J Adams, Esben Agerbo, Tracy M Air, Till M F Andlauer,[...]. Nat Genet 2018
50

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study.
Paul Lichtenstein, Benjamin H Yip, Camilla Björk, Yudi Pawitan, Tyrone D Cannon, Patrick F Sullivan, Christina M Hultman. Lancet 2009
37


Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits.
Andrew D Grotzinger, Mijke Rhemtulla, Ronald de Vlaming, Stuart J Ritchie, Travis T Mallard, W David Hill, Hill F Ip, Riccardo E Marioni, Andrew M McIntosh, Ian J Deary,[...]. Nat Hum Behav 2019
157
37

Genetic correlations of polygenic disease traits: from theory to practice.
Wouter van Rheenen, Wouter J Peyrot, Andrew J Schork, S Hong Lee, Naomi R Wray. Nat Rev Genet 2019
82
37

A global overview of pleiotropy and genetic architecture in complex traits.
Kyoko Watanabe, Sven Stringer, Oleksandr Frei, Maša Umićević Mirkov, Christiaan de Leeuw, Tinca J C Polderman, Sophie van der Sluis, Ole A Andreassen, Benjamin M Neale, Danielle Posthuma. Nat Genet 2019
256
37

Meta-analysis of the heritability of human traits based on fifty years of twin studies.
Tinca J C Polderman, Beben Benyamin, Christiaan A de Leeuw, Patrick F Sullivan, Arjen van Bochoven, Peter M Visscher, Danielle Posthuma. Nat Genet 2015
744
37

Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.
David M Howard, Mark J Adams, Toni-Kim Clarke, Jonathan D Hafferty, Jude Gibson, Masoud Shirali, Jonathan R I Coleman, Saskia P Hagenaars, Joey Ward, Eleanor M Wigmore,[...]. Nat Neurosci 2019
522
37

Psychiatric Genomics: An Update and an Agenda.
Patrick F Sullivan, Arpana Agrawal, Cynthia M Bulik, Ole A Andreassen, Anders D Børglum, Gerome Breen, Sven Cichon, Howard J Edenberg, Stephen V Faraone, Joel Gelernter,[...]. Am J Psychiatry 2018
234
25

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.
Michael J Gandal, Jillian R Haney, Neelroop N Parikshak, Virpi Leppa, Gokul Ramaswami, Chris Hartl, Andrew J Schork, Vivek Appadurai, Alfonso Buil, Thomas M Werge,[...]. Science 2018
448
25

Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders.
Min-Tzu Lo, David A Hinds, Joyce Y Tung, Carol Franz, Chun-Chieh Fan, Yunpeng Wang, Olav B Smeland, Andrew Schork, Dominic Holland, Karolina Kauppi,[...]. Nat Genet 2017
158
25

The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
488
25

The road to precision psychiatry: translating genetics into disease mechanisms.
Michael J Gandal, Virpi Leppa, Hyejung Won, Neelroop N Parikshak, Daniel H Geschwind. Nat Neurosci 2016
117
25

The Hierarchical Taxonomy of Psychopathology (HiTOP): A dimensional alternative to traditional nosologies.
Roman Kotov, Robert F Krueger, David Watson, Thomas M Achenbach, Robert R Althoff, R Michael Bagby, Timothy A Brown, William T Carpenter, Avshalom Caspi, Lee Anna Clark,[...]. J Abnorm Psychol 2017
758
25

Research review: Polygenic methods and their application to psychiatric traits.
Naomi R Wray, Sang Hong Lee, Divya Mehta, Anna A E Vinkhuyzen, Frank Dudbridge, Christel M Middeldorp. J Child Psychol Psychiatry 2014
345
25

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
S Hong Lee, Stephan Ripke, Benjamin M Neale, Stephen V Faraone, Shaun M Purcell, Roy H Perlis, Bryan J Mowry, Anita Thapar, Michael E Goddard, John S Witte,[...]. Nat Genet 2013
25

Diagnostic shifts during the decade following first admission for psychosis.
Evelyn J Bromet, Roman Kotov, Laura J Fochtmann, Gabrielle A Carlson, Marsha Tanenberg-Karant, Camilo Ruggero, Su-wei Chang. Am J Psychiatry 2011
162
25

All for One and One for All: Mental Disorders in One Dimension.
Avshalom Caspi, Terrie E Moffitt. Am J Psychiatry 2018
251
25


Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.
Jackson G Thorp, Andries T Marees, Jue-Sheng Ong, Jiyuan An, Stuart MacGregor, Eske M Derks. Psychol Med 2020
13
25

Polygenic dissection of major depression clinical heterogeneity.
Y Milaneschi, F Lamers, W J Peyrot, A Abdellaoui, G Willemsen, J-J Hottenga, R Jansen, H Mbarek, A Dehghan, C Lu,[...]. Mol Psychiatry 2016
111
25

The structure of genetic and environmental risk factors for syndromal and subsyndromal common DSM-IV axis I and all axis II disorders.
Kenneth S Kendler, Steven H Aggen, Gun Peggy Knudsen, Espen Røysamb, Michael C Neale, Ted Reichborn-Kjennerud. Am J Psychiatry 2011
235
25

Common disorders are quantitative traits.
Robert Plomin, Claire M A Haworth, Oliver S P Davis. Nat Rev Genet 2009
446
25

The heritability of bipolar affective disorder and the genetic relationship to unipolar depression.
Peter McGuffin, Fruhling Rijsdijk, Martin Andrew, Pak Sham, Randy Katz, Alastair Cardno. Arch Gen Psychiatry 2003
757
25

Disorders and borders: psychiatric genetics and nosology.
Jordan W Smoller. Am J Med Genet B Neuropsychiatr Genet 2013
34
25

Causal associations between risk factors and common diseases inferred from GWAS summary data.
Zhihong Zhu, Zhili Zheng, Futao Zhang, Yang Wu, Maciej Trzaskowski, Robert Maier, Matthew R Robinson, John J McGrath, Peter M Visscher, Naomi R Wray,[...]. Nat Commun 2018
289
25



Bivariate causal mixture model quantifies polygenic overlap between complex traits beyond genetic correlation.
Oleksandr Frei, Dominic Holland, Olav B Smeland, Alexey A Shadrin, Chun Chieh Fan, Steffen Maeland, Kevin S O'Connell, Yunpeng Wang, Srdjan Djurovic, Wesley K Thompson,[...]. Nat Commun 2019
59
25

Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems.
Amanda B Zheutlin, Jessica Dennis, Richard Karlsson Linnér, Arden Moscati, Nicole Restrepo, Peter Straub, Douglas Ruderfer, Victor M Castro, Chia-Yen Chen, Tian Ge,[...]. Am J Psychiatry 2019
60
25

Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders.
Enda M Byrne, Zhihong Zhu, Ting Qi, Nathan G Skene, Julien Bryois, Antonio F Pardinas, Eli Stahl, Jordan W Smoller, Marcella Rietschel, Michael J Owen,[...]. Mol Psychiatry 2021
19
25


Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.
Hunna J Watson, Zeynep Yilmaz, Laura M Thornton, Christopher Hübel, Jonathan R I Coleman, Héléna A Gaspar, Julien Bryois, Anke Hinney, Virpi M Leppä, Manuel Mattheisen,[...]. Nat Genet 2019
256
25

From genome-wide associations to candidate causal variants by statistical fine-mapping.
Daniel J Schaid, Wenan Chen, Nicholas B Larson. Nat Rev Genet 2018
234
25

Comparison of Sociodemographic and Health-Related Characteristics of UK Biobank Participants With Those of the General Population.
Anna Fry, Thomas J Littlejohns, Cathie Sudlow, Nicola Doherty, Ligia Adamska, Tim Sprosen, Rory Collins, Naomi E Allen. Am J Epidemiol 2017
821
25

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders.
Raymond K Walters, Renato Polimanti, Emma C Johnson, Jeanette N McClintick, Mark J Adams, Amy E Adkins, Fazil Aliev, Silviu-Alin Bacanu, Anthony Batzler, Sarah Bertelsen,[...]. Nat Neurosci 2018
214
25

Genomics of body fat percentage may contribute to sex bias in anorexia nervosa.
Christopher Hübel, Héléna A Gaspar, Jonathan R I Coleman, Hilary Finucane, Kirstin L Purves, Ken B Hanscombe, Inga Prokopenko, Mariaelisa Graff, Julius S Ngwa, Tsegaselassie Workalemahu,[...]. Am J Med Genet B Neuropsychiatr Genet 2019
37
25

Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
607
25

Genome-wide association study identifies 74 loci associated with educational attainment.
Aysu Okbay, Jonathan P Beauchamp, Mark Alan Fontana, James J Lee, Tune H Pers, Cornelius A Rietveld, Patrick Turley, Guo-Bo Chen, Valur Emilsson, S Fleur W Meddens,[...]. Nature 2016
570
25

10 Years of GWAS Discovery: Biology, Function, and Translation.
Peter M Visscher, Naomi R Wray, Qian Zhang, Pamela Sklar, Mark I McCarthy, Matthew A Brown, Jian Yang. Am J Hum Genet 2017
25

Family, twin, and adoption studies of bipolar disorder.
Jordan W Smoller, Christine T Finn. Am J Med Genet C Semin Med Genet 2003
410
25

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Ditte Demontis, Raymond K Walters, Joanna Martin, Manuel Mattheisen, Thomas D Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen,[...]. Nat Genet 2019
668
25

Genetic epidemiology of major depression: review and meta-analysis.
P F Sullivan, M C Neale, K S Kendler. Am J Psychiatry 2000
25


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.