A citation-based method for searching scientific literature

Alexander W Charney, Eli A Stahl, Elaine K Green, Chia-Yen Chen, Jennifer L Moran, Kimberly Chambert, Richard A Belliveau, Liz Forty, Katherine Gordon-Smith, Phil H Lee, Evelyn J Bromet, Peter F Buckley, Michael A Escamilla, Ayman H Fanous, Laura J Fochtmann, Douglas S Lehrer, Dolores Malaspina, Stephen R Marder, Christopher P Morley, Humberto Nicolini, Diana O Perkins, Jeffrey J Rakofsky, Mark H Rapaport, Helena Medeiros, Janet L Sobell, Lena Backlund, Sarah E Bergen, Anders Juréus, Martin Schalling, Paul Lichtenstein, James A Knowles, Katherine E Burdick, Ian Jones, Lisa A Jones, Christina M Hultman, Roy Perlis, Shaun M Purcell, Steven A McCarroll, Carlos N Pato, Michele T Pato, Ariana Di Florio, Nick Craddock, Mikael Landén, Jordan W Smoller, Douglas M Ruderfer, Pamela Sklar. Biol Psychiatry 2019
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


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
408
72

Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder.
A W Charney, D M Ruderfer, E A Stahl, J L Moran, K Chambert, R A Belliveau, L Forty, K Gordon-Smith, A Di Florio, P H Lee,[...]. Transl Psychiatry 2017
79
54

Copy number variation in bipolar disorder.
E K Green, E Rees, J T R Walters, K-G Smith, L Forty, D Grozeva, J L Moran, P Sklar, S Ripke, K D Chambert,[...]. Mol Psychiatry 2016
92
54



Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
506
45

Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations.
M Kataoka, N Matoba, T Sawada, A-A Kazuno, M Ishiwata, K Fujii, K Matsuo, A Takata, T Kato. Mol Psychiatry 2016
57
45

Exome Sequencing of Familial Bipolar Disorder.
Fernando S Goes, Mehdi Pirooznia, Jennifer S Parla, Melissa Kramer, Elena Ghiban, Senem Mavruk, Yun-Ching Chen, Eric T Monson, Virginia L Willour, Rachel Karchin,[...]. JAMA Psychiatry 2016
54
36

An examination of multiple classes of rare variants in extended families with bipolar disorder.
Claudio Toma, Alex D Shaw, Richard J N Allcock, Anna Heath, Kerrie D Pierce, Philip B Mitchell, Peter R Schofield, Janice M Fullerton. Transl Psychiatry 2018
18
36

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
732
36

Rare variants in neuronal excitability genes influence risk for bipolar disorder.
Seth A Ament, Szabolcs Szelinger, Gustavo Glusman, Justin Ashworth, Liping Hou, Nirmala Akula, Tatyana Shekhtman, Judith A Badner, Mary E Brunkow, Denise E Mauldin,[...]. Proc Natl Acad Sci U S A 2015
93
36


Prevalence and correlates of bipolar spectrum disorder in the world mental health survey initiative.
Kathleen R Merikangas, Robert Jin, Jian-Ping He, Ronald C Kessler, Sing Lee, Nancy A Sampson, Maria Carmen Viana, Laura Helena Andrade, Chiyi Hu, Elie G Karam,[...]. Arch Gen Psychiatry 2011
36

Association Between Schizophrenia-Related Polygenic Liability and the Occurrence and Level of Mood-Incongruent Psychotic Symptoms in Bipolar Disorder.
Judith Allardyce, Ganna Leonenko, Marian Hamshere, Antonio F Pardiñas, Liz Forty, Sarah Knott, Katherine Gordon-Smith, David J Porteous, Caroline Haywood, Arianna Di Florio,[...]. JAMA Psychiatry 2018
44
36

Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.
D T Chen, X Jiang, N Akula, Y Y Shugart, J R Wendland, C J M Steele, L Kassem, J-H Park, N Chatterjee, S Jamain,[...]. Mol Psychiatry 2013
134
36

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
371
36

Family, twin, and adoption studies of bipolar disorder.
Jordan W Smoller, Christine T Finn. Am J Med Genet C Semin Med Genet 2003
396
36

Genome-wide association study reveals two new risk loci for bipolar disorder.
Thomas W Mühleisen, Markus Leber, Thomas G Schulze, Jana Strohmaier, Franziska Degenhardt, Jens Treutlein, Manuel Mattheisen, Andreas J Forstner, Johannes Schumacher, René Breuer,[...]. Nat Commun 2014
199
36

Genome-wide association study of bipolar disorder in European American and African American individuals.
E N Smith, C S Bloss, J A Badner, T Barrett, P L Belmonte, W Berrettini, W Byerley, W Coryell, D Craig, H J Edenberg,[...]. Mol Psychiatry 2009
258
36

Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.
Erin N Smith, Daniel L Koller, Corrie Panganiban, Szabolcs Szelinger, Peng Zhang, Judith A Badner, Thomas B Barrett, Wade H Berrettini, Cinnamon S Bloss, William Byerley,[...]. PLoS Genet 2011
52
36

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar. Nature 2009
36

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
209
36

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
398
36

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
601
27

The penetrance of copy number variations for schizophrenia and developmental delay.
George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran,[...]. Biol Psychiatry 2014
194
27

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
802
27

An Integrative Genomic Study Implicates the Postsynaptic Density in the Pathogenesis of Bipolar Disorder.
Nirmala Akula, Jens R Wendland, Kwang H Choi, Francis J McMahon. Neuropsychopharmacology 2016
20
27

Bipolar disorder.
Iria Grande, Michael Berk, Boris Birmaher, Eduard Vieta. Lancet 2016
526
27

Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.
Giulio Genovese, Menachem Fromer, Eli A Stahl, Douglas M Ruderfer, Kimberly Chambert, Mikael Landén, Jennifer L Moran, Shaun M Purcell, Pamela Sklar, Patrick F Sullivan,[...]. Nat Neurosci 2016
211
27


Searching for missing heritability: designing rare variant association studies.
Or Zuk, Stephen F Schaffner, Kaitlin Samocha, Ron Do, Eliana Hechter, Sekar Kathiresan, Mark J Daly, Benjamin M Neale, Shamil R Sunyaev, Eric S Lander. Proc Natl Acad Sci U S A 2014
338
27

Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
S E Bergen, C T O'Dushlaine, S Ripke, P H Lee, D M Ruderfer, S Akterin, J L Moran, K D Chambert, R E Handsaker, L Backlund,[...]. Mol Psychiatry 2012
156
27

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
27

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.
Sven Cichon, Thomas W Mühleisen, Franziska A Degenhardt, Manuel Mattheisen, Xavier Miró, Jana Strohmaier, Michael Steffens, Christian Meesters, Stefan Herms, Moritz Weingarten,[...]. Am J Hum Genet 2011
191
27

High frequencies of de novo CNVs in bipolar disorder and schizophrenia.
Dheeraj Malhotra, Shane McCarthy, Jacob J Michaelson, Vladimir Vacic, Katherine E Burdick, Seungtai Yoon, Sven Cichon, Aiden Corvin, Sydney Gary, Elliot S Gershon,[...]. Neuron 2011
199
27

An Expanded View of Complex Traits: From Polygenic to Omnigenic.
Evan A Boyle, Yang I Li, Jonathan K Pritchard. Cell 2017
956
27

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
Liping Hou, Sarah E Bergen, Nirmala Akula, Jie Song, Christina M Hultman, Mikael Landén, Mazda Adli, Martin Alda, Raffaella Ardau, Bárbara Arias,[...]. Hum Mol Genet 2016
88
27

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.
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,[...]. Nat Genet 2008
845
27

A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder.
M Ikeda, A Takahashi, Y Kamatani, Y Okahisa, H Kunugi, N Mori, T Sasaki, T Ohmori, Y Okamoto, H Kawasaki,[...]. Mol Psychiatry 2018
70
27

Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia.
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,[...]. Mol Psychiatry 2014
209
27

High concordance of bipolar I disorder in a nationwide sample of twins.
Tuula Kieseppä, Timo Partonen, Jari Haukka, Jaakko Kaprio, Jouko Lönnqvist. Am J Psychiatry 2004
253
27

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
847
27

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
27

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum.
Andrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, Indraniel Das, Mitja I Kurki, Claire Churchhouse, Jessica Alfoldi, Alicia R Martin, Aki S Havulinna, Andrea Byrnes,[...]. Am J Hum Genet 2018
39
27

A family study of schizoaffective, bipolar I, bipolar II, unipolar, and normal control probands.
E S Gershon, J Hamovit, J J Guroff, E Dibble, J F Leckman, W Sceery, S D Targum, J I Nurnberger, L R Goldin, W E Bunney. Arch Gen Psychiatry 1982
759
18


De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
G Kirov, A J Pocklington, P Holmans, D Ivanov, M Ikeda, D Ruderfer, J Moran, K Chambert, D Toncheva, L Georgieva,[...]. Mol Psychiatry 2012
515
18

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
18


Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate.
Benjamin Georgi, David Craig, Rachel L Kember, Wencheng Liu, Ingrid Lindquist, Sara Nasser, Christopher Brown, Janice A Egeland, Steven M Paul, Maja Bućan. PLoS Genet 2014
54
18


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.