A citation-based method for searching scientific literature

Bàrbara Torrico, Ester Antón-Galindo, Noèlia Fernàndez-Castillo, Eva Rojo-Francàs, Sadaf Ghorbani, Laura Pineda-Cirera, Amaia Hervás, Isabel Rueda, Estefanía Moreno, Janice M Fullerton, Vicent Casadó, Jan K Buitelaar, Nanda Rommelse, Barbara Franke, Andreas Reif, Andreas G Chiocchetti, Christine Freitag, Rune Kleppe, Jan Haavik, Claudio Toma, Bru Cormand. J Clin Med 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity



A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system.
S Sasaki, A Shionoya, M Ishida, M J Gambello, J Yingling, A Wynshaw-Boris, S Hirotsune. Neuron 2000
409
50


Modulators of 14-3-3 Protein-Protein Interactions.
Loes M Stevers, Eline Sijbesma, Maurizio Botta, Carol MacKintosh, Tomas Obsil, Isabelle Landrieu, Ylenia Cau, Andrew J Wilson, Anna Karawajczyk, Jan Eickhoff,[...]. J Med Chem 2018
96
50

NUDEL is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein.
M Niethammer, D S Smith, R Ayala, J Peng, J Ko, M S Lee, M Morabito, L H Tsai. Neuron 2000
398
50

14-3-3-affinity purification of over 200 human phosphoproteins reveals new links to regulation of cellular metabolism, proliferation and trafficking.
Mercedes Pozuelo Rubio, Kathryn M Geraghty, Barry H C Wong, Nicola T Wood, David G Campbell, Nick Morrice, Carol Mackintosh. Biochem J 2004
355
50

14-3-3 proteins: a historic overview.
Alastair Aitken. Semin Cancer Biol 2006
575
50

Identification of YWHAE, a gene encoding 14-3-3epsilon, as a possible susceptibility gene for schizophrenia.
Masashi Ikeda, Takao Hikita, Shinichiro Taya, Junko Uraguchi-Asaki, Kazuhito Toyo-oka, Anthony Wynshaw-Boris, Hiroshi Ujike, Toshiya Inada, Keizo Takao, Tsuyoshi Miyakawa,[...]. Hum Mol Genet 2008
75
50

Inhibition of 14-3-3 Proteins Leads to Schizophrenia-Related Behavioral Phenotypes and Synaptic Defects in Mice.
Molly Foote, Haifa Qiao, Kourtney Graham, Yuying Wu, Yi Zhou. Biol Psychiatry 2015
35
50

14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome.
Kazuhito Toyo-oka, Aki Shionoya, Michael J Gambello, Carlos Cardoso, Richard Leventer, Heather L Ward, Ramses Ayala, Li-Huei Tsai, William Dobyns, David Ledbetter,[...]. Nat Genet 2003
296
50

Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.
Zafar Iqbal, Geert Vandeweyer, Monique van der Voet, Ali Muhammad Waryah, Muhammad Yasir Zahoor, Judith A Besseling, Laura Tomas Roca, Anneke T Vulto-van Silfhout, Bonnie Nijhof, Jamie M Kramer,[...]. Hum Mol Genet 2013
99
25

A rare missense variant in RCL1 segregates with depression in extended families.
N Amin, F M S de Vrij, M Baghdadi, R W W Brouwer, J G J van Rooij, O Jovanova, A G Uitterlinden, A Hofman, H L A Janssen, S Darwish Murad,[...]. Mol Psychiatry 2018
19
25

DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders.
Niamh M Ryan, Jayon Lihm, Melissa Kramer, Shane McCarthy, Stewart W Morris, Aleix Arnau-Soler, Gail Davies, Barbara Duff, Elena Ghiban, Caroline Hayward,[...]. Mol Psychiatry 2018
11
25

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
205
25

A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorder.
Kevin A Strauss, Sander Markx, Benjamin Georgi, Steven M Paul, Robert N Jinks, Toshinori Hoshi, Ann McDonald, Michael B First, Wencheng Liu, Abigail R Benkert,[...]. Hum Mol Genet 2014
32
25

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
56
25

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
858
25

Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes
Bàrbara Torrico, Alex D. Shaw, Roberto Mosca, Norma Vivó-Luque, Amaia Hervás, Noèlia Fernàndez-Castillo, Patrick Aloy, Mònica Bayés, Janice M. Fullerton, Bru Cormand,[...]. J Psychiatry Neurosci 2019
11
25

Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.
Liping Hou, Urs Heilbronner, Franziska Degenhardt, Mazda Adli, Kazufumi Akiyama, Nirmala Akula, Raffaella Ardau, Bárbara Arias, Lena Backlund, Claudio E M Banzato,[...]. Lancet 2016
163
25

Psychosis, Mood and Behavioral Disorders in Usher Syndrome: Review of the Literature.
Daniela Domanico, Serena Fragiotta, Alessandro Cutini, Pier Luigi Grenga, Enzo Maria Vingolo. Med Hypothesis Discov Innov Ophthalmol 2015
10
25



A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
25

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
57
25

Molecular Mechanisms of Bipolar Disorder: Progress Made and Future Challenges.
Yeni Kim, Renata Santos, Fred H Gage, Maria C Marchetto. Front Cell Neurosci 2017
44
25

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
25


Rediscovering the value of families for psychiatric genetics research.
David C Glahn, Vishwajit L Nimgaonkar, Henriette Raventós, Javier Contreras, Andrew M McIntosh, Pippa A Thomson, Assen Jablensky, Nina S McCarthy, Jac C Charlesworth, Nicholas B Blackburn,[...]. Mol Psychiatry 2019
27
25

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
25

Multiple rare inherited variants in a four generation schizophrenia family offer leads for complex mode of disease inheritance.
Jibin John, Upasana Bhattacharyya, Navneesh Yadav, Prachi Kukshal, Triptish Bhatia, V L Nimgaonkar, Smita N Deshpande, B K Thelma. Schizophr Res 2020
6
25

Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.
Y Liu, D H Blackwood, S Caesar, E J C de Geus, A Farmer, M A R Ferreira, I N Ferrier, C Fraser, K Gordon-Smith, E K Green,[...]. Mol Psychiatry 2011
125
25

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.
Gonçalo R Abecasis, Stacey S Cherny, William O Cookson, Lon R Cardon. Nat Genet 2002
25

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
25

Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal.
Mingyao Li, Michael Boehnke, Goncalo R Abecasis. Am J Hum Genet 2005
98
25

Common and rare variants of microRNA genes in autism spectrum disorders.
Claudio Toma, Bàrbara Torrico, Amaia Hervás, Marta Salgado, Isabel Rueda, Rafael Valdés-Mas, Jan K Buitelaar, Nanda Rommelse, Barbara Franke, Christine Freitag,[...]. World J Biol Psychiatry 2015
15
25

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
83
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
744
25

Dysregulation of miR-34a links neuronal development to genetic risk factors for bipolar disorder.
S Bavamian, N Mellios, J Lalonde, D M Fass, J Wang, S D Sheridan, J M Madison, Fen Zhou, E H Rueckert, D Barker,[...]. Mol Psychiatry 2015
87
25

In Vitro Modeling of the Bipolar Disorder and Schizophrenia Using Patient-Derived Induced Pluripotent Stem Cells with Copy Number Variations of PCDH15 and RELN.
Takaya Ishii, Mitsuru Ishikawa, Koki Fujimori, Takuji Maeda, Itaru Kushima, Yuko Arioka, Daisuke Mori, Yuhki Nakatake, Bun Yamagata, Shintaro Nio,[...]. eNeuro 2019
17
25

Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder.
Cristiana Cruceanu, Amirthagowri Ambalavanan, Dan Spiegelman, Julie Gauthier, Ronald G Lafrenière, Patrick A Dion, Martin Alda, Gustavo Turecki, Guy A Rouleau. Genome 2013
29
25

MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates.
Anne Guimier, George C Gabriel, Fanny Bajolle, Michael Tsang, Hui Liu, Aaron Noll, Molly Schwartz, Rajae El Malti, Laurie D Smith, Nikolai T Klena,[...]. Nat Genet 2015
46
25

Rare deleterious mutations are associated with disease in bipolar disorder families.
A R Rao, M Yourshaw, B Christensen, S F Nelson, B Kerner. Mol Psychiatry 2017
20
25


Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing.
Jordi Corominas, Marieke Klein, Tetyana Zayats, Olga Rivero, Georg C Ziegler, Marc Pauper, Kornelia Neveling, Geert Poelmans, Charline Jansch, Evgeniy Svirin,[...]. Mol Psychiatry 2020
8
25

Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes.
Abdul Noor, Anath C Lionel, Sarah Cohen-Woods, Narges Moghimi, James Rucker, Alanna Fennell, Bhooma Thiruvahindrapuram, Liana Kaufman, Bryan Degagne, John Wei,[...]. Am J Med Genet B Neuropsychiatr Genet 2014
48
25

Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders.
Marta Codina-Solà, Benjamín Rodríguez-Santiago, Aïda Homs, Javier Santoyo, Maria Rigau, Gemma Aznar-Laín, Miguel Del Campo, Blanca Gener, Elisabeth Gabau, María Pilar Botella,[...]. Mol Autism 2015
70
25

Gene-based segregation method for identifying rare variants in family-based sequencing studies.
Dandi Qiao, Christoph Lange, Nan M Laird, Sungho Won, Craig P Hersh, Jarrett Morrow, Brian D Hobbs, Sharon M Lutz, Ingo Ruczinski, Terri H Beaty,[...]. Genet Epidemiol 2017
9
25

Ankyrin-3 as a molecular marker of early-life stress and vulnerability to psychiatric disorders.
A Luoni, R Massart, V Nieratschker, Z Nemoda, G Blasi, M Gilles, S H Witt, M J Suderman, S J Suomi, A Porcelli,[...]. Transl Psychiatry 2016
16
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
148
25

Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder.
Timothy Hughes, Ida E Sønderby, Tatiana Polushina, Lars Hansson, Asbjørn Holmgren, Lavinia Athanasiu, Christian Melbø-Jørgensen, Sahar Hassani, Louise K Hoeffding, Stefan Herms,[...]. Transl Psychiatry 2018
8
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.