A citation-based method for searching scientific literature

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, Anjali Bhat, Richard Bruggeman, Wiepke Cahn, Stella Calafato, Benedicto Crespo-Facorro, Liewe de Haan, Sonja M C de Zwarte, Marta Di Forti, Álvaro Díez-Revuelta, Jeremy Hall, Mei-Hua Hall, Conrad Iyegbe, Assen Jablensky, Rene Kahn, Luba Kalaydjieva, Eugenia Kravariti, Stephen Lawrie, Jurjen J Luykx, Igancio Mata, Colm McDonald, Andrew M McIntosh, Andrew McQuillin, Rebecca Muir, Roel Ophoff, Marco Picchioni, Diana P Prata, Siri Ranlund, Dan Rujescu, Bart P F Rutten, Katja Schulze, Madiha Shaikh, Frederike Schirmbeck, Claudia J P Simons, Timothea Toulopoulou, Therese van Amelsvoort, Neeltje van Haren, Jim van Os, Ruud van Winkel, Evangelos Vassos, Muriel Walshe, Matthias Weisbrod, Eirini Zartaloudi, Vaughan Bell, John Powell, Cathryn M Lewis, Robin M Murray, Elvira Bramon. Mol Psychiatry 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.
Alexander Gusev, Nicholas Mancuso, Hyejung Won, Maria Kousi, Hilary K Finucane, Yakir Reshef, Lingyun Song, Alexias Safi, Steven McCarroll, Benjamin M Neale,[...]. Nat Genet 2018
144
50


Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
353
25

Alternative Applications of Genotyping Array Data Using Multivariant Methods.
David C Samuels, Jennifer E Below, Scott Ness, Hui Yu, Shuguang Leng, Yan Guo. Trends Genet 2020
2
50


An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations.
Paolo Guanciali-Franchi, Claudio Celentano, Melissa Alfonsi, Chiara Palka, Giulietta Di Pasqua, Barbara Matarrelli, Giandomenico Palka. Mol Syndromol 2017
1
100

Parallel detection of single nucleotide variants and copy number variants with exome analysis: Validation in a cohort of 700 undiagnosed patients.
Hisato Suzuki, Mamiko Yamada, Tomoko Uehara, Toshiki Takenouchi, Kenjiro Kosaki. Am J Med Genet A 2020
3
33

Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.
Lena Sagi-Dain, Lital Cohen Vig, Sarit Kahana, Shiri Yacobson, Tamar Tenne, Ifat Agmon-Fishman, Cochava Klein, Reut Matar, Lina Basel-Salmon, Idit Maya. Genet Med 2019
31
25

Copy number variation in schizophrenia in Sweden.
J P Szatkiewicz, C O'Dushlaine, G Chen, K Chambert, J L Moran, B M Neale, M Fromer, D Ruderfer, S Akterin, S E Bergen,[...]. Mol Psychiatry 2014
159
25

Exon-focused targeted oligonucleotide microarray design increases detection of clinically relevant variants across multiple NHS genomic centres.
Jana Jezkova, Jade Heath, Angharad Williams, Deborah Barrell, Jessica Norton, Morag N Collinson, Sarah J Beal, Sian Corrin, Sian Morgan. NPJ Genom Med 2020
1
100

The variability of genetic disease.
Han G Brunner. N Engl J Med 2012
6
25

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
632
25

Polymorphic variation of RPGRIP1L and IQCB1 as modifiers of X-linked retinitis pigmentosa caused by mutations in RPGR.
Abigail T Fahim, Sara J Bowne, Lori S Sullivan, Kaylie D Webb, Jessica T Williams, Dianna K Wheaton, David G Birch, Stephen P Daiger. Adv Exp Med Biol 2012
13
25

Rare or Overlooked? Structural Disruption of Regulatory Domains in Human Neurocristopathies.
Víctor Sánchez-Gaya, Maria Mariner-Faulí, Alvaro Rada-Iglesias. Front Genet 2020
4
25

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland,[...]. Genet Med 2020
136
25


Copy number variations and constitutional chromothripsis (Review).
Aldina Brás, António Sebastião Rodrigues, José Rueff. Biomed Rep 2020
3
33

Comparative proteomic approach in rat model of absence epilepsy.
Gönül Gürol, Duygu Özel Demiralp, Ayça Kasapoğlu Yılmaz, Özlem Akman, Nurbay Ateş, Ayşe Karson. J Mol Neurosci 2015
2
50

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.
Laura M Huckins, Amanda Dobbyn, Douglas M Ruderfer, Gabriel Hoffman, Weiqing Wang, Antonio F Pardiñas, Veera M Rajagopal, Thomas D Als, Hoang T Nguyen, Kiran Girdhar,[...]. Nat Genet 2019
64
25

Reevaluation of SNP heritability in complex human traits.
Doug Speed, Na Cai, Michael R Johnson, Sergey Nejentsev, David J Balding. Nat Genet 2017
175
25

Mismatch negativity and low frequency oscillations in schizophrenia families.
L Elliot Hong, Lauren V Moran, Xiaoming Du, Patricio O'Donnell, Ann Summerfelt. Clin Neurophysiol 2012
26
25


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
622
25

Differential contribution of frontal and temporal cortices to auditory change detection: fMRI and ERP results.
Bertram Opitz, Teemu Rinne, Axel Mecklinger, D Yves von Cramon, Erich Schröger. Neuroimage 2002
333
25

Screening of Methylation Signature and Gene Functions Associated With the Subtypes of Isocitrate Dehydrogenase-Mutation Gliomas.
XiaoYong Pan, Tao Zeng, Fei Yuan, Yu-Hang Zhang, Lei Chen, LiuCun Zhu, SiBao Wan, Tao Huang, Yu-Dong Cai. Front Bioeng Biotechnol 2019
6
25

Prediction of psychosis by mismatch negativity.
Mitja Bodatsch, Stephan Ruhrmann, Michael Wagner, Ralf Müller, Frauke Schultze-Lutter, Ingo Frommann, Jürgen Brinkmeyer, Wolfgang Gaebel, Wolfgang Maier, Joachim Klosterkötter,[...]. Biol Psychiatry 2011
189
25

Mismatch negativity: an index of a preattentive processing deficit in schizophrenia.
A M Shelley, P B Ward, S V Catts, P T Michie, S Andrews, N McConaghy. Biol Psychiatry 1991
321
25

The Bayesian brain: the role of uncertainty in neural coding and computation.
David C Knill, Alexandre Pouget. Trends Neurosci 2004
839
25

Knowing when to stop: Aberrant precision and evidence accumulation in schizophrenia.
Roberto Limongi, Bartosz Bohaterewicz, Magdalena Nowicka, Aleksandra Plewka, Karl J Friston. Schizophr Res 2018
11
25

GCTA: a tool for genome-wide complex trait analysis.
Jian Yang, S Hong Lee, Michael E Goddard, Peter M Visscher. Am J Hum Genet 2011
25

A reference panel of 64,976 haplotypes for genotype imputation.
Shane McCarthy, Sayantan Das, Warren Kretzschmar, Olivier Delaneau, Andrew R Wood, Alexander Teumer, Hyun Min Kang, Christian Fuchsberger, Petr Danecek, Kevin Sharp,[...]. Nat Genet 2016
969
25

The computational anatomy of psychosis.
Rick A Adams, Klaas Enno Stephan, Harriet R Brown, Christopher D Frith, Karl J Friston. Front Psychiatry 2013
336
25

Reference-based phasing using the Haplotype Reference Consortium panel.
Po-Ru Loh, Petr Danecek, Pier Francesco Palamara, Christian Fuchsberger, Yakir A Reshef, Hilary K Finucane, Sebastian Schoenherr, Lukas Forer, Shane McCarthy, Goncalo R Abecasis,[...]. Nat Genet 2016
443
25


A gene-based association method for mapping traits using reference transcriptome data.
Eric R Gamazon, Heather E Wheeler, Kaanan P Shah, Sahar V Mozaffari, Keston Aquino-Michaels, Robert J Carroll, Anne E Eyler, Joshua C Denny, Dan L Nicolae, Nancy J Cox,[...]. Nat Genet 2015
581
25

The mismatch negativity (MMN)--a unique window to disturbed central auditory processing in ageing and different clinical conditions.
R Näätänen, T Kujala, C Escera, T Baldeweg, K Kreegipuu, S Carlson, C Ponton. Clin Neurophysiol 2012
224
25

Mismatch Negativity in First-Episode Schizophrenia: A Meta-Analysis.
Sarah M Haigh, Brian A Coffman, Dean F Salisbury. Clin EEG Neurosci 2017
54
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

A qPCR expression assay of IFI44L gene differentiates viral from bacterial infections in febrile children.
Alberto Gómez-Carballa, Miriam Cebey-López, Jacobo Pardo-Seco, Ruth Barral-Arca, Irene Rivero-Calle, Sara Pischedda, María José Currás-Tuala, José Gómez-Rial, Francisco Barros, Federico Martinón-Torres,[...]. Sci Rep 2019
14
25

Evoker: a visualization tool for genotype intensity data.
James A Morris, Joshua C Randall, Julian B Maller, Jeffrey C Barrett. Bioinformatics 2010
23
25

Hallucinations both in and out of context: An active inference account.
David Benrimoh, Thomas Parr, Rick A Adams, Karl Friston. PLoS One 2019
7
25

Impaired prefrontal synaptic gain in people with psychosis and their relatives during the mismatch negativity.
Siri Ranlund, Rick A Adams, Álvaro Díez, Miguel Constante, Anirban Dutt, Mei-Hua Hall, Amparo Maestro Carbayo, Colm McDonald, Sabrina Petrella, Katja Schulze,[...]. Hum Brain Mapp 2016
31
25

Endophenotype best practices.
William G Iacono, Stephen M Malone, Scott I Vrieze. Int J Psychophysiol 2017
38
25



The mismatch negativity: a review of underlying mechanisms.
Marta I Garrido, James M Kilner, Klaas E Stephan, Karl J Friston. Clin Neurophysiol 2009
624
25

Multi-tissue transcriptome analyses identify genetic mechanisms underlying neuropsychiatric traits.
Eric R Gamazon, Aeilko H Zwinderman, Nancy J Cox, Damiaan Denys, Eske M Derks. Nat Genet 2019
33
25

Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues.
Heather E Wheeler, Kaanan P Shah, Jonathon Brenner, Tzintzuni Garcia, Keston Aquino-Michaels, Nancy J Cox, Dan L Nicolae, Hae Kyung Im. PLoS Genet 2016
70
25

Common SNPs explain a large proportion of the heritability for human height.
Jian Yang, Beben Benyamin, Brian P McEvoy, Scott Gordon, Anjali K Henders, Dale R Nyholt, Pamela A Madden, Andrew C Heath, Nicholas G Martin, Grant W Montgomery,[...]. Nat Genet 2010
25

Prefrontal cortex involvement in preattentive auditory deviance detection: neuroimaging and electrophysiological evidence.
Christian F Doeller, Bertram Opitz, Axel Mecklinger, Christoph Krick, Wolfgang Reith, Erich Schröger. Neuroimage 2003
233
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.