A citation-based method for searching scientific literature

Tanner Koomar, Jacob J Michaelson. Curr Psychiatry Rep 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Effect of CACNA1C rs1006737 on neural correlates of verbal fluency in healthy individuals.
Axel Krug, Vanessa Nieratschker, Valentin Markov, Sören Krach, Andreas Jansen, Klaus Zerres, Thomas Eggermann, Tony Stöcker, N Jon Shah, Jens Treutlein,[...]. Neuroimage 2010
87
66

Data quality control in genetic case-control association studies.
Carl A Anderson, Fredrik H Pettersson, Geraldine M Clarke, Lon R Cardon, Andrew P Morris, Krina T Zondervan. Nat Protoc 2010
622
66

Functional mapping and annotation of genetic associations with FUMA.
Kyoko Watanabe, Erdogan Taskesen, Arjen van Bochoven, Danielle Posthuma. Nat Commun 2017
748
66

METAL: fast and efficient meta-analysis of genomewide association scans.
Cristen J Willer, Yun Li, Gonçalo R Abecasis. Bioinformatics 2010
66

First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.
D Roeske, K U Ludwig, N Neuhoff, J Becker, J Bartling, J Bruder, F F Brockschmidt, A Warnke, H Remschmidt, P Hoffmann,[...]. Mol Psychiatry 2011
68
33

Robust relationship inference in genome-wide association studies.
Ani Manichaikul, Josyf C Mychaleckyj, Stephen S Rich, Kathy Daly, Michèle Sale, Wei-Min Chen. Bioinformatics 2010
925
33

Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100 Canadian families.
Jordana Tzenova, Bonnie J Kaplan, Tracey L Petryshen, L Leigh Field. Am J Med Genet B Neuropsychiatr Genet 2004
50
33

KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia.
Sara Mascheretti, Valentina Riva, Roberto Giorda, Silvana Beri, Lara Francesca Emilia Lanzoni, Maria Rosaria Cellino, Cecilia Marino. J Hum Genet 2014
34
33

Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors.
T Kidd, K Brose, K J Mitchell, R D Fetter, M Tessier-Lavigne, C S Goodman, G Tear. Cell 1998
688
33

The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant.
David A Koolen, Rolph Pfundt, Katrin Linda, Gea Beunders, Hermine E Veenstra-Knol, Jessie H Conta, Ana Maria Fortuna, Gabriele Gillessen-Kaesbach, Sarah Dugan, Sara Halbach,[...]. Eur J Hum Genet 2016
47
33


Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15.
E L Grigorenko, F B Wood, M S Meyer, L A Hart, W C Speed, A Shuster, D L Pauls. Am J Hum Genet 1997
308
33

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.
Natalie Cope, Denise Harold, Gary Hill, Valentina Moskvina, Jim Stevenson, Peter Holmans, Michael J Owen, Michael C O'Donovan, Julie Williams. Am J Hum Genet 2005
202
33

Whole-genome association study of bipolar disorder.
P Sklar, J W Smoller, J Fan, M A R Ferreira, R H Perlis, K Chambert, V L Nimgaonkar, M B McQueen, S V Faraone, A Kirby,[...]. Mol Psychiatry 2008
499
33


Modelling schizophrenia using human induced pluripotent stem cells.
Kristen J Brennand, Anthony Simone, Jessica Jou, Chelsea Gelboin-Burkhart, Ngoc Tran, Sarah Sangar, Yan Li, Yangling Mu, Gong Chen, Diana Yu,[...]. Nature 2011
877
33

The neurogenetics of alternative splicing.
Celine K Vuong, Douglas L Black, Sika Zheng. Nat Rev Neurosci 2016
136
33

The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort.
E B Robinson, A Kirby, K Ruparel, J Yang, L McGrath, V Anttila, B M Neale, K Merikangas, T Lehner, P M A Sleiman,[...]. Mol Psychiatry 2015
27
33

Relations among speech, language, and reading disorders.
Bruce F Pennington, Dorothy V M Bishop. Annu Rev Psychol 2009
256
33



Ontario Child Health Study: correlates of disorder.
D R Offord, M H Boyle, Y Racine. J Am Acad Child Adolesc Psychiatry 1989
168
33


Positive association between GRIN2B gene and bipolar disorder in the Chinese Han Population.
Qian Zhao, Ronglin Che, Zhao Zhang, Peng Wang, Jun Li, You Li, Ke Huang, Wei Tang, Guoyin Feng, Klaus Lindpaintner,[...]. Psychiatry Res 2011
19
33


Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development.
Nanako Hamada, Hidenori Ito, Takuma Nishijo, Ikuko Iwamoto, Rika Morishita, Hidenori Tabata, Toshihiko Momiyama, Koh-Ichi Nagata. Sci Rep 2016
34
33


Suggestive linkage of developmental dyslexia to chromosome 1p34-p36.
M Rabin, X L Wen, M Hepburn, H A Lubs, E Feldman, R Duara. Lancet 1993
111
33


SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.
Hans Matsson, Kristiina Tammimies, Marco Zucchelli, Heidi Anthoni, Päivi Onkamo, Jaana Nopola-Hemmi, Heikki Lyytinen, Paavo H T Leppanen, Nina Neuhoff, Andreas Warnke,[...]. Behav Genet 2011
20
33

Dyslexia-associated kiaa0319-like protein interacts with axon guidance receptor nogo receptor 1.
Ming-Wai Poon, Wan-Hong Tsang, Sun-On Chan, Hiu-Ming Li, Ho-Keung Ng, Mary Miu-Yee Waye. Cell Mol Neurobiol 2011
21
33

Uncoupling of UNC5C with Polymerized TUBB3 in Microtubules Mediates Netrin-1 Repulsion.
Qiangqiang Shao, Tao Yang, Huai Huang, Farrah Alarmanazi, Guofa Liu. J Neurosci 2017
18
33

A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.
C Tran, F Gagnon, K G Wigg, Y Feng, L Gomez, T D Cate-Carter, E N Kerr, L L Field, B J Kaplan, M W Lovett,[...]. Am J Med Genet B Neuropsychiatr Genet 2013
12
33

A genome-wide association study for reading and language abilities in two population cohorts.
M Luciano, D M Evans, N K Hansell, S E Medland, G W Montgomery, N G Martin, M J Wright, T C Bates. Genes Brain Behav 2013
51
33

Within-individual variability in neurocognitive performance: age- and sex-related differences in children and youths from ages 8 to 21.
David R Roalf, Raquel E Gur, Kosha Ruparel, Monica E Calkins, Theodore D Satterthwaite, Warren B Bilker, Hakon Hakonarson, Lauren Julius Harris, Ruben C Gur. Neuropsychology 2014
54
33

Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis.
Kimm J E van Hulzen, Claus J Scholz, Barbara Franke, Stephan Ripke, Marieke Klein, Andrew McQuillin, Edmund J Sonuga-Barke, John R Kelsoe, Mikael Landén, Ole A Andreassen,[...]. Biol Psychiatry 2017
54
33

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
Gail Davies, Max Lam, Sarah E Harris, Joey W Trampush, Michelle Luciano, W David Hill, Saskia P Hagenaars, Stuart J Ritchie, Riccardo E Marioni, Chloe Fawns-Ritchie,[...]. Nat Commun 2018
192
33

Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults.
Franck Ramus, Stuart Rosen, Steven C Dakin, Brian L Day, Juan M Castellote, Sarah White, Uta Frith. Brain 2003
656
33

Evidence that dyslexia may represent the lower tail of a normal distribution of reading ability.
S E Shaywitz, M D Escobar, B A Shaywitz, J M Fletcher, R Makuch. N Engl J Med 1992
322
33

Reading disability: evidence for a genetic etiology.
J Gayán, R K Olson. Eur Child Adolesc Psychiatry 1999
26
33

Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia.
Deborah K Sokol, Meredith R Golomb, Karen S Carvalho, Mary Edwards-Brown. Neurology 2006
10
33

The human genome browser at UCSC.
W James Kent, Charles W Sugnet, Terrence S Furey, Krishna M Roskin, Tom H Pringle, Alan M Zahler, David Haussler. Genome Res 2002
33

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.
David J Hunter, Peter Kraft, Kevin B Jacobs, David G Cox, Meredith Yeager, Susan E Hankinson, Sholom Wacholder, Zhaoming Wang, Robert Welch, Amy Hutchinson,[...]. Nat Genet 2007
33

De novo gene disruptions in children on the autistic spectrum.
Ivan Iossifov, Michael Ronemus, Dan Levy, Zihua Wang, Inessa Hakker, Julie Rosenbaum, Boris Yamrom, Yoon-Ha Lee, Giuseppe Narzisi, Anthony Leotta,[...]. Neuron 2012
916
33

Literacy difficulties and psychiatric disorders: evidence for comorbidity.
Julia M Carroll, Barbara Maughan, Robert Goodman, Howard Meltzer. J Child Psychol Psychiatry 2005
137
33

Individual common variants exert weak effects on the risk for autism spectrum disorders.
Richard Anney, Lambertus Klei, Dalila Pinto, Joana Almeida, Elena Bacchelli, Gillian Baird, Nadia Bolshakova, Sven Bölte, Patrick F Bolton, Thomas Bourgeron,[...]. Hum Mol Genet 2012
231
33


The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia.
Katariina Hannula-Jouppi, Nina Kaminen-Ahola, Mikko Taipale, Ranja Eklund, Jaana Nopola-Hemmi, Helena Kääriäinen, Juha Kere. PLoS Genet 2005
209
33

Differential genetic etiology of reading component processes as a function of IQ.
Valerie S Knopik, Shelley D Smith, Lon Cardon, Bruce Pennington, Javier Gayan, Richard K Olson, John C DeFries. Behav Genet 2002
24
33

Identification of NCAN as a candidate gene for developmental dyslexia.
Elisabet Einarsdottir, Myriam Peyrard-Janvid, Fahimeh Darki, Jetro J Tuulari, Harri Merisaari, Linnea Karlsson, Noora M Scheinin, Jani Saunavaara, Riitta Parkkola, Katri Kantojärvi,[...]. Sci Rep 2017
11
33


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.