A citation-based method for searching scientific literature

Alessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, Kristina Moll, Jessica Becker, Per Hoffmann, Kerstin U Ludwig, Darina Czamara, Beate St Pourcain, Ferenc Honbolygó, Dénes Tóth, Valéria Csépe, Guillaume Huguet, Yves Chaix, Stephanie Iannuzzi, Jean-Francois Demonet, Andrew P Morris, Jacqueline Hulslander, Erik G Willcutt, John C DeFries, Richard K Olson, Shelley D Smith, Bruce F Pennington, Anniek Vaessen, Urs Maurer, Heikki Lyytinen, Myriam Peyrard-Janvid, Paavo H T Leppänen, Daniel Brandeis, Milene Bonte, John F Stein, Joel B Talcott, Fabien Fauchereau, Arndt Wilcke, Holger Kirsten, Bent Müller, Clyde Francks, Thomas Bourgeron, Anthony P Monaco, Franck Ramus, Karin Landerl, Juha Kere, Thomas S Scerri, Silvia Paracchini, Simon E Fisher, Johannes Schumacher, Markus M Nöthen, Bertram Müller-Myhsok, Gerd Schulte-Körne. Mol Psychiatry 2020
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Alessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, Kristina Moll, Jessica Becker, Per Hoffmann, Kerstin U Ludwig, Darina Czamara, Beate St Pourcain, William Brandler,[...]. Transl Psychiatry 2019
26
80

Developmental dyslexia.
Robin L Peterson, Bruce F Pennington. Annu Rev Clin Psychol 2015
147
50

Genome-wide screening for DNA variants associated with reading and language traits.
A Gialluisi, D F Newbury, E G Wilcutt, R K Olson, J C DeFries, W M Brandler, B F Pennington, S D Smith, T S Scerri, N H Simpson,[...]. Genes Brain Behav 2014
58
50

Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth.
Dongnhu Thuy Truong, Andrew Kenneth Adams, Steven Paniagua, Jan C Frijters, Richard Boada, Dina E Hill, Maureen W Lovett, E Mark Mahone, Erik G Willcutt, Maryanne Wolf,[...]. J Med Genet 2019
7
57

Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms.
S Mascheretti, A De Luca, V Trezzi, D Peruzzo, A Nordio, C Marino, F Arrigoni. Transl Psychiatry 2017
41
40

Developmental dyslexia.
Robin L Peterson, Bruce F Pennington. Lancet 2012
239
40

Generalist genes and learning disabilities.
Robert Plomin, Yulia Kovas. Psychol Bull 2005
262
30

Dyslexia: a deficit in visuo-spatial attention, not in phonological processing.
Trichur R Vidyasagar, Kristen Pammer. Trends Cogn Sci 2010
291
30


An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes.
S Mascheretti, A Bureau, M Battaglia, D Simone, E Quadrelli, J Croteau, M R Cellino, R Giorda, S Beri, M Maziade,[...]. Genes Brain Behav 2013
31
30

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
206
30

Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language.
Ellen Verhoef, Ditte Demontis, Stephen Burgess, Chin Yang Shapland, Philip S Dale, Aysu Okbay, Benjamin M Neale, Stephen V Faraone, Evie Stergiakouli, George Davey Smith,[...]. Transl Psychiatry 2019
12
30

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
49
30

Genome-wide association study of shared components of reading disability and language impairment.
J D Eicher, N R Powers, L L Miller, N Akshoomoff, D G Amaral, C S Bloss, O Libiger, N J Schork, B F Darst, B J Casey,[...]. Genes Brain Behav 2013
53
30


Genetic influences on reading difficulties in boys and girls: the Colorado twin study.
Jesse L Hawke, Sally J Wadsworth, John C DeFries. Dyslexia 2006
24
20




Genetic and environmental influences on writing and their relations to language and reading.
Richard K Olson, Jacqueline Hulslander, Micaela Christopher, Janice M Keenan, Sally J Wadsworth, Erik G Willcutt, Bruce F Pennington, John C DeFries. Ann Dyslexia 2013
17
20

Heritability of non-speech auditory processing skills.
Carmen C Brewer, Christopher K Zalewski, Kelly A King, Oliver Zobay, Alison Riley, Melanie A Ferguson, Jonathan E Bird, Margaret M McCabe, Linda J Hood, Dennis Drayna,[...]. Eur J Hum Genet 2016
13
20


Genetic influences on early word recognition abilities and disabilities: a study of 7-year-old twins.
Nicole Harlaar, Frank M Spinath, Philip S Dale, Robert Plomin. J Child Psychol Psychiatry 2005
100
20

Specific reading disability (dyslexia): what have we learned in the past four decades?
Frank R Vellutino, Jack M Fletcher, Margaret J Snowling, Donna M Scanlon. J Child Psychol Psychiatry 2004
863
20

Reading skills in early readers: genetic and shared environmental influences.
Stephen A Petrill, Kirby Deater-Deckard, Lee Anne Thompson, Laura S Dethorne, Christopher Schatschneider. J Learn Disabil 2006
84
20


Strong motion deficits in dyslexia associated with DCDC2 gene alteration.
Guido Marco Cicchini, Cecilia Marino, Sara Mascheretti, Daniela Perani, Maria Concetta Morrone. J Neurosci 2015
22
20

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
32
20

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
682
20

Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure.
Fahimeh Darki, Myriam Peyrard-Janvid, Hans Matsson, Juha Kere, Torkel Klingberg. Biol Psychiatry 2012
103
20

From BDNF to reading: Neural activation and phonological processing as multiple mediators.
Sara Mascheretti, Meaghan V Perdue, Bei Feng, Chiara Andreola, Ginette Dionne, Kaja K Jasińska, Kenneth R Pugh, Elena L Grigorenko, Nicole Landi. Behav Brain Res 2021
3
66



Association of short-term memory with a variant within DYX1C1 in developmental dyslexia.
C Marino, A Citterio, R Giorda, A Facoetti, G Menozzi, L Vanzin, M L Lorusso, M Nobile, M Molteni. Genes Brain Behav 2007
59
20


A causal link between visual spatial attention and reading acquisition.
Sandro Franceschini, Simone Gori, Milena Ruffino, Katia Pedrolli, Andrea Facoetti. Curr Biol 2012
223
20

Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.
Cecilia Marino, Sara Mascheretti, Valentina Riva, Francesca Cattaneo, Catia Rigoletto, Marianna Rusconi, Jeffrey R Gruen, Roberto Giorda, Claudio Lazazzera, Massimo Molteni. Behav Genet 2011
24
20

GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia.
Sara Mascheretti, Andrea Facoetti, Roberto Giorda, Silvana Beri, Valentina Riva, Vittoria Trezzi, Maria R Cellino, Cecilia Marino. Psychiatr Genet 2015
18
20


Multiple Causal Links Between Magnocellular-Dorsal Pathway Deficit and Developmental Dyslexia.
Simone Gori, Aaron R Seitz, Luca Ronconi, Sandro Franceschini, Andrea Facoetti. Cereb Cortex 2016
75
20


Support for EKN1 as the susceptibility locus for dyslexia on 15q21.
K G Wigg, J M Couto, Y Feng, B Anderson, T D Cate-Carter, F Macciardi, R Tannock, M W Lovett, T W Humphries, C L Barr. Mol Psychiatry 2004
87
20

Action video games make dyslexic children read better.
Sandro Franceschini, Simone Gori, Milena Ruffino, Simona Viola, Massimo Molteni, Andrea Facoetti. Curr Biol 2013
171
20

Developmental dyslexia: genetic dissection of a complex cognitive trait.
Simon E Fisher, John C DeFries. Nat Rev Neurosci 2002
188
20

Coherent motion sensitivity and reading development in the transition from prereading to reading stage.
Bart Boets, Maaike Vandermosten, Piers Cornelissen, Jan Wouters, Pol Ghesquière. Child Dev 2011
45
20

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
Jessica Becker, Darina Czamara, Tom S Scerri, Franck Ramus, Valéria Csépe, Joel B Talcott, John Stein, Andrew Morris, Kerstin U Ludwig, Per Hoffmann,[...]. Eur J Hum Genet 2014
37
20


DCDC2 genetic variants and susceptibility to developmental dyslexia.
Cecilia Marino, Haiying Meng, Sara Mascheretti, Marianna Rusconi, Natalie Cope, Roberto Giorda, Massimo Molteni, Jeffrey R Gruen. Psychiatr Genet 2012
54
20

Neurobiological systems in dyslexia.
John R Kershner. Trends Neurosci Educ 2019
8
25

Neurobiology of dyslexia.
Elizabeth S Norton, Sara D Beach, John D E Gabrieli. Curr Opin Neurobiol 2015
90
20


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.