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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 5, 2023. (Total: 223688Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Dyslexia and C2orf3[original query]
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
Human molecular genetics 2007 Mar 16 (6): 667-77.
Anthoni Heidi, Zucchelli Marco, Matsson Hans, Müller-Myhsok Bertram, Fransson Ingegerd, Schumacher Johannes, Massinen Satu, Onkamo Päivi, Warnke Andreas, Griesemann Heide, Hoffmann Per, Nopola-Hemmi Jaana, Lyytinen Heikki, Schulte-Körne Gerd, Kere Juha, Nöthen Markus M, Peyrard-Janvid Myri
Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.
Genes, brain, and behavior 2011 Mar 10 (2): 158-65.
Paracchini S, Ang Q W, Stanley F J, Monaco A P, Pennell C E, Whitehouse A J
DCDC2, KIAA0319 and CMIP are associated with reading-related traits.
Biological psychiatry 2011 Aug 70 (3): 237-45.
Scerri Tom S, Morris Andrew P, Buckingham Lyn-Louise, Newbury Dianne F, Miller Laura L, Monaco Anthony P, Bishop Dorothy V M, Paracchini Silv
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.
PloS one 2012 7 (11): 11.
Scerri TS, Darki F, Newbury DF, Whitehouse AJ, Peyrard-Janvid M, Matsson H, Ang QW, Pennell CE, Ring S, Stein J, Morris AP, Monaco AP, Kere J, Talcott JB, Klingberg T, Paracchini S
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
European journal of human genetics : EJHG 2014 May 22 (5): 675-80.
Becker Jessica, Czamara Darina, Scerri Tom S, Ramus Franck, Csépe Valéria, Talcott Joel B, Stein John, Morris Andrew, Ludwig Kerstin U, Hoffmann Per, Honbolygó Ferenc, Tóth Dénes, Fauchereau Fabien, Bogliotti Caroline, Iannuzzi Stéphanie, Chaix Yves, Valdois Sylviane, Billard Catherine, George Florence, Soares-Boucaud Isabelle, Gérard Christophe-Loïc, van der Mark Sanne, Schulz Enrico, Vaessen Anniek, Maurer Urs, Lohvansuu Kaisa, Lyytinen Heikki, Zucchelli Marco, Brandeis Daniel, Blomert Leo, Leppänen Paavo H T, Bruder Jennifer, Monaco Anthony P, Müller-Myhsok Bertram, Kere Juha, Landerl Karin, Nöthen Markus M, Schulte-Körne Gerd, Paracchini Silvia, Peyrard-Janvid Myriam, Schumacher Johann
Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with developmental dyslexia.
Gene 2013 Oct 529 (2): 215-9.
Venkatesh Shyamala K, Siddaiah Anand, Padakannaya Prakash, Ramachandra Nallur
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
Journal of human genetics 2015 Jul 60 (7): 399-401.
Matsson Hans, Huss Mikael, Persson Helena, Einarsdottir Elisabet, Tiraboschi Ettore, Nopola-Hemmi Jaana, Schumacher Johannes, Neuhoff Nina, Warnke Andreas, Lyytinen Heikki, Schulte-Körne Gert, Nöthen Markus M, Leppänen Paavo Ht, Peyrard-Janvid Myriam, Kere Ju
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