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DCDC2 is associated with reading disability and modulates neuronal development in the brain.
Meng H, Smith SD, Hager K, Held M, Liu J, Olson RK, Pennington BF, DeFries JC, Gelernter J, O'Reilly-Pol T, Somlo S, Skudlarski P, Shaywitz SE, Shaywitz BA, Marchione K, Wang Y, Paramasivam M, LoTurco JJ, Page GP, Gruen JR. Meng H, et al. Among authors: gruen jr. Proc Natl Acad Sci U S A. 2005 Nov 22;102(47):17053-8. doi: 10.1073/pnas.0508591102. Epub 2005 Nov 8. Proc Natl Acad Sci U S A. 2005. PMID: 16278297 Free PMC article.
The genetics of bronchopulmonary dysplasia.
Bhandari V, Gruen JR. Bhandari V, et al. Among authors: gruen jr. Semin Perinatol. 2006 Aug;30(4):185-91. doi: 10.1053/j.semperi.2006.05.005. Semin Perinatol. 2006. PMID: 16860158 Review.
Genetic susceptibility to retinopathy of prematurity.
Bizzarro MJ, Hussain N, Jonsson B, Feng R, Ment LR, Gruen JR, Zhang H, Bhandari V. Bizzarro MJ, et al. Among authors: gruen jr. Pediatrics. 2006 Nov;118(5):1858-63. doi: 10.1542/peds.2006-1088. Pediatrics. 2006. PMID: 17079555
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.
Ludwig KU, Schumacher J, Schulte-Körne G, König IR, Warnke A, Plume E, Anthoni H, Peyrard-Janvid M, Meng H, Ziegler A, Remschmidt H, Kere J, Gruen JR, Müller-Myhsok B, Nöthen MM, Hoffmann P. Ludwig KU, et al. Among authors: gruen jr. Psychiatr Genet. 2008 Dec;18(6):310-2. doi: 10.1097/YPG.0b013e3283063a78. Psychiatr Genet. 2008. PMID: 19018237 Free PMC article.
109 results