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Items: 1 to 20 of 55

1.
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample
Kerstin U. Ludwig, Johannes Schumacher, Gerd Schulte-Körne, Inke R. König, Andreas Warnke, Ellen Plume, Heidi Anthoni, Myriam Peyrard-Janvid, Haiying Meng, Andreas Ziegler, Helmut Remschmidt, Juha Kere, Jeffrey R. Gruen, Bertram Müller-Myhsok, Markus M. Nöthen, Per Hoffmann
Psychiatr Genet. Author manuscript; available in PMC 2022 Dec 14.
Published in final edited form as: Psychiatr Genet. 2008 Dec; 18(6): 310–312. doi: 10.1097/YPG.0b013e3283063a78
PMCID:
PMC9748830
AbstractArticlePDF–55K
2.
Integration of GWAS and brain transcriptomic analyses in a multi-ethnic sample of 35,245 older adults identifies DCDC2 gene as predictor of episodic memory maintenance
Yizhe Gao, Daniel Felsky, Dolly Reyes-Dumeyer, Sanjeev Sariya, Miguel Arce Rentería, Yiyi Ma, Hans-Ulrich Klein, Stephanie Cosentino, Philip L. De Jager, David A. Bennett, Adam M. Brickman, Gerard D. Schellenberg, Richard Mayeux, Sandra Barral
Alzheimers Dement. Author manuscript; available in PMC 2022 Oct 24.
Published in final edited form as: Alzheimers Dement. 2022 Oct; 18(10): 1797–1811. Published online 2021 Dec 7. doi: 10.1002/alz.12524
PMCID:
PMC9170841
ArticlePDF–810K
3.
White matter deficits correlate with visual motion perception impairments in dyslexic carriers of the DCDC2 genetic risk variant
Daniela Perani, Paola Scifo, Guido M. Cicchini, Pasquale Della Rosa, Chiara Banfi, Sara Mascheretti, Andrea Falini, Cecilia Marino, Maria Concetta Morrone
Exp Brain Res. 2021; 239(9): 2725–2740. Published online 2021 Jul 6. doi: 10.1007/s00221-021-06137-1
PMCID:
PMC8448712
AbstractArticlePDF–1.3M
4.
Identifying dyslexia: Link between maze learning and dyslexia susceptibility gene, DCDC2, in young children
Lisa A. Gabel, Kelsey Voss, Evelyn Johnson, Esther R. Lindström, Dongnhu T. Truong, Erin M. Murray, Karla Carino, Christiana M. Nielsen, Steven Paniagua, Jeffrey R. Gruen
Dev Neurosci. Author manuscript; available in PMC 2022 Jun 29.
Published in final edited form as: Dev Neurosci. 2021; 43(2): 116–133. Published online 2021 Jun 29. doi: 10.1159/000516667
PMCID:
PMC8292181
AbstractArticlePDF–1.8M
5.
Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes
Miao Li, Dongnhu T. Truong, Mellissa DeMille, Jeffrey G. Malins, Maureen W. Lovett, Joan Bosson-Heenan, Jeffrey R Gruen, Jan C. Frijters
Child Neuropsychol. Author manuscript; available in PMC 2021 May 28.
Published in final edited form as: Child Neuropsychol. 2020 Feb; 26(2): 145–169. Published online 2019 Aug 14. doi: 10.1080/09297049.2019.1648642
PMCID:
PMC8163097
AbstractArticlePDF–269K
6.
DCDC2 READ1 regulatory element: how temporal processing differences may shape language
Kevin Tang, Mellissa M. C. DeMille, Jan C. Frijters, Jeffrey R. Gruen
Proc Biol Sci. 2020 Jun 10; 287(1928): 20192712. Published online 2020 Jun 3. doi: 10.1098/rspb.2019.2712
PMCID:
PMC7341942
AbstractArticlePDF–627K
7.
DCDC2 Polymorphism Is Associated with Left Temporoparietal Gray and White Matter Structures during Development
Fahimeh Darki, Myriam Peyrard-Janvid, Hans Matsson, Juha Kere, Torkel Klingberg
J Neurosci. 2014 Oct 22; 34(43): 14455–14462. doi: 10.1523/JNEUROSCI.1216-14.2014
PMCID:
PMC6608392
AbstractArticlePDF–911K
8.
The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia
Cecilia Marino, Paola Scifo, Pasquale A. Della Rosa, Sara Mascheretti, Andrea Facoetti, Maria L. Lorusso, Roberto Giorda, Monica Consonni, Andrea Falini, Massimo Molteni, Jeffrey R. Gruen, Daniela Perani
Cortex. Author manuscript; available in PMC 2018 May 30.
Published in final edited form as: Cortex. 2014 Aug; 57: 227–243. Published online 2014 May 9. doi: 10.1016/j.cortex.2014.04.016
PMCID:
PMC5975637
AbstractArticlePDF–502K
9.
Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages
Mellissa M. C. DeMille, Kevin Tang, Chintan M. Mehta, Christopher Geissler, Jeffrey G. Malins, Natalie R. Powers, Beatrice M. Bowen, Andrew K. Adams, Dongnhu T. Truong, Jan C. Frijters, Jeffrey R. Gruen
Proc Natl Acad Sci U S A. 2018 May 8; 115(19): 4951–4956. Published online 2018 Apr 16. doi: 10.1073/pnas.1710472115
Correction in:
Proc Natl Acad Sci U S A. 2018 May 29; 115(22): E5251.
PMCID:
PMC5948951
AbstractArticlePDF–1.0M
10.
The DCDC2 deletion is not a risk factor for dyslexia
T S Scerri, E Macpherson, A Martinelli, W C Wa, A P Monaco, J Stein, M Zheng, C Suk-Han Ho, C McBride, M Snowling, C Hulme, M E Hayiou-Thomas, M M Y Waye, J B Talcott, S Paracchini
Transl Psychiatry. 2017 Jul; 7(7): e1182. Published online 2017 Jul 25. doi: 10.1038/tp.2017.151
PMCID:
PMC5538127
AbstractArticlePDF–200K
11.
Mutations in DCDC2 (doublecortin domain-containing protein 2) in neonatal sclerosing cholangitis
Tassos Grammatikopoulos, Melissa Sambrotta, Sandra Strautnieks, Pierre Foskett, A S Knisely, Bart Wagner, Maesha Deheragoda, Chris Starling, Giorgina Mieli-Vergani, Joshua Smith, University of Washington Center for Mendelian Genomics, Laura Bull, Richard J Thompson
J Hepatol. Author manuscript; available in PMC 2017 Dec 1.
Published in final edited form as: J Hepatol. 2016 Dec; 65(6): 1179–1187. Published online 2016 Jul 25. doi: 10.1016/j.jhep.2016.07.017
PMCID:
PMC5116266
AbstractArticlePDF–3.0M
12.
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 May 27; 35(21): 8059–8064. doi: 10.1523/JNEUROSCI.5077-14.2015
PMCID:
PMC4888943
AbstractArticlePDF–336K
13.
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. Author manuscript; available in PMC 2013 Feb 1.
Published in final edited form as: Psychiatr Genet. 2012 Feb; 22(1): 25–30. doi: 10.1097/YPG.0b013e32834acdb2
PMCID:
PMC3232293
AbstractArticlePDF–296K
14.
GENETIC INFLUENCES OF CORTICAL GREY MATTER IN LANGUAGE-RELATED REGIONS IN HEALTHY CONTROLS AND SCHIZOPHRENIA
S. Jamadar, N.R. Powers, S.A. Meda, J. Gelernter, J.R. Gruen, G.D. Pearlson
Schizophr Res. Author manuscript; available in PMC 2012 Jul 1.
Published in final edited form as: Schizophr Res. 2011 Jul; 129(2-3): 141–148. Published online 2011 Apr 20. doi: 10.1016/j.schres.2011.03.027
PMCID:
PMC3110636
AbstractArticlePDF–477K
15.
A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression
Haiying Meng, Natalie R. Powers, Ling Tang, Natalie A. Cope, Ping-Xia Zhang, Ramsay Fuleihan, Christopher Gibson, Grier P. Page, Jeffrey R. Gruen
Behav Genet. Author manuscript; available in PMC 2012 Jan 1.
Published in final edited form as: Behav Genet. 2011 Jan; 41(1): 58–66. Published online 2010 Nov 2. doi: 10.1007/s10519-010-9408-3
PMCID:
PMC3053575
AbstractArticlePDF–376K
16.
PROGRESS TOWARDS A CELLULAR NEUROBIOLOGY OF READING DISABILITY
Lisa A Gabel, Christopher J. Gibson, Jeffrey R. Gruen, Joseph J. LoTurco
Neurobiol Dis. Author manuscript; available in PMC 2011 May 1.
Published in final edited form as: Neurobiol Dis. 2010 May; 38(2): 173–180. Published online 2009 Jul 17. doi: 10.1016/j.nbd.2009.06.019
PMCID:
PMC2854314
AbstractArticlePDF–545K
17.
Polymorphism of DCDC2 Reveals Differences in Cortical Morphology of Healthy Individuals—A Preliminary Voxel Based Morphometry Study
Shashwath A. Meda, Joel Gelernter, Jeffrey R. Gruen, Vince D. Calhoun, Haiying Meng, Natalie A. Cope, Godfrey D. Pearlson
Brain Imaging Behav. Author manuscript; available in PMC 2008 Dec 17.
Published in final edited form as: Brain Imaging Behav. 2008 Mar; 2(1): 21–26. doi: 10.1007/s11682-007-9012-1
PMCID:
PMC2605089
AbstractArticlePDF–620K
18.
Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia
Johannes Schumacher, Heidi Anthoni, Faten Dahdouh, Inke R. König, Axel M. Hillmer, Nadine Kluck, Malou Manthey, Ellen Plume, Andreas Warnke, Helmut Remschmidt, Jutta Hülsmann, Sven Cichon, Cecilia M. Lindgren, Peter Propping, Marco Zucchelli, Andreas Ziegler, Myriam Peyrard-Janvid, Gerd Schulte-Körne, Markus M. Nöthen, Juha Kere
Am J Hum Genet. 2006 Jan; 78(1): 52–62. Published online 2005 Nov 17. doi: 10.1086/498992
PMCID:
PMC1380223
AbstractArticlePDF–1.4M
19.
DCDC2 inhibits hepatic stellate cell activation and ameliorates CCl4-induced liver fibrosis by suppressing Wnt/β-catenin signaling
Qing-Qing Liu, Jing Chen, Tao Ma, Wei Huang, Cui-Hua Lu
Sci Rep. 2024; 14: 9425. Published online 2024 Apr 24. doi: 10.1038/s41598-024-59698-w
PMCID:
PMC11043443
AbstractArticlePDF–4.8M
20.
Do Genes Associated with Dyslexia of Chinese Characters Evolve Neutrally?
Kumiko V. Nishiyama, Yoko Satta, Jun Gojobori
Genes (Basel) 2020 Jun; 11(6): 658. Published online 2020 Jun 17. doi: 10.3390/genes11060658
PMCID:
PMC7349701
AbstractArticlePDF–1.6M

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