Schulte-Körne G - Search Results

1

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. Psychiatr Genet. 2008 Dec;18(6):310-2. doi: 10.1097/YPG.0b013e3283063a78. Psychiatr Genet. 2008. PMID: 19018237 Free PMC article.

2

Visual evoked potential elicited by coherenty moving dots in dyslexic children.

Schulte-Körne G, Bartling J, Deimel W, Remschmidt H. Schulte-Körne G, et al. Neurosci Lett. 2004 Mar 11;357(3):207-10. doi: 10.1016/j.neulet.2003.12.098. Neurosci Lett. 2004. PMID: 15003286

3

Motion-onset VEPs in dyslexia. Evidence for visual perceptual deficit.

Schulte-Körne G, Bartling J, Deimel W, Remschmidt H. Schulte-Körne G, et al. Neuroreport. 2004 Apr 29;15(6):1075-8. doi: 10.1097/00001756-200404290-00029. Neuroreport. 2004. PMID: 15076738

4

Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair design.

Ziegler A, König IR, Deimel W, Plume E, Nöthen MM, Propping P, Kleensang A, Müller-Myhsok B, Warnke A, Remschmidt H, Schulte-Körne G. Ziegler A, et al. Hum Hered. 2005;59(3):136-43. doi: 10.1159/000085572. Epub 2005 May 2. Hum Hered. 2005. PMID: 15867474

5

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.

Schumacher J, Anthoni H, Dahdouh F, König IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hülsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, Ziegler A, Peyrard-Janvid M, Schulte-Körne G, Nöthen MM, Kere J. Schumacher J, et al. Am J Hum Genet. 2006 Jan;78(1):52-62. doi: 10.1086/498992. Epub 2005 Nov 17. Am J Hum Genet. 2006. PMID: 16385449 Free PMC article.

6

[Genetics of dyslexia].

Schulte-Körne G, Warnke A, Remschmidt H. Schulte-Körne G, et al. Z Kinder Jugendpsychiatr Psychother. 2006 Nov;34(6):435-44. doi: 10.1024/1422-4917.34.6.435. Z Kinder Jugendpsychiatr Psychother. 2006. PMID: 17094062 Review. German.

7

[Influencing factors on the course of supervised visitations in a parental counselling office].

Richardt M, Schulte-Körne G, Remschmidt H. Richardt M, et al. Prax Kinderpsychol Kinderpsychiatr. 2006;55(9):724-38. Prax Kinderpsychol Kinderpsychiatr. 2006. PMID: 17212190 German.

8

Genetics of dyslexia: the evolving landscape.

Schumacher J, Hoffmann P, Schmäl C, Schulte-Körne G, Nöthen MM. Schumacher J, et al. J Med Genet. 2007 May;44(5):289-97. doi: 10.1136/jmg.2006.046516. Epub 2007 Feb 16. J Med Genet. 2007. PMID: 17307837 Free PMC article. Review.

9

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.

Anthoni H, Zucchelli M, Matsson H, Müller-Myhsok B, Fransson I, Schumacher J, Massinen S, Onkamo P, Warnke A, Griesemann H, Hoffmann P, Nopola-Hemmi J, Lyytinen H, Schulte-Körne G, Kere J, Nöthen MM, Peyrard-Janvid M. Anthoni H, et al. Hum Mol Genet. 2007 Mar 15;16(6):667-77. doi: 10.1093/hmg/ddm009. Epub 2007 Feb 19. Hum Mol Genet. 2007. PMID: 17309879

10

No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level.

Wermter AK, Kamp-Becker I, Strauch K, Schulte-Körne G, Remschmidt H. Wermter AK, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):535-7. doi: 10.1002/ajmg.b.30618. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18189281

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