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Works by Müller, Bent

Results: 5

1

Improved prediction of complex diseases by common genetic markers: state of the art and further perspectives.

Published in:

Human Genetics, 2016, v. 135, n. 3, p. 259, doi. 10.1007/s00439-016-1636-z

By:

Müller, Bent;
Wilcke, Arndt;
Boulesteix, Anne-Laure;
Brauer, Jens;
Passarge, Eberhard;
Boltze, Johannes;
Kirsten, Holger

Publication type:

Article

2

NRSN1 associated grey matter volume of the visual word form area reveals dyslexia before school.

Published in:

Brain: A Journal of Neurology, 2016, v. 139, n. 10, p. 2792, doi. 10.1093/brain/aww153

By:

Skeide, Michael A.;
Kraft, Indra;
Müller, Bent;
Schaadt, Gesa;
Neef, Nicole E.;
Brauer, Jens;
Wilcke, Arndt;
Kirsten, Holger;
Boltze, Johannes;
Friederici, Angela D.

Publication type:

Article

3

Cortical differences in preliterate children at familiar risk of dyslexia are similar to those observed in dyslexic readers.

Published in:

2015

By:

Kraft, Indra;
Cafiero, Riccardo;
Schaadt, Gesa;
Brauer, Jens;
Neef, Nicole E.;
Müller, Bent;
Kirsten, Holger;
Wilcke, Arndt;
Boltze, Johannes;
Friederici, Angela D.;
Skeide, Michael A.

Publication type:

journal article

4

ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMR.

Published in:

Brain & Behavior, 2017, v. 7, n. 11, p. n/a, doi. 10.1002/brb3.851

By:

Müller, Bent;
Schaadt, Gesa;
Boltze, Johannes;
Emmrich, Frank;
Skeide, Michael A.;
Neef, Nicole E.;
Kraft, Indra;
Brauer, Jens;
Friederici, Angela D.;
Kirsten, Holger;
Wilcke, Arndt

Publication type:

Article

5

Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort.

Published in:

Scientific Reports, 2016, p. 27901, doi. 10.1038/srep27901

By:

Müller, Bent;
Wilcke, Arndt;
Czepezauer, Ivonne;
Ahnert, Peter;
Boltze, Johannes;
Kirsten, Holger

Publication type:

Article