Works by Wilcke, Arndt

Results: 9

Non-destructive ZooMS identification reveals strategic bone tool raw material selection by Neandertals.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-64358-w

By:

Martisius, Naomi L.;
Welker, Frido;
Dogandžić, Tamara;
Grote, Mark N.;
Rendu, William;
Sinet-Mathiot, Virginie;
Wilcke, Arndt;
McPherron, Shannon J. P.;
Soressi, Marie;
Steele, Teresa E.

Publication type:

Article

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

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

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

Combining ZooMS and zooarchaeology to study Late Pleistocene hominin behaviour at Fumane (Italy).

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-48706-z

By:

Sinet-Mathiot, Virginie;
Smith, Geoff M.;
Romandini, Matteo;
Wilcke, Arndt;
Peresani, Marco;
Hublin, Jean-Jacques;
Welker, Frido

Publication type:

Article

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

Imaging genetics of FOXP2 in dyslexia.

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 6, p. 714, doi. 10.1038/ejhg.2012.31

By:

Wilcke, Arndt;
Jana Burkhardt, Carolin Ligges;
Alexander, Michael;
Wolf, Christiane;
Quente, Elfi;
Ahnert, Peter;
Hoffmann, Per;
Becker, Albert;
Müller-Myhsok, Bertram;
Cichon, Sven;
Boltze, Johannes;
Kirsten, Holger

Publication type:

Article

Imaging genetics of FOXP2 in dyslexia.

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 2, p. 224, doi. 10.1038/ejhg.2011.160

By:

Wilcke, Arndt;
Ligges, Carolin;
Burkhardt, Jana;
Alexander, Michael;
Wolf, Christiane;
Quente, Elfi;
Ahnert, Peter;
Hoffmann, Per;
Becker, Albert;
Müller-Myhsok, Bertram;
Cichon, Sven;
Boltze, Johannes;
Kirsten, Holger

Publication type:

Article

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