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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
2011 2
2012 4
2013 1
2014 1
2015 4
2016 5
2017 2
2018 1
2019 3
2020 7
2021 1
2024 0

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27 results

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Page 1
Multi-protease analysis of Pleistocene bone proteomes.
Lanigan LT, Mackie M, Feine S, Hublin JJ, Schmitz RW, Wilcke A, Collins MJ, Cappellini E, Olsen JV, Taurozzi AJ, Welker F. Lanigan LT, et al. Among authors: wilcke a. J Proteomics. 2020 Sep 30;228:103889. doi: 10.1016/j.jprot.2020.103889. Epub 2020 Jul 9. J Proteomics. 2020. PMID: 32652221 Free article.
Five-year results of a cementless short-hip-stem prosthesis.
Wittenberg RH, Steffen R, Windhagen H, Bücking P, Wilcke A. Wittenberg RH, et al. Among authors: wilcke a. Orthop Rev (Pavia). 2013 Mar 19;5(1):e4. doi: 10.4081/or.2013.e4. Print 2013 Feb 22. Orthop Rev (Pavia). 2013. PMID: 23705062 Free PMC article.
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, Hulslander J, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-Janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Francks C, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-Myhsok B, Schulte-Körne G. Gialluisi A, et al. Among authors: wilcke a. Transl Psychiatry. 2019 Feb 11;9(1):77. doi: 10.1038/s41398-019-0402-0. Transl Psychiatry. 2019. PMID: 30741946 Free PMC article.
The emergence of dyslexia in the developing brain.
Kuhl U, Neef NE, Kraft I, Schaadt G, Dörr L, Brauer J, Czepezauer I, Müller B, Wilcke A, Kirsten H, Emmrich F, Boltze J, Friederici AD, Skeide MA. Kuhl U, et al. Among authors: wilcke a. Neuroimage. 2020 May 1;211:116633. doi: 10.1016/j.neuroimage.2020.116633. Epub 2020 Feb 12. Neuroimage. 2020. PMID: 32061802 Free article.
Imaging genetics of FOXP2 in dyslexia.
Wilcke A, Ligges C, Burkhardt J, Alexander M, Wolf C, Quente E, Ahnert P, Hoffmann P, Becker A, Müller-Myhsok B, Cichon S, Boltze J, Kirsten H. Wilcke A, et al. Eur J Hum Genet. 2012 Feb;20(2):224-9. doi: 10.1038/ejhg.2011.160. Epub 2011 Sep 7. Eur J Hum Genet. 2012. PMID: 21897444 Free PMC article.
Genetic risk variants for dyslexia on chromosome 18 in a German cohort.
Mueller B, Ahnert P, Burkhardt J, Brauer J, Czepezauer I, Quente E, Boltze J, Wilcke A, Kirsten H. Mueller B, et al. Among authors: wilcke a. Genes Brain Behav. 2014 Mar;13(3):350-6. doi: 10.1111/gbb.12118. Epub 2014 Feb 3. Genes Brain Behav. 2014. PMID: 24373531 Free article.
27 results