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Journal Article
Bey, Katharina, Wolfsgruber, Steffen, Karaca, Ilker ORCID: 0000-0002-2139-0015, Wagner, Holger, Lardenoije, Roy, Becker, Julian, Milz, Esther, Kornhuber, Johannes
ORCID: 0000-0002-8096-3987, Peters, Oliver, Froelich, Lutz, Huell, Michael, Ruether, Eckart, Wiltfang, Jens
ORCID: 0000-0003-1492-5330, Riedel-Heller, Steffi, Scherer, Martin, Jessen, Frank, Maier, Wolfgang, van den Hove, Daniel L., Rutten, Bart P. F., Wagner, Michael
ORCID: 0000-0003-2589-6440 and Ramirez, Alfredo
ORCID: 0000-0003-4991-763X
(2016).
No association of the variant rs11887120 in DNMT3A with cognitive decline in individuals with mild cognitive impairment.
Epigenomics, 8 (5).
S. 593 - 599.
LONDON:
FUTURE MEDICINE LTD.
ISSN 1750-192X
Haertle, Larissa ORCID: 0000-0002-3927-9163, Mueller, Tobias, Lardenoije, Roy, Maierhofer, Anna, Dittrich, Marcus, Riemens, Renzo J. M., Stora, Samantha, Roche, Mathilde, Leber, Markus, Riedel-Heller, Steffi, Wagner, Michael
ORCID: 0000-0003-2589-6440, Scherer, Martin, Ravel, Aime, Mircher, Clotilde, Cieuta-Walti, Cecile, Durand, Sophie, van de Hove, Daniel L. A., Hoffmann, Per, Ramirez, Alfredo
ORCID: 0000-0003-4991-763X, Haaf, Thomas, El Hajj, Nady and Megarbane, Andre
(2019).
Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer's disease-related dysregulation.
Clin. Epigenetics, 11 (1).
LONDON:
BMC.
ISSN 1868-7083
Lardenoije, Roy, Roubroeks, Janou A. Y., Pishva, Ehsan, Leber, Markus, Wagner, Holger, Iatrou, Artemis, Smith, Adam R., Smith, Rebecca G., Eijssen, Lars M. T., Kleineidam, Luca, Kawalia, Amit, Hoffmann, Per, Luck, Tobias ORCID: 0000-0001-7551-4397, Riedel-Heller, Steffi, Jessen, Frank, Maier, Wolfgang, Wagner, Michael
ORCID: 0000-0003-2589-6440, Hurlemann, Rene
ORCID: 0000-0003-2628-565X, Kenis, Gunter, Ali, Muhammad, del Sol, Antonio, Mastroeni, Diego, Delvaux, Elaine, Coleman, Paul D., Mill, Jonathan
ORCID: 0000-0003-1115-3224, Rutten, Bart P. F., Lunnon, Katie, Ramirez, Alfredo
ORCID: 0000-0003-4991-763X and van den Hove, Daniel L. A.
(2019).
Alzheimer's disease-associated (hydroxy)methylomic changes in the brain and blood.
Clin. Epigenetics, 11 (1).
LONDON:
BMC.
ISSN 1868-7083