Publications by Andersen, Peter M.

Freischmidt, Axel, Goswami, Anand, Limm, Katharina, Zimyanin, Vitaly L., Demestre, Maria, Glaß, Hannes, Holzmann, Karlheinz, Helferich, Anika M., Brockmann, Sarah J., Tripathi, Priyanka, Yamoah, Alfred, Poser, Ina, Oefner, Peter J., Böckers, Tobias M., Aronica, Eleonora, Ludolph, Albert C., Andersen, Peter M., Hermann, Andreas, Weis, Joachim, Reinders, Jörg, Danzer, Karin M. and Weishaupt, Jochen H. (2021) A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis. Brain 144 (4), pp. 1214-1229. Fulltext not available.

Brockmann, Sarah J., Freischmidt, Axel, Oeckl, Patrick , Müller, Kathrin, Ponna, Srinivas K., Helferich, Anika M., Paone, Christoph, Reinders, Jörg, Kojer, Kerstin, Orth, Michael, Jokela, Manu, Auranen, Mari, Udd, Bjarne, Hermann, Andreas, Danzer, Karin M., Lichtner, Peter, Walther, Paul, Ludolph, Albert C., Andersen, Peter M., Otto, Markus , Kursula, Petri , Just, Steffen and Weishaupt, Jochen H. (2018) CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency. Human Molecular Genetics 27 (4), pp. 706-715. Fulltext not available.

Helferich, Anika M., Brockmann, Sarah J., Reinders, Jörg, Deshpande, Dhruva, Holzmann, Karlheinz, Brenner, David, Andersen, Peter M., Petri, Susanne, Thal, Dietmar R. , Michaelis, Jens, Otto, Markus , Just, Steffen, Ludolph, Albert C., Danzer, Karin M., Freischmidt, Axel and Weishaupt, Jochen H. (2018) Dysregulation of a novel miR-1825/TBCB/TUBA4A pathway in sporadic and familial ALS. Cellular and Molecular Life Sciences 75 (23), pp. 4301-4319. Fulltext not available.