Personal profile
Scientific Focus
- Multi-institutional outreach and in-house interdisciplinary specialist center
- Community care for neuromuscular, motoneuron and related rare diseases
- Quantitative D50 modelling of progression for global rare diseases cohorts for decision pathways, stratification, trial monitoring and biomarker research
- Pathophysiology of motoneuron and mitochondrial disorders, ER-mitochondria calcium signalling in murine and human iPSC derived models of MND/NMD
- Functional and structural pathology in MR imaging, neurophysiological and lab biomarkers in motoneuron diseases
- Mononuclear blood / microglial cells as biomarkers and therapeutic targets
- Development of clinical trial and outcome strategies in rare disorders
- Adherence factor analyses in ageing populations
- Connecting people from different research fields
Research Areas and Centers
- Centers: Center for Neuromuscular Diseases
- Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)
- Centers: Center for Rare Diseases (ZSE)
DFG Research Classification Scheme
- 2.23-07 Clinical Neurology, Neurosurgery and Neuroradiology
- 2.23-06 Molecular and Cellular Neurology and Neuropathology
- 2.23-05 Experimental Models for the Understanding of Nervous System Diseases
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
-
SDG 3 Good Health and Well-being
Fingerprint
Dive into the research topics where Julian Großkreutz is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Research output
-
Cathepsin D as biomarker in cerebrospinal fluid of nusinersen-treated patients with spinal muscular atrophy
the SMArtCARE consortium, 07.2022, In: European Journal of Neurology. 29, 7, p. 2084-2096 13 p.Research output: Journal Articles › Journal articles › Research › peer-review
24 Link opens in a new tab Citations (Scopus)
-
Uncovering novel causes and modifiers of amyotrophic lateral sclerosis by nuclear and mitochondrial genome sequencing
Erdmann, J. (Principal Investigator (PI)), Großkreutz, J. (Principal Investigator (PI)), Klein, C. (Principal Investigator (PI)), Weishaupt, J. H. (Principal Investigator (PI)), Westenberger, A. (Principal Investigator (PI)) & Spielmann, M. (Speaker)
01.01.22 → 31.12.26
Project: DFG Individual Projects