Skip to main navigation
Skip to search
Skip to main content
University of Luebeck Home
English
Deutsch
Home
Research Units
Experts
Publications
Projects
Prizes
Spin-Offs
Media
Activities
Datasets
Search by expertise, name or affiliation
RU 2488: Reduced penetrance in hereditary movement disorders: Elucidating mechanisms of endogenous disease protection
Klein, Christine
(Speaker, Coordinator)
Berg, Daniela
(Principal Investigator (PI))
Brüggemann, Norbert
(Principal Investigator (PI))
Lohmann, Katja
(Principal Investigator (PI))
Seibler, Philip
(Principal Investigator (PI))
König, Inke Regina
(Principal Investigator (PI))
Lill, Christina Maria
(Principal Investigator (PI))
Bertram, Lars
(Principal Investigator (PI))
Erdmann, Jeanette
(Principal Investigator (PI))
Grünewald, Anne Katrin
(Principal Investigator (PI))
Kasten, Meike
(Principal Investigator (PI))
Westenberger, Ana
(Principal Investigator (PI))
Rakovic, Aleksander
(Principal Investigator (PI))
Kaiser, Frank
(Principal Investigator (PI))
Caliebe, Amke
(Principal Investigator (PI))
Busch, Hauke Stephan
(Principal Investigator (PI))
Krawczak, Michael
(Principal Investigator (PI))
Spielmann, Malte
(Principal Investigator (PI))
Institute of Neurogenetics
Clinic of Neurology
Institute of Medical Biometry and Statistic
Institute of Cardiogenetics
Clinic of Psychiatry and Psychotherapy
Institute of Experimental Dermatology
Institute of Human Genetics
University of Kiel
Universitätsmedizin Essen
Project
:
DFG Joint Research
›
DFG Research Units (RU)
Overview
Fingerprint
Publications
(4)
Fingerprint
Explore the research topics touched on by this project. These labels are generated based on the underlying awards/grants. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Medicine and Dentistry
Stereotypic Movement Disorder
100%
Penetrance
50%
Spinocerebellar Ataxia
50%
Onset Age
30%
Identified Patient
25%
Brainstem
25%
Autosomal Recessive Inheritance
25%
Facial Muscle
25%
Strabismus
25%
Ataxia
25%
Patient Counseling
25%
Clinical Feature
25%
Biochemistry, Genetics and Molecular Biology
Random Forest
50%
Genotyping
50%
Penetrance
50%
Autosomal Recessive Inheritance
50%
Rare Variant
50%
THAP1
32%
Minor Allele Frequency
25%
GNAL
25%
DNA Methylation
25%
Next Generation Sequencing
25%
Pharmacology, Toxicology and Pharmaceutical Science
Motor Dysfunction
100%
Onset Age
50%
Dystonia
50%
Environmental Disease
25%
Ataxia
25%
Clinical Feature
25%
Parkin
25%
Strabismus
25%