Gertrud N. Eckstein
Neuherberg, BY, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 19 publications
Huntingtin CAG repeat size variations below the Huntington's disease threshold: associations with depression, anxiety and basal ganglia structure.
Journal: European journal of human genetics : EJHG
Published: June 01, 2024
Human skin-resident host T cells can persist long term after allogeneic stem cell transplantation and maintain recirculation potential.
Journal: Science immunology
Published: January 28, 2022
Riociguat attenuates the changes in left ventricular proteome and microRNA profile after experimental aortic stenosis in mice.
Journal: British journal of pharmacology
Published: July 08, 2021
Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders.
Journal: Human molecular genetics
Published: May 18, 2021
The rare and the common: An Austrian DRPLA family harboring the European haplotype.
Journal: Parkinsonism & related disorders
Published: February 16, 2021
Congenital heart disease risk loci identified by genome-wide association study in European patients.
Congenital heart disease risk loci identified by genome-wide association study in European patients.
Journal: The Journal of clinical investigation
Published: June 30, 2020
Stimulation of soluble guanylyl cyclase (sGC) by riociguat attenuates heart failure and pathological cardiac remodelling.
Journal: British journal of pharmacology
Published: June 12, 2020
Mitochondrial DNA mutation analysis from exome sequencing-A more holistic approach in diagnostics of suspected mitochondrial disease.
Journal: Journal of inherited metabolic disease
Published: April 15, 2019
Adult-onset variant ataxia-telangiectasia diagnosed by exome and cDNA sequencing.
Journal: Neurology. Genetics
Published: March 14, 2019
Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study.
Journal: Neurobiology of aging
Published: June 30, 2016
Eight Novel Mutations Confirm the Role of AAGAB in Punctate Palmoplantar Keratoderma Type 1 (Buschke-Fischer-Brauer) and Show Broad Phenotypic Variability.
Journal: Acta dermato-venereologica
Published: November 27, 2015
Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy.
Journal: American journal of human genetics
Published: October 05, 2015
Last Updated: 09/26/2026