Barbara Stiller
Munich, BY, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
ADAMTS-7 Modulates Atherosclerotic Plaque Formation by Degradation of TIMP-1.
Journal: Circulation research
Published: September 07, 2023
Functional investigation of the coronary artery disease gene SVEP1.
Journal: Basic research in cardiology
Published: August 15, 2020
Cis-epistasis at the LPA locus and risk of cardiovascular diseases.
Journal: Cardiovascular research
Published: July 23, 2020
Fifty generations of Icelanders help to explain a cause of aortic coarctation.
Journal: European heart journal
Published: April 27, 2018
Genetics of coronary artery disease in the light of genome-wide association studies.
Journal: Clinical research in cardiology : official journal of the German Cardiac Society
Published: April 24, 2018
A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction.
Journal: Human molecular genetics
Published: May 25, 2017
Increased copper toxicity in Saccharomyces cerevisiae lacking VPS35, a component of the retromer and monogenic Parkinson disease gene in humans.
Journal: Biochemical and biophysical research communications
Published: May 20, 2016
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.
Journal: American journal of human genetics
Published: August 02, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026