Publication on RealFast and StripAssays

ViennaLab Diagnostics offers a variety of easy-to-use in vitro diagnostic kits for the detection of genetic mutations, as well as genetic predispositions, pharmacogenetics and oncology.

Their genetics test are split in two different technologies. They offer the quick and cost efficient RealFast assays which are based on hydrolysis probes. ViennaLab also offers StripAssays which can cover more mutations in one assay due to reverse hybridisation.

Title	Author	Date
the natural history of alpha-1 antitrypsin deficiency, and associated liver disease	S. Townsend	2018
Risk of Lung Disease in PI MZ Heterozygotes	Edwin K. Silverman	2016
Multicenter Validation Study of a Novel StripAssay for Cystic Fibrosis	Helene Pühringer	2018
Alpha-1 antitrypsin deficiency: An underrecognized, treatable cause of COPD	James K. Stoller	2016
Genetic Testing for Familial Mediterranean Fever in Austria by Means of Reverse-Hybridization Teststrips	Christian Oberkanins	2003
Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common a-thalassemia point mutations and deletions	Helene Pühringer	2007
Reverse-hybridization assay for rapid detection of common CYP21A2 mutations in dried blood spots from newborns with elevated 17-OH progesterone	Stefan Németh	2012
Lactase Non-Persistence Genotyping: Comparison of Two Real-Time PCR Assays and Assessment of Concomitant Fructose/Sorbitol Malabsorption Rates	Dietmar Enko	2016
The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1 and Simvastatin-Induced Myopathy	LB Ramsey	2014
Duplex reverse-hybridization assay for the simultaneous detection of KRAS/BRAF mutations in FFPE-extracted genomic DNA from colorectal cancer specimens	Veronika Buxhofer-Ausch	2013
Diagnosing α1-antitrypsin deficiency: how to improve the current algorithm	Noel G. McElvaney	2015
Genetic Modiﬁers in b-Thalassemia Intermedia: A Study on 102 Iraqi Arab Patients	Nasir A.S. Al-Allawi	2015
Beta-thalassemia: from genotype to phenotype	Fabrice Danjou	2011
Variants in genetic modifiers of b-thalassemia can help to predict the major or intermedia type of the disease	Catherine Badens	2011
A genetic score for the prediction of beta-thalassemia severity	Fabrice Danjou	2015
Interferon Lambda 4 Polymorphism Predicts Sustained Viral Response in Hepatitis C Virus Patients Irrespective of Hepatitis C Virus Genotypes, Ethnicity or Treatment Regimen: Results From a Meta-Analysis	Qin Wu	2015
Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice	C. Castellani	2008
IL28B expression depends on a novel TT/-G polymorphism which improves HCV clearance prediction	Stéphanie Bibert	2013
IFNL4-ΔG Genotype Is Associated With Slower Viral Clearance in Hepatitis C, Genotype-1 Patients Treated With Sofosbuvirand Ribavirin	Eric G. Meissner	2014
Sensitive Detection of KRAS Mutations in Archived Formalin-Fixed Paraffin-Embedded Tissue Using Mutant-Enriched PCR and Reverse-Hybridization	Christoph Ausch	2009
Genetically Guided Statin Therapy on Statin Perceptions, Adherence, and Cholesterol Lowering: A Pilot Implementation Study in Primary Care Patients	Josephine H. Li	2014
Comprehensive analysis of CYP2D6 variants and copy numbers using reverse-hybridization and real-time PCR based assays	Anne Berndt	2017