Asper Biotech (Estonia)

Recent papers from Asper Biotech (Estonia)

1. The Prevalence and Molecular Landscape of Lynch Syndrome in the Affected and General PopulationCancers · 2023
2. A very early diagnosis of Alstrӧm syndrome by next generation sequencingBMC Medical Genetics · 2020
3. Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and LatviaGastroenterology Research and Practice · 2015
4. Mutational Screening of LCA Genes Emphasizing RPE65 in South Indian Cohort of PatientsPLoS ONE · 2013
5. Ace I/D polymorphism is associated with habitual physical activity in pubertal boysThe Journal of Physiological Sciences · 2013
6. Li2B4O7:Mn for dosimetry applications: traps and mechanisms; pp. 279–295Proceedings of the Estonian Academy of Sciences · 2012
7. Genetic assessment following increased nuchal translucency and normal karyotypePrenatal Diagnosis · 2011
8. Fluoride‐Cleavable, Fluorescently Labelled Reversible Terminators: Synthesis and Use in Primer ExtensionChemistry - A European Journal · 2011
9. Molecular diagnosis of Down syndrome using quantitative APEX‐2 microarraysPrenatal Diagnosis · 2010
10. Microarray-Based Mutation Analysis of 183 Spanish Families with Usher SyndromeInvestigative Ophthalmology & Visual Science · 2010
11. Genotyping Microarray for CSNB-Associated GenesInvestigative Ophthalmology & Visual Science · 2009
12. Screening 52 single nucleotide polymorphisms for extreme value of glycolytic potential and drip loss in pigsJournal of Animal Breeding and Genetics · 2009
13. Carrier of R14W in Carbonic Anhydrase IV Presents Bothnia Dystrophy Phenotype Caused by Two Allelic Mutations inRLBP1Investigative Ophthalmology & Visual Science · 2008
14. Genotyping microarray as a novel approach for the detection of ATP7B gene mutations in patients with Wilson diseaseClinical Genetics · 2008
15. Towards an integrated approach to study SNPs and expression of candidate genes associated with milk protein biosynthesisRussian Journal of Genetics · 2008
16. Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin geneMovement Disorders · 2007
17. Development of a genotyping microarray for Usher syndrome2007
18. Simultaneous Multigene Mutation Detection in Patients With Sensorineural Hearing Loss Through a Novel Diagnostic Microarray: A New Approach for Newborn Screening Follow-upPEDIATRICS · 2006
19. A quality assessment survey of SNP genotyping laboratoriesHuman Mutation · 2006
20. Out-of-hospital resuscitation in Estonia: a bystander-witnessed sudden cardiac arrestEuropean Journal of Emergency Medicine · 2005