Author

Norbert Niklas

Observed names: N. Niklas, Niklas, Norbert

Observed institution: Austrian Red Cross

ORCID: 0000-0002-2106-9379

Observed ORCID: 0000-0002-2106-9379

OpenAlex ID: A5057874320

Rapid, scalable and highly automated HLA genotyping using next-generation sequencing: a transition from research to diagnostics

2013 · Martin Danzer, Norbert Niklas, et al. · BMC Genomics · 68

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Overcoming methodical limits of standard RHD genotyping by next‐generation sequencing

2010 · S. Stabentheiner, M. Danzer, et al. · Vox Sanguinis · 52

Rapid identification of compound mutations in patients with Philadelphia-positive leukaemias by long-range next generation sequencing

2013 · R. Kastner, A. Zopf, et al. · European Journal of Cancer · 39

A cancer stem cell-like phenotype is associated with miR-10b expression in aggressive squamous cell carcinomas

2020 · Monika Wimmer, Roland Zauner, et al. · Cell Communication and Signaling · 29

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Human immunodeficiency virus type 1 drug resistance testing: Evaluation of a new ultra-deep sequencing-based protocol and comparison with the TRUGENE HIV-1 Genotyping Kit

2011 · Evelyn Stelzl, Johannes Pröll, et al. · Journal of Virological Methods · 29

Mutation Analysis of Nine Chordoma Specimens by Targeted Next-Generation Cancer Panel Sequencing

2015 · Carina Fischer, Susanne Scheipl, et al. · Journal of Cancer · 25

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Sequence Capture and Next Generation Resequencing of the MHC Region Highlights Potential Transplantation Determinants in HLA Identical Haematopoietic Stem Cell Transplantation

2011 · J. Proll, M. Danzer, et al. · DNA Research · 24

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Routine performance and errors of 454 HLA exon sequencing in diagnostics

2013 · Norbert Niklas, Johannes Pröll, et al. · BMC Bioinformatics · 22

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The Impact of Digital Transformation on Blood Donation and Donor Characteristics

2023 · Norbert Niklas, Claudia Loimayr, et al. · Transfusion Medicine and Hemotherapy · 16

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Machine learning-based prediction of fainting during blood donations using donor properties and weather data as features

2022 · Susanne Suessner, Norbert Niklas, et al. · BMC Medical Informatics and Decision Making · 16

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Qualifying high-throughput immune repertoire sequencing

2014 · Norbert Niklas, Johannes Pröll, et al. · Cellular Immunology · 11

Biomarker Discovery in Rare Malignancies: Development of a miRNA Signature for RDEB-cSCC

2023 · Roland Zauner, Monika Wimmer, et al. · Cancers · 8

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cFinder: definition and quantification of multiple haplotypes in a mixed sample

2015 · Norbert Niklas, Julia Hafenscher, et al. · BMC Research Notes · 6

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Introduction of the Hybcell-Based Compact Sequencing Technology and Comparison to State-of-the-Art Methodologies for KRAS Mutation Detection

2015 · Agnes Zopf, Roman Raim, et al. · BioTechniques · 4

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On the trail of anti‐CDE to unexpected highlights of the RHD*weak 4.3 allele in the Upper Austrian population

2012 · H. Polin, W. Gaszner, et al. · Vox Sanguinis · 3

High-Throughput Sequencing of the Major Histocompatibility Complex following Targeted Sequence Capture

2017 · Johannes Pröll, Carina Fischer, et al. · Methods in molecular biology · 1

599 Deregulation of miR-10b affects HOXD10 expression in squamous cell carcinoma from epidermolysis bullosa patients

2017 · M. Wimmer, R. Zauner, et al. · Journal of Investigative Dermatology

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155 Identification of isomiRs in recessive dystrophic epidermolysis bullosa

2016 · R. Zauner, M. Wimmer, et al. · Journal of Investigative Dermatology

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069 miRNA-10 as potential therapeutic target in recessive dystrophic epidermolysis bullosa

2016 · M. Wimmer, R. Zauner, et al. · Journal of Investigative Dermatology

Additional file 1: of cFinder: definition and quantification of multiple haplotypes in a mixed sample

2015 · Niklas, Norbert, Hafenscher, Julia, et al. · Figshare

Additional file 2: of cFinder: definition and quantification of multiple haplotypes in a mixed sample

2015 · Niklas, Norbert, Hafenscher, Julia, et al. · Figshare

Works count: 24

Citation count: 353

H-index: 11

I10-index: 11