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A. Mikulasova · SciRah

Researcher profile · Semantic Scholar

A. Mikulasova

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A. Mikulasova — researcher profile on SciRah

h-index: 16
Works: 72
Citations: 1,320

Most-cited papers

Mutational Spectrum, Copy Number Changes, and Outcome: Results of a Sequencing Study of Patients With Newly Diagnosed Myeloma
B. Walker, E. Boyle, C. Wardell, Alex Murison +23 more
2015Journal of Clinical Oncology518 citations Open access
Semantic Scholar
Whole-genome sequencing reveals progressive versus stable myeloma precursor conditions as two distinct entities
Bénedith Oben, G. Froyen, K. Maclachlan, D. Leongamornlert +23 more
2021Nature Communications106 citations Open access
Semantic Scholar
Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2
C. Duncan, B. Thompson, Rui Chen, G. Rice +34 more
2019Science immunology94 citations Open access
Semantic Scholar
The spectrum of somatic mutations in monoclonal gammopathy of undetermined significance indicates a less complex genomic landscape than that in multiple myeloma
A. Mikulasova, C. Wardell, Alex Murison, E. Boyle +13 more
2017Haematologica92 citations Open access
Semantic Scholar
Germline TET2 Loss-Of-Function Causes Childhood Immunodeficiency And Lymphoma.
Jarmila Stremenova Spegarova, Dylan Lawless, S. Mohamad, K. Engelhardt +23 more
2020Blood73 citations Open access
Semantic Scholar
Microhomology-mediated end joining drives complex rearrangements and overexpression of MYC and PVT1 in multiple myeloma
A. Mikulasova, C. Ashby, R. Tytarenko, Ping-Ping Qu +18 more
2019Haematologica58 citations Open access
Semantic Scholar
A de novo paradigm for male infertility
M. Oud, R. Smits, H. Smith, F. K. Mastrorosa +65 more
2021Nature Communications55 citations Open access
Semantic Scholar
Genomewide profiling of copy‐number alteration in monoclonal gammopathy of undetermined significance
A. Mikulasova, J. Smetana, M. Wayhelova, H. Janyšková +12 more
2016European Journal of Haematology28 citations Open access
Semantic Scholar
Genome-Wide Screening of Cytogenetic Abnormalities in Multiple Myeloma Patients Using Array-CGH Technique: A Czech Multicenter Experience
J. Smetana, Jan Frohlich, R. Zaoralova, V. Vallová +11 more
2014BioMed Research International26 citations Open access
Semantic Scholar
Gain(1)(q21) is an unfavorable genetic prognostic factor for patients with relapsed multiple myeloma treated with thalidomide but not for those treated with bortezomib.
J. Smetana, K. Beránková, R. Zaoralova, P. Němec +17 more
2013Clinical Lymphoma, Myeloma & Leukemia26 citations Open access
Semantic Scholar
Molecular characterization and clinical outcome of B-cell precursor acute lymphoblastic leukemia with IG-MYC rearrangement
S. Bomken, A. Enshaei, E. Schwalbe, A. Mikulasova +36 more
2022Haematologica22 citations Open access
Semantic Scholar
Dynamics of broad H3K4me3 domains uncover an epigenetic switch between cell identity and cancer-related genes
M. Belhocine, M. Simonin, J. Abad-Flores, A. Cieslak +15 more
2021Genome Research21 citations Open access
Semantic Scholar
Broad H3K4me3 domains: Maintaining cellular identity and their implication in super‐enhancer hijacking
D. Kent, L. Marchetti, A. Mikulasova, L. Russell +1 more
2023Bioessays19 citations Open access
Semantic Scholar
Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders
M. Wayhelova, V. Vallová, Petr Broz, A. Mikulasova +6 more
2024Orphanet Journal of Rare Diseases18 citations Open access
Semantic Scholar
Epigenomic translocation of H3K4me3 broad domains over oncogenes following hijacking of super-enhancers
A. Mikulasova, D. Kent, Marco Trevisan-Herraz, N. Karataraki +17 more
2020bioRxiv18 citations Open access
Semantic Scholar
Structural variants shape the genomic landscape and clinical outcome of multiple myeloma
C. Ashby, E. Boyle, M. Bauer, A. Mikulasova +12 more
2022Blood Cancer Journal17 citations Open access
Semantic Scholar
High-resolution simulations of chromatin folding at genomic rearrangements in malignant B cells provide mechanistic insights into proto-oncogene deregulation
D. Rico, D. Kent, N. Karataraki, A. Mikulasova +5 more
2022bioRxiv13 citations Open access
Semantic Scholar
A first Czech analysis of 1887 cases with monoclonal gammopathy of undetermined significance
V. Sandecká, R. Hájek, L. Pour, I. Špička +23 more
2017European Journal of Haematology12 citations Open access
Semantic Scholar
Prediction of Progression of Smouldering into Therapy Requiring Multiple Myeloma By Easily Accessible Clinical Factors [in 527 Patients]
R. Hájek, V. Sandecká, A. Seckinger, I. Špička +24 more
201412 citations
Semantic Scholar
Oligonucleotide-based array CGH as a diagnostic tool in multiple myeloma patients.
J. Smetana, Jan Frohlich, Vladimíra Vranová, A. Mikulasova +2 more
2011Klinicka onkologie10 citations
Semantic Scholar
Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype
J. Smetana, V. Vallová, M. Wayhelova, Eva Hladílková +6 more
2021Frontiers in Genetics8 citations Open access
Semantic Scholar
Analysis of B-cell subpopulations in monoclonal gammopathies.
P. Všianská, L. Říhová, T. Varmužová, R. Suská +7 more
2015Clinical Lymphoma, Myeloma & Leukemia7 citations Open access
Semantic Scholar
Novel de novo pathogenic variant in the GNAI1 gene as a cause of severe disorders of intellectual development
M. Wayhelova, V. Vallová, P. Brož, A. Mikulasova +6 more
2021Journal of Human Genetics6 citations
Semantic Scholar
Chromosomal abnormalities in multiple myeloma
A. Mikulasova, G. Morgan, B. Walker
2022Nature Reviews Disease Primers5 citations Open access
Semantic Scholar
GATA2 deficiency phenotype associated with tandem duplication of GATA2 and overexpression of GATA2-AS1
Preeti Singh, Maninder Heer, Anastasia Resteu, A. Mikulasova +12 more
2021Blood Advances5 citations Open access
Semantic Scholar
Whole genome sequencing provides evidence of two biologically and clinically distinct entities of asymptomatic monoclonal gammopathies: progressive versus stable myeloma precursor condition
Bénedith Oben, G. Froyen, K. Maclachlan, D. Leongamornlert +22 more
2020bioRxiv5 citations Open access
Semantic Scholar
Exome Sequencing To Define A Genetic Signature Of Plasma Cells In Systemic AL Amyloidosis
E. Boyle, B. Walker, Dorota Rowczienio, C. Wardell +12 more
20135 citations
Semantic Scholar
EpiATLAS – a reference for human epigenomic research
Quirin Manz, M. Bilenky, Dennis Hecker, Nihit Aggarwal +144 more
2026bioRxiv4 citations Open access
Semantic Scholar
Heterogenous mutation spectrum and deregulated cellular pathways in aberrant plasma cells underline molecular pathology of light-chain amyloidosis
Z. Chyra, T. Ševčíková, Petr Vojta, Janka Puterová +30 more
2020Haematologica4 citations Open access
Semantic Scholar
Chromothripsis and Chromoplexy Are Associated with DNA Instability and Adverse Clinical Outcome in Multiple Myeloma
C. Ashby, M. Bauer, Yan Wang, C. Wardell +17 more
2018Blood4 citations
Semantic Scholar
A unique case of Bloom syndrome with a combination of genetic hits: A lesson from trio‑based exome sequencing: A case report
M. Wayhelova, V. Vallová, P. Brož, A. Mikulasova +6 more
2023Molecular Medicine Reports3 citations Open access
Semantic Scholar
Unraveling Diverse Mechanisms of Complex Structural Variant Interactions through Multiomic Data in Multiple Myeloma
En-Ze Liu, Nathan J. Becker, Parvathi Sudha, A. Mikulasova +5 more
2023Blood3 citations Open access
Semantic Scholar
[Identification of a Family with SUFU Germline Deletion Based on a Case of Desmoplastic Medulloblastoma in an Infant].
J. Šoukalová, K. Vejmělková, T. Cermanová, K. Kašíková +11 more
2016Klinicka onkologie3 citations Open access
Semantic Scholar
Evolutionarily conserved enhancer-associated features within the MYEOV locus suggest a regulatory role for this non-coding DNA region in cancer
Brigid S. A. Davidson, Juliana E. Arcila-Galvis, Marco Trevisan-Herraz, A. Mikulasova +3 more
2024Frontiers in Cell and Developmental Biology2 citations Open access
Semantic Scholar
Somatic Hypermutation in Enhancer Regions Shapes Non-Coding Myeloma Genome, Generating DNA Breaks and Driving Etiology through Mutation and Structural Variation
Patrick Blaney, Brian A. Walker, A. Mikulasova, Dylan C Gagler +17 more
2023Blood2 citations Open access
Semantic Scholar
Whole-Genome Sequencing Reveals Evidence of Two Biologically and Clinically Distinct Entities: Progressive Versus Stable Myeloma Precursor Disease
Bénedith Oben, G. Froyen, K. Maclachlan, Binbin Zheng-Lin +20 more
2020Blood2 citations
Semantic Scholar
Abstract 5324: Intragenic DNA-hypomethylation promotes overexpression ofITGB7in MF subgroup of multiple myeloma
Samrat Roy Choudhury, C. Ashby, R. Tytarenko, Yan Wang +7 more
2018Molecular and Cellular Biology / Genetics2 citations
Semantic Scholar
Incidence of cytogenetic aberrations in two B lineage subpopulations in multiple myeloma patients analyzed by combination of whole-genome profiling and FISH.
J. Smetana, E. Dementyeva, F. Kryukov, P. Němec +6 more
2013Neoplasma (Bratislava)2 citations Open access
Semantic Scholar
Mutationally Enriched Regions of the Non-Coding Genome Harbor Functionally Impactful Mutations That Dysregulate Key Genes Involved in Multiple Myeloma Pathogenesis
Patrick Blaney, K. Maclachlan, Marios Papadimitriou, A. Mikulasova +28 more
2024Blood1 citations
Semantic Scholar
Multiomics Data Integration in the Complete Myeloma Genome Reveals Frequent Centromeric Rearrangements and Their Epigenomic Consequences
A. Mikulasova, En-Ze Liu, Nathan J. Becker, Parvathi Sudha +2 more
2024Blood1 citations
Semantic Scholar
The discovery of an evolutionarily conserved enhancer within the MYEOV locus suggests an unexpected role for this non-coding region in cancer
Brigid S. A. Davidson, Juliana E. Arcila-Galvis, Marco Trevisan-Herraz, A. Mikulasova +3 more
2023bioRxiv1 citations Open access
Semantic Scholar
Whole genome amplification effect on segmental copy-number changes and copy-number neutral loss of heterozygosity analysis by oligonucleotide-based array-comparative genomic hybridization in human myeloma cell line
A. Mikulasova, J. Smetana, M. Wayhelova, H. Janyšková +3 more
20161 citations
Semantic Scholar
Clonal cytogenetics changes in progression of multiple myelomato extramedullary relapse and plasmocellular leukemia: a casereport
J. Smetana, P. Kuglík, H. Grešliková, R. Kupská +9 more
20161 citations
Semantic Scholar
Detection of oncogenic mutations in cervical carcinoma using method High Resolution Melting (HRM).
M. Wayhelova, A. Mikulasova, J. Smetana, V. Vallová +4 more
2016Neoplasma (Bratislava)1 citations Open access
Semantic Scholar
Evaluation of Current Clinical Models for Risk of Progression from Monoclonal Gammopathy of Undetermined Significance to Multiple Myeloma or Related Malignancies in 2028 Persons Followed in the Czech Republic
V. Sandecká, Z. Adam, I. Špička, V. Ščudla +20 more
20141 citations
Semantic Scholar
Mutational Patterns and Copy Number Changes at Diagnosis Are a Powerful Tool to Predict Outcome: Result of the Sequencing Study of 463 Newly Diagnosed Myeloma Trial Patients
E. Boyle, B. Walker, C. Wardell, Alex Murison +20 more
20141 citations Open access
Semantic Scholar
Incidence of cytogenetic aberrations in two B lineage subpopulations in multiple myeloma patients analyzed by combination of whole-genome profiling and FISH.
J. Smetana, E. Dementyeva, F. Kryukov, P. Němec +6 more
2014Neoplasma (Bratislava)1 citations
Semantic Scholar
Somatic Mutation Spectrum in Monoclonal Gammopathy of Undetermined Significance Compared to Multiple Myeloma
A. Mikulasova, B. Walker, C. Wardell, E. Boyle +6 more
20141 citations
Semantic Scholar
Genomic characterization of patient derived xenograft models of multiple myeloma reveals selection of multiple pre-existing high risk clones
Nathan J. Becker, En-Ze Liu, Riya Sharma, Parvathi Sudha +22 more
2026bioRxiv0 citations Open access
Semantic Scholar
Abstract 5940: Chromosome-level phasing to resolve haplotypes using multiomic data in multiple myeloma reveals complex distal interactions between chromosomes that impacts epigenetic states and gene expression
Nathan J. Becker, En-Ze Liu, J. Sanborn, A. Suvannasankha +9 more
2026Cancer Research0 citations
Semantic Scholar

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