Brigid Davidson
Dr Juliana Arcila Galvis
Dr Marco Trevisan-Herraz
Dr Aneta Mikulasova
Dr Lisa Russell
et al. | Evolutionarily conserved enhancer-associated features within the MYEOV locus suggest a regulatory role for this non-coding DNA region in cancer | 2024 |
|
Dr Aneta Mikulasova
| Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders | 2024 |
|
Dr Aneta Mikulasova
| A unique case of Bloom syndrome with a combination of genetic hits: A lesson from trio‑based exome sequencing: A case report | 2023 |
|
Dan Kent
Dr Letizia Marchetti
Dr Aneta Mikulasova
Dr Lisa Russell
Dr Daniel Rico Rodriguez
et al. | Broad H3K4me3 domains: Maintaining cellular identity and their implication in super-enhancer hijacking | 2023 |
|
Dr Simon Bomken
Dr Amir Enshaei
Dr Ed Schwalbe
Dr Aneta Mikulasova
Dr Masood Zaka
et al. | Molecular characterisation and clinical outcome of B-cell precursor acute lymphoblastic leukaemia with IG-MYC rearrangement | 2023 |
|
Hannah Smith
Francesco Kumara Mastrorosa
Dr Giles Holt
Dr Brendan Houston
Dr Bilal Alobaidi
et al. | A de novo paradigm for male infertility | 2022 |
|
Dr Aneta Mikulasova
| Chromosomal abnormalities in multiple myeloma | 2022 |
|
Dr Aneta Mikulasova
Dr Lisa Russell
Dr Daniel Rico Rodriguez
| Dynamics of broad H3K4me3 domains uncover an epigenetic switch between cell identity and cancer-related genes | 2022 |
|
Dr Aneta Mikulasova
Dan Kent
Dr Marco Trevisan-Herraz
Nefeli Karataraki
Kent Fung
et al. | Epigenomic translocation of H3K4me3 broad domains over oncogenes following hijacking of super-enhancers | 2022 |
|
Dr Aneta Mikulasova
| Novel de novo pathogenic variant in the GNAI1 gene as a cause of severe disorders of intellectual development | 2022 |
|
Dr Aneta Mikulasova
| Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype | 2021 |
|
Dr Preeti Singh
Maninder Heer
Dr Anastasia Resteu
Dr Aneta Mikulasova
Dr Mojgan Reza
et al. | GATA2 deficiency phenotype associated with tandem duplication of GATA2 and overexpression of GATA2-AS1 | 2021 |
|
Dr Aneta Mikulasova
| Heterogenous mutation spectrum and deregulated cellular pathways in aberrant plasma cells underline molecular pathology of light-chain amyloidosis | 2021 |
|
Dr Daniel Leongamornlert
Dr Aneta Mikulasova
| Whole-genome sequencing reveals progressive versus stable myeloma precursor conditions as two distinct entities | 2021 |
|
Dr Jarmila Spegarova
Dr Karin Engelhardt
Dr Helen Griffin
Dr Aneta Mikulasova
Dr Meghan Acres
et al. | Germline TET2 loss-of-function causes childhood immunodeficiency and lymphoma | 2020 |
|
Dr Aneta Mikulasova
Professor Graham Jackson
| Microhomology-mediated end joining drives complex rearrangements and overexpression of MYC and PVT1 in multiple myeloma | 2020 |
|
Dr Christopher Duncan
Dr Benjamin Thompson
Dr Rui Chen
Dr Florian Gothe
Victoria Shuttleworth
et al. | Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2 | 2019 |
|
Dr Aneta Mikulasova
| A first Czech analysis of 1887 cases with monoclonal gammopathy of undetermined significance | 2017 |
|
Dr Aneta Mikulasova
Professor Graham Jackson
| The spectrum of somatic mutations in monoclonal gammopathy of undetermined significance indicates a less complex genomic landscape than that in multiple myeloma | 2017 |
|
Dr Aneta Mikulasova
| Detection of oncogenic mutations in cervical carcinoma using method High Resolution Melting (HRM) | 2016 |
|
Dr Aneta Mikulasova
| Genome-wide profiling of copy‑number alteration in monoclonal gammopathy of undetermined significance | 2016 |
|
Dr Aneta Mikulasova
| Analysis of B-cell subpopulations in monoclonal gammopathies | 2015 |
|
Dr Aneta Mikulasova
Professor Graham Jackson
| Mutational Spectrum, Copy Number Changes, and Outcome: Results of a Sequencing Study of Patients With Newly Diagnosed Myeloma | 2015 |
|
Dr Aneta Mikulasova
| Genome-wide screening of cytogenetic abnormalities in multiple myeloma patients using array-CGH technique: a Czech multicenter experience | 2014 |
|
Dr Aneta Mikulasova
| Incidence of cytogenetic aberrations in two B lineage subpopulations in multiple myeloma patients analyzed by combination of whole-genome profiling and FISH | 2014 |
|
