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Browsing publications by
Dr Aneta Mikulasova.
Newcastle Authors
Title
Year
Full text
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 H
3
K
4
me
3
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