Toggle Main Menu Toggle Search

Open Access padlockePrints

Browsing publications by Dr Aneta Mikulasova

Newcastle AuthorsTitleYearFull text
Brigid Davidson
Dr Juliana Arcila Galvis
Dr Marco Trevisan
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 cancer2024
Dr Aneta Mikulasova
Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders2024
Dr Aneta Mikulasova
A unique case of Bloom syndrome with a combination of genetic hits: A lesson from trio‑based exome sequencing: A case report2023
Dan Kent
Dr Letizia Marchetti
Dr Aneta Mikulasova
Dr Lisa Russell
Dr Daniel Rico Rodriguez
Broad H3K4me3 domains: Maintaining cellular identity and their implication in super-enhancer hijacking2023
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 rearrangement2023
Hannah Smith
Francesco Kumara Mastrorosa
Dr Giles Holt
Dr Brendan Houston
Dr Bilal Alobaidi
et al.
A de novo paradigm for male infertility2022
Dr Aneta Mikulasova
Chromosomal abnormalities in multiple myeloma2022
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 genes2022
Dr Aneta Mikulasova
Dan Kent
Dr Marco Trevisan
Nefeli Karataraki
Kent Fung
et al.
Epigenomic translocation of H3K4me3 broad domains over oncogenes following hijacking of super-enhancers2022
Dr Aneta Mikulasova
Novel de novo pathogenic variant in the GNAI1 gene as a cause of severe disorders of intellectual development2022
Dr Aneta Mikulasova
Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype2021
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-AS12021
Dr Aneta Mikulasova
Heterogenous mutation spectrum and deregulated cellular pathways in aberrant plasma cells underline molecular pathology of light-chain amyloidosis2021
Dr Daniel Leongamornlert
Dr Aneta Mikulasova
Whole-genome sequencing reveals progressive versus stable myeloma precursor conditions as two distinct entities2021
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 lymphoma2020
12