Publications by authors named "Judit Balog"

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DUX4 activates common and context-specific intergenic transcripts and isoforms.
Dongxu Zheng, Anita van den Heuvel, Judit Balog, Iris M Willemsen, Susan Kloet

Sci Adv· May 2025

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Lrif1 modulates Trim28-mediated repression of the locus in mouse embryonic stem cells.
Darina Šikrová, Román González-Prieto, Alfred C O Vertegaal, Judit Balog, Lucia Clemens-Daxinger

bioRxiv· November 2024

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Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophy.
Richard J L F Lemmers, Russell Butterfield, Patrick J van der Vliet, Jan L de Bleecker, Ludo van der Pol, Judit Balog

Brain· February 2024

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snRNA-seq analysis in multinucleated myogenic FSHD cells identifies heterogeneous FSHD transcriptome signatures associated with embryonic-like program activation and oxidative stress-induced apoptosis.
Dongxu Zheng, Annelot Wondergem, Susan Kloet, Iris Willemsen, Judit Balog

Hum Mol Genet· January 2024

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SMCHD1 and LRIF1 converge at the FSHD-associated D4Z4 repeat and LRIF1 promoter yet display different modes of action.
Darina Šikrová, Alessandra M Testa, Iris Willemsen, Anita van den Heuvel, Stephen J Tapscott, Judit Balog

Commun Biol· June 2023

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Facioscapulohumeral muscular dystrophy: the road to targeted therapies.
Mara S Tihaya, Karlien Mul, Judit Balog, Jessica C de Greef, Stephen J Tapscott

Nat Rev Neurol· February 2023

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Hippocampal glucocorticoid target genes associated with enhancement of memory consolidation.
Jacobus C Buurstede, Lisa T C M van Weert, Paola Colucci, Max Gentenaar, Eva M G Viho, Judit Balog

Eur J Neurosci· May 2022

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Chromosome 10q-linked FSHD identifies as principal disease gene.
Richard J L F Lemmers, Patrick J van der Vliet, Ana Blatnik, Judit Balog, Janez Zidar

J Med Genet· February 2022

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A proteomics study identifying interactors of the FSHD2 gene product SMCHD1 reveals RUVBL1-dependent DUX4 repression.
Remko Goossens, Mara S Tihaya, Anita van den Heuvel, Klorane Tabot-Ndip, Iris M Willemsen, Judit Balog

Sci Rep· December 2021

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Adenine base editing of the polyadenylation signal for targeted genetic therapy in facioscapulohumeral muscular dystrophy.
Darina Šikrová, Vlad A Cadar, Yavuz Ariyurek, Jeroen F J Laros, Judit Balog

Mol Ther Nucleic Acids· September 2021

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Premature termination codons in the gene cause reduced local mRNA synthesis.
Raquel García-Rodríguez, Monika Hiller, Laura Jiménez-Gracia, Zarah van der Pal, Judit Balog

Proc Natl Acad Sci U S A· July 2020

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Homozygous nonsense variant in associated with facioscapulohumeral muscular dystrophy.
Kohei Hamanaka, Darina Šikrová, Satomi Mitsuhashi, Hiroki Masuda, Yukari Sekiguchi, Judit Balog

Neurology· June 2020

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Intronic variants in FSHD: testing the potential for CRISPR-Cas9 genome editing.
Remko Goossens, Marlinde L van den Boogaard, Richard J L F Lemmers, Judit Balog, Patrick J van der Vliet

J Med Genet· December 2019

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Characterisation of transcription factor profiles in polycystic kidney disease (PKD): identification and validation of STAT3 and RUNX1 in the injury/repair response and PKD progression.
Chiara Formica, Tareq Malas, Judit Balog, Lotte Verburg, Peter A C 't Hoen

J Mol Med (Berl)· December 2019

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Single-cell RNA sequencing in facioscapulohumeral muscular dystrophy disease etiology and development.
Anita van den Heuvel, Ahmed Mahfouz, Susan L Kloet, Judit Balog, Baziel G M van Engelen

Hum Mol Genet· April 2019

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Monosomy 18p is a risk factor for facioscapulohumeral dystrophy.
Judit Balog, Remko Goossens, Richard J L F Lemmers, Kirsten R Straasheijm, Patrick J van der Vliet

J Med Genet· July 2018

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Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2.
Richard Jlf Lemmers, Patrick J van der Vliet, Judit Balog, Jelle J Goeman, Wibowo Arindrarto

Eur J Hum Genet· January 2018

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SMCHD1 regulates a limited set of gene clusters on autosomal chromosomes.
Amanda G Mason, Roderick C Slieker, Judit Balog, Richard J L F Lemmers, Chao-Jen Wong

Skelet Muscle· June 2017

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NeuroD Factors Discriminate Mineralocorticoid From Glucocorticoid Receptor DNA Binding in the Male Rat Brain.
Lisa T C M van Weert, Jacobus C Buurstede, Ahmed Mahfouz, Pamela S M Braakhuis, J Annelies E Polman, Judit Balog

Endocrinology· May 2017

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Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4.
Judit Balog, Peter E Thijssen, Sean Shadle, Kirsten R Straasheijm, Patrick J van der Vliet

Epigenetics· November 2016

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Corrigendum. Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4.
Judit Balog, Peter E Thijssen, Sean Shadle, Kirsten R Straasheijm, Patrick J van der Vliet

Epigenetics· August 2016

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Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy.
Marlinde L van den Boogaard, Richard J L F Lemmers, Judit Balog, Mariëlle Wohlgemuth, Mari Auranen

Am J Hum Genet· May 2016

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Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2.
Richard J L F Lemmers, Jelle J Goeman, Patrick J van der Vliet, Merlijn P van Nieuwenhuizen, Judit Balog

Hum Mol Genet· February 2015

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DUX4-induced gene expression is the major molecular signature in FSHD skeletal muscle.
Zizhen Yao, Lauren Snider, Judit Balog, Richard J L F Lemmers, Silvère M Van Der Maarel

Hum Mol Genet· October 2014

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Genetic and epigenetic characteristics of FSHD-associated 4q and 10q D4Z4 that are distinct from non-4q/10q D4Z4 homologs.
Weihua Zeng, Yen-Yun Chen, Daniel A Newkirk, Beibei Wu, Judit Balog

Hum Mutat· August 2014

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