Judit Balog

2.9k total citations
22 papers, 1.3k citations indexed

About

Judit Balog is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Judit Balog has authored 22 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 5 papers in Physiology and 5 papers in Genetics. Recurrent topics in Judit Balog's work include Muscle Physiology and Disorders (12 papers), RNA Research and Splicing (6 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Judit Balog is often cited by papers focused on Muscle Physiology and Disorders (12 papers), RNA Research and Splicing (6 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Judit Balog collaborates with scholars based in Netherlands, United States and Italy. Judit Balog's co-authors include Silvère M. van der Maarel, Rabi Tawil, Stephen J. Tapscott, Zizhen Yao, Lauren Snider, Richard J.L.F. Lemmers, Peter Thijssen, Heribert Hirt, László Bögre and Irute Meskiene and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Endocrinology and The American Journal of Human Genetics.

In The Last Decade

Judit Balog

22 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Judit Balog Netherlands 18 1.1k 197 193 183 178 22 1.3k
Jean‐Pierre Revelli United States 15 546 0.5× 104 0.5× 105 0.5× 85 0.5× 11 0.1× 22 852
Christopher J. Krebs United States 15 345 0.3× 175 0.9× 16 0.1× 103 0.6× 39 0.2× 23 815
Jeffrey Rothstein United States 6 630 0.6× 92 0.5× 329 1.7× 28 0.2× 113 0.6× 9 987
Grace M. Hobson United States 23 851 0.8× 297 1.5× 70 0.4× 79 0.4× 88 0.5× 42 1.2k
Jennifer A. Myers United States 13 777 0.7× 91 0.5× 89 0.5× 89 0.5× 19 0.1× 19 963
Michelle L. Brinkmeier United States 21 916 0.8× 488 2.5× 65 0.3× 48 0.3× 16 0.1× 44 1.5k
Charalambos Magoulas United Kingdom 16 420 0.4× 113 0.6× 22 0.1× 27 0.1× 36 0.2× 35 781
Margaret J. Kovach United States 14 895 0.8× 188 1.0× 174 0.9× 32 0.2× 63 0.4× 17 1.8k
Evgueni A. Ivakine Canada 19 769 0.7× 241 1.2× 26 0.1× 49 0.3× 23 0.1× 44 1.1k
Suneeta Madan‐Khetarpal United States 15 430 0.4× 521 2.6× 66 0.3× 24 0.1× 72 0.4× 38 797

Countries citing papers authored by Judit Balog

Since Specialization
Citations

This map shows the geographic impact of Judit Balog's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Judit Balog with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Judit Balog more than expected).

Fields of papers citing papers by Judit Balog

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judit Balog. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Judit Balog. The network helps show where Judit Balog may publish in the future.

Co-authorship network of co-authors of Judit Balog

This figure shows the co-authorship network connecting the top 25 collaborators of Judit Balog. A scholar is included among the top collaborators of Judit Balog based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Judit Balog. Judit Balog is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Buurstede, Jacobus C., Lisa T. C. M. van Weert, Paola Colucci, et al.. (2021). Hippocampal glucocorticoid target genes associated with enhancement of memory consolidation. European Journal of Neuroscience. 55(9-10). 2666–2683. 24 indexed citations
2.
Lemmers, Richard J.L.F., Patrick J. van der Vliet, Ana Blatnik, et al.. (2021). Chromosome 10q-linked FSHD identifies DUX4 as principal disease gene. Journal of Medical Genetics. 59(2). 180–188. 19 indexed citations
3.
Hiller, Monika, et al.. (2020). Premature termination codons in the DMD gene cause reduced local mRNA synthesis. Proceedings of the National Academy of Sciences. 117(28). 16456–16464. 44 indexed citations
5.
Heuvel, Anita van den, Ahmed Mahfouz, Susan L. Kloet, et al.. (2018). Single-cell RNA sequencing in facioscapulohumeral muscular dystrophy disease etiology and development. Human Molecular Genetics. 28(7). 1064–1075. 35 indexed citations
6.
Weert, Lisa T. C. M. van, Jacobus C. Buurstede, Ahmed Mahfouz, et al.. (2017). NeuroD Factors Discriminate Mineralocorticoid From Glucocorticoid Receptor DNA Binding in the Male Rat Brain. Endocrinology. 158(5). 1511–1522. 59 indexed citations
7.
Slieker, Roderick C., Judit Balog, Richard J.L.F. Lemmers, et al.. (2017). SMCHD1 regulates a limited set of gene clusters on autosomal chromosomes. Skeletal Muscle. 7(1). 12–12. 25 indexed citations
8.
Lemmers, Richard J.L.F., Patrick J. van der Vliet, Judit Balog, et al.. (2017). Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2. European Journal of Human Genetics. 26(1). 94–106. 20 indexed citations
9.
Yao, Zizhen, Lauren Snider, Judit Balog, et al.. (2014). DUX4-induced gene expression is the major molecular signature in FSHD skeletal muscle. Human Molecular Genetics. 23(20). 5342–5352. 161 indexed citations
10.
Thijssen, Peter, Judit Balog, Zizhen Yao, et al.. (2014). DUX4 promotes transcription of FRG2 by directly activating its promoter in facioscapulohumeral muscular dystrophy. Skeletal Muscle. 4(1). 19–19. 21 indexed citations
11.
Lemmers, Richard J.L.F., Pilar Camaño, Patrick J. van der Vliet, et al.. (2014). G.O.4. Neuromuscular Disorders. 24(9-10). 793–793. 1 indexed citations
12.
Thijssen, Peter, Elmar W. Tobi, Judit Balog, et al.. (2013). Chromatin remodeling of human subtelomeres and TERRA promoters upon cellular senescence. Epigenetics. 8(5). 512–521. 22 indexed citations
13.
Sacconi, Sabrina, Richard J.L.F. Lemmers, Judit Balog, et al.. (2013). The FSHD2 Gene SMCHD1 Is a Modifier of Disease Severity in Families Affected by FSHD1. The American Journal of Human Genetics. 93(4). 744–751. 119 indexed citations
14.
Young, Janet M., Zizhen Yao, Lauren Snider, et al.. (2013). DUX4 Binding to Retroelements Creates Promoters That Are Active in FSHD Muscle and Testis. PLoS Genetics. 9(11). e1003947–e1003947. 128 indexed citations
15.
Krom, Yvonne D., Peter Thijssen, Janet M. Young, et al.. (2013). Intrinsic Epigenetic Regulation of the D4Z4 Macrosatellite Repeat in a Transgenic Mouse Model for FSHD. PLoS Genetics. 9(4). e1003415–e1003415. 86 indexed citations
16.
Polman, Japke A.E., et al.. (2012). A genome-wide signature of glucocorticoid receptor binding in neuronal PC12 cells. BMC Neuroscience. 13(1). 118–118. 81 indexed citations
17.
Balog, Judit, Peter Thijssen, Jessica C. de Greef, et al.. (2012). Correlation analysis of clinical parameters with epigenetic modifications in the DUX4 promoter in FSHD. Epigenetics. 7(6). 579–584. 46 indexed citations
18.
Zeng, Weihua, Jessica C. de Greef, Richard Chien, et al.. (2009). Specific Loss of Histone H3 Lysine 9 Trimethylation and HP1γ/Cohesin Binding at D4Z4 Repeats Is Associated with Facioscapulohumeral Dystrophy (FSHD). PLoS Genetics. 5(7). e1000559–e1000559. 214 indexed citations
19.
Meskiene, Irute, Wilco Ligterink, László Bögre, et al.. (1998). The SAM kinase pathway: An integrated circuit for stress signaling in plants. Journal of Plant Research. 111(2). 339–344. 10 indexed citations
20.
Meskiene, Irute, László Bögre, Walter Glaser, et al.. (1998). MP2C, a plant protein phosphatase 2C, functions as a negative regulator of mitogen-activated protein kinase pathways in yeast and plants. Proceedings of the National Academy of Sciences. 95(4). 1938–1943. 140 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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