Ferenc Boldog

3.0k total citations · 1 hit paper
36 papers, 2.5k citations indexed

About

Ferenc Boldog is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Ferenc Boldog has authored 36 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Cancer Research. Recurrent topics in Ferenc Boldog's work include Epigenetics and DNA Methylation (11 papers), Renal and related cancers (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Ferenc Boldog is often cited by papers focused on Epigenetics and DNA Methylation (11 papers), Renal and related cancers (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Ferenc Boldog collaborates with scholars based in United States, Sweden and Russia. Ferenc Boldog's co-authors include Henri S. Lichenstein, Michael Jeffers, Harry A. Drabkin, János Sümegi, Rikard Erlandsson, Robert M. Gemmill, Craig Hackett, Sigurður Ingvarsson, Gunnar O. Klein and Gábor G. Kovács and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Cell Biology.

In The Last Decade

Ferenc Boldog

36 papers receiving 2.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Determination of the class and isoform selectivity of small-molecule histone deacetylase inhibitors

2007 599 citations Nagma Khan, Michael Jeffers et al. Biochemical Journal profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ferenc Boldog United States	21	1.8k	517	500	445	308	36	2.5k
Luciana Chessa Italy	28	2.1k 1.2×	693 1.3×	371 0.7×	722 1.6×	149 0.5×	75	2.7k
Henrik Vissing United States	25	2.0k 1.1×	419 0.8×	906 1.8×	331 0.7×	217 0.7×	48	2.8k
Harald von Melchner Germany	31	2.3k 1.2×	381 0.7×	868 1.7×	279 0.6×	234 0.8×	71	3.2k
Perry D. Nisen United States	31	1.8k 1.0×	870 1.7×	491 1.0×	455 1.0×	550 1.8×	55	3.0k
Cristiana Lo Nigro Italy	27	1.2k 0.7×	697 1.3×	389 0.8×	560 1.3×	430 1.4×	82	2.6k
Ann Johnsson Sweden	7	1.6k 0.8×	594 1.1×	410 0.8×	341 0.8×	236 0.8×	7	2.6k
Pierre de la Grange France	34	2.2k 1.2×	462 0.9×	273 0.5×	630 1.4×	163 0.5×	93	3.2k
Michael Dodge United States	12	1.8k 1.0×	648 1.3×	221 0.4×	277 0.6×	186 0.6×	16	2.2k
Olive S. Pettengill United States	24	1.1k 0.6×	758 1.5×	287 0.6×	264 0.6×	209 0.7×	63	2.0k
Alan H. Shih United States	25	2.7k 1.5×	694 1.3×	266 0.5×	618 1.4×	191 0.6×	37	3.8k

Countries citing papers authored by Ferenc Boldog

Since Specialization

Citations

This map shows the geographic impact of Ferenc Boldog'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 Ferenc Boldog with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ferenc Boldog more than expected).

Fields of papers citing papers by Ferenc Boldog

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ferenc Boldog. 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 Ferenc Boldog. The network helps show where Ferenc Boldog may publish in the future.

Co-authorship network of co-authors of Ferenc Boldog

This figure shows the co-authorship network connecting the top 25 collaborators of Ferenc Boldog. A scholar is included among the top collaborators of Ferenc Boldog 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 Ferenc Boldog. Ferenc Boldog is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Zhang, Bo, et al.. (2019). Leap-In Transposases and Transposons Accelerate Cell Line Development. Genetic Engineering & Biotechnology News. 39(9). 59–61. 5 indexed citations

Chapoval, Andrei I., Glennda Smithson, Mehdi Mesri, et al.. (2013). BTNL8, a butyrophilin-like molecule that costimulates the primary immune response. Molecular Immunology. 56(4). 819–828. 27 indexed citations

Khan, Nagma, Michael Jeffers, Sampath Kumar, et al.. (2007). Determination of the class and isoform selectivity of small-molecule histone deacetylase inhibitors. Biochemical Journal. 409(2). 581–589. 599 indexed citations breakdown →

Mesri, Mehdi, Glennda Smithson, Andrei I. Chapoval, et al.. (2006). Inhibition of in vitro and in vivo T cell responses by recombinant human Tim-1 extracellular domain proteins. International Immunology. 18(3). 473–484. 20 indexed citations

LaRochelle, William J., Michael Jeffers, William F. McDonald, et al.. (2001). PDGF-D, a new protease-activated growth factor. Nature Cell Biology. 3(5). 517–521. 300 indexed citations

Gemmill, Robert M., James West, Ferenc Boldog, et al.. (1998). The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched- related gene, TRC8. Proceedings of the National Academy of Sciences. 95(16). 9572–9577. 122 indexed citations

Boldog, Ferenc, Robert M. Gemmill, James West, et al.. (1997). Chromosome 3p14 Homozygous Deletions and Sequence Analysis of FRA3B. Human Molecular Genetics. 6(2). 193–203. 117 indexed citations

Кашуба, В. И., Rinat Gizatullin, Rando Allikmets, et al.. (1997). NotI linking/jumping clones of human chromosome 3: mapping of the TFRC, RAB7 and HAUSP genes to regions rearranged in leukemia and deleted in solid tumors. FEBS Letters. 419(2-3). 181–185. 34 indexed citations

Rassool, Feyruz V., Mei-Ling Shen, S. Tiong Ong, et al.. (1996). Direct Cloning of DNA Sequences from the Common Fragile Site Region at Chromosome Band 3p14.2. Genomics. 35(1). 109–117. 51 indexed citations

10.

Wilke, Charles M., Bryan K. Hall, Ferenc Boldog, et al.. (1994). Multicolor FISH Mapping of YAC Clones in 3p14 and Identification of a YAC Spanning both FRA3B and the t(3;8) Associated with Hereditary Renal Cell Carcinoma. Genomics. 22(2). 319–326. 59 indexed citations

11.

Boldog, Ferenc, B. Waggoner, Thomas W. Glover, et al.. (1994). Integrated YAC contig containing the 3pl4.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B. Genes Chromosomes and Cancer. 11(4). 216–221. 32 indexed citations

12.

Roche, Joëlle, Emily Whisenant, Ferenc Boldog, et al.. (1994). Dinucleotide repeats flanking the renal carcinoma breakpoint at 3p14.2. Human Molecular Genetics. 3(1). 215–215. 13 indexed citations

13.

Wang, Jiyi, Eugene R. Zabarovsky, Peter Berglund, et al.. (1994). Somatic Cell Hybrid Panel and NotI Linking Clones for Physical Mapping of Human Chromosome 3. Genomics. 20(1). 105–113. 15 indexed citations

14.

Zabarovsky, Eugene R., В. И. Кашуба, Veronika I. Zabarovska, et al.. (1993). Alu-PCR Approach to Isolating NotI-Linking Clones from the 3p14-p21 Region Frequently Deleted in Renal Cell Carcinoma. Genomics. 16(3). 713–719. 12 indexed citations

15.

Zabarovsky, Eugene R., Ferenc Boldog, Rikard Erlandsson, et al.. (1991). New strategy for mapping the human genome based on a novel procedure for construction of jumping libraries. Genomics. 11(4). 1030–1039. 22 indexed citations

16.

Boldog, Ferenc, Kristina Arheden, Stephan Imreh, et al.. (1991). Involvement of 3p Deletions in Sporadic and Hereditary Forms of Renal Cell Carcinoma. Genes Chromosomes and Cancer. 3(5). 403–406. 10 indexed citations

17.

Erlandsson, Rikard, J. Szpirer, M.Q. Islam, et al.. (1991). The most frequently lost allelic site in human renal cell carcinoma (D3F15S2) on the short arm of chromosome 3 has homologous sequences on rat chromosome 8. Cytogenetic and Genome Research. 57(2-3). 149–150. 6 indexed citations

18.

Szabó, Gábor, Ferenc Boldog, & Norbert Wikonkál. (1990). Disassembly of chromatin into ≅50 kb units by detergent. Biochemical and Biophysical Research Communications. 169(2). 706–712. 12 indexed citations

19.

Minárovits, János, Michael Steinitz, Ferenc Boldog, et al.. (1990). Differences in C‐myc and pvt‐1 amplification in sewa sarcoma sublines selected for adherent or non‐adherent growth. International Journal of Cancer. 45(3). 514–520. 11 indexed citations

20.

Zabarovsky, Eugene R., Ferenc Boldog, Terri G. Thompson, et al.. (1990). Construction of a human chromosome 3 specific Notl linking library using a novel cloning procedure. Nucleic Acids Research. 18(21). 6319–6324. 33 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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