Eva Bober

7.9k total citations · 2 hit papers
64 papers, 6.3k citations indexed

About

Eva Bober is a scholar working on Molecular Biology, Geriatrics and Gerontology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Eva Bober has authored 64 papers receiving a total of 6.3k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 13 papers in Geriatrics and Gerontology and 9 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Eva Bober's work include Muscle Physiology and Disorders (20 papers), Developmental Biology and Gene Regulation (14 papers) and Sirtuins and Resveratrol in Medicine (13 papers). Eva Bober is often cited by papers focused on Muscle Physiology and Disorders (20 papers), Developmental Biology and Gene Regulation (14 papers) and Sirtuins and Resveratrol in Medicine (13 papers). Eva Bober collaborates with scholars based in Germany, United States and France. Eva Bober's co-authors include Thomas Braun, Hans-Henning Arnold, Hans-Henning Arnold, Gregor Buschhausen-Denker, Egbert Tannich, Gary E. Lyons, Barbara Winter, Margaret Buckingham, Peter Gruß and Nadia Rosenthal and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Eva Bober

64 papers receiving 6.2k citations

Hit Papers

align trajectories sort by overperformance

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.

A novel human muscle factor related to but distinct from MyoD1 induces myogenic conversion in 10T1/2 fibroblasts.

1989 810 citations Thomas Braun, Gregor Buschhausen-Denker et al. The EMBO Journal profile →
Sirt7 Increases Stress Resistance of Cardiomyocytes and Prevents Apoptosis and Inflammatory Cardiomyopathy in Mice

2008 525 citations Olesya Vakhrusheva, Christian Smolka et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Eva Bober	5.1k	899	706	571	520	64	6.3k
Gregory A. Cox	3.3k 0.6×	582 0.6×	49 0.1×	479 0.8×	558 1.1×	82	4.4k
Hansell H. Stedman	3.7k 0.7×	1.2k 1.3×	44 0.1×	937 1.6×	698 1.3×	51	4.3k
Pascal Maire	4.9k 1.0×	1.3k 1.4×	35 0.0×	305 0.5×	756 1.5×	72	6.6k
Eijiro Ozawa	4.1k 0.8×	459 0.5×	50 0.1×	943 1.7×	915 1.8×	99	4.7k
Yuko Miyagoe‐Suzuki	3.6k 0.7×	612 0.7×	41 0.1×	284 0.5×	885 1.7×	70	4.4k
Andrew S. Brack	5.8k 1.1×	666 0.7×	39 0.1×	294 0.5×	1.7k 3.3×	34	7.0k
Vincenzo Nigro	5.7k 1.1×	1.5k 1.7×	27 0.0×	1.3k 2.4×	550 1.1×	224	7.1k
Francisco J. Naya	3.2k 0.6×	1.2k 1.3×	28 0.0×	560 1.0×	425 0.8×	42	4.3k
Douglas P. Millay	2.9k 0.6×	347 0.4×	29 0.0×	411 0.7×	657 1.3×	53	3.4k
Zipora Yablonka‐Reuveni	4.5k 0.9×	728 0.8×	36 0.1×	230 0.4×	1.2k 2.3×	78	5.5k

Countries citing papers authored by Eva Bober

Since Specialization

Citations

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

Fields of papers citing papers by Eva Bober

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eva Bober

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Bartkuhn, Marek, Stefan Günther, Carsten Künne, et al.. (2022). Inactivation of Sirt6 ameliorates muscular dystrophy in mdx mice by releasing suppression of utrophin expression. Nature Communications. 13(1). 4184–4184. 12 indexed citations

Bosch‐Presegué, Laia, Anna Marazuela-Duque, Carolina de la Torre, et al.. (2018). SIRT6-dependent cysteine monoubiquitination in the PRE-SET domain of Suv39h1 regulates the NF-κB pathway. Nature Communications. 9(1). 101–101. 49 indexed citations

Ianni, Alessandro, Soraya Hoelper, Marcus Krüeger, Thomas Braun, & Eva Bober. (2017). Sirt7 stabilizes rDNA heterochromatin through recruitment of DNMT1 and Sirt1. Biochemical and Biophysical Research Communications. 492(3). 434–440. 23 indexed citations

Hölper, Soraya, Hendrik Nolte, Eva Bober, Thomas Braun, & Marcus Krüger. (2014). Dissection of metabolic pathways in the Db/Db mouse model by integrative proteome and acetylome analysis. Molecular BioSystems. 11(3). 908–922. 18 indexed citations

Studencka‐Turski, Maja, Christian Smolka, Tobias Baumann, et al.. (2013). The sirtuin SIRT6 regulates stress granules formation in C. elegans and in mammals. Journal of Cell Science. 126(Pt 22). 5166–77. 54 indexed citations

Buniello, Annalisa, Rachel E. Hardisty-Hughes, Johanna Pass, et al.. (2013). Headbobber: A Combined Morphogenetic and Cochleosaccular Mouse Model to Study 10qter Deletions in Human Deafness. PLoS ONE. 8(2). e56274–e56274. 7 indexed citations

Araki, Satoshi, Yasuhiro Izumiya, Takafumi Senokuchi, et al.. (2011). Abstract 9663: Sirt7 Contributes to Proper Wound Healing After Murine Model of Myocardial Infarction by Modulating the Fibroblast Differentiation. Circulation. 124(suppl_21). 1 indexed citations

Vakhrusheva, Olesya, Izabela Piotrowska, Wiesław Ziółkowski, et al.. (2009). Different extent of cardiac malfunction and resistance to oxidative stress in heterozygous and homozygous manganese-dependent superoxide dismutase-mutant mice. Cardiovascular Research. 82(3). 448–457. 46 indexed citations

Krüger, Marcus, Thomas Schmid, Sonja Krüger, Eva Bober, & Thomas Braun. (2006). Functional redundancy of NSCL‐1 and NeuroD during development of the petrosal and vestibulocochlear ganglia. European Journal of Neuroscience. 24(6). 1581–1590. 30 indexed citations

10.

Merlo, Giorgio R., Laura Paleari, Stefano Mantero, et al.. (2002). The Dlx5 Homeobox Gene Is Essential for Vestibular Morphogenesis in the Mouse Embryo through a BMP4-Mediated Pathway. Developmental Biology. 248(1). 157–169. 84 indexed citations

11.

Adamska, Maja, Heike Herbrand, Marcin Adamski, et al.. (2001). FGFs control the patterning of the inner ear but are not able to induce the full ear program. Mechanisms of Development. 109(2). 303–313. 62 indexed citations

12.

Adamska, Maja, S. Léger, Michael Brand, et al.. (2000). Inner ear and lateral line expression of a zebrafish Nkx5-1 gene and its downregulation in the ears of FGF8 mutant, ace. Mechanisms of Development. 97(1-2). 161–165. 45 indexed citations

13.

Mennerich, Detlev, et al.. (1999). Two Highly Related Homeodomain Proteins, Nkx5-1 and Nkx5-2, Display Different DNA Binding Specificities. Biological Chemistry. 380(9). 1041–8. 11 indexed citations

14.

Tajbakhsh, Shahragim, Eva Bober, Charles Babinet, et al.. (1996). Gene targeting themyf-5 locus withnlacZ reveals expression of this myogenic factor in mature skeletal muscle fibres as well as early embryonic muscle. Developmental Dynamics. 206(3). 291–300. 137 indexed citations

15.

Arnold, Hans-Henning, et al.. (1995). Distinct temporal expression of mouse Nkx-5.1 and Nkx-5.2 homeo☐ genes during brain and ear development. Mechanisms of Development. 52(2-3). 371–381. 48 indexed citations

16.

Bober, Eva, Gary E. Lyons, Thomas Braun, et al.. (1991). The muscle regulatory gene, Myf-6, has a biphasic pattern of expression during early mouse development.. The Journal of Cell Biology. 113(6). 1255–1265. 233 indexed citations

17.

Rosenthal, Nadia, Bruce M. Wentworth, Maria J. Donoghue, et al.. (1990). A highly conserved enhancer downstream of the human MLC1/3 locus is a target for multiple myogenic determination factors. Nucleic Acids Research. 18(21). 6239–6246. 90 indexed citations

18.

Seharaseyon, Jegatheesan, Eva Bober, Chih‐Lin Hsieh, et al.. (1990). Human embryonic/atrial myosin alkali light chain gene: Characterization, sequence, and chromosomal location. Genomics. 7(2). 289–293. 24 indexed citations

19.

Braun, Thomas, Gregor Buschhausen-Denker, Eva Bober, Egbert Tannich, & Hans-Henning Arnold. (1989). A novel human muscle factor related to but distinct from MyoD1 induces myogenic conversion in 10T1/2 fibroblasts.. The EMBO Journal. 8(3). 701–709. 810 indexed citations breakdown →

20.

Arnold, Hans-Henning, et al.. (1988). A novel human myosin alkali light chain is developmentally regulated. European Journal of Biochemistry. 178(1). 53–60. 21 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.

Explore authors with similar magnitude of impact