Thomas Brand

5.4k total citations
110 papers, 3.4k citations indexed

About

Thomas Brand is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Thomas Brand has authored 110 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Molecular Biology, 35 papers in Cardiology and Cardiovascular Medicine and 16 papers in Genetics. Recurrent topics in Thomas Brand's work include Congenital heart defects research (51 papers), Cardiomyopathy and Myosin Studies (17 papers) and Developmental Biology and Gene Regulation (15 papers). Thomas Brand is often cited by papers focused on Congenital heart defects research (51 papers), Cardiomyopathy and Myosin Studies (17 papers) and Developmental Biology and Gene Regulation (15 papers). Thomas Brand collaborates with scholars based in Germany, United Kingdom and United States. Thomas Brand's co-authors include Hans-Henning Arnold, Jan Schlueter, Birgit Andrée, Michael Schneider, R. Schindler, Thomas Schlange, Jörg Männer, W. Robb MacLellan, André Schneider and Kar Lai Poon and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Circulation.

In The Last Decade

Thomas Brand

103 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Brand Germany 33 2.8k 773 508 412 292 110 3.4k
Anthony B. Firulli United States 38 3.3k 1.2× 634 0.8× 567 1.1× 713 1.7× 226 0.8× 85 4.0k
Yunfu Sun China 27 3.3k 1.2× 672 0.9× 1.0k 2.0× 308 0.7× 344 1.2× 48 4.1k
Dieter Weichenhan Germany 34 2.4k 0.9× 653 0.8× 315 0.6× 517 1.3× 143 0.5× 93 3.5k
Lucile Miquerol France 31 2.3k 0.8× 725 0.9× 598 1.2× 274 0.7× 351 1.2× 62 3.1k
Yuka Morikawa United States 26 2.2k 0.8× 616 0.8× 922 1.8× 297 0.7× 781 2.7× 47 3.2k
Ivan P. Moskowitz United States 36 2.9k 1.1× 1.1k 1.4× 413 0.8× 666 1.6× 249 0.9× 71 3.7k
Yan‐Shan Dai United States 20 2.0k 0.7× 838 1.1× 379 0.7× 271 0.7× 144 0.5× 37 2.6k
Manvendra K. Singh United States 29 2.0k 0.7× 445 0.6× 427 0.8× 538 1.3× 609 2.1× 73 3.1k
Pingzhu Zhou United States 21 2.1k 0.8× 522 0.7× 538 1.1× 284 0.7× 428 1.5× 31 2.6k
An Zwijsen Belgium 35 3.4k 1.2× 272 0.4× 539 1.1× 454 1.1× 512 1.8× 87 4.7k

Countries citing papers authored by Thomas Brand

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Brand

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Brand

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Brand. A scholar is included among the top collaborators of Thomas Brand 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 Thomas Brand. Thomas Brand 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.
2.
Savarese, Marco, Susanne Rinné, Anne Schänzer, et al.. (2023). Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking. Acta Neuropathologica Communications. 11(1). 4–4. 4 indexed citations
3.
Baldwin, Tanya A., Susanne Rinné, Anibal Garza Carbajal, et al.. (2022). POPDC1 scaffolds a complex of adenylyl cyclase 9 and the potassium channel TREK‐1 in heart. EMBO Reports. 23(12). e55208–e55208. 13 indexed citations
4.
Shetty, Mahesh Shivarama, Laurence Ris, R. Schindler, et al.. (2021). Mice lacking the cAMP effector protein POPDC1 show enhanced hippocampal synaptic plasticity. Cerebral Cortex. 32(16). 3457–3471. 4 indexed citations
5.
Choksi, Yash A., Vishruth K. Reddy, Kshipra Singh, et al.. (2018). BVES is required for maintenance of colonic epithelial integrity in experimental colitis by modifying intestinal permeability. Mucosal Immunology. 11(5). 1363–1374. 15 indexed citations
6.
Yu, Joseph Kwong‐Leung, Padmini Sarathchandra, Adrian H. Chester, et al.. (2018). Cardiac regeneration following cryoinjury in the adult zebrafish targets a maturation-specific biomechanical remodeling program. Scientific Reports. 8(1). 15661–15661. 15 indexed citations
7.
Liebling, Michael, et al.. (2016). Development of the cardiac conduction system in zebrafish. Gene Expression Patterns. 21(2). 89–96. 16 indexed citations
8.
Da’as, Sahar, Joseph Kwong‐Leung Yu, Jonathan T. Butcher, et al.. (2014). Abstract 17545: Different Human Mutations in the Myosin Binding Protein C3 (MYBPC3) Produce Specific Cardiac Phenotypes in the Zebrafish. Circulation. 130. 4 indexed citations
9.
Brand, Thomas, et al.. (2011). Die Berechnung von Baugruben mit dem Bettungsmodulverfahren nach EB 102. Bautechnik. 88(10). 694–706. 1 indexed citations
10.
Schlueter, Jan & Thomas Brand. (2009). A right-sided pathway involving FGF8 / Snai1 controls asymmetric development of the proepicardium in the chick embryo. Proceedings of the National Academy of Sciences. 106(18). 7485–7490. 38 indexed citations
11.
Brand, Thomas. (2008). Le rôle des agences de notation. Regards croisés sur l'économie. n° 3(1). 265–266.
12.
Froese, Alexander & Thomas Brand. (2008). Expression pattern of Popdc2 during mouse embryogenesis and in the adult. Developmental Dynamics. 237(3). 780–787. 18 indexed citations
13.
Schlueter, Jan, Jörg Männer, & Thomas Brand. (2006). BMP is an important regulator of proepicardial identity in the chick embryo. Developmental Biology. 295(2). 546–558. 81 indexed citations
14.
Brand, Thomas. (2003). Heart development: molecular insights into cardiac specification and early morphogenesis. Developmental Biology. 258(1). 1–19. 341 indexed citations
15.
Schlange, Thomas, Birgit Andrée, Andreas D. Ebert, et al.. (2001). Chick CFC Controls Lefty1 Expression in the Embryonic Midline and Nodal Expression in the Lateral Plate. Developmental Biology. 234(2). 376–389. 35 indexed citations
16.
Schlange, Thomas, Birgit Andrée, Hans-Henning Arnold, & Thomas Brand. (2000). BMP2 is required for early heart development during a distinct time period. Mechanisms of Development. 91(1-2). 259–270. 160 indexed citations
17.
18.
Andrée, Birgit, Tina Hillemann, Gania Kessler‐Icekson, et al.. (2000). Isolation and Characterization of the Novel Popeye Gene Family Expressed in Skeletal Muscle and Heart. Developmental Biology. 223(2). 371–382. 98 indexed citations
19.
Brand, Thomas, Hari S. Sharma, & Wolfgang Schäper. (1993). Expression of Nuclear Proto-oncogenes in Isoproterenol-induced Cardiac Hypertrophy. Journal of Molecular and Cellular Cardiology. 25(11). 1325–1337. 41 indexed citations
20.
Sharma, Hari Shanker, M. Wunsch, Thomas Brand, Pieter D. Verdouw, & Wolfgang Schäper. (1992). Molecular Biology of the Coronary Vascular and Myocardial Responses to Ischemia. Journal of Cardiovascular Pharmacology. 20. S23–S31. 23 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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