Hans-Peter Vosberg

6.0k total citations · 2 hit papers
51 papers, 4.7k citations indexed

About

Hans-Peter Vosberg is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Hans-Peter Vosberg has authored 51 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 25 papers in Cardiology and Cardiovascular Medicine and 5 papers in Genetics. Recurrent topics in Hans-Peter Vosberg's work include Cardiomyopathy and Myosin Studies (25 papers), RNA Research and Splicing (9 papers) and Congenital heart defects research (8 papers). Hans-Peter Vosberg is often cited by papers focused on Cardiomyopathy and Myosin Studies (25 papers), RNA Research and Splicing (9 papers) and Congenital heart defects research (8 papers). Hans-Peter Vosberg collaborates with scholars based in Germany, United States and France. Hans-Peter Vosberg's co-authors include Christine E. Seidman, William J. McKenna, G Tanigawa, Susan Kass, Anja A. T. Geisterfer-Lowrance, J G Seidman, Jerome Vinograd, Ludwig Thierfelder, Hugh Watkins and Calum A. MacRae and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Hans-Peter Vosberg

51 papers receiving 4.5k 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.

A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation

1990 975 citations Susan Kass, G Tanigawa et al. Cell profile →
α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere

1994 779 citations Ludwig Thierfelder, Hugh Watkins et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hans-Peter Vosberg Germany	29	3.1k	2.7k	405	330	319	51	4.7k
Roger J.A. Grand United Kingdom	40	3.3k 1.1×	804 0.3×	419 1.0×	1.0k 3.1×	1.3k 4.0×	130	5.0k
Stéphan Vagner France	41	4.9k 1.6×	589 0.2×	247 0.6×	820 2.5×	381 1.2×	86	5.8k
Jamal Tazi France	43	5.3k 1.7×	187 0.1×	186 0.5×	497 1.5×	457 1.4×	87	6.0k
Henrik Ørum Denmark	29	3.6k 1.2×	116 0.0×	358 0.9×	201 0.6×	207 0.6×	52	4.7k
Inger Helene Madshus Norway	34	2.8k 0.9×	175 0.1×	254 0.6×	845 2.6×	261 0.8×	67	4.3k
J.S. Sussenbach Netherlands	39	3.1k 1.0×	185 0.1×	178 0.4×	548 1.7×	2.1k 6.7×	123	4.6k
Shinya Satoh Japan	27	1.2k 0.4×	216 0.1×	749 1.8×	72 0.2×	178 0.6×	96	2.5k
Anton Poliakov United States	20	3.8k 1.2×	175 0.1×	348 0.9×	271 0.8×	243 0.8×	31	4.8k
Reinout Raijmakers Netherlands	32	3.0k 1.0×	151 0.1×	391 1.0×	396 1.2×	177 0.6×	57	4.3k
Maria K. Vartiainen Finland	33	2.4k 0.8×	307 0.1×	82 0.2×	219 0.7×	179 0.6×	56	3.7k

Countries citing papers authored by Hans-Peter Vosberg

Since Specialization

Citations

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

Fields of papers citing papers by Hans-Peter Vosberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hans-Peter Vosberg. 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 Hans-Peter Vosberg. The network helps show where Hans-Peter Vosberg may publish in the future.

Co-authorship network of co-authors of Hans-Peter Vosberg

This figure shows the co-authorship network connecting the top 25 collaborators of Hans-Peter Vosberg. A scholar is included among the top collaborators of Hans-Peter Vosberg 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 Hans-Peter Vosberg. Hans-Peter Vosberg 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

Budde, Birgit, Priska Binner, Stephan Waldmüller, et al.. (2007). Noncompaction of the Ventricular Myocardium Is Associated with a De Novo Mutation in the β-Myosin Heavy Chain Gene. PLoS ONE. 2(12). e1362–e1362. 98 indexed citations

Vosberg, Hans-Peter. (2000). Genetic counselling for hypertrophic cardiomyopathy: are we ready for it?. Trials. 1(1). 41–44. 5 indexed citations

Sadayappan, Sakthivel, et al.. (2000). A novel missense mutation (R712L) adjacent to the ?active thiol? region of the cardiac ?-myosin heavy chain gene causing hypertrophic cardiomyopathy in an Indian family. Human Mutation. 15(3). 298–299. 9 indexed citations

Döhlemann, C, Joachim Hebe, Thomas Meitinger, & Hans-Peter Vosberg. (2000). Apical hypertrophic cardiomyopathy due to a de novo mutation Arg719Trp of the b-myosin heavy chain gene and cardiac arrest in childhood A case report and family study. Zeitschrift für Kardiologie. 89(7). 612–619. 7 indexed citations

Schröder, Dirk, et al.. (1998). A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated β-myosin heavy chain genes. Human Genetics. 102(3). 299–304. 51 indexed citations

Coviello, Domenico, Barry J. Maron, Paolo Spirito, et al.. (1997). Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin Gene. Journal of the American College of Cardiology. 29(3). 635–640. 80 indexed citations

Vosberg, Hans-Peter, et al.. (1995). Simultaneous assessment of type I collagen synthesis and degradation for detection of bone metastases. Calcified Tissue International. 56(5). 463. 1 indexed citations

Bonne, Gisèle, Lucie Carrier, J. Bercovici, et al.. (1995). Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. Nature Genetics. 11(4). 438–440. 336 indexed citations

Thierfelder, Ludwig, Calum A. MacRae, Hugh Watkins, et al.. (1994). FAMILIAL HYPERTROPHIC CARDIOMYOPATHY IS A DISEASE OF THE SARCOMERE. Circulation. 90. 519–519. 3 indexed citations

10.

Vosberg, Hans-Peter. (1994). Identification of Gene Defects by Linkage Analysis: Use in Inherited Cardiomyopathies. European Heart Journal. 15(suppl D). 20–23. 2 indexed citations

11.

Thierfelder, Ludwig, Hugh Watkins, Calum A. MacRae, et al.. (1994). α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere. Cell. 77(5). 701–712. 779 indexed citations breakdown →

12.

Dufour, Cécile, Eric Dausse, Luc Fetler, et al.. (1994). Identification of a Mutation Near a Functional Site of the β cardiac myosin Heavy Chain Gene in a Family with Hypertrophic Cardiomyopathy. Journal of Molecular and Cellular Cardiology. 26(9). 1241–1247. 13 indexed citations

13.

Eldin, Patrick, et al.. (1994). Mapping of the actomyosin interfaces.. Proceedings of the National Academy of Sciences. 91(7). 2772–2776. 4 indexed citations

14.

Thierfelder, Ludwig, Calum A. MacRae, Hugh Watkins, et al.. (1993). 2 NEW LOCI FOR HYPERTROPHIC CARDIOMYOPATHY MAP TO CHROMOSOME-15Q2 (CMH3) AND CHROMOSOME-11Q (CMH4). Circulation. 88. 573–573. 2 indexed citations

15.

Vosberg, Hans-Peter, et al.. (1992). The regulation of the human β myosin heavy-chain gene. Steinkopff eBooks. 87 Suppl 1. 161–173. 2 indexed citations

16.

Jaenicke, Thomas, K W Diederich, Walter Haas, et al.. (1990). The complete sequence of the human β-myosin heavy chain gene and a comparative analysis of its product. Genomics. 8(2). 194–206. 150 indexed citations

17.

Tanigawa, G, John A. Jarcho, Susan Kass, et al.. (1990). A molecular basis for familial hypertrophic cardiomyopathy: An αβ cardiac myosin heavy chain hybrid gene. Cell. 62(5). 991–998. 167 indexed citations

18.

Ried, Thomas, et al.. (1989). Isolation and characterization of the complete human ?-myosin heavy chain gene. Human Genetics. 81(3). 214–20. 15 indexed citations

19.

Vosberg, Hans-Peter, et al.. (1988). Enzymatic Amplification of Myosin Heavy-Chain mRNA Sequences In Vitro. DNA. 7(4). 297–306. 27 indexed citations

20.

Nakamaye, Kay L., Gerald Gish, Fritz Eckstein, & Hans-Peter Vosberg. (1988). Direct sequencing of polymerase chain reaction amplified DNA fragments through the incorporation of deoxynucleoside α-thiotriphosphates. Nucleic Acids Research. 16(21). 9947–9959. 57 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