Susanne Probst

992 total citations
7 papers, 662 citations indexed

About

Susanne Probst is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Susanne Probst has authored 7 papers receiving a total of 662 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cardiology and Cardiovascular Medicine, 4 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Susanne Probst's work include Cardiomyopathy and Myosin Studies (5 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Congenital heart defects research (2 papers). Susanne Probst is often cited by papers focused on Cardiomyopathy and Myosin Studies (5 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Congenital heart defects research (2 papers). Susanne Probst collaborates with scholars based in Germany, Netherlands and Canada. Susanne Probst's co-authors include Sabine Klaassen, Ludwig Thierfelder, Erwin Oechslin, Rolf Jenni, Felix Berger, Matthias Greutmann, Pia Schuler, Arnd Heuser, Brenda Gerull and Gregor Krings and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and Circulation Cardiovascular Genetics.

In The Last Decade

Susanne Probst

6 papers receiving 640 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Susanne Probst Germany	5	587	388	144	104	86	7	662
Yvonne M. Hoedemaekers Netherlands	12	701 1.2×	350 0.9×	104 0.7×	66 0.6×	70 0.8×	23	759
M. Yegitbasi Germany	3	290 0.5×	175 0.5×	78 0.5×	35 0.3×	64 0.7×	3	361
Brian C. Weiford United States	3	363 0.6×	126 0.3×	92 0.6×	27 0.3×	107 1.2×	6	396
Samantha Barratt Ross Australia	11	327 0.6×	211 0.5×	34 0.2×	35 0.3×	34 0.4×	24	406
Hiroshi Mito Japan	4	495 0.8×	218 0.6×	173 1.2×	14 0.1×	121 1.4×	6	534
Jean Cavanaugh United States	8	365 0.6×	340 0.9×	19 0.1×	45 0.4×	27 0.3×	10	574
Alexa M.C. Vermeer Netherlands	8	309 0.5×	167 0.4×	19 0.1×	45 0.4×	26 0.3×	14	345
Ingrid A.W. van Rijsingen Netherlands	8	698 1.2×	287 0.7×	26 0.2×	15 0.1×	39 0.5×	11	783
Anna Gaertner Germany	14	443 0.8×	244 0.6×	28 0.2×	13 0.1×	21 0.2×	21	595
Sulekha Rajagopalan Australia	8	149 0.3×	145 0.4×	12 0.1×	35 0.3×	27 0.3×	13	303

Countries citing papers authored by Susanne Probst

Since Specialization

Citations

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

Fields of papers citing papers by Susanne Probst

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susanne Probst

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

All Works

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7 of 7 papers shown

1.

Probst, Susanne, Erwin Oechslin, Pia Schuler, et al.. (2011). Sarcomere Gene Mutations in Isolated Left Ventricular Noncompaction Cardiomyopathy Do Not Predict Clinical Phenotype. Circulation Cardiovascular Genetics. 4(4). 367–374. 120 indexed citations

2.

Postma, Alex V., Klaartje van Engelen, Thahira Rahman, et al.. (2010). Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly. Circulation Cardiovascular Genetics. 4(1). 43–50. 129 indexed citations

3.

Klaassen, Sabine, Susanne Probst, Erwin Oechslin, et al.. (2008). Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction. Circulation. 117(22). 2893–2901. 304 indexed citations

4.

Probst, Susanne, et al.. (2008). Frauendichtung in Rom. Die Elegien der Sulpicia. heiDOK (Heidelberg University).

5.

Probst, Susanne. (2007). Bedeutung der Visite in der Psychosomatischen Medizin. PPmP - Psychotherapie · Psychosomatik · Medizinische Psychologie. 59(2). 1 indexed citations

6.

Ellinor, Patrick T., Sabine Klaassen, Susanne Probst, et al.. (2006). A Novel Locus for Dilated Cardiomyopathy, Diffuse Myocardial Fibrosis, and Sudden Death on Chromosome 10q25-26. Journal of the American College of Cardiology. 48(1). 106–111. 23 indexed citations

7.

Klaassen, Sabine, Susanne Probst, Brenda Gerull, et al.. (2004). Novel Gene Locus for Autosomal Dominant Left Ventricular Noncompaction Maps to Chromosome 11p15. Circulation. 109(22). 2720–2723. 85 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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