Stephan Waldmüller

951 total citations
14 papers, 387 citations indexed

About

Stephan Waldmüller is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Stephan Waldmüller has authored 14 papers receiving a total of 387 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Cardiology and Cardiovascular Medicine and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Stephan Waldmüller's work include Cardiomyopathy and Myosin Studies (9 papers), Congenital heart defects research (6 papers) and Aortic Disease and Treatment Approaches (3 papers). Stephan Waldmüller is often cited by papers focused on Cardiomyopathy and Myosin Studies (9 papers), Congenital heart defects research (6 papers) and Aortic Disease and Treatment Approaches (3 papers). Stephan Waldmüller collaborates with scholars based in Germany, United States and Austria. Stephan Waldmüller's co-authors include Thomas Scheffold, Priska Binner, Hans-Peter Vosberg, Kirsten Rackebrandt, Melanie Müller, Wulf Blankenfeldt, Michael Bonin, Roland Toder, Melanie Müller and Erik May and has published in prestigious journals such as PLoS ONE, Clinical Chemistry and Journal of Molecular and Cellular Cardiology.

In The Last Decade

Stephan Waldmüller

14 papers receiving 385 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephan Waldmüller Germany	9	233	232	88	66	57	14	387
Sabine Haßfeld Germany	8	157 0.7×	238 1.0×	19 0.2×	41 0.6×	42 0.7×	12	329
Javier T Granados-Riveron United Kingdom	8	399 1.7×	140 0.6×	75 0.9×	176 2.7×	56 1.0×	10	478
Jessica Woodley United Kingdom	3	277 1.2×	343 1.5×	106 1.2×	44 0.7×	8 0.1×	3	519
Tim McQuinn United States	7	273 1.2×	137 0.6×	45 0.5×	113 1.7×	52 0.9×	11	368
Sophie Julia France	12	163 0.7×	36 0.2×	241 2.7×	42 0.6×	29 0.5×	27	372
Jeffrey D. Steimle United States	10	321 1.4×	79 0.3×	68 0.8×	93 1.4×	39 0.7×	15	371
Anna R. Duncan United States	8	182 0.8×	39 0.2×	52 0.6×	33 0.5×	22 0.4×	9	287
Karel van Duijvenboden Netherlands	12	442 1.9×	234 1.0×	72 0.8×	67 1.0×	46 0.8×	23	566
Anna Baroncini Italy	13	149 0.6×	45 0.2×	256 2.9×	64 1.0×	50 0.9×	29	458
Donna K. Mahnke United States	11	300 1.3×	62 0.3×	70 0.8×	129 2.0×	44 0.8×	14	392

Countries citing papers authored by Stephan Waldmüller

Since Specialization

Citations

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

Fields of papers citing papers by Stephan Waldmüller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephan Waldmüller

This figure shows the co-authorship network connecting the top 25 collaborators of Stephan Waldmüller. A scholar is included among the top collaborators of Stephan Waldmüller 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 Stephan Waldmüller. Stephan Waldmüller 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:

14 of 14 papers shown

Weiß, Birgit, Tim Ott, Philipp Vick, et al.. (2023). Identification of novel genes including NAV2 associated with isolated tall stature. Frontiers in Endocrinology. 14. 1258313–1258313. 1 indexed citations

Bader, Ingrid, Michael Freilinger, Franz Landauer, et al.. (2022). A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathy. Orphanet Journal of Rare Diseases. 17(1). 279–279. 2 indexed citations

Averdunk, Luisa, Sandra Donkervoort, Denise Horn, et al.. (2022). Recognizable Pattern of Arthrogryposis and Congenital Myopathy Caused by the Recurrent TTN Metatranscript-only c.39974-11T > G Splice Variant. Neuropediatrics. 53(5). 309–320. 5 indexed citations

Hofbeck, Michael, G. Wiegand, Renate Kaulitz, et al.. (2021). MEK-Inhibition Treatment with Trametinib in a 7.7-Year-Old Girl with Noonan's Syndrome and Life-Threatening Lymphangiopathy. The Thoracic and Cardiovascular Surgeon. 69. 2 indexed citations

Waldmüller, Stephan, Christopher Schroeder, Marc Sturm, et al.. (2015). Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies. Molecular and Cellular Probes. 29(5). 308–314. 33 indexed citations

Keyser, Britta, Sabine Hoffjan, Melanie Müller, et al.. (2012). High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections. Molecular and Cellular Probes. 27(2). 103–108. 9 indexed citations

Hoffjan, Sabine, Stephan Waldmüller, Wulf Blankenfeldt, et al.. (2011). Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections. European Journal of Human Genetics. 19(5). 520–524. 28 indexed citations

Posch, Maximilian, Stephan Waldmüller, Melanie Müller, et al.. (2011). Cardiac Alpha-Myosin (MYH6) Is the Predominant Sarcomeric Disease Gene for Familial Atrial Septal Defects. PLoS ONE. 6(12). e28872–e28872. 69 indexed citations

Waldmüller, Stephan, Melanie Müller, Kirsten Rackebrandt, et al.. (2008). Array-Based Resequencing Assay for Mutations Causing Hypertrophic Cardiomyopathy. Clinical Chemistry. 54(4). 682–687. 35 indexed citations

10.

Waldmüller, Stephan, Michael Müller, H. Warnecke, et al.. (2007). Genetic testing in patients with aortic aneurysms/dissections: a novel genotype/phenotype correlation?☆. European Journal of Cardio-Thoracic Surgery. 31(6). 970–975. 21 indexed citations

11.

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

12.

Waldmüller, Stephan. (2003). Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy. Journal of Molecular and Cellular Cardiology. 35(6). 623–636. 52 indexed citations

13.

Waldmüller, Stephan, et al.. (2002). Low-density DNA microarrays are versatile tools to screen for known mutations in hypertrophic cardiomyopathy. Human Mutation. 19(5). 560–569. 29 indexed citations

14.

Waldmüller, Stephan, Padmakumar Ramachandran, Pascale Richard, et al.. (2001). Novel mutations in MYH7 and MYBPC3 of an Indian family causing hypertrophic cardiomyopathy. Journal of Molecular and Cellular Cardiology. 33(6). A105–A105. 3 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