Ellen Schulze-Bahr

705 total citations
6 papers, 515 citations indexed

About

Ellen Schulze-Bahr is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Sensory Systems. According to data from OpenAlex, Ellen Schulze-Bahr has authored 6 papers receiving a total of 515 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Cardiology and Cardiovascular Medicine and 2 papers in Sensory Systems. Recurrent topics in Ellen Schulze-Bahr's work include Cardiac electrophysiology and arrhythmias (4 papers), Ion channel regulation and function (3 papers) and Congenital heart defects research (2 papers). Ellen Schulze-Bahr is often cited by papers focused on Cardiac electrophysiology and arrhythmias (4 papers), Ion channel regulation and function (3 papers) and Congenital heart defects research (2 papers). Ellen Schulze-Bahr collaborates with scholars based in Germany, Poland and United States. Ellen Schulze-Bahr's co-authors include Birgit Stallmeyer, Eric Schulze‐Bahr, Olaf Pongs, Iris Ohmert, Martin Kruse, Valerie A. Corfield, Alf Beckmann, Paul A. Brink, Ulrike Nowak‐Göttl and Sven Zumhagen and has published in prestigious journals such as Journal of Clinical Investigation, Circulation Research and Human Mutation.

In The Last Decade

Ellen Schulze-Bahr

6 papers receiving 509 citations

Peers

Ellen Schulze-Bahr

MB

CCM

SS

EPIDE

ND

Tim S. Munsey United Kingdom

Helen E. Collins United States

Yaopeng Hu Japan

Leonid Tyan United States

Mahmut Ay Germany

Lutz Sternfeld Germany

Juan E. Camacho Londoño Germany

Vishal Yadav United States

Yasuhiro Kawarabayashi Japan

Shailesh Deshpande India

Tim S. Munsey United Kingdom

Ellen Schulze-Bahr

212 ×0.6

MB

68 ×0.3

CCM

77 ×0.4

SS

22 ×0.3

EPIDE

60 ×0.9

ND

Citations per year, relative to Ellen Schulze-Bahr Ellen Schulze-Bahr (= 1×) peers Tim S. Munsey

Countries citing papers authored by Ellen Schulze-Bahr

Since Specialization

Citations

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

Fields of papers citing papers by Ellen Schulze-Bahr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ellen Schulze-Bahr. 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 Ellen Schulze-Bahr. The network helps show where Ellen Schulze-Bahr may publish in the future.

Co-authorship network of co-authors of Ellen Schulze-Bahr

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

All Works

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6 of 6 papers shown

1.

Frank, Derk, Ashraf Yusuf Rangrez, Corinna Friedrich, et al.. (2019). Cardiac α-Actin ( ACTC1 ) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy. Circulation Genomic and Precision Medicine. 12(8). e002491–e002491. 39 indexed citations

2.

Stallmeyer, Birgit, S. Kotthoff, Sven Zumhagen, et al.. (2017). A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction. Circulation Research. 120(10). e33–e44. 32 indexed citations

3.

Stallmeyer, Birgit, Sven Zumhagen, Isabelle Denjoy, et al.. (2011). Mutational spectrum in the Ca2+-activated cation channel gene TRPM4 in patients with cardiac conductance disturbances. Human Mutation. 33(1). 109–117. 125 indexed citations

4.

Stallmeyer, Birgit, et al.. (2010). Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease. Clinical Genetics. 78(6). 533–540. 75 indexed citations

5.

Kruse, Martin, Eric Schulze‐Bahr, Valerie A. Corfield, et al.. (2009). Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I. Journal of Clinical Investigation. 119(9). 2737–2744. 234 indexed citations

6.

Wedekind, Horst, Martin Schwarz, Wilhelm Haverkamp, et al.. (2004). Effective long‐term control of cardiac events with β‐blockers in a family with a common LQT1 mutation. Clinical Genetics. 65(3). 233–241. 10 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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