Ulrike Esslinger

602 total citations
3 papers, 34 citations indexed

About

Ulrike Esslinger is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Ulrike Esslinger has authored 3 papers receiving a total of 34 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Cardiology and Cardiovascular Medicine and 2 papers in Genetics. Recurrent topics in Ulrike Esslinger's work include Genetic Associations and Epidemiology (2 papers), Viral Infections and Immunology Research (1 paper) and Protein Tyrosine Phosphatases (1 paper). Ulrike Esslinger is often cited by papers focused on Genetic Associations and Epidemiology (2 papers), Viral Infections and Immunology Research (1 paper) and Protein Tyrosine Phosphatases (1 paper). Ulrike Esslinger collaborates with scholars based in France and Germany. Ulrike Esslinger's co-authors include Stefanie Ebert, Wibke Reinhard, Klaus Stark, Christian Hengstenberg, Christa Zollbrecht, Thomas Langmann, Pascal Challande, Stéphane Laurent, Pierre Boutouyrie and Frédérique Thomas and has published in prestigious journals such as Atherosclerosis, Clinical Genetics and Circulation Cardiovascular Genetics.

In The Last Decade

Ulrike Esslinger

3 papers receiving 34 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ulrike Esslinger France	2	18	13	10	6	5	3	34
Thirupugal Govindarajan United States	2	18 1.0×	10 0.8×	7 0.7×	6 1.0×	3 0.6×	4	34
Yujing Xia United Kingdom	2	34 1.9×	6 0.5×	8 0.8×	7 1.2×	4 0.8×	2	44
Tobias Reinberger Germany	4	10 0.6×	8 0.6×	3 0.3×	11 1.8×	3 0.6×	7	33
Bart Loeys Belgium	4	19 1.1×	26 2.0×	6 0.6×	3 0.5×	11 2.2×	6	39
Emeline Davoine Switzerland	4	18 1.0×	5 0.4×	5 0.5×	9 1.5×	3 0.6×	4	32
Mark C. Thel United States	3	10 0.6×	5 0.4×	3 0.3×	7 1.2×	7 1.4×	5	35
Sharon Senchanthisai United States	2	22 1.2×	11 0.8×	4 0.4×	2 0.3×	13 2.6×	2	37
Baishali Maskeri United States	3	25 1.4×	10 0.8×	6 0.6×	16 2.7×	4 0.8×	4	58
Neha Hafeez United States	4	38 2.1×	26 2.0×	6 0.6×	2 0.3×	13 2.6×	8	81
Lindsay Guare United States	3	18 1.0×	6 0.5×	3 0.3×	18 3.0×	3 0.6×	6	56

Countries citing papers authored by Ulrike Esslinger

Since Specialization

Citations

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

Fields of papers citing papers by Ulrike Esslinger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulrike Esslinger

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

All Works

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3 of 3 papers shown

1.

Perret, Claire, Carole Proust, Ulrike Esslinger, et al.. (2023). DNA ‐pools targeted‐sequencing as a robust cost‐effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis. Clinical Genetics. 105(2). 185–189. 1 indexed citations

2.

Proust, Carole, Jean‐Philippe Empana, Pierre Boutouyrie, et al.. (2015). Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry. Circulation Cardiovascular Genetics. 8(4). 628–636. 15 indexed citations

3.

Zollbrecht, Christa, Wibke Reinhard, Ulrike Esslinger, et al.. (2013). Expression pattern in human macrophages dependent on 9p21.3 coronary artery disease risk locus. Atherosclerosis. 227(2). 244–249. 18 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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