Ingrid Brænne

3.7k total citations
16 papers, 437 citations indexed

About

Ingrid Brænne is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Epidemiology. According to data from OpenAlex, Ingrid Brænne has authored 16 papers receiving a total of 437 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Cardiology and Cardiovascular Medicine and 3 papers in Epidemiology. Recurrent topics in Ingrid Brænne's work include Genomics and Rare Diseases (2 papers), Lipoproteins and Cardiovascular Health (2 papers) and Protein Kinase Regulation and GTPase Signaling (2 papers). Ingrid Brænne is often cited by papers focused on Genomics and Rare Diseases (2 papers), Lipoproteins and Cardiovascular Health (2 papers) and Protein Kinase Regulation and GTPase Signaling (2 papers). Ingrid Brænne collaborates with scholars based in Germany, United Kingdom and United States. Ingrid Brænne's co-authors include J. Hardt, K. Wulff, Lars Steinmüller‐Magin, Guenther Witzke, Petra Staubach, Konrad Bork, Jeanette Erdmann, Heribert Schunkert, Benedikt Reiz and Christian Hengstenberg and has published in prestigious journals such as Circulation, Nature Communications and PLoS ONE.

In The Last Decade

Ingrid Brænne

16 papers receiving 429 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ingrid Brænne Germany 8 199 142 93 87 70 16 437
Michel Cailleret France 12 49 0.2× 351 2.5× 36 0.4× 11 0.1× 55 0.8× 17 551
J.M. Martínez-Peñuela Spain 13 59 0.3× 195 1.4× 142 1.5× 25 0.3× 7 0.1× 35 572
Rania Shamekh United States 12 39 0.2× 100 0.7× 35 0.4× 29 0.3× 27 0.4× 21 329
Akatsuki Kubota Japan 11 46 0.2× 215 1.5× 23 0.2× 44 0.5× 27 0.4× 35 442
Sébastien Toffoli Belgium 9 42 0.2× 281 2.0× 43 0.5× 12 0.1× 46 0.7× 14 576
João N. Stávale Brazil 12 279 1.4× 104 0.7× 81 0.9× 12 0.1× 25 0.4× 23 538
Michaela Hanneder Austria 9 83 0.4× 458 3.2× 43 0.5× 14 0.2× 40 0.6× 10 615
Ankush Bhatia United States 10 92 0.5× 71 0.5× 40 0.4× 37 0.4× 47 0.7× 23 417
Anna Křepelová Czechia 13 49 0.2× 238 1.7× 82 0.9× 13 0.1× 27 0.4× 26 465
Yalda Nilipour Iran 12 70 0.4× 219 1.5× 26 0.3× 90 1.0× 19 0.3× 61 426

Countries citing papers authored by Ingrid Brænne

Since Specialization
Citations

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

Fields of papers citing papers by Ingrid Brænne

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingrid Brænne

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

All Works

16 of 16 papers shown
1.
Qiu, Jiajun, Li Li, A. Mesut Erzurumluoglu, et al.. (2025). Deep representation learning for clustering longitudinal survival data from electronic health records. Nature Communications. 16(1). 2534–2534. 2 indexed citations
2.
Brodt, Michael D., et al.. (2020). Old Mice Have Less Transcriptional Activation But Similar Periosteal Cell Proliferation Compared to Young-Adult Mice in Response to in vivo Mechanical Loading. Journal of Bone and Mineral Research. 35(9). 1751–1764. 31 indexed citations
3.
Demal, Till, Benedikt Reiz, Ingrid Brænne, et al.. (2019). A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A. Scientific Reports. 9(1). 2959–2959. 12 indexed citations
4.
Bork, Konrad, K. Wulff, Lars Steinmüller‐Magin, et al.. (2017). Hereditary angioedema with a mutation in the plasminogen gene. Allergy. 73(2). 442–450. 198 indexed citations
5.
Brænne, Ingrid, Lingyao Zeng, Christina Willenborg, et al.. (2017). Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk. PLoS ONE. 12(8). e0182999–e0182999. 5 indexed citations
6.
Brænne, Ingrid, Christina Willenborg, Benedikt Reiz, et al.. (2016). Pleiotropic molecular targets of coxibs reveals novel genomic loci conferring coronary artery disease risk. Atherosclerosis. 252. e252–e253. 1 indexed citations
7.
Brænne, Ingrid, Benedikt Reiz, Elisabeth Graf, et al.. (2015). Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction. European Journal of Human Genetics. 24(2). 191–197. 56 indexed citations
8.
Domingo, Aloysius, Ana Westenberger, Lillian V. Lee, et al.. (2015). New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3). European Journal of Human Genetics. 23(10). 1334–1340. 52 indexed citations
9.
Dang, Tan An, Jana Wobst, Thorsten Kessler, et al.. (2015). Investigating the impact of a mutation in PDE5A on myocardial infarction. BMC Pharmacology and Toxicology. 16(S1). 4 indexed citations
10.
Asl, Hassan Foroughi, Husain A. Talukdar, Alida Kindt, et al.. (2015). Expression Quantitative Trait Loci Acting Across Multiple Tissues Are Enriched in Inherited Risk for Coronary Artery Disease. Circulation Cardiovascular Genetics. 8(2). 305–315. 29 indexed citations
11.
Braunholz, Diana, Ilaria Parenti, Jelena Pozojevic, et al.. (2015). Hidden Mutations in Cornelia de Lange Syndrome Limitations of Sanger Sequencing in Molecular Diagnostics. Human Mutation. 36(2). 279–280. 3 indexed citations
12.
Wilcox, Robert A., Ingrid Brænne, Norbert Brüggemann, et al.. (2014). Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only. Journal of Neurology. 262(1). 187–193. 6 indexed citations
13.
Braunholz, Diana, Ilaria Parenti, Jelena Pozojevic, et al.. (2014). Hidden Mutations in Cornelia de Lange Syndrome Limitations of Sanger Sequencing in Molecular Diagnostics. Human Mutation. 36(1). 26–29. 19 indexed citations
14.
Brænne, Ingrid, Benedikt Reiz, Anja Medack, et al.. (2014). Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia. BMC Cardiovascular Disorders. 14(1). 108–108. 17 indexed citations
15.
Dang, Tan An, Ingrid Brænne, Rédouane Aherrahrou, et al.. (2014). Abstract 19944: A PDE5A Gene Mutation Affecting Risk of Myocardial Infarction. Circulation. 130(suppl_2). 1 indexed citations
16.
Brænne, Ingrid, Anja Medack, Klaus Stark, et al.. (2012). Abstract 19823: Whole-Exome Sequencing in an Extended Family with Myocardial Infarction Identified a Potential Functional Mutation in PDE5A. Circulation. 126(suppl_21). 1 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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