Verena Rupp

486 total citations
7 papers, 336 citations indexed

About

Verena Rupp is a scholar working on Molecular Biology, Cell Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Verena Rupp has authored 7 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Cell Biology and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Verena Rupp's work include RNA modifications and cancer (2 papers), Microtubule and mitosis dynamics (2 papers) and Acute Myeloid Leukemia Research (1 paper). Verena Rupp is often cited by papers focused on RNA modifications and cancer (2 papers), Microtubule and mitosis dynamics (2 papers) and Acute Myeloid Leukemia Research (1 paper). Verena Rupp collaborates with scholars based in Austria, Pakistan and Germany. Verena Rupp's co-authors include Christian Windpassinger, Muhammad Ansar, John B. Vincent, Muzammil Ahmad Khan, Dan Doherty, Ghazanfar Ali, Falak Sher Khan, Gisele E. Ishak, Michaela Frye and Abdul Noor and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

Verena Rupp

7 papers receiving 333 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Verena Rupp Austria	6	269	92	55	54	48	7	336
Petra Zeisberger Germany	5	268 1.0×	58 0.6×	24 0.4×	99 1.8×	15 0.3×	11	349
Candace J. Poole United States	7	234 0.9×	51 0.6×	29 0.5×	29 0.5×	33 0.7×	10	298
Nina Weichert‐Leahey United States	6	334 1.2×	100 1.1×	37 0.7×	16 0.3×	34 0.7×	10	427
Alix Rousseau France	5	199 0.7×	30 0.3×	56 1.0×	75 1.4×	19 0.4×	6	281
Dimitris Karamitros Greece	9	201 0.7×	37 0.4×	21 0.4×	100 1.9×	36 0.8×	14	306
Brynelle Myers United Kingdom	3	204 0.8×	79 0.9×	19 0.3×	52 1.0×	20 0.4×	6	280
Michael Spencer Chapman United Kingdom	7	155 0.6×	105 1.1×	69 1.3×	74 1.4×	9 0.2×	15	277
Caila Ryan United States	9	385 1.4×	51 0.6×	39 0.7×	38 0.7×	15 0.3×	9	456
Lisa von Paleske Germany	4	245 0.9×	51 0.6×	21 0.4×	86 1.6×	11 0.2×	6	316

Countries citing papers authored by Verena Rupp

Since Specialization

Citations

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

Fields of papers citing papers by Verena Rupp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Verena Rupp

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

7 of 7 papers shown

Xue, Yuan, Benedikt Schoser, Roberto Quadrelli, et al.. (2016). Exome Sequencing Identified a Splice Site Mutation in FHL1 that Causes Uruguay Syndrome, an X-Linked Disorder With Skeletal Muscle Hypertrophy and Premature Cardiac Death. Circulation Cardiovascular Genetics. 9(2). 130–135. 6 indexed citations

Khan, Muzammil Ahmad, Verena Rupp, Meritxell Orpinell, et al.. (2014). A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family. Human Molecular Genetics. 23(22). 5940–5949. 50 indexed citations

Khan, Muzammil Ahmad, et al.. (2014). Genetic analysis of a consanguineous Pakistani family with Leber congenital amaurosis identifies a novel mutation in GUCY2D gene. Journal of Genetics. 93(2). 527–530. 3 indexed citations

Rupp, Verena, et al.. (2014). A novel single base pair duplication in WDR62 causes primary microcephaly. BMC Medical Genetics. 15(1). 107–107. 12 indexed citations

Neubauer, Björn, Katharina Machura, Verena Rupp, et al.. (2013). Development of renal renin-expressing cells does not involve PDGF-B-PDGFR-βsignaling. Physiological Reports. 1(5). e00132–e00132. 7 indexed citations

Schulz, Eduard, Angelika Valentin, Peter Ulz, et al.. (2012). Germline mutations in the DNA damage response genes BRCA1, BRCA2, BARD1 and TP53 in patients with therapy related myeloid neoplasms. Journal of Medical Genetics. 49(7). 422–428. 76 indexed citations

Khan, Muzammil Ahmad, Muhammad Rafiq, Abdul Noor, et al.. (2012). Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability. The American Journal of Human Genetics. 90(5). 856–863. 182 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