Franziska Kause

762 total citations
3 papers, 20 citations indexed

About

Franziska Kause is a scholar working on Surgery, Urology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Franziska Kause has authored 3 papers receiving a total of 20 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Surgery, 1 paper in Urology and 1 paper in Pulmonary and Respiratory Medicine. Recurrent topics in Franziska Kause's work include Esophageal and GI Pathology (2 papers), Congenital Anomalies and Fetal Surgery (1 paper) and Head and Neck Anomalies (1 paper). Franziska Kause is often cited by papers focused on Esophageal and GI Pathology (2 papers), Congenital Anomalies and Fetal Surgery (1 paper) and Head and Neck Anomalies (1 paper). Franziska Kause collaborates with scholars based in Germany, Switzerland and United States. Franziska Kause's co-authors include Heiko Reutter, Rong Zhang, Hölger Thiele, Michael Ludwig, Alina C. Hilger, Stefan Herms, Janine Altmueller, Eberhard Schmiedeke, Friedhelm Hildebrandt and Anke Rißmann and has published in prestigious journals such as Molecular Medicine Reports, Birth Defects Research and Journal of Pediatric Genetics.

In The Last Decade

Franziska Kause

3 papers receiving 20 citations

Peers

Franziska Kause

SURGE

MB

PRM

GENET

Yui Nomiya Japan

Naoto Kondo Japan

Sabine Specht United Kingdom

Regina Fritsche Danielson Sweden

Michael Abern United States

Hyung Joon Kim South Korea

Lara Hawkes United Kingdom

Simon Imm Australia

Gabrielle Archer France

Marian Streško Slovakia

Yui Nomiya Japan

Franziska Kause

8 ×0.7

SURGE

19 ×1.7

MB

7 ×1.2

PRM

4 ×1.3

GENET

1 ×0.5

GENET

Citations per year, relative to Franziska Kause Franziska Kause (= 1×) peers Yui Nomiya

Countries citing papers authored by Franziska Kause

Since Specialization

Citations

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

Fields of papers citing papers by Franziska Kause

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Franziska Kause

This figure shows the co-authorship network connecting the top 25 collaborators of Franziska Kause. A scholar is included among the top collaborators of Franziska Kause 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 Franziska Kause. Franziska Kause 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.

Kause, Franziska, Rong Zhang, Michael Ludwig, et al.. (2019). HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum. Birth Defects Research. 111(10). 591–597. 16 indexed citations

2.

Zhang, Rong, Michael Knapp, Franziska Kause, Heiko Reutter, & Michael Ludwig. (2017). Role of the LF-SINE–Derived Distal ISL1 Enhancer in Patients with Classic Bladder Exstrophy. Journal of Pediatric Genetics. 6(3). 169–173. 1 indexed citations

3.

Kause, Franziska, et al.. (2017). Whole exome sequencing identifies a mutation in EYA1 and GLI3 in a patient with branchio‑otic syndrome and esophageal atresia: Coincidence or a digenic mode of inheritance?. Molecular Medicine Reports. 17(2). 3200–3205. 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.

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