Gunda Schwaninger

614 total citations
7 papers, 472 citations indexed

About

Gunda Schwaninger is a scholar working on Genetics, Pathology and Forensic Medicine and General Health Professions. According to data from OpenAlex, Gunda Schwaninger has authored 7 papers receiving a total of 472 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Pathology and Forensic Medicine and 2 papers in General Health Professions. Recurrent topics in Gunda Schwaninger's work include BRCA gene mutations in cancer (5 papers), Genetic factors in colorectal cancer (2 papers) and Ethics in medical practice (2 papers). Gunda Schwaninger is often cited by papers focused on BRCA gene mutations in cancer (5 papers), Genetic factors in colorectal cancer (2 papers) and Ethics in medical practice (2 papers). Gunda Schwaninger collaborates with scholars based in Austria, Germany and Switzerland. Gunda Schwaninger's co-authors include Jeffery L. Kutok, Alicia Y. Zhou, Mary W. Brooks, Naoyuki Miura, Jing Yang, Sendurai A. Mani, Kimberly A. Hartwell, Andrea L. Richardson, Robert A. Weinberg and Johannes Zschocke and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Clinical Genetics.

In The Last Decade

Gunda Schwaninger

5 papers receiving 468 citations

Peers

Gunda Schwaninger

MB

ONCOL

CR

CB

GENET

Nicholas Jette Canada

May Yin Lee Singapore

Rosa Viñas-Castells Spain

Jingxin Feng China

Erika López‐Arribillaga Spain

Robyn T. Sussman United States

Anne Kovochich United States

Ran‐Ju Kim South Korea

Kazunobu Isogaya Japan

Wei Zong China

Nicholas Jette Canada

Gunda Schwaninger

448 ×1.3

MB

301 ×1.1

ONCOL

76 ×0.6

CR

36 ×0.6

CB

44 ×0.9

GENET

Citations per year, relative to Gunda Schwaninger Gunda Schwaninger (= 1×) peers Nicholas Jette

Countries citing papers authored by Gunda Schwaninger

Since Specialization

Citations

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

Fields of papers citing papers by Gunda Schwaninger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gunda Schwaninger

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

All Works

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7 of 7 papers shown

1.

Schwaninger, Gunda, et al.. (2024). Workshop report: Clinical training and integration of genetic counselors into interprofessional teams in the German-speaking countries. SHILAP Revista de lepidopterología. 2(Suppl 2). 101855–101855.

2.

Schwaninger, Gunda, Simone Heidemann, Sabine Rudnik‐Schöneborn, & Johannes Zschocke. (2024). The current state of the genetic counselor profession in the German-speaking countries. SHILAP Revista de lepidopterología. 2(Suppl 2). 101849–101849.

3.

Schwaninger, Gunda, Lukas Forer, Christoph Ebenbichler, et al.. (2023). Filling the gap: Genetic risk assessment in hypercholesterolemia using LDL‐C and LPA genetic scores. Clinical Genetics. 104(3). 334–343. 3 indexed citations

4.

Witsch‐Baumgartner, Martina, et al.. (2022). Array genotyping as diagnostic approach in medical genetics. Molecular Genetics & Genomic Medicine. 10(9). e2016–e2016. 3 indexed citations

5.

Schwaninger, Gunda, Caroline Benjamin, Sabine Rudnik‐Schöneborn, & Johannes Zschocke. (2021). The genetic counseling profession in Austria: Stakeholders’ perspectives. Journal of Genetic Counseling. 30(3). 861–871. 8 indexed citations

6.

Schwaninger, Gunda, et al.. (2021). Prospects and challenges for the genetic counsellor profession in the German-speaking countries: report of a workshop. Medizinische Genetik. 33(1). 35–44. 3 indexed citations

7.

Mani, Sendurai A., Jing Yang, Mary W. Brooks, et al.. (2007). Mesenchyme Forkhead 1 ( FOXC2 ) plays a key role in metastasis and is associated with aggressive basal-like breast cancers. Proceedings of the National Academy of Sciences. 104(24). 10069–10074. 455 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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