Katharina Schwarze

803 total citations · 1 hit paper
8 papers, 501 citations indexed

About

Katharina Schwarze is a scholar working on Pathology and Forensic Medicine, Genetics and General Health Professions. According to data from OpenAlex, Katharina Schwarze has authored 8 papers receiving a total of 501 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Pathology and Forensic Medicine, 3 papers in Genetics and 2 papers in General Health Professions. Recurrent topics in Katharina Schwarze's work include Genomics and Rare Diseases (3 papers), Genetic factors in colorectal cancer (3 papers) and Patient Satisfaction in Healthcare (2 papers). Katharina Schwarze is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetic factors in colorectal cancer (3 papers) and Patient Satisfaction in Healthcare (2 papers). Katharina Schwarze collaborates with scholars based in Germany, United Kingdom and Austria. Katharina Schwarze's co-authors include James Buchanan, Sarah Wordsworth, Jenny C. Taylor, Jilles M. Fermont, Pavlos Antoniou, Melissa M. Pentony, Niko Popitsch, John Taylor, Anna Schuh and Hélène Dreau and has published in prestigious journals such as SHILAP Revista de lepidopterología, Genetics in Medicine and Value in Health.

In The Last Decade

Katharina Schwarze

5 papers receiving 494 citations

Hit Papers

Are whole-exome and whole-genome sequencing approaches co... 2018 2026 2020 2023 2018 100 200 300
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature
    2018 349 citations Katharina Schwarze, James Buchanan et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katharina Schwarze Germany 3 243 162 129 78 55 8 501
Megan McDonald United States 17 179 0.7× 353 2.2× 116 0.9× 31 0.4× 63 1.1× 59 879
Christina Hubbart United Kingdom 11 111 0.5× 136 0.8× 73 0.6× 36 0.5× 29 0.5× 18 597
Ken H. Buetow United States 5 132 0.5× 236 1.5× 79 0.6× 26 0.3× 18 0.3× 8 413
Daniel Backenroth United States 12 143 0.6× 140 0.9× 73 0.6× 15 0.2× 110 2.0× 28 448
Borbála Mifsud United Kingdom 13 231 1.0× 808 5.0× 104 0.8× 28 0.4× 35 0.6× 26 1.1k
Mine Cicek United States 16 156 0.6× 205 1.3× 150 1.2× 202 2.6× 66 1.2× 21 717
Karen Dubois‐Camacho Chile 11 135 0.6× 180 1.1× 73 0.6× 25 0.3× 24 0.4× 20 471
Jinyoung Byun United States 13 73 0.3× 188 1.2× 65 0.5× 30 0.4× 82 1.5× 37 417
Rita D. Brandão Netherlands 10 275 1.1× 374 2.3× 232 1.8× 95 1.2× 94 1.7× 18 717

Countries citing papers authored by Katharina Schwarze

Since Specialization
Citations

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

Fields of papers citing papers by Katharina Schwarze

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katharina Schwarze

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

All Works

8 of 8 papers shown
1.
2.
Wasmuth, Susanne, Ross Parfitt, Werner Brannath, et al.. (2025). Evaluating the Hearing‐Related Quality of Life in People With Intellectual Disabilities. Journal of Intellectual Disability Research. 69(12). 1413–1424.
3.
Wasem, Jürgen, et al.. (2024). Preference-Based Implementation of Video Consultations in Urban and Rural Regions in Outpatient Care in Germany: Protocol for a Mixed Methods Study. JMIR Research Protocols. 13. e50932–e50932. 2 indexed citations
4.
Schwarze, Katharina, et al.. (2024). Evaluation of a cross-sectoral care model including novel telemedical concepts for diagnosis and treatment of obstructive sleep apnea (SLEEP WELL). Somnologie - Schlafforschung und Schlafmedizin. 28(3). 203–211.
5.
6.
Schwarze, Katharina, James Buchanan, Jilles M. Fermont, et al.. (2019). The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United Kingdom. Genetics in Medicine. 22(1). 85–94. 140 indexed citations
7.
Schwarze, Katharina, et al.. (2018). Are whole Exome and whole Genome Sequencing Approaches Cost-Effective? A Systematic Review of the Literature. Value in Health. 21. S100–S100. 8 indexed citations
8.
Schwarze, Katharina, James Buchanan, Jenny C. Taylor, & Sarah Wordsworth. (2018). Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature. Genetics in Medicine. 20(10). 1122–1130. 349 indexed citations breakdown →

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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