Ulrike Faust

1.5k citations
14 papers · 88 · h-index 5

Impact in

    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Cancer Genomics and Diagnostics

Papers in

Ulrike Faust

12 papers receiving 87 citations

Peers

Ulrike Faust
Comparison fields: 5 of 26
  • Genetics 43
  • Cancer Research 19
  • Pathology and Forensic Medicine 12
  • Ophthalmology 5
  • Oncology 15
Replace Mattias Van Heetvelde with:
Mattias Van Heetvelde Belgium
Sophie Allen United Kingdom
A. Kulkarni United Kingdom
Tom Van Maerken Belgium
Sofie Joris Belgium
Virginie Moncoutier France
Seema Rego United States
Tjoung-Won Park-Simon Germany
Jeffrey Conroy United States
Martina Zimovjanová Czechia
Ulrike Faust relative to Mattias Van Heetvelde Belgium Mattias Van Heetvelde's profile →
Citations per field
00.5×1.5×
Mattias Van Heetvelde · 1×
Citations per year

Countries citing papers authored by Ulrike Faust

Since Specialization
Citations

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

Fields of papers citing papers by Ulrike Faust

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Ulrike Faust, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ulrike Faust Line = papers co-authored together Ulrike Faust links everyone, so they are left out of the graph.

All Works

14 of 14 papers shown
#Work
1 201535
2 202014
3 20189
4 20219
5 20137
6 20233
7 20213
8 20232
9 20252
10 20192
11 20251
12 20171
13 20250
14 20240

About Ulrike Faust

Ulrike Faust is a scholar working on Genetics, Pathology and Forensic Medicine, Cancer Research, Oncology and Surgery, having authored 14 papers that have together received 88 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Genetic factors in colorectal cancer (4 papers), Cancer Genomics and Diagnostics (3 papers), Genomics and Rare Diseases (2 papers), Vascular Tumors and Angiosarcomas (2 papers), DNA Repair Mechanisms (1 paper), Neurological disorders and treatments (1 paper) and Vascular Malformations and Hemangiomas (1 paper). The work is most often cited by research in Genetics (43 citations), Cancer Research (19 citations), Pathology and Forensic Medicine (12 citations), Ophthalmology (5 citations) and Oncology (15 citations). Ulrike Faust has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Andreas Rump, Olaf Rieß, Peter Bauer, Luisa Mackenroth, Kathrin Grundmann, Evelin Schröck, Marc Sturm, Karin Kast, Martin Kehrer and Christopher Schroeder. Their work appears in journals such as Journal of Clinical Oncology, Clinical Cancer Research, Breast Cancer Research and Treatment, Prenatal Diagnosis and Lung Cancer.

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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