Markus Mayrhofer

1.4k citations
22 papers · 536 · h-index 12

Impact in

Papers in

    • Cancer Genomics and Diagnostics 5
    • Genomic variations and chromosomal abnormalities 3
    • Diabetes and associated disorders 2

Markus Mayrhofer

21 papers receiving 530 citations

Peers

Markus Mayrhofer
Comparison fields: 5 of 44
  • Cancer Research 142
  • Pulmonary and Respiratory Medicine 164
  • Endocrinology, Diabetes and Metabolism 82
  • Genetics 127
  • Hematology 45
Replace Roelof Koster with:
Roelof Koster Netherlands
Justine N. McCutcheon United States
Mary Buchta Germany
Jiu-Cun Wang China
Joana Vieira Portugal
Ulla Aspenblad Sweden
Audrey Gros France
Samuel Suzuki United States
Rieke Fischer Germany
Anke Dam Netherlands
Markus Mayrhofer relative to Roelof Koster Netherlands Roelof Koster's profile →
Citations per field
00.5×2.8×
Roelof Koster · 1×
Citations per year

Countries citing papers authored by Markus Mayrhofer

Since Specialization
Citations

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

Fields of papers citing papers by Markus Mayrhofer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Markus Mayrhofer, 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 Markus Mayrhofer Line = papers co-authored together Markus Mayrhofer links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 22 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201798
2 199389
3 201647
4 201341
5 202135
6 201534
7 201533
8 201526
9 201224
10 201723
11 202122
12 201819
13 201410
14 202510
15 20257
16 20127
17 20245
18 20092
19 19972
20 20241

About Markus Mayrhofer

Markus Mayrhofer is a scholar working on Cancer Research, Genetics, Molecular Biology, Pathology and Forensic Medicine and Surgery, having authored 22 papers that have together received 536 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetic factors in colorectal cancer (3 papers), Diabetes and associated disorders (2 papers), Acute Myeloid Leukemia Research (2 papers), Pancreatic and Hepatic Oncology Research (2 papers), Prostate Cancer Treatment and Research (2 papers) and Pancreatic function and diabetes (2 papers). The work is most often cited by research in Cancer Research (142 citations), Pulmonary and Respiratory Medicine (164 citations), Endocrinology, Diabetes and Metabolism (82 citations), Genetics (127 citations) and Hematology (45 citations). Markus Mayrhofer has collaborated with scholars based in Sweden, Germany and Norway. Frequent co-authors include Anders Isaksson, Sebastian DiLorenzo, Johan Lindberg, Henrik Grönberg, Anette‐Gabriele Ziegler, Eberhard Standl, Wolfgang Rabl, Anne Lenz, U. Mollenhauer and Michael Hummel. Their work appears in journals such as BMC Cancer, Clinical Cancer Research, Scientific Reports, Blood Advances and Diabetologia.

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