Andreas Thimm

585 citations
24 papers · 409 · h-index 13

Impact in

  • Genetics top 5%
    • Neurogenetic and Muscular Disorders Research
    • Genomics and Rare Diseases
    • Amyloidosis: Diagnosis, Treatment, Outcomes
    • Gut microbiota and health

Papers in

    • Neurogenetic and Muscular Disorders Research 9
    • Amyloidosis: Diagnosis, Treatment, Outcomes 11
    • Gut microbiota and health 1

Andreas Thimm

22 papers receiving 400 citations

Peers

Andreas Thimm
Comparison fields: 5 of 36
  • Genetics 189
  • Molecular Biology 153
  • Neurology 25
  • Clinical Biochemistry 7
  • Speech and Hearing 4
Replace Ylva Mende with:
Ylva Mende Germany
C.L. de Winter Netherlands
Jena M. Krueger United States
Tomoki T. Nomakuchi United States
Carla Gliubizzi Italy
C. Cini Italy
Natalie F. Reash United States
Melissa A. Goddard United States
Mary S. Sedra United States
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Andreas Thimm relative to Ylva Mende Germany Ylva Mende's profile →
Citations per field
00.5×2×4×6×8×9.5×
Ylva Mende · 1×
Citations per year

Countries citing papers authored by Andreas Thimm

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Thimm

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201946
2 202441
3 202239
4 202232
5 202130
6 202129
7 202228
8 202324
9 202121
10 202121
11 202218
12 202117
13 202014
14 202113
15 202212
16 20228
17 20235
18 20234
19 20193
20 20252

About Andreas Thimm

Andreas Thimm is a scholar working on Genetics, Molecular Biology, Neurology, Cellular and Molecular Neuroscience and Oncology, having authored 24 papers that have together received 409 indexed citations. Recurring topics across this work include Amyloidosis: Diagnosis, Treatment, Outcomes (11 papers), Neurogenetic and Muscular Disorders Research (9 papers), Cancer Immunotherapy and Biomarkers (1 paper), Gut microbiota and health (1 paper), Hereditary Neurological Disorders (1 paper) and Myasthenia Gravis and Thymoma (1 paper). The work is most often cited by research in Genetics (189 citations), Molecular Biology (153 citations), Neurology (25 citations), Clinical Biochemistry (7 citations) and Speech and Hearing (4 citations). Andreas Thimm has collaborated with scholars based in Germany, United Kingdom and Austria. Frequent co-authors include Tim Hagenacker, Christoph Kleinschnitz, Benjamin Stolte, Kathrin Kizina, Andreas Totzeck, Alexander Carpinteiro, Tienush Rassaf, Μαρία Παπαθανασίου, Christoph Rischpler and Lukas Kessler. Their work appears in journals such as Journal of Neurology, Orphanet Journal of Rare Diseases, Journal of Clinical Medicine, European Journal Of Haematology and Frontiers in Neurology.

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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