Sven Hoffmeyer

19 papers receiving 3.6k citations

Sven Hoffmeyer's Hit Papers

Functional polymorphisms of the human multidrug-resistance gene: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo 2000 · 2.0k citations
2.0k0+8+17Years since publication50010001.5k2.0k

Peers

Sven Hoffmeyer
Comparison fields: 5 of 92
  • Oncology 2.1k
  • Transplantation 197
  • Pharmacology 636
  • Pediatrics, Perinatology and Child Health 1.2k
  • Neurology 410
Replace Peter Kuehl with:
Peter Kuehl United States
Horst Schran United States
Susan J. Johns United States
Ludger Banken Switzerland
Michael Cole United Kingdom
Norihiko Tsuchiya Japan
Ryan Owen United States
Shigeru Horita Japan
Nicolas Pallet France
Jamie L. Renbarger United States
Sven Hoffmeyer relative to Peter Kuehl United States Peter Kuehl's profile →
Citations per field
00.5×2×3.0×
Peter Kuehl · 1×
Citations per year

Countries citing papers authored by Sven Hoffmeyer

Since Specialization
Citations

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

Fields of papers citing papers by Sven Hoffmeyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

19 of 19 papers shown
#Work
1
Functional polymorphisms of the human multidrug-resistance gene: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo
Hit paper breakdown →
20002028
2 2000490
3 2002273
4 2000247
5 2002215
6 2001163
7 199756
8 199848
9 199541
10 199436
11
Aberrant splicing in several human tumors in the tumor suppressor genes neurofibromatosis type 1, neurofibromatosis type 2, and tuberous sclerosis 2.
200231
12 199429
13 199924
14 199919
15 199912
16 199411
17 19996
18 19953
19 19992

About Sven Hoffmeyer

Sven Hoffmeyer is a scholar working on Neurology, Pulmonary and Respiratory Medicine, Molecular Biology, Oncology and Rheumatology, having authored 19 papers that have together received 3.7k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (14 papers), Sarcoma Diagnosis and Treatment (6 papers), Drug Transport and Resistance Mechanisms (5 papers), Soft tissue tumor case studies (4 papers), Chromatin Remodeling and Cancer (3 papers), Hippo pathway signaling and YAP/TAZ (3 papers), Soft tissue tumors and treatment (2 papers) and Meningioma and schwannoma management (2 papers). The work is most often cited by research in Oncology (2.1k citations), Transplantation (197 citations), Pharmacology (636 citations), Pediatrics, Perinatology and Child Health (1.2k citations) and Neurology (410 citations). Sven Hoffmeyer has collaborated with scholars based in Germany, Iran and China. Frequent co-authors include Ulrich Brinkmann, Ingolf Cascorbi, Andreas Johne, Ivar Roots, Thomas Gerloff, Oliver Burk, Michel Eichelbaum, Oliver von Richter, J. Brockmöller and Reinhold Kerb. Their work appears in journals such as The American Journal of Human Genetics, Proceedings of the National Academy of Sciences, Archives of Dermatological Research, Human Genetics and Journal of the American Society of Nephrology.

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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