Sven Hoffmeyer

4.4k total citations · 1 hit paper
19 papers, 3.6k citations indexed

About

Sven Hoffmeyer is a scholar working on Neurology, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Sven Hoffmeyer has authored 19 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Neurology, 6 papers in Pulmonary and Respiratory Medicine and 5 papers in Molecular Biology. Recurrent topics in Sven Hoffmeyer's work include Neurofibromatosis and Schwannoma Cases (14 papers), Sarcoma Diagnosis and Treatment (6 papers) and Drug Transport and Resistance Mechanisms (5 papers). Sven Hoffmeyer is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (14 papers), Sarcoma Diagnosis and Treatment (6 papers) and Drug Transport and Resistance Mechanisms (5 papers). Sven Hoffmeyer collaborates with scholars based in Germany, United States and Iran. Sven Hoffmeyer's co-authors include Ulrich Brinkmann, Ivar Roots, Thomas Gerloff, Andreas Johne, Ingolf Cascorbi, Oliver Burk, Michel Eichelbaum, J. Brockmöller, Oliver von Richter and Reinhold Kerb and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Biochemical and Biophysical Research Communications and Journal of the American Society of Nephrology.

In The Last Decade

Sven Hoffmeyer

19 papers receiving 3.5k citations

Hit Papers

align trajectories

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.

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 Sven Hoffmeyer, Oliver Burk et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sven Hoffmeyer Germany	14	2.4k	1.5k	736	724	438	19	3.6k
Horst Schran United States	28	1.1k 0.5×	231 0.2×	186 0.3×	626 0.9×	87 0.2×	70	3.0k
Susan J. Johns United States	23	1.4k 0.6×	656 0.4×	324 0.4×	733 1.0×	306 0.7×	33	2.3k
Conny Bakker Netherlands	17	1.2k 0.5×	1.7k 1.1×	388 0.5×	1.3k 1.8×	139 0.3×	27	3.0k
Jamie L. Renbarger United States	20	806 0.3×	360 0.2×	311 0.4×	507 0.7×	53 0.1×	65	1.8k
Shigeru Horita Japan	29	716 0.3×	374 0.2×	191 0.3×	616 0.9×	70 0.2×	123	2.7k
William R. Crom United States	22	556 0.2×	533 0.4×	165 0.2×	445 0.6×	28 0.1×	37	1.7k
Nicolas Pallet France	34	295 0.1×	380 0.3×	94 0.1×	1.2k 1.7×	137 0.3×	123	3.4k
Ursula Amstutz Switzerland	24	948 0.4×	337 0.2×	524 0.7×	603 0.8×	34 0.1×	50	2.1k
Ryan Owen United States	17	535 0.2×	280 0.2×	293 0.4×	719 1.0×	157 0.4×	35	2.4k
Kimberly L. Napoli United States	25	275 0.1×	471 0.3×	140 0.2×	434 0.6×	174 0.4×	56	2.1k

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-authorship network of co-authors of Sven Hoffmeyer

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

All Works

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19 of 19 papers shown

1.

Johne, Andreas, Karla Köpke, Thomas Gerloff, et al.. (2002). Modulation of steady‐state kinetics of digoxin by haplotypes of the P‐glycoprotein MDR1 gene. Clinical Pharmacology & Therapeutics. 72(5). 584–594. 267 indexed citations

2.

Siegsmund, M., Ulrich Brinkmann, Gregor Weirich, et al.. (2002). Association of the P-Glycoprotein Transporter MDR1 C3435T Polymorphism with the Susceptibility to Renal Epithelial Tumors. Journal of the American Society of Nephrology. 13(7). 1847–1854. 210 indexed citations

3.

Kaufmann, Dieter, et al.. (2002). Aberrant splicing in several human tumors in the tumor suppressor genes neurofibromatosis type 1, neurofibromatosis type 2, and tuberous sclerosis 2.. PubMed. 62(5). 1503–9. 30 indexed citations

4.

Kerb, Reinhold, Sven Hoffmeyer, & Ulrich Brinkmann. (2001). ABC drug transporters: hereditary polymorphisms and pharmacological impact in MDR1, MRP1 and MRP2. Pharmacogenomics. 2(1). 51–64. 157 indexed citations

5.

Fahsold, Raimund, Sven Hoffmeyer, Claudia Mischung, et al.. (2000). Minor Lesion Mutational Spectrum of the Entire NF1 Gene Does Not Explain Its High Mutability but Points to a Functional Domain Upstream of the GAP-Related Domain. The American Journal of Human Genetics. 66(3). 790–818. 231 indexed citations

6.

Hoffmeyer, Sven, Oliver Burk, Oliver von Richter, et al.. (2000). Functional polymorphisms of the human multidrug-resistance gene: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proceedings of the National Academy of Sciences. 97(7). 3473–3478. 1951 indexed citations breakdown →

7.

Hoffmeyer, Sven. (2000). Functional polymorphisms of the human multidrug-resistance gene: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proceedings of the National Academy of Sciences. 97(7). 3473–3478. 470 indexed citations

8.

Kaufmann, Dieter, et al.. (1999). EVI2B, a Gene Lying in an Intron of the Neurofibromatosis Type 1 (NF1) Gene, Is As the NF1 Gene Involved in Differentiation of Melanocytes and Keratinocytes and Is Overexpressed in Cells Derived from NF1 Neurofibromas. DNA and Cell Biology. 18(5). 345–356. 18 indexed citations

9.

Harder, Anja, Hartmut Peters, Sven Hoffmeyer, et al.. (1999). Two independent mutations in a family with neurofibromatosis type 1 (NF1). American Journal of Medical Genetics. 83(1). 6–12. 22 indexed citations

10.

Harder, Anja, Hartmut Peters, Sven Hoffmeyer, et al.. (1999). Two independent mutations in a family with neurofibromatosis type 1 (NF1). American Journal of Medical Genetics. 83(1). 6–12. 2 indexed citations

11.

Peters, Nils, Ruth Wellenreuther, Reinhard E. Friedrich, et al.. (1999). Quantitative analysis of NF1 and OMGP gene transcripts in sporadic gliomas, sporadic meningiomas and neurofibromatosis type 1-associated plexiform neurofibromas. Acta Neuropathologica. 97(6). 547–551. 6 indexed citations

12.

Kaufmann, Dieter, Britta Bartelt‐Kirbach, Sven Hoffmeyer, & Ralf Müller-Xing. (1999). Posttranslational regulation of neurofibromin content in melanocytes of neurofibromatosis type 1 patients. Archives of Dermatological Research. 291(6). 312–317. 9 indexed citations

13.

Hoffmeyer, Sven, et al.. (1998). Nearby Stop Codons in Exons of the Neurofibromatosis Type 1 Gene Are Disparate Splice Effectors. The American Journal of Human Genetics. 62(2). 269–277. 45 indexed citations

14.

Assum, Günter, Ingrid Eisenbarth, W. Krone, et al.. (1997). Clonal Origin of Tumor Cells in a Plexiform Neurofibroma with LOH in NF1 Intron 38 and in Dermal Neurofibromas without LOH of the NF1 Gene. Biochemical and Biophysical Research Communications. 234(2). 346–350. 49 indexed citations

15.

Eisenbarth, Ingrid, et al.. (1995). Analysis of an alternatively spliced exon of the neurofibromatosis type 1 gene in cultured melanocytes from patients with neurofibromatosis 1. Archives of Dermatological Research. 287(5). 413–416. 3 indexed citations

16.

Hoffmeyer, Sven, et al.. (1995). On unequal allelic expression of the neurofibromin gene in neurofibromatosis type 1. Human Molecular Genetics. 4(8). 1267–1272. 40 indexed citations

17.

Hoffmeyer, Sven, et al.. (1994). An RsaI polymorphism in the transcribed region of the neurofibromatosis (NF1)-gene. Human Genetics. 93(4). 36 indexed citations

18.

Hoffmeyer, Sven, et al.. (1994). A deletion in the 5 ′-region of the neurofibromatosis type 1 (NF1) gene. Human Genetics. 94(1). 97–100. 11 indexed citations

19.

Kaufmann, Dieter, Frank Braun, Ingrid Eisenbarth, et al.. (1994). Investigations of neurofibromin expression in the skin of patients with NF 1 (neurofibromatosis type 1). Melanoma Research. 4(2). 45–45. 28 indexed citations

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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