Vinzenz Oji

5.5k total citations
67 papers, 1.9k citations indexed

About

Vinzenz Oji is a scholar working on Cell Biology, Molecular Biology and Genetics. According to data from OpenAlex, Vinzenz Oji has authored 67 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Cell Biology, 28 papers in Molecular Biology and 20 papers in Genetics. Recurrent topics in Vinzenz Oji's work include Skin and Cellular Biology Research (44 papers), Dermatological and Skeletal Disorders (14 papers) and Dermatology and Skin Diseases (11 papers). Vinzenz Oji is often cited by papers focused on Skin and Cellular Biology Research (44 papers), Dermatological and Skeletal Disorders (14 papers) and Dermatology and Skin Diseases (11 papers). Vinzenz Oji collaborates with scholars based in Germany, Austria and France. Vinzenz Oji's co-authors include Heiko Traupe, Ingrid Haußer, Karin Aufenvenne, Judith Fischer, Hans Christian Hennies, Katja‐Martina Eckl, Alberto Sánchez‐Guijo, Stefan A. Wudy, Michaela F. Hartmann and Dieter Metze and has published in prestigious journals such as Nature Genetics, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Vinzenz Oji

62 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vinzenz Oji Germany 26 970 828 490 461 212 67 1.9k
B. Bouadjar Algeria 21 608 0.6× 943 1.1× 354 0.7× 306 0.7× 59 0.3× 27 1.8k
Masako Mizoguchi Japan 28 819 0.8× 615 0.7× 108 0.2× 746 1.6× 81 0.4× 111 2.3k
Muriel Cario France 27 907 0.9× 575 0.7× 111 0.2× 626 1.4× 55 0.3× 71 1.8k
Anders Vahlquist Sweden 17 764 0.8× 613 0.7× 235 0.5× 284 0.6× 148 0.7× 27 1.4k
Toshifumi Nomura Japan 21 380 0.4× 421 0.5× 154 0.3× 954 2.1× 67 0.3× 100 1.8k
Amir Tavakkol United States 20 322 0.3× 803 1.0× 285 0.6× 487 1.1× 64 0.3× 27 1.5k
Barbara Gilbert Belgium 17 440 0.5× 1.3k 1.5× 111 0.2× 276 0.6× 38 0.2× 20 2.0k
Alan N. Moshell United States 22 354 0.4× 810 1.0× 214 0.4× 565 1.2× 413 1.9× 40 1.9k
H. Iizuka Japan 21 372 0.4× 454 0.5× 123 0.3× 402 0.9× 49 0.2× 77 1.4k
Minao Furumura Japan 28 910 0.9× 640 0.8× 138 0.3× 534 1.2× 52 0.2× 71 2.1k

Countries citing papers authored by Vinzenz Oji

Since Specialization
Citations

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

Fields of papers citing papers by Vinzenz Oji

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vinzenz Oji

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

All Works

20 of 20 papers shown
1.
Hotz, Alrun, Regina Fölster‐Holst, Vinzenz Oji, et al.. (2024). Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying ABCA12 Mutations. Genes. 15(3). 288–288. 2 indexed citations
2.
Oji, Vinzenz, et al.. (2023). Acral keratoderma and sudden death. Diagnostic histopathology. 30(1). 77–80.
3.
Aßmann, G., Michaela Köhm, Volker Schuster, et al.. (2020). Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups. BMC Medical Genetics. 21(1). 102–102. 11 indexed citations
4.
Sánchez‐Guijo, Alberto, Vinzenz Oji, Michaela F. Hartmann, Heiko Traupe, & Stefan A. Wudy. (2015). Simultaneous quantification of cholesterol sulfate, androgen sulfates, and progestagen sulfates in human serum by LC-MS/MS. Journal of Lipid Research. 56(9). 1843–1851. 64 indexed citations
5.
Hotz, Alrun, Vinzenz Oji, E. Bourrat, et al.. (2015). Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis. Acta Dermato Venereologica. 96(4). 473–478. 40 indexed citations
6.
Eckl, Katja‐Martina, Rotem Tidhar, Holger Thiele, et al.. (2013). Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length. Journal of Investigative Dermatology. 133(9). 2202–2211. 130 indexed citations
7.
Blaydon, Diana C., Daniela Nitoiu, Katja‐Martina Eckl, et al.. (2011). Mutations in CSTA, Encoding Cystatin A, Underlie Exfoliative Ichthyosis and Reveal a Role for This Protease Inhibitor in Cell-Cell Adhesion. The American Journal of Human Genetics. 89(4). 564–571. 67 indexed citations
8.
Oji, Vinzenz, et al.. (2010). rAAV2-mediated restoration of LEKTI in LEKTI-deficient cells from Netherton patients. Journal of Dermatological Science. 61(3). 194–198. 21 indexed citations
9.
Arin, Meral J., Vinzenz Oji, Steffen Emmert, et al.. (2010). Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis. British Journal of Dermatology. 164(2). 442–447. 54 indexed citations
10.
Oji, Vinzenz. (2010). Klinik und Ätiologie der Ichthyosen. Der Hautarzt. 61(10). 891–905. 9 indexed citations
11.
Oji, Vinzenz, Katja‐Martina Eckl, Karin Aufenvenne, et al.. (2010). Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin Disease. The American Journal of Human Genetics. 87(2). 274–281. 146 indexed citations
12.
Pasternack, Sandra M., Ivar von Kügelgen, Melanie Müller, et al.. (2009). In Vitro Analysis of LIPH Mutations Causing Hypotrichosis Simplex: Evidence Confirming the Role of Lipase H and Lysophosphatidic Acid in Hair Growth. Journal of Investigative Dermatology. 129(12). 2772–2776. 27 indexed citations
13.
Oji, Vinzenz & Heiko Traupe. (2009). Ichthyosis. American Journal of Clinical Dermatology. 10(6). 351–364. 81 indexed citations
14.
Geel, Michel van, Jos L. V. Broers, Fares Chedid, et al.. (2008). A newly identified splice site mutation inZMPSTE24causes restrictive dermopathy in the Middle East. British Journal of Dermatology. 159(4). 961–967. 10 indexed citations
15.
Haenssle, Holger A., Ingrid Haußer, Vinzenz Oji, et al.. (2008). Effective treatment of severe thermodysregulation by oral retinoids in a patient with recessive congenital lamellar ichthyosis. Clinical and Experimental Dermatology. 33(5). 578–581. 13 indexed citations
16.
Grzeschik, Karl‐Heinz, Dorothea Bornholdt, Frank Oeffner, et al.. (2007). Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia. Nature Genetics. 39(7). 833–835. 181 indexed citations
17.
Hüffmeier, Ulrike, Heiko Traupe, Vinzenz Oji, et al.. (2007). Loss-of-Function Variants of the Filaggrin Gene Are Not Major Susceptibility Factors for Psoriasis Vulgaris or Psoriatic Arthritis in German Patients. Journal of Investigative Dermatology. 127(6). 1367–1370. 36 indexed citations
18.
19.
Böhm, Markus, Zhuo Li, Stefan W. Schneider, et al.. (2005). Detection of Functionally Active Melanocortin Receptors and Evidence for an Immunoregulatory Activity of α-Melanocyte-Stimulating Hormone in Human Dermal Papilla Cells. Endocrinology. 146(11). 4635–4646. 46 indexed citations
20.
Raghunath, Michael, Vinzenz Oji, Karin Aufenvenne, et al.. (2004). SPINK5 and Netherton Syndrome: Novel Mutations, Demonstration of Missing LEKTI, and Differential Expression of Transglutaminases. Journal of Investigative Dermatology. 123(3). 474–483. 82 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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