Alrun Hotz

532 total citations
22 papers, 211 citations indexed

About

Alrun Hotz is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Alrun Hotz has authored 22 papers receiving a total of 211 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Cell Biology and 11 papers in Genetics. Recurrent topics in Alrun Hotz's work include Skin and Cellular Biology Research (14 papers), Wnt/β-catenin signaling in development and cancer (8 papers) and Dermatological and Skeletal Disorders (6 papers). Alrun Hotz is often cited by papers focused on Skin and Cellular Biology Research (14 papers), Wnt/β-catenin signaling in development and cancer (8 papers) and Dermatological and Skeletal Disorders (6 papers). Alrun Hotz collaborates with scholars based in Germany, France and Sweden. Alrun Hotz's co-authors include Andreas Zimmer, Johannes Fischer, E. Bourrat, Judith Fischer, A. Vahlquist, Anette Bygum, F Brandrup, Vinzenz Oji, Agneta Gånemo and Marie Virtanen and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Investigative Dermatology and British Journal of Dermatology.

In The Last Decade

Alrun Hotz

18 papers receiving 199 citations

Peers

Alrun Hotz

GENET

UROLO

DERMA

N. Malchin Israel

Diane Gleeson United Kingdom

Jay Krachmer United States

Tom Rabinowitz Israel

Roberta Contin Italy

Dulce Lima Cunha United Kingdom

Anne-Katrin Kortüm Germany

Anissa Edir France

Emine Bolat Netherlands

Ana-Maria Cujba United Kingdom

N. Malchin Israel

Alrun Hotz

71 ×0.5

116 ×0.9

55 ×0.6

GENET

11 ×0.6

UROLO

53 ×3.5

DERMA

Citations per year, relative to Alrun Hotz Alrun Hotz (= 1×) peers N. Malchin

Countries citing papers authored by Alrun Hotz

Since Specialization

Citations

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

Fields of papers citing papers by Alrun Hotz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alrun Hotz

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

All Works

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20 of 20 papers shown

Tomasini, Dario, Carlo Tomasini, Andrea Michelerio, et al.. (2025). Genetic and Phenotypic Features of 2 Northern Italy Families with Dowling-Degos Disease Type 4. JID Innovations. 5(4). 100364–100364. 1 indexed citations

Schreml, Julia, Judith Fischer, Alrun Hotz, et al.. (2024). Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein‐1 mutation: A case report. SHILAP Revista de lepidopterología. 12(5). e8881–e8881.

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

Komlósi, Katalin, Cristina Glocker, Svenja Alter, et al.. (2024). Autosomal Dominant Lamellar Ichthyosis Due to a Missense Variant in the Gene NKPD1. Journal of Investigative Dermatology. 144(12). 2754–2763.e6. 2 indexed citations

Hotz, Alrun, et al.. (2024). Pseudoainhum and universal alopecia. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 22(9). 1287–1289.

Wang, Yao, Alrun Hotz, Philipp R. Esser, Judith Fischer, & Cristina Has. (2023). Amino Acid Substitution in the Cysteine-Rich Region of the Integrin β4 Subunit Causes Late-Onset Mild Junctional Epidermolysis Bullosa without Extracutaneous Involvement. Journal of Investigative Dermatology. 143(11). 2233–2242.e3. 1 indexed citations

Fischer, Judith, Alrun Hotz, & Katalin Komlósi. (2023). Syndromic ichthyoses. Medizinische Genetik. 35(1). 23–32.

Feige, Bernd, Kimon Runge, Kathrin Nickel, et al.. (2022). Obsessive–compulsive symptoms in ACTG1-associated Baraitser-Winter cerebrofrontofacial syndrome. Journal of Neural Transmission. 129(11). 1387–1391. 3 indexed citations

Hotz, Alrun, et al.. (2021). Plantar involvement correlates with obesity, pain and impaired mobility in epidermolysis bullosa simplex: a retrospective cohort study. Journal of the European Academy of Dermatology and Venereology. 35(10). 2097–2104. 4 indexed citations

10.

Hotz, Alrun, et al.. (2021). High rate of self‐improving phenotypes in children with non‐syndromic congenital ichthyosis: case series from south‐western Germany. Journal of the European Academy of Dermatology and Venereology. 35(11). 2293–2299. 6 indexed citations

11.

Has, Cristina, et al.. (2021). Maternal Isodisomy of Chromosome 3 Combined with a De Novo Mutation in the ABHD5 Gene Causes Autosomal Recessive Chanarin-Dorfman Syndrome. Genes. 12(8). 1164–1164. 2 indexed citations

12.

Komlósi, Katalin, Alrun Hotz, Svenja Alter, et al.. (2020). Neonatal presentation of COG6‐CDG with prominent skin phenotype. JIMD Reports. 55(1). 51–58. 9 indexed citations

13.

Alter, Svenja, Alrun Hotz, Arne Jahn, et al.. (2018). Novel VPS33B mutation in a patient with autosomal recessive keratoderma‐ichthyosis‐deafness syndrome. American Journal of Medical Genetics Part A. 176(12). 2862–2866. 8 indexed citations

14.

Bourrat, E., P. Vabres, Julien Thévenon, et al.. (2018). Mosaicism due to postzygotic mutations in women with focal dermal hypoplasia. British Journal of Dermatology. 180(3). 657–661. 1 indexed citations

15.

Hotz, Alrun, E. Bourrat, Vinzenz Oji, et al.. (2018). Mutation update for CYP4F22 variants associated with autosomal recessive congenital ichthyosis. Human Mutation. 39(10). 1305–1313. 17 indexed citations

16.

Hotz, Alrun, Christina Fagerberg, A. Vahlquist, et al.. (2017). Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosis. British Journal of Dermatology. 178(3). e207–e209. 12 indexed citations

17.

Zimmer, Andreas, Alrun Hotz, E. Bourrat, et al.. (2017). Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function. British Journal of Dermatology. 177(2). 445–455. 22 indexed citations

18.

Pigg, Maritta Hellström, Anette Bygum, Agneta Gånemo, et al.. (2016). Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients. Acta Dermato Venereologica. 96(7). 932–937. 55 indexed citations

19.

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

20.

Hotz, Alrun, Yorck Hellenbroich, Jürgen Sperner, et al.. (2013). Microdeletion 5q14.3 and anomalies of brain development. American Journal of Medical Genetics Part A. 161(9). 2124–2133. 25 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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