Judith Fischer

7.4k total citations
119 papers, 3.7k citations indexed

About

Judith Fischer is a scholar working on Cell Biology, Molecular Biology and Genetics. According to data from OpenAlex, Judith Fischer has authored 119 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Cell Biology, 71 papers in Molecular Biology and 41 papers in Genetics. Recurrent topics in Judith Fischer's work include Skin and Cellular Biology Research (70 papers), Wnt/β-catenin signaling in development and cancer (32 papers) and Dermatological and Skeletal Disorders (22 papers). Judith Fischer is often cited by papers focused on Skin and Cellular Biology Research (70 papers), Wnt/β-catenin signaling in development and cancer (32 papers) and Dermatological and Skeletal Disorders (22 papers). Judith Fischer collaborates with scholars based in Germany, France and United States. Judith Fischer's co-authors include Mark Lathrop, Caroline Lefèvre, B. Bouadjar, Jean-François Prud’homme, Florence Jobard, Franz P.W. Radner, Anders Vahlquist, Robert Salvayre, Hans Törmä and Meral Özgüç and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Judith Fischer

109 papers receiving 3.6k citations

Peers

Judith Fischer

BIOCH

GENET

PHYSI

Heiko Traupe Germany

T. Mohandas United States

M.G. Byers United States

L. Marty France

Mohamed Elalfy Canada

T.B. Shows United States

Jesper T. Troelsen Denmark

Craig L. Bennett United States

A Kahn France

Jacques Picard France

Heiko Traupe Germany

Judith Fischer

2.0k ×1.0

2.0k ×1.2

66 ×0.1

BIOCH

1.3k ×1.6

GENET

417 ×0.7

PHYSI

Citations per year, relative to Judith Fischer Judith Fischer (= 1×) peers Heiko Traupe

Countries citing papers authored by Judith Fischer

Since Specialization

Citations

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

Fields of papers citing papers by Judith Fischer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judith Fischer

This figure shows the co-authorship network connecting the top 25 collaborators of Judith Fischer. A scholar is included among the top collaborators of Judith Fischer 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 Judith Fischer. Judith Fischer 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

Chiavérini, C., Fanny Morice‐Picard, Hélène Texier, et al.. (2024). French national protocol for the management of congenital ichthyosis. Annales de Dermatologie et de Vénéréologie. 151(1). 103247–103247.

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.

Klein, Christoph, Rachel Sommer, Matthias Augustin, et al.. (2024). Personal, financial and time burden in inherited ichthyoses: A survey of 144 patients in a university‐based setting. Journal of the European Academy of Dermatology and Venereology. 38(9). 1809–1817. 1 indexed citations

Giehl, Kathrin, Svenja Alter, Iliana Tantcheva‐Poór, et al.. (2024). Epidermolytic ichthyosis: Clinical spectrum and burden of disease in a large German cohort. Journal of the European Academy of Dermatology and Venereology. 39(5). 1028–1037. 1 indexed citations

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

Beck‐Woedl, Stefanie, Katalin Komlósi, Matthias Eckenweiler, et al.. (2023). Novel homozygous LAMB1 in‐frame deletion in a pediatric patient with brain anomalies and cerebrovascular event. American Journal of Medical Genetics Part A. 191(10). 2656–2663. 1 indexed citations

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, et al.. (2022). Lipoid proteinosis: Novel ECM1 pathogenic variants and intrafamilial variability in four unrelated Arab families. Pediatric Dermatology. 40(1). 113–119.

Lay, Kenneth, Andreas Zimmer, Kristin Technau‐Hafsi, et al.. (2022). A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings. British Journal of Dermatology. 188(2). 259–267. 7 indexed citations

10.

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

11.

Mintoff, Dillon, et al.. (2021). A novel SPINK5 donor splice site variant in a child with Netherton syndrome. Molecular Genetics & Genomic Medicine. 9(3). e1611–e1611. 2 indexed citations

12.

Komlósi, Katalin, Jürgen Neesen, Paul Dremsek, et al.. (2021). Marfan Syndrome Caused by Disruption of the FBN1 Gene due to A Reciprocal Chromosome Translocation. Genes. 12(11). 1836–1836. 16 indexed citations

13.

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

14.

Marrakchi, Slaheddine, Franz P.W. Radner, Gerd Zolles, et al.. (2019). A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation. Journal of Investigative Dermatology. 139(10). 2154–2163.e5. 16 indexed citations

15.

Emmert, Steffen, Sebastian Iben, Judith Fischer, et al.. (2019). Ein neues Forum für seltene Hauterkrankungen. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 17(6). 672–673.

16.

Weber, Juliane, Lars Frings, Michel Rijntjes, et al.. (2019). Chorea-Acanthocytosis Presenting as Autosomal Recessive Epilepsy in a Family With a Novel VPS13A Mutation. Frontiers in Neurology. 9. 1168–1168. 8 indexed citations

17.

Niculescu, Liviu, Cristel Ruini, Jerome Srour, et al.. (2018). Tazarotene 0.015% Cream as a Potential Topical Agent for Management of Ichthyosis in Dorfman-Chanarin Syndrome. Acta Dermato Venereologica. 99(3). 345–346. 4 indexed citations

18.

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

19.

Has, Cristina & Judith Fischer. (2018). Inherited epidermolysis bullosa: New diagnostics and new clinical phenotypes. Experimental Dermatology. 28(10). 1146–1152. 43 indexed citations

20.

Radner, Franz P.W., Slaheddine Marrakchi, Gwang-Jin Kim, et al.. (2013). Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans. PLoS Genetics. 9(6). 37 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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