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

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

#	Work	Indexed citations
1	French national protocol for the management of congenital ichthyosis 2024 ·Annales de Dermatologie et de Vénéréologie ·(unknown), (unknown), C. Chiavérini, (unknown), Fanny Morice‐Picard, Hélène Texier, I. Dreyfus, (unknown), S. Mallet, Christine Bodemer, Judith Fischer, Nathalie Jonca, J. Mazereeuw‐Hautier	0
2	Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein‐1 mutation: A case report 2024 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), Julia Schreml, Judith Fischer, Alrun Hotz, Christoph M. Hammers, Mark Berneburg, Dennis Niebel, Stephan Schreml	0
3	Personal, financial and time burden in inherited ichthyoses: A survey of 144 patients in a university‐based setting 2024 ·Journal of the European Academy of Dermatology and Venereology ·Christoph Klein, (unknown), Rachel Sommer, Matthias Augustin, Sonja Ständer, Stefan Salzmann, (unknown), (unknown), (unknown), Heiko Traupe, Judith Fischer, S. Steinke, (unknown)	1
4	Epidermolytic ichthyosis: Clinical spectrum and burden of disease in a large German cohort 2024 ·Journal of the European Academy of Dermatology and Venereology ·(unknown), Kathrin Giehl, (unknown), (unknown), (unknown), (unknown), (unknown), Svenja Alter, Iliana Tantcheva‐Poór, Hagen Ott, Judith Fischer, Cristina Has	1
5	Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying ABCA12 Mutations 2024 ·Genes ·Alrun Hotz, Regina Fölster‐Holst, Vinzenz Oji, E. Bourrat, Jorge Frank, Slaheddine Marrakchi, (unknown), (unknown), Katalin Komlósi, Svenja Alter, Judith Fischer	2
6	Novel homozygous LAMB1 in‐frame deletion in a pediatric patient with brain anomalies and cerebrovascular event 2023 ·American Journal of Medical Genetics Part A ·(unknown), Stefanie Beck‐Woedl, (unknown), (unknown), Katalin Komlósi, Matthias Eckenweiler, (unknown), Tobias B. Haack, Judith Fischer, Ingrid Bader, Andreas Tzschach	1
7	Amino Acid Substitution in the Cysteine-Rich Region of the Integrin β4 Subunit Causes Late-Onset Mild Junctional Epidermolysis Bullosa without Extracutaneous Involvement 2023 ·Journal of Investigative Dermatology ·Yao Wang, Alrun Hotz, Philipp R. Esser, Judith Fischer, Cristina Has	1
8	Lipoid proteinosis: Novel ECM1 pathogenic variants and intrafamilial variability in four unrelated Arab families 2022 ·Pediatric Dermatology ·(unknown), Judith Fischer, (unknown), (unknown), (unknown), Svenja Alter, Cristina Has, Ebtesam Abdalla	0
9	A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings 2022 ·British Journal of Dermatology ·(unknown), Kenneth Lay, Andreas Zimmer, Kristin Technau‐Hafsi, Jasmine C. Wong, (unknown), Jan Rohr, Ebtesam Abdalla, Judith Fischer, Bruno Reversade, Cristina Has	7
10	Plantar involvement correlates with obesity, pain and impaired mobility in epidermolysis bullosa simplex: a retrospective cohort study 2021 ·Journal of the European Academy of Dermatology and Venereology ·(unknown), (unknown), Alrun Hotz, Judith Fischer, Leena Bruckner‐Tuderman, Cristina Has	4
11	A novel SPINK5 donor splice site variant in a child with Netherton syndrome 2021 ·Molecular Genetics & Genomic Medicine ·Dillon Mintoff, Isabella Borg, (unknown), (unknown), (unknown), (unknown), Susan Aquilina, Nikolai Paul Pace, Judith Fischer	2
12	Marfan Syndrome Caused by Disruption of the FBN1 Gene due to A Reciprocal Chromosome Translocation 2021 ·Genes ·(unknown), Katalin Komlósi, (unknown), Jürgen Neesen, Paul Dremsek, Thomas Schwarz, Andreas Tzschach, (unknown), Ekkehart Lausch, Judith Fischer, Birgitta Gläser	16
13	High rate of self‐improving phenotypes in children with non‐syndromic congenital ichthyosis: case series from south‐western Germany 2021 ·Journal of the European Academy of Dermatology and Venereology ·(unknown), (unknown), (unknown), Alrun Hotz, (unknown), (unknown), (unknown), Birgit Zirn, Judith Fischer, Cristina Has	6
14	A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation 2019 ·Journal of Investigative Dermatology ·(unknown), Slaheddine Marrakchi, Franz P.W. Radner, Gerd Zolles, (unknown), Thomas O. Eichmann, Cristina Has, (unknown), Nadia Mahfoudh, H. Turki, Andreas Zimmer, Judith Fischer	16
15	Ein neues Forum für seltene Hauterkrankungen 2019 ·JDDG Journal der Deutschen Dermatologischen Gesellschaft ·Steffen Emmert, Sebastian Iben, Judith Fischer, Katalin Komlósi, Regina C. Betz, (unknown), Cristina Has	0
16	Chorea-Acanthocytosis Presenting as Autosomal Recessive Epilepsy in a Family With a Novel VPS13A Mutation 2019 ·Frontiers in Neurology ·Juliane Weber, Lars Frings, Michel Rijntjes, Horst Urbach, Judith Fischer, Cornelius Weiller, Philipp T. Meyer, Stephan Klebe	8
17	Tazarotene 0.015% Cream as a Potential Topical Agent for Management of Ichthyosis in Dorfman-Chanarin Syndrome 2018 ·Acta Dermato Venereologica ·Liviu Niculescu, Cristel Ruini, Jerome Srour, (unknown), Ines Schönbuchner, Tanja von Braunmühl, Thomas Ruzicka, (unknown), Kathrin Giehl, Judith Fischer, Andreas Wollenberg	4
18	Novel VPS33B mutation in a patient with autosomal recessive keratoderma‐ichthyosis‐deafness syndrome 2018 ·American Journal of Medical Genetics Part A ·Svenja Alter, Alrun Hotz, Arne Jahn, Nataliya Di Donato, Evelin Schröck, Martin Smitka, Maja von der Hagen, Jens Schallner, Mario Menschikowski, (unknown), Martin W. Laaß, Judith Fischer, Andreas Tzschach	8
19	Inherited epidermolysis bullosa: New diagnostics and new clinical phenotypes 2018 ·Experimental Dermatology ·Cristina Has, Judith Fischer	43
20	Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans 2013 ·PLoS Genetics ·Franz P.W. Radner, Slaheddine Marrakchi, (unknown), Gwang-Jin Kim, Florence Ribiérre, (unknown), Leïla Abid, M. Leipoldt, H. Turki, W. Schempp, Roland Heilig, Mark Lathrop, Judith Fischer	37

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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