Manuela Pigors

587 total citations
17 papers, 305 citations indexed

About

Manuela Pigors is a scholar working on Pathology and Forensic Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Manuela Pigors has authored 17 papers receiving a total of 305 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Pathology and Forensic Medicine, 7 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Manuela Pigors's work include Autoimmune Bullous Skin Diseases (8 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (7 papers) and Skin and Cellular Biology Research (5 papers). Manuela Pigors is often cited by papers focused on Autoimmune Bullous Skin Diseases (8 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (7 papers) and Skin and Cellular Biology Research (5 papers). Manuela Pigors collaborates with scholars based in Germany, United Kingdom and United States. Manuela Pigors's co-authors include Cristina Has, Leena Bruckner‐Tuderman, Jürgen Kohlhase, Dimitra Kiritsi, Ingrid Haußer, Maurizio Podda, David P. Kelsell, Agnes Schwieger‐Briel, Andreas Arnold and Nicola Wagner and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Frontiers in Immunology.

In The Last Decade

Manuela Pigors

16 papers receiving 300 citations

Peers

Manuela Pigors

PFM

GENET

Albane A. Bizet Canada

Ajoy Bardhan United Kingdom

Jeannette Reinartz Germany

Jouni Uitto United States

J. L. Holton United Kingdom

Anna Zielinska‐Kwiatkowska United States

Marie‐Therese Abdou Switzerland

Beverley Anderson United Kingdom

Thomas Magg Germany

Naomi De Luca Italy

Albane A. Bizet Canada

Manuela Pigors

69 ×0.6

279 ×2.6

31 ×0.3

PFM

56 ×0.8

GENET

19 ×0.3

GENET

Citations per year, relative to Manuela Pigors Manuela Pigors (= 1×) peers Albane A. Bizet

Countries citing papers authored by Manuela Pigors

Since Specialization

Citations

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

Fields of papers citing papers by Manuela Pigors

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Pigors

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

All Works

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17 of 17 papers shown

Kasperkiewicz, Michael, Manuela Pigors, Maike M. Holtsche, Stephanie Goletz, & Enno Schmidt. (2025). Anti-p200 pemphigoid. British Journal of Dermatology. 194(1). 10–17.

Pigors, Manuela, Stephanie Goletz, Yao Wang, et al.. (2024). Anti-Laminin β4 IgG Drives Tissue Damage in Anti-p200 Pemphigoid and Shows Interactions with Laminin α3 and γ1/2 Chains. Journal of Investigative Dermatology. 145(4). 821–830.e3. 2 indexed citations

Goletz, Stephanie, Manuela Pigors, Christoph M. Hammers, et al.. (2023). Laminin β4 is a constituent of the cutaneous basement membrane zone and additional autoantigen of anti-p200 pemphigoid. Journal of the American Academy of Dermatology. 90(4). 790–797. 13 indexed citations

Pigors, Manuela, Shirin Emtenani, Katja Bieber, et al.. (2023). Bullous pemphigoid induced by IgG targeting type XVII collagen non‐NC16A / NC15A extracellular domains is driven by Fc gamma receptor‐ and complement‐mediated effector mechanisms and is ameliorated by neonatal Fc receptor blockade. The Journal of Pathology. 262(2). 161–174. 12 indexed citations

Pigors, Manuela, Heiko Steenbock, Katharina Boch, et al.. (2022). Increased Fibrosis in a Mouse Model of Anti-Laminin 332 Mucous Membrane Pemphigoid Remains Unaltered by Inhibition of Aldehyde Dehydrogenase. Frontiers in Immunology. 12. 812627–812627. 7 indexed citations

Emtenani, Shirin, Manuela Pigors, Anika Kasprick, et al.. (2022). Cutaneous kinase activity correlates with treatment outcomes following PI3K delta inhibition in mice with experimental pemphigoid diseases. Frontiers in Immunology. 13. 865241–865241. 6 indexed citations

Holtsche, Maike M., Stephanie Goletz, Nina van Beek, et al.. (2020). Serologic characterization of anti-p200 pemphigoid: Epitope spreading as a common phenomenon. Journal of the American Academy of Dermatology. 84(4). 1155–1157. 15 indexed citations

McDonald, Bryan, Manuela Pigors, David P. Kelsell, et al.. (2018). Noonan syndrome with multiple lentigines and associated craniosynostosis. Clinical and Experimental Dermatology. 43(3). 357–359. 8 indexed citations

Russell, Mark A., Manuela Pigors, Maha E. Houssen, et al.. (2017). A novel de novo activating mutation in STAT3 identified in a patient with common variable immunodeficiency (CVID). Clinical Immunology. 187. 132–136. 21 indexed citations

10.

Pigors, Manuela, Ofer Sarig, Vincent Plagnol, et al.. (2016). Loss-of-Function Mutations in SERPINB8 Linked to Exfoliative Ichthyosis with Impaired Mechanical Stability of Intercellular Adhesions. The American Journal of Human Genetics. 99(2). 430–436. 22 indexed citations

11.

Pigors, Manuela, Agnes Schwieger‐Briel, Raluca Cosgarea, et al.. (2015). Desmoplakin Mutations with Palmoplantar Keratoderma, Woolly Hair and Cardiomyopathy. Acta Dermato Venereologica. 95(3). 337–340. 28 indexed citations

12.

Has, Cristina, Lauretta Levati, Iria Neri, et al.. (2014). FERMT1 promoter mutations in patients with Kindler syndrome. Clinical Genetics. 88(3). 248–254. 12 indexed citations

13.

Schumann, Hauke, Dimitra Kiritsi, Manuela Pigors, et al.. (2013). Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutations. British Journal of Dermatology. 169(1). 115–124. 46 indexed citations

14.

Pigors, Manuela, Dimitra Kiritsi, Agnes Schwieger‐Briel, et al.. (2012). TGM5 Mutations Impact Epidermal Differentiation in Acral Peeling Skin Syndrome. Journal of Investigative Dermatology. 132(10). 2422–2429. 20 indexed citations

15.

Arnold, Andreas, Johannes S. Kern, Peter Itin, et al.. (2012). Acromelanosis Albo-Punctata: A Distinct Inherited Dermatosis with Acral Spotty Dyspigmentation without Systemic Involvement. Dermatology. 224(4). 331–339. 2 indexed citations

16.

Pigors, Manuela, Dimitra Kiritsi, Nicola Wagner, et al.. (2011). Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity. Human Molecular Genetics. 20(9). 1811–1819. 55 indexed citations

17.

Arnold, Andreas, Peter Itin, Manuela Pigors, et al.. (2010). Poikiloderma with neutropenia: a novelC16orf57mutation and clinical diagnostic criteria. British Journal of Dermatology. 163(4). 866–869. 36 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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