Jouni Uitto

901 total citations
14 papers, 692 citations indexed

About

Jouni Uitto is a scholar working on Cell Biology, Immunology and Allergy and Pathology and Forensic Medicine. According to data from OpenAlex, Jouni Uitto has authored 14 papers receiving a total of 692 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cell Biology, 9 papers in Immunology and Allergy and 7 papers in Pathology and Forensic Medicine. Recurrent topics in Jouni Uitto's work include Skin and Cellular Biology Research (12 papers), Cell Adhesion Molecules Research (9 papers) and Autoimmune Bullous Skin Diseases (6 papers). Jouni Uitto is often cited by papers focused on Skin and Cellular Biology Research (12 papers), Cell Adhesion Molecules Research (9 papers) and Autoimmune Bullous Skin Diseases (6 papers). Jouni Uitto collaborates with scholars based in United States, India and Austria. Jouni Uitto's co-authors include Angela M. Christiano, Angela M. Christiano, Alain Mauviel, Franziska Ringpfeil, Leena Pulkkinen, John A. McGrath, Aoi Nakano, Jo‐David Fine, Patricia Rousselle and Reza F. Ghohestani and has published in prestigious journals such as Oncogene, FEBS Letters and The American Journal of Human Genetics.

In The Last Decade

Jouni Uitto

14 papers receiving 675 citations

Peers

Jouni Uitto
Leena Pulkkinen United States
J Ryynänen United States
Biljana Gatalica United States
Ngon T. Nguyen United States
Tod A. Brown United States
Jouni Uitto United States
Laurence Cadalbert United Kingdom
K Heeres Netherlands
Y Sarret France
Leena Pulkkinen United States
Jouni Uitto
Citations per year, relative to Jouni Uitto Jouni Uitto (= 1×) peers Leena Pulkkinen

Countries citing papers authored by Jouni Uitto

Since Specialization
Citations

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

Fields of papers citing papers by Jouni Uitto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jouni Uitto

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

All Works

14 of 14 papers shown
1.
Uitto, Jouni. (2009). Progress in Heritable Skin Diseases: Translational Implications of Mutation Analysis and Prospects of Molecular Therapies*. Acta Dermato Venereologica. 89(3). 228–235. 20 indexed citations
2.
Ghohestani, Reza F., Kehua Li, Patricia Rousselle, & Jouni Uitto. (2001). Molecular organization of the cutaneous basement membrane zone. Clinics in Dermatology. 19(5). 551–562. 42 indexed citations
3.
Ringpfeil, Franziska, Aoi Nakano, Jouni Uitto, & Leena Pulkkinen. (2001). Compound Heterozygosity for a Recurrent 16.5-kb Alu-Mediated Deletion Mutation and Single-Base-Pair Substitutions in the ABCC6 Gene Results in Pseudoxanthoma Elasticum. The American Journal of Human Genetics. 68(3). 642–652. 66 indexed citations
4.
Ringpfeil, Franziska, Mark Lebwohl, & Jouni Uitto. (2000). Mutations in the MRP6 Gene Cause Pseudoxanthoma Elasticum.. Journal of Investigative Dermatology. 115(2). 332–332. 3 indexed citations
5.
Kon, Atsushi, Laurence Vindevoghel, David J. Kouba, et al.. (1999). Cooperation between SMAD and NF-κB in growth factor regulated type VII collagen gene expression. Oncogene. 18(10). 1837–1844. 58 indexed citations
6.
Wallerstein, Robert, Maria C. Garzón, Tod A. Brown, et al.. (1998). Novel ITGB4 Mutations in Lethal and Nonlethal Variants of Epidermolysis Bullosa with Pyloric Atresia: Missense versus Nonsense. The American Journal of Human Genetics. 63(5). 1376–1387. 92 indexed citations
7.
Takizawa, Yasuko, Hiroshi Shimizu, John A. McGrath, et al.. (1998). Novel Mutations in the LAMB3 Gene Shared by Two Japanese Unrelated Families with Herlitz Junctional Epidermolysis Bullosa, and Their Application for Prenatal Testing. Journal of Investigative Dermatology. 110(2). 174–178. 18 indexed citations
8.
Christiano, Angela M., Jo‐David Fine, & Jouni Uitto. (1997). Genetic Basis of Dominantly Inherited Transient Bullous Dermolysis of the Newborn: A Splice Site Mutation in the Type VII Collagen Gene. Journal of Investigative Dermatology. 109(6). 811–814. 44 indexed citations
9.
Mellerio, Jemima E., M. G. S. Dunnill, G H S Ashton, et al.. (1997). Recurrent Mutations in the Type VII Collagen Gene (COL7A1) in Patients with Recessive Dystrophic Epidermolysis Bullosa. Journal of Investigative Dermatology. 109(2). 246–249. 44 indexed citations
10.
McGrath, John A., Thomas N. Darling, Biljana Gatalica, et al.. (1996). A Homozygous Deletion Mutation in the Gene Encoding the 180-kDa Bullous Pemphigoid Antigen (BPAG2) in a Family with Generalized Atrophic Benign Epidermolysis Bullosa. Journal of Investigative Dermatology. 106(4). 771–774. 52 indexed citations
11.
Christiano, Angela M. & Jouni Uitto. (1996). Molecular complexity of the cutaneous basement membrane zone. Experimental Dermatology. 5(1). 1–11. 163 indexed citations
13.
McGrath, John A., James R. McMillan, M. G. S. Dunnill, et al.. (1995). Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: Implications for prenatal diagnosis in one family. Prenatal Diagnosis. 15(7). 647–654. 23 indexed citations
14.
Hickok, Noreen J. & Jouni Uitto. (1992). Regulation of Ornithine Decarboxylase Gene Expression, Polyamine Levels, and DNA Synthetic Rates by All-Trans-Retinoic Acid in Cultured Human Keratinocytes. Journal of Investigative Dermatology. 98(3). 327–332. 8 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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