Francesca Pasutto

5.1k total citations
41 papers, 1.3k citations indexed

About

Francesca Pasutto is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Francesca Pasutto has authored 41 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 23 papers in Ophthalmology and 9 papers in Genetics. Recurrent topics in Francesca Pasutto's work include Glaucoma and retinal disorders (22 papers), Retinal Diseases and Treatments (10 papers) and Microbial metabolism and enzyme function (8 papers). Francesca Pasutto is often cited by papers focused on Glaucoma and retinal disorders (22 papers), Retinal Diseases and Treatments (10 papers) and Microbial metabolism and enzyme function (8 papers). Francesca Pasutto collaborates with scholars based in Germany, United States and Italy. Francesca Pasutto's co-authors include André Reis, Friedrich E. Kruse, Matthias Zenkel, Ursula Schlötzer‐Schrehardt, Christian Y. Mardin, Bernhard H. F. Weber, Nicole Weisschuh, E. Gramer, Bernd Rautenstrauß and Heinrich Sticht and has published in prestigious journals such as Genes & Development, International Journal of Molecular Sciences and Ophthalmology.

In The Last Decade

Francesca Pasutto

40 papers receiving 1.3k citations

Peers

Francesca Pasutto
Allan R. Shepard United States
Jacoline B. ten Brink Netherlands
J. Cameron Millar United States
Nicole Weisschuh Germany
Panagiotis I. Sergouniotis United Kingdom
Bernard Arnaud France
Deborah Wallace Ireland
Neil D. Ebenezer United Kingdom
Ola Sandgren Sweden
Bruce A. Pfeffer United States
Allan R. Shepard United States
Francesca Pasutto
Citations per year, relative to Francesca Pasutto Francesca Pasutto (= 1×) peers Allan R. Shepard

Countries citing papers authored by Francesca Pasutto

Since Specialization
Citations

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

Fields of papers citing papers by Francesca Pasutto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Pasutto

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

All Works

20 of 20 papers shown
1.
Hirbo, Jibril, Francesca Pasutto, Eric R. Gamazon, et al.. (2023). Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome. BMC Genomics. 24(1). 75–75. 6 indexed citations
2.
Burdon, Kathryn P., John D. Hulleman, Francesca Pasutto, et al.. (2022). Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panel. Human Mutation. 43(12). 2170–2186. 11 indexed citations
3.
Zenkel, Matthias, Ursula Hoja, Andreas Gießl, et al.. (2022). Dysregulated Retinoic Acid Signaling in the Pathogenesis of Pseudoexfoliation Syndrome. International Journal of Molecular Sciences. 23(11). 5977–5977. 11 indexed citations
4.
Zenkel, Matthias, Ursula Schlötzer‐Schrehardt, Daniel Berner, et al.. (2017). Dysregulated expression of POMP and TMEM136 may contribute to impaired proteasome function and endothelial dysfunction in eyes with pseudoexfoliation syndrome/glaucoma. Investigative Ophthalmology & Visual Science. 58(8). 4902–4902. 1 indexed citations
5.
Berner, Daniel, Matthias Zenkel, Francesca Pasutto, et al.. (2017). Alternative splicing and nonsense-mediated mRNA decay contribute to regulation of LOXL1 expression in response to cellular stress in pseudoexfoliation. Investigative Ophthalmology & Visual Science. 58(8). 4909–4909. 1 indexed citations
6.
Zenkel, Matthias, Francesca Pasutto, Antonio Bergua, et al.. (2016). Expression of CACNA1A in Patients with Pseudoexfoliation Syndrome. Investigative Ophthalmology & Visual Science. 57(12). 5997–5997. 1 indexed citations
7.
Schlötzer‐Schrehardt, Ursula, Matthias Zenkel, Ursula Hoja, et al.. (2016). LOXL1 intronic variants influence LOXL1 expression through differential transcription factor binding in pseudoexfoliation syndrome/glaucoma. Investigative Ophthalmology & Visual Science. 57(12). 789–789. 1 indexed citations
8.
Mauri, Lucia, Steffen Uebe, Heinrich Sticht, et al.. (2016). Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma. Orphanet Journal of Rare Diseases. 11(1). 108–108. 28 indexed citations
9.
Pasutto, Francesca, Lucia Mauri, Bernt Popp, et al.. (2015). Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld–Rieger syndrome and glaucoma. Gene. 568(1). 76–80. 7 indexed citations
10.
Zenkel, Matthias, et al.. (2013). Candidate regulatory lysyl oxidase-like 1 (LOXL1) variants in pseudoexfoliation syndrome/glaucoma are associated with differential LOXL1 expression. Investigative Ophthalmology & Visual Science. 54(15). 6243–6243. 1 indexed citations
11.
Ng, Wy Ching, Francesca Pasutto, Geoffrey Watson, et al.. (2012). A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family. Clinical Genetics. 83(2). 162–168. 13 indexed citations
12.
Krumbiegel, Mandy, Francesca Pasutto, Ursula Schlötzer‐Schrehardt, et al.. (2010). Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome. European Journal of Human Genetics. 19(2). 186–193. 45 indexed citations
13.
Pasutto, Francesca & André Reis. (2010). Response to Liu et al.. The American Journal of Human Genetics. 86(3). 500–500.
14.
Krumbiegel, Mandy, Francesca Pasutto, Christian Y. Mardin, et al.. (2010). Apolipoprotein E Genotypes in Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma. Journal of Glaucoma. 19(8). 561–565. 22 indexed citations
15.
Wolf, Christiane, E. Gramer, Bertram Müller‐Myhsok, et al.. (2010). Lysyl Oxidase-like 1 Gene Polymorphisms in German Patients With Normal Tension Glaucoma, Pigmentary Glaucoma and Exfoliation Glaucoma. Journal of Glaucoma. 19(2). 136–141. 27 indexed citations
16.
Wolf, Christiane, E. Gramer, Bertram Müller‐Myhsok, et al.. (2009). Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study. BMC Medical Genetics. 10(1). 91–91. 42 indexed citations
17.
Segel, Reeval, Ephrat Levy‐Lahad, Francesca Pasutto, et al.. (2009). Pulmonary hypoplasia–diaphragmatic hernia–anophthalmia–cardiac defect (PDAC) syndrome due to STRA6 mutations—What are the minimal criteria?. American Journal of Medical Genetics Part A. 149A(11). 2457–2463. 31 indexed citations
18.
Pasutto, Francesca, Tomoya Matsumoto, Christian Y. Mardin, et al.. (2009). Heterozygous NTF4 Mutations Impairing Neurotrophin-4 Signaling in Patients with Primary Open-Angle Glaucoma. The American Journal of Human Genetics. 85(4). 447–456. 104 indexed citations
19.
Schlötzer‐Schrehardt, Ursula, Francesca Pasutto, Pascal Sommer, et al.. (2008). Genotype-Correlated Expression of Lysyl Oxidase-Like 1 in Ocular Tissues of Patients with Pseudoexfoliation Syndrome/Glaucoma and Normal Patients. American Journal Of Pathology. 173(6). 1724–1735. 101 indexed citations
20.
Bergstrom, Rebecca A., Francesca Pasutto, Philipp Wabnitz, et al.. (2004). Vestibular defects in head-tilt mice result from mutations inNox3, encoding an NADPH oxidase. Genes & Development. 18(5). 486–491. 213 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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