Marina D’Alessio

2.6k total citations
34 papers, 2.1k citations indexed

About

Marina D’Alessio is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Marina D’Alessio has authored 34 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 16 papers in Molecular Biology and 14 papers in Cell Biology. Recurrent topics in Marina D’Alessio's work include Connective tissue disorders research (16 papers), Skin and Cellular Biology Research (14 papers) and Wnt/β-catenin signaling in development and cancer (10 papers). Marina D’Alessio is often cited by papers focused on Connective tissue disorders research (16 papers), Skin and Cellular Biology Research (14 papers) and Wnt/β-catenin signaling in development and cancer (10 papers). Marina D’Alessio collaborates with scholars based in United States, Italy and France. Marina D’Alessio's co-authors include Francesco Ramirez, Jennifer Lynch, Bryan Sykes, Lygia V. Pereira, Giovanna Zambruno, Manfred Frasch, J Bonadio, Michael Solursh, Jean‐Yves Exposito and David W. Hollister and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Marina D’Alessio

34 papers receiving 2.0k citations

Peers

Countries citing papers authored by Marina D’Alessio

Since Specialization

Citations

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

Fields of papers citing papers by Marina D’Alessio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marina D’Alessio. 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 Marina D’Alessio. The network helps show where Marina D’Alessio may publish in the future.

Co-authorship network of co-authors of Marina D’Alessio

This figure shows the co-authorship network connecting the top 25 collaborators of Marina D’Alessio. A scholar is included among the top collaborators of Marina D’Alessio 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 Marina D’Alessio. Marina D’Alessio 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	The 420K LEKTI variant alters LEKTI proteolytic activation and results in protease deregulation: implications for atopic dermatitis 2012 ·Human Molecular Genetics ·Paola Fortugno, Laetitia Furio, Massimo Teson, (unknown), May El Hachem, Giovanna Zambruno, Alain Hovnanian, Marina D’Alessio	67
2	Proteolytic Activation Cascade of the Netherton Syndrome–Defective Protein, LEKTI, in the Epidermis: Implications for Skin Homeostasis 2011 ·Journal of Investigative Dermatology ·Paola Fortugno, Alberto Bresciani, Chantal Paolini, Chiara Pazzagli, May El Hachem, Marina D’Alessio, Giovanna Zambruno	57
3	Immunofluorescence Analysis of Villous Trophoblasts: A Tool for Prenatal Diagnosis of Inherited Epidermolysis Bullosa with Pyloric Atresia 2008 ·Journal of Investigative Dermatology ·Marina D’Alessio, Giovanna Zambruno, A. Charlesworth, J.‐P. Lacour, Guerrino Meneguzzi	20
4	Corneodesmosomal Cadherins Are Preferential Targets of Stratum Corneum Trypsin- and Chymotrypsin-like Hyperactivity in Netherton Syndrome 2006 ·Journal of Investigative Dermatology ·Pascal Descargues, Céline Deraison, Cathérine Prost, Sylvie Fraitag, J. Mazereeuw‐Hautier, Marina D’Alessio, Akemi Ishida‐Yamamoto, Christine Bodemer, Giovanna Zambruno, Alain Hovnanian	143
5	Characterization and expression analysis of the Spink5 gene, the mouse ortholog of the defective gene in Netherton syndrome 2005 ·Genomics ·(unknown), Rosa Maria Roccasecca, Pascal Descargues, (unknown), Elaine R. Levy, Giovanna Zambruno, Marina D’Alessio, Alain Hovnanian	7
6	SPINK5, the Defective Gene in Netherton Syndrome, Encodes Multiple LEKTI Isoforms Derived from Alternative Pre-mRNA Processing 2005 ·Journal of Investigative Dermatology ·(unknown), Chrystelle Bonnart, (unknown), Francesca Cianfarani, (unknown), Giovanna Zambruno, Alain Hovnanian, Marina D’Alessio	31
7	Intracellular degradation of beta4 integrin in lethal junctional epidermolysis bullosa with pyloric atresia 2004 ·British Journal of Dermatology ·(unknown), Naomi De Luca, Gianluca Tadini, Giovanna Zambruno, Marina D’Alessio	18
8	Novel and recurrent mutations in the integrin beta 4 subunit gene causing lethal junctional epidermolysis bullosa with pyloric atresia 2003 ·Experimental Dermatology ·S. Iacovacci, (unknown), Teresa Odorisio, Evelina Silvestri, Hülya Kayserili, Giovanna Zambruno, Pietro Puddu, Marina D’Alessio	18
9	A Homozygous Nonsense Mutation in Type XVII Collagen Gene (COL17A1) Uncovers an Alternatively Spliced mRNA Accounting for an Unusually Mild Form of Non-Herlitz Junctional Epidermolysis Bullosa 2001 ·Journal of Investigative Dermatology ·(unknown), Patrizia Posteraro, Giovanna Zambruno, Daniele Castiglia, Marina D’Alessio, Hendri H. Pas, Chiara Maria Mazzanti, Biagio Didona, Katsushi Owaribe, Guerrino Meneguzzi	32
10	Genomic organization of the human integrin β4 gene 1997 ·Mammalian Genome ·S. Iacovacci, G Laurent, Giovanna Zambruno, Guerrino Meneguzzi, Marina D’Alessio	10
11	A homozygous mutation in the integrin alpha6 gene in junctional epidermolysis bullosa with pyloric atresia. 1997 ·Journal of Clinical Investigation ·(unknown), (unknown), Mari Pinola, Susana Belli, Guerrino Meneguzzi, Marina D’Alessio, Giovanna Zambruno	140
12	Comparative Analysis of Fibrillar and Basement Membrane Collagen Expression in Embryos of the Sea Urchin, Strongylocentrotus purpuratus 1997 ·ZOOLOGICAL SCIENCE ·Hiroaki Suzuki, Rebecca S. Reiter, Marina D’Alessio, Maurizio Di Liberto, Francesco Ramirez, Jean‐Yves Exposito, Roberto Gambino, Michael Solursh	14
13	msh may play a conserved role in dorsoventral patterning of the neuroectoderm and mesoderm 1996 ·Mechanisms of Development ·Marina D’Alessio, Manfred Frasch	111
14	A Common Insertion Mutation in COL7A1 in Two Italian Families With Recessive Dystrophic Epidermolysis Bullosa 1996 ·Journal of Investigative Dermatology ·(unknown), Marina D’Alessio, Mauro Paradisi, (unknown), Chiara Maria Mazzanti, Pietro Puddu, Jouni Uitto	21
15	Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome 1993 ·Human Molecular Genetics ·Lygia V. Pereira, Marina D’Alessio, Francesco Ramirez, Jennifer Lynch, Bryan Sykes, (unknown), Jeffrey Bonadio	267
16	Complete primary structure of a sea urchin type IV collagen alpha chain and analysis of the 5' end of its gene. 1993 ·Journal of Biological Chemistry ·Jean‐Yves Exposito, Marina D’Alessio, (unknown), Francesco Ramirez	32
17	Fibrillar Collagen Genes 1990 ·Annals of the New York Academy of Sciences ·Francesco Ramirez, Sharon Boast, Marina D’Alessio, Brendan Lee, James P. Prince, Mingwan Su, Henrik Vissing, Hidekatsu Yoshioka	10
18	A glycine to serine polymorphism in the C-propeptide of the human type II procollagen 1990 ·Nucleic Acids Research ·Henrik Vissing, Mette Rasmussen, Marina D’Alessio, (unknown), Carl Dobkin, Francesco Ramirez	9
19	Structure and developmental expression of a sea urchin fibrillar collagen gene. 1989 ·Proceedings of the National Academy of Sciences ·Marina D’Alessio, Francesco Ramirez, Hiroaki Suzuki, Michael Solursh, Roberto Gambino	52
20	Complete nucleotide sequence of the region encompassing the first twenty-five exons of the human proα 1(I) collagen gene (COL1A1) 1988 ·Gene ·Marina D’Alessio, Michael P. Bernard, (unknown), Wouter de Wet, Francesco Ramirez	80

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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