Marina Colombi

7.9k total citations
181 papers, 3.7k citations indexed

About

Marina Colombi is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Marina Colombi has authored 181 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 94 papers in Genetics, 64 papers in Molecular Biology and 36 papers in Cell Biology. Recurrent topics in Marina Colombi's work include Connective tissue disorders research (82 papers), Dermatological and Skeletal Disorders (39 papers) and Cell Adhesion Molecules Research (31 papers). Marina Colombi is often cited by papers focused on Connective tissue disorders research (82 papers), Dermatological and Skeletal Disorders (39 papers) and Cell Adhesion Molecules Research (31 papers). Marina Colombi collaborates with scholars based in Italy, United States and Switzerland. Marina Colombi's co-authors include Marco Ritelli, Nicoletta Zoppi, Sergio Barlati, Nicola Chiarelli, Chiara Dordoni, Rita Gardella, Marco Castori, Marina Venturini, Paola Grammatico and Silvia Morlino and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Marina Colombi

179 papers receiving 3.6k citations

Peers

Countries citing papers authored by Marina Colombi

Since Specialization

Citations

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

Fields of papers citing papers by Marina Colombi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marina Colombi

This figure shows the co-authorship network connecting the top 25 collaborators of Marina Colombi. A scholar is included among the top collaborators of Marina Colombi 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 Colombi. Marina Colombi 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	Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome 2025 ·European Journal of Human Genetics ·(unknown), Shadi Albaba, Glenda Sobey, Jessica Bowen, Deirdre E. Donnelly, Marina Colombi, Marco Ritelli, (unknown), Neeti Ghali, Fleur S. van Dijk, Emma Hobson, (unknown), Esther Kinning, Abhijit Dixit, (unknown), Duncan Baker, Diana Johnson	0
2	Integrative Multi-Omics Approach in Vascular Ehlers–Danlos Syndrome: Further Insights into the Disease Mechanisms by Proteomic Analysis of Patient Dermal Fibroblasts 2024 ·Biomedicines ·Nicola Chiarelli, Valeria Cinquina, Nicoletta Zoppi, (unknown), (unknown), Chiara De Leonibus, (unknown), Marina Venturini, Marina Colombi, Marco Ritelli	1
3	Looking back and beyond the 2017 diagnostic criteria for hypermobile Ehlers‐Danlos syndrome: A retrospective cross‐sectional study from an Italian reference center 2023 ·American Journal of Medical Genetics Part A ·Marco Ritelli, Nicola Chiarelli, Valeria Cinquina, Marika Vezzoli, Marina Venturini, Marina Colombi	8
4	Matrix Metalloproteinases Inhibition by Doxycycline Rescues Extracellular Matrix Organization and Partly Reverts Myofibroblast Differentiation in Hypermobile Ehlers-Danlos Syndrome Dermal Fibroblasts: A Potential Therapeutic Target? 2021 ·Cells ·Nicola Chiarelli, Nicoletta Zoppi, Marina Venturini, Daniele Capitanio, Cecilia Gelfi, Marco Ritelli, Marina Colombi	7
5	TAB2 c.1398dup variant leads to haploinsufficiency and impairs extracellular matrix homeostasis 2019 ·Human Mutation ·Silvia Morlino, Annalucia Carbone, Marco Ritelli, Carmela Fusco, Vincenzo Giambra, (unknown), Angelo Notarangelo, (unknown), Gianluigi Mazzoccoli, Nicoletta Zoppi, Paola Grammatico, (unknown), Marina Colombi, Marco Castori, Lucia Micale	4
6	Absence of Collagen Flowers on Electron Microscopy and Identification of (Likely) Pathogenic COL5A1 Variants in Two Patients 2019 ·Genes ·(unknown), Angela F. Brady, Marina Colombi, David Ferguson, Rebecca C. Pollitt, F. Michael Pope, Marco Ritelli, Sofie Symoens, Neeti Ghali, Fleur S. van Dijk	11
7	Further Defining the Phenotypic Spectrum of B3GAT3 Mutations and Literature Review on Linkeropathy Syndromes 2019 ·Genes ·Marco Ritelli, Valeria Cinquina, Edoardo Giacopuzzi, Marina Venturini, Nicola Chiarelli, Marina Colombi	25
8	Delineation of Ehlers–Danlos syndrome phenotype due to the c.934C>T, p.(Arg312Cys) mutation in COL1A1: Report on a three‐generation family without cardiovascular events, and literature review 2016 ·American Journal of Medical Genetics Part A ·Marina Colombi, Chiara Dordoni, Marina Venturini, Arianna Zanca, Piergiacomo Calzavara‐Pinton, Marco Ritelli	33
9	Further delineation of FKBP14‐related Ehlers–Danlos syndrome: A patient with early vascular complications and non‐progressive kyphoscoliosis, and literature review 2016 ·American Journal of Medical Genetics Part A ·Chiara Dordoni, Claudia Ciaccio, Marina Venturini, Piergiacomo Calzavara‐Pinton, Marco Ritelli, Marina Colombi	12
10	Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers‐Danlos syndrome, hypermobility type 2015 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Marco Castori, Chiara Dordoni, Silvia Morlino, Isabella Sperduti, Marco Ritelli, (unknown), Nicola Chiarelli, Arianna Zanca, Claudia Celletti, Marina Venturini, Filippo Camerota, Piergiacomo Calzavara‐Pinton, Paola Grammatico, Marina Colombi	29
11	Arterial Tortuosity Syndrome: homozygosity for two novel and one recurrent SLC2A10missense mutations in three families with severe cardiopulmonary complications in infancy and a literature review 2014 ·BMC Medical Genetics ·Marco Ritelli, Nicola Chiarelli, Chiara Dordoni, Elena Reffo, Marina Venturini, (unknown), Matteo Della Monica, Gioacchino Scarano, Giuseppe Santoro, Maria Giovanna Russo, Piergiacomo Calzavara‐Pinton, Ornella Milanesi, Marina Colombi	27
12	Late diagnosis of lateral meningocele syndrome in a 55‐year‐old woman with symptoms of joint instability and chronic musculoskeletal pain 2013 ·American Journal of Medical Genetics Part A ·Marco Castori, Silvia Morlino, Marco Ritelli, Francesco Brancati, Carmelilia De Bernardo, Marina Colombi, Paola Grammatico	15
13	Recurring and Generalized Visceroptosis in Ehlers–Danlos Syndrome Hypermobility Type 2013 ·American Journal of Medical Genetics Part A ·Chiara Dordoni, Marco Ritelli, Marina Venturini, Nicola Chiarelli, Lidia Pezzani, (unknown), Piergiacomo Calzavara‐Pinton, Marina Colombi	21
14	Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio 2011 ·The International Journal of Developmental Biology ·Nicola Chiarelli, Marco Ritelli, Nicoletta Zoppi, Anna Benini, Giuseppe Borsani, Sergio Barlati, Marina Colombi	8
15	Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients 2009 ·Orphanet Journal of Rare Diseases ·Bruno Drera, Marco Ritelli, Nicoletta Zoppi, Anita Wischmeijer, Maria Gnoli, Rossella Fattori, Piergiacomo Calzavara‐Pinton, Sergio Barlati, Marina Colombi	18
16	The Italian Registry of Hereditary Epidermolysis Bullosa 2005 ·Redia-Giornale Di Zoologia ·Gianluca Tadini, Lorenzo Gualandri, Marina Colombi	19
17	Collagen type VII (COL7A1) mutation survey and genotype-phenotype correlation in Italian patients affected by dystrophic epidermolysis bullosa 2002 ·Journal of Investigative Dermatology ·(unknown), Rita Gardella, Brunella Posteraro, Gianluca Tadini, Sergio Barlati, John A. McGrath, Marina Colombi, Giovanna Zambruno	1
18	Poor prognosis in non‐villous splenic marginal zone cell lymphoma is associated with p53 mutations 1997 ·British Journal of Haematology ·Luca Baldini, Andrea Guffanti, Lilla Cro, Nicola Stefano Fracchiolla, Marina Colombi, Maddalena Motta, Anna Teresa Maiolo, Antonino Neri	22
19	RT‐PCR detection of fibronectin EDA⁺ and EDB⁺ mRNA isoforms: Molecular markers for hepatocellular carcinoma 1994 ·International Journal of Cancer ·Daniela Tavian, Giuseppina De Petro, Marina Colombi, Nazario Portolani, Stefano Maria Giulini, Rita Gardella, (unknown)	41
20	Quantitative Evaluation of mRNAs by In Situ Hybridization and Image Analysis: Principles and Applications 1993 ·DNA and Cell Biology ·Marina Colombi, Laura Moro, Nicoletta Zoppi, Sergio Barlati	13

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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