Rita Gardella

1.3k total citations
32 papers, 968 citations indexed

About

Rita Gardella is a scholar working on Cell Biology, Genetics and Immunology and Allergy. According to data from OpenAlex, Rita Gardella has authored 32 papers receiving a total of 968 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cell Biology, 15 papers in Genetics and 14 papers in Immunology and Allergy. Recurrent topics in Rita Gardella's work include Cell Adhesion Molecules Research (14 papers), Skin and Cellular Biology Research (10 papers) and Connective tissue disorders research (7 papers). Rita Gardella is often cited by papers focused on Cell Adhesion Molecules Research (14 papers), Skin and Cellular Biology Research (10 papers) and Connective tissue disorders research (7 papers). Rita Gardella collaborates with scholars based in Italy, United States and Belgium. Rita Gardella's co-authors include Sergio Barlati, Marina Colombi, Nicoletta Zoppi, Emilio Sacchetti, Paolo Valsecchi, Chiara Magri, Anne De Paepe, Anne De Paepe, Paul Coucke and Joyce E. Fox and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Rita Gardella

31 papers receiving 942 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Rita Gardella Italy 16 479 373 265 185 143 32 968
Elizabeth E. Gerber United States 9 447 0.9× 280 0.8× 92 0.3× 74 0.4× 221 1.5× 11 847
John R.W. Yates United Kingdom 19 490 1.0× 802 2.2× 171 0.6× 53 0.3× 135 0.9× 30 1.7k
Luitgard M. Neumann Germany 20 1.0k 2.1× 708 1.9× 189 0.7× 73 0.4× 208 1.5× 46 1.7k
Abdulrahman Alswaid Saudi Arabia 16 698 1.5× 509 1.4× 155 0.6× 67 0.4× 70 0.5× 29 1.1k
Delfien Syx Belgium 22 770 1.6× 537 1.4× 319 1.2× 57 0.3× 63 0.4× 51 1.3k
Susana de Vega Japan 18 258 0.5× 717 1.9× 201 0.8× 129 0.7× 51 0.4× 37 1.2k
Ann‐Charlotte Thuresson Sweden 20 485 1.0× 655 1.8× 120 0.5× 101 0.5× 53 0.4× 34 1.1k
Shazia S. Chaudhry United Kingdom 7 345 0.7× 307 0.8× 96 0.4× 104 0.6× 128 0.9× 7 750
Katrien Janssens Belgium 19 514 1.1× 1.0k 2.8× 297 1.1× 64 0.3× 64 0.4× 43 1.8k
Louise Brueton United Kingdom 24 604 1.3× 908 2.4× 72 0.3× 61 0.3× 75 0.5× 34 1.5k

Countries citing papers authored by Rita Gardella

Since Specialization
Citations

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

Fields of papers citing papers by Rita Gardella

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rita Gardella

This figure shows the co-authorship network connecting the top 25 collaborators of Rita Gardella. A scholar is included among the top collaborators of Rita Gardella 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 Rita Gardella. Rita Gardella 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.
Giacopuzzi, Edoardo, Massimo Gennarelli, Alessandra Minelli, et al.. (2017). Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways. PLoS ONE. 12(8). e0182778–e0182778. 15 indexed citations
2.
Magri, Chiara, Emilio Sacchetti, Michele Traversa, et al.. (2010). New Copy Number Variations in Schizophrenia. PLoS ONE. 5(10). e13422–e13422. 70 indexed citations
3.
Iatropoulos, Paraskevas, Rita Gardella, Paolo Valsecchi, et al.. (2009). Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia. Psychiatric Genetics. 19(5). 237–243. 8 indexed citations
4.
Magri, Chiara, Rita Gardella, Paolo Valsecchi, et al.. (2007). Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(6). 745–753. 30 indexed citations
5.
Magri, Chiara, Rita Gardella, Sergio Barlati, et al.. (2006). Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM‐IV‐TR schizophrenia: A pilot case‐control association study in an Italian sample. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(3). 287–293. 37 indexed citations
6.
Drera, Bruno, Andrea Guala, Nicoletta Zoppi, et al.. (2006). Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity syndrome. American Journal of Medical Genetics Part A. 143A(2). 216–218. 24 indexed citations
7.
Zoppi, Nicoletta, Rita Gardella, Anne De Paepe, Sergio Barlati, & Marina Colombi. (2004). Human Fibroblasts with Mutations in COL5A1 and COL3A1 Genes Do Not Organize Collagens and Fibronectin in the Extracellular Matrix, Down-regulate α2β1 Integrin, and Recruit αvβ3 Instead of α5β1 Integrin. Journal of Biological Chemistry. 279(18). 18157–18168. 82 indexed citations
8.
Gardella, Rita, Nicoletta Zoppi, Deodato Assanelli, et al.. (2003). Exclusion of candidate genes in a family with arterial tortuosity syndrome. American Journal of Medical Genetics Part A. 126A(3). 221–228. 32 indexed citations
9.
Gardella, Rita, Brunella Posteraro, Gianluca Tadini, et al.. (2002). Collagen type VII (COL7A1) mutation survey and genotype-phenotype correlation in Italian patients affected by dystrophic epidermolysis bullosa. Journal of Investigative Dermatology. 119(3). 719–719. 1 indexed citations
10.
Gardella, Rita, Daniele Castiglia, Patrizia Posteraro, et al.. (2002). Genotype–Phenotype Correlation in Italian Patients with Dystrophic Epidermolysis Bullosa. Journal of Investigative Dermatology. 119(6). 1456–1462. 54 indexed citations
11.
Gardella, Rita, Lieve Nuytinck, Sergio Barlati, et al.. (2001). Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient. Clinical and Experimental Dermatology. 26(8). 710–713.
12.
Gardella, Rita, Sergio Barlati, Nicoletta Zoppi, Gianluca Tadini, & Marina Colombi. (2000). A -96C?T mutation in the promoter of the collagen type VII gene (COL7A1) abolishing transcription in a patient affected by recessive dystrophic epidermolysis bullosa. Human Mutation. 16(3). 275–275. 10 indexed citations
13.
Tavian, Daniela, Giuseppina De Petro, Marina Colombi, et al.. (1994). RT‐PCR detection of fibronectin EDA+ and EDB+ mRNA isoforms: Molecular markers for hepatocellular carcinoma. International Journal of Cancer. 56(6). 820–825. 41 indexed citations
14.
Gardella, Rita, Marina Colombi, & Sergio Barlati. (1993). Human fibronectin gene (FN1) RFLPs: Mapping and linkage disequilibrium analysis. Human Genetics. 92(6). 639–641. 4 indexed citations
15.
Gardella, Rita, et al.. (1993). The type III‐9 repeat of human fibronectin is encoded by a single exon which is not alternatively spliced.. Cell Biology International. 17(11). 989–992. 2 indexed citations
16.
17.
Gardella, Rita, Marina Colombi, & Sergio Barlati. (1989). A new TaqI RFLP of the human fibronectin (FNI) gene. Nucleic Acids Research. 17(24). 10520–10520. 3 indexed citations
18.
Gardella, Rita, Marina Colombi, & Sergio Barlati. (1988). A common MspI RFLP of the human fibronectin gene (FN1). Nucleic Acids Research. 16(4). 1651–1651. 5 indexed citations
19.
Gardella, Rita, Marina Colombi, & Sergio Barlati. (1988). A TaqI RFLP for the human fibronectin (FN1) gene. Nucleic Acids Research. 16(23). 11388–11388. 3 indexed citations
20.
Colombi, Marina, Rita Gardella, & Sergio Barlati. (1988). A frequent HindIII RFLP of the human fibronectin gene (FN1). Nucleic Acids Research. 16(18). 9074–9074. 7 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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