M. Crippa

643 total citations
37 papers, 396 citations indexed

About

M. Crippa is a scholar working on Molecular Biology, Genetics and Dermatology. According to data from OpenAlex, M. Crippa has authored 37 papers receiving a total of 396 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 18 papers in Genetics and 11 papers in Dermatology. Recurrent topics in M. Crippa's work include Contact Dermatitis and Allergies (11 papers), Genomic variations and chromosomal abnormalities (11 papers) and Occupational exposure and asthma (10 papers). M. Crippa is often cited by papers focused on Contact Dermatitis and Allergies (11 papers), Genomic variations and chromosomal abnormalities (11 papers) and Occupational exposure and asthma (10 papers). M. Crippa collaborates with scholars based in Italy, Israel and United Kingdom. M. Crippa's co-authors include I Sures, Palma Finelli, Lidia Larizza, Chiara Castronovo, Maria Teresa Bonati, Silvia Russo, L Alessio, Emma Sala, Daniela Toniolo and Anna Marozzi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Science of The Total Environment and Scientific Reports.

In The Last Decade

M. Crippa

35 papers receiving 387 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Crippa Italy 12 203 145 72 46 43 37 396
Renata M. J. Hamvas United Kingdom 14 267 1.3× 254 1.8× 34 0.5× 21 0.5× 34 0.8× 26 521
Zhongyou Li United States 13 297 1.5× 150 1.0× 134 1.9× 6 0.1× 12 0.3× 20 569
Angelika Stammler Germany 12 142 0.7× 47 0.3× 47 0.7× 5 0.1× 6 0.1× 16 354
Kenneth J. Eilertsen United States 14 563 2.8× 228 1.6× 339 4.7× 57 1.2× 50 1.2× 21 781
Nathalie Marle France 11 170 0.8× 237 1.6× 53 0.7× 10 0.2× 56 1.3× 23 373
A Rinaldi Italy 12 215 1.1× 191 1.3× 64 0.9× 3 0.1× 128 3.0× 35 476
Thomas Papenbrock United States 10 304 1.5× 89 0.6× 72 1.0× 21 0.5× 140 3.3× 10 495
Ada Rosenmann Israel 16 347 1.7× 252 1.7× 31 0.4× 33 0.7× 91 2.1× 36 650
Theodore F. Thurmon United States 12 111 0.5× 122 0.8× 14 0.2× 4 0.1× 39 0.9× 29 393
Rossana Sapiro Uruguay 13 287 1.4× 308 2.1× 283 3.9× 2 0.0× 86 2.0× 25 780

Countries citing papers authored by M. Crippa

Since Specialization
Citations

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

Fields of papers citing papers by M. Crippa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Crippa

This figure shows the co-authorship network connecting the top 25 collaborators of M. Crippa. A scholar is included among the top collaborators of M. Crippa 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 M. Crippa. M. Crippa 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.
Tannorella, Pierpaola, Luciano Calzari, Mirella Moro, et al.. (2023). Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum. Frontiers in Genetics. 14. 1198821–1198821.
2.
Crippa, M., Maria Teresa Bonati, Luciano Calzari, et al.. (2019). Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes. Frontiers in Genetics. 10. 955–955. 10 indexed citations
3.
4.
Bonati, Maria Teresa, Chiara Castronovo, M. Crippa, et al.. (2019). 9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression. Neurogenetics. 20(3). 145–154. 11 indexed citations
5.
6.
Crippa, M., Roberta Villa, Tiziana de Filippis, et al.. (2018). A balanced reciprocal translocation t(10;15)(q22.3;q26.1) interrupting ACAN gene in a family with proportionate short stature. Journal of Endocrinological Investigation. 41(8). 929–936. 9 indexed citations
7.
Cirello, Valentina, Roberta Rizzo, M. Crippa, et al.. (2015). Fetal cell microchimerism: a protective role in autoimmune thyroid diseases. European Journal of Endocrinology. 173(1). 111–118. 17 indexed citations
8.
Roversi, Gaia, M. Crippa, Daniela Perotti, et al.. (2015). Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors. Scientific Reports. 5(1). 15454–15454. 7 indexed citations
9.
Crippa, M., Chiara Castronovo, Silvia Russo, et al.. (2015). Familial intragenic duplication of ANKRD11 underlying three patients of KBG syndrome. Molecular Cytogenetics. 8(1). 20–20. 11 indexed citations
10.
Castronovo, Chiara, M. Crippa, Silvia Russo, et al.. (2014). Complex de novo chromosomal rearrangement at 15q11–q13 involving an intrachromosomal triplication in a patient with a severe neuropsychological phenotype: Clinical report and review of the literature. American Journal of Medical Genetics Part A. 167(1). 221–230. 12 indexed citations
11.
Castronovo, Chiara, M. Crippa, Daniela Giardino, et al.. (2013). A novel mosaic NSD1 intragenic deletion in a patient with an atypical phenotype. American Journal of Medical Genetics Part A. 161(3). 611–618. 5 indexed citations
12.
Castronovo, Chiara, Emanuele Valtorta, M. Crippa, et al.. (2013). Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes. Molecular Cytogenetics. 6(1). 45–45. 8 indexed citations
13.
Elli, Francesca Marta, Stefano Ghirardello, Claudia Giavoli, et al.. (2012). A new structural rearrangement associated to Wolfram syndrome in a child with a partial phenotype. Gene. 509(1). 168–172. 19 indexed citations
14.
Finelli, Palma, Silvia Maria Sirchia, Maura Masciadri, et al.. (2012). Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype. Molecular Cytogenetics. 5(1). 16–16. 21 indexed citations
15.
Crippa, M., Maria Luisa Gelmi, Emma Sala, et al.. (2004). [Latex allergy in health care workers: frequency, exposure quantification, efficacy of criteria used for job fitness assessment].. PubMed. 95(1). 62–71. 8 indexed citations
16.
Moscato, Gianna, Antonio Dellabianca, Piero Maestrelli, et al.. (2002). Features and severity of occupational asthma upon diagnosis: an Italian multicentric case review. Allergy. 57(3). 236–242. 18 indexed citations
17.
Crippa, M., et al.. (2002). Occupational exposure to pectinase. Allergy. 57(8). 755–755. 2 indexed citations
18.
Crippa, M., et al.. (2001). Occupational dermatitis in a highly industrialized Italian region: the experience of four occupational health departments. The Science of The Total Environment. 270(1-3). 89–96. 7 indexed citations
19.
Crippa, M., et al.. (1997). Allergic reactions due to glove-lubricant-powder in health-care workers. International Archives of Occupational and Environmental Health. 70(6). 399–402. 16 indexed citations
20.
Crippa, M., et al.. (1990). Contact dermatitis from animal proteins in a milker. Contact Dermatitis. 22(4). 240–240. 3 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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