Paola Carrera

5.0k total citations
128 papers, 2.3k citations indexed

About

Paola Carrera is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Paola Carrera has authored 128 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 32 papers in Neurology and 28 papers in Genetics. Recurrent topics in Paola Carrera's work include Amyotrophic Lateral Sclerosis Research (16 papers), Neonatal Respiratory Health Research (14 papers) and Genetic Neurodegenerative Diseases (11 papers). Paola Carrera is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (16 papers), Neonatal Respiratory Health Research (14 papers) and Genetic Neurodegenerative Diseases (11 papers). Paola Carrera collaborates with scholars based in Italy, United States and France. Paola Carrera's co-authors include Maurizio Ferrari, Stefania Stenirri, Nica Borgese, Grazia Pietrini, Cecilia Gelfi, Pier Giorgio Righetti, Marco Somaschini, Chiara Di Resta, Silvia Galbiati and Marco Piatti and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Paola Carrera

118 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Paola Carrera Italy	27	936	491	383	377	275	128	2.3k
Marcela V. Karpuj United States	20	1.3k 1.4×	276 0.6×	370 1.0×	254 0.7×	87 0.3×	26	2.9k
George E. Farmer United States	17	957 1.0×	299 0.6×	206 0.5×	199 0.5×	76 0.3×	41	2.2k
Atsushi Watanabe Japan	29	1.1k 1.2×	221 0.5×	438 1.1×	117 0.3×	75 0.3×	137	3.0k
Saeed Bohlega Saudi Arabia	34	1.3k 1.4×	1.2k 2.4×	431 1.1×	224 0.6×	157 0.6×	130	3.8k
Fred Lühder Germany	36	630 0.7×	284 0.6×	495 1.3×	104 0.3×	83 0.3×	93	3.2k
Mary Anna Venneri Italy	30	2.6k 2.8×	168 0.3×	550 1.4×	235 0.6×	120 0.4×	71	5.3k
Alexandre Montpetit Canada	33	1.4k 1.5×	214 0.4×	897 2.3×	215 0.6×	65 0.2×	66	3.5k
J F Bach France	18	795 0.8×	1.1k 2.3×	343 0.9×	148 0.4×	118 0.4×	38	3.0k
Ronen Spiegel Israel	26	884 0.9×	172 0.4×	335 0.9×	110 0.3×	159 0.6×	97	1.9k
Dani Bercovich Israel	28	1.2k 1.2×	200 0.4×	696 1.8×	213 0.6×	46 0.2×	74	2.9k

Countries citing papers authored by Paola Carrera

Since Specialization

Citations

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

Fields of papers citing papers by Paola Carrera

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paola Carrera

This figure shows the co-authorship network connecting the top 25 collaborators of Paola Carrera. A scholar is included among the top collaborators of Paola Carrera 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 Paola Carrera. Paola Carrera 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

Recalcati, Maria Paola, et al.. (2023). APC-Related Phenotypes and Intellectual Disability in 5q Interstitial Deletions: A New Case and Review of the Literature. Genes. 14(7). 1505–1505. 4 indexed citations

Sferruzza, Giacomo, Laura Pozzi, Federica Agosta, et al.. (2023). Unveiling the SOD1-mediated ALS phenotype: insights from a comprehensive meta-analysis. Journal of Neurology. 271(3). 1342–1354. 6 indexed citations

Salvarani, Nicolò, Giovanni Peretto, Silvia Crasto, et al.. (2023). Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells. International Journal of Molecular Sciences. 24(11). 9548–9548. 2 indexed citations

Carrera, Paola, et al.. (2023). Congenital solitary kidney in autosomal dominant polycystic kidney disease: Where do known genes end and the unknown begin?. SHILAP Revista de lepidopterología. 11(11). e7917–e7917. 2 indexed citations

Micaglio, Emanuele, Andrea Ghiroldi, Anna Binda, et al.. (2023). Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights. International Journal of Molecular Sciences. 24(20). 15089–15089.

Brunetto, Emanuela, Alice Bergamini, Greta Grassini, et al.. (2022). Locally Performed HRD Testing for Ovarian Cancer? Yes, We Can!. Cancers. 15(1). 43–43. 8 indexed citations

Agosta, Federica, Edoardo Gioele Spinelli, Nilo Riva, et al.. (2020). Deep Grey Matter and Hippocampal Involvement in Genetic Cases of Frontotemporal Lobar Degeneration (1508). Neurology. 94(15_supplement). 1 indexed citations

Domi, Teuta, Laura Pozzi, Alessandro Romano, et al.. (2020). Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS Cohort. International Journal of Molecular Sciences. 21(9). 3346–3346. 15 indexed citations

Resta, Chiara Di, et al.. (2020). Current scenario of the genetic testing for rare neurological disorders exploiting next generation sequencing. Neural Regeneration Research. 16(3). 475–475. 14 indexed citations

10.

Somaschini, Marco, et al.. (2017). Genetic surfactant dysfunction in newborn infants and children with acute and chronic lung disease. SHILAP Revista de lepidopterología. 1 indexed citations

11.

Cotton, Richard G.H., Arleen D. Auerbach, A. F. Brown, et al.. (2007). A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases. Human Mutation. 28(10). 931–932. 9 indexed citations

12.

Cameron, H. Scott, Marco Somaschini, Paola Carrera, et al.. (2005). A common mutation in the surfactant protein C gene associated with lung disease. The Journal of Pediatrics. 146(3). 370–375. 127 indexed citations

13.

Battistini, Stefania, Fabio Giannini, Giuseppe Greco, et al.. (2005). The” D90A” still an enigma among SOD1 gene mutations. Report of three italian cases.. Use Siena air (University of Siena). 78–78. 1 indexed citations

14.

Cinque, Paola, Arabella Bestetti, Sara Racca, et al.. (2001). Effect of Genotypic Resistance on the Virological Response to Highly Active Antiretroviral Therapy in Cerebrospinal Fluid. AIDS Research and Human Retroviruses. 17(5). 377–383. 36 indexed citations

15.

Angeli, Silvia, Paola Carrera, Massimo Del Sette, et al.. (2001). Very High Prevalence of Right-to-Left Shunt on Transcranial Doppler in an Italian Family with Cerebral Autosomal Dominant Angiopathy with Subcortical Infarcts and Leukoencephalopathy. European Neurology. 46(4). 198–201. 24 indexed citations

16.

Corradini, Paolo, Corrado Tarella, Marco Bregni, et al.. (2000). Allografting for patients with advanced hematological malignancies: non-myeloablative conditioning followed by the reinfusion of lymphocytes engineered with hsv thymidine kinase gene. Blood. 96. 1 indexed citations

17.

Parisi, Vincenzo, Francesco Pierelli, Alessandro Malandrini, et al.. (2000). Visual electrophysiological responses in subjects with cerebral autosomal arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Clinical Neurophysiology. 111(9). 1582–1588. 23 indexed citations

18.

Ferrari, Maurizio, Paola Carrera, & Laura Cremonesi. (1996). Different approaches of molecular scanning of point mutations in genetic diseases. Pure and Applied Chemistry. 68(10). 1913–1918. 4 indexed citations

19.

Lampasona, Vito, Maurizio Ferrari, Ezio Bonifacio, et al.. (1995). HLA-DQ screening for risk assessment of insulin dependent diabetes in northern Italy. Acta Diabetologica. 32(3). 137–142. 3 indexed citations

20.

Gelfi, Cecilia, et al.. (1995). Amplification of 18 dystrophin gene exons in DMD/BMD patients: simultaneous resolution by capillary electrophoresis in sieving liquid polymers.. PubMed. 19(2). 254–8, 260. 25 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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