Lorena Mosca

1.6k total citations
27 papers, 477 citations indexed

About

Lorena Mosca is a scholar working on Neurology, Genetics and Neurology. According to data from OpenAlex, Lorena Mosca has authored 27 papers receiving a total of 477 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Neurology, 12 papers in Genetics and 6 papers in Neurology. Recurrent topics in Lorena Mosca's work include Amyotrophic Lateral Sclerosis Research (15 papers), Neurogenetic and Muscular Disorders Research (12 papers) and Parkinson's Disease Mechanisms and Treatments (8 papers). Lorena Mosca is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (15 papers), Neurogenetic and Muscular Disorders Research (12 papers) and Parkinson's Disease Mechanisms and Treatments (8 papers). Lorena Mosca collaborates with scholars based in Italy, United Kingdom and United States. Lorena Mosca's co-authors include Christian Lunetta, Silvana Penco, Alessandro Marocchi, Claudia Tarlarini, Fabio Coppedè, Andrea Stoccoro, Lucia Migliore, Francesca Avemaria, Massimo Corbo and Eleonora Maestri and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Lorena Mosca

27 papers receiving 473 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lorena Mosca Italy 14 310 180 171 108 58 27 477
J Rafałowska Poland 12 188 0.6× 137 0.8× 101 0.6× 82 0.8× 51 0.9× 44 390
T. Sprovieri Italy 14 225 0.7× 197 1.1× 145 0.8× 124 1.1× 19 0.3× 39 533
Kon‐Ping Lin Taiwan 13 263 0.8× 163 0.9× 96 0.6× 91 0.8× 41 0.7× 31 480
Dorota Dziewulska Poland 12 329 1.1× 142 0.8× 66 0.4× 189 1.8× 63 1.1× 62 607
C Ungaro Italy 12 207 0.7× 138 0.8× 126 0.7× 94 0.9× 19 0.3× 29 367
Afagh Alavi Iran 13 134 0.4× 236 1.3× 125 0.7× 146 1.4× 36 0.6× 60 535
Nicolas Dupré France 12 199 0.6× 150 0.8× 89 0.5× 82 0.8× 32 0.6× 23 429
Emily P. McCann Australia 12 373 1.2× 213 1.2× 156 0.9× 89 0.8× 57 1.0× 18 508
André Bento‐Abreu Belgium 12 372 1.2× 383 2.1× 231 1.4× 144 1.3× 118 2.0× 18 833
Yuriy Shapovalov United States 6 300 1.0× 254 1.4× 121 0.7× 163 1.5× 84 1.4× 6 616

Countries citing papers authored by Lorena Mosca

Since Specialization
Citations

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

Fields of papers citing papers by Lorena Mosca

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lorena Mosca

This figure shows the co-authorship network connecting the top 25 collaborators of Lorena Mosca. A scholar is included among the top collaborators of Lorena Mosca 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 Lorena Mosca. Lorena Mosca 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.
Ćorić, Marijana, Laura Calabresi, Chiara Pavanello, et al.. (2022). Two novel variants in the lecithin:cholesterol acyltransferase gene resulted in classic LCAT deficiency. SHILAP Revista de lepidopterología. 49. 28–31. 1 indexed citations
2.
Conti, Elisa, Gessica Sala, Susanna Diamanti, et al.. (2021). Serum naturally occurring anti-TDP-43 auto-antibodies are increased in amyotrophic lateral sclerosis. Scientific Reports. 11(1). 1978–1978. 15 indexed citations
3.
Stoccoro, Andrea, Adam R. Smith, Lorena Mosca, et al.. (2020). Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis. Clinical Epigenetics. 12(1). 137–137. 37 indexed citations
4.
Lunetta, Christian, Andrea Lizio, Francesca Gerardi, et al.. (2020). Urinary neopterin, a new marker of the neuroinflammatory status in amyotrophic lateral sclerosis. Journal of Neurology. 267(12). 3609–3616. 13 indexed citations
5.
Tondo, Giacomo, Leonardo Iaccarino, Chiara Cerami, et al.. (2020). 11C‐PK11195 PET–based molecular study of microglia activation in SOD1 amyotrophic lateral sclerosis. Annals of Clinical and Translational Neurology. 7(9). 1513–1523. 35 indexed citations
6.
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
7.
Pavanello, Chiara, Carlo Pirazzi, Joakim Sandstedt, et al.. (2019). Individuals with familial hypercholesterolemia and cardiovascular events have higher circulating Lp(a) levels. Journal of clinical lipidology. 13(5). 778–787.e6. 21 indexed citations
8.
Talotta, Rossella, Lorena Mosca, Antonio Brucato, et al.. (2019). AB1106 PREVALENCE AND EPIDEMIOLOGY OF FAMILIAL MEDITERRANEAN FEVER AND TUMOR NECROSIS FACTORRECEPTOR-ASSOCIATED PERIODIC SYNDROME: RESULTS FROM AN ITALIAN CENTER. Annals of the Rheumatic Diseases. 78. 2016–2017. 1 indexed citations
9.
Stoccoro, Andrea, Lorena Mosca, Vittoria Carnicelli, et al.. (2018). Mitochondrial DNA Copy Number and D-Loop Region Methylation in Carriers of Amyotrophic Lateral Sclerosis Gene Mutations. Epigenomics. 10(11). 1431–1443. 61 indexed citations
10.
Lattante, Serena, Maria Grazia Pomponi, Amelia Conte, et al.. (2017). ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis. Neurobiology of Aging. 64. 157.e1–157.e5. 31 indexed citations
11.
Mosca, Lorena, Francesca Rivieri, Raffaella Tanel, et al.. (2014). Mutational Screening of NOTCH3 Gene Reveals Two Novel Mutations: Complexity of CADASIL Diagnosis. Journal of Molecular Neuroscience. 54(4). 723–729. 2 indexed citations
12.
Moccia, Marcello, Lorena Mosca, Roberto Erro, et al.. (2014). Hypomorphic NOTCH3 mutation in an Italian family with CADASIL features. Neurobiology of Aging. 36(1). 547.e5–547.e11. 28 indexed citations
13.
Lunetta, Christian, Valeria Sansone, Silvana Penco, et al.. (2014). Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype. European Journal of Neurology. 21(4). 594–598. 10 indexed citations
14.
Mosca, Lorena, Silvana Pileggi, Francesca Avemaria, et al.. (2012). De Novo MGC4607 Gene Heterozygous Missense Variants in a Child with Multiple Cerebral Cavernous Malformations. Journal of Molecular Neuroscience. 47(3). 475–480. 6 indexed citations
15.
16.
Ricci, Claudia, Silvana Penco, Lorena Mosca, et al.. (2011). No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population. Neurobiology of Aging. 33(1). 208.e7–208.e8. 5 indexed citations
17.
Avemaria, Francesca, Christian Lunetta, Claudia Tarlarini, et al.. (2011). Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression. Amyotrophic Lateral Sclerosis. 12(3). 228–230. 20 indexed citations
18.
Mosca, Lorena, Silvana Penco, Maria Cristina Patrosso, et al.. (2011). Genetic variability of the fructosamine 3-kinase gene in diabetic patients. Clinical Chemistry and Laboratory Medicine (CCLM). 49(5). 803–808. 11 indexed citations
19.
Mosca, Lorena, Raffaella Marazzi, Alfonso Ciccone, et al.. (2011). NOTCH3 gene mutations in subjects clinically suspected of CADASIL. Journal of the Neurological Sciences. 307(1-2). 144–148. 10 indexed citations
20.
Penco, Silvana, Christian Lunetta, Lorena Mosca, et al.. (2010). Phenotypic Heterogeneity in a SOD1 G93D Italian ALS Family: An Example of Human Model to Study a Complex Disease. Journal of Molecular Neuroscience. 44(1). 25–30. 17 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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