Annabella Marozza

969 total citations
11 papers, 287 citations indexed

About

Annabella Marozza is a scholar working on Molecular Biology, Ophthalmology and Oncology. According to data from OpenAlex, Annabella Marozza has authored 11 papers receiving a total of 287 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Ophthalmology and 4 papers in Oncology. Recurrent topics in Annabella Marozza's work include Cancer-related Molecular Pathways (4 papers), Ocular Oncology and Treatments (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Annabella Marozza is often cited by papers focused on Cancer-related Molecular Pathways (4 papers), Ocular Oncology and Treatments (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Annabella Marozza collaborates with scholars based in Italy and Finland. Annabella Marozza's co-authors include Alessandra Renieri, Maria Antonietta Mencarelli, Francesca Ariani, Francesca Mari, Marzia Pollazzon, Theodora Hadjistilianou, Paolo Toti, Sonia De Francesco, Maria Carmela Epistolato and Mariangela Amenduni and has published in prestigious journals such as Journal of Neurology, Cancer Science and European Journal of Human Genetics.

In The Last Decade

Annabella Marozza

10 papers receiving 286 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Annabella Marozza Italy	9	163	108	77	69	39	11	287
Irene Marcos Spain	11	212 1.3×	85 0.8×	53 0.7×	34 0.5×	25 0.6×	21	290
Virginie G. Peter Switzerland	10	198 1.2×	121 1.1×	65 0.8×	22 0.3×	6 0.2×	17	325
Anand Saggar United Kingdom	8	280 1.7×	231 2.1×	22 0.3×	13 0.2×	11 0.3×	15	415
Kyle S. Yau Australia	7	145 0.9×	44 0.4×	33 0.4×	32 0.5×	76 1.9×	10	250
Venkateswara R. Potluri United States	7	141 0.9×	195 1.8×	45 0.6×	58 0.8×	3 0.1×	10	321
Marie‐Louise Bondeson Sweden	10	202 1.2×	108 1.0×	5 0.1×	32 0.5×	20 0.5×	13	305
Tatiana Ferreira de Almeida Brazil	6	182 1.1×	129 1.2×	6 0.1×	27 0.4×	10 0.3×	10	306
Kristin McDonald Gibson United States	8	272 1.7×	118 1.1×	20 0.3×	12 0.2×	86 2.2×	9	424
Kaoru Tsujikawa Japan	11	151 0.9×	29 0.3×	138 1.8×	19 0.3×	10 0.3×	15	352
B. Horsthemke Germany	9	326 2.0×	321 3.0×	18 0.2×	30 0.4×	8 0.2×	13	444

Countries citing papers authored by Annabella Marozza

Since Specialization

Citations

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

Fields of papers citing papers by Annabella Marozza

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annabella Marozza

This figure shows the co-authorship network connecting the top 25 collaborators of Annabella Marozza. A scholar is included among the top collaborators of Annabella Marozza 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 Annabella Marozza. Annabella Marozza is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Ammar, Oumaïma, Francesca Gensini, Annabella Marozza, et al.. (2025). Foetal cardiac rhabdomyoma due to paternal TSC1 Mutation: a case report and literature review. Pathologica. 117(1). 33–38.

Paganini, Irene, Roberta Sestini, Gabriele Lorenzo Capone, et al.. (2017). A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency. Clinical Genetics. 92(6). 664–668. 39 indexed citations

Amitrano, Sara, Annabella Marozza, Theodora Hadjistilianou, et al.. (2015). Next generation sequencing in sporadic retinoblastoma patients reveals somatic mosaicism. European Journal of Human Genetics. 23(11). 1523–1530. 34 indexed citations

Mucciolo, Mafalda, Pamela Magini, Annabella Marozza, et al.. (2013). 9q31.1q31.3 deletion in two patients with similar clinical features: A newly recognized microdeletion syndrome?. American Journal of Medical Genetics Part A. 164(3). 685–690. 7 indexed citations

Epistolato, Maria Carmela, Mariangela Amenduni, Vittoria Disciglio, et al.. (2012). Epigenetic and Copy Number Variation Analysis in Retinoblastoma by MS-MLPA. Pathology & Oncology Research. 18(3). 703–712. 38 indexed citations

Epistolato, Maria Carmela, Vittoria Disciglio, Paola Berchialla, et al.. (2011). p53 Arg72Pro and MDM2 309 SNPs in hereditary retinoblastoma. Journal of Human Genetics. 56(9). 685–686. 10 indexed citations

Uliana, Vera, Salvatore Grosso, M. Cioni, et al.. (2010). 3.2 Mb microdeletion in chromosome 7 bands q22.2–q22.3 associated with overgrowth and delayed bone age. European Journal of Medical Genetics. 53(3). 168–170. 14 indexed citations

Sampieri, Katia, Mariangela Amenduni, Filomena Tiziana Papa, et al.. (2009). Array comparative genomic hybridization in retinoma and retinoblastoma tissues. Cancer Science. 100(3). 465–471. 29 indexed citations

Pollazzon, Marzia, Salvatore Grosso, Filomena Tiziana Papa, et al.. (2009). A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb. European Journal of Medical Genetics. 52(2-3). 131–133. 16 indexed citations

10.

Pollazzon, Marzia, Tiina Suominen, Sini Penttilä, et al.. (2009). The first Italian family with tibial muscular dystrophy caused by a novel titin mutation. Journal of Neurology. 257(4). 575–579. 40 indexed citations

11.

Artuso, Rosangela, Maria Antonietta Mencarelli, Roberta Polli, et al.. (2009). Early-onset seizure variant of Rett syndrome: Definition of the clinical diagnostic criteria. Brain and Development. 32(1). 17–24. 60 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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