Manuela Oppo

798 total citations
8 papers, 129 citations indexed

About

Manuela Oppo is a scholar working on Molecular Biology, Genetics and Developmental Biology. According to data from OpenAlex, Manuela Oppo has authored 8 papers receiving a total of 129 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 1 paper in Developmental Biology. Recurrent topics in Manuela Oppo's work include Genomics and Rare Diseases (2 papers), Bone Metabolism and Diseases (2 papers) and RNA regulation and disease (2 papers). Manuela Oppo is often cited by papers focused on Genomics and Rare Diseases (2 papers), Bone Metabolism and Diseases (2 papers) and RNA regulation and disease (2 papers). Manuela Oppo collaborates with scholars based in Italy, United Kingdom and Spain. Manuela Oppo's co-authors include Anna Villa, Andrea Angius, Paolo Vezzoni, Paolo Uva, Cristina Sobacchi, Francesco Cucca, Maria Consuelo Valentini, Laura Crisponi, Luca Zammataro and Rossano Atzeni and has published in prestigious journals such as Journal of Bone and Mineral Research, Bone and Metabolism.

In The Last Decade

Manuela Oppo

8 papers receiving 127 citations

Peers

Manuela Oppo

MB

GENET

ONCOL

SS

RHEUM

Alka V. Ekbote India

Emiel Baten Belgium

Bita Bozorgmehr Iran

Milena Mariani Italy

Céline Poirsier France

Aaron Hardin United States

Stephanie Cox United States

Theresa Mihalic Mosher United States

Charles Van Goethem France

Sebastian Röner Germany

Alka V. Ekbote India

Manuela Oppo

136 ×1.5

MB

102 ×2.0

GENET

17 ×0.8

ONCOL

8 ×0.6

SS

22 ×2.2

RHEUM

Citations per year, relative to Manuela Oppo Manuela Oppo (= 1×) peers Alka V. Ekbote

Countries citing papers authored by Manuela Oppo

Since Specialization

Citations

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

Fields of papers citing papers by Manuela Oppo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Oppo

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

All Works

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8 of 8 papers shown

1.

Angius, Andrea, Paolo Uva, Manuela Oppo, et al.. (2019). Exome sequencing in Crisponi/cold‐induced sweating syndrome–like individuals reveals unpredicted alternative diagnoses. Clinical Genetics. 95(5). 607–614. 9 indexed citations

2.

Uva, Paolo, Manuela Oppo, Ivana Persico, et al.. (2019). Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report. BMC Medical Genetics. 20(1). 16–16. 15 indexed citations

3.

Angius, Andrea, Paolo Uva, Manuela Oppo, et al.. (2019). Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of CREBBP. American Journal of Medical Genetics Part A. 179(4). 634–638. 11 indexed citations

4.

Palagano, Eleonora, Paolo Prontera, Renato Borgatti, et al.. (2018). Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1. Bone. 114. 125–136. 16 indexed citations

5.

Palombo, Flavia, Guido Alberto Gnecchi‐Ruscone, Manuela Oppo, et al.. (2016). A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman. Journal of Human Genetics. 62(2). 259–264. 18 indexed citations

6.

Palagano, Eleonora, S. P. Lucia, Ciro Menale, et al.. (2016). Synonymous Mutations Add a Layer of Complexity in the Diagnosis of Human Osteopetrosis. Journal of Bone and Mineral Research. 32(1). 99–105. 12 indexed citations

7.

Reinier, Frédéric, Magdalena Żołędziewska, D. Hanna, et al.. (2015). Mandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome in the context of inherited lipodystrophies. Metabolism. 64(11). 1530–1540. 22 indexed citations

8.

Pangrazio, Alessandra, Manuela Oppo, Maria Consuelo Valentini, et al.. (2013). Exome sequencing identifies CTSK mutations in patients originally diagnosed as intermediate osteopetrosis. Bone. 59. 122–126. 26 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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