Olga Calabrese

1.1k total citations
29 papers, 605 citations indexed

About

Olga Calabrese is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Olga Calabrese has authored 29 papers receiving a total of 605 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 11 papers in Molecular Biology and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Olga Calabrese's work include Prenatal Screening and Diagnostics (7 papers), Genetic Neurodegenerative Diseases (7 papers) and Mitochondrial Function and Pathology (5 papers). Olga Calabrese is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genetic Neurodegenerative Diseases (7 papers) and Mitochondrial Function and Pathology (5 papers). Olga Calabrese collaborates with scholars based in Italy, United Kingdom and United States. Olga Calabrese's co-authors include Imma Castaldo, Alessandro Filla, Giuseppe De Michele, Elisa Calzolari, Luigi Di Maio, G Campanella, Sergio Cocozza, Marco Fichera, Stefania Bigoni and Mariangela Lo Giudice and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and CHEST Journal.

In The Last Decade

Olga Calabrese

25 papers receiving 592 citations

Peers

Olga Calabrese

CMN

NEURO

GENET

PPCH

Tena Varvil United States

Laurence E. Walsh United States

Yoshio Morimatsu Japan

Eugènia Monrós Spain

Hanna Mierzewska Poland

María A. Ramos‐Arroyo Spain

Anne‐Sophie Lia France

Dong-Hui Chen United States

H. Grehl Germany

Simon Holden United Kingdom

Tena Varvil United States

Olga Calabrese

198 ×0.5

217 ×0.6

CMN

85 ×0.6

NEURO

174 ×1.6

GENET

43 ×0.7

PPCH

Citations per year, relative to Olga Calabrese Olga Calabrese (= 1×) peers Tena Varvil

Countries citing papers authored by Olga Calabrese

Since Specialization

Citations

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

Fields of papers citing papers by Olga Calabrese

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olga Calabrese

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

Lugli, Licia, Cecilia Rossi, Alberto Berardi, et al.. (2024). Prenatal multidisciplinary counseling for fetal congenital anomalies: A narrative review. International Journal of Gynecology & Obstetrics. 169(2). 498–510. 2 indexed citations

Paganelli, Alessia, Elena Rossi, Olga Calabrese, et al.. (2024). Unveiling new entities in the PAPA spectrum. Italian Journal of Dermatology and Venereology. 159(6). 677–678. 1 indexed citations

Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2022). Atypical, Composite, or Blended Phenotypes: How Different Molecular Mechanisms Could Associate in Double-Diagnosed Patients. Genes. 13(7). 1275–1275. 17 indexed citations

Astolfi, Gianni, Stefania Bigoni, Anna Baroncini, et al.. (2022). Prenatal genetic counselling: issues and perspectives for pre-conceptional health care in Emilia Romagna (Northern Italy). SHILAP Revista de lepidopterología. 11(2).

Baroncini, Anna, Olga Calabrese, Marco Colotto, et al.. (2022). Knowledge and attitude of general pratictioners towards direct-to-consumer genomic tests: a survey conducted in Italy. SHILAP Revista de lepidopterología. 12(4). 2 indexed citations

Lugli, Licia, Cecilia Rossi, Pier Luca Ceccarelli, et al.. (2022). Townes-Brocks syndrome with craniosynostosis in two siblings. European Journal of Medical Genetics. 65(12). 104642–104642. 3 indexed citations

Lugli, Licia, Emma Bertucci, Laura Lucaccioni, et al.. (2021). Homozygous n.64C>T mutation in mitochondrial RNA-processing endoribonuclease gene causes cartilage hair hypoplasia syndrome in two siblings. European Journal of Medical Genetics. 64(2). 104136–104136.

Mengoli, Maria Cecilia, Olga Calabrese, Giovanni Della Casa, et al.. (2019). Cannonball-Like Lung Nodules in a Patient With a Colorectal Tumor. CHEST Journal. 156(4). e85–e89. 2 indexed citations

Ritelli, Marco, Andrea Zini, Marina Colombi, et al.. (2019). Novel pathogenic TGFBR1 and SMAD3 variants identified after cerebrovascular events in adult patients with Loeys-dietz syndrome. European Journal of Medical Genetics. 62(10). 103727–103727. 7 indexed citations

10.

Athanasakis, Emmanouil, Sophie Dahoun, Ambroise Wonkam, et al.. (2013). Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations. European Journal of Medical Genetics. 56(8). 404–410. 7 indexed citations

11.

Diggle, Christine P., Ian Carr, Emanuel Zitt, et al.. (2010). Common and recurrent HPGD mutations in Caucasian individuals with primary hypertrophic osteoarthropathy. Lara D. Veeken. 49(6). 1056–1062. 40 indexed citations

12.

Brussino, Alessandro, Giovanna Vaula, Cinzia Cagnoli, et al.. (2009). A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy. Journal of Neurology Neurosurgery & Psychiatry. 80(2). 237–240. 32 indexed citations

13.

Filla, Alessandro, Caterina Mariotti, Giuseppe Caruso, et al.. (2000). Relative Frequencies of CAG Expansions in Spinocerebellar Ataxia and Dentatorubropallidoluysian Atrophy in 116 Italian Families. European Neurology. 44(1). 31–36. 49 indexed citations

14.

Gualandi, Francesca, Maria Carla Pittalis, Olga Calabrese, et al.. (2000). Mole maker phenotype: possible narrowing of the candidate region. European Journal of Human Genetics. 8(8). 641–644. 44 indexed citations

15.

Filla, Alessandro, Giuseppe De Michele, Lucio Santoro, et al.. (1999). Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families. Journal of Neurology. 246(6). 467–471. 48 indexed citations

16.

Trojano, Luigi, Laura Chiacchio, Dario Grossi, et al.. (1998). Determinants of cognitive disorders in Autosomal Dominant Cerebellar Ataxia type 1. Journal of the Neurological Sciences. 157(2). 162–167. 14 indexed citations

17.

Giovannone, Barbara, G. Sabbadini, Luigi Di Maio, et al.. (1997). Analysis of (CAG)n size heterogeneity in somatic and sperm cell DNA from intermediate and expanded Huntington disease gene carriers. Human Mutation. 10(6). 458–464. 25 indexed citations

18.

Vesce, Fortunato, et al.. (1997). Increased Incidence of Preeclampsia in Pregnancies Complicated by Fetal Malformation. Gynecologic and Obstetric Investigation. 44(2). 107–111. 19 indexed citations

19.

Vesce, Fortunato, et al.. (1996). Raised Level of Amniotic Endothelin in Pregnancies with Fetal Aneuploidy. Fetal Diagnosis and Therapy. 11(2). 94–98. 6 indexed citations

20.

Telenius, H., E. Almqvist, B Kremer, et al.. (1995). Somatic mosaicism in sperm is associated with intergenerational (CAG)_n changes in Huntington disease. Human Molecular Genetics. 4(2). 189–195. 67 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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