Elisa Contini

672 total citations
17 papers, 280 citations indexed

About

Elisa Contini is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Elisa Contini has authored 17 papers receiving a total of 280 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Surgery. Recurrent topics in Elisa Contini's work include Forensic and Genetic Research (3 papers), Acute Myeloid Leukemia Research (2 papers) and Molecular Biology Techniques and Applications (2 papers). Elisa Contini is often cited by papers focused on Forensic and Genetic Research (3 papers), Acute Myeloid Leukemia Research (2 papers) and Molecular Biology Techniques and Applications (2 papers). Elisa Contini collaborates with scholars based in Italy, China and United Kingdom. Elisa Contini's co-authors include Francesca Torricelli, Matteo Benelli, Mario Maggi, Laura Papi, Roberta Sestini, Irene Paganini, Gabriele Lorenzo Capone, N. A. Hatch, Giovanni M. Colpi and Antoni Riera‐Escamilla and has published in prestigious journals such as Blood, PLoS ONE and Monthly Notices of the Royal Astronomical Society.

In The Last Decade

Elisa Contini

17 papers receiving 276 citations

Peers

Elisa Contini

GENET

CCM

GENET

Özge Özalp Yüreğir Türkiye

Ana Blanco Spain

Emmanouil Manolakos Greece

Hiroto Ueda Japan

Igor Nazarov Russia

Mari Miiluniemi Finland

Hadia Hijazi Saudi Arabia

Alper Gezdirici Türkiye

Jenifer P. Suntharalingham United Kingdom

Silvia Genovese Italy

Özge Özalp Yüreğir Türkiye

Elisa Contini

137 ×1.0

133 ×1.4

GENET

9 ×0.2

CCM

35 ×0.9

GENET

19 ×0.6

Citations per year, relative to Elisa Contini Elisa Contini (= 1×) peers Özge Özalp Yüreğir

Countries citing papers authored by Elisa Contini

Since Specialization

Citations

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

Fields of papers citing papers by Elisa Contini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisa Contini

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

All Works

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17 of 17 papers shown

Contini, Elisa, Andrea Valeri, Massimiliano Chetta, et al.. (2020). Germline Mutation in KIF1Bβ Gene Associated with Loss of Heterozygosity: Usefulness of Next-Generation Sequencing in the Genetic Screening of Patients with Pheochromocytoma. International Journal of Endocrinology. 2020. 1–8. 2 indexed citations

Bartalucci, Niccolò, Francesco Mannelli, Elisa Contini, et al.. (2019). THIRD GENERATION SEQUENCING OF NORMAL KARYOTYPE ACUTE MYELOID LEUKEMIA: IMPLICATIONS FOR PROGNOSIS. Haematologica. 104. 12–12. 1 indexed citations

Guglielmelli, Paola, Niccolò Bartalucci, Elisa Contini, et al.. (2019). Involvement of RUNX1 Pathway Is a Common Event in the Leukemic Transformation of Chronic Myeloproliferative Neoplasms (MPNs). Blood. 134(Supplement_1). 2968–2968. 4 indexed citations

Riera‐Escamilla, Antoni, Daniel Moreno‐Mendoza, Chiara Chianese, et al.. (2019). Sequencing of a ‘mouse azoospermia’ gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest. Human Reproduction. 34(6). 978–988. 58 indexed citations

Cappelli, Francesco, Francesco Mazzarotto, Sabrina Frusconi, et al.. (2019). P2731Genetic ancestry analysis of the Italian founder population carrying the cardiac amyloidosis-causing variant Val122Ile in the transthyretin gene. European Heart Journal. 40(Supplement_1). 1 indexed citations

Pacilli, Annalisa, Giada Rotunno, Carmela Mannarelli, et al.. (2018). Mutation landscape in patients with myelofibrosis receiving ruxolitinib or hydroxyurea. Blood Cancer Journal. 8(12). 122–122. 24 indexed citations

Mazzarotto, Francesco, Francesca Girolami, Beatrice Boschi, et al.. (2018). Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center. Genetics in Medicine. 21(2). 284–292. 51 indexed citations

Mucciolo, Dario Pasquale, Andrea Sodi, Ilaria Passerini, et al.. (2018). Fundus phenotype in retinitis pigmentosa associated with EYS mutations. Ophthalmic Genetics. 39(5). 589–602. 8 indexed citations

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

10.

Contini, Elisa, G. De Lucia, N. A. Hatch, S. Borgani, & Xi Kang. (2015). Semi-analytic model predictions of the galaxy population in protoclusters. Monthly Notices of the Royal Astronomical Society. 456(2). 1924–1935. 18 indexed citations

11.

Contini, Elisa, Irene Paganini, Roberta Sestini, et al.. (2015). A Systematic Assessment of Accuracy in Detecting Somatic Mosaic Variants by Deep Amplicon Sequencing: Application to NF2 Gene. PLoS ONE. 10(6). e0129099–e0129099. 15 indexed citations

12.

Contini, Elisa, et al.. (2015). Forensic genetics in NGS era: New frontiers for massively parallel typing. Forensic science international. Genetics supplement series. 5. e418–e419. 10 indexed citations

13.

Fattorini, Paolo, Carlo Previderè, Elisa Contini, et al.. (2015). Evaluation of the reliability of the data generated by Next Generation Sequencing from artificially degraded DNA samples. Forensic science international. Genetics supplement series. 5. e83–e85. 6 indexed citations

14.

Ricci, U., Elisa Contini, Francesca Torricelli, et al.. (2015). Genetic identification of burned corpses as a part of disaster victim identification effort. Forensic science international. Genetics supplement series. 5. e447–e448. 3 indexed citations

15.

Marini, Carla, Antonella Cecconi, Elisa Contini, et al.. (2013). Clinical and genetic study of a family with a paternally inherited 15q11–q13 duplication. American Journal of Medical Genetics Part A. 161(6). 1459–1464. 18 indexed citations

16.

Michelini, Sandro, D. Degiorgio, Maria Francesca Cardone, et al.. (2012). Clinical and genetic study of 46 Italian patients with primary lymphedema.. PubMed. 45(1). 3–12. 20 indexed citations

17.

Giglio, Sabrina, Elisa Contini, Sonia Toni, & I. Pela. (2010). Growth hormone therapy-related hyperglycaemia in a boy with renal cystic hypodysplasia and a new mutation of the HNF1 gene. Nephrology Dialysis Transplantation. 25(9). 3116–3119. 2 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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