Emanuela Scarano

2.5k total citations
67 papers, 1.6k citations indexed

About

Emanuela Scarano is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Emanuela Scarano has authored 67 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 25 papers in Genetics and 9 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Emanuela Scarano's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers), Galectins and Cancer Biology (7 papers) and Growth Hormone and Insulin-like Growth Factors (7 papers). Emanuela Scarano is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers), Galectins and Cancer Biology (7 papers) and Growth Hormone and Insulin-like Growth Factors (7 papers). Emanuela Scarano collaborates with scholars based in Italy, United States and United Kingdom. Emanuela Scarano's co-authors include Maurizio Iaccarino, P. Grippo, Emmanuele Parisi, Laura Mazzanti, Vincenzo Scardi, P. Scotto, Alessandro Cicognani, Mauro Rossi, E Cacciari and Rosalba Bergamaschi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Molecular Biology and The FASEB Journal.

In The Last Decade

Emanuela Scarano

62 papers receiving 1.5k citations

Peers

Countries citing papers authored by Emanuela Scarano

Since Specialization

Citations

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

Fields of papers citing papers by Emanuela Scarano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emanuela Scarano

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

#	Title	Journal	Authors	Indexed citations
1	Integrating vosoritide therapy with limb surgery in paediatric patients with achondroplasia: real-life experiences	Orphanet Journal of Rare Diseases	Anna Elsa Maria Allegri, Maria Francesca Bedeschi et al.	0
2	Impact of pubertal timing on growth progression and final height in subjects affected by RASopathies	Frontiers in Endocrinology	Federica Tamburrino, Laura Mazzanti et al.	0
3	Growth Hormone Treatment in Patients With KBG Syndrome: Novel Insights, Challenges and Recommendations From Six New Patients and Literature Review	American Journal of Medical Genetics Part A	Sietse Aukema, Emanuela Scarano et al.	1
4	Lipid profile in Noonan syndrome and related disorders: trend by age, sex and genotype	Frontiers in Endocrinology	Federica Tamburrino, Laura Mazzanti et al.	2
5	Real-life long-term efficacy and safety of recombinant human growth hormone therapy in children with short stature homeobox-containing deficiency	Endocrine Connections	Patrizia Bruzzi, Silvia Vannelli et al.	2
6	Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome	Epilepsia Open	Floor E. Jansen, Charlotte W. Ockeloen et al.	7
7	Chromosomal Microarray Analysis Identifies a Novel SALL1 Deletion, Supporting the Association of Haploinsufficiency with a Mild Phenotype of Townes–Brocks Syndrome	Genes	Emanuela Scarano, Antonella Pragliola et al.	3
8	Obesity in Prader–Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches	Journal of Endocrinological Investigation	Giovanna Muscogiuri, Luigi Barrea et al.	60
9	Is there any gender difference in epidemiology, clinical presentation and co-morbidities of non-functioning pituitary adenomas? A prospective survey of a National Referral Center and review of the literature	Journal of Endocrinological Investigation	Carolina Di Somma, Emanuela Scarano et al.	18
10	Challenges in the clinical interpretation of small de novo copy number variants in neurodevelopmental disorders	Gene	Pamela Magini, Emanuela Scarano et al.	8
11	<b><i>HDAC8</i></b> Loss of Function and <b><i>SHOX</i></b> Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype	Cytogenetic and Genome Research	Elena Bonora, Annamaria Perri et al.	3
12	New insights on diabetes in Turner syndrome: results from an observational study in adulthood	Endocrine	Paola Altieri, Emanuela Scarano et al.	17
13	Disorders of glucose metabolism in Prader–Willi syndrome: Results of a multicenter Italian cohort study	Nutrition Metabolism and Cardiovascular Diseases	Danilo Fintini, Graziano Grugni et al.	46
14	Prevalence of hypovitaminosis D in adult patients with hypopituitarism	15th International & 14th European Congress of Endocrinology	Ralph Esposito, Maria Cristina Savanelli et al.	0
15	Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria	European Journal of Histochemistry	Vittoria Cenni, Cristina Capanni et al.	72
16	Developmental Syndromes: Growth Hormone Deficiency and Treatment	Endocrine development	Laura Mazzanti, Federica Tamburrino et al.	13
17	Strawberry plant relationship through the stolon	Physiologia Plantarum	G. Savini, Veronica Giorgi et al.	31
18	A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation	American Journal of Medical Genetics Part A	Claudio Graziano, Angela D’Elia et al.	25
19	Noonan‐like syndrome with loose anagen hair: A new syndrome?	American Journal of Medical Genetics Part A	Laura Mazzanti, E Cacciari et al.	62
20	The control of gene function in cell differentiation and in embryogenesis.	PubMed	Emanuela Scarano	25

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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