Elena Cellini

2.5k total citations
52 papers, 1.4k citations indexed

About

Elena Cellini is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Elena Cellini has authored 52 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 18 papers in Physiology and 11 papers in Genetics. Recurrent topics in Elena Cellini's work include Alzheimer's disease research and treatments (18 papers), Eating Disorders and Behaviors (9 papers) and Mitochondrial Function and Pathology (7 papers). Elena Cellini is often cited by papers focused on Alzheimer's disease research and treatments (18 papers), Eating Disorders and Behaviors (9 papers) and Mitochondrial Function and Pathology (7 papers). Elena Cellini collaborates with scholars based in Italy, United States and Spain. Elena Cellini's co-authors include Benedetta Nacmias, Sandro Sorbi, Silvia Bagnoli, Andrea Tedde, Renzo Guerrini, Laura Bracco, Valdo Ricca, Silvia Piacentini, Milena Di Bernardo and Davide Mei and has published in prestigious journals such as Neurology, British Journal Of Nutrition and Epilepsia.

In The Last Decade

Elena Cellini

52 papers receiving 1.3k citations

Peers

Elena Cellini

PHYSI

GENET

PMH

CMN

Andrea Tedde Italy

R.H. Belmaker Israel

Lingjun Zuo United States

Caroline Nothdurfter Germany

Patricia Gassó Spain

Jasminka Štefulj Croatia

Ding‐Lieh Liao Taiwan

Vanessa Ota Brazil

Hugh B. Hughes United States

Sarah Bertelsen United States

Andrea Tedde Italy

Elena Cellini

455 ×0.9

490 ×1.5

PHYSI

189 ×0.6

GENET

157 ×0.5

PMH

237 ×0.9

CMN

Citations per year, relative to Elena Cellini Elena Cellini (= 1×) peers Andrea Tedde

Countries citing papers authored by Elena Cellini

Since Specialization

Citations

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

Fields of papers citing papers by Elena Cellini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Cellini

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

Miceli, Francesco, Renzo Guerrini, Maria Virginia Soldovieri, et al.. (2021). Distinct epilepsy phenotypes and response to drugs in KCNA1 gain‐ and loss‐of function variants. Epilepsia. 63(1). e7–e14. 25 indexed citations

Cellini, Elena, Annalisa Vetro, Valerio Conti, et al.. (2019). Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity. European Journal of Human Genetics. 27(6). 909–918. 21 indexed citations

Vincenzetti, Silvia, et al.. (2017). Determination of some water-soluble vitamins in donkey milk.. Italian Journal of Animal Science. 16. 922–922. 1 indexed citations

Marini, Carla, Katia Hardies, Tiziana Pisano, et al.. (2017). Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects. American Journal of Medical Genetics Part A. 173(4). 1119–1123. 16 indexed citations

Penelo, Eva, Roser Granero, Isabel Krug, et al.. (2010). Factors of risk and maintenance for eating disorders: psychometric exploration of the cross‐cultural questionnaire (CCQ) across five European countries. Clinical Psychology & Psychotherapy. 18(6). 535–552. 12 indexed citations

Cellini, Elena, Giovanni Castellini, Valdo Ricca, et al.. (2010). Glucocorticoid receptor gene polymorphisms in Italian patients with eating disorders and obesity. Psychiatric Genetics. 20(6). 282–288. 30 indexed citations

Krug, Isabel, Janet Treasure, Marija Anderluh, et al.. (2008). Present and lifetime comorbidity of tobacco, alcohol and drug use in eating disorders: A European multicenter study. Drug and Alcohol Dependence. 97(1-2). 169–179. 70 indexed citations

Poleggi, Anna, Alessandra Bizzarro, Piero Antuono, et al.. (2008). Codon 129 polymorphism of prion protein gene in sporadic Alzheimer’s disease. European Journal of Neurology. 15(2). 173–178. 14 indexed citations

Ginestroni, Andrea, Laura Guerrini, Riccardo Della Nave, et al.. (2007). Morphometry and 1H-MR Spectroscopy of the Brain Stem and Cerebellum in Three Patients with Fragile X-Associated Tremor/Ataxia Syndrome. American Journal of Neuroradiology. 28(3). 486–488. 8 indexed citations

10.

Tedde, Andrea, Silvia Bagnoli, Elena Cellini, et al.. (2007). No Association Between the LRRK2 G2019S Mutation and Alzheimer’s disease in Italy. Cellular and Molecular Neurobiology. 27(7). 877–881. 12 indexed citations

11.

Tedde, Andrea, Elena Cellini, Silvia Bagnoli, Sandro Sorbi, & Alessandro Peri. (2007). Mutational screening analysis of DHCR24/seladin‐1 gene in Italian familial Alzheimer's disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(1). 117–119. 8 indexed citations

12.

Bagnoli, Silvia, Elena Cellini, Andrea Tedde, et al.. (2007). Association of IL10 promoter polymorphism in Italian Alzheimer's disease. Neuroscience Letters. 418(3). 262–265. 31 indexed citations

13.

Cellini, Elena, Andrea Tedde, Silvia Bagnoli, et al.. (2006). Association analysis of the paraoxonase-1 gene with Alzheimer's disease. Neuroscience Letters. 408(3). 199–202. 29 indexed citations

14.

Tedde, Andrea, Mario Rotondi, Elena Cellini, et al.. (2005). Lack of association between the CYP46 gene polymorphism and Italian late-onset sporadic Alzheimer's disease. Neurobiology of Aging. 27(5). 773.e1–773.e3. 20 indexed citations

15.

Nacmias, Benedetta, Silvia Bagnoli, Andrea Tedde, et al.. (2005). Cystatin C and apoe polymorphisms in Italian Alzheimer's disease. Neuroscience Letters. 392(1-2). 110–113. 10 indexed citations

16.

Ricca, Valdo, Benedetta Nacmias, Maura Boldrini, et al.. (2004). Psychopathological traits and 5-HT2A receptor promoter polymorphism (−1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa. Neuroscience Letters. 365(2). 92–96. 30 indexed citations

17.

Tedde, Andrea, Benedetta Nacmias, Paolo Forleo, et al.. (2003). Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease. Archives of Neurology. 60(11). 1541–1541. 40 indexed citations

18.

Ricca, Valdo, Benedetta Nacmias, Elena Cellini, et al.. (2002). 5-HT2A receptor gene polymorphism and eating disorders. Neuroscience Letters. 323(2). 105–108. 67 indexed citations

19.

Cellini, Elena, Silvia Piacentini, Benedetta Nacmias, et al.. (2002). A Family With Spinocerebellar Ataxia Type 8 Expansion and Vitamin E Deficiency Ataxia. Archives of Neurology. 59(12). 1952–1952. 10 indexed citations

20.

Sorbi, Sandro, Paolo Forleo, Andrea Tedde, et al.. (2001). Genetic risk factors in familial Alzheimer's disease. Mechanisms of Ageing and Development. 122(16). 1951–1960. 23 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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