Mara Giordano

2.4k total citations
83 papers, 1.3k citations indexed

About

Mara Giordano is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Mara Giordano has authored 83 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 32 papers in Genetics and 23 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Mara Giordano's work include Growth Hormone and Insulin-like Growth Factors (21 papers), Genetic Syndromes and Imprinting (10 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Mara Giordano is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (21 papers), Genetic Syndromes and Imprinting (10 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Mara Giordano collaborates with scholars based in Italy, United States and France. Mara Giordano's co-authors include Patricia Momigliano‐Richiardi, Sandra D’Alfonso, Gianni Bona, Simona Mellone, Marta Mellai, P. Richiardi, Simonetta Bellone, Flavia Prodam, Umberto Dianzani and Antonella Petri and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Diabetes.

In The Last Decade

Mara Giordano

78 papers receiving 1.3k citations

Peers

Mara Giordano

GENET

EDM

IMMUN

Ulrike Baschant Germany

Chela James United Kingdom

Angela F. Brady United Kingdom

N. P. Groome United Kingdom

Rozen Le Panse France

Takeshi Taketani Japan

Tony Antakly Canada

Wassila Carpentier France

Sawako Minami Japan

Claude Besmond France

Ulrike Baschant Germany

Mara Giordano

468 ×0.9

146 ×0.4

GENET

152 ×0.5

EDM

291 ×1.3

IMMUN

123 ×1.0

Citations per year, relative to Mara Giordano Mara Giordano (= 1×) peers Ulrike Baschant

Countries citing papers authored by Mara Giordano

Since Specialization

Citations

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

Fields of papers citing papers by Mara Giordano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mara Giordano

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

Waśniewska, Małgorzata, Mara Giordano, Giorgia Pepe, et al.. (2025). Cumulative Effects of Genetic Variants Detected in a Child with Early-Onset Non-Syndromic Obesity Due to SIM-1 Gene Mutation. Genes. 16(5). 588–588.

Puricelli, Chiara, Elena Boggio, Casimiro Luca Gigliotti, et al.. (2023). Platelets, Protean Cells with All-Around Functions and Multifaceted Pharmacological Applications. International Journal of Molecular Sciences. 24(5). 4565–4565. 23 indexed citations

Mellone, Simona, Chiara Puricelli, Cinzia Peruzzi, et al.. (2022). The Usefulness of a Targeted Next Generation Sequencing Gene Panel in Providing Molecular Diagnosis to Patients With a Broad Spectrum of Neurodevelopmental Disorders. Frontiers in Genetics. 13. 875182–875182. 12 indexed citations

Prodam, Flavia, Giulia Genoni, Giorgio Bellomo, et al.. (2021). The Prevalence of Thyroid Autoimmunity in Children with Developmental Dyslexia. BioMed Research International. 2021(1). 7656843–7656843.

Prodam, Flavia, Simona Mellone, Roberta Ricotti, et al.. (2021). Retrospective Diagnosis of a Novel ACAN Pathogenic Variant in a Family With Short Stature: A Case Report and Review of the Literature. Frontiers in Genetics. 12. 708864–708864. 7 indexed citations

Rolla, Roberta, Alessandro Lupi, Patrizia Pergolini, et al.. (2018). Cardiovascular Risk Profile of Patients Hospitalized for Myocardial Infarction is Undestimated by Traditional Risk Factors and is Better Estimated by a Genetic Analysis Based Upon Single Nucleotide Polymorphisms: A Retrospective Study. 54(98). 1–8.

Dellepiane, Rosa Maria, Laura Dell’Era, Paolo Macor, et al.. (2016). Invasive meningococcal disease in three siblings with hereditary deficiency of the 8th component of complement: evidence for the importance of an early diagnosis. Orphanet Journal of Rare Diseases. 11(1). 64–64. 8 indexed citations

Rienzo, Francesca De, Simona Mellone, Simonetta Bellone, et al.. (2015). Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort. Clinical Endocrinology. 83(6). 849–860. 60 indexed citations

Giordano, Mara, et al.. (2015). A 5.8 Mb interstitial deletion on chromosome Xq21.1 in a boy with intellectual disability, cleft palate, hearing impairment and combined growth hormone deficiency. BMC Medical Genetics. 16(1). 74–74. 9 indexed citations

10.

Prodam, Flavia, Silvia Savastio, Giulia Genoni, et al.. (2014). Effects of Growth Hormone (GH) Therapy Withdrawal on Glucose Metabolism in Not Confirmed GH Deficient Adolescents at Final Height. PLoS ONE. 9(1). e87157–e87157. 15 indexed citations

11.

Rossi, Elisabetta, et al.. (2012). Diels–Alder Reactions of 2-Vinylindoles with Cyclic Dienophiles: Synthesis of [c]-Annulated Tetrahydrocarbazoles. Synlett. 23(20). 2913–2918. 14 indexed citations

12.

Vivenza, Daniela, Michela Godi, Maria Felicia Faienza, et al.. (2011). A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing. European Journal of Endocrinology. 164(5). 705–713. 11 indexed citations

13.

Giordano, Mara, Marta Mellai, M.G. Limongelli, et al.. (2006). A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population. Genes and Immunity. 7(7). 606–608. 24 indexed citations

14.

Chiocchetti, Annalisa, Cristoforo Comi, Manuela Indelicato, et al.. (2005). Osteopontin gene haplotypes correlate with multiple sclerosis development and progression. Journal of Neuroimmunology. 163(1-2). 172–178. 60 indexed citations

15.

Mellai, Marta, Mara Giordano, Sandra D’Alfonso, et al.. (2003). Prolactin and prolactin receptor gene polymorphisms in multiple sclerosis and systemic lupus erythematosus. Human Immunology. 64(2). 274–284. 29 indexed citations

16.

D’Alfonso, Sandra, Marta Mellai, Mara Giordano, et al.. (2002). Identification of single nucleotide variations in the coding and regulatory regions of the myelin-associated glycoprotein gene and study of their association with multiple sclerosis. Journal of Neuroimmunology. 126(1-2). 196–204. 11 indexed citations

17.

D’Alfonso, Sandra, Mara Giordano, Marta Mellai, et al.. (2002). Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5′ regulatory region. Genes and Immunity. 3(8). 454–463. 30 indexed citations

18.

Giordano, Mara, Elisabetta Bolognesi, Sandra D’Alfonso, et al.. (1999). Linkage disequilibrium between intra‐locus variants in the aminopeptidase n gene and test of their association with coeliac disease. Annals of Human Genetics. 63(3). 207–215. 6 indexed citations

19.

Giordano, Mara, et al.. (1996). Reassessment of the Specificity of Lens Opacities in Myotonic Dystrophy. Ophthalmic Research. 28(4). 224–229. 5 indexed citations

20.

Giordano, Mara, et al.. (1995). Problems arising in correlating clinical and molecular data in myotonic dystrophy. Clinical Genetics. 47(6). 302–304. 6 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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