Francesca Frangipane

1.7k total citations
17 papers, 253 citations indexed

About

Francesca Frangipane is a scholar working on Physiology, Molecular Biology and Neurology. According to data from OpenAlex, Francesca Frangipane has authored 17 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Physiology, 8 papers in Molecular Biology and 8 papers in Neurology. Recurrent topics in Francesca Frangipane's work include Alzheimer's disease research and treatments (10 papers), Amyotrophic Lateral Sclerosis Research (5 papers) and Prion Diseases and Protein Misfolding (4 papers). Francesca Frangipane is often cited by papers focused on Alzheimer's disease research and treatments (10 papers), Amyotrophic Lateral Sclerosis Research (5 papers) and Prion Diseases and Protein Misfolding (4 papers). Francesca Frangipane collaborates with scholars based in Italy, Belgium and Türkiye. Francesca Frangipane's co-authors include Rosanna Colao, Amalia C. Bruni, Gianfranco Puccio, Raffaele Maletta, Sabrina A.M. Curcio, Maria Mirabelli, Livia Bernardi, Nicoletta Smirne, Maura Gallo and Maria Anfossi and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurobiology of Aging and Journal of Alzheimer s Disease.

In The Last Decade

Francesca Frangipane

15 papers receiving 228 citations

Peers

Francesca Frangipane

PHYSI

PMH

NEURO

Nicoletta Smirne Italy

Gianfranco Puccio Italy

Sabrina A.M. Curcio Italy

Roberto Lopez-Alberola United States

Malia Rumbaugh United States

Ubaldo Bonuccelli Italy

Kaj Blennow Sweden

Jason Lockrow United States

Donald Schmechel United States

Rachel L. Henson United States

Nicoletta Smirne Italy

Francesca Frangipane

162 ×1.2

PHYSI

120 ×1.3

81 ×1.3

PMH

93 ×1.5

NEURO

56 ×1.0

NEURO

Citations per year, relative to Francesca Frangipane Francesca Frangipane (= 1×) peers Nicoletta Smirne

Countries citing papers authored by Francesca Frangipane

Since Specialization

Citations

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

Fields of papers citing papers by Francesca Frangipane

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Frangipane

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

All Works

Sort: Min cites: Since: Top N: Style:

17 of 17 papers shown

Bruno, Francesco, Paolo Abondio, Rosanna Colao, et al.. (2023). Using the Theory of Planned Behavior and Past Behavior to Explain the Intention to Receive a Seasonal Influenza Vaccine among Family Caregivers of People with Dementia. SHILAP Revista de lepidopterología. 3(2). 246–254.

Bruno, Francesco, Giulia Innocenti Bruni, Nicoletta Smirne, et al.. (2022). Neuropsychiatric or Behavioral and Psychological Symptoms of Dementia (BPSD): Focus on Prevalence and Natural History in Alzheimer's Disease and Frontotemporal Dementia. Frontiers in Neurology. 13. 832199–832199. 52 indexed citations

Bruno, Francesco, Maria Elena Conidi, Gianfranco Puccio, et al.. (2021). A Novel Mutation (D395A) in Valosin-Containing Protein Gene Is Associated With Early Onset Frontotemporal Dementia in an Italian Family. Frontiers in Genetics. 12. 795029–795029. 12 indexed citations

Abondio, Paolo, Stefania Sarno, Cristina Giuliani, et al.. (2021). Amyloid Precursor Protein A713T Mutation in Calabrian Patients with Alzheimer’s Disease: A Population Genomics Approach to Estimate Inheritance from a Common Ancestor. Biomedicines. 10(1). 20–20. 15 indexed citations

Montesanto, Alberto, Paolina Crocco, Serena Dato, et al.. (2018). Uncoupling protein 4 (UCP4) gene variability in neurodegenerative disorders: further evidence of association in Frontotemporal dementia. Aging. 10(11). 3283–3293. 10 indexed citations

Bernardi, Livia, Chiara Cupidi, Francesca Frangipane, et al.. (2014). Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome. Neurobiology of Aging. 35(11). 2657.e7–2657.e11. 12 indexed citations

Anfossi, Maria, Rosanna Colao, Maura Gallo, et al.. (2013). Identification of Three Novel LRRK2 Mutations associated with Parkinson's Disease in a Calabrian Population. Journal of Alzheimer s Disease. 38(2). 351–357. 5 indexed citations

Bernardi, Livia, Maura Gallo, Maria Anfossi, et al.. (2013). Role of TOMM40 rs10524523 Polymorphism in Onset of Alzheimer's Disease Caused by the PSEN1 M146L Mutation. Journal of Alzheimer s Disease. 37(2). 285–289. 9 indexed citations

Clodomiro, Alessandra, Pietro Gareri, Gianfranco Puccio, et al.. (2013). Somatic comorbidities and Alzheimer’s disease treatment. Neurological Sciences. 34(9). 1581–1589. 20 indexed citations

10.

Anfossi, Maria, Romina Vuono, Raffaele Maletta, et al.. (2011). Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia. Neurobiology of Aging. 32(4). 757.e1–757.e11. 16 indexed citations

11.

Bernardi, Livia, Maria Anfossi, Maura Gallo, et al.. (2011). PSEN1 and PRNP Gene Mutations Co-occurrence Makes Onset Very Early in a Family with FTD Phenotype. Journal of Alzheimer s Disease. 24(3). 415–419. 8 indexed citations

12.

Anfossi, Maria, Livia Bernardi, Maura Gallo, et al.. (2010). MAPT V363I Variation in a Sporadic Case of Frontotemporal Dementia. Alzheimer Disease & Associated Disorders. 25(1). 96–99. 12 indexed citations

13.

Gallo, Maura, Carmine Tomaino, Gianfranco Puccio, et al.. (2009). Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia. Neurological Sciences. 31(1). 65–70. 17 indexed citations

14.

Bernardi, Livia, Silvana Geracitano, Rosanna Colao, et al.. (2009). AβPP A713T Mutation in Late Onset Alzheimer's Disease with Cerebrovascular Lesions. Journal of Alzheimer s Disease. 17(2). 383–389. 17 indexed citations

15.

Bruni, Amalia C., Francesca Frangipane, Rosanna Colao, et al.. (2009). P3‐166: Epidemiology of Frontotemporal dementia in southern Italy. Alzheimer s & Dementia. 5(4S_Part_13). 1 indexed citations

16.

Bernardi, Livia, Carmine Tomaino, Maria Anfossi, et al.. (2008). Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia. Neurobiology of Aging. 30(11). 1825–1833. 46 indexed citations

17.

Gallo, Maura, Carmine Tomaino, Livia Bernardi, et al.. (2008). P3‐220: PS1 polymorphism and a novel PS2 mutation in a patient with late‐onset familial Alzheimer's disease. Alzheimer s & Dementia. 4(4S_Part_18). 1 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.

Explore authors with similar magnitude of impact