Giacomina Rossi

10.9k citations

71 papers · 2.6k indexed · h-index 27

Co-authors: Fabrizio Tagliavini Giorgio Giaccone Orso Bugiani Mario Salmona Gianfranco Puoti Michela Morbin Barbara Canciani Gianluigi Forloni
Topics: Alzheimer's disease research and treatments (29 papers)Amyotrophic Lateral Sclerosis Research (26 papers)Neurological diseases and metabolism (24 papers)
Cited by: Neurology Physiology
Journals: Cell Proceedings of the National Academy of Sciences Journal of Biological Chemistry
Partner nations: Italy United States United Kingdom

In The Last Decade

Giacomina Rossi

70 papers receiving 2.6k citations

Peers

Countries citing papers authored by Giacomina Rossi

Since Specialization

Citations

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

Fields of papers citing papers by Giacomina Rossi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giacomina Rossi

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

#	Work	Indexed citations
1	A novel SORL1 mutation in a pedigree affected by early-onset Alzheimer's disease 2025 ·Journal of Alzheimer s Disease Reports ·Veronica Redaelli,(unknown),Angelo Del Sole,(unknown),Sara Prioni,Giacomina Rossi	0
2	Plasma Small Extracellular Vesicle Cathepsin D Dysregulation in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration 2022 ·International Journal of Molecular Sciences ·(unknown),Claudia Saraceno,Luisa Benussi,(unknown),(unknown),(unknown),(unknown),(unknown),Laura Canafoglia,Cinzia Coppola,(unknown),Giuliano Binetti,Giacomina Rossi,Roberta Ghidoni	5
3	Plasma Small Extracellular Vesicles with Complement Alterations in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration 2022 ·Cells ·(unknown),Claudia Saraceno,Luisa Benussi,Rosanna Squitti,(unknown),(unknown),Laura Canafoglia,Cinzia Coppola,Gianfranco Puoti,Clarissa Ferrari,(unknown),(unknown),Marta Lombardi,Giulia D’Arrigo,Claudia Verderio,Giuliano Binetti,Giacomina Rossi,Roberta Ghidoni	8
4	The PINK1 p.Asn521Thr Variant Is Associated with Earlier Disease Onset in GRN/C9orf72 Frontotemporal Lobar Degeneration 2022 ·International Journal of Molecular Sciences ·Giacomina Rossi,Erika Salvi,Luisa Benussi,(unknown),(unknown),(unknown),(unknown),(unknown),Matteo Carrara,Cristian Bonvicini,(unknown),Claudia Saraceno,(unknown),Giorgio Giaccone,Giuliano Binetti,Roberta Ghidoni	2
5	Pathological 25 kDa C-Terminal Fragments of TDP-43 Are Present in Lymphoblastoid Cell Lines and Extracellular Vesicles from Patients Affected by Frontotemporal Lobar Degeneration and Neuronal Ceroidolipofuscinosis Carrying a GRN Mutation 2022 ·International Journal of Molecular Sciences ·(unknown),(unknown),Claudia Saraceno,Luisa Benussi,Roberta Ghidoni,Silvia Giliani,(unknown),Laura Canafoglia,Giorgio Giaccone,Giacomina Rossi	4
6	GRN−/− iPSC-derived cortical neurons recapitulate the pathological findings of both frontotemporal lobar degeneration and neuronal ceroidolipofuscinosis 2022 ·Neurobiology of Disease ·Patrizia Bossolasco,(unknown),Emanuela Maderna,Donatella Bardelli,Laura Canafoglia,Tiziana Cavallaro,(unknown),Vincenzo Silani,Gianluca Marucci,Giacomina Rossi	6
7	A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain) 2019 ·Neurobiology of Aging ·Leire Palencia-Madrid,Raquel Sánchez‐Valle,(unknown),(unknown),Oriol Grau‐Rivera,Ramón Reñé,Isabel de la Torre Díez,(unknown),Giacomina Rossi,Paola Caroppo,Veronica Redaelli,Isabelle Le Ber,Agnès Camuzat,Alexis Brice,Anna Antonell,Mircea Balasa,Ellen Gelpí,Albert Lladó,Marian M. de Pancorbo	5
8	Tau Mutations Serve as a Novel Risk Factor for Cancer 2018 ·UCL Discovery (University College London) ·Giacomina Rossi,Veronica Redaelli,Paolo Contiero,Sabrina Fabiano,Giovanna Tagliabue,Paola Perego,Luisa Benussi,Amalia C. Bruni,Graziella Filippini,Mariangela Farinotti,Giorgio Giaccone,(unknown),Claudia Manzoni,Raffaele Ferrari,Fabrizio Tagliavini	20
9	Missense mutation in GRN gene affecting RNA splicing and plasma progranulin level in a family affected by frontotemporal lobar degeneration 2017 ·Neurobiology of Aging ·Simona Luzzi,(unknown),(unknown),(unknown),(unknown),(unknown),Mauro Silvestrini,Paola Caroppo,Giorgio Giaccone,Fabrizio Tagliavini,Giacomina Rossi	5
10	Missense mutations in progranulin gene associated with frontotemporal lobar degeneration: study of pathogenetic features 2015 ·Neurobiology of Aging ·Celeste M. Karch,Lubov Ezerskiy,Veronica Redaelli,Anna Rıta Gıovagnolı,Pietro Tiraboschi,Giuseppe Pelliccioni,(unknown),Dimos Kapetis,Ilaria D’Amato,Elena Piccoli,(unknown),Fabrizio Tagliavini,Giacomina Rossi	17
11	Frontotemporal lobar degeneration: old knowledge and new insight into the pathogenetic mechanisms of tau mutations 2015 ·Frontiers in Aging Neuroscience ·Giacomina Rossi,Fabrizio Tagliavini	40
12	Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features 2013 ·Neurobiology of Aging ·Giacomina Rossi,Antonio Bastone,Elena Piccoli,Michela Morbin,Giulia Mazzoleni,Valeria Fugnanesi,Marten Beeg,Elena Del Favero,Laura Cantù,(unknown),Ettore Salsano,Davide Pareyson,Alessandra Erbetta,Antonio Emanuele Elia,Francesca Del Sorbo,Vincenzo Silani,Claudia Morelli,Mario Salmona,Fabrizio Tagliavini	31
13	Mutations in MAPT Gene Cause Chromosome Instability and Introduce Copy Number Variations Widely in the Genome 2013 ·Journal of Alzheimer s Disease ·Giacomina Rossi,Donatella Conconi,Elena Panzeri,Serena Redaelli,Elena Piccoli,(unknown),Leda Dalprà,Fabrizio Tagliavini	37
14	Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage 2012 ·The American Journal of Human Genetics ·Katherine R. Smith,John A. Damiano,Silvana Franceschetti,Stirling Carpenter,Laura Canafoglia,Michela Morbin,Giacomina Rossi,Davide Pareyson,Sara Mole,John F. Staropoli,Katherine B. Sims,Jada Lewis,Wen-Lang Lin,Dennis W. Dickson,Hans‐Henrik M. Dahl,Melanie Bahlo,Samuel F. Berkovic	356
15	Optimal Plasma Progranulin Cutoff Value for Predicting Null Progranulin Mutations in Neurodegenerative Diseases: A Multicenter Italian Study 2011 ·Neurodegenerative Diseases ·Roberta Ghidoni,Elena Stoppani,Giacomina Rossi,Elena Piccoli,Valentina Albertini,Anna Paterlini,Michela Glionna,(unknown),Luigi F. Agnati,Chiara Fenoglio,Elio Scarpini,Daniela Galimberti,Michela Morbin,Fabrizio Tagliavini,Giuliano Binetti,Luisa Benussi	74
16	The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome 2008 ·Movement Disorders ·Giacomina Rossi,Cécilia Marelli,Laura Farina,(unknown),Anna Basile,(unknown),Fabrizio Tagliavini,Davide Pareyson	36
17	A 7-kDa Prion Protein (PrP) Fragment, an Integral Component of the PrP Region Required for Infectivity, Is the Major Amyloid Protein in Gerstmann-Sträussler-Scheinker Disease A117V 2001 ·Journal of Biological Chemistry ·Fabrizio Tagliavini,Patricia Lievens,Christine Tranchant,(unknown),Michel Mohr,Giorgio Giaccone,Francesco Perini,Giacomina Rossi,Mario Salmona,Pedro Piccardo,Bernardino Ghetti,Ronald C. Beavis,Orso Bugiani,Blas Frangione,Frances Prelli	107
18	Tetracycline affects abnormal properties of synthetic PrP peptides and PrPSc in vitro11Edited by J. Karn 2000 ·Journal of Molecular Biology ·Fabrizio Tagliavini,Gianluigi Forloni,Laura Colombo,Giacomina Rossi,(unknown),Barbara Canciani,Nadia Angeretti,(unknown),(unknown),(unknown),Luca De Gioia,Enzio Ragg,Orso Bugiani,Mario Salmona	130
19	Creutzfeldt‐Jakob Disease: Carnoy's Fixative Improves the Immunohistochemistry of the Proteinase K‐ Resistant Prion Protein 2000 ·Brain Pathology ·Giorgio Giaccone,Barbara Canciani,Gianfranco Puoti,Giacomina Rossi,Donato Goffredo,Selina Iussich,Paolo Fociani,Fabrizio Tagliavini,Orso Bugiani	43
20	Diffuse thalamic degeneration in fatal familial insomnia. A morphometric study 1997 ·Brain Research ·G Macchi,Giacomina Rossi,Anna Laura Abbamondi,Giorgio Giaccone,(unknown),Fabrizio Tagliavini,Orso Bugiani	24

About Giacomina Rossi

Giacomina Rossi is a scholar working on Neurology, Neurology and Physiology, having authored 71 papers that have together received 2.6k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (29 papers), Amyotrophic Lateral Sclerosis Research (26 papers) and Neurological diseases and metabolism (24 papers). The work is most often cited by research in Neurology (878 citations), Neurology (816 citations) and Physiology (960 citations). Giacomina Rossi has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Fabrizio Tagliavini, Giorgio Giaccone, Orso Bugiani, Mario Salmona, Gianfranco Puoti, Michela Morbin, Barbara Canciani, Gianluigi Forloni, Laura Colombo and Davide Pareyson. Their work appears in journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

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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