Guja Astrea

2.6k total citations
53 papers, 655 citations indexed

About

Guja Astrea is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Guja Astrea has authored 53 papers receiving a total of 655 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 16 papers in Cellular and Molecular Neuroscience and 11 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Guja Astrea's work include Muscle Physiology and Disorders (17 papers), Genetic Neurodegenerative Diseases (11 papers) and Cardiomyopathy and Myosin Studies (11 papers). Guja Astrea is often cited by papers focused on Muscle Physiology and Disorders (17 papers), Genetic Neurodegenerative Diseases (11 papers) and Cardiomyopathy and Myosin Studies (11 papers). Guja Astrea collaborates with scholars based in Italy, United Kingdom and United States. Guja Astrea's co-authors include Filippo M. Santorelli, Roberta Battini, Chiara Fiorillo, Claudio Bruno, Stefania Bargagna, Carlo Minetti, Fabio Coppedè, Renato Colognato, Giacomo Brisca and Lucia Migliore and has published in prestigious journals such as PLoS ONE, Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Guja Astrea

48 papers receiving 644 citations

Peers

Countries citing papers authored by Guja Astrea

Since Specialization

Citations

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

Fields of papers citing papers by Guja Astrea

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guja Astrea

This figure shows the co-authorship network connecting the top 25 collaborators of Guja Astrea. A scholar is included among the top collaborators of Guja Astrea 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 Guja Astrea. Guja Astrea 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:

20 of 20 papers shown

#	Work	Indexed citations
1	Expanding the Clinical Spectrum Associated with the Recurrent Arg203Trp Variant in PACS1: An Italian Cohort Study 2025 ·Genes ·Stefano Pagano, Diego Lopergolo, Alessandro De Falco, (unknown), (unknown), Rosa Pasquariello, Rosanna Trovato, Alessandra Tessa, Claudia Casalini, Lucia Pfanner, Guja Astrea, (unknown), Filippo M. Santorelli	0
2	KLHL40-Related Myopathy: A Systematic Review and Insight into a Follow-up Biomarker via a New Case Report 2024 ·Genes ·(unknown), (unknown), Rosa Pasquariello, (unknown), Silvia Frosini, Filippo M. Santorelli, Alessandro Orsini, Roberta Battini, Guja Astrea	3
3	Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up Study 2024 ·Journal of Neuromuscular Diseases ·Giulia Ricci, Alessandra Govoni, (unknown), Guja Astrea, (unknown), (unknown), Roberta Battini, Maria Laura Manca, Vincenzo Castiglione, Alberto Giannoni, Michele Emdin, Gabriele Siciliano	2
4	Parental diagnostic delay and developmental outcomes in congenital and childhood‐onset myotonic dystrophy type 1 2024 ·Developmental Medicine & Child Neurology ·Federica Trucco, Emilio Albamonte, Marika Pane, Federica Ricci, Adele D’Amico, Guja Astrea, Isabella Moroni, Antonella Pini, Chiara Fiorillo, Angela Berardinelli, Nicholas E. Johnson, Valeria Sansone, (unknown)	2
5	Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiency 2024 ·Human Genomics ·Viola Alesi, Silvia Genovese, (unknown), (unknown), Silvia Di Tommaso, Sara Loddo, (unknown), Dario Pompili, (unknown), (unknown), Elisa Pisaneschi, (unknown), (unknown), Corrado Mammì, Guja Astrea, Roberta Battini, Manuela Priolo, Maria Lisa Dentici, (unknown), Antonio Novelli	1
6	Combined generalized and focal epilepsy with reflex features in Adaptor protein complex 4-associated hereditary spastic paraplegias: A cohort observational study 2024 ·Seizure ·Emanuele Bartolini, Anna Rita Ferrari, Filippo M. Santorelli, (unknown), Guja Astrea, (unknown), (unknown), Alessandro Orsini, Roberta Battini	0
7	Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature 2023 ·Genes ·(unknown), Alessandro Orsini, (unknown), Elisa Costa, Andrea Santangelo, Guja Astrea, Silvia Frosini, Rosa Pasquariello, Anna Rubegni, (unknown), Martina Corsi, Alice Bonuccelli, Roberta Battini	3
8	Neural substrates of neuropsychological profiles in dystrophynopathies: A pilot study of diffusion tractography imaging 2021 ·PLoS ONE ·Laura Biagi, (unknown), (unknown), Simona Fiori, Paolo Bosco, (unknown), Guja Astrea, Antonella Pini, Giovanni Cioni, Eugenio Mercuri, Michela Tosetti, Roberta Battini	4
9	Muscle “islands”: An MRI signature distinguishing neurogenic from myopathic causes of early onset distal weakness 2021 ·Neuromuscular Disorders ·Guja Astrea, Jasper M. Morrow, (unknown), Roxana Gunny, Roberta Battini, Eugenio Mercuri, Mary M. Reilly, Francesco Muntoni, Tarek Yousry	8
10	Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants 2019 ·Journal of Neurology ·Francesco Nicita, Fabrizia Stregapede, Alessandra Tessa, Maria Teresa Bassi, Aleksandra Jezela‐Stanek, Guido Primiano, Antonio Pizzuti, Melissa Barghigiani, (unknown), Ginevra Zanni, Serenella Servidei, Guja Astrea, Elena Panzeri, Cristina Maghini, Luciana Losito, Rafał Płoski, Piotr Gasperowicz, Filippo M. Santorelli, Enrico Bertini, Lorena Travaglini	13
11	Italian recommendations for diagnosis and management of congenital myasthenic syndromes 2018 ·Neurological Sciences ·Lorenzo Maggi, Pia Bernasconi, Adele D’Amico, Raffaella Brugnoni, Chiara Fiorillo, Matteo Garibaldi, Guja Astrea, Claudio Bruno, Filippo M. Santorelli, Rocco Liguori, Giovanni Antonini, Amelia Evoli, Enrico Bertini, Carmelo Rodolico, Renato Mantegazza	24
12	Congenital myopathies: clinical phenotypes and new diagnostic tools 2017 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·(unknown), Denise Cassandrini, Rosanna Trovato, Anna Rubegni, (unknown), Chiara Fiorillo, (unknown), Carlo Minetti, Guja Astrea, Claudio Bruno, Filippo M. Santorelli	70
13	TMEM5-associated dystroglycanopathy presenting with CMD and mild limb-girdle muscle involvement 2016 ·Neuromuscular Disorders ·Guja Astrea, Ilaria Pezzini, (unknown), Rosa Pasquariello, Francesca Moro, Manuela Ergoli, Paola D′Ambrosio, Adele D’Amico, Luisa Politano, Filippo M. Santorelli	12
14	A Diagnostic Dilemma in a Family With Cystinuria Type B Resolved by Muscle Magnetic Resonance 2015 ·Pediatric Neurology ·Guja Astrea, Iulia Munteanu, Denise Cassandrini, Suzanne Lillis, Rosanna Trovato, Elena Pegoraro, Giovanni Cioni, Eugenio Mercuri, Francesco Muntoni, Roberta Battini	4
15	Friedreich’s Ataxia Presenting as Isolated Spastic Paraparesis 2014 ·Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Alessandra Tessa, Chiara Fiorillo, D. De Grandis, Guja Astrea, Silvia Perazza, Alessandro Filla, Filippo M. Santorelli	1
16	Novel mutations in the fukutin gene in a boy with asymptomatic hyperCKemia 2013 ·Neuromuscular Disorders ·Chiara Fiorillo, Francesca Moro, Guja Astrea, Maria Aurora Morales, (unknown), Maria Marchese, Sara Scapolan, Claudio Bruno, Roberta Battini, Filippo M. Santorelli	4
17	Polymorphisms in folate and homocysteine metabolising genes and chromosome damage in young mothers of Down syndrome children and in controls 2007 ·American Journal of Medical Genetics Part A ·Fabio Coppedè, Renato Colognato, (unknown), Guja Astrea, Stefania Bargagna, Gabriele Siciliano, Lucia Migliore	2
18	Polymorphisms in folate and homocysteine metabolizing genes and chromosome damage in mothers of Down syndrome children 2007 ·American Journal of Medical Genetics Part A ·Fabio Coppedè, Renato Colognato, (unknown), Guja Astrea, Stefania Bargagna, Gabriele Siciliano, Lucia Migliore	35
19	Folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women 2006 ·American Journal of Medical Genetics Part A ·Fabio Coppedè, Giulia Marini, Stefania Bargagna, Liborio Stuppia, Fabrizio Minichilli, (unknown), Renato Colognato, Guja Astrea, Giandomenico Palka, Lucia Migliore	69
20	Rapporti tra abilità linguistiche, cognitive e profili di sviluppo adattivo in giovani adulti con Sindrome di Down 2004 ·Psicologia clinica dello sviluppo ·Stefania Bargagna, (unknown), Anastasia Dressler, (unknown), (unknown), Guja Astrea, (unknown), Anna Maria Chilosi	3

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