Bruno Bembi

8.4k total citations
133 papers, 5.4k citations indexed

About

Bruno Bembi is a scholar working on Physiology, Organic Chemistry and Cell Biology. According to data from OpenAlex, Bruno Bembi has authored 133 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 115 papers in Physiology, 43 papers in Organic Chemistry and 40 papers in Cell Biology. Recurrent topics in Bruno Bembi's work include Lysosomal Storage Disorders Research (115 papers), Carbohydrate Chemistry and Synthesis (42 papers) and Cellular transport and secretion (40 papers). Bruno Bembi is often cited by papers focused on Lysosomal Storage Disorders Research (115 papers), Carbohydrate Chemistry and Synthesis (42 papers) and Cellular transport and secretion (40 papers). Bruno Bembi collaborates with scholars based in Italy, United States and United Kingdom. Bruno Bembi's co-authors include Andrea Dardis, Giovanni Ciana, María Gabriela Pittis, Eugen Mengel, Stefania Zampieri, Mirella Filocamo, Neal J. Weinreb, Mercedes Roca‐Espiau, Richard Wenstrup and Anders Erikson and has published in prestigious journals such as The Lancet, Nucleic Acids Research and SHILAP Revista de lepidopterología.

In The Last Decade

Bruno Bembi

133 papers receiving 5.2k citations

Peers

Countries citing papers authored by Bruno Bembi

Since Specialization

Citations

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

Fields of papers citing papers by Bruno Bembi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bruno Bembi

This figure shows the co-authorship network connecting the top 25 collaborators of Bruno Bembi. A scholar is included among the top collaborators of Bruno Bembi 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 Bruno Bembi. Bruno Bembi 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	Twelve Years of the Gaucher Outcomes Survey (GOS): Insights, Achievements, and Lessons Learned from a Global Patient Registry 2024 ·Journal of Clinical Medicine ·Deborah Elstein, Nadia Belmatoug, Bruno Bembi, Patrick Deegan, (unknown), Pilar Giraldo, Özlem Göker-Alpan, Derralynn Hughes, Heather Lau, Elena Lukina, Shoshana Revel‐Vilk, Ida Vanessa Döederlein Schwartz, (unknown), Jaco Botha, Noga Gadir, (unknown), Ari Zimran	2
2	Mechanistic convergence and shared therapeutic targets in Niemann‐Pick disease 2019 ·Journal of Inherited Metabolic Disease ·Alexandria Colaço, (unknown), Elias Adriaenssens, Lianne C. Davis, Stefania Zampieri, (unknown), Chong Yew Tan, Patrick Deegan, Forbes D. Porter, (unknown), Bruno Bembi, Andrea Dardis, Frances M. Platt	15
3	A genetic modifier of symptom onset in Pompe disease 2019 ·EBioMedicine ·Atze J. Bergsma, Stijn L.M. in ‘t Groen, (unknown), (unknown), Nadine A. M. E. van der Beek, Benedikt Schoser, António Toscano, Olimpia Musumeci, Bruno Bembi, Andrea Dardis, Amelia Morrone, Albina Tummolo, Elisabetta Pasquini, Ans T. van der Ploeg, W.W.M. Pim Pijnappel	33
4	Glycogen Reduction in Myotubes of Late-Onset Pompe Disease Patients Using Antisense Technology 2017 ·Molecular Therapy ·(unknown), Paolo Peruzzo, Bruno Bembi, Andrea Dardis, Emanuele Buratti	25
5	Altered localization and functionality of TAR DNA Binding Protein 43 (TDP-43) in niemann- pick disease type C 2016 ·Acta Neuropathologica Communications ·Andrea Dardis, Stefania Zampieri, Sonia Canterini, Kathy L. Newell, Cristiana Stuani, Jill R. Murrell, Bernardino Ghetti, Maria Teresa Fiorenza, Bruno Bembi, Emanuele Buratti	29
6	Changing Characteristics of Late-Onset Pompe Disease Patients in Italy: Data from the Pompe Registry 2015 ·Journal of Neuromuscular Diseases ·C. Angelini, Bruno Bembi, Alberto Burlina, Massimiliano Filosto, Maria Antonietta Maioli, Lucía Morandi, Rossella Parini, Elena Pegoraro, Sabrina Ravaglia, Serenella Servidei, António Toscano, V. Tugnoli	1
7	Efficacy of Miglustat in Niemann–Pick C disease: A single centre experience 2013 ·Molecular Genetics and Metabolism ·(unknown), Adele D’Amico, Enrico Bertini, (unknown), Andrea Dardis, Daniela Verrigni, Bruno Bembi, Carlo Dionisi‐Vici, Federica Deodato	16
8	The angiotensin-converting enzyme insertion/deletion polymorphism modifies the clinical outcome in patients with Pompe disease 2010 ·Genetics in Medicine ·Paola De Filippi, Sabrina Ravaglia, Bruno Bembi, Alfredo Costa, Arrigo Moglia, G. Piccolo, Alessandra Repetto, Andrea Dardis, Giuseppe Greco, Giovanni Ciana, (unknown), Cesare Danesino	24
9	Identification and characterization of 15 novel GALC gene mutations causing Krabbe disease 2010 ·Human Mutation ·Barbara Tappino, Roberta Biancheri, Matthew Mort, Stefano Regis, Fabio Corsolini, Andrea Rossi, Marina Stroppiano, Susanna Lualdi, Agata Fiumara, Bruno Bembi, Maja Di Rocco, D.N. Cooper, Mirella Filocamo	90
10	Oxidative stress in NPC1 deficient cells: protective effect of allopregnanolone 2008 ·Journal of Cellular and Molecular Medicine ·Stefania Zampieri, Synthia H. Mellon, Terry D. Butters, (unknown), Douglas F. Covey, Bruno Bembi, Andrea Dardis	99
11	Post-marketing surveillance of miglustat in type 1 Gaucher disease (GD1) 2007 ·UCL Discovery (University College London) ·Derralynn Hughes, (unknown), Barbara Schwierin, Bruno Bembi	1
12	Mutation profile of theGAA gene in 40 Italian patients with late onset glycogen storage disease type II 2006 ·Human Mutation ·(unknown), Bruno Bembi, (unknown), Mirella Filocamo, Giancarlo Parenti, Massimiliano Rossi, Luciano Merlini, Emanuele Buratti, Paola De Filippi, Andrea Dardis, Marina Stroppiano, Giovanni Ciana, María Gabriela Pittis	103
13	Skeletal aspects of Gaucher disease: a review 2002 ·British Journal of Radiology ·Richard Wenstrup, Mercedes Roca‐Espiau, Neal J. Weinreb, Bruno Bembi	182
14	Response of Gaucher bone disease to enzyme replacement therapy 2002 ·British Journal of Radiology ·L. Poll, Mario Maas, Michael R. Terk, Mercedes Roca‐Espiau, Bruno Bembi, Giovanni Ciana, Neal J. Weinreb	67
15	Two novel mutations of the human Δ7-sterol reductase (DHCR7) gene in children with Smith–Lemli–Opitz syndrome 2002 ·Molecular and Cellular Probes ·Carlo Patrono, Carlo Dionisi‐Vici, Aldo Giannotti, Bruno Bembi, M. Cristina Digilio, Cristiano Rizzo, Cristina Purificato, C. Martini, (unknown), Filippo M. Santorelli	13
16	Sea-blue histiocytosis secondary to Niemann-Pick disease type B: a case report 2001 ·Annals of Hematology ·Anna Candoni, (unknown), Paolo Doretto, Renato Fanin, (unknown), Bruno Bembi	13
17	Intravenous pamidronate treatment in osteogenesis imperfecta 1997 ·The Journal of Pediatrics ·Bruno Bembi, (unknown), (unknown), (unknown), Mirko Zanatta, Carmen Martini, Giovanni Ciana	100
18	A rare G6490 → substitution at the last nucleotide of exon 10 of the glucocerebrosidase gene in two unrelated Italian Gaucher patients 1995 ·Clinical Genetics ·Marco Seri, Mirella Filocamo, Fabio Corsolini, Bruno Bembi, (unknown), Rosanna Gatti	9
19	Enzyme replacement treatment in type 1 and type 3 Gaucher's disease 1994 ·The Lancet ·Bruno Bembi, (unknown), Mirko Zanatta, Marco Carrozzi, Rosalba Gornati, B. Berra, Francisco E. Baralle	53
20	Y418C: a novel mutation in exon 9 of the glucocerebrosidase gene of a patient with Gaucher disease creates a new Bgl I site 1994 ·Human Genetics ·Renu Tuteja, Narendra Tuteja, Franco Lilliu, Bruno Bembi, Renzo Galanello, Antonio Cao, Francisco E. Baralle	11

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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