Cecilia Giunta

6.1k total citations
69 papers, 2.4k citations indexed

About

Cecilia Giunta is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Cecilia Giunta has authored 69 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Genetics, 24 papers in Molecular Biology and 20 papers in Rheumatology. Recurrent topics in Cecilia Giunta's work include Connective tissue disorders research (44 papers), Dermatological and Skeletal Disorders (17 papers) and Bone and Dental Protein Studies (10 papers). Cecilia Giunta is often cited by papers focused on Connective tissue disorders research (44 papers), Dermatological and Skeletal Disorders (17 papers) and Bone and Dental Protein Studies (10 papers). Cecilia Giunta collaborates with scholars based in Switzerland, Italy and United States. Cecilia Giunta's co-authors include Beat Steinmann, Marianne Rohrbach, Fransiska Malfait, Tomoki Kosho, Marius Kraenzlin, Clair A. Francomano, Peter H. Byers, Marco Castori, David R. Eyre and Uschi Lindert and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Bone and Joint Surgery.

In The Last Decade

Cecilia Giunta

67 papers receiving 2.3k citations

Peers

Countries citing papers authored by Cecilia Giunta

Since Specialization

Citations

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

Fields of papers citing papers by Cecilia Giunta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cecilia Giunta

This figure shows the co-authorship network connecting the top 25 collaborators of Cecilia Giunta. A scholar is included among the top collaborators of Cecilia Giunta 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 Cecilia Giunta. Cecilia Giunta 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	Physiological cell bioprinting density in human bone-derived cell-laden scaffolds enhances matrix mineralization rate and stiffness under dynamic loading 2024 ·Frontiers in Bioengineering and Biotechnology ·(unknown), (unknown), Pei Jin Lim, Jianhua Zhang, (unknown), (unknown), Marianne Rohrbach, Cecilia Giunta, (unknown), Marina Rubert, Ralph Müller	6
2	COL1-Related Disorders: Case Report and Review of Overlapping Syndromes 2021 ·Frontiers in Genetics ·Maria Gnoli, Evelise Brizola, Morena Tremosini, Elena Pedrini, (unknown), Massimiliano Mosca, (unknown), Paola Castronovo, Cecilia Giunta, Luca Sangiorgi	13
3	Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers‐Danlos syndrome 2020 ·American Journal of Medical Genetics Part A ·(unknown), Neeti Ghali, (unknown), Duncan Baker, (unknown), Angela F. Brady, Maria Luisa Giovannucci Uzielli, Cecilia Giunta, Diana Johnson, Tomoki Kosho, Katherine Neas, F M Pope, Frank Rutsch, (unknown), Glenda Sobey, Anthony Vandersteen, Fleur S. van Dijk	14
4	Obstructive Sleep Apnoea in Children and Adolescents with Ehlers-Danlos Syndrome 2018 ·Respiration ·(unknown), Thomas Gaisl, Cecilia Giunta, Noriane A. Sievi, Florian Singer, Alexander Möller, Marianne Rohrbach, Malcolm Kohler	14
5	Arterial fragility in kyphoscoliotic Ehlers-Danlos syndrome 2018 ·BMJ Case Reports ·Pierrick Henneton, Anne Debost‐Legrand, Cecilia Giunta, Michael Frank	8
6	Expanding the clinical and mutational spectrum of the Ehlers–Danlos syndrome, dermatosparaxis type 2016 ·Genetics in Medicine ·Tim Van Damme, Alain Colige, Delfien Syx, Cecilia Giunta, Uschi Lindert, Marianne Rohrbach, Omid Aryani, Yasemin Alanay, Pelin Özlem Şimşek‐Kiper, Hester Y. Kroes, Koenraad Devriendt, Marc Thiry, Sofie Symoens, Anne De Paepe, Fransiska Malfait	34
7	Urinary pyridinoline cross-links as biomarkers of osteogenesis imperfecta 2015 ·Orphanet Journal of Rare Diseases ·Uschi Lindert, Marius Kraenzlin, Belinda Campos‐Xavier, Matthias R. Baumgartner, Luisa Bonafé, Cecilia Giunta, Marianne Rohrbach	6
8	Bruch’s membrane abnormalities in PRDM5-related brittle cornea syndrome 2015 ·Orphanet Journal of Rare Diseases ·Louise F. Porter, Roberto Gallego‐Pinazo, (unknown), (unknown), Nicoletta Zoppi, Marina Colombi, Cecilia Giunta, R E Bonshek, Forbes Manson, Graeme C. Black	20
9	Hallazgos bucales en niños con enfermedad renal 2013 ·Acta odontológica venezolana ·(unknown), (unknown), Cecilia Giunta, (unknown), (unknown)	1
10	Genotype–phenotype study in type V osteogenesis imperfecta 2013 ·Clinical Dysmorphology ·Meena Balasubramanian, Michael Parker, Ann Dalton, Cecilia Giunta, Uschi Lindert, Luíz César Peres, Bart Wagner, Paul Arundel, Amaka C Offiah, Nicholas Bishop	32
11	Promotion of vesicular zinc efflux by ZIP13 and its implications for spondylocheiro dysplastic Ehlers–Danlos syndrome 2012 ·Proceedings of the National Academy of Sciences ·Jeeyon Jeong, Joel M. Walker, Fudi Wang, J. Genevieve Park, Amy E. Palmer, Cecilia Giunta, Marianne Rohrbach, Beat Steinmann, David Eide	91
12	Recessive osteogenesis imperfecta: Clinical, radiological, and molecular findings 2012 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Marianne Rohrbach, Cecilia Giunta	38
13	Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta 2011 ·Human Mutation ·Víctor Martínez‐Glez, Eulalia Valencia, José A. Caparrós‐Martín, Mona Aglan, Samia A. Temtamy, Jair Tenorio, Verónica Pulido, Uschi Lindert, Marianne Rohrbach, David R. Eyre, Cecilia Giunta, Pablo Lapunzina, Víctor L. Ruiz‐Pérez	155
14	Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency 2010 ·European Journal of Human Genetics ·Janine Meienberg, Marianne Rohrbach, Stefan Neuenschwander, Katharina Spanaus, Cecilia Giunta, (unknown), (unknown), (unknown), Stephan Regenass, Andrea Patrignani, Silvia Azzarello‐Burri, Bernhard Steiner, Anders O.H. Nygren, Thierry Carrel, Beat Steinmann, Gábor Mátyás	28
15	Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13 2008 ·The American Journal of Human Genetics ·Cecilia Giunta, Nursel Elçioğlu, Beate Albrecht, Georg Eich, Céline Chambaz, Andreas Janecke, Heather N. Yeowell, MaryAnn Weis, David R. Eyre, Marius Kraenzlin, Beat Steinmann	149
16	Nevo syndrome is allelic to the kyphoscoliotic type of the Ehlers–Danlos syndrome (EDS VIA) 2005 ·American Journal of Medical Genetics Part A ·Cecilia Giunta, Ann Randolph, (unknown), Han G. Brunner, Marius Kraenzlin, Beat Steinmann	47
17	Brittle cornea syndrome and its delineation from the kyphoscoliotic type of Ehlers–Danlos syndrome (EDS VI): Report on 23 patients and review of the literature 2003 ·American Journal of Medical Genetics Part A ·Hailah Al‐Hussain, Steffen M. Zeisberger, Peter Huber, Cecilia Giunta, Beat Steinmann	52
18	COL5A1 Haploinsufficiency Is a Common Molecular Mechanism Underlying the Classical Form of EDS 2000 ·The American Journal of Human Genetics ·Richard Wenstrup, Jane B. Florer, Marcia Willing, Cecilia Giunta, Beat Steinmann, Felix Young, Miki Susic, William G. Cole	91
19	Sibs affected with both Ehlers-Danlos syndrome type VI and cystic fibrosis 1998 ·American Journal of Medical Genetics ·Andrea Jarisch, Cecilia Giunta, Stefan Zielen, (unknown), Beat Steinmann	15
20	RAPD analysis of systematic relationships among the Cervidae 1996 ·Heredity ·Sergio Comincini, (unknown), Claudio Bandi, Cecilia Giunta, Michele Rubini, Francesco Fontana	37

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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