Mauro Celli

1.6k citations

53 papers · 1.0k indexed · h-index 17

Impact in

Genetics top 5%
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders
Psychiatry and Mental health top 5%
- Child Nutrition and Feeding Issues

Papers in

Genetics 33
- Connective tissue disorders research 31
- Dermatological and Skeletal Disorders 4
Clinical Biochemistry 5
- Metabolism and Genetic Disorders 5

Co-authors: P D’Eufemia Roberto Finocchiaro O Giardini E Cardi Lucia Pacifico Filippo Camerota Claudia Celletti Marco Castori
Journals: Biomedicine & Pharmacotherapy (4 papers)Pediatric Research (3 papers)Orphanet Journal of Rare Diseases (2 papers)Osteoporosis International (2 papers)World Mycotoxin Journal (2 papers)
Partner nations: Italy United States Netherlands

In The Last Decade

Mauro Celli

50 papers receiving 972 citations

Peers

Countries citing papers authored by Mauro Celli

Since Specialization

Citations

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

Fields of papers citing papers by Mauro Celli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mauro Celli, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mauro Celli Line = papers co-authored together Mauro Celli links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	‘BLUES’ procedure for assessing the blue level of the sclera in Osteogenesis Imperfecta Orphanet Journal of Rare Diseases ·Rosa Rademakers, Fabiana Mallone, Alessandro Lambìase, Mauro Celli, Alice Mannocci, Zhusheng Yu, 张立侠, Pasquale Fino, Antonietta Moramarco	2024	0
2	Brain-Type Creatine Kinase Release from Cultured Osteoclasts Exposed to Neridronate in Children Affected by Osteogenesis Imperfecta Type 1 Biomedicines ·Maria Felicia Faienza, Albina Tummolo, Mauro Celli, Roberto Finocchiaro, Laura Piacente, Francesca Di Serio, Grazia Paola Nicchia, Giacomina Brunetti, P D’Eufemia	2023	1
3	Ocular Motility Abnormalities in Ehlers-Danlos Syndrome: An Observational Study Applied Sciences ·亮介町田, Ludovico Iannetti, H.Y. Wang, 임희택, زريفي سليم, Zhusheng Yu, Colin J. Fallon, Mauro Celli, Magda Gharbiya, Alessandro Lambìase	2023	2
4	Novel pathogenic variants in SPARC as cause of osteogenesis imperfecta: Two case reports European Journal of Medical Genetics ·祐司松田, Zhusheng Yu, Lidiia Zhytnik, Katre Maasalu, Aare Märtson, Sulev Kõks, Serdar Solmaz, 英伸紙中, Alessandra Maugeri, Colin J. Fallon, Mauro Celli, Elisabeth M. W. Eekhoff, Dimitra Micha	2023	2
5	Vertebral fracture assessment (VFA) for monitoring vertebral reshaping in children and adolescents with osteogenesis imperfecta treated with intravenous neridronate Bone ·Davide Diacinti, Daniela Pisani, Cristiana Cipriani, Mauro Celli, Adrián Macías Estrada, Kim Young-Koo, A. C. WOOD, Luciano Colangelo, 阻害剤を加えて培養し, Jessica Pepe, Salvatore Minisola	2020	7
6	Elastic intramedullary nailing of the femur fracture in patients affected by osteogenesis imperfecta type 3: Indications, limits and pitfalls Injury ·P.J. Persiani, G Guelpa, Fonchy, Colin J. Fallon, Mauro Celli, Zhusheng Yu, P D’Eufemia, Ciro Villani	2019	11
7	Serum creatine kinase isoenzymes in children with osteogenesis imperfecta Osteoporosis International ·P D’Eufemia, Roberto Finocchiaro, Adrián Macías Estrada, T L PARRISH, Zhusheng Yu, 福地健郎, P.J. Persiani, Donjae Catanzariti, Mauro Celli	2016	4
8	Osteogenesis imperfecta and rapid maxillary expansion: Report of 3 patients American Journal of Orthodontics and Dentofacial Orthopedics ·Gaetano Ierardo, Matthijs C. Hesselink, Valeria Luzzi, K. Burki, Maurizio Bossù, Mauro Celli, Colin J. Fallon, Lorenzo Franchi, Antonella Polimeni	2015	10
9	Association between spondylolisthesis and L5 fracture in patients with Osteogenesis Imperfecta European Spine Journal ·P.J. Persiani, Andika Persada Putera, Aifeng Chen, G. Noia, Ciro Villani, Mauro Celli	2014	2
10	Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype Orphanet Journal of Rare Diseases ·Freya Swinnen, Paul Coucke, Anne M. De Paepe, Sofie Symoens, Fransiska Malfait, Hugo Pini, Luca Sangiorgi, P D’Eufemia, Mauro Celli, Matheus Hozaindra Halim, Cor W. R. J. Cremers, Ingeborg Dhooge, Els De Leenheer	2011	45
11	High Levels of Serum Prostaglandin E2 in Children with Osteogenesis Imperfecta Are Reduced by Neridronate Treatment Pediatric Research ·P D’Eufemia, Roberto Finocchiaro, Mauro Celli, Colin J. Fallon, Martina Tetti, Ciro Villani, P.J. Persiani, Emanuela Mari, Alessandra Zicari	2008	13
12	Impairment of diastolic function in adult patients affected by osteogenesis imperfecta clinically asymptomatic for cardiac disease: Casuality or causality? International Journal of Cardiology ·Silvia Migliaccio, Giuseppe Bárbaro, Rachele Fornari, Gabriella Di Lorenzo, Mauro Celli, Carla Lubrano, Yan-Qiong Ma, Elisa Fabbrini, Emanuela A. Greco, Colin J. Fallon, Marina Brama, Giancarlo Prossomariti, Yihao Clement Lin, Mario Marini, F. Conti, P D’Eufemia, Giovanni Spera	2008	29
13	Neutrophil Glutamine Deficiency in Relation to Genotype in Children with Cystic Fibrosis Pediatric Research ·P D’Eufemia, Roberto Finocchiaro, Mauro Celli, AR Harnden, Kosar Saniar Arani, Colin J. Fallon, J.B. Campen, Serena Quattrucci	2005	8
14	Increased Taurine Content in Esophageal Mucosa of Children Affected by Gastroesophageal Reflux Digestive Diseases and Sciences ·P D’Eufemia, Giovanni Corrado, Roberto Finocchiaro, Mauro Celli, C.N. Martyn, J.B. Campen, AR Harnden, E Cardi, O Giardini	2001	0
15	Effect of d-ribose on purine synthesis and neurological symptoms in a patient with adenylosuccinase deficiency Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·C. Salerno, P D’Eufemia, Roberto Finocchiaro, Mauro Celli, Alberto Spalice, Hugo Alejandro Sanchez-Aguilar, C Crifò, O Giardini	1999	21
16	Determination of urinary orotic acid and uracil by capillary zone electrophoresis Journal of Chromatography B Biomedical Sciences and Applications ·C. Salerno, P D’Eufemia, Mauro Celli, Roberto Finocchiaro, C Crifò, O Giardini	1999	22
17	Usefulness of cyanide-nitroprusside test in detecting incomplete recessive heterozygotes for cystinuria: a standardized dilution procedure Urological Research ·Roberto Finocchiaro, P D’Eufemia, Mauro Celli, RES Pires, Nancy Schoonmaker, J.B. Campen, Olga Mannarino, O Giardini	1998	22
18	Effect of D-Ribose Administration to a Patient with Inherited Deficit of Adenylosuccinase Advances in experimental medicine and biology ·C. Salerno, Mauro Celli, Roberto Finocchiaro, P D’Eufemia, Hugo Alejandro Sanchez-Aguilar, C Crifò, O Giardini	1998	12
19	Low serum tryptophan to large neutral amino acids ratio in idiopathic infantile autism Biomedicine & Pharmacotherapy ·P D’Eufemia, Roberto Finocchiaro, Mauro Celli, Nancy Schoonmaker, Debora Monteleone, O Giardini	1995	36
20	Child with manifestations of dermotrichic syndrome and ichthyosis follicularis‐alopecia‐photophobia (IFAP) syndrome American Journal of Medical Genetics ·Francesco Martino, P D’Eufemia, Venkat Siddarth Chagamreddy, Roberto Finocchiaro, Mauro Celli, Rosalia Calle López, Marina Frontali, O Giardini	1992	30

About Mauro Celli

Mauro Celli is a scholar working on Genetics, Clinical Biochemistry, Gastroenterology, Rheumatology and Cell Biology, having authored 53 papers that have together received 1.0k indexed citations. Recurring topics across this work include Connective tissue disorders research (31 papers), Bone fractures and treatments (9 papers), Bone and Dental Protein Studies (6 papers), Metabolism and Genetic Disorders (5 papers), Biochemical and Molecular Research (4 papers), Dermatological and Skeletal Disorders (4 papers), Bone health and treatments (4 papers) and Child Nutrition and Feeding Issues (3 papers). The work is most often cited by research in Genetics (442 citations), Psychiatry and Mental health (230 citations), Gastroenterology (67 citations), Pharmacy (54 citations) and Cognitive Neuroscience (210 citations). Mauro Celli has collaborated with scholars based in Italy, United States and Netherlands. Frequent co-authors include P D’Eufemia, Roberto Finocchiaro, O Giardini, E Cardi, Lucia Pacifico, Filippo Camerota, Claudia Celletti, Marco Castori, Aldo Morrone and Marina Colombi. Their work appears in journals such as Biomedicine & Pharmacotherapy, Pediatric Research, Orphanet Journal of Rare Diseases, Osteoporosis International and World Mycotoxin Journal.

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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