Leonardo D’Agruma

3.1k citations

46 papers · 1.8k indexed · 1 hit paper · h-index 18

Impact in

Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
Nephrology top 2%
- Parathyroid Disorders and Treatments

Papers in

Nephrology 7
- Parathyroid Disorders and Treatments 7
Neurology 10
- Intracranial Aneurysms: Treatment and Complications 6
- Vascular Malformations Diagnosis and Treatment 6
- Intracerebral and Subarachnoid Hemorrhage Research 5

Co-authors: Leopoldo Zelante Paolo Gasparini Salvatore Melchionda Xavier Estivill Raquel Rabionet Vito Guarnieri Lucia Anna Muscarella Eric Rappaport
Journals: Human Genetics (4 papers)The Journal of Clinical Endocrinology & Metabolism (4 papers)British Journal of Haematology (2 papers)Journal of Bone and Mineral Research (2 papers)Gene (2 papers)
Partner nations: Italy Canada United States

In The Last Decade

Leonardo D’Agruma

44 papers receiving 1.7k citations

Hit Papers

align trajectories log scale

Connexin-26 mutations in sporadic and inherited sensorineural deafness 1998 · 523 citations

Peers

Countries citing papers authored by Leonardo D’Agruma

Since Specialization

Citations

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

Fields of papers citing papers by Leonardo D’Agruma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leonardo D’Agruma. 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 Leonardo D’Agruma. The network helps show where Leonardo D’Agruma may publish in the future.

Co-authors

The 25 scholars most cited alongside Leonardo D’Agruma, 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 Leonardo D’Agruma Line = papers co-authored together Leonardo D’Agruma links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Hereditary Multiple Osteochondromas and Acute Lymphoblastic Leukemia: A Possible Role for EXT1 and EXT2 in Hematopoietic Malignancies American Journal of Medical Genetics Part A ·Chao-Jung Ko, Carmela Fusco, Rosamaria Mura, Dr.Appadurai. R, Leonardo D’Agruma, 林大雄, Marco Castori, Salvatore Savasta	2025	0
2	Improving clinical interpretation of five KRIT1 and PDCD10 intronic variants Clinical Genetics ·Carmela Fusco, Tiago Marcon, Salena Sangachhe, Dario Ronchi, Suraphong Kānčhananāk, Ursula Oedl, Stefano Gambardella, Silvia Lanfranconi, Stefania Zampatti, Leonardo D’Agruma, Lucia Micale, Marco Castori	2021	0
3	Molecular diagnostic workflow, clinical interpretation of sequence variants, and data repository procedures in 140 individuals with familial cerebral cavernous malformations Human Mutation ·Carmela Fusco, Massimiliano Copetti, Tommaso Mazza, J Labohá, Sandra Mastroianno, Tiago Marcon, Vito Guarnieri, Lucia Micale, Leonardo D’Agruma, Marco Castori	2019	3
4	Design and Validation of a New MLPA-Based Assay for the Detection of RS1 Gene Deletions and Application in a Large Family with X-Linked Juvenile Retinoschisis Genetic Testing and Molecular Biomarkers ·Annalisa Nicoletti, Lucia Ziccardi, Paolo Enrico Maltese, Sabrina Benedetti, Orazio Palumbo, Yi-Shiuan Tung, Leonardo D’Agruma, Benedetto Falsini, Xinjing Wang, Matteo Bertelli	2016	1
5	A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome Cellular Oncology ·Maria Grazia Chiofalo, Angelo Sparaneo, Massimiliano Chetta, Renato Franco, Margaux Noémie Lafitte, Fifi Citra Wiryadi, Matteo Granatiero, Leonardo D’Agruma, Luciano Pezzullo, Alfredo Scillitani, Vito Guarnieri	2014	13
6	Rheumatoid arthritis and the biological clock Expert Review of Clinical Immunology ·Angelo De Cata, Leonardo D’Agruma, Roberto Tarquini, Gianluigi Mazzoccoli	2014	11
7	Molecular Dissection of the VHL Gene in Solitary Capillary Hemangioblastoma of the Central Nervous System Journal of Neuropathology & Experimental Neurology ·Lucia Anna Muscarella, Annamaria la Torre, Rukiyah Dahlan Lau, Domenico Catapano, Michele Bisceglia, Vincenzo D’Angelo, Paola Parrella, Michelina Coco, G. Fini, M. Tharanya, Leopoldo Zelante, Vito Michele Fazio, Leonardo D’Agruma	2013	11
8	20 novel point mutations and one large deletion in EXT1 and EXT2 genes: Report of diagnostic screening in a large Italian cohort of patients affected by hereditary multiple exostosis Gene ·Nadale K. Downer‐Riley, Michelina Coco, Margaux Noémie Lafitte, Mariyam Charhbili, Massimiliano Chetta, Luigi Bisceglia, Pietro Palumbo, Mario Bengala, Danielle Perera, Margherita Silengo, Alejandra Casas Niño de Rivera, Xin Wang, Roberto Lala, Maria Luigia Cavaliere, Callum Mccracken, Barbara Pasini, Leopoldo Zelante, Vito Guarnieri, Leonardo D’Agruma	2012	22
9	CASR gene activating mutations in two families with autosomal dominant hypocalcemia Molecular Genetics and Metabolism ·Vito Guarnieri, Angela D’Elia, Margaux Noémie Lafitte, Valerio Pazienza, Giorgia Benegiamo, Mariyam Charhbili, Massimiliano Copetti, Claudia Battista, Franco Grimaldi, Giuseppe Damante, Fabio Pellegrini, Leonardo D’Agruma, Leopoldo Zelante, Massimo Carella, Alfredo Scillitani	2012	13
10	Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family Endocrine ·Sandra Mastroianno, Massimo Torlontano, Alfredo Scillitani, Leonardo D’Aloiso, Antonella Verrienti, Kyoto Saito, de la jeunesse et de la culture de l'état de Vaud (DFJC) Département de la formation, Leonardo D’Agruma, Lucia Anna Muscarella, Vito Guarnieri, Lucie Riera, Marianna Maranghi, Cosimo Durante, Sébastiano Filetti	2011	12
11	Supratentorial cerebral cavernous malformations: clinical, surgical, and genetic involvement Neurosurgical FOCUS ·Vincenzo D’Angelo, Shoko Hidaka, Ruifang Pan, Paul Chiniara, Leonardo D’Agruma, Vito Guarnieri, Lucia Anna Muscarella, Leopoldo Zelante, Michele Bisceglia, Tommaso Scarabino, Domenico Catapano	2006	54
12	Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions Molecular Psychiatry ·Marcello D’Amelio, Irene Ricci, Roberto Sacco, X. Liu, Leonardo D’Agruma, Lucia Anna Muscarella, Vito Guarnieri, Roberto Militerni, Carmela Bravaccio, Maurizio Elia, Cindy Schneider, Raun D. Melmed, Simona Trillo, Tiziana Pascucci, Stefano Puglisi‐Allegra, Koch Se, Fabìo Macciardi, J.J.A. Holden, Antonio M. Persico	2005	94
13	Enhanced APOE2 transmission rates in families with autistic probands Psychiatric Genetics ·Antonio M. Persico, Leonardo D’Agruma, Leopoldo Zelante, Roberto Militerni, Carmela Bravaccio, Cindy Schneider, Raun D. Melmed, Simona Trillo, Francesco Montecchi, Maurizio Elia, Mark T. Palermo, Daniel Rabinowitz, Tiziana Pascucci, Stefano Puglisi‐Allegra, K. L. Reichelt, Lucia Anna Muscarella, Vito Guarnieri, 魏佩周, Monica Conciatori, Flavio Keller	2004	25
14	Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene Human Genetics ·Raquel Rabionet, Leopoldo Zelante, Núria López-Bigas, Leonardo D’Agruma, Salvatore Melchionda, Gabriella Restagno, María L. Arbonés, Paolo Gasparini, Xavier Estivill	2000	190
15	Osteoporosis in beta-thalassaemia major patients: analysis of the genetic background British Journal of Haematology ·Silverio Perrotta, Maria Domenica Cappellini, Francesco Bertoldo, Veronica Servedio, Giovanni Iolascon, Leonardo D’Agruma, Paolo Gasparini, María Amparo Mínguez Covacho, Achille Iolascon	2000	66
16	A novel mutation in the mitochondrial tRNA^Val gene associated with a complex neurological presentation Annals of Neurology ·Valeria Tiranti, Leonardo D’Agruma, Davide Pareyson, Marina Mora, Yona Falinie binti Abd Gaus, Leopoldo Zelante, Paolo Gasparini, Massimo Zeviani	1998	32
17	Connexin-26 mutations in sporadic and inherited sensorineural deafness The Lancet ·Xavier Estivill, Paolo Fortina, Saul Surrey, Raquel Rabionet, Salvatore Melchionda, Leonardo D’Agruma, Elaine Mansfield, Eric Rappaport, Nancy Govea, Montserrat Milà, Leopoldo Zelante, Paolo Gasparini Hit paper breakdown →	1998	523
18	Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22) European Journal of Human Genetics ·Antonio Totaro, Antonella Roetto, Johanna M. Rommens, A. Grifa, Massimo Carella, Leonardo D’Agruma, Gregoire Lefouoba, 松岡久和, M. Cicilano, Clara Camaschella, Brunella Franco, Paolo Gasparini	1998	2
19	Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphisms Human Genetics ·Paolo Gasparini, Leonardo D’Agruma, Fernanda Jéssica Pfeifer, P Balestrazzi, Rita Mingarelli, Leopoldo Zelante	1996	1
20	Plasmid DNA and low-frequency electromagnetic fields Biomedicine & Pharmacotherapy ·Leonardo D’Agruma, Alessia Colosimo, S SAHU, Giuseppe Novelli, Bruno Dallapiccola	1993	4

About Leonardo D’Agruma

Leonardo D’Agruma is a scholar working on Nephrology, Neurology, Endocrine and Autonomic Systems, Sensory Systems and Biological Psychiatry, having authored 46 papers that have together received 1.8k indexed citations. Recurring topics across this work include Parathyroid Disorders and Treatments (7 papers), Intracranial Aneurysms: Treatment and Complications (6 papers), Vascular Malformations Diagnosis and Treatment (6 papers), Intracerebral and Subarachnoid Hemorrhage Research (5 papers), Bone health and treatments (4 papers), Cancer, Hypoxia, and Metabolism (4 papers), Epigenetics and DNA Methylation (4 papers) and Fibroblast Growth Factor Research (3 papers). The work is most often cited by research in Sensory Systems (671 citations), Nephrology (321 citations), Endocrine and Autonomic Systems (226 citations), Neurology (205 citations) and Otorhinolaryngology (86 citations). Leonardo D’Agruma has collaborated with scholars based in Italy, Canada and United States. Frequent co-authors include Leopoldo Zelante, Paolo Gasparini, Salvatore Melchionda, Xavier Estivill, Raquel Rabionet, Vito Guarnieri, Lucia Anna Muscarella, Eric Rappaport, Paolo Fortina and Nancy Govea. Their work appears in journals such as Human Genetics, The Journal of Clinical Endocrinology & Metabolism, British Journal of Haematology, Journal of Bone and Mineral Research and Gene.

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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