Renata Bocciardi

4.4k total citations · 1 hit paper
64 papers, 2.3k citations indexed

About

Renata Bocciardi is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Rheumatology. According to data from OpenAlex, Renata Bocciardi has authored 64 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 21 papers in Pulmonary and Respiratory Medicine and 19 papers in Rheumatology. Recurrent topics in Renata Bocciardi's work include Heterotopic Ossification and Related Conditions (18 papers), Medical Imaging and Pathology Studies (17 papers) and Parathyroid Disorders and Treatments (13 papers). Renata Bocciardi is often cited by papers focused on Heterotopic Ossification and Related Conditions (18 papers), Medical Imaging and Pathology Studies (17 papers) and Parathyroid Disorders and Treatments (13 papers). Renata Bocciardi collaborates with scholars based in Italy, France and United States. Renata Bocciardi's co-authors include Isabella Ceccherini, Roberto Ravazzolo, Barbara Pasini, Marco Seri, Virginia Barone, Giovanni Romeo, Margherita Lerone, Yin Luo, Giuseppe Martucciello and Patrizia Ronchetto and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Renata Bocciardi

61 papers receiving 2.3k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

1994 532 citations Giovanni Romeo, Yin Luo et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Renata Bocciardi Italy	26	1.0k	852	641	337	299	64	2.3k
M. Le Merrer France	23	983 1.0×	227 0.3×	919 1.4×	164 0.5×	320 1.1×	93	1.8k
Nicolas Chassaing France	25	1.1k 1.1×	392 0.5×	1.2k 1.8×	151 0.4×	175 0.6×	83	2.1k
Yisrael Sidis United States	32	2.1k 2.1×	192 0.2×	568 0.9×	100 0.3×	211 0.7×	47	4.1k
Kelly L. Walton Australia	25	1.4k 1.3×	186 0.2×	285 0.4×	170 0.5×	215 0.7×	53	2.3k
Hatem El‐Shanti United States	28	1.7k 1.6×	475 0.6×	618 1.0×	135 0.4×	604 2.0×	84	2.7k
Satyajit Karnik United States	12	844 0.8×	713 0.8×	556 0.9×	312 0.9×	48 0.2×	15	2.0k
Nadia Sakati Saudi Arabia	22	819 0.8×	215 0.3×	546 0.9×	111 0.3×	123 0.4×	78	1.7k
Emily L. Germain‐Lee United States	24	1.1k 1.1×	236 0.3×	905 1.4×	93 0.3×	195 0.7×	56	1.8k
Donna Y. Deng United States	18	1.1k 1.1×	622 0.7×	244 0.4×	464 1.4×	976 3.3×	36	2.6k
Jussi Merenmies Finland	21	925 0.9×	284 0.3×	263 0.4×	240 0.7×	106 0.4×	44	1.9k

Countries citing papers authored by Renata Bocciardi

Since Specialization

Citations

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

Fields of papers citing papers by Renata Bocciardi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renata Bocciardi

This figure shows the co-authorship network connecting the top 25 collaborators of Renata Bocciardi. A scholar is included among the top collaborators of Renata Bocciardi 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 Renata Bocciardi. Renata Bocciardi 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

Conteduca, Giuseppina, Chiara Baldo, Renata Bocciardi, et al.. (2025). Derivation of the IGGi006-A stem cell line from a patient with CAPRIN1 haploinsufficiency. Stem Cell Research. 85. 103696–103696. 1 indexed citations

Scala, Marcello, Yu Zhang, Mariasavina Severino, et al.. (2025). A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcifications. European Journal of Human Genetics. 34(3). 324–332. 1 indexed citations

Bocciardi, Renata, Nicoletta Pedemonte, Elisabetta Volpe, et al.. (2025). Interplay between ALK2R206H mutant receptor and autophagy signaling regulates receptor stability and its chondrogenic functions. Cell Death Discovery. 11(1). 117–117. 1 indexed citations

Volpedo, Greta, Loretta Ferrera, Federico Zara, et al.. (2024). Antisense oligonucleotides as a precision therapy for developmental and epileptic encephalopathies. CNS Neuroscience & Therapeutics. 30(11). e70050–e70050. 7 indexed citations

Aloi, Concetta, Alessandro Salina, Francesco Caroli, et al.. (2023). Next Generation Sequencing (NGS) Target Approach for Undiagnosed Dysglycaemia. Life. 13(5). 1080–1080. 1 indexed citations

Salina, Alessandro, Marta Bassi, Concetta Aloi, et al.. (2023). “Pesto” Mutation: Phenotypic and Genotypic Characteristics of Eight GCK/MODY Ligurian Patients. International Journal of Molecular Sciences. 24(4). 4034–4034.

Sondo, Elvira, Federico Cresta, Valeria Tomati, et al.. (2022). The L467F-F508del Complex Allele Hampers Pharmacological Rescue of Mutant CFTR by Elexacaftor/Tezacaftor/Ivacaftor in Cystic Fibrosis Patients: The Value of the Ex Vivo Nasal Epithelial Model to Address Non-Responders to CFTR-Modulating Drugs. International Journal of Molecular Sciences. 23(6). 3175–3175. 31 indexed citations

Monti, Paola, et al.. (2021). Evaluating the Influence of a G-Quadruplex Prone Sequence on the Transactivation Potential by Wild-Type and/or Mutant P53 Family Proteins through a Yeast-Based Functional Assay. Genes. 12(2). 277–277. 6 indexed citations

Monti, Paola, Yari Ciribilli, Giorgia Foggetti, et al.. (2019). P63 modulates the expression of theWDFY2gene which is implicated in cancer regulation and limb development. Bioscience Reports. 39(12). 7 indexed citations

10.

Cuoco, Cristina, et al.. (2015). Hypogonadotropic hypogonadism in a trisomy X carrier: phenotype description and genotype correlation. Gynecological Endocrinology. 32(1). 14–17. 1 indexed citations

11.

Tassano, Elisa, Jens Buttgereit, Michael Bäder, et al.. (2013). Genotype-Phenotype Correlation of 2q37 Deletions Including NPPC Gene Associated with Skeletal Malformations. PLoS ONE. 8(6). e66048–e66048. 33 indexed citations

12.

Giacopelli, Francesca, et al.. (2012). The Role of the 3′UTR Region in the Regulation of the ACVR1/Alk-2 Gene Expression. PLoS ONE. 7(12). e50958–e50958. 26 indexed citations

13.

Bocciardi, Renata, Roberto Giorda, Jens Buttgereit, et al.. (2007). Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation. Human Mutation. 28(7). 724–731. 100 indexed citations

14.

Martucciello, Giuseppe, Antonella Brizzolara, A. Favre, et al.. (2007). Neural Crest Neuroblasts Can Colonise Aganglionic and Ganglionic Gut In Vivo. European Journal of Pediatric Surgery. 17(1). 34–40. 30 indexed citations

15.

Gimelli, Giorgio, Stefania Gimelli, Nazzareno Dimasi, et al.. (2006). Identification and molecular modelling of a novel familial mutation in the SRY gene implicated in the pure gonadal dysgenesis. European Journal of Human Genetics. 15(1). 76–80. 24 indexed citations

16.

Musso, Marco, Renata Bocciardi, Sara Parodi, Roberto Ravazzolo, & Isabella Ceccherini. (2006). Betaine, Dimethyl Sulfoxide, and 7-Deaza-dGTP, a Powerful Mixture for Amplification of GC-Rich DNA Sequences. Journal of Molecular Diagnostics. 8(5). 544–550. 92 indexed citations

17.

Griseri, Paola, Renata Bocciardi, Robert M.W. Hofstra, et al.. (2000). A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease. European Journal of Human Genetics. 8(9). 721–724. 37 indexed citations

18.

Griseri, Paola, Renata Bocciardi, Robert M.W. Hofstra, et al.. (1999). Decreased frequency of a neutral sequence variant of the RET proto-oncogene in sporadic Hirschsprung disease.. Data Archiving and Networked Services (DANS). 1 indexed citations

19.

Mograbi, Baharia, Nathalie Rochet, Véronique Imbert, et al.. (1997). Human monocytes express amphiregulin and heregulin growth factors upon activation.. PubMed. 8(1). 73–81. 40 indexed citations

20.

Pasini, Barbara, Maria Grazia Borrello, Angela Greco, et al.. (1995). Loss of function effect of RET mutations causing Hirschsprung disease. Nature Genetics. 10(1). 35–40. 159 indexed citations

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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