Chiara Baldo

1.7k total citations
31 papers, 947 citations indexed

About

Chiara Baldo is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Chiara Baldo has authored 31 papers receiving a total of 947 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 15 papers in Molecular Biology and 7 papers in Oncology. Recurrent topics in Chiara Baldo's work include Genomics and Rare Diseases (6 papers), Genetic Syndromes and Imprinting (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Chiara Baldo is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetic Syndromes and Imprinting (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Chiara Baldo collaborates with scholars based in Italy, United Kingdom and United States. Chiara Baldo's co-authors include Domizia Debernardis, C. Aschele, G Tunesi, Alberto Sobrero, Rita Lionetto, Frank Maley, Giovanna Antonelli, Anna Maria Baldelli, F. Dagna Bricarelli and Paolo Giordani and has published in prestigious journals such as Journal of Clinical Oncology, Biomaterials and Neurology.

In The Last Decade

Chiara Baldo

29 papers receiving 918 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chiara Baldo Italy 15 371 322 228 156 133 31 947
Avinash Mohan United States 14 956 2.6× 306 1.0× 188 0.8× 141 0.9× 371 2.8× 34 1.5k
Gary S. Gottesman United States 20 542 1.5× 209 0.6× 394 1.7× 61 0.4× 148 1.1× 55 1.6k
Jean-Michel Foidart Belgium 14 308 0.8× 256 0.8× 250 1.1× 96 0.6× 62 0.5× 20 1.1k
Tadayuki Akagi Japan 23 766 2.1× 138 0.4× 185 0.8× 114 0.7× 91 0.7× 48 1.2k
Satkiran S. Grewal United States 12 368 1.0× 243 0.8× 93 0.4× 149 1.0× 58 0.4× 16 1.2k
Minjie Luo United States 18 460 1.2× 126 0.4× 306 1.3× 35 0.2× 86 0.6× 65 1.0k
Stephen Tonna Australia 13 609 1.6× 105 0.3× 178 0.8× 29 0.2× 94 0.7× 18 1.3k
Lars Palmqvist Sweden 23 722 1.9× 251 0.8× 117 0.5× 306 2.0× 112 0.8× 67 1.6k
Kazuo Asanoma Japan 21 670 1.8× 235 0.7× 139 0.6× 100 0.6× 35 0.3× 59 1.3k
Shinji Itoyama Japan 20 353 1.0× 478 1.5× 102 0.4× 42 0.3× 337 2.5× 64 1.3k

Countries citing papers authored by Chiara Baldo

Since Specialization
Citations

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

Fields of papers citing papers by Chiara Baldo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chiara Baldo

This figure shows the co-authorship network connecting the top 25 collaborators of Chiara Baldo. A scholar is included among the top collaborators of Chiara Baldo 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 Chiara Baldo. Chiara Baldo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
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
2.
Danesino, Cesare, Federico Biglioli, Laura Moneghini, et al.. (2024). Pleomorphic Parotid Adenoma in a Child Affected with Cri du Chat Syndrome: Clinical, Cytogenetic, and Molecular Analysis. International Journal of Molecular Sciences. 25(19). 10664–10664.
3.
Conteduca, Giuseppina, Davide Cangelosi, Chiara Baldo, et al.. (2024). Impact of NSD1 Alternative Transcripts in Actin Filament Formation and Cellular Division Pathways in Fibroblasts. Genes. 15(9). 1117–1117.
4.
Conteduca, Giuseppina, Chiara Baldo, Sımona Baldassari, et al.. (2024). Generation of IGGi003-A induced pluripotent stem cell line from a patient with Sotos Syndrome carrying c.1633delA NSD1 variant in exon 5. Stem Cell Research. 76. 103324–103324. 1 indexed citations
5.
Conteduca, Giuseppina, Marina Grasso, Maurizio Cecconi, et al.. (2023). Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome. Genes. 14(2). 295–295. 9 indexed citations
6.
Conteduca, Giuseppina, Davide Cangelosi, Simona Coco, et al.. (2022). NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint. Life. 12(7). 988–988. 6 indexed citations
7.
Conteduca, Giuseppina, Chiara Baldo, Michela Malacarne, et al.. (2022). Identification of alternative transcripts of NSD1 gene in Sotos Syndrome patients and healthy subjects. Gene. 851. 146970–146970. 7 indexed citations
8.
Conteduca, Giuseppina, Chiara Baldo, Monica Traverso, et al.. (2022). Generation of induced pluripotent stem cell lines from a patient with Sotos syndrome carrying 5q35 microdeletion. Stem Cell Research. 66. 103007–103007. 1 indexed citations
9.
Capra, Anna Paola, Silvana Briuglia, Chiara Baldo, et al.. (2021). 8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature. Genes. 12(5). 652–652. 12 indexed citations
10.
Ivanovski, Ivan, Stefano Giuseppe Caraffi, Elisa Magnani, et al.. (2019). Alazami syndrome: the first case of papillary thyroid carcinoma. Journal of Human Genetics. 65(2). 133–141. 15 indexed citations
11.
Ehresmann, Sophie, Cinzia Magnani, Francesca Forzano, et al.. (2018). Lowry-Wood syndrome: further evidence of association with RNU4ATAC, and correlation between genotype and phenotype. Human Genetics. 137(11-12). 905–909. 9 indexed citations
12.
Cho, Sung Yoon, Nayoung K. D. Kim, Francesca Forzano, et al.. (2016). BGN Mutations in X-Linked Spondyloepimetaphyseal Dysplasia. The American Journal of Human Genetics. 98(6). 1243–1248. 30 indexed citations
13.
Baldo, Chiara, Alessandra Renieri, Giuseppe Merla, et al.. (2016). The alliance between genetic biobanks and patient organisations: the experience of the telethon network of genetic biobanks. Orphanet Journal of Rare Diseases. 11(1). 142–142. 27 indexed citations
14.
Cavani, Simona, Michela Malacarne, Chiara Baldo, et al.. (2013). First-trimester euploid miscarriages analysed by array-CGH. Journal of Applied Genetics. 54(3). 353–359. 40 indexed citations
15.
Filocamo, Mirella, Chiara Baldo, Stefano Goldwurm, et al.. (2013). Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases. Orphanet Journal of Rare Diseases. 8(1). 129–129. 36 indexed citations
16.
Mirabella, Teodelinda, Alessandro Poggi, Massimo Mogni, et al.. (2011). Recruitment of host’s progenitor cells to sites of human amniotic fluid stem cells implantation. Biomaterials. 32(18). 4218–4227. 26 indexed citations
17.
Vita, Serena De, Claudia Canzonetta, Catherine Mulligan, et al.. (2010). Trisomic dose of several chromosome 21 genes perturbs haematopoietic stem and progenitor cell differentiation in Down's syndrome. Oncogene. 29(46). 6102–6114. 35 indexed citations
18.
Prandini, Paola, Samuel Deutsch, Robert Lyle, et al.. (2007). Natural Gene-Expression Variation in Down Syndrome Modulates the Outcome of Gene-Dosage Imbalance. The American Journal of Human Genetics. 81(2). 252–263. 145 indexed citations
19.
Pastorino, Lorenza, Roberto Cusano, Chiara Baldo, et al.. (2005). Nevoid Basal Cell Carcinoma Syndrome in infants: improving diagnosis. Child Care Health and Development. 31(3). 351–354. 8 indexed citations
20.
McElwaine, Suzanne, Claire Mulligan, Jürgen Groet, et al.. (2004). Microarray transcript profiling distinguishes the transient from the acute type of megakaryoblastic leukaemia (M7) in Down's syndrome, revealing PRAME as a specific discriminating marker. British Journal of Haematology. 125(6). 729–742. 48 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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