Bruno Dallapiccola

52.9k total citations · 1 hit paper
766 papers, 22.9k citations indexed

About

Bruno Dallapiccola is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Bruno Dallapiccola has authored 766 papers receiving a total of 22.9k indexed citations (citations by other indexed papers that have themselves been cited), including 397 papers in Molecular Biology, 294 papers in Genetics and 103 papers in Epidemiology. Recurrent topics in Bruno Dallapiccola's work include Genomic variations and chromosomal abnormalities (140 papers), Congenital heart defects research (117 papers) and Congenital Heart Disease Studies (63 papers). Bruno Dallapiccola is often cited by papers focused on Genomic variations and chromosomal abnormalities (140 papers), Congenital heart defects research (117 papers) and Congenital Heart Disease Studies (63 papers). Bruno Dallapiccola collaborates with scholars based in Italy, United States and France. Bruno Dallapiccola's co-authors include Giuseppe Novelli, M. Cristina Digilio, Enza Maria Valente, Rita Mingarelli, Aldo Giannotti, Bruno Marino, Francesco Brancati, Anna Sárközy, Antonio Pizzuti and Lorenza Putignani and has published in prestigious journals such as Nature, New England Journal of Medicine and The Lancet.

In The Last Decade

Bruno Dallapiccola

754 papers receiving 22.3k citations

Hit Papers

align trajectories

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.

Gut microbiota profiling of pediatric nonalcoholic fatty liver disease and obese patients unveiled by an integrated meta‐omics‐based approach

2016 557 citations Federica Del Chierico, Valério Nobili et al. profile →

Peers

Bruno Dallapiccola

GENET

EPIDE

PPCH

NEURO

Wayne W. Grody United States

Wendy K. Chung United States

Richard P. Lifton United States

Arnold Münnich France

Elaine Lyon United States

Xavier Estivill Spain

Thomas J. Hudson Canada

Daniel J. Schaid United States

David R. Clemmons United States

John Burn United Kingdom

Wayne W. Grody United States

Bruno Dallapiccola

11.9k ×1.0

12.1k ×1.8

GENET

1.2k ×0.3

EPIDE

2.8k ×1.2

PPCH

1.0k ×0.5

NEURO

Citations per year, relative to Bruno Dallapiccola Bruno Dallapiccola (= 1×) peers Wayne W. Grody

Countries citing papers authored by Bruno Dallapiccola

Since Specialization

Citations

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

Fields of papers citing papers by Bruno Dallapiccola

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bruno Dallapiccola

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Marzano, Valeria, Stefano Levi Mortera, Pamela Vernocchi, et al.. (2023). Williams–Beuren syndrome shapes the gut microbiota metaproteome. Scientific Reports. 13(1). 18963–18963. 3 indexed citations

Dallapiccola, Bruno, Massimo Rugge, Massimo Cardillo, et al.. (2022). Organ donation from patients with a rare disease is often safe: the italian guidelines. Clinical Transplantation. 36(9). e14769–e14769. 1 indexed citations

Priolo, Manuela, Andrea Ciolfi, Luca Pannone, et al.. (2022). SHP2 's gain‐of‐function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction. Clinical Genetics. 102(1). 12–21. 2 indexed citations

Agolini, Emanuele, Elena Botta, M. Cristina Digilio, et al.. (2021). Expansion of the clinical and molecular spectrum of an XPD ‐related disorder linked to biallelic mutations in ERCC2 gene. Clinical Genetics. 99(6). 842–848. 5 indexed citations

Alesi, Viola, Maria Lisa Dentici, Silvia Genovese, et al.. (2021). Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Growth Hormone Deficiency and Early Onset Osteoporosis. International Journal of Molecular Sciences. 22(2). 750–750. 1 indexed citations

Dentici, Maria Lisa, Sabina Barresi, Marcello Niceta, et al.. (2019). Expanding the clinical spectrum associated with PACS2 mutations. Clinical Genetics. 95(4). 525–531. 17 indexed citations

Niceta, Marcello, Domenico Barbuti, Neerja Gupta, et al.. (2019). Skeletal abnormalities are common features in Aymé‐Gripp syndrome. Clinical Genetics. 97(2). 362–369. 10 indexed citations

Luciano, Rosa, Blegina Shashaj, Andrea Del Fattore, et al.. (2017). Percentiles of serum uric acid and cardiometabolic abnormalities in obese Italian children and adolescents. The Italian Journal of Pediatrics/Italian journal of pediatrics. 43(1). 3–3. 26 indexed citations

Lepri, Francesca Romana, Dario Cocciadiferro, Bartolomeo Augello, et al.. (2017). Clinical and Neurobehavioral Features of Three Novel Kabuki Syndrome Patients with Mosaic KMT2D Mutations and a Review of Literature. International Journal of Molecular Sciences. 19(1). 82–82. 17 indexed citations

10.

Morini, Eleonora, Vittorio Tassi, Ornella Ludovico, et al.. (2008). Interaction Between PPARγ2 Variants and Gender on the Modulation of Body Weight. Obesity. 16(6). 1467–1470. 40 indexed citations

11.

Prudente, Sabrina, Manisha Chandalia, Eleonora Morini, et al.. (2007). The Q121/Q121 Genotype of ENPP1/PC-1 Is Associated with Lower BMI in Non-diabetic Whites*. Obesity. 15(1). 1–4.

12.

Ferraris, Alessandro, et al.. (2006). Combined Test for UGT1A1 –3279T→G and A(TA)nTAA Polymorphisms Best Predicts Gilbert's Syndrome in Italian Pediatric Patients. Genetic Testing. 10(2). 121–125. 22 indexed citations

13.

Schirinzi, Annalisa, Snezana Drmanac, Bruno Dallapiccola, et al.. (2006). Combinatorial Sequencing-by-Hybridization: Analysis of the NF1 Gene. Genetic Testing. 10(1). 8–17. 5 indexed citations

14.

Sárközy, Anna, et al.. (2006). Noonan's syndrome and related disorders: Clinical-molecular update and guidelines. The Italian Journal of Pediatrics/Italian journal of pediatrics. 32(3). 145–155. 3 indexed citations

15.

Bertolino, Alessandro, Giuseppe Blasi, Valeria Latorre, et al.. (2006). Additive Effects of Genetic Variation in Dopamine Regulating Genes on Working Memory Cortical Activity in Human Brain. Journal of Neuroscience. 26(15). 3918–3922. 172 indexed citations

16.

Colosimo, Alessia, Valentina Guida, Alessandro De Luca, et al.. (2003). Validation of dHPLC for Molecular Diagnosis of β-Thalassemia in Southern Italy. Genetic Testing. 7(3). 269–275. 8 indexed citations

17.

Semprini, Sabrina, Alessandra Tacconelli, Francesca Capon, et al.. (2001). A Single Strand Conformation Polymorphism-Based Carrier Test for Spinal Muscular Atrophy. Genetic Testing. 5(1). 33–37. 11 indexed citations

18.

Amselem, Serge, Marie‐Laure Sobrier, Philippe Duquesnoy, et al.. (1991). Recurrent nonsense mutations in the growth hormone receptor from patients with Laron dwarfism.. Journal of Clinical Investigation. 87(3). 1098–1102. 72 indexed citations

19.

Dallapiccola, Bruno, et al.. (1984). Regional Mapping of Hexokinase-1 within the Short Arm of Chromosome 10. Human Heredity. 34(3). 156–160. 5 indexed citations

20.

Forabosco, Antonino, et al.. (1979). Ovarian dys function in balanced x autosome translocations 2 cases involving band xq 21. Annales de Génétique. 22(1). 11–16. 3 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.

Explore authors with similar magnitude of impact