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

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

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20 of 20 papers shown

#	Title	Journal	Authors	Indexed citations
1	Williams–Beuren syndrome shapes the gut microbiota metaproteome	Scientific Reports	Valeria Marzano, Stefano Levi Mortera et al.	3
2	Organ donation from patients with a rare disease is often safe: the italian guidelines	Clinical Transplantation	Bruno Dallapiccola, Massimo Rugge et al.	1
3	SHP2 's gain‐of‐function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction	Clinical Genetics	Manuela Priolo, Andrea Ciolfi et al.	2
4	Expansion of the clinical and molecular spectrum of an XPD ‐related disorder linked to biallelic mutations in ERCC2 gene	Clinical Genetics	Emanuele Agolini, Elena Botta et al.	5
5	Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Growth Hormone Deficiency and Early Onset Osteoporosis	International Journal of Molecular Sciences	Viola Alesi, Maria Lisa Dentici et al.	1
6	Expanding the clinical spectrum associated with PACS2 mutations	Clinical Genetics	Maria Lisa Dentici, Sabina Barresi et al.	17
7	Skeletal abnormalities are common features in Aymé‐Gripp syndrome	Clinical Genetics	Marcello Niceta, Domenico Barbuti et al.	10
8	Percentiles of serum uric acid and cardiometabolic abnormalities in obese Italian children and adolescents	The Italian Journal of Pediatrics/Italian journal of pediatrics	Rosa Luciano, Blegina Shashaj et al.	26
9	Clinical and Neurobehavioral Features of Three Novel Kabuki Syndrome Patients with Mosaic KMT2D Mutations and a Review of Literature	International Journal of Molecular Sciences	Francesca Romana Lepri, Dario Cocciadiferro et al.	17
10	Interaction Between PPARγ2 Variants and Gender on the Modulation of Body Weight	Obesity	Eleonora Morini, Vittorio Tassi et al.	40
11	The Q121/Q121 Genotype of ENPP1/PC-1 Is Associated with Lower BMI in Non-diabetic Whites*	Obesity	Sabrina Prudente, Manisha Chandalia et al.	0
12	Combined Test for UGT1A1 –3279T→G and A(TA)nTAA Polymorphisms Best Predicts Gilbert's Syndrome in Italian Pediatric Patients	Genetic Testing	Alessandro Ferraris, Valério Nobili et al.	22
13	Combinatorial Sequencing-by-Hybridization: Analysis of the NF1 Gene	Genetic Testing	Annalisa Schirinzi, Snezana Drmanac et al.	5
14	Noonan's syndrome and related disorders: Clinical-molecular update and guidelines	The Italian Journal of Pediatrics/Italian journal of pediatrics	Anna Sárközy, Bruno Marino et al.	3
15	Additive Effects of Genetic Variation in Dopamine Regulating Genes on Working Memory Cortical Activity in Human Brain	Journal of Neuroscience	Alessandro Bertolino, Giuseppe Blasi et al.	172
16	Validation of dHPLC for Molecular Diagnosis of β-Thalassemia in Southern Italy	Genetic Testing	Alessia Colosimo, Valentina Guida et al.	8
17	A Single Strand Conformation Polymorphism-Based Carrier Test for Spinal Muscular Atrophy	Genetic Testing	Sabrina Semprini, Alessandra Tacconelli et al.	11
18	Recurrent nonsense mutations in the growth hormone receptor from patients with Laron dwarfism.	Journal of Clinical Investigation	Serge Amselem, Marie‐Laure Sobrier et al.	72
19	Regional Mapping of Hexokinase-1 within the Short Arm of Chromosome 10	Human Heredity	Bruno Dallapiccola, Giulietta Micara et al.	5
20	Ovarian dys function in balanced x autosome translocations 2 cases involving band xq 21	Annales de Génétique	Antonino Forabosco, E Tarantino et al.	3

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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