Roberto Giorda

9.4k total citations
157 papers, 5.1k citations indexed

About

Roberto Giorda is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Roberto Giorda has authored 157 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Genetics, 60 papers in Molecular Biology and 25 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Roberto Giorda's work include Genomic variations and chromosomal abnormalities (33 papers), Genetics and Neurodevelopmental Disorders (32 papers) and Child and Adolescent Psychosocial and Emotional Development (17 papers). Roberto Giorda is often cited by papers focused on Genomic variations and chromosomal abnormalities (33 papers), Genetics and Neurodevelopmental Disorders (32 papers) and Child and Adolescent Psychosocial and Emotional Development (17 papers). Roberto Giorda collaborates with scholars based in Italy, United States and Canada. Roberto Giorda's co-authors include Orsetta Zuffardi, María Clara Bonaglia, Silvana Beri, Massimo Trucco, Cecilia Marino, Renato Borgatti, Massimo Molteni, Roberto Ciccone, Giorgio Gimelli and Livio Provenzi and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Roberto Giorda

154 papers receiving 4.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Roberto Giorda Italy	41	2.0k	2.0k	765	668	622	157	5.1k
Anjali K. Henders Australia	35	1.8k 0.9×	3.3k 1.7×	411 0.5×	364 0.5×	498 0.8×	83	6.5k
Jane A. Hurst United Kingdom	34	2.6k 1.3×	3.1k 1.6×	447 0.6×	139 0.2×	277 0.4×	85	7.7k
Marcus Pembrey United Kingdom	53	4.3k 2.2×	3.5k 1.8×	2.6k 3.4×	354 0.5×	250 0.4×	161	10.2k
Julie R. Korenberg United States	51	5.5k 2.8×	2.5k 1.3×	631 0.8×	350 0.5×	763 1.2×	167	10.5k
Bryan H. King United States	49	2.3k 1.2×	1.6k 0.8×	413 0.5×	649 1.0×	427 0.7×	136	8.0k
Judith L. Ross United States	59	4.3k 2.2×	5.9k 3.0×	1.4k 1.9×	188 0.3×	340 0.5×	212	10.0k
Santhosh Girirajan United States	34	2.5k 1.3×	3.4k 1.7×	390 0.5×	168 0.3×	596 1.0×	82	5.0k
J. P. Fryns Belgium	39	2.8k 1.4×	4.3k 2.2×	997 1.3×	275 0.4×	728 1.2×	280	6.2k
Leena Peltonen Finland	51	3.3k 1.7×	2.9k 1.5×	452 0.6×	681 1.0×	194 0.3×	146	9.6k
Ana C. D’Alessio United States	19	6.7k 3.4×	2.2k 1.1×	2.5k 3.3×	303 0.5×	131 0.2×	25	11.9k

Countries citing papers authored by Roberto Giorda

Since Specialization

Citations

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

Fields of papers citing papers by Roberto Giorda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberto Giorda

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

Bonanni, Paolo, Roberto Giorda, Roberto Michelucci, Carlo Nobile, & Emanuela Dazzo. (2024). A de novo pathogenic variant in MICAL‐1 causes epilepsy with auditory features. Epilepsia Open. 9(3). 1083–1087. 2 indexed citations

Zanotta, Nicoletta, Elena Panzeri, Sara Minghetti, et al.. (2023). A case of a childhood onset developmental encephalopathy with a novel de novo truncating variant in the Membrane Protein Palmitoylated 5 (MPP5) gene. Seizure. 116. 151–155.

Errichiello, Edoardo, Roberto Giorda, Antonella Gambale, et al.. (2020). RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanism. Molecular Genetics & Genomic Medicine. 9(1). e1561–e1561. 3 indexed citations

Provenzi, Livio, Serena Grumi, Roberto Giorda, et al.. (2020). Measuring the Outcomes of Maternal COVID-19-related Prenatal Exposure (MOM-COPE): study protocol for a multicentric longitudinal project. BMJ Open. 10(12). e044585–e044585. 15 indexed citations

Montirosso, Rosario, Roberto Giorda, Elisa Fazzi, et al.. (2020). Early Parenting Intervention – Biobehavioral Outcomes in infants with Neurodevelopmental Disabilities (EPI-BOND): study protocol for an Italian multicentre randomised controlled trial. BMJ Open. 10(7). e035249–e035249. 18 indexed citations

Marino, Cecilia, Paola Scifo, Pasquale Anthony Della Rosa, et al.. (2014). The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia. Cortex. 57. 227–243. 39 indexed citations

Rolando, Antonio & Roberto Giorda. (2013). MALE INTERSEXES IN OPHRYOTROCHA LABRONICA LA GRECA & BACCI (ANNELIDA POLYCHAETA). Monitore Zoologico Italiano-Italian Journal of Zoology. 16(1). 67–73. 1 indexed citations

Nobile, Maria, Andrea Greco, Giampaolo Perna, et al.. (2013). Effect of the serotonin transporter gene and of environment on the continuity of anxiety and depression traits throughout adolescence. Epidemiology and Psychiatric Sciences. 23(4). 399–409. 7 indexed citations

Novara, Francesca, Enrico Alfei, Stefano D’Arrigo, et al.. (2012). 5p13 microduplication syndrome: A new case and better clinical definition of the syndrome. European Journal of Medical Genetics. 56(1). 54–58. 24 indexed citations

10.

Esch, Hilde Van, Francesca Novara, Silvana Beri, et al.. (2010). Refining the phenotype associated with MEF2C haploinsufficiency. European Journal of Human Genetics. 18. 85–85. 4 indexed citations

11.

Bonaglia, María Clara, Roberto Ciccone, Giorgio Gimelli, et al.. (2008). Detailed phenotype–genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader–Willi-like phenotype. European Journal of Human Genetics. 16(12). 1443–1449. 75 indexed citations

12.

Rossi, Elena, Anna Verri, Maria Grazia Patricelli, et al.. (2008). A 12 Mb deletion at 7q33–q35 associated with autism spectrum disorders and primary amenorrhea. European Journal of Medical Genetics. 51(6). 631–638. 59 indexed citations

13.

Gimelli, Giorgio, Roberto Giorda, Silvana Beri, Stefania Gimelli, & Orsetta Zuffardi. (2005). A 46,X,inv(Y) young woman with gonadal dysgenesis and gonadoblastoma: Cytogenetics, molecular, and methylation studies. American Journal of Medical Genetics Part A. 140A(1). 40–45. 14 indexed citations

14.

Marino, Cecilia, Roberto Giorda, Laura Vanzin, et al.. (2004). CORRECTION. Journal of Medical Genetics. 41(1). 46–46.

15.

Marino, Cecilia, Laura Vanzin, Roberto Giorda, et al.. (2004). An Assessment of Transmission Disequilibrium Between Quantitative Measures of Childhood Problem Behaviors and DRD2/Taql and DRD4/48bp-Repeat Polymorphisms. Behavior Genetics. 34(5). 495–502. 26 indexed citations

16.

Cagliani, Rachele, Francesco Fortunato, Roberto Giorda, et al.. (2003). Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population. Neuromuscular Disorders. 13(10). 788–795. 38 indexed citations

17.

Giglio, Sabrina, Karl W. Broman, Naomichi Matsumoto, et al.. (2001). Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements. The American Journal of Human Genetics. 68(4). 874–883. 288 indexed citations

18.

Kerrison, John, et al.. (2001). Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1). Ophthalmic Genetics. 22(4). 241–248. 22 indexed citations

19.

Bonaglia, María Clara, Roberto Giorda, Maria Elisabetta Raggi, et al.. (2000). Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q. European Journal of Human Genetics. 8(8). 597–603. 53 indexed citations

20.

Ohmachi, Tetsuo, Roberto Giorda, David Shaw, & Herbert L. Ennis. (1989). Molecular organization of developmentally regulated Dictyostelium discoideum ubiquitin cDNAs. Biochemistry. 28(12). 5226–5231. 38 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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