Giuseppe Barrano

946 total citations
11 papers, 442 citations indexed

About

Giuseppe Barrano is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Giuseppe Barrano has authored 11 papers receiving a total of 442 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Giuseppe Barrano's work include Fetal and Pediatric Neurological Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic and Kidney Cyst Diseases (2 papers). Giuseppe Barrano is often cited by papers focused on Fetal and Pediatric Neurological Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic and Kidney Cyst Diseases (2 papers). Giuseppe Barrano collaborates with scholars based in Italy, Switzerland and United States. Giuseppe Barrano's co-authors include Francesco Brancati, Bruno Dallapiccola, Enza Maria Valente, Eugen Boltshauser, Enrico Bertini, Loredana Boccone, Carrie M Louie, Jennifer L. Silhavy, Emanuele Bellacchio and Lihadh Al‐Gazali and has published in prestigious journals such as Nature Genetics, International Journal of Molecular Sciences and Gene.

In The Last Decade

Giuseppe Barrano

11 papers receiving 435 citations

Peers

Giuseppe Barrano

GENET

PPCH

NEURO

CMN

Tatjana Bierhals Germany

Sven Poths Germany

Christine Massicotte Canada

Alexander Paciorkowski United States

Saghar Ghasemi Firouzabadi Iran

Shino Shimada Japan

Sara Loddo Italy

Patrick Yu‐Wai‐Man United Kingdom

Philip H. Iffland United States

Tatjana Bierhals Germany

Giuseppe Barrano

201 ×0.6

GENET

271 ×0.9

55 ×0.6

PPCH

11 ×0.2

NEURO

51 ×1.0

CMN

Citations per year, relative to Giuseppe Barrano Giuseppe Barrano (= 1×) peers Tatjana Bierhals

Countries citing papers authored by Giuseppe Barrano

Since Specialization

Citations

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

Fields of papers citing papers by Giuseppe Barrano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giuseppe Barrano

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

All Works

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11 of 11 papers shown

Barrano, Giuseppe, S Meli, Paola Santalucia, et al.. (2023). Monitoring of SARS-CoV-2 Infection in Ragusa Area: Next Generation Sequencing and Serological Analysis. International Journal of Molecular Sciences. 24(5). 4742–4742. 4 indexed citations

Alesi, Viola, Anna Maria Nardone, Silvia Di Tommaso, et al.. (2021). Clinical Application of Easychip 8x15K Platform in 4106 Pregnancies Without Ultrasound Anomalies. Reproductive Sciences. 28(4). 1142–1149. 1 indexed citations

Antona, Vincenzo, et al.. (2020). What is the impact of a novel MED12 variant on syndromic conotruncal heart defects? Analysis of case report on two male sibs. The Italian Journal of Pediatrics/Italian journal of pediatrics. 46(1). 98–98. 5 indexed citations

Zampatti, Stefania, G. Pagliaroli, Giuseppe Barrano, et al.. (2018). Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis. Prenatal Diagnosis. 38(13). 1096–1102. 5 indexed citations

Ferese, Rosangela, Stefania Zampatti, Anna Maria Griguoli, et al.. (2016). A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS). Journal of Molecular Neuroscience. 59(3). 376–381. 11 indexed citations

Alesi, Viola, Marta Bertoli, Giuseppe Barrano, et al.. (2012). 335.4kb microduplication in chromosome band Xp11.2p11.3 associated with developmental delay, growth retardation, autistic disorder and dysmorphic features. Gene. 505(2). 384–387. 11 indexed citations

Alesi, Viola, Giuseppe Barrano, Anna Capalbo, et al.. (2011). A previously undescribed de novo 4p15 deletion in a patient with apparently isolated metopic craniosynostosis. American Journal of Medical Genetics Part A. 155(10). 2543–2551. 6 indexed citations

Suppa, Antonio, Alfredo Berardelli, Francesco Brancati, et al.. (2009). Clinical, neuropsychological, neurophysiologic, and genetic features of a new Italian pedigree with familial cortical myoclonic tremor with epilepsy. Epilepsia. 50(5). 1284–1288. 29 indexed citations

Brancati, Francesco, Lorena Travaglini, Eugen Boltshauser, et al.. (2008). RPGRIP1L mutations are mainly associated with the cerebello‐renal phenotype of Joubert syndrome‐related disorders. Clinical Genetics. 74(2). 164–170. 50 indexed citations

10.

Valente, Enza Maria, Jennifer L. Silhavy, Francesco Brancati, et al.. (2006). Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome. Nature Genetics. 38(6). 623–625. 291 indexed citations

11.

Gambarin, Mattia, Enza Maria Valente, Paolo Liberini, et al.. (2006). Atypical phenotypes and clinical variability in a large Italian family with DYT1–primary torsion dystonia. Movement Disorders. 21(10). 1782–1784. 29 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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