Roberto Zori

882 total citations
12 papers, 198 citations indexed

About

Roberto Zori is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Roberto Zori has authored 12 papers receiving a total of 198 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Neurology. Recurrent topics in Roberto Zori's work include Chromosomal and Genetic Variations (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Roberto Zori is often cited by papers focused on Chromosomal and Genetic Variations (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Roberto Zori collaborates with scholars based in United States, Italy and Russia. Roberto Zori's co-authors include Charles A. Williams, Margaret R. Wallace, Daniel J. Driscoll, Boris G. Kousseff, Heather J. Stalker, Sonja A. Rasmussen, Brian A. Gray, Vasilisa Aksenova, Amanda D. Rice and Elisena Morizio and has published in prestigious journals such as PEDIATRICS, Journal of Immunological Methods and Oncotarget.

In The Last Decade

Roberto Zori

12 papers receiving 196 citations

Peers

Roberto Zori

GENET

IMMUN

NEURO

RHEUM

Martin A. Haagmans Netherlands

Birutė Burnytė Lithuania

Maja Dembić Denmark

Florence Renaldo France

Eyby Leon United States

Hirofumi Ohashi Japan

Leïla Lazaro France

Ruolan Guo China

Marie‐Louise Bondeson Sweden

Sonia Nizard France

Martin A. Haagmans Netherlands

Roberto Zori

157 ×1.9

43 ×0.8

GENET

19 ×0.5

IMMUN

51 ×1.5

NEURO

23 ×0.7

RHEUM

Citations per year, relative to Roberto Zori Roberto Zori (= 1×) peers Martin A. Haagmans

Countries citing papers authored by Roberto Zori

Since Specialization

Citations

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

Fields of papers citing papers by Roberto Zori

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberto Zori

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

All Works

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12 of 12 papers shown

Díaz, George A., Andreas Schulze, Nicola Longo, et al.. (2019). Long-term safety and efficacy of glycerol phenylbutyrate for the management of urea cycle disorder patients. Molecular Genetics and Metabolism. 127(4). 336–345. 10 indexed citations

Marsh, Kevin, Adrian Quartel, Haoling H. Weng, et al.. (2019). A benefit-risk analysis of pegvaliase for the treatment of phenylketonuria: A study of patients' preferences. Molecular Genetics and Metabolism Reports. 21. 100507–100507. 14 indexed citations

Larimore, Kevin, Roberto Zori, Gillian Shepherd, et al.. (2019). Depletion of interfering IgG and IgM is critical to determine the role of IgE in pegvaliase-associated hypersensitivity. Journal of Immunological Methods. 468. 20–28. 7 indexed citations

Giovinazzi, Serena, Pietro Sirleto, Vasilisa Aksenova, et al.. (2014). Usp7 protects genomic stability by regulating Bub3. Oncotarget. 5(11). 3728–3742. 20 indexed citations

Palka, Chiara, Elisena Morizio, Barbara Matarrelli, et al.. (2011). Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus. European Journal of Medical Genetics. 54(3). 333–336. 4 indexed citations

Palka, Chiara, Paolo Guanciali Franchi, Donatella Fantasia, et al.. (2011). Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment. PEDIATRICS. 129(1). e183–e188. 30 indexed citations

Zhuang, Haoyang, Pui Y. Lee, Amanda D. Rice, et al.. (2006). Lupus‐like disease and high interferon levels corresponding to trisomy of the type I interferon cluster on chromosome 9p. Arthritis & Rheumatism. 54(5). 1573–1579. 34 indexed citations

Stalker, Heather, et al.. (2004). Reply to Unger: The mildest form of campomelic dysplasia. American Journal of Medical Genetics Part A. 132A(1). 114–115. 1 indexed citations

Johnson, Jennifer, Charles A. Williams, Daniel J. Driscoll, et al.. (1998). Analysis of CpG C‐to‐T mutations in neurofibromatosis type 1. Human Mutation. 11(5). 411–411. 1 indexed citations

10.

Rasmussen, Sonja A., Heather J. Stalker, Roberto Zori, et al.. (1997). NF1 mutation analysis using a combined heteroduplex/SSCP approach. Human Mutation. 9(6). 548–554. 40 indexed citations

11.

Mancuso, Anthony, et al.. (1995). Association of anophthalmia and esophageal atresia. American Journal of Medical Genetics. 59(4). 484–491. 12 indexed citations

12.

Gray, Brian A., Stephen W. Scherer, L.-C. Tsui, et al.. (1995). Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient.. PubMed. 56(6). 1411–6. 25 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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