Stefania Zappata

410 total citations
14 papers, 338 citations indexed

About

Stefania Zappata is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Stefania Zappata has authored 14 papers receiving a total of 338 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Genetics. Recurrent topics in Stefania Zappata's work include Neurogenetic and Muscular Disorders Research (9 papers), RNA modifications and cancer (7 papers) and RNA Research and Splicing (5 papers). Stefania Zappata is often cited by papers focused on Neurogenetic and Muscular Disorders Research (9 papers), RNA modifications and cancer (7 papers) and RNA Research and Splicing (5 papers). Stefania Zappata collaborates with scholars based in Italy, Netherlands and United States. Stefania Zappata's co-authors include Christina Brahe, Giovanni Neri, Francesco Danilo Tiziano, P. Tonali, Serenella Servidei, Enzo Ricci, Johan T. den Dunnen, Hans Scheffer, G J van Ommen and P.M. Grootscholten and has published in prestigious journals such as The Lancet, Human Molecular Genetics and Genomics.

In The Last Decade

Stefania Zappata

14 papers receiving 325 citations

Peers

Countries citing papers authored by Stefania Zappata

Since Specialization

Citations

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

Fields of papers citing papers by Stefania Zappata

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefania Zappata

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	SMN protein analysis in fibroblast, amniocyte and CVS cultures from spinal muscular atrophy patients and its relevance for diagnosis 1999 ·European Journal of Human Genetics ·(unknown), Francesco Danilo Tiziano, Stefania Zappata, Maria Alice Donati, Giovanni Neri, Christina Brahe	41
2	Detection of the Survival Motor Neuron (SMN) Genes by FISH: Further Evidence for a Role for SMN2 in the Modulation of Disease Severity in SMA Patients 1999 ·Human Molecular Genetics ·Tiziana Vitali, Vesna Sossi, Francesco Danilo Tiziano, Stefania Zappata, (unknown), Maria Paravatou‐Petsotas, Giovanni Neri, Christina Brahe	54
3	Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation 1997 ·American Journal of Medical Genetics ·Angelo Serra, (unknown), (unknown), (unknown), Stefania Zappata, Christina Brahe	4
4	Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation 1997 ·American Journal of Medical Genetics ·Angelo Serra, (unknown), (unknown), (unknown), Stefania Zappata, Christina Brahe	1
5	Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21) (p16.3;q22.1): Relevance to the Wolf-Hirschhorn and Down syndrome critical regions 1996 ·American Journal of Medical Genetics ·Gianfranco Sebastio, Lucia Perone, Vito Guzzetta, (unknown), (unknown), Roberto Della Casa, Fiorella Gurrieri, Stefania Zappata, Maria Grazia Pomponi, (unknown), Giovanni Neri, Generoso Andria, Christina Brahe	2
6	Deletions in the SMN gene in infantile and adult spinal muscular atrophy patients from the same family 1996 ·Human Genetics ·Stefania Zappata, Francesco Danilo Tiziano, Giovanni Neri, Christina Brahe	8
7	Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5. 1996 ·PubMed ·(unknown), P.M. Grootscholten, J. M. Cobben, Stefania Zappata, Hans Scheffer, Johan T. den Dunnen, G J van Ommen, Christina Brahe, C.H.C.M. Buys	86
8	Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy 1995 ·The Lancet ·Christina Brahe, Stefania Zappata, Giovanni Neri, Serenella Servidei, Enzo Ricci, P. Tonali	88
9	Highly polymorphic repeat marker within the ?-amyloid precursor protein gene 1994 ·Human Genetics ·Stefania Zappata, (unknown), (unknown), (unknown), (unknown), Flora Tassone, Angelo Serra, Stylianos E. Antonarakis, Christina Brahe	2
10	Mapping of two new markers within the smallest interval harboring the spinal muscular atrophy locus by family and radiation hybrid analysis 1994 ·Human Genetics ·Christina Brahe, (unknown), Gerrit van der Steege, Stefania Zappata, (unknown), Jan Osinga, Carli M.J. Tops, Riccardo Fodde, P. Meera Khan, Charles H.C.M. Buys, Giovanni Neri	25
11	Identification of Key Recombinants in Multiplex SMA Families 1994 ·Genomics ·Gerrit van der Steege, Jan-Maarten Cobben, Christina Brahe, Jan Osinga, Stefania Zappata, Hans Scheffer, Giovanni Neri, Gert‐Jan B. van Ommen, Leo P. ten Kate, Charles H.C.M. Buys	4
12	Presymptomatic diagnosis of SMA III by genotype analysis 1993 ·American Journal of Medical Genetics ·Christina Brahe, Stefania Zappata, (unknown), Enrico Bertini, Serenella Servidei, Pietro Tonali, Giovanni Neri	5
13	Dinucleotide repeat polymorphism proximal to the spinal muscular atrophy region at the D5S524 locus 1993 ·Human Molecular Genetics ·(unknown), Stefania Zappata, (unknown), Riccardo Fodde, P. Meera Khan, Giovanni Neri, Christina Brahe	2
14	Ultrastructure of the mature sperm and spermiogenesis inCallista chione(Mollusca, Bivalvia) 1991 ·Invertebrate Reproduction & Development ·Antonietta Nicotra, Stefania Zappata	16

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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