Anna Ruggeri

701 total citations
13 papers, 402 citations indexed

About

Anna Ruggeri is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Anna Ruggeri has authored 13 papers receiving a total of 402 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pediatrics, Perinatology and Child Health, 6 papers in Genetics and 3 papers in Molecular Biology. Recurrent topics in Anna Ruggeri's work include Prenatal Screening and Diagnostics (7 papers), Genetic Syndromes and Imprinting (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Anna Ruggeri is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genetic Syndromes and Imprinting (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Anna Ruggeri collaborates with scholars based in Italy, United States and Australia. Anna Ruggeri's co-authors include Francesca Romana Grati, Giuseppe Simoni, Federico Maggi, Beatrice Grimi, Francesca Dulcetti, Simona De Toffol, Francesca Malvestiti, Monica Miozzo, Cristina Agrati and Elisa Gaetani and has published in prestigious journals such as Cancer Research, Transplantation and Journal of Medical Genetics.

In The Last Decade

Anna Ruggeri

13 papers receiving 353 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anna Ruggeri Italy	10	255	197	122	76	45	13	402
Simona De Toffol Italy	11	303 1.2×	216 1.1×	84 0.7×	79 1.0×	22 0.5×	15	412
Francesca Dulcetti Italy	10	301 1.2×	203 1.0×	83 0.7×	84 1.1×	26 0.6×	12	387
Dan Diego‐Álvarez Spain	11	360 1.4×	228 1.2×	151 1.2×	61 0.8×	13 0.3×	16	509
Pascale Kleinfinger France	12	244 1.0×	153 0.8×	93 0.8×	63 0.8×	29 0.6×	27	334
Marios Ioannides Cyprus	13	216 0.8×	233 1.2×	218 1.8×	51 0.7×	55 1.2×	25	443
Cristina Agrati Italy	8	415 1.6×	231 1.2×	116 1.0×	108 1.4×	32 0.7×	11	497
Ioannis Papoulidis Greece	13	195 0.8×	251 1.3×	116 1.0×	24 0.3×	11 0.2×	52	388
Matthew Hoi Kin Chau Hong Kong	13	271 1.1×	250 1.3×	93 0.8×	41 0.5×	34 0.8×	28	387
G. Gemelos United States	5	633 2.5×	300 1.5×	148 1.2×	113 1.5×	60 1.3×	10	702

Countries citing papers authored by Anna Ruggeri

Since Specialization

Citations

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

Fields of papers citing papers by Anna Ruggeri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Ruggeri

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

All Works

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13 of 13 papers shown

Grati, Francesca Romana, Francesca Malvestiti, José Carlos Ferreira, et al.. (2014). Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results. Genetics in Medicine. 16(8). 620–624. 144 indexed citations

Malvestiti, Francesca, Simona De Toffol, Beatrice Grimi, et al.. (2014). De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches. Prenatal Diagnosis. 34(5). 460–468. 17 indexed citations

Grati, Francesca Romana, Francesca Malvestiti, Beatrice Grimi, et al.. (2013). QF‐PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first‐trimester prenatal diagnoses. Prenatal Diagnosis. 33(5). 502–508. 14 indexed citations

Grati, Francesca Romana, D. Molina Gomes, Devika Ganesamoorthy, et al.. (2012). Application of a new molecular technique for the genetic evaluation of products of conception. Prenatal Diagnosis. 33(1). 32–41. 15 indexed citations

Toffol, Simona De, Emilia Bellone, Francesca Dulcetti, et al.. (2010). Quantitative Fluorescence-Polymerase Chain Reaction Assay for the Detection of the Duplication of the Charcot Marie Tooth Disease Type 1A Critical Region. Genetic Testing and Molecular Biomarkers. 14(2). 225–231. 1 indexed citations

Grati, Francesca Romana, Beatrice Grimi, Silvia Milani, et al.. (2010). Chromosome abnormalities investigated by non‐invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypes. American Journal of Medical Genetics Part A. 152A(6). 1434–1442. 41 indexed citations

Grati, Francesca Romana, Marci M. Lesperance, Simona De Toffol, et al.. (2009). Pure monosomy and pure trisomy of 13q21.2–31.1 consequent to a familial insertional translocation: Exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1). American Journal of Medical Genetics Part A. 149A(5). 906–913. 10 indexed citations

Grati, Francesca Romana, Licia Turolla, Anna Ruggeri, et al.. (2007). Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele: new highlights on phenotype–genotype correlations in Beckwith–Wiedemann syndrome. Journal of Medical Genetics. 44(4). 257–263. 27 indexed citations

Sirchia, Silvia Maria, Francesca Romana Grati, Floriana Barbera, et al.. (2005). Loss of the Inactive X Chromosome and Replication of the Active X in BRCA1-Defective and Wild-type Breast Cancer Cells. Cancer Research. 65(6). 2139–2146. 76 indexed citations

10.

Ruggeri, Anna, Francesca Dulcetti, Monica Miozzo, et al.. (2004). Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations. Prenatal Diagnosis. 24(12). 997–1000. 33 indexed citations

11.

Conti, Gabriella, et al.. (1980). Effect of cytotoxic agents on suppressor cells in mice. European Journal of Cancer (1965). 16(1). 53–58. 8 indexed citations

12.

Ruggeri, Anna, et al.. (1980). In vivo and in vitro immunosuppressive effect of two batroxobin preparations in mice. Thrombosis Research. 18(1-2). 253–258. 2 indexed citations

13.

Moras, Maria Luisa, et al.. (1979). IN VITRO GENERATION OF NONSPECIFIC SUPPRESSOR CELLS AND THEIR CHARACTERIZATION. Transplantation. 27(5). 329–332. 14 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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