Valeria Romanelli

1.5k total citations
21 papers, 649 citations indexed

About

Valeria Romanelli is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Valeria Romanelli has authored 21 papers receiving a total of 649 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Valeria Romanelli's work include Genetic Syndromes and Imprinting (10 papers), Prenatal Screening and Diagnostics (10 papers) and Epigenetics and DNA Methylation (7 papers). Valeria Romanelli is often cited by papers focused on Genetic Syndromes and Imprinting (10 papers), Prenatal Screening and Diagnostics (10 papers) and Epigenetics and DNA Methylation (7 papers). Valeria Romanelli collaborates with scholars based in Spain, Italy and United States. Valeria Romanelli's co-authors include Pablo Lapunzina, Antonio Capalbo, Laura Rienzi, Danilo Cimadomo, Filippo Maria Ubaldi, David Monk, Cristina Patassini, Laura Girardi, Víctor Martínez‐Glez and Franck Court and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Clinical Endocrinology & Metabolism and Human Reproduction.

In The Last Decade

Valeria Romanelli

21 papers receiving 637 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valeria Romanelli Spain 16 345 340 339 126 41 21 649
Volkan Baltacı Türkiye 12 178 0.5× 153 0.5× 189 0.6× 238 1.9× 4 0.1× 42 539
N.D. Watson United Kingdom 10 113 0.3× 144 0.4× 200 0.6× 31 0.2× 9 0.2× 16 515
Xiu‐An Yang China 12 207 0.6× 129 0.4× 35 0.1× 55 0.4× 9 0.2× 22 412
G. Schiliró Italy 15 167 0.5× 83 0.2× 170 0.5× 74 0.6× 23 0.6× 78 900
Robin M. Flatley United States 9 207 0.6× 46 0.1× 120 0.4× 128 1.0× 4 0.1× 9 538
Manuela Langbein Germany 5 208 0.6× 62 0.2× 150 0.4× 25 0.2× 4 0.1× 5 414
Yuqi Wu China 11 422 1.2× 48 0.1× 43 0.1× 147 1.2× 9 0.2× 30 583
R. Holanda Da Silva Sanches France 5 218 0.6× 108 0.3× 50 0.1× 16 0.1× 5 0.1× 7 344
Kathryn Owens United States 9 127 0.4× 25 0.1× 165 0.5× 74 0.6× 20 0.5× 9 538

Countries citing papers authored by Valeria Romanelli

Since Specialization
Citations

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

Fields of papers citing papers by Valeria Romanelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valeria Romanelli

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

All Works

20 of 20 papers shown
1.
Arias, Pedro, Valeria Romanelli, Piranit Nik Kantaputra, et al.. (2022). Clinical Spectrum and Tumour Risk Analysis in Patients with Beckwith-Wiedemann Syndrome Due to CDKN1C Pathogenic Variants. Cancers. 14(15). 3807–3807. 2 indexed citations
2.
Poli, Maurizio, Laura Girardi, Marco Fabiani, et al.. (2019). Past, Present, and Future Strategies for Enhanced Assessment of Embryo's Genome and Reproductive Competence in Women of Advanced Reproductive Age. Frontiers in Endocrinology. 10. 154–154. 17 indexed citations
3.
Romanelli, Valeria, Maurizio Poli, & Antonio Capalbo. (2019). Preimplantation genetic testing in assisted reproductive technology. Panminerva Medica. 61(1). 30–41. 3 indexed citations
4.
Girardi, Laura, Valeria Romanelli, Marco Fabiani, et al.. (2019). 8. SEGMENTAL ANEUPLOIDIES SHOW MOSAIC PATTERN REDUCING PREDICTIVE VALUE COMPARED TO HIGH WHOLE CHROMOSOME ANEUPLOIDIES REPRESENTATIVENESS. Reproductive BioMedicine Online. 39. e18–e19. 1 indexed citations
5.
Capalbo, Antonio, Valeria Romanelli, Cristina Patassini, et al.. (2018). Diagnostic efficacy of blastocoel fluid and spent media as sources of DNA for preimplantation genetic testing in standard clinical conditions. Fertility and Sterility. 110(5). 870–879.e5. 75 indexed citations
6.
Capalbo, Antonio, Valeria Romanelli, Maurizio Poli, et al.. (2018). Non invasive analysis of the embryonic genome: a critical review of non invasive approaches for PGD and PGS. Reproductive BioMedicine Online. 36. e7–e8. 1 indexed citations
7.
Capalbo, Antonio, Valeria Romanelli, Danilo Cimadomo, et al.. (2016). Implementing PGD/PGD-A in IVF clinics: considerations for the best laboratory approach and management. Journal of Assisted Reproduction and Genetics. 33(10). 1279–1286. 29 indexed citations
8.
Romanelli, Valeria, Kazuhiko Nakabayashi, Miguel Vizoso, et al.. (2014). Variable maternal methylation overlapping thenc886/vtRNA2-1locus is locked between hypermethylated repeats and is frequently altered in cancer. Epigenetics. 9(5). 783–790. 33 indexed citations
9.
Court, Franck, Álex Martín-Trujillo, Valeria Romanelli, et al.. (2013). Genome-Wide Allelic Methylation Analysis Reveals Disease-Specific Susceptibility to Multiple Methylation Defects in Imprinting Syndromes. Human Mutation. 34(4). n/a–n/a. 71 indexed citations
10.
Kantaputra, Piranit Nik, et al.. (2012). A novel mutation in CDKN1C in sibs with Beckwith–Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases. American Journal of Medical Genetics Part A. 161(1). 192–197. 10 indexed citations
11.
Nanclares, Gustavo Pérez de, Valeria Romanelli, Sonia Mayo, et al.. (2012). Detection of Hypomethylation Syndrome among Patients with Epigenetic Alterations at theGNASLocus. The Journal of Clinical Endocrinology & Metabolism. 97(6). E1060–E1067. 27 indexed citations
12.
Lapunzina, Pablo, Jennifer Gentile, Nina Tolkoff‐Rubin, et al.. (2011). Adults with Sotos syndrome: Review of 21 adults with molecularly confirmed NSD1 alterations, including a detailed case report of the oldest person. American Journal of Medical Genetics Part A. 155(9). 2105–2111. 23 indexed citations
13.
Romanelli, Valeria, Víctor Martínez‐Glez, Mario F. Fraga, et al.. (2011). Beckwith–Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques. European Journal of Human Genetics. 19(4). 416–421. 36 indexed citations
14.
Romanelli, Valeria, Julián Nevado, Mario F. Fraga, et al.. (2010). Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanism. Journal of Medical Genetics. 48(3). 212–216. 28 indexed citations
15.
Martínez‐Glez, Víctor, Valeria Romanelli, María Ángeles Mori, et al.. (2010). Macrocephaly–capillary malformation: Analysis of 13 patients and review of the diagnostic criteria. American Journal of Medical Genetics Part A. 152A(12). 3101–3106. 38 indexed citations
16.
Benito‐Sanz, Sara, Eva Barroso, Damián Heine‐Suñer, et al.. (2010). Clinical and Molecular Evaluation of SHOX/PAR1 Duplications in Léri-Weill Dyschondrosteosis (LWD) and Idiopathic Short Stature (ISS). The Journal of Clinical Endocrinology & Metabolism. 96(2). E404–E412. 58 indexed citations
17.
Romanelli, Valeria, Ángel Campos‐Barros, Karen E. Heath, et al.. (2009). CDKN1C Mutations in HELLP/Preeclamptic Mothers of Beckwith–Wiedemann Syndrome (BWS) Patients. Placenta. 30(6). 551–554. 34 indexed citations
18.
Lamanna, Raffaele, et al.. (2008). A preliminary study of soft cheese degradation in different packaging conditions by 1H‐NMR. Magnetic Resonance in Chemistry. 46(9). 828–831. 20 indexed citations
19.
Busico, Vincenzo, et al.. (2005). Reactivity of Secondary Metal−Alkyls in Catalytic Propene Polymerization:  How Dormant Are “Dormant Chains”?. Journal of the American Chemical Society. 127(6). 1608–1609. 45 indexed citations
20.
Stabile, Achille, et al.. (1988). Intravenous immunoglobulin for prophylaxis of neonatal sepsis in premature infants.. Archives of Disease in Childhood. 63(4). 441–443. 45 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Volkan Baltacı Breakdown of academic impact, for papers by N.D. Watson Breakdown of academic impact, for papers by Xiu‐An Yang Breakdown of academic impact, for papers by G. Schiliró Breakdown of academic impact, for papers by Robin M. Flatley Breakdown of academic impact, for papers by Manuela Langbein Breakdown of academic impact, for papers by Yuqi Wu Breakdown of academic impact, for papers by R. Holanda Da Silva Sanches Breakdown of academic impact, for papers by Kathryn Owens
Rankless by CCL
2026