Elena Andreucci

3.2k total citations
32 papers, 742 citations indexed

About

Elena Andreucci is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Elena Andreucci has authored 32 papers receiving a total of 742 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Psychiatry and Mental health. Recurrent topics in Elena Andreucci's work include Cerebral Palsy and Movement Disorders (6 papers), Botulinum Toxin and Related Neurological Disorders (3 papers) and Autism Spectrum Disorder Research (3 papers). Elena Andreucci is often cited by papers focused on Cerebral Palsy and Movement Disorders (6 papers), Botulinum Toxin and Related Neurological Disorders (3 papers) and Autism Spectrum Disorder Research (3 papers). Elena Andreucci collaborates with scholars based in Italy, United States and Switzerland. Elena Andreucci's co-authors include Ermellina Fedrizzi, Emanuela Pagliano, Sara Bulgheroni, R. Bono, Daria Riva, Sabrina Giglio, Lucía Morandi, Maria Luisa Bianchi, Maurizio Genuardi and Chiara Vago and has published in prestigious journals such as Osteoporosis International, Nephrology Dialysis Transplantation and Developmental Medicine & Child Neurology.

In The Last Decade

Elena Andreucci

31 papers receiving 726 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elena Andreucci Italy	18	357	203	153	129	103	32	742
Richard O. Robinson United Kingdom	16	700 2.0×	92 0.5×	219 1.4×	266 2.1×	163 1.6×	38	1.0k
Anna‐Karin Kroksmark Sweden	19	201 0.6×	695 3.4×	51 0.3×	119 0.9×	98 1.0×	39	1.2k
Loretta A. Staudt United States	15	581 1.6×	122 0.6×	115 0.8×	394 3.1×	31 0.3×	26	879
Laura McAdam Canada	16	108 0.3×	466 2.3×	46 0.3×	64 0.5×	72 0.7×	44	873
Lucia Ruggiero Italy	15	524 1.5×	234 1.2×	54 0.4×	143 1.1×	35 0.3×	53	1.1k
Delphine Viguier France	16	343 1.0×	88 0.4×	418 2.7×	124 1.0×	103 1.0×	16	1.1k
Eva Pontén Sweden	15	425 1.2×	149 0.7×	65 0.4×	213 1.7×	16 0.2×	44	681
Nelci Zanon Brazil	15	142 0.4×	43 0.2×	142 0.9×	97 0.8×	63 0.6×	37	735
Nancy J. Clegg United States	16	244 0.7×	458 2.3×	485 3.2×	195 1.5×	309 3.0×	33	957
Ilona A. Barash United States	10	287 0.8×	357 1.8×	40 0.3×	303 2.3×	59 0.6×	13	979

Countries citing papers authored by Elena Andreucci

Since Specialization

Citations

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

Fields of papers citing papers by Elena Andreucci

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Andreucci

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Peppicelli, Silvia, Lido Calorini, Francesca Bianchini, et al.. (2024). Acidity and hypoxia of tumor microenvironment, a positive interplay in extracellular vesicle release by tumor cells. Cellular Oncology. 48(1). 27–41. 19 indexed citations

Formicola, Daniela, Elena Andreucci, Sabrina Giglio, et al.. (2024). Expanding the molecular landscape of childhood apraxia of speech: evidence from a single-center experience. Frontiers in Neuroscience. 18. 1396240–1396240. 3 indexed citations

Pignata, Laura, Angela Sparago, Orazio Palumbo, et al.. (2021). Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome. Genes. 12(4). 581–581. 5 indexed citations

Bargiacchi, Sara, Matteo Della Monica, Roberto Biagiotti, et al.. (2017). Metatropic dysplasia in third trimester of pregnancy and a novel causative variant in the TRPV4 gene. European Journal of Medical Genetics. 60(7). 365–368. 2 indexed citations

Delvecchio, Maurizio, Paola Primignani, Roberto Caputo, et al.. (2016). A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency. Journal of Pediatric Endocrinology and Metabolism. 29(5). 603–5. 3 indexed citations

Straniero, Letizia, Valeria Rimoldi, Giulia Soldà, et al.. (2015). Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites. Journal of Human Genetics. 60(9). 467–471. 5 indexed citations

Artuso, Rosangela, Aldesia Provenzano, Benedetta Mazzinghi, et al.. (2014). Therapeutic implications of novel mutations of the RFX6 gene associated with early-onset diabetes. The Pharmacogenomics Journal. 15(1). 49–54. 17 indexed citations

Garavelli, Livia, Simonetta Rosato, Anita Wischmeijer, et al.. (2012). Simpson–Golabi–Behmel syndrome type 1 in a 27‐week macrosomic preterm newborn: The diagnostic value of rib malformations and index nail and finger hypoplasia. American Journal of Medical Genetics Part A. 158A(9). 2245–2249. 13 indexed citations

Vultaggio, Alessandra, Andrea Matucci, Mario Milco D’Elios, et al.. (2012). Multiorgan Infiltration by CD8+ T Cells and 1p;16p Translocation in a Patient with Hypogammaglobulinemia and a Reduced Number of B Cells. International Archives of Allergy and Immunology. 158(2). 206–210. 2 indexed citations

10.

Bedeschi, Maria Francesca, Vera Bianchi, Barbara Gentilin, et al.. (2011). Prenatal manifestation and management of a mother and child affected by spondyloperipheral dysplasia with a C-propeptide mutation in COL2A1: case report. Orphanet Journal of Rare Diseases. 6(1). 7–7. 8 indexed citations

11.

Pozza, Laura Visonà Dalla, et al.. (2010). The perception of involved professionals towards research feasibility and usefulness: lessons from the Multi-Site Trial on Efficacy of Constraint Induced Movement Therapy in Children with Hemiplegia.. PubMed. 46(3). 369–76. 4 indexed citations

12.

Andreucci, Elena, Benedetta Bianchi, Giancarlo Lavoratti, et al.. (2009). Inner ear abnormalities in four patients with dRTA and SNHL: clinical and genetic heterogeneity. Pediatric Nephrology. 24(11). 2147–2153. 26 indexed citations

13.

Andreucci, Elena, Rosa Caruso, Roberto Ciccone, et al.. (2009). Medullary sponge kidney associated with primary distal renal tubular acidosis and mutations of the H+-ATPase genes. Nephrology Dialysis Transplantation. 24(9). 2734–2738. 26 indexed citations

14.

Giunti, Laura, Valentina Cetica, U. Ricci, et al.. (2009). Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome. European Journal of Human Genetics. 17(7). 919–927. 24 indexed citations

15.

Pagliano, Emanuela, Ermellina Fedrizzi, Alessandra Erbetta, et al.. (2007). Cognitive Profiles and Visuoperceptual Abilities in Preterm and Term Spastic Diplegic Children With Periventricular Leukomalacia. Journal of Child Neurology. 22(3). 282–288. 56 indexed citations

16.

Crenna, P., Ermellina Fedrizzi, Elena Andreucci, C. Frigo, & R. Bono. (2004). The heel-contact gait pattern of habitual toe walkers. Gait & Posture. 21(3). 311–317. 24 indexed citations

17.

Savino, Michelangelo, Maria D’Apolito, Francesca Mari, et al.. (2004). Spectrum ofPTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: Identification of thirteen novel alleles. Human Mutation. 24(5). 441–441. 19 indexed citations

18.

Giunti, Laura, Silvia Guarducci, Elisabetta Lapi, et al.. (2001). Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlation. Brain and Development. 23. S242–S245. 18 indexed citations

19.

Pagliano, Emanuela, et al.. (2001). Evolution of upper limb function in children with congenital hemiplegia. Neurological Sciences. 22(5). 371–375. 21 indexed citations

20.

Ricci, U., Ilaria Sani, Silvia Guarducci, et al.. (2000). Infrared fluorescent automated detection of thirteen short tandem repeat polymorphisms and one gender-determining system of the CODIS core system. Electrophoresis. 21(17). 3564–3570. 20 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