Amedea Mencarelli

2.8k total citations · 1 hit paper
38 papers, 2.3k citations indexed

About

Amedea Mencarelli is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Amedea Mencarelli has authored 38 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 17 papers in Genetics and 8 papers in Hematology. Recurrent topics in Amedea Mencarelli's work include Retinoids in leukemia and cellular processes (13 papers), Acute Myeloid Leukemia Research (8 papers) and Genomic variations and chromosomal abnormalities (4 papers). Amedea Mencarelli is often cited by papers focused on Retinoids in leukemia and cellular processes (13 papers), Acute Myeloid Leukemia Research (8 papers) and Genomic variations and chromosomal abnormalities (4 papers). Amedea Mencarelli collaborates with scholars based in Italy, United States and Canada. Amedea Mencarelli's co-authors include Myriam Alcalay, F Grignani, Pier Giuseppe Pelicci, Andrea Biondi, M Fagioli, P P Pandolfi, Alessandro Rambaldi, D Zangrilli, Fausto Grignani and Pier Francesco Ferrucci and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Amedea Mencarelli

37 papers receiving 2.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The acute promyelocytic leukemia-specific PML-RARα fusion protein inhibits differentiation and promotes survival of myeloid precursor cells

1993 519 citations F Grignani, Pier Francesco Ferrucci et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amedea Mencarelli Italy	17	1.9k	1.3k	479	322	268	38	2.3k
Xiangyuan Wang United States	24	1.5k 0.8×	126 0.1×	553 1.2×	27 0.1×	99 0.4×	43	2.0k
Eda Yildirim United States	16	1.0k 0.5×	52 0.0×	290 0.6×	97 0.3×	163 0.6×	23	1.8k
Lisa Holmgren United States	7	560 0.3×	239 0.2×	148 0.3×	18 0.1×	357 1.3×	7	1.4k
Roger Belizaire United States	16	740 0.4×	156 0.1×	91 0.2×	17 0.1×	323 1.2×	30	1.7k
Rūta Navakauskienė Lithuania	20	626 0.3×	99 0.1×	46 0.1×	31 0.1×	97 0.4×	92	1.0k
Emmanuel Richard France	21	845 0.4×	36 0.0×	268 0.6×	77 0.2×	38 0.1×	57	1.2k
Oliver Bell United States	15	1.4k 0.7×	156 0.1×	196 0.4×	10 0.0×	60 0.2×	21	1.7k
Diana Hernandez United Kingdom	19	748 0.4×	56 0.0×	311 0.6×	12 0.0×	105 0.4×	51	1.4k
K Tanaka Japan	20	1.7k 0.9×	121 0.1×	121 0.3×	8 0.0×	266 1.0×	32	2.1k
Meritxell Alberich-Jordà Czechia	25	1.3k 0.7×	450 0.3×	96 0.2×	6 0.0×	258 1.0×	60	2.0k

Countries citing papers authored by Amedea Mencarelli

Since Specialization

Citations

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

Fields of papers citing papers by Amedea Mencarelli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amedea Mencarelli

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

All Works

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20 of 20 papers shown

Verrotti, Alberto, Paolo Gorello, Duccio Maria Cordelli, et al.. (2023). NFIA haploinsufficiency: case series and literature review. Frontiers in Pediatrics. 11. 1292654–1292654. 6 indexed citations

Rooney, Kathleen, Michael A. Levy, Sadegheh Haghshenas, et al.. (2021). Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome. International Journal of Molecular Sciences. 22(16). 8611–8611. 13 indexed citations

Lonardo, Fortunato, M. Cristina Digilio, Daniela Rogaia, et al.. (2021). Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype. American Journal of Medical Genetics Part A. 185(4). 1204–1210. 5 indexed citations

Flex, Elisabetta, Giovanna Carpentieri, Alessandro Bruselles, et al.. (2021). A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3. Genes. 12(9). 1406–1406. 3 indexed citations

Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2019). Schilbach–Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene. European Journal of Human Genetics. 27(8). 1260–1266. 1 indexed citations

Prontera, Paolo, Amedea Mencarelli, Marta Cofini, et al.. (2018). Report of a Novel SHOX Missense Variant in a Boy With Short Stature and His Mother With Leri–Weill Dyschondrosteosis. Frontiers in Endocrinology. 9. 163–163. 3 indexed citations

Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2017). Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature. International Journal of Molecular Sciences. 18(9). 1998–1998. 8 indexed citations

Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2016). A novel MED12 mutation: Evidence for a fourth phenotype. American Journal of Medical Genetics Part A. 170(9). 2377–2382. 23 indexed citations

Prontera, Paolo, et al.. (2016). A Clinical and Molecular Survey of 62 Cystic Fibrosis Patients from Umbria (Central Italy) Disclosing a High Frequency (2.4%) of the 2184insA Allele: Implications for Screening. Public Health Genomics. 19(6). 336–341.

10.

Prontera, Paolo, et al.. (2013). Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression?. Molecular Syndromology. 4(4). 197–202. 8 indexed citations

11.

Prontera, Paolo, et al.. (2011). Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia. American Journal of Medical Genetics Part A. 155(4). 928–930. 20 indexed citations

12.

Prontera, Paolo, Emanuela Garelli, Amedea Mencarelli, et al.. (2011). Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome. American Journal of Medical Genetics Part A. 155(11). 2746–2749. 21 indexed citations

13.

Cavani, Simona, Paolo Prontera, Marina Grasso, et al.. (2010). FMR1, FMR2, and SLITRK2 deletion inside a paracentric inversion involving bands Xq27.3–q28 in a male and his mother. American Journal of Medical Genetics Part A. 155(1). 221–224. 8 indexed citations

14.

Prontera, Paolo, et al.. (2009). Encephalocraniocutaneous lipomatosis (ECCL) in a patient with history of familial multiple lipomatosis (FML). American Journal of Medical Genetics Part A. 149A(3). 543–545. 7 indexed citations

15.

Barocci, Simone, Sandro Sonnino, Amedea Mencarelli, et al.. (2000). Linalool modifies the nicotinic receptor–ion channel kinetics at the mouse neuromuscular junction. Pharmacological Research. 42(2). 177–181. 161 indexed citations

16.

Fagioli, M, Myriam Alcalay, Pier Francesco Ferrucci, et al.. (1998). Cooperation between the RING+B1-B2 and coiled-coil domains of PML is necessary for its effects on cell survival. Oncogene. 16(22). 2905–2913. 61 indexed citations

17.

Grignani, F, Pier Francesco Ferrucci, Ugo Testa, et al.. (1993). The acute promyelocytic leukemia-specific PML-RARα fusion protein inhibits differentiation and promotes survival of myeloid precursor cells. Cell. 74(3). 423–431. 519 indexed citations breakdown →

18.

Alcalay, Myriam, D Zangrilli, M Fagioli, et al.. (1992). Expression pattern of the RAR alpha-PML fusion gene in acute promyelocytic leukemia.. Proceedings of the National Academy of Sciences. 89(11). 4840–4844. 125 indexed citations

19.

Longo, Letizia, P P Pandolfi, Andrea Biondi, et al.. (1990). Rearrangements and aberrant expression of the retinoic acid receptor alpha gene in acute promyelocytic leukemias.. The Journal of Experimental Medicine. 172(6). 1571–1575. 156 indexed citations

20.

Longo, Letizia, Emilio Donti, Amedea Mencarelli, et al.. (1990). Mapping of chromosome 17 breakpoints in acute myeloid leukemias.. PubMed. 5(10). 1557–63. 29 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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