Emilia Vitale

2.5k total citations · 1 hit paper
38 papers, 1.6k citations indexed

About

Emilia Vitale is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Emilia Vitale has authored 38 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 12 papers in Genetics and 7 papers in Genetics. Recurrent topics in Emilia Vitale's work include RNA modifications and cancer (6 papers), Connective tissue disorders research (5 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Emilia Vitale is often cited by papers focused on RNA modifications and cancer (6 papers), Connective tissue disorders research (5 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Emilia Vitale collaborates with scholars based in Italy, United States and Germany. Emilia Vitale's co-authors include Francesco Ramirez, Petros Tsipouras, Maurice Godfrey, Hisae Hori, Mansoor Sarfarazi, Brendan Lee, Marie‐Geneviève Mattéi, David W. Hollister, B Steinmann and B Lee and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Emilia Vitale

37 papers receiving 1.5k 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.

Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

1991 515 citations Brendan Lee, Maurice Godfrey et al. Nature profile →

Peers

Countries citing papers authored by Emilia Vitale

Since Specialization

Citations

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

Fields of papers citing papers by Emilia Vitale

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emilia Vitale

This figure shows the co-authorship network connecting the top 25 collaborators of Emilia Vitale. A scholar is included among the top collaborators of Emilia Vitale 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 Emilia Vitale. Emilia Vitale 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

#	Work	Indexed citations
1	Sustained Depolarization Induces Gene Expression Pattern Changes Related to Synaptic Plasticity in a Human Cholinergic Cellular Model 2024 ·Molecular Neurobiology ·(unknown), (unknown), (unknown), (unknown), Francesco Aniello, Emilia Vitale, Aldo Donizetti	0
2	CD33 rs2455069 SNP: Correlation with Alzheimer’s Disease and Hypothesis of Functional Role 2022 ·International Journal of Molecular Sciences ·(unknown), (unknown), Antonella Angiolillo, Alfonso Di Costanzo, Francesco Aniello, Aldo Donizetti, Ferdinando Febbraio, Emilia Vitale	13
3	LINC00473 as an Immediate Early Gene under the Control of the EGR1 Transcription Factor 2020 ·Non-Coding RNA ·(unknown), Emilia Vitale, Francesco Aniello, Aldo Donizetti	3
4	GRN deletion in familial frontotemporal dementia showing association with clinical variability in 3 familial cases 2017 ·Neurobiology of Aging ·Graziella Milan, (unknown), Sabina Pappatà, Maria Teresa Gentile, Luca Colucci-D’Amato, (unknown), Anna Maciąg, (unknown), Laura Fucci, Annibale Alessandro Puca, Dario Grossi, Alfredo Postiglione, Emilia Vitale	10
5	Metabolic response of SH-SY5Y cells to gold nanoparticles by NMR-based metabolomics analyses 2016 ·Biomedical Physics & Engineering Express ·Debora Paris, Dominique Melck, Angela Longo, (unknown), G. Carotenuto, L. Nicolais, Andréa Motta, Emilia Vitale	6
6	Molecular responses of cells to 2-mercapto-1-methylimidazole gold nanoparticles (AuNPs)-mmi: investigations of histone methylation changes 2014 ·Journal of Nanoparticle Research ·Arianna Polverino, Angela Longo, Aldo Donizetti, (unknown), Maria Frucci, (unknown), G. Carotenuto, L. Nicolais, Marina Piscopo, Emilia Vitale, Laura Fucci	3
7	Cortical Metabolic Deficits in a Rat Model of Cholinergic Basal Forebrain Degeneration 2013 ·Neurochemical Research ·Francesca Gelfo, Laura Petrosini, Alessandro Graziano, Paola De Bartolo, (unknown), Emilia Vitale, Arianna Polverino, (unknown), Giuseppe Sorrentino, Laura Mandolesi	7
8	Role of Cytosolic Calcium-Dependent Phospholipase A2 in Alzheimer's Disease Pathogenesis 2012 ·Molecular Neurobiology ·Maria Teresa Gentile, (unknown), Pierpaolo Sorrentino, Emilia Vitale, Giuseppe Sorrentino, Annibale Alessandro Puca, Luca Colucci-D’Amato	35
9	Structural Chromosomal Variations in Neurological Diseases 2009 ·The Neurologist ·Bernadette Kálmán, Emilia Vitale	8
10	Arvanil and anandamide up-regulate CD36 expression in human peripheral blood mononuclear cells 2007 ·Immunology Letters ·Anna Maria Malfitano, Gökçe Törüner, Patrizia Gazzerro, Chiara Laezza, Seema Husain, Davide Eletto, Pierangelo Orlando, Luciano De Petrocellis, (unknown), Marvin N. Schwalb, Emilia Vitale, Maurizio Bifulco	8
11	Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations 2007 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Fernando Gianfrancesco, Milena Cannella, Tiziana Martino, Vittorio Maglione, Teresa Esposito, Gualtiero Innocenzi, Emilia Vitale, Christina L. Liquori, Douglas A. Marchuk, Ferdinando Squitieri	29
12	A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema‐distichiasis syndrome associated with renal disease and diabetes mellitus 2004 ·American Journal of Medical Genetics Part A ·Cagri Yildirim‐Toruner, (unknown), (unknown), Emily Chen, Stanley Goldstein, Emilia Vitale	29
13	Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation 2002 ·European Journal of Human Genetics ·Farhad Mirghomizadeh, (unknown), Marcella Devoto, Markus Pfister, Jens Oeken, (unknown), Emilia Vitale, Antonio Riccio, Assunta De Rienzo, H. P. Zenner, Nikolaus Blin	8
14	Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12 2002 ·Human Molecular Genetics ·Emilia Vitale	27
15	Novel X-linked mental retardation syndrome with short stature maps to Xq24 2001 ·American Journal of Medical Genetics ·Emilia Vitale, Claudia Specchia, Marcella Devoto, Andrea Angius, Rong Sun, Mariano Rocchi, Marvin N. Schwalb, (unknown), (unknown), Salvatorica Manca, C Mastropaolo, (unknown)	15
16	Genomic Cloning and Characterization of the Human Thrombin Receptor Gene 1996 ·Journal of Biological Chemistry ·Valentina A. Schmidt, Emilia Vitale, Wadie F. Bahou	37
17	Genetic Linkage of the Marfan Syndrome, Ectopia Lentis, and Congenital Contractural Arachnodactyly to the Fibrillin Genes on Chromosomes 15 and 5 1992 ·New England Journal of Medicine ·Petros Tsipouras, (unknown), M. Sarfarazi, B Lee, Emilia Vitale, A. H. Child, Maurice Godfrey, Richard B. Devereux, D. Hewett, B Steinmann, (unknown), (unknown), (unknown), (unknown)	205
18	Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes breakdown → 1991 ·Nature ·Brendan Lee, Maurice Godfrey, Emilia Vitale, Hisae Hori, Marie‐Geneviève Mattéi, Mansoor Sarfarazi, Petros Tsipouras, Francesco Ramirez, David W. Hollister	515
19	Repating developmental expression of G-Hox 7, a novel homeobox-containing gene in the chicken 1991 ·Developmental Biology ·Hiroaki Suzuki, Babu J. Padanilam, Emilia Vitale, Francesco Ramirez, Michael Solursh	91
20	Assignment of human aldolase C gene to chromosome 17, region cen?q21.1 1989 ·Human Genetics ·Mariano Rocchi, Emilia Vitale, Angela Elvira Covone, Giovanni Romeo, Rita Santamaria, Pasqualina Buono, Giovanni Paolella, Francesco Salvatore	11

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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