Emanuela Manfredini

1.8k total citations
27 papers, 1.1k citations indexed

About

Emanuela Manfredini is a scholar working on Molecular Biology, Neurology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Emanuela Manfredini has authored 27 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Neurology and 5 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Emanuela Manfredini's work include Peripheral Neuropathies and Disorders (8 papers), Glycosylation and Glycoproteins Research (4 papers) and melanin and skin pigmentation (4 papers). Emanuela Manfredini is often cited by papers focused on Peripheral Neuropathies and Disorders (8 papers), Glycosylation and Glycoproteins Research (4 papers) and melanin and skin pigmentation (4 papers). Emanuela Manfredini collaborates with scholars based in Italy, United States and Switzerland. Emanuela Manfredini's co-authors include Eduardo Nobile‐Orazio, M. Carpo, Sergio Barbieri, G. Scarlato, Bruno Bonetti, Salvatore Monaco, Sérgio Ferrari, Walter Vegetti, S. Allaria and Anna Marozzi and has published in prestigious journals such as New England Journal of Medicine, Annals of Neurology and Gene.

In The Last Decade

Emanuela Manfredini

27 papers receiving 1.1k citations

Peers

Emanuela Manfredini
Jean‐Christophe Antoine France
A. Sebastian López‐Chiriboga United States
Michael L. Nordlund United States
Αναστασία Ζεκερίδου United States
Vesa Juvonen Finland
Roxanne Cofiell United States
B. de Leeuw Netherlands
Chris Amos United States
J.P. Louboutin France
Bastien Joubert France
Jean‐Christophe Antoine France
Emanuela Manfredini
Citations per year, relative to Emanuela Manfredini Emanuela Manfredini (= 1×) peers Jean‐Christophe Antoine

Countries citing papers authored by Emanuela Manfredini

Since Specialization
Citations

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

Fields of papers citing papers by Emanuela Manfredini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emanuela Manfredini

This figure shows the co-authorship network connecting the top 25 collaborators of Emanuela Manfredini. A scholar is included among the top collaborators of Emanuela Manfredini 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 Emanuela Manfredini. Emanuela Manfredini 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.
Maloberti, Alessandro, Paola Vallerio, Francesca Spanò, et al.. (2019). Could two-dimensional radial strain be considered as a novel tool to identify pre-clinical hypertrophic cardiomyopathy mutation carriers?. International journal of cardiac imaging. 35(12). 2167–2175. 3 indexed citations
2.
Mauri, Lucia, Emanuela Manfredini, Alessandra Longo, et al.. (2016). Clinical evaluation and molecular screening of a large consecutive series of albino patients. Journal of Human Genetics. 62(2). 277–290. 16 indexed citations
3.
Mauri, Lucia, Steffen Uebe, Heinrich Sticht, et al.. (2016). Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma. Orphanet Journal of Rare Diseases. 11(1). 108–108. 28 indexed citations
4.
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
5.
Mosca, Lorena, Francesca Rivieri, Raffaella Tanel, et al.. (2014). Mutational Screening of NOTCH3 Gene Reveals Two Novel Mutations: Complexity of CADASIL Diagnosis. Journal of Molecular Neuroscience. 54(4). 723–729. 2 indexed citations
6.
Mauri, Lucia, Alessandra Franzoni, Livia Garavelli, et al.. (2014). SOX2, OTX2 and PAX6 analysis in subjects with anophthalmia and microphthalmia. European Journal of Medical Genetics. 58(2). 66–70. 15 indexed citations
7.
Rimoldi, Valeria, Letizia Straniero, Rosanna Asselta, et al.. (2013). Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II. Gene. 537(1). 79–84. 15 indexed citations
8.
Mauri, Lucia, Alessandra Longo, Elena Piozzi, et al.. (2013). SLC45A2 mutation frequency in Oculocutaneous Albinism Italian patients doesn't differ from other European studies. Gene. 533(1). 398–402. 7 indexed citations
9.
Recalcati, Maria Paola, Emanuele Valtorta, Lorenza Romitti, et al.. (2010). Characterisation of complex chromosome 18p rearrangements in two syndromic patients with immunological deficits. European Journal of Medical Genetics. 53(4). 186–191. 10 indexed citations
10.
Nobile‐Orazio, Eduardo, Sergio Barbieri, Luca Baldini, et al.. (2009). Peripheral neuropathy in monoclonal gammopathy of undetermined significance: prevalence and immunopathogenetic studies. Acta Neurologica Scandinavica. 85(6). 383–390. 59 indexed citations
11.
Marozzi, Anna, Walter Vegetti, Emanuela Manfredini, et al.. (2000). Association between idiopathic premature ovarian failure and fragile X premutation. Human Reproduction. 15(1). 197–202. 105 indexed citations
12.
Vegetti, Walter, Anna Marozzi, Emanuela Manfredini, et al.. (2000). Premature ovarian failure. Molecular and Cellular Endocrinology. 161(1-2). 53–57. 65 indexed citations
13.
Marozzi, Anna, Emanuela Manfredini, Maria Grazia Tibiletti, et al.. (2000). Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure. Human Genetics. 107(4). 304–311. 78 indexed citations
14.
Carpo, M., N. Meucci, C. Pellegrino, et al.. (1999). Clinical features and anti-neural reactivity in neuropathy associated with IgG monoclonal gammopathy of undetermined significance. Journal of the Neurological Sciences. 164(1). 64–71. 46 indexed citations
15.
16.
Berg, Leonard H. van den, Arthur P. Hays, Eduardo Nobile‐Orazio, et al.. (1996). Anti-MAG and anti-SGPG antibodies in neuropathy. Muscle & Nerve. 19(5). 637–643. 88 indexed citations
17.
Manfredini, Emanuela, Eduardo Nobile‐Orazio, S. Allaria, & G. Scarlato. (1995). Anti-alpha- and beta-tubulin IgM antibodies in dysimmune neuropathies. Journal of the Neurological Sciences. 133(1-2). 79–84. 20 indexed citations
18.
Nobile‐Orazio, Eduardo, Emanuela Manfredini, M. Carpo, et al.. (1994). Frequency and clinical correlates of anti–neural IgM antibodies in neuropathy associated with IgM monoclonal gammopathy. Annals of Neurology. 36(3). 416–424. 201 indexed citations
19.
Monaco, Salvatore, Bruno Bonetti, Sérgio Ferrari, et al.. (1990). Complement-Mediated Demyelination in Patients with IgM Monoclonal Gammopathy and Polyneuropathy. New England Journal of Medicine. 322(10). 649–652. 132 indexed citations
20.
Nobile‐Orazio, Eduardo, Erik Francomano, Rita Daverio, et al.. (1989). Anti–myelin‐associated glycoprotein IgM antibody titers in neuropathy associated with macroglobulinemia. Annals of Neurology. 26(4). 543–550. 70 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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