Manuela Fanciulli

1.2k total citations
13 papers, 726 citations indexed

About

Manuela Fanciulli is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Manuela Fanciulli has authored 13 papers receiving a total of 726 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Manuela Fanciulli's work include Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Manuela Fanciulli is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Manuela Fanciulli collaborates with scholars based in Italy, United Kingdom and United States. Manuela Fanciulli's co-authors include Enrico Petretto, Timothy J. Aitman, Timothy J. Vyse, Philippe Froguel, H. Terence Cook, Stephen Gough, Simon H. S. Pearce, Charles D. Pusey, Loı̈c Guillevin and Lavanya Kamesh and has published in prestigious journals such as Nature Genetics, Neurology and The American Journal of Human Genetics.

In The Last Decade

Manuela Fanciulli

13 papers receiving 716 citations

Peers

Countries citing papers authored by Manuela Fanciulli

Since Specialization

Citations

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

Fields of papers citing papers by Manuela Fanciulli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Fanciulli

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

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations 2017 ·Epilepsy & Behavior ·Roberto Michelucci, Patrizia Pulitano, Carlo Di Bonaventura, S. Binelli, Concetta Luisi, Elena Pasini, Salvatore Striano, Pasquale Striano, Giangennaro Coppola, Angela La Neve, Anna Teresa Giallonardo, Oriano Mecarelli, (unknown), Emanuela Dazzo, Manuela Fanciulli, Carlo Nobile	25
2	Copy number variations and susceptibility to lateral temporal epilepsy: A study of 21 pedigrees 2014 ·Epilepsia ·Manuela Fanciulli, Elena Pasini, Sandro Malacrida, Pasquale Striano, Salvatore Striano, Roberto Michelucci, Ruth Ottman, Carlo Nobile	10
3	Suggestive linkage of familial mesial temporal lobe epilepsy to chromosome 3q26 2013 ·Epilepsy Research ·Manuela Fanciulli, Carlo Di Bonaventura, Gabriella Egeo, Jinane Fattouch, Emanuela Dazzo, Slobodanka Radović, Alessandro Spadotto, Anna Teresa Giallonardo, Carlo Nobile	11
4	Molecular changes induced by the curcumin analogue D6 in human melanoma cells 2013 ·Molecular Cancer ·Carla Rozzo, Manuela Fanciulli, Cristina Fraumene, (unknown), Tiziana Cubeddu, (unknown), (unknown), (unknown), Grazia Galleri, Emanuela Azara, Maria Antonietta Dettori, Davide Fabbri, Giuseppe Palmieri, Marina Pisano	23
5	Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy 2013 ·European Journal of Human Genetics ·(unknown), Barbara Bauce, Andrea Nava, Manuela Fanciulli, Giovanni Vazza, Elisa Mazzotti, Ilaria Rigato, Marzia De Bortoli, Giorgia Beffagna, Alessandra Lorenzon, Martina Calore, Emanuela Dazzo, Carlo Nobile, Maria Luisa Mostacciuolo, Domenico Corrado, Cristina Basso, Luciano Daliento, Gaetano Thiene, Alessandra Rampazzo	28
6	LGI1 microdeletion in autosomal dominant lateral temporal epilepsy 2012 ·Neurology ·Manuela Fanciulli, Lia Santulli, (unknown), Chiara Barozzi, Luciana Tomasi, Laura Rigon, Tiziana Cubeddu, (unknown), Alessandra Rampazzo, Roberto Michelucci, Sergio Uzzau, Salvatore Striano, De Falco Fa, Pasquale Striano, Carlo Nobile	24
7	FCGR3B copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans 2011 ·Lara D. Veeken ·Mariam Molokhia, Manuela Fanciulli, Enrico Petretto, Alan L. Patrick, Paul McKeigue, Amy L. Roberts, Timothy J. Vyse, Timothy J. Aitman	25
8	Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations 2009 ·BMC Medical Genetics ·Evelina Mocci, Maria Pina Concas, Manuela Fanciulli, Nicola Pirastu, Mauro F. A. Adamo, (unknown), Cristina Fraumene, Ivana Persico, Alessandro Sassu, (unknown), Dionigio Antonio Prodi, (unknown), Ginevra Biino, Mario Pirastu, Andrea Angius	10
9	Gene copy number variation and common human disease 2009 ·Clinical Genetics ·Manuela Fanciulli, Enrico Petretto, Timothy J. Aitman	82
10	Copy number variation of Fc gamma receptor genes and disease predisposition 2008 ·Cytogenetic and Genome Research ·Manuela Fanciulli, Timothy J. Vyse, Timothy J. Aitman	18
11	FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity 2007 ·Nature Genetics ·Manuela Fanciulli, Penny J. Norsworthy, Enrico Petretto, Rong Dong, Lorraine Harper, Lavanya Kamesh, J. M. Heward, Stephen Gough, Adam J. de Smith, Alexandra I. F. Blakemore, Philippe Froguel, Catherine Owen, Simon H. S. Pearce, Luís Teixeira, Loı̈c Guillevin, Deborah S. Cunninghame Graham, Charles D. Pusey, H. Terence Cook, Timothy J. Vyse, Timothy J. Aitman	352
12	Ocular refraction: heritability and genome-wide search for eye morphometry traits in an isolated Sardinian population 2004 ·Human Genetics ·Ginevra Biino, Maria Antonietta Palmas, (unknown), Dionigio Antonio Prodi, Manuela Fanciulli, (unknown), (unknown), Maurizio Fossarello, Mario Pirastu	53
13	A New Essential Hypertension Susceptibility Locus on Chromosome 2p24-p25, Detected by Genomewide Search 2002 ·The American Journal of Human Genetics ·Andrea Angius, Enrico Petretto, (unknown), Paola Forabosco, Giuseppina Casu, Daniela Piras, Manuela Fanciulli, Mario Falchi, Paola Melis, Mario Palermo, Mario Pirastu	65

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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