Giovanni Neri

3.6k total citations · 2 hit papers
56 papers, 2.2k citations indexed

About

Giovanni Neri is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Giovanni Neri has authored 56 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 17 papers in Molecular Biology and 15 papers in Genetics. Recurrent topics in Giovanni Neri's work include Neurogenetic and Muscular Disorders Research (15 papers), Prenatal Screening and Diagnostics (13 papers) and RNA modifications and cancer (9 papers). Giovanni Neri is often cited by papers focused on Neurogenetic and Muscular Disorders Research (15 papers), Prenatal Screening and Diagnostics (13 papers) and RNA modifications and cancer (9 papers). Giovanni Neri collaborates with scholars based in Italy, United States and Netherlands. Giovanni Neri's co-authors include Alfonso Bellacosa, Maurizio Genuardi, Valeria Masciullo, Deborah A. Altomare, Louis Dubeau, Salvatore Mancuso, Minghong Wan, Andrew K. Godwin, Daphne W. Bell and Jin Q. Cheng and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and International Journal of Molecular Sciences.

In The Last Decade

Giovanni Neri

55 papers receiving 2.1k 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.

Molecular alterations of the AKT2 oncogene in ovarian and breast carcinomas

1995 691 citations Alfonso Bellacosa, Andrew K. Godwin et al. International Journal of Cancer profile →
Suicidal risk among adolescent psychiatric inpatients: the role of insomnia, depression, and social-personal factors

2025 20 citations Valentina Baldini, Giorgia Varallo et al. European Psychiatry profile →

Peers

Countries citing papers authored by Giovanni Neri

Since Specialization

Citations

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

Fields of papers citing papers by Giovanni Neri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giovanni Neri

This figure shows the co-authorship network connecting the top 25 collaborators of Giovanni Neri. A scholar is included among the top collaborators of Giovanni Neri 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 Giovanni Neri. Giovanni Neri 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	Suicidal risk among adolescent psychiatric inpatients: the role of insomnia, depression, and social-personal factors breakdown → 2025 ·European Psychiatry ·Valentina Baldini, (unknown), (unknown), (unknown), (unknown), (unknown), Giorgia Varallo, (unknown), Giovanni Neri, Andrea Fiorillo, Giuseppe Plazzi	20
2	SMN transcript levels in leukocytes of SMA patients determined by absolute real-time PCR 2009 ·European Journal of Human Genetics ·Francesco Danilo Tiziano, Anna Maria Pinto, Stefania Fiori, (unknown), Sonia Messina, Claudio Bruno, Antonella Pini, Marika Pane, Adele D’Amico, Alessandro Ghezzo, Enrico Bertini, Eugenio Mercuri, Giovanni Neri, Christina Brahe	42
3	A case of Beckwith–Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus 2009 ·Journal of Medical Genetics ·Marcella Zollino, Daniela Orteschi, Giuseppe Marangi, Agostina De Crescenzo, Vanna Pecile, Andrea Riccio, Giovanni Neri	39
4	A New Susceptibility Locus for Migraine with Aura in the 15q11-q13 Genomic Region Containing Three GABA-A Receptor Genes 2005 ·The American Journal of Human Genetics ·Luisa Russo, Paolo Mariotti, Eugenio Sangiorgi, Tiziana Giordano, (unknown), Francesca R. Lupi, (unknown), Andrea Guzzetta, Giovanni Neri, Fiorella Gurrieri	64
5	Upregulation of SMN2 gene expression by 4-phenylbutyrate: relevance for a therapeutic approach to spinal muscular atrophy. 2002 ·UCL Discovery (University College London) ·(unknown), Catia Andreassi, Carla Angelozzi, Tiziana Vitali, (unknown), Alma Boninsegna, Marcello Villanova, Giovanni Neri, Christina Brahe	2
6	Premature termination mutations in exon 3 of the SMN1 gene are associated with exon skipping and a relatively mild SMA phenotype 2001 ·European Journal of Human Genetics ·(unknown), (unknown), Tiziana Vitali, Francesco Danilo Tiziano, Massimiliano Mirabella, A. Antonelli, Giovanni Neri, Christina Brahe	38
7	Survival analysis in families affected by hereditary non-polyposis colorectal cancer 1997 ·International Journal of Cancer ·Antonio Percesepe, Piero Benatti, Luca Roncucci, Romano Sassatelli, Rossella Fante, D. Ganazzi, Alfonso Bellacosa, Maurizio Genuardi, Giovanni Neri, Alessandra Viel, Maurizio Ponz de Leòn	49
8	A three years follow-up of a group of «everyday patients» in a mental health centre 1997 ·Epidemiologia e Psichiatria Sociale ·(unknown), (unknown), (unknown), Giovanni Neri	1
9	Limb-pelvis hypoplasia/aplasia: A discrete entity in the fibuloulnar developmental field complex 1997 ·American Journal of Medical Genetics ·Maurizio Genuardi, Paolo Gasparini, Giovanni Neri, Leopoldo Zelante	4
10	Characterization ofMSH2 andMLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer 1997 ·Genes Chromosomes and Cancer ·Alessandra Viel, Maurizio Genuardi, E Capozzi, Francesca Leonardi, Alfonso Bellacosa, Maria Paravatou‐Petsotas, Maria Grazia Pomponi, Mara Fornasarig, Antonio Percesepe, Luca Roncucci, Maria Grazia Tamassia, Piero Benatti, Maurizio Ponz de Leòn, (unknown), Marcello Covino, M. Anti, (unknown), Mauro Boiocchi, Giovanni Neri	65
11	Molecular alterations of the AKT2 oncogene in ovarian and breast carcinomas breakdown → 1995 ·International Journal of Cancer ·Alfonso Bellacosa, (unknown), Andrew K. Godwin, Daphne W. Bell, Jin Q. Cheng, Deborah A. Altomare, Minghong Wan, Louis Dubeau, Giovanni Scambia, Valeria Masciullo, Gabriella Ferrandina, Pierluigi Benedetti Panici, Salvatore Mancuso, Giovanni Neri, Joseph R. Testa	691
12	Mapping of two new markers within the smallest interval harboring the spinal muscular atrophy locus by family and radiation hybrid analysis 1994 ·Human Genetics ·Christina Brahe, (unknown), Gerrit van der Steege, Stefania Zappata, (unknown), Jan Osinga, Carli M.J. Tops, Riccardo Fodde, P. Meera Khan, Charles H.C.M. Buys, Giovanni Neri	25
13	Presymptomatic diagnosis of SMA III by genotype analysis 1993 ·American Journal of Medical Genetics ·Christina Brahe, Stefania Zappata, (unknown), Enrico Bertini, Serenella Servidei, Pietro Tonali, Giovanni Neri	5
14	Neu‐Laxova syndrome: Pathological, radiological, and prenatal findings in a stillborn female 1989 ·American Journal of Medical Genetics ·Rosa Russo, Maria DʼArmiento, Pasquale Martinelli, V. Ventruto, Giovanni Neri, James F. Reynolds	22
15	Further delineation of a syndrome of cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, coloboma, and hepatic fibrosis 1989 ·American Journal of Medical Genetics ·Alain Verloès, C Lambotte, Giovanni Neri, James F. Reynolds	61
16	Simpson‐Golabi‐Behmel syndrome: An X‐linked encephalo‐trophoschisis syndrome 1988 ·American Journal of Medical Genetics ·Giovanni Neri, (unknown), Marco Cappa, P. Borrelli, John M. Opitz	68
17	Prevalence of a novel epileptogenic EEG pattern in the Martin‐Bell syndrome 1988 ·American Journal of Medical Genetics ·S Musumeci, Raffaele Ferri, (unknown), Giovanni Neri, (unknown), P Bergonzi	22
18	IVIC Syndrome. Report of a second family 1988 ·American Journal of Medical Genetics ·(unknown), (unknown), (unknown), (unknown), Giovanni Neri, John M. Optiz, James F. Reynolds	9
19	Partial tetrasomy 9 in an infant with clinical and radiological evidence of multiple joint dislocations 1988 ·European Journal of Pediatrics ·(unknown), (unknown), (unknown), (unknown), (unknown), Maurizio Genuardi, Giovanni Neri	21
20	Complex chromosomal rearrangement in a woman with multiple miscarriages 1988 ·American Journal of Medical Genetics ·Katrin Kausch, Thomas Haaf, Julia R. Köhler, Michael Schmid, Giovanni Neri, James F. Reynolds	70

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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