Lidia Larizza

11.0k citations

271 papers · 6.3k indexed · h-index 43

Impact in

Developmental Biology top 1%
Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders

Papers in

Developmental Biology 16
Genetics 132
- Genomic variations and chromosomal abnormalities 79
- Genetic Syndromes and Imprinting 28
- Genetics and Neurodevelopmental Disorders 25

Co-authors: Alessandro Beghini Silvia Russo Gaia Roversi Cristina Gervasini Enrica Morra Roberto Cairoli Angelo Selicorni Palma Finelli
Journals: International Journal of Cancer (14 papers)Clinical Genetics (13 papers)European Journal of Medical Genetics (10 papers)European Journal of Human Genetics (9 papers)International Journal of Molecular Sciences (8 papers)
Partner nations: Italy United States France

In The Last Decade

Lidia Larizza

265 papers receiving 6.1k citations

Peers

Countries citing papers authored by Lidia Larizza

Since Specialization

Citations

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

Fields of papers citing papers by Lidia Larizza

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Lidia Larizza, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Lidia Larizza Line = papers co-authored together Lidia Larizza links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Low‐grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis‐like syndrome American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Francesca Cogliati, Letizia Straniero, Valeria Rimoldi, Maura Masciadri, 楚林, Berardo Rinaldi, Donatella Milani, Davide Gentilini, Lidia Larizza, Rosanna Asselta, Silvia Russo, Maria Francesca Bedeschi	2024	2
2	A Novel KIDINS220 Pathogenic Variant Associated with the Syndromic Spastic Paraplegia SINO: An Expansion of the Brain Malformation Spectrum and a Literature Review Genes ·Maria Teresa Bonati, Cristina Baldoli, Cheng-Jen Liu, 李英善, Lidia Larizza, Palma Finelli, Maria Iascone	2024	0
3	Germline NUP98 Variants in Two Siblings with a Rothmund–Thomson-Like Spectrum: Protein Functional Changes Predicted by Molecular Modeling International Journal of Molecular Sciences ·Elisa Adele Colombo, A Riahi Medvar, 吴江航朱怀球, Alessandro Orro, Silvia Majore, Paola Grammatico, Davide Gentilini, Palma Finelli, Cristina Gervasini, Pasqualina D’Ursi, Lidia Larizza	2023	3
4	8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature Genes ·Dustin Galer, Hai Yun Zhu, Anna Paola Capra, Silvana Briuglia, Chiara Baldo, Maria Paola Canevini, R. Arumugam, G. G. Frenkel', Francesca Forzano, Ornella Galesi, Enrico Grosso, Michela Malacarne, Angela Peron, Corrado Romano, Monica Saccani, Lidia Larizza, Maria Paola Recalcati	2021	12
5	Insights into Mutation Effect in Three Poikiloderma with Neutropenia Patients by Transcript Analysis and Disease Evolution of Reported Patients with the Same Pathogenic Variants Journal of Clinical Immunology ·Elisa Adele Colombo, Nursel Elçioğlu, Claudio Graziano, You-Juo Chung, 成本仁, Iria Neri, Elena Facchini, Mariangela Greco, Cristina Gervasini, Lidia Larizza	2018	6
6	Complex de novo chromosomal rearrangement at 15q11–q13 involving an intrachromosomal triplication in a patient with a severe neuropsychological phenotype: Clinical report and review of the literature American Journal of Medical Genetics Part A ·Chiara Castronovo, M. Crippa, Luis Marcelo Vilches Herrera, Beatrice Schmidt Giusti, Silvia Russo, Lidia Larizza, L. M. Ishutina, Maria Teresa Bonati, Palma Finelli	2014	12
7	Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrum American Journal of Medical Genetics Part A ·Cristina Gervasini, Silvia Russo, Anna Cereda, Ilaria Parenti, Maura Masciadri, Jacopo Azzollini, Daniela Melis, Lingfeng Zhang, Bérénice Doray, Alessandra Ferrarini, Livia Garavelli, Angelo Selicorni, Lidia Larizza	2013	24
8	Rothmund-Thomson syndrome Orphanet Journal of Rare Diseases ·Lidia Larizza, Gaia Roversi, Ludovica Volpi	2010	182
9	SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome Genetics in Medicine ·Cristina Gervasini, Francesca Romana Grati, Faustina Lalatta, Silvia Tabano, Barbara Gentilin, Patrizia Colapietro, Simona De Toffol, Giada Frontino, F. Motta, Silvia Maitz, Laura Bernardini, Bruno Dallapiccola, Luigi Fedele, Lidia Larizza, Monica Miozzo	2010	55
10	Functional analysis of splicing mutations in exon 7 of NF1gene BMC Medical Genetics ·Irene Bottillo, Alessandro De Luca, Annalisa Schirinzi, Valentina Guida, Isabella Torrente, Stefano Calvieri, Cristina Gervasini, Lidia Larizza, Antonio Pizzuti, Bruno Dallapiccola	2007	27
11	Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs Prenatal Diagnosis ·Daniela Giardino, Toshiyasu Hibino, Lucia Ballarati, Palma Finelli, Metin PİRİ, Giovanni Botta, K. Reddy Bhargavi, Enrico Grosso, Lidia Larizza	2006	31
12	STI 571 inhibition effect on KITAsn822Lys-mediated signal transduction cascade Experimental Hematology ·Alessandro Beghini, Melissa Bellini, Ivana Magnani, Patrizia Colapietro, Roberto Cairoli, Enrica Morra, Lidia Larizza	2005	18
13	Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions Human Genetics ·Cristina Gervasini, Francesca Orzan, Angela Bentivegna, Patrizia Colapietro, María Isabel Solarana Cabezuela, Romano Tenconi, Meena Upadhyaya, Lidia Larizza, Lucia Corrado, Marco Venturin, Paola Riva	2004	31
14	Unbalanced segregation of a complex four-break 5q23–31 insertion in the 5p13 band in a malformed child European Journal of Human Genetics ·Daniela Giardino, Palma Finelli, Francesco Amico, Thür Cecconi, Jerzy T. Petrus, Huage Hei, G. Nocera, Lidia Larizza	2004	3
15	KL/KIT co-expression in mouse fetal oocytes The International Journal of Developmental Biology ·Luisa Doneda, Francesca Gioia Klinger, Lidia Larizza, Massimo De Felici	2002	27
16	Genotype-phenotype correlation in patients with NF1 microdeletion syndrome: identification of candidate genes for mental retardation The American Journal of Human Genetics ·Paola Riva, Marco Venturin, Paolo Guarnieri, Francesca Orzan, Federica Natacci, Cristina Gervasini, R. Yturriaga Atarranz, Angela Bentivegna, M Stabile, Romano Tenconi, Meena Upadhyaya, Carmen Hernández, Lidia Larizza	2002	0
17	C-kit mutations in core binding factor leukemias Blood ·Alessandro Beghini, Paolo Peterlongo, Carla B. Ripamonti, Lidia Larizza, Roberto Cairoli, Enrica Morra, Cristina Mecucci	2000	240
18	A rapid and simple method for the generation of locus-specific probes for fish analysis Paola Riva, Lucia Corrado, Patrizia Colapietro, Lidia Larizza	1999	8
19	Detection of aneuploid cells in fibroblast cultures from the father of two trisomy 21 patients. PubMed ·Giuseppe Simoni, T. Kinone, Martina Stefanini, Lidia Larizza, P Maraschio, Fiorella Nuzzo	1976	1
20	Induced heteroploidy and cell transformation Lidia Larizza, Giuseppe Simoni, M. Stefanini	1976	3

About Lidia Larizza

Lidia Larizza is a scholar working on Developmental Biology, Genetics, Molecular Biology, Cancer Research and Genetics, having authored 271 papers that have together received 6.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (79 papers), Genomics and Chromatin Dynamics (43 papers), Prenatal Screening and Diagnostics (34 papers), Chromosomal and Genetic Variations (33 papers), RNA Research and Splicing (29 papers), Genetic Syndromes and Imprinting (28 papers), Genetics and Neurodevelopmental Disorders (25 papers) and RNA modifications and cancer (18 papers). The work is most often cited by research in Developmental Biology (244 citations), Genetics (2.3k citations), Molecular Biology (3.7k citations), Hematology (578 citations) and Pediatrics, Perinatology and Child Health (780 citations). Lidia Larizza has collaborated with scholars based in Italy, United States and France. Frequent co-authors include Alessandro Beghini, Silvia Russo, Gaia Roversi, Cristina Gervasini, Enrica Morra, Roberto Cairoli, Angelo Selicorni, Palma Finelli, Ivana Magnani and Paola Riva. Their work appears in journals such as International Journal of Cancer, Clinical Genetics, European Journal of Medical Genetics, European Journal of Human Genetics and International Journal of Molecular Sciences.

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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