2026 Paolo Radice: Medicine Researcher – H-Index, Publications & Awards

Discipline name	D-Index	World Ranking	Current World Ranking	National Ranking	Current National Ranking	Publications	Citations
Medicine	101	7853	7383	263	248	462	46946

Overview

Paolo Radice is affiliated with the Fondazione IRCCS Istituto Nazionale dei Tumori in Italy. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology with significant contributions in Medicine as well. Subfields of focus include Genetics, Molecular Biology, Ophthalmology, Radiology, Nuclear Medicine and Imaging, and Oncology.

Their main topics of work comprise:

BRCA gene mutations in cancer
Genetic Associations and Epidemiology
Retinal and Macular Surgery
Genomics and Rare Diseases
Intraocular Surgery and Lenses
Retinal Diseases and Treatments
DNA Repair Mechanisms

Among recent publications from Paolo Radice are the following papers:

Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes, 2022, published in JAMA Oncology
OCT Biomarkers in Neovascular Age-Related Macular Degeneration: A Narrative Review, 2021, published in Journal of Ophthalmology
Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants, 2020, published in JAMA Oncology
Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel, 2024, published in The American Journal of Human Genetics
Breast cancer risks associated with missense variants in breast cancer susceptibility genes, 2022, published in Genome Medicine

They frequently collaborate with other researchers, notably:

Paolo Peterlongo
Irene L. Andrulis
Thilo Dörk
Heli Nevanlinna
Anna Jakubowska

Paolo Radice's work is commonly published in venues such as:

UNC Libraries
bioRxiv (Cold Spring Harbor Laboratory)
Cancers
Human Mutation
Retina

Best Publications

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies

A. Antoniou;P.D.P. Pharoah;S. Narod;H.A. Risch

4611
Citations
Association analysis identifies 65 new breast cancer risk loci

Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley

1400
Citations
Large-scale genotyping identifies 41 new loci associated with breast cancer risk

Kyriaki Michailidou;Per Hall;Anna Gonzalez-Neira;Maya Ghoussaini

1271
Citations
Breast-Cancer Risk in Families with Mutations in PALB2

A. C. Antoniou;S. Casadei;T. Heikkinen;D. Barrowdale

1023
Citations
RAD51B in Familial Breast Cancer

Liisa M. Pelttari;Sofia Khan;Mikko Vuorela;Johanna I. Kiiski

1015
Citations
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

Nasim Mavaddat;Kyriaki Michailidou;Kyriaki Michailidou;Joe Dennis;Michael Lush

940
Citations
Associations of Breast Cancer Risk Factors With Tumor Subtypes: A Pooled Analysis From the Breast Cancer Association Consortium Studies

Xiaohong R. Yang;Jenny Chang-Claude;Ellen L. Goode;Fergus J. Couch

916
Citations
Oral Contraceptives and the Risk of Hereditary Ovarian Cancer

S. A. Narod;H. Risch;R. Moslehi;A. Dorum

860
Citations
Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype

Sunil R. Lakhani;Jorge S. Reis-Filho;Laura Fulford;Frederique Penault-Llorca

810
Citations
Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women

Leila Dorling;Sara Carvalho;Jamie Allen

783
Citations
Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA).

Nasim Mavaddat;Daniel Barrowdale;Irene L. Andrulis;Susan M. Domchek

732
Citations
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

John R.B. Perry;Felix Day;Cathy E. Elks;Patrick Sulem

681
Citations
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

Kyriaki Michailidou;Jonathan Beesley;Sara Lindstrom;Sander Canisius

663
Citations
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Stig E. Bojesen;Stig E. Bojesen;Karen A. Pooley;Sharon E. Johnatty;Jonathan Beesley

643
Citations
Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants

Nasim Mavaddat;Paul D.P. Pharoah;Kyriaki Michailidou;Jonathan Tyrer

643
Citations
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

Felix R. Day;Deborah J. Thompson;Hannes Helgason;Hannes Helgason;Daniel I. Chasman

641
Citations
MicroRNA related polymorphisms and breast cancer risk

Sofia Khan;Dario Greco;Dario Greco;Kyriaki Michailidou;Roger L. Milne;Roger L. Milne

632
Citations
The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions.

A C Antoniou;A P Cunningham;J Peto;D G Evans

610
Citations
A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene: Implications for Presymptomatic Testing and Screening

Donna Shattuck Eidens;Melody Mcclure;Jacques Simard;Fernand Labrie

591
Citations
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

Timothy R. Rebbeck;Nandita Mitra;Fei Wan;Olga M. Sinilnikova

513
Citations

Frequent Co-Authors

Paolo Peterlongo Memorial Sloan Kettering Cancer Center

Irene L. Andrulis University of Toronto

Graham G. Giles University of Melbourne

Hiltrud Brauch German Cancer Research Center

Melissa C. Southey Monash University

Roger L. Milne Cancer Council Victoria

Fergus J. Couch Mayo Clinic

Douglas F. Easton University of Cambridge

Heli Nevanlinna University of Helsinki

Georgia Chenevix-Trench QIMR Berghofer Medical Research Institute

External Links

Personal website of Paolo Radice

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