P. Lagomarsini - Concepedia

Author

P. Lagomarsini

Istituto di Genetica Molecolare

Also Known As

P Lagomarsini, P. Lagomarsini, Paola Lagomarsini

Publications

447

Citations

H-Index

Concepts

All Affiliations

Istituto di Genetica Molecolare University of Pavia Policlinico San Matteo Fondazione University of Sussex

About

P. Lagomarsini is an author at Istituto di Genetica Molecolare specializing in pathology, medicine, and dermatology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	228
2	Health Sciences	2	2	68
3	Public Health	1	1	16
4	Cell Biology	1	1	47
5	Molecular Medicine	1	1	137

P. Lagomarsini

Publications

416

Citations

H-Index

Page 1

	Year	Citations
Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity Miria Stefanini, P. Lagomarsini, C.F. Arlett, Human Genetics Complementation Group DXeroderma PigmentosumMendelian DisorderGenetic DisorderPathology	1986	137
Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy Miria Stefanini, P. Lagomarsini, Silvia Giliani, Carcinogenesis	1993	115
Chromosome instability in lymphocytes from a patient with Werner's syndrome is not associated with DNA repair defects Miria Stefanini, Susi Scappaticci, P. Lagomarsini, Mutation Research/DNAging ChromatinGenome InstabilityChromosome InstabilityDna DamageCell Division	1989	47
Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivity Miria Stefanini, P. Lagomarsini, R. Giorgi, Mutation Research Letters Complement SystemEnhanced Uv PhotosensitivityMedicinePhotocarcinogenesisComplementation Studies	1987	28
Response of mammalian ADP-ribosyl transferase to lymphocyte stimulation, mutagen treatment and cell cycling A. Ivana Scovassi, Miria Stefanini, P. Lagomarsini, Carcinogenesis	1987	28
Trichothiodystrophy without photosensitivity A. Fois, Paolo Balestri, Stefano Calvieri, European Journal of Pediatrics PhotochemistryPhototoxicityDegenerative DiseasePhotoprotectionDermatology	1988	21
Search for consanguinity within and among families of patients with trichothiodystrophy associated with xeroderma pigmentosum. Fiorella Nuzzo, G. Zei, Miria Stefanini, Journal of Medical Genetics Genetic TestingGeneticsGenetic EpidemiologyLinkage AnalysisPathology	1990	16
Normal sensitivity to mutagens, spontaneous chromosome breakage, and mutation frequency in nevoid basal cell carcinoma syndrome. Miria Stefanini, P. Lagomarsini, Enzo Berardesca, PubMed	1988	14
Chromosomal fragility in the cancer-prone disease xeroderma pigmentosum preferentially involves bands relevant for cutaneous carcinogenesis A Lanza, P. Lagomarsini, Alessandra Casati, International Journal of Cancer	1997	10

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