Search Results - "Modafferi, Clarissa"

Genetic Testing in Periodontitis: A Narrative Review on Current Applications, Limitations, and Future Perspectives.

Authors: Modafferi, Clarissa Grippaudo, Cristina Corvaglia, Andrea et al.

Source: Genes. Nov2025, Vol. 16 Issue 11, p1308. 24p.

Genetic Aspects of Tooth Agenesis.

Authors: Modafferi, Clarissa Tucci, Ilaria Bogliardi, Francesco Maria et al.

Source: Genes. May2025, Vol. 16 Issue 5, p582. 14p.

Syndromic and Non-Syndromic Primary Failure of Tooth Eruption: A Genetic Overview.

Authors: Modafferi, Clarissa Tabolacci, Elisabetta Grippaudo, Cristina et al.

Source: Genes. Feb2025, Vol. 16 Issue 2, p147. 14p.

Clinical-Genetic Approach to Conditions with Macrocephaly and ASD/Behaviour Abnormalities: Variants in PTEN and PPP2R5D Are the Most Recurrent Gene Mutations in a Patient-Oriented Diagnostic Strategy.

Authors: L'Erario, Federica Francesca Gazzellone, Annalisa Contaldo, Ilaria et al.

Source: Genes. Apr2025, Vol. 16 Issue 4, p469. 11p.

Two new cases of fragile X syndrome without CGG triplet expansion. Clinical-molecular characterization and review of the literature.

Authors: Lauretti G Pietrobono R Niccolini B et al.

Source: European journal of medical genetics [Eur J Med Genet] 2026 Jul 15; Vol. 83, pp. 105093. Date of Electronic Publication: 2026 Jul 15.

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE

FMR1 RNA interaction with DNMT1 blocks DNA methylation at the FMR1 locus.

Authors: Nobile V Niccolini B Pucci C et al.

Source: NAR molecular medicine [NAR Mol Med] 2026 Jan 14; Vol. 3 (1), pp. ugag004. Date of Electronic Publication: 2026 Jan 14 (Print Publication: 2026).

Publication Type: Journal Article

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 9918752080106676 Publication Model: eCollection Cited Medium: Internet ISSN: 2976-856X (Electronic) Linking ISSN: 2976856X NLM ISO Abbreviation: NAR Mol Med Subsets: PubMed not MEDLINE

GAPO syndrome: a comprehensive examination and review of 105 clinical cases.

Authors: Modafferi C D'Ambrosio P Andaloro S et al.

Source: Journal of medical genetics [J Med Genet] 2025 Sep 17. Date of Electronic Publication: 2025 Sep 17.

Publication Type: Journal Article

Journal Info: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

New Insight into the genotype-phenotype correlation of PTH1R variants and primary failure of tooth eruption on an Italian Cohort.

Authors: Modafferi C Tabolacci E Lo Vecchio F et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2024 Nov; Vol. 32 (11), pp. 1402-1411. Date of Electronic Publication: 2024 Sep 26.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE