Pierpaola Tannorella - Search Results

Year	Number of Results
2011	1
2012	2
2013	1
2014	1
2015	1
2016	4
2017	2
2019	2
2020	2
2021	1
2022	2

1

Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases.

Tannorella P, Minervino D, Guzzetti S, Vimercati A, Calzari L, Patti G, Maghnie M, Allegri AEM, Milani D, Scuvera G, Mariani M, Modena P, Selicorni A, Larizza L, Russo S. Tannorella P, et al. Genes (Basel). 2021 Apr 17;12(4):588. doi: 10.3390/genes12040588. Genes (Basel). 2021. PMID: 33920573 Free PMC article.

2

Polymorphisms of genes required for methionine synthesis and DNA methylation influence mitochondrial DNA methylation.

Stoccoro A, Tannorella P, Migliore L, Coppedè F. Stoccoro A, et al. Among authors: tannorella p. Epigenomics. 2020 Jun;12(12):1003-1012. doi: 10.2217/epi-2020-0041. Epub 2020 May 12. Epigenomics. 2020. PMID: 32393056

3

Methylation analysis of DNA repair genes in Alzheimer's disease.

Coppedè F, Tannorella P, Stoccoro A, Chico L, Siciliano G, Bonuccelli U, Migliore L. Coppedè F, et al. Among authors: tannorella p. Mech Ageing Dev. 2017 Jan;161(Pt A):105-111. doi: 10.1016/j.mad.2016.04.003. Epub 2016 Apr 11. Mech Ageing Dev. 2017. PMID: 27080585 Clinical Trial.

4

Association of Polymorphisms in Genes Involved in One-Carbon Metabolism with MTHFR Methylation Levels.

Coppedè F, Stoccoro A, Tannorella P, Gallo R, Nicolì V, Migliore L. Coppedè F, et al. Among authors: tannorella p. Int J Mol Sci. 2019 Jul 31;20(15):3754. doi: 10.3390/ijms20153754. Int J Mol Sci. 2019. PMID: 31370354 Free PMC article.

5

Increased MTHFR promoter methylation in mothers of Down syndrome individuals.

Coppedè F, Denaro M, Tannorella P, Migliore L. Coppedè F, et al. Among authors: tannorella p. Mutat Res. 2016 May;787:1-6. doi: 10.1016/j.mrfmmm.2016.02.008. Epub 2016 Feb 22. Mutat Res. 2016. PMID: 26926955

6

Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms.

Pensato V, Magri S, Bella ED, Tannorella P, Bersano E, Sorarù G, Gatti M, Ticozzi N, Taroni F, Lauria G, Mariotti C, Gellera C. Pensato V, et al. Among authors: tannorella p. J Clin Med. 2020 Feb 3;9(2):412. doi: 10.3390/jcm9020412. J Clin Med. 2020. PMID: 32028661 Free PMC article.

7

Plasma Homocysteine and Polymorphisms of Genes Involved in Folate Metabolism Correlate with DNMT1 Gene Methylation Levels.

Coppedè F, Stoccoro A, Tannorella P, Migliore L. Coppedè F, et al. Among authors: tannorella p. Metabolites. 2019 Dec 7;9(12):298. doi: 10.3390/metabo9120298. Metabolites. 2019. PMID: 31817852 Free PMC article.

8

Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences.

Eggermann T, Yapici E, Bliek J, Pereda A, Begemann M, Russo S, Tannorella P, Calzari L, de Nanclares GP, Lombardi P, Temple IK, Mackay D, Riccio A, Kagami M, Ogata T, Lapunzina P, Monk D, Maher ER, Tümer Z. Eggermann T, et al. Among authors: tannorella p. Clin Epigenetics. 2022 Mar 16;14(1):41. doi: 10.1186/s13148-022-01259-x. Clin Epigenetics. 2022. PMID: 35296332 Free PMC article.

9

Artificial Neural Networks Link One-Carbon Metabolism to Gene-Promoter Methylation in Alzheimer's Disease.

Grossi E, Stoccoro A, Tannorella P, Migliore L, Coppedè F. Grossi E, et al. Among authors: tannorella p. J Alzheimers Dis. 2016 Jul 1;53(4):1517-22. doi: 10.3233/JAD-160210. J Alzheimers Dis. 2016. PMID: 27392858

10

Methylation analysis of multiple genes in blood DNA of Alzheimer's disease and healthy individuals.

Tannorella P, Stoccoro A, Tognoni G, Petrozzi L, Salluzzo MG, Ragalmuto A, Siciliano G, Haslberger A, Bosco P, Bonuccelli U, Migliore L, Coppedè F. Tannorella P, et al. Neurosci Lett. 2015 Jul 23;600:143-7. doi: 10.1016/j.neulet.2015.06.009. Epub 2015 Jun 12. Neurosci Lett. 2015. PMID: 26079324

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