Pierpaola Tannorella

Author

University of Pisa ORCID

Also Known As

P Tannorella, Pierpaola Tannorella, Tannorella, Pierpaola

Publications

591

Citations

H-Index

Concepts

All Affiliations

University of Pisa Istituti di Ricovero e Cura a Carattere Scientifico IRCCS Istituto Auxologico Italiano University of Siena University of Campania "Luigi Vanvitelli"

About

Pierpaola Tannorella is an author at University of Pisa specializing in medicine, genetics, and epigenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	135
2	Molecular Biology	2	2	97
3	Natural Sciences	1	1	75
4	Public Health	1	1	13
5	Molecular Medicine	1	1	13

Pierpaola Tannorella

Publications

537

Citations

H-Index

Page 1

	Year	Citations
Methylation analysis of multiple genes in blood DNA of Alzheimer’s disease and healthy individuals Pierpaola Tannorella, Andrea Stoccoro, Gloria Tognoni, Neuroscience Letters Neurodegenerative DiseasesAlzheimer's DiseaseEpigenetic RegulationBlood DnaGenetics	2015	75
Folate, Homocysteine, Vitamin B12, and Polymorphisms of Genes Participating in One-Carbon Metabolism in Late-Onset Alzheimer's Disease Patients and Healthy Controls Fabio Coppedè, Pierpaola Tannorella, Ilaria Pezzini, Antioxidants and Redox Signaling	2011	72
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences Thomas Eggermann, Elzem Yapici, Jet Bliek, Clinical Epigenetics	2022	51
Association of Polymorphisms in Genes Involved in One-Carbon Metabolism with MTHFR Methylation Levels Fabio Coppedè, Andrea Stoccoro, Pierpaola Tannorella, International Journal of Molecular Sciences	2019	50
Artificial Neural Networks Link One-Carbon Metabolism to Gene-Promoter Methylation in Alzheimer’s Disease Enzo Grossi, Andrea Stoccoro, Pierpaola Tannorella, Journal of Alzheimer s Disease	2016	45
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 Viviana Pensato, Stefania Magri, Eleonora Dalla Bella, Journal of Clinical Medicine	2020	36
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders Deborah Mackay, Jet Bliek, Masayo Kagami, Clinical Epigenetics	2022	33
DNMT3B promoter polymorphisms and maternal risk of birth of a child with Down syndrome Fabio Coppedè, Paolo Bosco, Pierpaola Tannorella, Human Reproduction	2012	28
The Methylenetetrahydrofolate Reductase C677T Polymorphism and Risk for Late-Onset Alzheimer’s disease: Further Evidence in an Italian Multicenter Study Andrea Stoccoro, Pierpaola Tannorella, Maria Grazia Salluzzo, Journal of Alzheimer s Disease	2017	27
Increased MTHFR promoter methylation in mothers of Down syndrome individuals Fabio Coppedè, Maria Denaro, Pierpaola Tannorella, Mutation research. Fundamental and molecular mechanisms of mutagenesis Down SyndromeGenetic DisorderMedicineGeneticsDna Methylation	2016	25

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