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Pierpaola Tannorella

Observed names: P Tannorella, TANNORELLA, PIERPAOLA, Tannorella, Pierpaola
ORCID: 0000-0003-1367-9860
Observed ORCID: 0000-0003-1367-9860
OpenAlex ID: A5036025922
Methylation analysis of multiple genes in blood DNA of Alzheimer’s disease and healthy individuals
2015 · Pierpaola Tannorella, Andrea Stoccoro, et al. · Neuroscience Letters · 74
Folate, Homocysteine, Vitamin B12, and Polymorphisms of Genes Participating in One-Carbon Metabolism in Late-Onset Alzheimer's Disease Patients and Healthy Controls
2011 · Fabio Coppedè, Pierpaola Tannorella, et al. · Antioxidants and Redox Signaling · 74
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences
2022 · Thomas Eggermann, Elzem Yapici, et al. · Clinical Epigenetics · 57
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Association of Polymorphisms in Genes Involved in One-Carbon Metabolism with MTHFR Methylation Levels
2019 · Fabio Coppedè, Andrea Stoccoro, et al. · International Journal of Molecular Sciences · 50
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Artificial Neural Networks Link One-Carbon Metabolism to Gene-Promoter Methylation in Alzheimer’s Disease
2016 · Enzo Grossi, Andrea Stoccoro, et al. · Journal of Alzheimer s Disease · 46
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders
2022 · Deborah Mackay, Jet Bliek, et al. · Clinical Epigenetics · 34
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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
2020 · Viviana Pensato, Stefania Magri, et al. · Journal of Clinical Medicine · 33
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DNMT3B promoter polymorphisms and maternal risk of birth of a child with Down syndrome
2012 · Fabio Coppedè, Paolo Bosco, et al. · Human Reproduction · 30
The Methylenetetrahydrofolate Reductase C677T Polymorphism and Risk for Late-Onset Alzheimer’s disease: Further Evidence in an Italian Multicenter Study
2017 · Andrea Stoccoro, Pierpaola Tannorella, et al. · Journal of Alzheimer s Disease · 27
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis
2024 · Deborah J. G. Mackay, Gabriella Gazdagh, et al. · Clinical Epigenetics · 25
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Increased MTHFR promoter methylation in mothers of Down syndrome individuals
2016 · Fabio Coppedè, Maria Denaro, et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 23
Methylation analysis of DNA repair genes in Alzheimer’s disease
2016 · Fabio Coppedè, Pierpaola Tannorella, et al. · Mechanisms of Ageing and Development · 22
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith–Wiedemann progeny
2022 · Pierpaola Tannorella, Luciano Calzari, et al. · Clinical Epigenetics · 19
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Plasma Homocysteine and Polymorphisms of Genes Involved in Folate Metabolism Correlate with DNMT1 Gene Methylation Levels
2019 · Fabio Coppedè, Andrea Stoccoro, et al. · Metabolites · 19
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Clinical and molecular characterization of patients affected by Beckwith‐Wiedemann spectrum conceived through assisted reproduction techniques
2022 · Diana Carli, Matteo Operti, et al. · Clinical Genetics · 15
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Polymorphisms of Genes Required for Methionine Synthesis and DNA Methylation Influence Mitochondrial DNA Methylation
2020 · Andrea Stoccoro, Pierpaola Tannorella, et al. · Epigenomics · 14
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases
2021 · Pierpaola Tannorella, Daniele Minervino, et al. · Genes · 13
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Prenatal testing for imprinting disorders: A laboratory perspective
2023 · Jasmin Beygo, Silvia Russo, et al. · Prenatal Diagnosis · 11
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Performance Metrics of the Scoring System for the Diagnosis of the Beckwith–Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development
2023 · Maria Luca, Diana Carli, et al. · Cancers · 9
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Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver–Russell Syndrome and Focus on the IGF1R Gene
2024 · Alessandro Vimercati, Pierpaola Tannorella, et al. · The Journal of Clinical Endocrinology & Metabolism · 8
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Exploring NEK1 genetic variability in Italian amyotrophic lateral sclerosis patients
2025 · Viviana Pensato, Silvia Peverelli, et al. · Journal of Neurology · 6
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Association study between the DNMT3A -448A>G polymorphism and risk of Alzheimer's disease in Caucasians of Italian origin.
2016 · Pierpaola Tannorella, Andrea Stoccoro, et al. · PubMed · 6
Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum
2023 · Alessandro Vimercati, Pierpaola Tannorella, et al. · Frontiers in Genetics · 3
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Beckwith-Wiedemann spectrum (BWSp): an update on diagnosis, management, and follow-up from the scientific committee of the Italian BWSp association
2025 · Silvia Russo, Donatella Milani, et al. · ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics · 2
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A Pilot Study Evaluating the Contribution ofSLC19A1(RFC-1) 80G>A Polymorphism to Alzheimer’s Disease in Italian Caucasians
2014 · Fabio Coppedè, Pierpaola Tannorella, et al. · BioMed Research International · 2
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Works count: 43
Citation count: 622
H-index: 15
I10-index: 18
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