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A

Andrea Stoccoro

University of Pisa

H指数:23

被引数:1,870

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Mitochondrial epigenetic mechanisms in cancer: an updated overview

Frontiers in Cell and Developmental Biology

IF4.3

2026-01-170

OAAI

Increased methylation levels of the MTHFR gene promoter in Down syndrome

唐氏综合征中MTHFR基因启动子的甲基化水平升高

IF2.6

2025-09-010

PRE

Epigenetic Mechanisms Underlying Sex Differences in Neurodegenerative Diseases

IF3.5

2025-01-190

OAAI

DNA methylation analysis of multiple genes in thymic epithelial tumors

IF2.6

2024-11-080

PRE

Mitochondrial D-loop methylation levels inversely correlate with disease duration in amyotrophic lateral sclerosis

IF2.6

2024-02-053

PRE

Editorial: Role of genetics, epigenetics, and environmental factors in human complex diseases from the mitochondrial point of view

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2023-05-171

OAAI

The Potential Role of Dysregulated miRNAs in Adolescent Idiopathic Scoliosis and 22q11.2 Deletion Syndrome

失调的miRNAs在青少年特发性脊柱侧凸和22 q11.2缺失综合征中的潜在作用

JOURNAL OF PERSONALIZED MEDICINE

IF3

2022-11-187

OAAI

Artificial neural networks reveal sex differences in gene methylation, and connections between maternal risk factors and symptom severity in autism spectrum disorder

人工神经网络揭示了自闭症谱系障碍中基因甲基化的性别差异，以及母亲危险因素与症状严重程度之间的联系

IF2.6

2022-11-038

PRE

A perspective on diet, epigenetics and complex diseases: where is the field headed next?

IF2.6

2022-11-037

PRE

Editorial: Epigenetics of Neurodevelopmental, Neuromuscular and Neurodegenerative Disorders

FRONTIERS IN MOLECULAR NEUROSCIENCE

IF3.8

2022-06-101

OAAI

Correlation among maternal risk factors, gene methylation and disease severity in females with autism spectrum disorder

母亲危险因素、基因甲基化与女性孤独症谱系障碍疾病严重程度的相关性研究

IF2.6

2022-01-277

PRE

Gender Specific Differences in Disease Susceptibility: The Role of Epigenetics

IF3.9

2021-06-0857

OAAI

Autism Spectrum Disorder from the Womb to Adulthood: Suggestions for a Paradigm Shift

从子宫到成年的自闭症谱系障碍: 范式转变的建议

JOURNAL OF PERSONALIZED MEDICINE

IF3

2021-01-2545

OAAI

Panisi, Cristina; Guerini, Franca Rosa; Abruzzo, Provvidenza Maria; Balzola, Federico; Biava, Pier Mario; Bolotta, Alessandra; Brunero, Marco; Burgio, Ernesto; Chiara, Alberto; Clerici, Mario; Croce, Luigi; Ferreri, Carla; Giovannini, Niccolo; Ghezzo, Alessandro; Grossi, Enzo; Keller, Roberto; Manzotti, Andrea; Marini, Marina; Migliore, Lucia; Moderato, Lucio; Moscone, Davide; Mussap, Michele; Parmeggiani, Antonia; Pasin, Valentina; Perotti, Monica; Piras, Cristina; Saresella, Marina; Stoccoro, Andrea; Toso, Tiziana; Vacca, Rosa Anna; Vagni, David; Vendemmia, Salvatore; Villa, Laura; Politi, Pierluigi; Fanos, Vassilios

Investigation of MLH1, MGMT, CDKN2A, and RASSF1A Gene Methylation in Thymomas From Patients With Myasthenia Gravis

FRONTIERS IN MOLECULAR NEUROSCIENCE

IF3.8

2020-10-234

OAAI

Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis

CLINICAL EPIGENETICS

IF4.4

2020-09-1131

OAAI

Genetic and epigenetic MTHFR gene variants in the mothers of attention-deficit/hyperactivity disorder affected children as possible risk factors for neurodevelopmental disorders

IF2.6

2020-06-022

PREAI

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

IF2.6

2020-05-1212

PREAI

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

IF3.7

2019-12-077

OAAI

Mitoepigenetics and Neurodegenerative Diseases

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2019-02-1955

OAAI

Activation of the interferon type I response rather than autophagy contributes to myogenesis inhibition in congenital DM1 myoblasts

CELL DEATH & DISEASE

IF9.6

2018-10-1914

OAAI