Author

Margherita Mutarelli

Observed names: M Mutarelli, M. Mutarelli, Mutarelli, Margherita

Institutions: Institute of Applied Science and Intelligent Systems, National Research Council

Observed institutions: Radboud University Nijmegen, University of Campania "Luigi Vanvitelli", Istituto Superiore di Sanità, Radboud University Medical Center, Institute of Food Science, Institute of Applied Science and Intelligent Systems, Federico II University Hospital, Italian Association for Cancer Research, Telethon Institute Of Genetics And Medicine, National Research Council, University of Naples Federico II

ORCID: 0000-0002-2168-5059

Observed ORCID: 0000-0002-2168-5059

OpenAlex ID: A5010286920

Global analysis of estrogen receptor beta binding to breast cancer cell genome reveals an extensive interplay with estrogen receptor alpha for target gene regulation

2011 · Oli MV Grober, Margherita Mutarelli, et al. · BMC Genomics · 177

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Autophagosome–lysosome fusion triggers a lysosomal response mediated by TLR9 and controlled by OCRL

2016 · Maria Giovanna De Leo, Leopoldo Staiano, et al. · Nature Cell Biology · 173

Estrogen Receptor α Controls a Gene Network in Luminal-Like Breast Cancer Cells Comprising Multiple Transcription Factors and MicroRNAs

2010 · Luigi Cicatiello, Margherita Mutarelli, et al. · American Journal Of Pathology · 163

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Triple Vectors Expand AAV Transfer Capacity in the Retina

2017 · Andrea Maddalena, Patrizia Tornabene, et al. · Molecular Therapy · 137

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High-resolution analysis of the human retina miRNome reveals isomiR variations and novel microRNAs

2016 · Marianthi Karali, Maria Persico, et al. · Nucleic Acids Research · 120

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Time-course analysis of genome-wide gene expression data from hormone-responsive human breast cancer cells

2008 · Margherita Mutarelli, Luigi Cicatiello, et al. · BMC Bioinformatics · 109

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The genetic basis of undiagnosed muscular dystrophies and myopathies: Results from 504 patients

2016 · Marco Savarese, Giuseppina Di Fruscio, et al. · Neurology · 103

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Next-Generation Sequencing Identifies Transportin 3 as the Causative Gene for LGMD1F

2013 · Annalaura Torella, Marina Fanin, et al. · PLoS ONE · 91

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Direct generation of human naive induced pluripotent stem cells from somatic cells in microfluidics

2018 · Stefano Giulitti, Marco Pellegrini, et al. · Nature Cell Biology · 90

Nutrient‐sensitive transcription factors TFEB and TFE3 couple autophagy and metabolism to the peripheral clock

2019 · Nunzia Pastore, Anna Vainshtein, et al. · The EMBO Journal · 88

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Quantitative expression profiling of highly degraded RNA from formalin-fixed, paraffin-embedded breast tumor biopsies by oligonucleotide microarrays

2008 · Maria Ravo, Margherita Mutarelli, et al. · Laboratory Investigation · 81

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An atlas of gene expression and gene co-regulation in the human retina

2016 · Michele Pinelli, Annamaria Carissimo, et al. · Nucleic Acids Research · 78

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MotorPlex provides accurate variant detection across large muscle genes both in single myopathic patients and in pools of DNA samples

2014 · Marco Savarese, Giuseppina Di Fruscio, et al. · Acta Neuropathologica Communications · 73

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Massive-Scale RNA-Seq Analysis of Non Ribosomal Transcriptome in Human Trisomy 21

2011 · Valerio Costa, Claudia Angelini, et al. · PLoS ONE · 71

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Lysoplex: An efficient toolkit to detect DNA sequence variations in the autophagy-lysosomal pathway

2015 · Giuseppina Di Fruscio, Angela Schulz, et al. · Autophagy · 63

Genetic Association of ARHGAP21 Gene Variant with Mandibular Prognathism

2015 · L. Perillo, A. Monsurrò, et al. · Journal of Dental Research · 60

Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes

2022 · Marcello Scala, Masashi Nishikawa, et al. · Brain · 57

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HOCTAR database: A unique resource for microRNA target prediction

2011 · Vincenzo Alessandro Gennarino, Marco Sardiello, et al. · Gene · 57

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BATS: a Bayesian user-friendly software for Analyzing Time Series microarray experiments

2008 · Claudia Angelini, Luisa Cutillo, et al. · BMC Bioinformatics · 57

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TFEB regulates murine liver cell fate during development and regeneration

2020 · Nunzia Pastore, Tuong Huynh, et al. · Nature Communications · 56

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De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides–Baraitser syndrome

2020 · Gerarda Cappuccio, Camille Sayou, et al. · Genetics in Medicine · 53

Myopalladin promotes muscle growth through modulation of the serum response factor pathway

2019 · Maria Carmela Filomena, Daniel L. Yamamoto, et al. · Journal of Cachexia Sarcopenia and Muscle · 49

Computational drugs repositioning identifies inhibitors of oncogenic PI3K/AKT/P70S6K-dependent pathways among FDA-approved compounds

2016 · Diego Carrella, Isabella Manni, et al. · Oncotarget · 48

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YAP contributes to DNA methylation remodeling upon mouse embryonic stem cell differentiation

2020 · Fabiana Passaro, Ilaria De Martino, et al. · Journal of Biological Chemistry · 47

The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy

2013 · Ivana Peluso, Ivan Conte, et al. · Orphanet Journal of Rare Diseases · 47

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Works count: 86

Citation count: 2,709

H-index: 30

I10-index: 46