Claudia Angelini

ResearcherID Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 25

Top Topics

Dna Methylation

Induced Pluripotent Stem Cells

Top Venues

Genome research

Journal of translational medicine

Bioinformatics (Oxford, England)

This page only lists publications with an associated author ORCID identifier.

Publications

Anna Plaksienko, Pietro Di Lena, Christine Nardini, Claudia Angelini
methyLImp2: faster missing value estimation for DNA methylation data. Bioinformatics (Oxford, England) 40 (1) (2024)
Anna Plaksienko, Pietro Di Lena, Christine Nardini, Claudia Angelini
methyLImp2: faster missing value estimation for DNA methylation data. Bioinformatics (Oxford, England) 40 (1) (2024)
Maria Claudia Costa, Claudia Angelini, Monica Franzese, Concetta Iside, Marco Salvatore, Luigi Laezza, Francesco Napolitano, Michele Ceccarelli
Identification of therapeutic targets in osteoarthritis by combining heterogeneous transcriptional datasets, drug-induced expression profiles, and known drug-target interactions. Journal of translational medicine 22 (1) (2024)
Claudia Angelini, Daniela De Canditiis, Italia De Feis, Antonella Iuliano
A Network-Constrain Weibull AFT Model for Biomarkers Discovery. Biometrical journal. Biometrische Zeitschrift 66 (7) (2024)
Maria Claudia Costa, Claudia Angelini, Monica Franzese, Concetta Iside, Marco Salvatore, Luigi Laezza, Francesco Napolitano, Michele Ceccarelli
Identification of therapeutic targets in osteoarthritis by combining heterogeneous transcriptional datasets, drug-induced expression profiles, and known drug-target interactions. Journal of translational medicine 22 (1) (2024)
Maria Claudia Costa, Claudia Angelini, Monica Franzese, Concetta Iside, Marco Salvatore, Luigi Laezza, Francesco Napolitano, Michele Ceccarelli
Identification of therapeutic targets in osteoarthritis by combining heterogeneous transcriptional datasets, drug-induced expression profiles, and known drug-target interactions. Journal of translational medicine 22 (1) (2024)
Maria Claudia Costa, Claudia Angelini, Monica Franzese, Concetta Iside, Marco Salvatore, Luigi Laezza, Francesco Napolitano, Michele Ceccarelli
Identification of therapeutic targets in osteoarthritis by combining heterogeneous transcriptional datasets, drug-induced expression profiles, and known drug-target interactions. Journal of translational medicine 22 (1) (2024)
Anna Plaksienko, Pietro Di Lena, Christine Nardini, Claudia Angelini
methyLImp2: faster missing value estimation for DNA methylation data. Bioinformatics (Oxford, England) 40 (1) (2024)
Varsha Poondi-Krishnan, Barbara Morone, Shir Toubiana, Monika Krzak, Salvatore Fioriniello, Floriana Della Ragione, Maria Strazzullo, Claudia Angelini, Sara Selig, Maria R Matarazzo
The aberrant epigenome of DNMT3B -mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory. Genome research 33 (2) (2023)
Ankit Verma, Varsha Poondi-Krishnan, Francesco Cecere, Emilia D'Angelo, Vincenzo Lullo, Maria Strazzullo, Sara Selig, Claudia Angelini, Maria R Matarazzo, Andrea Riccio
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming. Biomolecules 13 (12) (2023)
Varsha Poondi-Krishnan, Barbara Morone, Shir Toubiana, Monika Krzak, Salvatore Fioriniello, Floriana Della Ragione, Maria Strazzullo, Claudia Angelini, Sara Selig, Maria R Matarazzo
The aberrant epigenome of DNMT3B -mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory. Genome research (2023)
Varsha Poondi-Krishnan, Barbara Morone, Shir Toubiana, Monika Krzak, Salvatore Fioriniello, Floriana Della Ragione, Maria Strazzullo, Claudia Angelini, Sara Selig, Maria R Matarazzo
The aberrant epigenome of DNMT3B -mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory. Genome research 33 (2) (2023)
Varsha Poondi-Krishnan, Barbara Morone, Shir Toubiana, Monika Krzak, Salvatore Fioriniello, Floriana Della Ragione, Maria Strazzullo, Claudia Angelini, Sara Selig, Maria R Matarazzo
The aberrant epigenome of DNMT3B -mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory. Genome research 33 (2) (2023)
Ankit Verma, Varsha Poondi-Krishnan, Francesco Cecere, Emilia D'Angelo, Vincenzo Lullo, Maria Strazzullo, Sara Selig, Claudia Angelini, Maria R Matarazzo, Andrea Riccio
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming. Biomolecules 13 (12) (2023)
Francesco Cecere, Laura Pignata, Bruno Hay Mele, Abu Saadat, Emilia D'Angelo, Orazio Palumbo, Pietro Palumbo, Massimo Carella, Gioacchino Scarano, Giovanni Battista Rossi, Claudia Angelini, Angela Sparago, Flavia Cerrato, Andrea Riccio
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer. Cancers 15 (7) (2023)
Varsha Poondi-Krishnan, Barbara Morone, Shir Toubiana, Monika Krzak, Salvatore Fioriniello, Floriana Della Ragione, Maria Strazzullo, Claudia Angelini, Sara Selig, Maria R Matarazzo
The aberrant epigenome of DNMT3B -mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory. Genome research 33 (2) (2023)
Ankit Verma, Varsha Poondi-Krishnan, Francesco Cecere, Emilia D'Angelo, Vincenzo Lullo, Maria Strazzullo, Sara Selig, Claudia Angelini, Maria R Matarazzo, Andrea Riccio
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming. Biomolecules 13 (12) (2023)
Ye Cui, Mehdi Benamar, Klaus Schmitz-Abe, Varsha Poondi-Krishnan, Qian Chen, Bat-Erdene Jugder, Benoit Fatou, Jason Fong, Yuelin Zhong, Stuti Mehta, Altantsetseg Buyanbat, Beray Selver Eklioglu, Esra Karabiber, Safa Barış, Ayça Kiykim, Sevgi Keles, Emmanuel Stephen-Victor, Claudia Angelini, Louis-Marie Charbonnier, Talal A Chatila
A Stk4-Foxp3-NF-κB p65 transcriptional complex promotes T reg cell activation and homeostasis. Science immunology 7 (75) (2022)
Gabriella Lania, Monica Franzese, Noritaka Adachi, Marchesa Bilio, Gemma Flore, Annalaura Russo, Erika D'Agostino, Claudia Angelini, Robert G Kelly, Antonio Baldini
A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome. Disease models & mechanisms 15 (9) (2022)
Sara Terreri, Sara Mancinelli, Matteo Ferro, Maria Concetta Vitale, Sisto Perdonà, Luigi Castaldo, Vincenzo Gigantino, Vincenzo Mercadante, Rossella De Cecio, Gabriella Aquino, Marco Montella, Claudia Angelini, Eugenio Del Prete, Marianna Aprile, Angelo Ciaramella, Giovanna Lucia Liguori, Valerio Costa, George A Calin, Evelina La Civita, Daniela Terracciano, Ferdinando Febbraio, Amelia Cimmino
Subcellular Localization of uc.8+ as a Prognostic Biomarker in Bladder Cancer Tissue. Cancers 13 (4) (2021)
Nicola G Criscuolo, Claudia Angelini
StructuRly: A novel shiny app to produce comprehensive, detailed and interactive plots for population genetic analysis. PloS one 15 (2) (2020)
Mariangela Valletta, Rosita Russo, Ilaria Baglivo, Veronica Russo, Sara Ragucci, Annamaria Sandomenico, Emanuela Iaccarino, Menotti Ruvo, Italia De Feis, Claudia Angelini, Sara Iachettini, Annamaria Biroccio, Paolo Vincenzo Pedone, Angela Nebbioso
Exploring the Interaction between the SWI/SNF Chromatin Remodeling Complex and the Zinc Finger Factor CTCF. International journal of molecular sciences 21 (23) (2020)
Roberto Defez, Anna Andreozzi, Silvia Romano, Gabriella Pocsfalvi, Immacolata Fiume, Roberta Esposito, Claudia Angelini, Carmen Bianco
Bacterial IAA-Delivery into Medicago Root Nodules Triggers a Balanced Stimulation of C and N Metabolism Leading to a Biomass Increase. Microorganisms 7 (10) (2019)
Francesco Russo, Dario Righelli, Claudia Angelini
Advancements in RNASeqGUI towards a Reproducible Analysis of RNA-Seq Experiments. BioMed research international 2016 (2016)
Alessandro Fiorenzano, Emilia Pascale, Cristina D'Aniello, Dario Acampora, Cecilia Bassalert, Francesco Russo, Gennaro Andolfi, Mauro Biffoni, Federica Francescangeli, Ann Zeuner, Claudia Angelini, Claire Chazaud, Eduardo J Patriarca, Annalisa Fico, Gabriella Minchiotti
Cripto is essential to capture mouse epiblast stem cell and human embryonic stem cell pluripotency. Nature communications 7 (2016)