Emanuela Abiusi

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 9

Top Topics

Intellectual Disability

Candida Albicans

Congenital Heart Disease

Ejection Fraction

Top Venues

European journal of human genetics : EJHG

European heart journal

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology

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

Publications

Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG 32 (2) (2023)
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG 32 (2) (2023)
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG (2023)
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG 32 (2) (2023)
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG 32 (2) (2023)
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG 32 (2) (2023)
Roberta Pastorino, Michele Sassano, Danilo Francesco Tiziano, Luca Giraldi, Rosarita Amore, Dario Arzani, Emanuela Abiusi, Wolfgang Ahrens, Laia Alemany Vilches, Cristina Canova, Claire Mary Healy, Ivana Holcatova, Pagona Lagiou, Jerry Polesel, Maja Popović, Ståle Nygard, Gabriella Cadoni, Ariana Znaor, Paolo Boffetta, Keitaro Matsuo, Isao Oze, Paul J Brennan, Stefania Boccia
Plasma miR-151-3p as a Candidate Diagnostic Biomarker for Head and Neck Cancer: A Cross-sectional Study within the INHANCE Consortium. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 31 (12) (2022)
Roddy Walsh, Arnon Adler, Ahmad S Amin, Emanuela Abiusi, Melanie Care, Hennie Bikker, Simona Amenta, Harriet Feilotter, Eline A Nannenberg, Francesco Mazzarotto, Valentina Trevisan, John Garcia, Ray E Hershberger, Marco Valentin Perez, Amy C Sturm, James Simon Ware, Wojciech Zareba, Valeria Novelli, Arthur A M Wilde, Michael H Gollob
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death. European heart journal (2021)
Emanuela Abiusi, Paola Infante, Cinzia Cagnoli, Ludovica Lospinoso Severini, Marika Pane, Giorgia Coratti, Maria Carmela Pera, Adele D'Amico, Federica Diano, Agnese Novelli, Serena Spartano, Stefania Fiori, Giovanni Baranello, Isabella Moroni, Marina Mora, Maria Barbara Pasanisi, Krizia Pocino, Loredana Le Pera, Davide D'Amico, Lorena Travaglini, Francesco Ria, Claudio Bruno, Denise Locatelli, Enrico Silvio Bertini, Lucia Ovidia Morandi, Eugenio Mercuri, Lucia Di Marcotullio, Danilo Francesco Tiziano
SMA-miRs (miR-181a-5p, -324-5p, and -451a) are overexpressed in spinal muscular atrophy skeletal muscle and serum samples. eLife 10 (2021)