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Frontiers in Aging Neuroscience
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June 27, 2022
C9orf72-Related Neurodegenerative Diseases: From Clinical Diagnosis to Therapeutic Strategies
Stefania Zampatti, Cristina Peconi, Rosa Campopiano, et al.
Electrophoresis
|
December 5, 2008
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15
Emiliano Giardina, Cristina Peconi, Raffaella Cascella, et al.
Frontiers in Pharmacology
|
August 5, 2025
Pharmacogenetics or predictive genetics? APOE testing blurs the lines
Stefania Zampatti, Cristina Peconi, Juliette Farro, et al.
Genes
|
August 26, 2023
Co-Inheritance of Pathogenic Variants in <i>PKD1</i> and <i>PKD2</i> Genes Determined by Parental Segregation and De Novo Origin: A Case Report
Ludovico Graziani, Stefania Zampatti, Miriam Lucia Carriero, et al.
Electrophoresis
|
June 12, 2009
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7
Emiliano Giardina, Cristina Peconi, Raffaella Cascella, et al.
Genes
|
April 27, 2024
Innovations in Medicine: Exploring ChatGPT's Impact on Rare Disorder Management
Stefania Zampatti, Cristina Peconi, Domenica Megalizzi, et al.
Genes
|
January 25, 2025
AI-Powered Neurogenetics: Supporting Patient's Evaluation with Chatbot
Stefania Zampatti, Juliette Farro, Cristina Peconi, et al.
Genes
|
August 26, 2023
A Splicing Variant in RDH8 Is Associated with Autosomal Recessive Stargardt Macular Dystrophy
Stefania Zampatti, Cristina Peconi, Giulia Calvino, et al.
Journal of Personalized Medicine
|
June 2, 2021
Genetic Counselling Improves the Molecular Characterisation of Dementing Disorders
Stefania Zampatti, Michele Ragazzo, Cristina Peconi, et al.
Genes
|
January 8, 2025
Federated Learning: Breaking Down Barriers in Global Genomic Research
Giulia Calvino, Cristina Peconi, Claudia Strafella, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 28) with videos related to
Sort By:
Page
of 3
Frontiers in Aging Neuroscience
|
June 27, 2022
C9orf72-Related Neurodegenerative Diseases: From Clinical Diagnosis to Therapeutic Strategies
Stefania Zampatti, Cristina Peconi, Rosa Campopiano, et al.
Electrophoresis
|
December 5, 2008
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15
Emiliano Giardina, Cristina Peconi, Raffaella Cascella, et al.
Frontiers in Pharmacology
|
August 5, 2025
Pharmacogenetics or predictive genetics? APOE testing blurs the lines
Stefania Zampatti, Cristina Peconi, Juliette Farro, et al.
Genes
|
August 26, 2023
Co-Inheritance of Pathogenic Variants in <i>PKD1</i> and <i>PKD2</i> Genes Determined by Parental Segregation and De Novo Origin: A Case Report
Ludovico Graziani, Stefania Zampatti, Miriam Lucia Carriero, et al.
Electrophoresis
|
June 12, 2009
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7
Emiliano Giardina, Cristina Peconi, Raffaella Cascella, et al.
Genes
|
April 27, 2024
Innovations in Medicine: Exploring ChatGPT's Impact on Rare Disorder Management
Stefania Zampatti, Cristina Peconi, Domenica Megalizzi, et al.
Genes
|
January 25, 2025
AI-Powered Neurogenetics: Supporting Patient's Evaluation with Chatbot
Stefania Zampatti, Juliette Farro, Cristina Peconi, et al.
Genes
|
August 26, 2023
A Splicing Variant in RDH8 Is Associated with Autosomal Recessive Stargardt Macular Dystrophy
Stefania Zampatti, Cristina Peconi, Giulia Calvino, et al.
Journal of Personalized Medicine
|
June 2, 2021
Genetic Counselling Improves the Molecular Characterisation of Dementing Disorders
Stefania Zampatti, Michele Ragazzo, Cristina Peconi, et al.
Genes
|
January 8, 2025
Federated Learning: Breaking Down Barriers in Global Genomic Research
Giulia Calvino, Cristina Peconi, Claudia Strafella, et al.
Page
of 3