Alessandro Mattiaccio
Bologna, 40138, Italy
Last Updated: 09/26/2026
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Found 9 publications
A polygenic etiology for inherited thrombocytopenias of unknown origin.
Journal: HemaSphere
Published: March 06, 2026
Distribution of Sequencing Coverage Gaps in Exomes and Genomes: Potential Implications for Diagnostic Accuracy in Neurodevelopmental Disorder Genes.
Journal: Genes
Published: January 16, 2026
Activated FGFR2 signalling as a biomarker for selection of intrahepatic cholangiocarcinoma patients candidate to FGFR targeted therapies.
Journal: Scientific reports
Published: August 29, 2023
Molecular and Clinical Links between Drug-Induced Cholestasis and Familial Intrahepatic Cholestasis.
Molecular and Clinical Links between Drug-Induced Cholestasis and Familial Intrahepatic Cholestasis.
Journal: International journal of molecular sciences
Published: February 16, 2023
Genetics in Familial Intrahepatic Cholestasis: Clinical Patterns and Development of Liver and Biliary Cancers: A Review of the Literature.
Journal: Cancers
Published: May 31, 2022
Gene Panel Analysis in a Large Cohort of Patients With Autosomal Dominant Polycystic Kidney Disease Allows the Identification of 80 Potentially Causative Novel Variants and the Characterization of a Complex Genetic Architecture in a Subset of Families.
Journal: Frontiers in genetics
Published: December 04, 2019
Association between CANCA1C gene rs1034936 polymorphism and alcohol dependence in bipolar disorder.
Journal: Journal of affective disorders
Published: June 11, 2019
Cryptogenic cholestasis in young and adults: ATP8B1, ABCB11, ABCB4, and TJP2 gene variants analysis by high-throughput sequencing.
Journal: Journal of gastroenterology
Published: October 25, 2017
Showing 1-9 of 9
Last Updated: 09/26/2026