Malvestiti, Francesco

Exome-wide association study on alanine aminotransferase identifies sequence variants in the GPAM and APOE associated with fatty liver disease

Jamialahmadi, O., Mancina, R. M., Ciociola, E., Tavaglione, F., Luukkonen, P. K., Baselli, G., Malvestiti, F., Thuillier, D., Raverdy, V., Männistö, V., et al. (2021) · Gastroenterology

Liver Disease Diagnosis and TreatmentGenetic Associations and Epidemiology

Cited by 148

Interaction between estrogen receptor-α and PNPLA3 p.I148M variant drives fatty liver disease susceptibility in women

Cherubini, A., Ostadreza, M., Jamialahmadi, O., Pelusi, S., Rrapaj, E., Casirati, E., Passignani, G., Norouziesfahani, M., Sinopoli, E., Baselli, G., et al. (2023) · Nature Medicine

Liver Disease Diagnosis and TreatmentLiver physiology and pathology

Cited by 136

Rare ATG7 genetic variants predispose patients to severe fatty liver disease

Baselli, G. A., Jamialahmadi, O., Pelusi, S., Ciociola, E., Malvestiti, F., Saracino, M., Santoro, L., Cherubini, A., Dongiovanni, P., Maggioni, M., et al. (2022) · Journal of Hepatology

Liver Disease Diagnosis and TreatmentAutophagy in Disease and Therapy

Cited by 97

Definition of healthy ranges for alanine aminotransferase levels: a 2021 update

Valenti, L., Pelusi, S., Bianco, C., Ceriotti, F., Berzuini, A., Iogna Prat, L., Trotti, R., Malvestiti, F., D’Ambrosio, R., Lampertico, P., et al. (2021) · Hepatology Communications

Liver Disease Diagnosis and TreatmentClinical Laboratory Practices and Quality Control

Cited by 77

Clinical exome sequencing for diagnosing severe cryptogenic liver disease in adults: a case series

Pelusi, S., Ronzoni, L., Malvestiti, F., Bianco, C., Marini, I., D'Ambrosio, R., Giannotta, J. A., Soardo, G., Maggioni, M., Prati, D., et al. (2022) · Liver International

Liver Disease Diagnosis and TreatmentGenomics and Rare Diseases

Cited by 18