Claudia Lamanna

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Davina J. Hensman Moss, Antonio F. Pardiñas, Douglas R. Langbehn et al. · The Lancet Neurology · 2017 · 332 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

An exploratory double‐blind, randomized clinical trial with selisistat, a <scp>SirT1</scp> inhibitor, in patients with <scp>H</scp>untington's disease

Sigurd D. Süßmuth, Salman Haider, G. Bernhard Landwehrmeyer et al. · British Journal of Clinical Pharmacology · 2014 · 164 citations · Full text

Medicine, Neurology, Pharmacology +17

Straightforward Recursive Partitioning Model for Discarding Insoluble Compounds in the Drug Discovery Process

Claudia Lamanna, Marta Bellini, Alessandro Padova et al. · Journal of Medicinal Chemistry · 2008 · 82 citations

Pharmacy, Medicinal Chemistry, Computational Chemistry +13

Linked Registries: Connecting Rare Diseases Patient Registries through a Semantic Web Layer

Pedro Sernadela, Lorena González-Castro, Claudio Carta et al. · BioMed Research International · 2017 · 56 citations · Full text

Computing, Biomedical Informatics, Health Informatics +13

Clinical manifestations of intermediate allele carriers in Huntington disease

Esther Cubo, María A. Ramos-Arroyo, Saül Martínez‐Horta et al. · Neurology · 2016 · 54 citations

Life Sciences, Genetics, Neurology +13