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The Journal of Rheumatology|January 27, 2000
Anti-ganglioside antibodies in a large cohort of European patients with systemic lupus erythematosus: clinical, serological, and HLA class II gene associations. European Concerted Action on the Immunogenetics of SLEM Galeazzi, P Annunziata, G D Sebastiani, et al.
JMIR Medical Informatics|March 5, 2021
A Personal Health System for Self-Management of Congestive Heart Failure (HeartMan): Development, Technical Evaluation, and Proof-of-Concept Randomized Controlled TrialMitja Luštrek, Marko Bohanec, Carlos Cavero Barca, et al.
Cell Genomics|August 21, 2023
Large-scale exome sequence analysis identifies sex- and age-specific determinants of obesityLena R Kaisinger, Katherine A Kentistou, Stasa Stankovic, et al.
Scientific Reports|March 12, 2021
Proof-of-concept trial results of the HeartMan mobile personal health system for self-management in congestive heart failureEls Clays, Paolo Emilio Puddu, Mitja Luštrek, et al.
Scientific Reports|January 18, 2020
Morphological Neural Computation Restores Discrimination of Naturalistic Textures in Trans-radial AmputeesAlberto Mazzoni, Calogero M Oddo, Giacomo Valle, et al.
Nature Structural & Molecular Biology|March 29, 2025
OGT prevents DNA demethylation and suppresses the expression of transposable elements in heterochromatin by restraining TET activity genome-wideHugo Sepulveda, Xiang Li, Leo J Arteaga-Vazquez, et al.
Journal of Neurology|August 16, 2015
C9ORF72 intermediate repeat expansion in patients affected by atypical parkinsonian syndromes or Parkinson's disease complicated by psychosis or dementia in a Sardinian populationAntonino Cannas, Paolo Solla, Giuseppe Borghero, et al.
JACC. Cardiovascular Imaging|May 15, 2025
The Cardiovascular Magnetic Resonance Phenotype of Lamin Heart DiseaseConstantin-Cristian Topriceanu, Mashael Al-Farih, George Joy, et al.
Research Square|July 29, 2024
Epigenome-wide DNA Methylation Association Study of CHIP Provides Insight into Perturbed Gene RegulationDaniel Levy, Sara Kirmani, Tianxiao Huan, et al.
American Journal of Human Genetics|July 9, 2016
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis PigmentosaAndrea Angius, Paolo Uva, Insa Buers, et al.
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