Manuela Fanciulli

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

Manuela Fanciulli, Penny J. Norsworthy, Enrico Petretto et al. · Nature Genetics · 2007 · 462 citations · Full text

Immunogenetics, Autoimmune Disease, Autoantibody Production +9

Heterozygous Reelin Mutations Cause Autosomal-Dominant Lateral Temporal Epilepsy

Emanuela Dazzo, Manuela Fanciulli, Elena Serioli et al. · The American Journal of Human Genetics · 2015 · 121 citations · Full text

Mendelian Disorder, Neurological Disorder, Genetic Disorder +4

A New Essential Hypertension Susceptibility Locus on Chromosome 2p24-p25, Detected by Genomewide Search

Andrea Angius, Enrico Petretto, Giovanni Battista Maestrale et al. · The American Journal of Human Genetics · 2002 · 76 citations · Full text

Genetic Determinant, Genetic Disorder, Genetics +9

Ocular refraction: heritability and genome-wide search for eye morphometry traits in an isolated Sardinian population

Ginevra Biino, Maria Antonietta Palmas, Carla Corona et al. · Human Genetics · 2004 · 65 citations

Biology, Ocular Refraction, Genotype-phenotype Association +12

Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy

Ilena Egle Astrid Li Mura, Barbara Bauce, Andrea Nava et al. · European Journal of Human Genetics · 2013 · 41 citations · Full text

Cardiac Muscle, Cardiomyopathy, Heart Failure +8