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

Manuela Fanciulli, Penny J. Norsworthy, Enrico Petretto, +16

Nature Genetics

ImmunogeneticsAutoimmune DiseaseAutoantibody ProductionImmunodeficienciesImmunology +7

Heterozygous Reelin Mutations Cause Autosomal-Dominant Lateral Temporal Epilepsy

Emanuela Dazzo, Manuela Fanciulli, Elena Serioli, +20

The American Journal of Human Genetics

Mendelian DisorderNeurological DisorderGenetic DisorderNeurologyNeuroscience +2

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

Andrea Angius, Enrico Petretto, Giovanni Battista Maestrale, +8

The American Journal of Human Genetics

Genetic DeterminantGenetic DisorderGeneticsGenetic EpidemiologyHuman Polymorphism +7

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

Ginevra Biino, Maria Antonietta Palmas, Carla Corona, +6

Human Genetics

BiologyOcular RefractionGenotype-phenotype AssociationNatural SciencesGenetics +10

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

Ilena Egle Astrid Li Mura, Barbara Bauce, Andrea Nava, +16

European Journal of Human Genetics

Cardiac MuscleCardiomyopathyHeart FailureCardiovascular DiseasePkp2 Gene Deletion +6

The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations

Roberto Michelucci, Patrizia Pulitano, Carlo Di Bonaventura, +13

Epilepsy & Behavior

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without<i><scp>LGI</scp>1</i>mutations

Roberto Michelucci, Elena Pasini, Sandro Malacrida, +29

Epilepsia

FCGR3B copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans

Mariam Molokhia, Manuela Fanciulli, Enrico Petretto, +5

Lara D. Veeken

<i>LGI1</i> microdeletion in autosomal dominant lateral temporal epilepsy

Manuela Fanciulli, Lia Santulli, Luca Errichiello, +12

Neurology

Molecular changes induced by the curcumin analogue D6 in human melanoma cells

Carla Rozzo, Manuela Fanciulli, Cristina Fraumene, +11

Molecular Cancer