Leonardo D’Agruma

Connexin-26 mutations in sporadic and inherited sensorineural deafness

Xavier Estivill, Paolo Fortina, Saul Surrey et al. · The Lancet · 1998 · 642 citations · Full text

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

Antonio M. Persico, Leonardo D’Agruma, Nunzia Maiorano et al. · Molecular Psychiatry · 2001 · 337 citations · Full text

Reelin Gene Alleles, Developmental Biology, Syndromic Autism +8

Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene

Raquel Rabionet, Leopoldo Zelante, Núria López-Bigas et al. · Human Genetics · 2000 · 219 citations

Developmental Biology, Genetic Disorder, Childhood Deafness +6

Sporadic and MEN1-Related Primary Hyperparathyroidism: Differences in Clinical Expression and Severity

Cristina Eller-Vainicher, Iacopo Chiodini, Claudia Battista et al. · Journal of Bone and Mineral Research · 2009 · 154 citations · Full text

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions

Marcello D’Amelio, Irene Ricci, Roberto Sacco et al. · Molecular Psychiatry · 2005 · 125 citations · Full text

Paraoxonase Gene Variants, Gene–environment Interactions, Syndromic Autism +8