Romeo Carrozzo

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Brunella Franco, Silvana Guioli, Antonella Pragliola et al. · Nature · 1991 · 850 citations

Developmental Biology, Molecular Neuroscience, Mendelian Disorder +14

Olfactory receptor gene cluster on human chromosome 17: possible duplication of an ancestral receptor repertoire

Nissim Ben‐Arie, Doron Lancet, Clare Taylor et al. · Human Molecular Genetics · 1994 · 199 citations

Autosomal recessive Rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: Delineation of the syndrome and gene mapping to chromosome 16p12-11.2

Renzo Guerrini, Paolo Bonanni, Nardo Nardocci et al. · Annals of Neurology · 1999 · 157 citations

Chromosome 20 Ring: A Chromosomal Disorder Associated with a Particular Electroclinical Pattern

Maria Paola Canevini, V. Sgrò, Orsetta Zuffardi et al. · Epilepsia · 1998 · 145 citations · Full text

Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing

Renzo Guerrini, Romeo Carrozzo · Seizure · 2001 · 97 citations · Full text

Developmental Anomaly, Genetic Testing, Neurological Disorder +9