Carla Babalini

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis

Antonio Orlacchio, Carla Babalini, Antonella Borreca et al. · Brain · 2010 · 261 citations · Full text

Genetics, Pathology, Disease Gene Identification +16

Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12

Gladys Montenegro, Adriana Rebelo, James W. Connell et al. · Journal of Clinical Investigation · 2012 · 168 citations

Neurodegenerative Diseases, Mendelian Disorder, Er Localization +14

The population history of the Croatian linguistic minority of Molise (southern Italy): a maternal view

Carla Babalini, Cristina Martínez‐Labarga, Helle-Viivi Tolk et al. · European Journal of Human Genetics · 2005 · 29 citations · Full text

Population History, Sociolinguistics, Linguistic Diversity +9

Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity

Tommaso Pippucci, Emanuele Panza, Eva Pompilii et al. · European Journal of Neurology · 2008 · 15 citations

Restriction Fragment Length Polymorphisms of Type I Collagen Locus 2 (COL1A2) in Two Communities of African Ancestry and Other Mixed Populations of Northwestern Ecuador

Olga Rickards, Cristina Martínez‐Labarga, Emiliano Trucchi et al. · Human Biology · 2005 · 12 citations

Genetics, Genetic Epidemiology, Linkage Analysis +18