Armando Cama

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly

Silvia Brunelli, A. Faiella, Valeria Capra et al. · Nature Genetics · 1996 · 305 citations

Mendelian Disorder, Genetic Disorder, Homeobox Gene Emx2 +11

Medulloblastoma Variants: Age-Dependent Occurrence and Relation to Gorlin Syndrome—A New Clinical Perspective

Maria Luisa Garrè, Armando Cama, Francesca Bagnasco et al. · Clinical Cancer Research · 2009 · 120 citations

VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase<i>Pcsk5</i>

Dorota Szumska, Guido Pieles, Rachid Essalmani et al. · Genes & Development · 2008 · 119 citations · Full text

Knockout Mouse, Recessive Mouse Mutation, Developmental Biology +13

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

Patrizia De Marco, Maria Grazia Calevo, Anna Moroni et al. · Journal of Human Genetics · 2002 · 115 citations · Full text

Polygenic Risk, Genetic Epidemiology, Human Polymorphism +7

Segmental spinal dysgenesis: neuroradiologic findings with clinical and embryologic correlation.

Paolo Tortori‐Donati, M. P. Fondelli, Andrea Rossi et al. · PubMed · 1999 · 114 citations · Full text