| Characterization of a murine gene expressed from the inactive X chromosome G Borsani, R Tonlorenzi, MC Simmler, L Dandolo, D Arnaud, V Capra, ... Nature 351 (6324), 325-329, 1991 | 676 | 1991 |
| Mutations in VANGL1 associated with neural-tube defects Z Kibar, E Torban, JR McDearmid, A Reynolds, J Berghout, M Mathieu, ... New England Journal of Medicine 356 (14), 1432-1437, 2007 | 364 | 2007 |
| Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly S Brunelli, A Faiella, V Capra, V Nigro, A Simeone, A Cama, E Boncinelli Nature genetics 12 (1), 94-96, 1996 | 361 | 1996 |
| Frequent hSNF5/INI1 Germline Mutations in Patients with Rhabdoid Tumor F Bourdeaut, D Lequin, L Brugieres, S Reynaud, C Dufour, F Doz, ... Clinical Cancer Research 17 (1), 31-38, 2011 | 244 | 2011 |
| AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ... Nature communications 10 (1), 3094, 2019 | 227 | 2019 |
| Leukotrienes as mediators of asthma S Nicosia, V Capra, GE Rovati Pulmonary pharmacology & therapeutics 14 (1), 3-19, 2001 | 181 | 2001 |
| Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population P De Marco, MG Calevo, A Moroni, L Arata, E Merello, RH Finnell, H Zhu, ... Journal of human genetics 47 (6), 319-324, 2002 | 179 | 2002 |
| Toward understanding the genetic basis of neural tube defects Z Kibar, V Capra, P Gros Clinical genetics 71 (4), 295-310, 2007 | 171 | 2007 |
| VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5 D Szumska, G Pieles, R Essalmani, M Bilski, D Mesnard, K Kaur, ... Genes & development 22 (11), 1465-1477, 2008 | 164 | 2008 |
| Contribution of VANGL2 mutations to isolated neural tube defects Z Kibar, S Salem, CM Bosoi, E Pauwels, P De Marco, E Merello, ... Clinical genetics 80 (1), 76-82, 2011 | 145 | 2011 |
| Novel mutations in VANGL1 in neural tube defects Z Kibar, CM Bosoi, M Kooistra, S Salem, RH Finnell, P De Marco, ... Human mutation 30 (7), E706-E715, 2009 | 144 | 2009 |
| Segmental spinal dysgenesis: neuroradiologic findings with clinical and embryologic correlation P Tortori-Donati, MP Fondelli, A Rossi, CA Raybaud, A Cama, V Capra American journal of neuroradiology 20 (3), 445-456, 1999 | 138 | 1999 |
| Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome—a new clinical perspective ML Garre, A Cama, F Bagnasco, G Morana, F Giangaspero, M Brisigotti, ... Clinical Cancer Research 15 (7), 2463-2471, 2009 | 137 | 2009 |
| Loss of tubulin deglutamylase CCP 1 causes infantile‐onset neurodegeneration V Shashi, MM Magiera, D Klein, M Zaki, K Schoch, S Rudnik‐Schöneborn, ... The EMBO journal 37 (23), e100540, 2018 | 123 | 2018 |
| Reduced folate carrier polymorphism (80A→ G) and neural tube defects P De Marco, MG Calevo, A Moroni, E Merello, A Raso, RH Finnell, H Zhu, ... European journal of human genetics 11 (3), 245-252, 2003 | 118 | 2003 |
| Role of the planar cell polarity gene CELSR1 in neural tube defects and caudal agenesis R Allache, P De Marco, E Merello, V Capra, Z Kibar Birth Defects Research Part A: Clinical and Molecular Teratology 94 (3), 176-181, 2012 | 114 | 2012 |
| FZD6 is a novel gene for human neural tube defects P De Marco, E Merello, A Rossi, G Piatelli, A Cama, Z Kibar, V Capra Human mutation 33 (2), 384-390, 2012 | 113 | 2012 |
| Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans JH Seo, Y Zilber, S Babayeva, JJ Liu, P Kyriakopoulos, P De Marco, ... Human molecular genetics 20 (22), 4324-4333, 2011 | 106 | 2011 |
| Cysteinyl-leukotriene receptor antagonists: present situation and future opportunities V Capra, M Ambrosio, G Riccioni, GE Rovati Current medicinal chemistry 13 (26), 3213-3226, 2006 | 106 | 2006 |
| Impact of vascular thromboxane prostanoid receptor activation on hemostasis, thrombosis, oxidative stress, and inflammation V Capra, M Bäck, DJ Angiolillo, M Cattaneo, KS Sakariassen Journal of Thrombosis and Haemostasis 12 (2), 126-137, 2014 | 104 | 2014 |