| Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22 NA Quaderi, S Schweiger, K Gaudenz, B Franco, EI Rugarli, W Berger, ... Nature genetics 17 (3), 285-291, 1997 | 423 | 1997 |
| The UTX Gene Escapes X Inactivation in Mice and Humans A Greenfield, L Carrel, D Pennisi, C Philippe, N Quaderi, P Siggers, ... Human molecular genetics 7 (4), 737-742, 1998 | 304 | 1998 |
| Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 M D’esposito, NA Quaderi, A Ciccodicola, P Bruni, T Esposito, M D’Urso, ... Mammalian Genome 7, 533-535, 1996 | 182 | 1996 |
| Expression pattern of the Tbr2 (Eomesodermin) gene during mouse and chick brain development A Bulfone, S Martinez, V Marigo, M Campanella, A Basile, N Quaderi, ... Mechanisms of development 84 (1-2), 133-138, 1999 | 172 | 1999 |
| The Mouse Mid1 Gene: Implications for the Pathogenesis of Opitz Syndrome and the Evolution of the Mammalian Pseudoautosomal Region L Dal Zotto, NA Quaderi, R Elliott, PA Lingerfelter, L Carrel, V Valsecchi, ... Human molecular genetics 7 (3), 489-499, 1998 | 89 | 1998 |
| Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome NA Quaderi, RR Meehan, PH Tate, SH Cross, AP Bird, A Chatterjee, ... Genomics 22 (3), 648-651, 1994 | 82 | 1994 |
| Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domain K Gaudenz, E Roessler, N Quaderi, B Franco, G Feldman, DL Gasser, ... The American Journal of Human Genetics 63 (3), 703-710, 1998 | 80 | 1998 |
| MID2, a Homologue of the Opitz Syndrome Gene MID1: Similarities in Subcellular Localization and Differences in Expression During Development G Buchner, E Montini, G Andolfi, N Quaderi, S Cainarca, S Messali, ... Human molecular genetics 8 (8), 1397-1407, 1999 | 79 | 1999 |
| The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouse DA Adler, NA Quaderi, SDM Brown, VM Chapman, J Moore, P Tate, ... Mammalian Genome 6, 491-492, 1995 | 64 | 1995 |
| The Opitz syndrome gene MID1 is essential for establishing asymmetric gene expression in Hensen’s node A Granata, NA Quaderi Developmental biology 258 (2), 397-405, 2003 | 62 | 2003 |
| Identification of a new EGF-repeat-containing gene from human Xp22: a candidate for developmental disorders G Buchner, U Orfanelli, N Quaderi, MT Bassi, G Andolfi, A Ballabio, ... Genomics 65 (1), 16-23, 2000 | 45 | 2000 |
| Evidence of functional redundancy between MID proteins: implications for the presentation of Opitz syndrome A Granata, D Savery, J Hazan, BMF Cheung, A Lumsden, NA Quaderi Developmental biology 277 (2), 417-424, 2005 | 35 | 2005 |
| Identification and characterization of a novel member of the dystrobrevin gene family AA Puca, V Nigro, G Piluso, A Belsito, S Sampaolo, N Quaderi, E Rossi, ... FEBS letters 425 (1), 7-13, 1998 | 32 | 1998 |
| Differential Expression Pattern of XqPAR-Linked Genes SYBL1 and IL9R Correlates with the Structure and Evolution of the Region M D'Esposito, MR Matarazzo, A Ciccodicola, M Strazzullo, R Mazzarella, ... Human molecular genetics 6 (11), 1917-1923, 1997 | 32 | 1997 |
| Mouse X chromosome. GE Herman, HJ Blair, Y Boyd, SDM Brown, B Gouyon, A Haynes, ... | 15 | 1996 |
| Asymmetric expression of Gli transcription factors in Hensen's node A Granata, NA Quaderi Gene expression patterns 5 (4), 529-531, 2005 | 10 | 2005 |
| Comparative mapping on the mouse X chromosome defines a myotubular myopathy equivalent region B De Gouyon, A Chatterjee, A Monaco, N Quaderi, SDM Brown, ... Mammalian Genome 7, 575-579, 1996 | 5 | 1996 |
| Microphthalmia, Linear Skin Defects, Callosal Agenesis, and Cleft Palate in a Patient with Deletion at Xp22. 3p22. 2 S Vendramini-Pittoli, RM Candido-Souza, RG Quiezi, RM Zechi-Ceide, ... Journal of Pediatric Genetics 9 (04), 258-262, 2020 | 1 | 2020 |
| A defect of midline development, Opitz syndrome, is due to mutations in a novel RING finger gene on Xp22 N Quaderi, S Schweiger, K Gaudenz, B Franco, E Rugarli, W Berger, ... NATURE GENETICS 17, 285-291, 1997 | 1 | 1997 |
| Genetic mapping of a gene encoding an atypical protein kinase C, protein kinase C lambda, to the proximal region of mouse chromosome 3 NA Quaderi, SDM Brown, F Gianfrancesco, M DUrso, M DEsposito Genomics 29 (3), 1995 | 1 | 1995 |
