| Alopecia Universalis Associated with a Mutation in the Human hairless Gene W Ahmad, M Faiyaz ul Haque, V Brancolini, HC Tsou, S Ul Haque, ... Science 279 (5351), 720-724, 1998 | 417 | 1998 |
| The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative cases HC Tsou, DHF Teng, XL Ping, V Brancolini, T Davis, R Hu, XX Xie, ... The American Journal of Human Genetics 61 (5), 1036-1043, 1997 | 156 | 1997 |
| Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype … A Bolino, V Brancolini, F Bono, A Bruni, A Gambardella, G Romeo, ... Human molecular genetics 5 (7), 1051-1054, 1996 | 147 | 1996 |
| A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12. 1 W Ahmad, V Brancolini, MF ul Haque, HM Lam, S ul Haque, M Haider, ... The American Journal of Human Genetics 62 (4), 987-991, 1998 | 114 | 1998 |
| The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28. A Auricchio, V Brancolini, G Casari, PJ Milla, VV Smith, M Devoto, ... American journal of human genetics 58 (4), 743, 1996 | 95 | 1996 |
| Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease LJ Andrew, V Brancolini, LS De la Pena, M Devoto, F Caeiro, ... The American Journal of Human Genetics 64 (1), 136-145, 1999 | 72 | 1999 |
| Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B) A Gambardella, A Bolino, M Muglia, P Valentino, F Bono, RL Oliveri, ... Neurology 50 (3), 799-801, 1998 | 53 | 1998 |
| Five families with arginine519‐cysteine mutation in COL2A1: Evidence for three distinct founders JF Bleasel, D Holderbaum, V Brancolini, RW Moskowitz, EL Considine, ... Human mutation 12 (3), 172-176, 1998 | 39 | 1998 |
| Capillary zone electrophoresis of polymerase chain reaction‐amplified DNA fragments in polymer networks: The case of GATT microsatellites in cystic fibrosis C Gelfi, A Orsi, PG Righetti, V Brancolini, L Cremonesi, M Ferrari Electrophoresis 15 (1), 640-643, 1994 | 39 | 1994 |
| ul Haque W Ahmad, V Brancolini S., Haider, M., Maimon, A., Aita, VM, Owen, J., Brown, D., et al, 987-991, 1998 | 37 | 1998 |
| Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy A Malandrini, P Carrera, S Palmeri, T Cavallaro, GM Fabrizi, M Villanova, ... Acta neuropathologica 92, 115-122, 1996 | 36 | 1996 |
| Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy A Malandrini, P Carrera, G Ciacci, S Gonnelli, M Villanova, S Palmeri, ... Neurology 48 (5), 1200-1203, 1997 | 34 | 1997 |
| Capillary electrophoresis in polymer networks for analysis of PCR products: detection of delta F508 mutation in cystic fibrosis C Gelfi, PG Righetti, V Brancolini, L Cremonesi, M Ferrari Clinical chemistry 40 (8), 1603-1605, 1994 | 31 | 1994 |
| Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutations V Brancolini, L Cremonesi, E Belloni, E Pappalardo, R Bordoni, M Seia, ... Human genetics 96, 312-318, 1995 | 28 | 1995 |
| Exclusion of linkage between RET and neuronal intestinal dysplasia type B V Barone, D Weber, Y Luo, V Brancolini, M Devoto, G Romeo American journal of medical genetics 62 (2), 195-198, 1996 | 26 | 1996 |
| Suggestive linkage of situs inversus and other left-right axis anomalies to chromosome 6p E Vitale, V Brancolini, A De Rienzo, L Bird, V Allada, M Sklansky, ... Journal of medical genetics 38 (3), 182-185, 2001 | 21 | 2001 |
| Arg519‐Cys Mutation in COL2A1: Evidence for Multiple Foundersa ARG519‐CYS MUTATION IN COL2A1 JF Bleasel, D Holderaum, V Brancolini, RW Moskowitz, TM Haqqi, ... Annals of the New York Academy of Sciences 785 (1), 215-218, 1996 | 13 | 1996 |
| Antiochian genealogies in which idiopathic epilepsy presents familial conglomeration. Simulations of power for the detection of genetic linkage M Arcos-Burgos, LG Palacio, I Jimenez, N Pineda, O Mora, JL Sanchez, ... Revista de Neurologia 26 (149), 50-52, 1998 | 4 | 1998 |
| Genetic linkage studies for the identification of cancer-related genes V Brancolini, M Devoto ANNALI-ISTITUTO SUPERIORE DI SANITA 32, 173-180, 1996 | 4 | 1996 |
| Genealogías antioqueñas en las que la epilepsia idiomática presenta conglomeración familiar M Arcos-Burgos, LG Palacio, I Jiménez, N Pineda, O Mora, JL Sánchez, ... Rev. de Neurol 26, 50, 1998 | 2 | 1998 |
