| Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies DT Miller, MP Adam, S Aradhya, LG Biesecker, AR Brothman, NP Carter, ... The American Journal of Human Genetics 86 (5), 749-764, 2010 | 3293 | 2010 |
| Mutations in the APC tumour suppressor gene cause chromosomal instability R Fodde, J Kuipers, C Rosenberg, R Smits, M Kielman, C Gaspar, ... Nature cell biology 3 (4), 433-438, 2001 | 965 | 2001 |
| TRPC1, a human homolog of a Drosophila store-operated channel. PD Wes, J Chevesich, A Jeromin, C Rosenberg, G Stetten, C Montell Proceedings of the National Academy of Sciences 92 (21), 9652-9656, 1995 | 843 | 1995 |
| Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability C Shaw-Smith, AM Pittman, L Willatt, H Martin, L Rickman, S Gribble, ... Nature genetics 38 (9), 1032-1037, 2006 | 425 | 2006 |
| Array CGH identifies reciprocal 16p13. 1 duplications and deletions that predispose to autism and/or mental retardation R Ullmann, G Turner, M Kirchhoff, W Chen, B Tonge, C Rosenberg, ... Human mutation 28 (7), 674-682, 2007 | 350 | 2007 |
| Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents C Rosenberg, J Knijnenburg, E Bakker, AM Vianna-Morgante, W Sloos, ... Journal of medical genetics 43 (2), 180-186, 2006 | 268 | 2006 |
| Clinical and molecular delineation of the 17q21. 31 microdeletion syndrome DA Koolen, AJ Sharp, JA Hurst, HV Firth, SJL Knight, A Goldenberg, ... Journal of medical genetics 45 (11), 710-720, 2008 | 260 | 2008 |
| Identification of genetic markers for prostatic cancer progression JC Alers, J Rochat, PJ Krijtenburg, WCJ Hop, R Kranse, C Rosenberg, ... Laboratory investigation 80 (6), 931-942, 2000 | 250 | 2000 |
| Comparative genomic hybridization of cancer of the gastroesophageal junction: deletion of 14Q31–32.1 discriminates between esophageal (Barrett’s) and gastric cardia adenocarcinomas H van Dekken, E Geelen, WNM Dinjens, BPL Wijnhoven, HW Tilanus, ... Cancer research 59 (3), 748-752, 1999 | 181 | 1999 |
| Overrepresentation of the short arm of chromosome 12 is related to invasive growth of human testicular seminomas and nonseminomas C Rosenberg, R Van Gurp, E Geelen, JW Oosterhuis, LHJ Looijenga Oncogene 19 (51), 5858-5862, 2000 | 169 | 2000 |
| Molecular genetic characterization of both components of a dedifferentiated chondrosarcoma, with implications for its histogenesis JVMG Bovée, AM Cleton‐Jansen, C Rosenberg, AHM Taminiau, ... The Journal of pathology 189 (4), 454-462, 1999 | 156 | 1999 |
| Genomic imbalances associated with müllerian aplasia C Cheroki, ACV Krepischi-Santos, K Szuhai, V Brenner, CAE Kim, PA Otto, ... Journal of medical genetics 45 (4), 228-232, 2008 | 155 | 2008 |
| Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair M Bauters, H Van Esch, MJ Friez, O Boespflug-Tanguy, M Zenker, ... Genome research 18 (6), 847-858, 2008 | 152 | 2008 |
| A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome CJ Haven, FK Wong, EWCM Van Dam, R Van Der Luijt, C Van Asperen, ... The Journal of Clinical Endocrinology & Metabolism 85 (4), 1449-1454, 2000 | 148 | 2000 |
| Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization J Dierlamm, C Rosenberg, M Stul, S Pittaluga, I Wlodarska, L Michaux, ... Leukemia 11 (5), 747-758, 1997 | 146 | 1997 |
| Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations ACV Krepischi-Santos, AM Vianna-Morgante, FS Jehee, ... Cytogenetic and genome research 115 (3-4), 254-261, 2006 | 141 | 2006 |
| Array-based comparative genomic hybridization analysis reveals recurrent chromosomal alterations and prognostic parameters in primary cutaneous large B-cell lymphoma R Dijkman, CP Tensen, ES Jordanova, J Knijnenburg, JJ Hoefnagel, ... Journal of clinical oncology 24 (2), 296-305, 2006 | 138 | 2006 |
| Germline DNA copy number variation in familial and early-onset breast cancer ACV Krepischi, MIW Achatz, EMM Santos, SS Costa, BCG Lisboa, ... Breast Cancer Research 14, 1-8, 2012 | 136 | 2012 |
| Genetic alterations on chromosome 16 and 17 are important features of ductal carcinoma in situ of the breast and are associated with histologic type CBJ Vos, NT Ter Haar, C Rosenberg, JL Peterse, AM Cleton-Jansen, ... British journal of cancer 81 (8), 1410-1418, 1999 | 126 | 1999 |
| Identification of the critical region of 12p over-representation in testicular germ cell tumors of adolescents and adults MC Mostert, AJMH Verkerk, M van de Pol, J Heighway, P Marynen, ... Oncogene 16 (20), 2617-2627, 1998 | 123 | 1998 |
Ana C V KrepischiInstitute of Biosciences - University of São Paulo - BrazilDirección de correo verificada de ib.usp.br
