| Differentially expressed genes in eutopic and ectopic endometrium of women with endometriosis J Meola, JCR e Silva, DB Dentillo, WA da Silva Jr, LC Veiga-Castelli, ... Fertility and sterility 93 (6), 1750-1773, 2010 | 140 | 2010 |
| Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome JF Mazzeu, E Pardono, AM Vianna‐Morgante, A Richieri‐Costa, ... American journal of medical genetics Part A 143 (4), 320-325, 2007 | 119 | 2007 |
| Recurrent 22q11. 2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome P Sandrin‐Garcia, C Macedo, LR Martelli, ES Ramos, ML Guion‐Almeida, ... Clinical genetics 61 (5), 380-383, 2002 | 56 | 2002 |
| SRY-negative true hermaphrodites and an XX male in two generations of the same family ES Ramos, CA Moreira-Filho, YA Vicente, MAS Llorach-Velludo, S Tucci, ... Human genetics 97, 596-598, 1996 | 56 | 1996 |
| Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes TF Araujo, C Friedrich, CHP Grangeiro, LR Martelli, JD Grzesiuk, J Emich, ... Andrology 8 (2), 434-441, 2020 | 47 | 2020 |
| Messenger RNAs in metaphase II oocytes correlate with successful embryo development to the blastocyst stage FH Biase, RE Everts, R Oliveira, WKF Santos-Biase, GKF Merighe, ... Zygote 22 (1), 69-79, 2014 | 45 | 2014 |
| Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11. 2 P Sandrin-Garcia, DVM Abramides, LR Martelli, ES Ramos, ... Molecular and cellular biochemistry 303, 9-17, 2007 | 38 | 2007 |
| Deregulation of LOXL1 and HTRA1 Gene Expression in Endometriosis DB Dentillo, J Meola, JC Rosa e Silva, S Giuliatti, WA Silva, RA Ferriani, ... Reproductive Sciences 17, 1016-1023, 2010 | 34 | 2010 |
| Is MUC1 polymorphism associated with female infertility? LR Goulart, GS Vieira, L Martelli, J Inacio, IMB Goulart, JG Franco Jr Reproductive biomedicine online 8 (4), 477-482, 2004 | 33 | 2004 |
| Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability C Zhang, A Jolly, BJ Shayota, JF Mazzeu, H Du, M Dawood, PC Soper, ... Human Genetics and Genomics Advances 3 (1), 2022 | 29 | 2022 |
| Three new cases of spondylocarpotarsal synostosis syndrome: clinical and radiographic studies KÉFA Coêlho, ES Ramos, TM Felix, L Martelli, JM de Pina‐Neto, ... American journal of medical genetics 77 (1), 12-15, 1998 | 28 | 1998 |
| Prenatal diagnosis of Charcot‐Marie‐Tooth disease type 1a by multicolor in situ hybridization RV Lebo, L Martelli, Y Su, L Li, E Lynch, E Mansfield, KH Pua, DF Watson, ... American journal of medical genetics 47 (3), 441-450, 1993 | 28 | 1993 |
| Global poly (A) mRNA expression profile measured in individual bovine oocytes and cleavage embryos FH Biase, GKF Merighe, WKFS Biase, L Martelli, FV Meirelles Zygote 16 (1), 29-38, 2008 | 27 | 2008 |
| Use of the TSPY gene for sexing cattle DC Lemos, ÁFL Rios, LC Caetano, RB Lôbo, RA Vila, L Martelli, ... Genetics and Molecular Biology 28, 117-119, 2005 | 27 | 2005 |
| Glycodelin expression in the endometrium of healthy women and in the eutopic and ectopic endometrium of women with endometriosis J Meola, DB Dentillo, JCR e Silva, RA Ferriani, LC Veiga, CCP de Paz, ... Fertility and sterility 91 (5), 1676-1680, 2009 | 26 | 2009 |
| Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas LC Veiga-Castelli, JC Rosa e Silva, J Meola, RA Ferriani, M Yoshimoto, ... Brazilian Journal of Medical and Biological Research 43, 799-805, 2010 | 23 | 2010 |
| Smoking-induced chromosomal segregation anomalies identified by FISH analysis of sperm CS Pereira, MS Juchniuk de Vozzi, SA Dos Santos, MAC Vasconcelos, ... Molecular cytogenetics 7, 1-8, 2014 | 22 | 2014 |
| No evidence of association of MUC-1 genetic polymorphism with embryo implantation failure DB Dentillo, FRP Souza, J Meola, GS Vieira, MEHD Yazlle, LR Goulart, ... Brazilian Journal of Medical and Biological Research 40, 793-797, 2007 | 21 | 2007 |
| Analysis of restriction fragment length polymorphism in the kappa-casein gene related to weight expected progeny difference in Nellore cattle FH Biase, ADV Garnero, LAF Bezerra, AJM Rosa, RB Lôbo, L Martelli Genetics and Molecular Biology 28, 84-87, 2005 | 21 | 2005 |
| Karyotype/phenotype correlation in partial trisomies of the long arm of chromosome 16: case report and review of literature AC Laus, WAR Baratela, LAF Laureano, SA Santos, J Huber, ES Ramos, ... American Journal of Medical Genetics Part A 158 (4), 821-827, 2012 | 15 | 2012 |
Ester Silveira RamosFaculdade de Medicina de Ribeirão Preto-Universidade de São Paulo在 fmrp.usp.br 的电子邮件经过验证
