Follow
Ester Silveira Ramos
Ester Silveira Ramos
Faculdade de Medicina de Ribeirão Preto-Universidade de São Paulo
Verified email at fmrp.usp.br
Title
Cited by
Cited by
Year
Abnormal methylation at the KvDMR1 imprinting control region in clinically normal children conceived by assisted reproductive technologies
MV Gomes, J Huber, RA Ferriani, AM Amaral Neto, ES Ramos
Molecular human reproduction 15 (8), 471-477, 2009
1382009
eNOS haplotypes associated with gestational hypertension or preeclampsia
VC Sandrim, ACT Palei, RC Cavalli, FM Araújo, ES Ramos, G Duarte, ...
Future Medicine Ltd 9 (10), 1467-1473, 2008
1112008
Why do older women have poor implantation rates? A possible role of the mitochondria
AK Bartmann, GS Romao, E da Silveira Ramos, RA Ferriani
Journal of Assisted Reproduction and Genetics 21, 79-83, 2004
1082004
Vascular endothelial growth factor genotypes and haplotypes are associated with pre-eclampsia but not with gestational hypertension
VC Sandrim, ACT Palei, RC Cavalli, FM Araujo, ES Ramos, G Duarte, ...
Molecular human reproduction 15 (2), 115-120, 2009
952009
Familial risk among patients with endometriosis
RM Dos Reis, MF Silva De Sá, MD De Moura, AA Nogueira, JU Ribeiro, ...
Journal of assisted Reproduction and Genetics 16, 500-503, 1999
691999
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
571996
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
562002
Association between birth weight, body mass index and IGF2/ApaI polymorphism
MVM Gomes, MR Soares, A Pasqualim-Neto, CR Marcondes, RB Lôbo, ...
Growth hormone & IGF research 15 (5), 360-362, 2005
492005
Mutations in PCYT1A cause spondylometaphyseal dysplasia with cone-rod dystrophy
GL Yamamoto, WAR Baratela, TF Almeida, M Lazar, CL Afonso, ...
The American Journal of Human Genetics 94 (1), 113-119, 2014
472014
Methylation pattern at the KvDMR in a child with Beckwith-Wiedemann syndrome conceived by ICSI
MV Gomes, CC Gomes, W Pinto, ES Ramos
American journal of medical genetics. Part A 143 (6), 625, 2007
452007
Low levels of exosomal-miRNAs in maternal blood are associated with early pregnancy loss in cloned cattle
THC De Bem, JC Da Silveira, RV Sampaio, JR Sangalli, MLF Oliveira, ...
Scientific reports 7 (1), 14319, 2017
442017
5meCpG Epigenetic Marks Neighboring a Primate-Conserved Core Promoter Short Tandem Repeat Indicate X-Chromosome Inactivation
FB Machado, FB Machado, MA Faria, VL Lovatel, AF Alves da Silva, ...
PloS one 9 (7), e103714, 2014
392014
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
392007
The relationship among sperm global DNA methylation, telomere length, and DNA fragmentation in varicocele: a cross-sectional study of 20 cases
VP Santana, CL Miranda-Furtado, DCC Pedroso, MC Eiras, ...
Systems Biology in Reproductive Medicine 65 (2), 95-104, 2019
342019
The interactive effect of GHR-exon 3 and− 202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner syndrome
AF Braz, EF Costalonga, LR Montenegro, EB Trarbach, SRR Antonini, ...
The Journal of Clinical Endocrinology & Metabolism 97 (4), E671-E677, 2012
322012
Differential expression of the MHM region and of sex-determining-related genes during gonadal development in chicken embryos.
LC Caetano, FGO Gennaro, K Coelho, FM Araújo, RA Vila, A Araújo, ...
Genetics and Molecular Research, v. 13, n. 1, p. 838-849, 2014., 2014
302014
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
281998
The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma
J Huber, ES Ramos
Brazilian journal of medical and biological research 39, 237-241, 2006
262006
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
262005
Bovine fetal DNA in the maternal circulation: applications and implications
DC Lemos, PL Takeuchi, ÁFL Rios, A Araujo, HC Lemos, ES Ramos
Placenta 32 (11), 912-913, 2011
242011
The system can't perform the operation now. Try again later.
Articles 1–20