Published in Fertil Steril on June 07, 2009
Extended in vitro maturation of immature oocytes from stimulated cycles: an analysis of fertilization potential, embryo development, and reproductive outcomes. J Assist Reprod Genet (2010) 1.50
The effect of human cumulus cells on the maturation and developmental potential of immature oocytes in ICSI cycles. J Assist Reprod Genet (2012) 0.78
Chromosomal aberrations in in-vitro matured oocytes influence implantation and ongoing pregnancy rates in a mouse model undergoing intracytoplasmic sperm injection. PLoS One (2014) 0.78
In vitro maturation, fertilization, embryo development & clinical outcome of human metaphase-I oocytes retrieved from stimulated intracytoplasmic sperm injection cycles. Indian J Med Res (2013) 0.78
Expression profiles of cohesins, shugoshins and spindle assembly checkpoint genes in rhesus macaque oocytes predict their susceptibility for aneuploidy during embryonic development. Cell Cycle (2012) 0.76
Delayed intracytoplasmic sperm injection (ICSI) with trophectoderm biopsy and preimplantation genetic screening (PGS) show increased aneuploidy rates but can lead to live births with single thawed euploid embryo transfer (STEET). J Assist Reprod Genet (2016) 0.75
Vitrification of Human Germinal Vesicle Oocytes: before or after In Vitro Maturation? Int J Fertil Steril (2017) 0.75
Intracytoplasmic sperm injection outcome of ejaculated versus extracted testicular spermatozoa in cryptozoospermic men. Fertil Steril (2013) 2.70
Loss-of-function mutation in the dioxygenase-encoding FTO gene causes severe growth retardation and multiple malformations. Am J Hum Genet (2009) 2.09
Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities. Am J Hum Genet (2009) 2.07
Favorable influence of local injury to the endometrium in intracytoplasmic sperm injection patients with high-order implantation failure. Fertil Steril (2007) 1.51
In vitro fertilization is a risk factor for vasa previa. Fertil Steril (2002) 1.50
Ovarian pregnancy-a 12-year experience of 19 cases in one institution. Eur J Obstet Gynecol Reprod Biol (2004) 1.44
Is there an increased rate of anencephaly in twins? Prenat Diagn (2005) 1.44
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy. J Med Genet (2007) 1.43
Mosaic compound heterozygosity of SHOX resulting in Leri-Weill dyschondrosteosis with marked short stature: implications for disease mechanisms and recurrence risks. Am J Med Genet A (2010) 1.43
Ultrasonographic-guided percutaneous transabdominal puncture for oocyte retrieval in a rare patient with Rokitansky syndrome in an in vitro fertilization surrogacy program. Fertil Steril (2006) 1.40
Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease. Am J Hum Genet (2009) 1.39
De novo occurrence of novel SPG3A/atlastin mutation presenting as cerebral palsy. Arch Neurol (2006) 1.37
Cone-rod dystrophy and a frameshift mutation in the PROM1 gene. Mol Vis (2009) 1.32
Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients. Eur J Hum Genet (2010) 1.27
Ovarian response to stimulation for fertility preservation in women with malignant disease: a systematic review and meta-analysis. Fertil Steril (2011) 1.23
Insulin resistance in patients with polycystic ovary syndrome is associated with elevated plasma homocysteine. Hum Reprod (2003) 1.06
Increased frequency of female partner chromosomal abnormalities in patients with high-order implantation failure after in vitro fertilization. Fertil Steril (2002) 1.00
The effect of medical clowning on pregnancy rates after in vitro fertilization and embryo transfer. Fertil Steril (2011) 0.97
In vivo maturation of oocytes by extending the interval between human chorionic gonadotropin administration and oocyte retrieval. Fertil Steril (2006) 0.97
The clinical spectrum of fetal Niemann-Pick type C. Am J Med Genet A (2009) 0.95
Fetal abnormalities leading to termination of singleton pregnancy: the 7-year experience of a single medical center. Prenat Diagn (2006) 0.95
Can pregnancy rate be improved in gonadotropin-releasing hormone (GnRH) antagonist cycles by administering GnRH agonist before oocyte retrieval? A prospective, randomized study. Fertil Steril (2007) 0.94
Oocyte maturity and preimplantation development in relation to follicle diameter in gonadotropin-releasing hormone agonist or antagonist treatments. Fertil Steril (2006) 0.93
Vertical transmission of a mutation in exon 1 of the WT1 gene: lessons for genetic counseling. Am J Med Genet A (2008) 0.92
The effect of two distinct levels of oxygen concentration on embryo development in a sibling oocyte study. J Assist Reprod Genet (2013) 0.89
Congenital myopathy is caused by mutation of HACD1. Hum Mol Genet (2013) 0.89
Morphological and ultrastructural evaluation of cultured frozen-thawed human fetal ovarian tissue. Fertil Steril (2006) 0.87
Neurodevelopmental and behavioral abnormalities associated with deletion of chromosome 9p. J Child Neurol (2002) 0.86
Differential expression of genes coding for EGF-like factors and ADAMTS1 following gonadotropin stimulation in normal and transformed human granulosa cells. Biochem Biophys Res Commun (2005) 0.86
Increased early pregnancy loss in IVF patients with severe ovarian hyperstimulation syndrome. Hum Reprod (2002) 0.84
Sporadic aneuploidy in PHA-stimulated lymphocytes of Turner's syndrome patients. Chromosome Res (2006) 0.83
Eight years' experience with an IVF surrogate gestational pregnancy programme. Reprod Biomed Online (2005) 0.82
Prenatal diagnosis of sex chromosome abnormalities: the 8-year experience of a single medical center. Fetal Diagn Ther (2007) 0.82
The role of pigment epithelium-derived factor in the pathophysiology and treatment of ovarian hyperstimulation syndrome in mice. J Clin Endocrinol Metab (2013) 0.82
Novel function of ovarian growth factors: combined studies by DNA microarray, biochemical and physiological approaches. Mol Hum Reprod (2006) 0.82
The aberrant asynchronous replication - characterizing lymphocytes of cancer patients - is erased following stem cell transplantation. BMC Cancer (2010) 0.81
Prospective, randomized trial of metformin and vitamins for the reduction of plasma homocysteine in insulin-resistant polycystic ovary syndrome. Fertil Steril (2007) 0.81
Nationwide use of postmortem retrieved sperm in Israel: a follow-up report. Fertil Steril (2011) 0.79
Autosomal dominant congenital cataract in a Libyan Jewish family: cosegregation with a reciprocal chromosomal translocation [t(3;5)(p22.3; p15.1)]. Mol Vis (2008) 0.78
Hormonal regulation of pigment epithelium-derived factor (PEDF) in granulosa cells. Mol Hum Reprod (2012) 0.78
[Prenatal diagnosis of triploidy: the experience of Assaf-Harofe Medical Center]. Harefuah (2014) 0.78
Prenatal diagnosis of Down syndrome: ten year experience in the Israeli population. Am J Med Genet A (2003) 0.78
Congenital hypothyroidism with Prader-Willi syndrome. J Pediatr Endocrinol Metab (2002) 0.77
Diagnosis of conjoined twins before 16 weeks' gestation: the 4-year experience of one medical center. Prenat Diagn (2005) 0.77
A comparison of the incidence, presentation, and management of ovarian pregnancies between two periods of time. J Am Assoc Gynecol Laparosc (2004) 0.77
Chorioangioma and its severe infantile sequelae: case report. Prenat Diagn (2003) 0.77
In vitro fertilization surrogacy in rare coexisting Mayer-Rokitansky-Kuster-Hauser syndrome and triple X karyotype. Fertil Steril (2010) 0.77
Fetal abnormalities leading to third trimester abortion: nine-year experience from a single medical center. Prenat Diagn (2009) 0.77
Computerized cell-scanning system for evaluating human spermatogenesis in non-obstructive azoospermic patients. Reprod Biomed Online (2011) 0.77
Asynchronous replication of alleles in genomes carrying a microdeletion. Isr Med Assoc J (2002) 0.76
Epigenetic analyses in blood cells of men suspected of prostate cancer predict the outcome of biopsy better than serum PSA levels. Clin Epigenetics (2011) 0.76
Termination of pregnancy due to fetal abnormalities performed after 23 weeks' gestation: analysis of indications in 144 cases from a single medical center. Fetal Diagn Ther (2009) 0.76
Conventional IVF versus ICSI in sibling oocytes from couples with endometriosis and normozoospermic semen. J Assist Reprod Genet (2012) 0.76
Preimplantation genetic diagnosis (PGD) for SHOX-related haploinsufficiency in conjunction with trisomy 21 detection by molecular analysis. J Assist Reprod Genet (2010) 0.75
Ploidy of spermatogenic cells of men with non-mosaic Klinefelter's syndrome as measured by a computerized cell scanning system. J Assist Reprod Genet (2015) 0.75
Birth of healthy twins resulting from donated oocytes and posthumous use of frozen-thawed spermatozoa obtained prior to chemotherapy. J Assist Reprod Genet (2003) 0.75
Reply of the authors. Fertil Steril (2013) 0.75
Correlation and overlapping between nuchal translucency and triple test among Down syndrome-affected pregnancies. Fetal Diagn Ther (2003) 0.75
Analysis of mesenchymal cells derived from an chondrodysplasia punctuate patient and donors. J Cell Biochem (2004) 0.75
Preimplantation genetic diagnosis in genomic regions with duplications and pseudogenes: long-range PCR in the single-cell assay. Hum Mutat (2013) 0.75
Predicting the result of additional second-trimester markers from a woman's first-trimester marker profile: a new concept in Down syndrome screening. Prenat Diagn (2005) 0.75
Using sperm posthumously: national guidelines versus practice. Fertil Steril (2009) 0.75
Chromosome aberration and environmental physical activity: Down syndrome and solar and cosmic ray activity, Israel, 1990-2000. Int J Biometeorol (2005) 0.75
Symposium--Update on prediction and management of OHSS: introduction to guest symposium. Reprod Biomed Online (2009) 0.75
A founder COL17A1 splice site mutation leading to generalized atrophic benign epidermolysis bullosa in an extended inbred Palestinian family from Israel. Genet Med (2003) 0.75
The best marker combination using the integrated screening test approach for detecting various chromosomal aneuploidies. J Perinat Med (2005) 0.75
A non-pathogenic pseudoautosomal region 1 (PAR1) copy number variant downstream of SHOX. Am J Med Genet A (2011) 0.75
Outcome of IVF pregnancies following severe OHSS. Reprod Biomed Online (2009) 0.75
Bitterness of glucose/galactose: novel mutations in the SLC5A1 gene. J Pediatr Gastroenterol Nutr (2014) 0.75
[Fetal abnormalities leading to termination of pregnancy: the experience at the Assaf Harofeh Medical Center between the years 1999-2000]. Harefuah (2003) 0.75
Dynamic modification strategy of the Israeli prenatal carrier screening protocol: inclusion of the oriental Jewish group to the cystic fibrosis panel-update. Genet Med (2009) 0.75