Published in Reprod Biomed Online on April 01, 2007
Whole genome amplification in preimplantation genetic diagnosis. J Zhejiang Univ Sci B (2011) 1.00
Female sex bias in human embryonic stem cell lines. Stem Cells Dev (2011) 0.99
The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge. Clin Biochem Rev (2011) 0.91
Improving preimplantation genetic diagnosis for Fragile X syndrome: two new powerful single-round multiplex indirect and direct tests. Eur J Hum Genet (2015) 0.76
Improving preimplantation genetic diagnosis (PGD) reliability by selection of sperm donor with the most informative haplotype. Reprod Biol Endocrinol (2017) 0.75
The effect of a germline mutation in the APC gene on β-catenin in human embryonic stem cells. BMC Cancer (2016) 0.75
Clinical and Technical Overview of Preimplantation Genetic Diagnosis for Fragile X Syndrome: Experience at the University Hospital Virgen del Rocio in Spain. Biomed Res Int (2015) 0.75
Fragile X syndrome: A review of clinical management. Intractable Rare Dis Res (2016) 0.75
Fragile X-Associated Diminished Ovarian Reserve and Primary Ovarian Insufficiency from Molecular Mechanisms to Clinical Manifestations. Front Mol Neurosci (2017) 0.75
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes. Nat Genet (2010) 3.66
Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos. Cell Stem Cell (2007) 2.87
Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis. Prenat Diagn (2013) 2.87
A novel founder mutation in the RNASEL gene, 471delAAAG, is associated with prostate cancer in Ashkenazi Jews. Am J Hum Genet (2002) 2.24
Effects of cancer on ovarian response in controlled ovarian stimulation for fertility preservation. Fertil Steril (2012) 1.61
Prenatal Detection of Down Syndrome using Massively Parallel Sequencing (MPS): a rapid response statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011. Prenat Diagn (2012) 1.45
Multiple genes in human 20q13 chromosomal region are involved in an advanced prostate cancer xenograft. Cancer Res (2002) 1.40
Retrieval of immature oocytes after chemotherapy for Hodgkin's disease and prolonged ovarian down-regulation with gonadotropin-releasing hormone agonist. Fertil Steril (2009) 1.39
Preimplantation aneuploid embryos undergo self-correction in correlation with their developmental potential. Fertil Steril (2008) 1.28
Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature. Hum Mutat (2009) 1.18
Increased rates of thrombophilia in women with repeated IVF failures. Hum Reprod (2004) 1.15
Prenatal detection of congenital bilateral cataract leading to the diagnosis of Nance-Horan syndrome in the extended family. Prenat Diagn (2007) 1.06
Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog. Eur J Hum Genet (2009) 1.04
Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutations. Hum Mutat (2002) 1.03
Third-trimester unexplained intrauterine fetal death is associated with inherited thrombophilia. Obstet Gynecol (2002) 1.02
Carrier testing for spinal muscular atrophy. Genet Med (2010) 1.02
Rett syndrome: clinical manifestations in males with MECP2 mutations. J Child Neurol (2002) 1.00
Female sex bias in human embryonic stem cell lines. Stem Cells Dev (2011) 0.99
Unpredicted gender preference of obstetricians and gynecologists by Muslim Israeli-Arab women. Patient Educ Couns (2011) 0.98
Elucidating the origin of chromosomal aberrations in IVF embryos by preimplantation genetic analysis. Mol Cell Endocrinol (2007) 0.98
Ovarian stimulation and emergency in vitro fertilization for fertility preservation in cancer patients. Eur J Obstet Gynecol Reprod Biol (2010) 0.97
Screening for familial dysautonomia in Israel: evidence for higher carrier rate among Polish Ashkenazi Jews. Genet Test (2003) 0.94
Large-scale population screening for spinal muscular atrophy: clinical implications. Genet Med (2011) 0.94
Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform. Mol Vis (2008) 0.92
Clinical evaluation of isolated nonvisualized fetal gallbladder. Prenat Diagn (2007) 0.92
Effects of salpingectomy on ovarian response in controlled ovarian hyperstimulation for in vitro fertilization: a reappraisal. Fertil Steril (2011) 0.91
Maternal serum HCG is higher in the presence of a female fetus as early as week 3 post-fertilization. Hum Reprod (2002) 0.91
Follicular fluid levels of anti-Mullerian hormone as a predictor of oocyte maturation, fertilization rate, and embryonic development in patients with polycystic ovary syndrome. Fertil Steril (2009) 0.91
Aneuploidy screening: a position statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, January 2011. Prenat Diagn (2011) 0.91
Human embryonic stem cells carrying mutations for severe genetic disorders. In Vitro Cell Dev Biol Anim (2010) 0.90
Genomic analysis of hESC pedigrees identifies de novo mutations and enables determination of the timing and origin of mutational events. Cell Rep (2013) 0.90
Current controversies in prenatal diagnosis 3: For prenatal diagnosis, should we offer less or more than metaphase karyotyping? Prenat Diagn (2009) 0.90
Histologic evaluation of fresh human ovarian tissue before cryopreservation. Int J Gynecol Pathol (2010) 0.89
Regulation of vascular endothelial growth factor-A and its soluble receptor sFlt-1 by luteinizing hormone in vivo: implication for ovarian follicle angiogenesis. Fertil Steril (2008) 0.89
Circulating angiogenic proteins in trisomy 13. Am J Obstet Gynecol (2006) 0.88
Genetic and physiological study of morphologically abnormal human zona pellucida. Eur J Obstet Gynecol Reprod Biol (2012) 0.87
Two novel translocations, t(2;4)(q35;q31) and t(X;12)(q22;q24), as the only karyotypic abnormalities in a malignant peripheral nerve sheath tumor of the skull base. Cancer Genet Cytogenet (2003) 0.87
2nd-trimester maternal serum human chorionic gonadotropin and alpha-fetoprotein levels in male and female fetuses with Down syndrome. Fetal Diagn Ther (2005) 0.86
Higher C-reactive protein levels during IVF stimulation are associated with ART failure. J Reprod Immunol (2007) 0.86
Virtual azoospermia and cryptozoospermia--fresh/frozen testicular or ejaculate sperm for better IVF outcome? J Androl (2010) 0.86
Prospective randomized comparison of two embryo culture systems: P1 medium by Irvine Scientific and the Cook IVF Medium. J Assist Reprod Genet (2004) 0.86
Does high serum progesterone level on the day of human chorionic gonadotropin administration affect pregnancy rate after intracytoplasmic sperm injection and embryo transfer? Gynecol Endocrinol (2008) 0.85
The effect of CGG repeat number on ovarian response among fragile X premutation carriers undergoing preimplantation genetic diagnosis. Fertil Steril (2009) 0.85
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction. J Med Genet (2012) 0.84
MECP2 mutations in Israel: implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome. Hum Mutat (2002) 0.83
Effects of laser polar-body biopsy on embryo quality. Fertil Steril (2012) 0.83
Recombinant luteinizing hormone induces increased production of ovarian follicular adiponectin in vivo: implications for enhanced insulin sensitivity. Fertil Steril (2008) 0.83
Insight into the intrinsic sensitivity of the PCR assay used to detect CMV infection in amniotic fluid specimens. J Clin Virol (2004) 0.83
First live birth following IVF-embryo transfer and use of GnRHa alone for ovarian stimulation. Reprod Biomed Online (2009) 0.82
Loeys-Dietz syndrome in pregnancy: a case description and report of a novel mutation. Fetal Diagn Ther (2009) 0.82
Obstetricians and gynecologists: which characteristics do Israeli lesbians prefer? J Obstet Gynaecol Res (2014) 0.82
Adverse obstetric outcome for the vanishing twin syndrome. Reprod Biomed Online (2009) 0.81
Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCR. Prenat Diagn (2005) 0.81
Multiplex nested PCR for preimplantation genetic diagnosis of spinal muscular atrophy. Fetal Diagn Ther (2004) 0.81
Undiagnosed systemic lupus erythematosus in a cohort of infertile women. Am J Reprod Immunol (2004) 0.80
GnRH-agonist induced depressive and anxiety symptoms during in vitro fertilization-embryo transfer cycles. Fertil Steril (2011) 0.79
Surrogate pregnancy in a patient who underwent radical hysterectomy and bilateral transposition of ovaries. Fertil Steril (2003) 0.79
Israeli Society of Medical Genetics NIPT Committee Opinion 072013: Non-invasive prenatal testing of cell-free DNA in maternal plasma for detection of fetal aneuploidy. Fetal Diagn Ther (2014) 0.79
An embryo cleavage pattern based on the relative blastomere size as a function of cell number for predicting implantation outcome. Fertil Steril (2012) 0.78
Preimplantation genetic diagnosis of Canavan disease. Fetal Diagn Ther (2005) 0.78
Feasibility of nuchal translucency in triplet pregnancies. J Ultrasound Med (2004) 0.78
Elucidation of abnormal fertilization by single-cell analysis with fluorescence in situ hybridization and polymorphic marker analysis. Fertil Steril (2008) 0.78
Cytogenetic analysis of three variants of clival chordoma. Cancer Genet Cytogenet (2004) 0.77
Embryo quality in controlled ovarian stimulation for in vitro fertilization in young poor responders. Gynecol Endocrinol (2014) 0.77
Psychological response and cortisol reactivity to in vitro fertilization treatment in women with a lifetime anxiety or unipolar mood disorder diagnosis. J Clin Psychiatry (2013) 0.77
Combined cytogenetic and array-based comparative genomic hybridization analyses of Wilms tumors: amplification and overexpression of the multidrug resistance associated protein 1 gene (MRP1) in a metachronous tumor. Cancer Genet Cytogenet (2003) 0.77
Divalent cation levels in serum and preovulatory follicular fluid of women undergoing in vitro fertilization embryo transfer. Gynecol Obstet Invest (2003) 0.77
Successful transfer of frozen-thawed embryos obtained after subtotal colectomy for colorectal cancer and before fluorouracil-based chemotherapy. Gynecol Oncol (2004) 0.77
[Anti mullerian hormone (AMH)--is it a new reliable marker of the ovarian reserve? Its role in predicting the ovarian response in assisted reproductive technology (ART)]. Harefuah (2012) 0.77
Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes? Prenat Diagn (2009) 0.77
Screening for Down syndrome--incidental diagnosis of other aneuploidies. Prenat Diagn (2014) 0.77
Assessment of ovarian reserve following ovarian tissue banking and/or GnRH-a co-treatment prior to chemotherapy in patients with Hodgkin's disease. J Assist Reprod Genet (2008) 0.77
Detection of spinal muscular atrophy carriers by nested polymerase chain reaction of single sperm cells. Genet Test (2006) 0.77
Dynamic modification strategy of the Israeli carrier screening protocol: inclusion of the Oriental Jewish Group to the cystic fibrosis panel. Genet Med (2009) 0.77
The mitochondrial DNA mutation (deltamtDNA5286) in human oocytes: correlation with age and IVF outcome. J Assist Reprod Genet (2002) 0.76
Case report: pregnancy outcome following ICSI of oocytes with abnormal cytoplasm and zona pellucida. Hum Reprod (2004) 0.76
Severe hypospermatogenesis in cases of nonobstructive azoospermia: should we use fresh or frozen testicular spermatozoa? J Androl (2005) 0.76
[The involvement of the zona pellucida in unexplained infertile women]. Harefuah (2008) 0.76
Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia. Prenat Diagn (2010) 0.76