Published in BJOG on August 01, 2004
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response. Nat Genet (2009) 5.84
Clinical and molecular phenotype of Aicardi-Goutieres syndrome. Am J Hum Genet (2007) 2.81
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study. Lancet Neurol (2013) 2.36
The incidence of large fetomaternal hemorrhage and the Kleihauer-Betke test. Obstet Gynecol (2005) 2.29
Precesarean Prophylactic Balloon Catheters for Suspected Placenta Accreta: A Randomized Controlled Trial. Obstet Gynecol (2015) 2.23
Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome). Nat Genet (2005) 2.04
NEK1 mutations cause short-rib polydactyly syndrome type majewski. Am J Hum Genet (2011) 1.56
Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration--a late onset variant of PCH-1? Eur J Paediatr Neurol (2007) 1.52
Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9. Am J Hum Genet (2008) 1.52
Graves' disease in pregnancy: prospective evaluation of a selective invasive treatment protocol. Am J Obstet Gynecol (2003) 1.50
Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasis. Dev Med Child Neurol (2010) 1.47
Expression and importance of matrix metalloproteinase 2 and 9 (MMP-2 and -9) in human trophoblast invasion. Reprod Biol Endocrinol (2004) 1.44
Exome sequencing identifies INPPL1 mutations as a cause of opsismodysplasia. Am J Hum Genet (2012) 1.36
Human trophoblast function during the implantation process. Reprod Biol Endocrinol (2005) 1.34
Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosa. Am J Hum Genet (2010) 1.29
Autosomal-recessive early-onset retinitis pigmentosa caused by a mutation in PDE6G, the gene encoding the gamma subunit of rod cGMP phosphodiesterase. Am J Hum Genet (2010) 1.13
Clinical characterization of a newly described neonatal diabetes syndrome caused by RFX6 mutations. Am J Med Genet A (2011) 1.11
The matrix metalloproteinases (MMPS) in the decidua and fetal membranes. Front Biosci (2007) 1.08
A randomized study of thromboprophylaxis in women with unexplained consecutive recurrent miscarriages. Fertil Steril (2006) 1.06
For how long should oxytocin be continued during induction of labour? BJOG (2004) 1.06
MMPS and TIMPS in ovarian physiology and pathophysiology. Front Biosci (2004) 1.04
SLC25A19 mutation as a cause of neuropathy and bilateral striatal necrosis. Ann Neurol (2009) 1.02
A targeted population carrier screening program for severe and frequent genetic diseases in Israel. Eur J Hum Genet (2008) 1.01
Progesterone receptor expression in human decidua and fetal membranes before and after contractions: possible mechanism for functional progesterone withdrawal. Mol Hum Reprod (2005) 1.01
The significance of coasting duration during ovarian stimulation for conception in assisted fertilization cycles. Hum Reprod (2002) 1.00
The Coffin-Siris syndrome: a proposed diagnostic approach and assessment of 15 overlapping cases. Am J Med Genet A (2012) 1.00
Health implications resulting from the timing of elective cesarean delivery. Reprod Biol Endocrinol (2010) 0.98
Suggested approach for management of placenta percreta invading the urinary bladder. Obstet Gynecol (2007) 0.96
The clinical spectrum of fetal Niemann-Pick type C. Am J Med Genet A (2009) 0.95
The consequences of consanguinity on the rates of malformations and major medical conditions at birth and in early childhood in inbred populations. Am J Med Genet A (2010) 0.94
Continuous compared with intermittent epidural infusion on progress of labor and patient satisfaction. Obstet Gynecol (2005) 0.92
Genetic disorders among Palestinian Arabs. 4: Genetic clinics in the community. Am J Med Genet A (2006) 0.91
Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog. J Med Genet (2012) 0.88
A novel splice site mutation of CDHR1 in a consanguineous Israeli Christian Arab family segregating autosomal recessive cone-rod dystrophy. Mol Vis (2012) 0.88
The effects of decidual injury on the invasion potential of trophoblastic cells. Obstet Gynecol (2011) 0.87
Novel mutations of MYO7A and USH1G in Israeli Arab families with Usher syndrome type 1. Mol Vis (2011) 0.87
Myotonia congenita in a large consanguineous Arab family: insight into the clinical spectrum of carriers and double heterozygotes of a novel mutation in the chloride channel CLCN1 gene. Muscle Nerve (2010) 0.86
Comparison between amniotomy, oxytocin or both for augmentation of labor in prolonged latent phase: a randomized controlled trial. Reprod Biol Endocrinol (2010) 0.86
The role of the matrix metalloproteinases in human endometrial and ovarian cycles. Eur J Obstet Gynecol Reprod Biol (2003) 0.86
Expression of plexin-B1 in the mouse ovary and its possible role in follicular development. Fertil Steril (2005) 0.86
TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome. J Med Genet (2010) 0.85
Expanding the clinical spectrum of SLC29A3 gene defects. Eur J Med Genet (2010) 0.85
Human amniotic epithelial cells differentiate into cells expressing germ cell specific markers when cultured in medium containing serum substitute supplement. Reprod Biol Endocrinol (2012) 0.85
The effect of serum from women with preeclampsia on JAR (trophoblast-like) cell line. J Soc Gynecol Investig (2005) 0.85
Timing of elective repeat cesarean delivery at term. N Engl J Med (2009) 0.85
Human uterine epithelial RL95-2 and HEC-1A cell-line adhesiveness: the role of plexin B1. Fertil Steril (2007) 0.84
Epidemiologic risk factors for preterm delivery. Isr Med Assoc J (2002) 0.84
Effect of interventions in reducing the rate of infection after cesarean delivery. Am J Infect Control (2011) 0.84
Tumor chemoconversion following surgery, chemotherapy, and normalization of serum tumor markers in a woman with a mixed type germ cell ovarian tumor. Gynecol Oncol (2002) 0.84
Difference in progesterone-receptor isoforms ratio between early and late first-trimester human trophoblast is associated with differential cell invasion and matrix metalloproteinase 2 expression. Biol Reprod (2005) 0.84
The efficacy of specific IVIG anti-idiotypic antibodies in antiphospholipid syndrome (APS): trophoblast invasiveness and APS animal model. Int Immunol (2007) 0.84
Ets-2 and p53 mediate cAMP-induced MMP-2 expression, activity and trophoblast invasion. Reprod Biol Endocrinol (2009) 0.83
Hydrops fetalis: an unusual prenatal presentation of hereditary congenital lymphedema. Prenat Diagn (2005) 0.83
Clinical and ultrasonographic weight estimation in large for gestational age fetus. Eur J Obstet Gynecol Reprod Biol (2002) 0.83
Limb-girdle muscular dystrophy 2I: phenotypic variability within a large consanguineous Bedouin family associated with a novel FKRP mutation. Eur J Hum Genet (2004) 0.83
Matrix metalloproteinase-2 is elevated in midtrimester amniotic fluid prior to the development of preeclampsia. Reprod Biol Endocrinol (2009) 0.82
A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia. Eur J Clin Invest (2012) 0.82
Mutated NDUFS6 is the cause of fatal neonatal lactic acidemia in Caucasus Jews. Eur J Hum Genet (2009) 0.82
Single-balloon compared with double-balloon catheters for induction of labor: a randomized controlled trial. Obstet Gynecol (2011) 0.82
Comparison of intrapartum outcome among immigrant women from Ethiopia and the general obstetric population in Israel. Int J Gynaecol Obstet (2012) 0.82
Plexin-B1, glycodelin and MMP7 expression in the human fallopian tube and in the endometrium. Reprod Biol Endocrinol (2009) 0.81
Acrocallosal syndrome: identification of a novel KIF7 mutation and evidence for oligogenic inheritance. Eur J Med Genet (2012) 0.81
A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathy. Gene (2012) 0.81
Progesterone receptor isoforms profile, modulate matrix metalloproteinase 2 expression in the decidua. Am J Obstet Gynecol (2007) 0.81
Human amniotic epithelial cells cultured in substitute serum medium maintain their stem cell characteristics for up to four passages. Int J Stem Cells (2011) 0.80
Chronic recurrent multifocal osteomyelitis and deficiency of interleukin-1-receptor antagonist. Pediatr Infect Dis J (2013) 0.80
Mechanisms of matrix metalloproteinase-2 (mmp-2) transcriptional repression by progesterone in jar choriocarcinoma cells. Reprod Biol Endocrinol (2009) 0.80
Marriage patterns and reproductive decision-making in the inhabitants of a single Muslim village during a 50-year period. Hum Hered (2014) 0.80
Nifedipine compared with atosiban for treating preterm labor: a randomized controlled trial. Obstet Gynecol (2012) 0.80
[ABANDONED EMBRYOS OR SURPLUS FERTILIZED OOCYTES--SEEKING THE SOLUTION FOR A FROZEN BURNING PROBLEM]. Harefuah (2015) 0.80
ANE syndrome caused by mutated RBM28 gene: a novel etiology of combined pituitary hormone deficiency. Eur J Endocrinol (2010) 0.80
Umbilical-placental blood flow gradient during the early second trimester of pregnancy. J Matern Fetal Neonatal Med (2005) 0.79
Bacterial colonization of the uterine cervix and success rate in assisted reproduction: results of a prospective survey. Hum Reprod (2002) 0.79
Semaphorin-4D (Sema-4D), the Plexin-B1 ligand, is involved in mouse ovary follicular development. Reprod Biol Endocrinol (2007) 0.79
Progesterone receptor A and c-Met mediates spheroids-endometrium attachment. Reprod Biol Endocrinol (2009) 0.79
The effects of gonadotropin-releasing hormone (GnRH) I and GnRH II on the urokinase-type plasminogen activator/plasminogen activator inhibitor system in human extravillous cytotrophoblasts in vitro. J Clin Endocrinol Metab (2002) 0.79
A proposed mechanism for progesterone regulation of trophoblast MMP2 transcription independent of classical progesterone response elements on its promoter. J Exp Clin Assist Reprod (2006) 0.78
Assessment of uterine placental circulation in thrombophilic women. Semin Thromb Hemost (2003) 0.78
Establishment of fetal biometric charts using quantile regression analysis. J Ultrasound Med (2013) 0.78
High incidence of deafness from three frequent connexin 26 mutations in an isolated community. Genet Test (2006) 0.78
The effect of progesterone on gelatinase expression in the decidua and fetal membranes before and after contractions. Am J Obstet Gynecol (2007) 0.78
Progesterone receptor profile in the decidua and fetal membrane. Front Biosci (2007) 0.78
Origin and expansion of four different beta globin mutations in a single Arab village. Am J Hum Biol (2005) 0.78
Regulation of matrix metalloproteinase-9 (MMP-9), tissue inhibitor of MMP, and progesterone secretion in luteinized granulosa cells from normally ovulating women with polycystic ovary disease. Fertil Steril (2003) 0.77
Founder effect with variable age at onset in Arab families with Lafora disease and EPM2A mutation. Epilepsia (2007) 0.77
Prenatal diagnosis of 5p deletion syndrome following abnormally low maternal serum human chorionic gonadotrophin. Prenat Diagn (2003) 0.77
Holoprosencephaly and craniosynostosis: A report of two siblings and review of the literature. Am J Med Genet C Semin Med Genet (2010) 0.77
The association of umbilical cord hemangioma with fetal vascular birthmarks. Prenat Diagn (2005) 0.77
Diagnosis of congenital cardiac defects between 11 and 14 weeks' gestation in high-risk patients. J Ultrasound Med (2002) 0.77
Anthropometric parameters in infants of gestational diabetic women with strict glycemic control. Obstet Gynecol (2004) 0.77
[Employing a balloon catheter for occlusion and/or embolization of the pelvic vasculature as an adjuvant therapy in cases of abnormal placentation]. Harefuah (2010) 0.77
Risk factors for infection following cesarean delivery: an interventional study. J Matern Fetal Neonatal Med (2012) 0.76
[Progesterone receptor's profile and the effect of the hormone and its derivatives on invasiveness and MMP2 secretion in endometrial carcinoma cell lines]. Harefuah (2009) 0.76
Extreme clinical variability of dilated cardiomyopathy in two siblings with Alström syndrome. Pediatr Cardiol (2012) 0.76