Published in J Assist Reprod Genet on May 03, 2015
The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. PLoS Med (2007) 8.46
Revised American Society for Reproductive Medicine classification of endometriosis: 1996. Fertil Steril (1997) 7.19
Strengthening the reporting of genetic association studies (STREGA): an extension of the strengthening the reporting of observational studies in epidemiology (STROBE) statement. J Clin Epidemiol (2009) 2.45
Immunobiology of endometriosis. Fertil Steril (2001) 2.29
High rates of autoimmune and endocrine disorders, fibromyalgia, chronic fatigue syndrome and atopic diseases among women with endometriosis: a survey analysis. Hum Reprod (2002) 1.76
Follicular oestrogen synthesis: the 'two-cell, two-gonadotrophin' model revisited. Mol Cell Endocrinol (1994) 1.63
Heritable aspects of endometriosis. I. Genetic studies. Am J Obstet Gynecol (1980) 1.60
Ovarian response to follicle-stimulating hormone (FSH) stimulation depends on the FSH receptor genotype. J Clin Endocrinol Metab (2000) 1.60
The search for genes contributing to endometriosis risk. Hum Reprod Update (2008) 1.58
Genetic and functional analyses of polymorphisms in the human FSH receptor gene. Mol Hum Reprod (2002) 1.56
Economic burden of endometriosis. Fertil Steril (2006) 1.43
Pathogenic mechanisms in endometriosis-associated infertility. Fertil Steril (2008) 1.40
Definitions of infertility and recurrent pregnancy loss. Fertil Steril (2008) 1.31
The International Endogene Study: a collection of families for genetic research in endometriosis. Fertil Steril (2002) 1.28
Endometriosis and infertility. Fertil Steril (2006) 1.27
Mutational analysis of the follicle-stimulating hormone (FSH) receptor in normal and infertile men: identification and characterization of two discrete FSH receptor isoforms. J Clin Endocrinol Metab (1999) 1.20
Genetic polymorphisms influence the ovarian response to rFSH stimulation in patients undergoing in vitro fertilization programs with ICSI. PLoS One (2012) 1.12
Decreased anti-Müllerian hormone and altered ovarian follicular cohort in infertile patients with mild/minimal endometriosis. Fertil Steril (2007) 1.09
A common single nucleotide polymorphism in exon 10 of the human follicle stimulating hormone receptor is a major determinant of length and hormonal dynamics of the menstrual cycle. J Clin Endocrinol Metab (2005) 1.09
Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis. Hum Reprod Update (2008) 1.07
Role of follicle-stimulating hormone receptor Ser680Asn polymorphism in the efficacy of follicle-stimulating hormone. Fertil Steril (2003) 1.05
Genetic complexity of FSH receptor function. Trends Endocrinol Metab (2005) 1.05
Significance of a common single nucleotide polymorphism in exon 10 of the follicle-stimulating hormone (FSH) receptor gene for the ovarian response to FSH: a pharmacogenetic approach to controlled ovarian hyperstimulation. Pharmacogenet Genomics (2005) 1.02
Occurrence and biological properties of a common genetic variant of luteinizing hormone. J Clin Endocrinol Metab (1995) 1.00
Endometriosis and mechanisms of pelvic pain. J Minim Invasive Gynecol (2009) 0.99
Suboptimal response to GnRHa long protocol is associated with a common LH polymorphism. Reprod Biomed Online (2009) 0.97
Worldwide frequency of a common genetic variant of luteinizing hormone: an international collaborative research. International Collaborative Research Group. Fertil Steril (1997) 0.96
The role of cell-mediated immunity in pathogenesis of endometriosis. Acta Obstet Gynecol Scand Suppl (1994) 0.96
A common polymorphism renders the luteinizing hormone receptor protein more active by improving signal peptide function and predicts adverse outcome in breast cancer patients. J Clin Endocrinol Metab (2006) 0.95
Structure of the human luteinizing hormone-choriogonadotropin receptor gene: unusual promoter and 5' non-coding regions. Mol Cell Endocrinol (1995) 0.93
Body mass index in endometriosis. Eur J Obstet Gynecol Reprod Biol (2005) 0.92
The role of luteinizing hormone-beta gene polymorphism in the onset and progression of puberty in healthy boys. J Clin Endocrinol Metab (1996) 0.92
Increased prevalence of luteinizing hormone beta-subunit variant in Japanese infertility patients. Hum Reprod (1998) 0.91
The role of luteinizing hormone in folliculogenesis and ovulation induction. Fertil Steril (1999) 0.91
A new contributing factor to polycystic ovary syndrome: the genetic variant of luteinizing hormone. J Clin Endocrinol Metab (1999) 0.90
Increased prevalence of luteinizing hormone beta-subunit variant in patients with premature ovarian failure. Fertil Steril (1999) 0.88
Genetics of endometriosis: heritability and candidate genes. Best Pract Res Clin Obstet Gynaecol (2004) 0.88
Current concepts and novel applications of LH activity in ovarian stimulation. Trends Endocrinol Metab (2003) 0.88
Prevalence of an immunological LH beta-subunit variant in a UK population of healthy women and women with polycystic ovary syndrome. Clin Endocrinol (Oxf) (1995) 0.87
Genetics of endometriosis: current status and prospects. Front Biosci (2007) 0.87
Evaluation of serum CA 125 levels in patients with pelvic pain related to endometriosis. Int J Biol Markers (2007) 0.87
Luteinizing hormone signaling and breast cancer: polymorphisms and age of onset. J Clin Endocrinol Metab (2003) 0.86
Study in 1790 Baltic men: FSHR Asn680Ser polymorphism affects total testes volume. Andrology (2012) 0.84
Polymorphisms in gonadotropin and gonadotropin receptor genes as markers of ovarian reserve and response in in vitro fertilization. Fertil Steril (2013) 0.84
There is no complete linkage between the polymorphisms N680S and T307A of the follicular stimulating hormone receptor gene in fertile women. J Assist Reprod Genet (2010) 0.83
Assessment of ovarian reserve. Ovarian biopsy is not a valid method for the prediction of ovarian reserve. Hum Reprod (2004) 0.82
Hyperprolactinemia and luteal insufficiency in infertile patients with mild and minimal endometriosis. Horm Metab Res (2001) 0.82
Physiopathological aspects of corpus luteum defect in infertile patients with mild/minimal endometriosis. J Assist Reprod Genet (2003) 0.81
Role of the mutations Trp8 => Arg and Ile15 => Thr of the human luteinizing hormone beta-subunit in women with polycystic ovary syndrome. Fertil Steril (1999) 0.81
A common genetic variant of luteinizing hormone; relation to normal and aberrant pituitary-gonadal function. Eur J Pharmacol (2001) 0.79
A mutant single nucleotide polymorphism of follicle-stimulating hormone receptor is associated with a lower risk of endometriosis. Fertil Steril (2011) 0.78
Lack of association of the common immunologically anomalous LH with endometriosis. Hum Reprod (2002) 0.78
Evidences for an allelic variant of the human LC/CG receptor rather than a gene duplication: functional comparison of wild-type and variant receptors. J Clin Endocrinol Metab (1998) 0.77
Medical treatment of endometriosis. Clin Obstet Gynecol (1999) 0.76
Avoiding type II errors--simulation studies? Fertil Steril (2007) 1.39
Laparoscopic excision of endometriomas and ovarian reserve. Fertil Steril (2012) 1.39
Acid and Weakly Acidic Gastroesophageal Reflux and Pepsin Isoforms (A and C) in Tracheal Secretions of Critically Ill Children. Chest (2015) 1.38
Guidelines for the management of mucopolysaccharidosis type I. J Pediatr (2009) 1.15
Decreased anti-Müllerian hormone and altered ovarian follicular cohort in infertile patients with mild/minimal endometriosis. Fertil Steril (2007) 1.09
Macrophages, inflammation and risk of cervical intraepithelial neoplasia (CIN) progression--clinicopathological correlation. Gynecol Oncol (2007) 1.00
Coordination of early antral follicles by luteal estradiol administration provides a basis for alternative controlled ovarian hyperstimulation regimens. Fertil Steril (2003) 0.96
The Latin-American network of human genetics. Community Genet (2004) 0.95
Coordination of antral follicle growth: basis for innovative concepts of controlled ovarian hyperstimulation. Semin Reprod Med (2005) 0.95
Up-regulation of VEGF, c-fms and COX-2 expression correlates with severity of cervical cancer precursor (CIN) lesions and invasive disease. Gynecol Oncol (2008) 0.92
Enzyme replacement therapy started at birth improves outcome in difficult-to-treat organs in mucopolysaccharidosis I mice. Mol Genet Metab (2013) 0.91
Luteal estradiol administration strengthens the relationship between day 3 follicle-stimulating hormone and inhibin B levels and ovarian follicular status. Fertil Steril (2003) 0.90
Mutations, clinical findings and survival estimates in South American patients with X-linked adrenoleukodystrophy. PLoS One (2012) 0.89
Placenta analysis of prenatally diagnosed patients reveals early GAG storage in mucopolysaccharidoses II and VI. Mol Genet Metab (2011) 0.89
Plasmin-mediated proteolysis is required for hepatocyte growth factor activation during liver repair. J Biol Chem (2009) 0.88
Effects of FTO RS9939906 and MC4R RS17782313 on obesity, type 2 diabetes mellitus and blood pressure in patients with hypertension. Cardiovasc Diabetol (2013) 0.87
Recombinant encapsulated cells overexpressing alpha-L-iduronidase correct enzyme deficiency in human mucopolysaccharidosis type I cells. Cells Tissues Organs (2011) 0.87
Evidence of a progressive motor dysfunction in Mucopolysaccharidosis type I mice. Behav Brain Res (2012) 0.86
New GLB1 mutation in siblings with Morquio type B disease presenting with mental regression. Mol Genet Metab (2008) 0.86
UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association? Pediatr Res (2012) 0.85
Hormonal manipulations in the luteal phase to coordinate subsequent antral follicle growth during ovarian stimulation. Reprod Biomed Online (2005) 0.85
Infected and noninfected ascites in pediatric patients. J Pediatr Gastroenterol Nutr (2005) 0.84
DNMT3A Mutations in Patients with Acute Myeloid Leukemia in South Brazil. Adv Hematol (2012) 0.84
Kidney function and 24-hour proteinuria in patients with Fabry disease during 36 months of agalsidase alfa enzyme replacement therapy: a Brazilian experience. Ren Fail (2009) 0.83
There is no complete linkage between the polymorphisms N680S and T307A of the follicular stimulating hormone receptor gene in fertile women. J Assist Reprod Genet (2010) 0.83
Early use of cardiac troponin-I and echocardiography imaging for prediction of myocardial infarction size in Wistar rats. Life Sci (2013) 0.82
Intraperitoneal implant of recombinant encapsulated cells overexpressing alpha-L-iduronidase partially corrects visceral pathology in mucopolysaccharidosis type I mice. Cytotherapy (2012) 0.82
Transcoronary gradient of plasma microRNA 423-5p in heart failure: evidence of altered myocardial expression. Biomarkers (2014) 0.82
Further cases of "neighbor" mutations in mucopolysaccharidosis type II. Am J Med Genet A (2006) 0.81
N-acetylcysteine improves antitumoural response of Interferon alpha by NF-kB downregulation in liver cancer cells. Comp Hepatol (2012) 0.81
Bone marrow derived cells decrease inflammation but not oxidative stress in an experimental model of acute myocardial infarction. Life Sci (2010) 0.81
Germinative testicular cells and bone marrow mononuclear cells transplanted to a rat model of testicular degeneration. Cloning Stem Cells (2008) 0.81
Adult derived mononuclear bone marrow cells improve survival in a model of acetaminophen-induced acute liver failure in rats. Toxicology (2008) 0.81
Amplification of bacterial DNA does not distinguish patients with ascitic fluid infection from those colonized by bacteria. J Pediatr Gastroenterol Nutr (2007) 0.80
Cationic Nanoemulsions as a Gene Delivery System: Proof of Concept in the Mucopolysaccharidosis I Murine Model. J Nanosci Nanotechnol (2015) 0.80
Neurological impairment among heterozygote women for X-linked Adrenoleukodystrophy: a case control study on a clinical, neurophysiological and biochemical characteristics. Orphanet J Rare Dis (2014) 0.79
Genotypic and phenotypic characterization of Brazilian patients with GM1 gangliosidosis. Gene (2012) 0.79
Serum and tissue transforming [corrected] growth factor β1 in children with biliary atresia. J Pediatr Surg (2010) 0.79
Immunolocalization of VEGF A and its receptors, VEGFR1 and VEGFR2, in the liver from patients with biliary atresia. Appl Immunohistochem Mol Morphol (2011) 0.79
Platelet increases survival in a model of 90% hepatectomy in rats. Liver Int (2013) 0.79
T helper (Th)1, Th2, and Th17 interleukin pathways in infertile patients with minimal/mild endometriosis. Fertil Steril (2011) 0.79
Fabry disease in hemodialysis patients in southern Brazil: prevalence study and clinical report. Ren Fail (2008) 0.79
Bone marrow mononuclear cell transplantation improves survival and induces hepatocyte proliferation in rats after CCl(4) acute liver damage. Dig Dis Sci (2010) 0.79
Effects of cryopreservation and hypothermic storage on cell viability and enzyme activity in recombinant encapsulated cells overexpressing alpha-L-iduronidase. Artif Organs (2010) 0.78
Influence of phospholipid composition on cationic emulsions/DNA complexes: physicochemical properties, cytotoxicity, and transfection on Hep G2 cells. Int J Nanomedicine (2011) 0.78
Frequent polymorphisms of FSH receptor do not influence antral follicle responsiveness to follicle-stimulating hormone administration as assessed by the Follicular Output RaTe (FORT). J Assist Reprod Genet (2012) 0.78
Computer-assisted immunohistochemical analysis of cervical cancer biomarkers using low-cost and simple software. Appl Immunohistochem Mol Morphol (2007) 0.78
Characterization of joint disease in mucopolysaccharidosis type I mice. Int J Exp Pathol (2013) 0.78
Freshly isolated hepatocyte transplantation in acetaminophen-induced hepatotoxicity model in rats. Arq Gastroenterol (2012) 0.78
Gene delivery strategies for the treatment of mucopolysaccharidoses. Expert Opin Drug Deliv (2014) 0.78
Ontogenetic changes in serum S100B in Down syndrome patients. Clin Biochem (2005) 0.77
In vitro correction of ARSA deficiency in human skin fibroblasts from metachromatic leukodystrophy patients after treatment with microencapsulated recombinant cells. Metab Brain Dis (2008) 0.77
Treatment of MPS I mice with microencapsulated cells overexpressing IDUA: effect of the prednisolone administration. J Microencapsul (2013) 0.77
miRNA-21 and miRNA-34a Are Potential Minimally Invasive Biomarkers for the Diagnosis of Pancreatic Ductal Adenocarcinoma. Pancreas (2016) 0.77
Intestinal permeability assessed by 51Cr-EDTA in rats with CCl4 - induced cirrhosis. Arq Gastroenterol (2010) 0.77
Twin Town in South Brazil: a Nazi's experiment or a genetic founder effect? PLoS One (2011) 0.77
References to alcohol consumption and alcoholism in medical records of a general hospital of Porto Alegre, Brazil--a comparison between samples with a 20 year gap. Subst Abus (2004) 0.76
Chloramphenicol enhances IDUA activity on fibroblasts from mucopolysaccharidosis I patients. Curr Pharm Biotechnol (2013) 0.75
Ethics, genetics and public policies in Uruguay: newborn and infant screening as a paradigm. J Community Genet (2015) 0.75
Population analysis of the GLB1 gene in South Brazil. Genet Mol Biol (2011) 0.75
The Latin American School of Human and Medical Genetics: promoting education and collaboration in genetics and ethics applied to health sciences across the continent. J Community Genet (2015) 0.75
ESR1 rs9340799 is associated with endometriosis-related infertility and in vitro fertilization failure. Dis Markers (2013) 0.75
Vascular endothelial growth factor gene therapy induces early re-establishment of canine bronchial circulation. Eur J Cardiothorac Surg (2008) 0.75
Dopamine receptor D2 genotype (3438) is associated with moderate/severe endometriosis in infertile women in Brazil. Fertil Steril (2012) 0.75
Laronidase-functionalized multiple-wall lipid-core nanocapsules: promising formulation for a more effective treatment of mucopolysaccharidosis type I. Pharm Res (2014) 0.75
Genetic diagnosis in recently transfused patients. Diagn Mol Pathol (2013) 0.75
Progression rate of myelopathy in X-linked adrenoleukodystrophy heterozygotes. Metab Brain Dis (2015) 0.75
Alpha-mannosidase activity in goats fed with Sida carpinifolia. Exp Toxicol Pathol (2009) 0.75
Analysis of cDNA molecules is not suitable for the molecular diagnosis of Mucopolysaccharidosis type I. Diagn Mol Pathol (2012) 0.75
Relationship between serum transforming growth factor ß1 and liver collagen content in rats treated with carbon tetrachloride. Arq Gastroenterol (2012) 0.75
Office hysteroscopy study in consecutive miscarriage patients. Rev Assoc Med Bras (2011) 0.75