Published in Eur Heart J on February 01, 2004
Estrogen receptors and human disease. J Clin Invest (2006) 4.91
Hot flushes, coronary heart disease, and hormone therapy in postmenopausal women. Menopause (2009) 2.07
Sex/gender medicine. The biological basis for personalized care in cardiovascular medicine. Circ J (2009) 1.01
Association between arterial stiffness and variations in oestrogen-related genes. J Hum Hypertens (2009) 0.88
Nonlinear association between serum testosterone levels and coronary artery disease in Iranian men. Eur J Epidemiol (2009) 0.85
Variation in estrogen-related genes associated with cardiovascular phenotypes and circulating estradiol, testosterone, and dehydroepiandrosterone sulfate levels. J Clin Endocrinol Metab (2008) 0.85
Genetic determinants of osteoporosis: common bases to cardiovascular diseases? Int J Hypertens (2010) 0.83
Association between low serum magnesium level and major adverse cardiac events in patients treated with drug-eluting stents for acute myocardial infarction. PLoS One (2014) 0.81
Implications for reproductive medicine: Sex differences in cardiovascular disease. Sex Reprod Menopause (2011) 0.78
Risk factors for long-term outcome of drug-eluting stenting in adults with early-onset coronary artery disease. Int J Med Sci (2014) 0.77
Systems Pharmacology Dissecting Holistic Medicine for Treatment of Complex Diseases: An Example Using Cardiocerebrovascular Diseases Treated by TCM. Evid Based Complement Alternat Med (2015) 0.77
PPAR transcriptional activator complex polymorphisms and the promise of individualized therapy for heart failure. Heart Fail Rev (2008) 0.76
Correlation of oestrogen receptor gene polymorphism with gouty arthritis. Ann Rheum Dis (2006) 0.75
Polymorphism analysis in estrogen receptors alpha and beta genes and their association with infertile population in Pakistan. EXCLI J (2015) 0.75
Toll-like receptor 4 rs11536889 is associated with angiographic extent and severity of coronary artery disease in a Chinese population. Oncotarget (2017) 0.75
Comparative analysis of estrogen receptor gene polymorphisms in apes. Primates (2006) 0.75
Smoking status and long-term survival after first acute myocardial infarction a population-based cohort study. J Am Coll Cardiol (2009) 1.12
Refractive profile in oculocutaneous albinism and its correlation with final visual outcome. Br J Ophthalmol (2011) 1.06
Amelogenin, a major structural protein in mineralizing enamel, is also expressed in soft tissues: brain and cells of the hematopoietic system. Eur J Oral Sci (2006) 1.05
Amelogenin in cranio-facial development: the tooth as a model to study the role of amelogenin during embryogenesis. J Exp Zool B Mol Dev Evol (2009) 1.04
Homozygosity for a novel ABCA4 founder splicing mutation is associated with progressive and severe Stargardt-like disease. Invest Ophthalmol Vis Sci (2007) 1.00
Amelogenin expression in long bone and cartilage cells and in bone marrow progenitor cells. Anat Rec (Hoboken) (2007) 0.97
Regeneration of bone and periodontal ligament induced by recombinant amelogenin after periodontitis. J Cell Mol Med (2009) 0.96
High yield of biologically active recombinant human amelogenin using the baculovirus expression system. Protein Expr Purif (2005) 0.96
Identification of the first non-Jewish mutation in familial Dysautonomia. Am J Med Genet A (2003) 0.91
Estrogen receptor alpha gene polymorphisms are associated with the angiographic extent of coronary artery disease. J Clin Endocrinol Metab (2005) 0.88
A new genetic isolate with a unique phenotype of syndromic oculocutaneous albinism: clinical, molecular, and cellular characteristics. Hum Mutat (2006) 0.87
Association of an estrogen receptor-alpha gene polymorphism with left ventricular mass. Blood Press (2006) 0.81
Localization, quantification, and characterization of tuftelin in soft tissues. Anat Rec (Hoboken) (2007) 0.80
Ethnic differences in patterns of secondhand smoke exposure among adolescents in Israel. Nicotine Tob Res (2012) 0.80
A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridia. Mol Vis (2008) 0.78
Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra-ocular features. Acta Ophthalmol (2014) 0.78
Biphasic influence of hypoxia on tuftelin expression in mouse mesenchymal C3H10T1/2 stem cells. Eur J Oral Sci (2011) 0.77
Ectopic pancreatic pseudocyst and cyst presenting as a cervical and mediastinal mass: case report and review of the literature. Diagn Pathol (2013) 0.77
Fetal inherited thrombophilias influence the severity of preeclampsia, IUGR and placental abruption. Eur J Obstet Gynecol Reprod Biol (2004) 0.77
The induction of tuftelin expression in PC12 cell line during hypoxia and NGF-induced differentiation. J Cell Physiol (2011) 0.76
Crush-related injury after disasters. N Engl J Med (2006) 0.75
Combined Occurrence of Autosomal Dominant Aniridia and Autosomal Recessive Albinism in Several Members of a Family. Ophthalmic Genet (2015) 0.75
Prenatal molecular diagnosis of oculocutaneous albinism (OCA) in a large cohort of Israeli families. Prenat Diagn (2009) 0.75
[Going forward--five years experience in pulmonary rehabilitation]. Harefuah (2014) 0.75
Avoiding Routine Chest Radiography after Transbronchial Biopsy Is Safe. Respiration (2016) 0.75
The acts of terrorism. N Engl J Med (2002) 0.75