Published in Reprod Toxicol on July 11, 2005
Folic acid supplements and risk of facial clefts: national population based case-control study. BMJ (2007) 3.67
Developmental origins of health and disease: environmental exposures. Semin Reprod Med (2009) 1.44
The mandatory fortification of staple foods with folic acid: a current controversy in Germany. Dtsch Arztebl Int (2011) 1.09
Folate deficiency and folic acid supplementation: the prevention of neural-tube defects and congenital heart defects. Nutrients (2013) 1.02
Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defects. J Med Genet (2010) 0.93
Maternal periconceptional factors affect the risk of spina bifida-affected pregnancies: an Italian case-control study. Childs Nerv Syst (2011) 0.92
Folic acid and human reproduction-ten important issues for clinicians. J Exp Clin Assist Reprod (2011) 0.90
Association between MTHFD1 G1958A polymorphism and neural tube defects susceptibility: a meta-analysis. PLoS One (2014) 0.87
Ten years after the Dutch public health campaign on folic acid: the continuing challenge. Eur J Clin Pharmacol (2008) 0.85
Polymorphism 677C → T MTHFR gene in Mexican mothers of children with complex congenital heart disease. Pediatr Cardiol (2012) 0.84
Knowledge and periconceptional use of folic acid for the prevention of neural tube defects in ethnic communities in the United Kingdom: systematic review and meta-analysis. Birth Defects Res A Clin Mol Teratol (2013) 0.83
Prevention of congenital malformations and other adverse pregnancy outcomes with 4.0 mg of folic acid: community-based randomized clinical trial in Italy and the Netherlands. BMC Pregnancy Childbirth (2014) 0.80
Dihydrofolate reductase gene variations in susceptibility to disease and treatment outcomes. Curr Genomics (2010) 0.79
EE-drospirenone-levomefolate calcium versus EE-drospirenone + folic acid: folate status during 24 weeks of treatment and over 20 weeks following treatment cessation. Int J Womens Health (2013) 0.78
A cost-of-illness study of spina bifida in Italy. Clinicoecon Outcomes Res (2013) 0.78
Primary prevention of neural-tube defects and some other congenital abnormalities by folic acid and multivitamins: history, missed opportunity and tasks. Ther Adv Drug Saf (2011) 0.77
Imaging the course of a hypoplastic cerebellum in a spina bifida newborn. Childs Nerv Syst (2013) 0.77
MTHFD1 polymorphism as maternal risk for neural tube defects: a meta-analysis. Neurol Sci (2014) 0.76
Folic Acid Intake and Neural Tube Defects: Two Egyptian Centers Experience. Medicine (Baltimore) (2015) 0.75
Vitamins and minerals for women: recent programs and intervention trials. Nutr Res Pract (2011) 0.75
Development of a wheelchair mobility skills test for children and adolescents: combining evidence with clinical expertise. BMC Pediatr (2017) 0.75
Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet (2012) 41.47
Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet (2012) 26.95
Urinary incontinence after vaginal delivery or cesarean section. N Engl J Med (2003) 6.32
UK health performance: findings of the Global Burden of Disease Study 2010. Lancet (2013) 6.11
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response. Nat Genet (2009) 5.84
Self-selection and bias in a large prospective pregnancy cohort in Norway. Paediatr Perinat Epidemiol (2009) 4.78
Selective serotonin reuptake inhibitors and risk for major congenital anomalies. Obstet Gynecol (2011) 4.53
International study of temperature, heat and urban mortality: the 'ISOTHURM' project. Int J Epidemiol (2008) 4.13
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat Genet (2003) 3.96
Children born after assisted fertilization have an increased rate of major congenital anomalies. Fertil Steril (2005) 3.89
An overview of methods for calculating the burden of disease due to specific risk factors. Epidemiology (2006) 3.83
Long-term effects of traffic-related air pollution on mortality in a Dutch cohort (NLCS-AIR study). Environ Health Perspect (2008) 3.70
Impact of high temperatures on mortality: is there an added heat wave effect? Epidemiology (2006) 3.69
Are smoking and other lifestyle factors associated with female urinary incontinence? The Norwegian EPINCONT Study. BJOG (2003) 2.99
Valproic acid monotherapy in pregnancy and major congenital malformations. N Engl J Med (2010) 2.94
Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C. Am J Hum Genet (2002) 2.90
Adrenocortical carcinomas and adrenal pheochromocytomas: mass and enhancement loss evaluation at delayed contrast-enhanced CT. Radiology (2005) 2.87
Clinical and molecular phenotype of Aicardi-Goutieres syndrome. Am J Hum Genet (2007) 2.81
Socioeconomic differentials in the temperature-mortality relationship in São Paulo, Brazil. Int J Epidemiol (2003) 2.77
Chlamydia pneumoniae seropositivity and the risk of nonarteritic ischemic optic neuropathy. Ophthalmology (2002) 2.77
Intrauterine exposure to carbamazepine and specific congenital malformations: systematic review and case-control study. BMJ (2010) 2.77
Vulnerability to winter mortality in elderly people in Britain: population based study. BMJ (2004) 2.65
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature (2011) 2.59
Time series regression studies in environmental epidemiology. Int J Epidemiol (2013) 2.52
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
Effects of long-term exposure to traffic-related air pollution on respiratory and cardiovascular mortality in the Netherlands: the NLCS-AIR study. Res Rep Health Eff Inst (2009) 2.26
Transjugular intrahepatic portosystemic shunt creation with the Viatorr expanded polytetrafluoroethylene-covered stent-graft. J Vasc Interv Radiol (2004) 2.21
The impact of heat waves on mortality. Epidemiology (2011) 2.20
Calibration and discriminatory accuracy of prognosis calculation for breast cancer with the online Adjuvant! program: a hospital-based retrospective cohort study. Lancet Oncol (2009) 2.17
Reductions in serum lipids with a 4-year decline in serum perfluorooctanoic acid and perfluorooctanesulfonic acid. Epidemiology (2013) 2.13
Cerebral palsy and intrauterine growth in single births: European collaborative study. Lancet (2003) 2.11
Association between climate variability and hospital visits for non-cholera diarrhoea in Bangladesh: effects and vulnerable groups. Int J Epidemiol (2007) 2.10
The effect of high temperatures on cause-specific mortality in England and Wales. Occup Environ Med (2011) 2.04
Declining vulnerability to temperature-related mortality in London over the 20th century. Am J Epidemiol (2006) 2.00
Effect of 20 mph traffic speed zones on road injuries in London, 1986-2006: controlled interrupted time series analysis. BMJ (2009) 1.96
Calcinosis cutis: part I. Diagnostic pathway. J Am Acad Dermatol (2011) 1.95
Genetic predisposition for adult lactose intolerance and relation to diet, bone density, and bone fractures. J Bone Miner Res (2004) 1.93
The effects of hourly differences in air pollution on the risk of myocardial infarction: case crossover analysis of the MINAP database. BMJ (2011) 1.88
Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene. Am J Hum Genet (2010) 1.86
Poland syndrome with bilateral features: case description with review of the literature. Am J Med Genet A (2009) 1.82
Calcinosis cutis: part II. Treatment options. J Am Acad Dermatol (2011) 1.79
Time series analysis on the health effects of temperature: advancements and limitations. Environ Res (2010) 1.77
The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis. Hum Mol Genet (2010) 1.73
Trends in prenatal diagnosis, pregnancy termination, and perinatal mortality of newborns with congenital heart disease in France, 1983-2000: a population-based evaluation. Pediatrics (2005) 1.72
Prescription drug use among fathers and mothers before and during pregnancy. A population-based cohort study of 106,000 pregnancies in Norway 2004-2006. Br J Clin Pharmacol (2008) 1.69
Long-term exposure to traffic-related air pollution and lung cancer risk. Epidemiology (2008) 1.68
Congenital anomalies in children with cerebral palsy: a population-based record linkage study. Dev Med Child Neurol (2009) 1.63
Copy-number disorders are a common cause of congenital kidney malformations. Am J Hum Genet (2012) 1.63
Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population. Eur J Hum Genet (2005) 1.62
Risk factors for hypospadias in Norwegian boys - association with testicular dysgenesis syndrome? Int J Androl (2004) 1.61
Myasthenia gravis: consequences for pregnancy, delivery, and the newborn. Neurology (2003) 1.59
The effect of rainfall on the incidence of cholera in Bangladesh. Epidemiology (2008) 1.58
Home energy efficiency and radon related risk of lung cancer: modelling study. BMJ (2014) 1.58
Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly. Am J Hum Genet (2012) 1.57
Macrosomia: mode of delivery and pregnancy outcome. Acta Obstet Gynecol Scand (2010) 1.56
One naive T cell, multiple fates in CD8+ T cell differentiation. J Exp Med (2010) 1.55
Global variation in the effects of ambient temperature on mortality: a systematic evaluation. Epidemiology (2014) 1.55
Familial occurrence of multiple pterygium syndrome: expression in a heterozygote of the recessive form or variability of the dominant form? Am J Med Genet A (2006) 1.54
Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome. J Bone Miner Res (2011) 1.53
Survival analysis of 254 patients after manifestation of spinal metastases: evaluation of seven preoperative scoring systems. Spine (Phila Pa 1976) (2011) 1.53
A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome. Hum Genet (2006) 1.51
Twenty-year trends in the prevalence of Down syndrome and other trisomies in Europe: impact of maternal age and prenatal screening. Eur J Hum Genet (2012) 1.51
Systematic review and meta-analysis of short-acting insulin analogues in patients with diabetes mellitus. Arch Intern Med (2005) 1.49
Male periconceptional ribavir-ininterferon alpha-2b exposure with no adverse fetal effects. Birth Defects Res A Clin Mol Teratol (2003) 1.47
The short-term influence of temperature on daily mortality in the temperate climate of Montreal, Canada. Environ Res (2011) 1.46
Coenzyme Q-responsive Leigh's encephalopathy in two sisters. Ann Neurol (2002) 1.45
Reducing and meta-analysing estimates from distributed lag non-linear models. BMC Med Res Methodol (2013) 1.45
Toward the effective surveillance of hypospadias. Environ Health Perspect (2004) 1.45
Paper 6: EUROCAT member registries: organization and activities. Birth Defects Res A Clin Mol Teratol (2011) 1.42
Paper 1: The EUROCAT network--organization and processes. Birth Defects Res A Clin Mol Teratol (2011) 1.40
Microtia in Finland: comparison of characteristics in different populations. Int J Pediatr Otorhinolaryngol (2007) 1.39
International retrospective cohort study of neural tube defects in relation to folic acid recommendations: are the recommendations working? BMJ (2005) 1.39
Science, art, and mistery in the statues and in the anatomical machines of the prince of sansevero: the masterpieces of the "Sansevero Chapel". Am J Med Genet A (2013) 1.39
Preventing neural tube defects in Europe: population based study. BMJ (2005) 1.38
Conjoined twins: a worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and Research. Am J Med Genet C Semin Med Genet (2011) 1.37
Deletion and point mutations of PTHLH cause brachydactyly type E. Am J Hum Genet (2010) 1.35
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy. Physiol Genomics (2005) 1.34