Published in Am J Epidemiol on January 01, 1996
Epidemiologic and genetic aspects of spina bifida and other neural tube defects. Dev Disabil Res Rev (2010) 1.96
Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals. Birth Defects Res A Clin Mol Teratol (2008) 1.07
Correlates of intake of folic acid-containing supplements among pregnant women. Am J Obstet Gynecol (2006) 1.02
Folic acid and human reproduction-ten important issues for clinicians. J Exp Clin Assist Reprod (2011) 0.90
Risk for neural tube defect-affected pregnancies among women of Mexican descent and white women in California. Am J Public Health (1997) 0.88
Markers of acculturation and risk of NTDs among Hispanic women in California. Birth Defects Res A Clin Mol Teratol (2008) 0.79
Prevalence of anencephaly in the region of Rijeka, Croatia. Eur J Epidemiol (2001) 0.79
Decreased incidence of myelomeningocele at birth: effect of folic acid recommendations or prenatal diagnostics? Childs Nerv Syst (2011) 0.75
Incidence and Risk Factors of Neural Tube Defects in Kashan, Central Iran. Iran J Child Neurol (2015) 0.75
Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935-1984. Epilepsia (1993) 6.32
Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder. N Engl J Med (1999) 5.82
Prader-Willi syndrome: consensus diagnostic criteria. Pediatrics (1993) 4.86
Incidence of premature ovarian failure. Obstet Gynecol (1986) 4.64
Remission of seizures and relapse in patients with epilepsy. Epilepsia (1979) 4.17
Diagnostic criteria for Walker-Warburg syndrome. Am J Med Genet (1989) 3.74
The incidence, causes, and secular trends of head trauma in Olmsted County, Minnesota, 1935-1974. Neurology (1980) 3.23
Factors prognostic of unprovoked seizures after febrile convulsions. N Engl J Med (1987) 3.21
Prevalence of epilepsy in Rochester, Minnesota: 1940-1980. Epilepsia (1991) 3.02
Seizures after head trauma: a population study. Neurology (1980) 2.87
Risk of recurrent seizures after two unprovoked seizures. N Engl J Med (1998) 2.74
Long-term mortality after a first episode of status epilepticus. Neurology (2002) 2.60
Descriptive epidemiology of epilepsy: contributions of population-based studies from Rochester, Minnesota. Mayo Clin Proc (1996) 2.46
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis. Hum Mol Genet (1992) 2.35
The cost of epilepsy in the United States: an estimate from population-based clinical and survey data. Epilepsia (2000) 2.23
The association of the DiGeorge anomalad with partial monosomy of chromosome 22. J Pediatr (1982) 2.21
Incidence and risk factors in sudden unexpected death in epilepsy: a prospective cohort study. Neurology (2001) 2.19
A population study of the VACTERL association: evidence for its etiologic heterogeneity. Pediatrics (1983) 2.09
Major depression is a risk factor for seizures in older adults. Ann Neurol (2000) 2.05
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy. Hum Mol Genet (1993) 2.02
Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly. Am J Med Genet (1984) 1.95
Familial DiGeorge syndrome and associated partial monosomy of chromosome 22. Hum Genet (1984) 1.86
Higher risk of seizures in offspring of mothers than of fathers with epilepsy. Am J Hum Genet (1988) 1.84
Traumatic brain injury and time to onset of Alzheimer's disease: a population-based study. Am J Epidemiol (1999) 1.81
Seizure recurrence after a 1st unprovoked seizure: an extended follow-up. Neurology (1990) 1.76
Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome. Am J Hum Genet (1997) 1.74
Incidence and prevalence of dementia in a multiethnic cohort of municipal retirees. Neurology (1997) 1.72
Incidence of status epilepticus in Rochester, Minnesota, 1965-1984. Neurology (1998) 1.72
Population-based study of the incidence of sudden unexplained death in epilepsy. Neurology (1998) 1.72
Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome. Am J Hum Genet (1995) 1.68
Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4. Am J Hum Genet (1991) 1.67
Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A. Nat Genet (1992) 1.66
Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome. J Pediatr (1986) 1.65
Serum organochlorine pesticide levels in patients with colorectal cancer in Egypt. Arch Environ Health (1998) 1.63
Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15. Am J Hum Genet (1991) 1.62
The risk of epilepsy following febrile convulsions. Neurology (1979) 1.61
The lifetime cost of bipolar disorder in the US: an estimate for new cases in 1998. Pharmacoeconomics (2001) 1.59
Mortality in patients with epilepsy. Epilepsia (1980) 1.56
Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients. Am J Hum Genet (1996) 1.56
Air pollution and lung cancer mortality in Harris County, Texas, 1979-1981. Am J Epidemiol (1988) 1.55
Effect of follow-up time on risk estimates: a longitudinal examination of the relative risks of leukemia and multiple myeloma in a rubber hydrochloride cohort. Am J Ind Med (2002) 1.53
Population-based study of seizure disorders after cerebral infarction. Neurology (1996) 1.52
Reproductive history in women with coronary heart disease. A case-control study. Am J Epidemiol (1984) 1.50
Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region. Am J Med Genet (1995) 1.49
Short-term mortality after a first episode of status epilepticus. Epilepsia (1997) 1.49
The Rochester Coronary Heart Disease Project: effect of cigarette smoking, hypertension, diabetes, and steroidal estrogen use on coronary heart disease among 40- to 59-year-old women, 1960 through 1982. Mayo Clin Proc (1989) 1.48
Relations of genetic and environmental factors in the etiology of epilepsy. Ann Neurol (1996) 1.47
Ophthalmic manifestations of Smith-Magenis syndrome. Ophthalmology (1996) 1.47
Miller-Dieker syndrome: lissencephaly and monosomy 17p. J Pediatr (1983) 1.46
Risk of unprovoked seizure after acute symptomatic seizure: effect of status epilepticus. Ann Neurol (1998) 1.46
Williams syndrome: autosomal dominant inheritance. Am J Med Genet (1993) 1.45
Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome. Am J Med Genet (1986) 1.44
Fiber intake and childhood appendicitis. Am J Public Health (1985) 1.41
Excess leukemia and multiple myeloma in a mining county in northeast Texas. Tex Med (1994) 1.39
Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21. Am J Hum Genet (1992) 1.38
Clinicopathologic review of 118 granulosa and 82 theca cell tumors. Obstet Gynecol (1980) 1.38
Dementia and adult-onset unprovoked seizures. Neurology (1996) 1.37
Sleep disturbance in Smith-Magenis syndrome (del 17 p11.2). Am J Med Genet (1998) 1.34
Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q). Am J Med Genet (1988) 1.33
Mortality in achondroplasia. Am J Hum Genet (1987) 1.33
Incidence of neonatal seizures in Harris County, Texas, 1992-1994. Am J Epidemiol (1999) 1.32
Risk of recurrence after an initial unprovoked seizure. Epilepsia (1986) 1.31
Prognosis of amyotrophic lateral sclerosis and the effect of referral selection. J Neurol Sci (1995) 1.29
Sudden unexplained death in epilepsy: observations from a large clinical development program. Epilepsia (1997) 1.29
Exogenous estrogen and endometrial carcinoma: case-control and incidence study. Am J Obstet Gynecol (1977) 1.28
Disability days associated with detection and treatment in a hypertension control program. Am J Epidemiol (1984) 1.28
Cigarette smoking and alcohol consumption as risk factors for colorectal adenomatous polyps. J Natl Cancer Inst (1995) 1.27
The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2. Am J Hum Genet (1995) 1.26
Risk factors for seizure recurrence in children with febrile seizures: a pooled analysis of individual patient data from five studies. J Pediatr (1994) 1.25
Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2). Am J Med Genet (1998) 1.24
Cohort study of incidence of sudden unexplained death in persons with seizure disorder treated with antiepileptic drugs in Saskatchewan, Canada. Epilepsia (1995) 1.23
The familial aggregation of rheumatoid arthritis and its relationship to the HLA-DR4 association. Am J Epidemiol (1984) 1.21
Incidence of skull fractures in Olmsted County, Minnesota. Neurosurgery (1984) 1.21
Severe, uncontrolled hypertension and adult-onset seizures: a case-control study in Rochester, Minnesota. Epilepsia (1996) 1.20
Child and adolescent drownings in Harris County, Texas, 1983 through 1990. Am J Public Health (1994) 1.20
Epidemiology and the genetics of epilepsy. Res Publ Assoc Res Nerv Ment Dis (1983) 1.19
Childhood appendicitis: factors associated with perforation. Pediatrics (1985) 1.17
Ovarian cancer: incidence and case-control study. Cancer (1979) 1.17
The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients. Hum Mol Genet (1995) 1.15
Heart disease mortality and morbidity in patients with epilepsy. Epilepsia (1984) 1.15
Acute health effects in a community after a release of hydrofluoric acid. Arch Environ Health (1991) 1.14
Seizure risk in offspring of parents with generalized versus partial epilepsy. Epilepsia (1989) 1.13
Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17. Am J Med Genet (1986) 1.13
Risk factors for ectopic pregnancy. A population-based study. JAMA (1988) 1.12
Are standardized mortality ratios valid for public health data analysis? Stat Med (2000) 1.11
The risks of seizure disorders among relatives of patients with childhood onset epilepsy. Neurology (1982) 1.11
Epidemiologic study of primary intracranial neoplasms. Arch Neurol (1981) 1.11
The relationship between rheumatoid arthritis and reproductive function. Br J Rheumatol (1989) 1.10
Brain injury and neurologic sequelae: a cohort study of dementia, parkinsonism, and amyotrophic lateral sclerosis. Neurology (1991) 1.10
A surveillance system for assessing health effects from hazardous exposures. Am J Epidemiol (1990) 1.10
De novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic, and molecular characterization. Am J Med Genet (1995) 1.10
Molecular studies of DiGeorge syndrome. Am J Hum Genet (1990) 1.09
Is Bendectin a teratogen? JAMA (1981) 1.09
Do anticonvulsants reduce the efficacy of oral contraceptives? Epilepsia (1979) 1.09
Case-control study of the risk factors for eclampsia. Am J Epidemiol (1995) 1.07
Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathy. Hum Genet (1996) 1.06
Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin. Am J Med Genet (1998) 1.06
Complex segregation analysis of febrile convulsions. Am J Hum Genet (1987) 1.06
Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p. Genomics (1992) 1.06
The risk of seizure disorders among relatives of children with febrile convulsions. Neurology (1985) 1.06