Published in Am J Med Genet on July 11, 1997
Clinical and Genetic Studies of VACTERL Association | NCT00766571
Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology. J Med Genet (2005) 2.28
Analysis of component findings in 79 patients diagnosed with VACTERL association. Am J Med Genet A (2010) 2.03
VACTERL/VATER Association. Orphanet J Rare Dis (2011) 1.87
The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches. J Negat Results Biomed (2006) 1.64
Clinical geneticists' views of VACTERL/VATER association. Am J Med Genet A (2012) 1.08
Analysis of genitourinary anomalies in patients with VACTERL (Vertebral anomalies, Anal atresia, Cardiac malformations, Tracheo-Esophageal fistula, Renal anomalies, Limb abnormalities) association. Congenit Anom (Kyoto) (2011) 1.08
Ephrin-B reverse signaling controls septation events at the embryonic midline through separate tyrosine phosphorylation-independent signaling avenues. Dev Biol (2011) 1.06
Familial occurrence of the VATER/VACTERL association. Pediatr Surg Int (2012) 1.05
Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype? Ital J Pediatr (2013) 1.02
VACTERL-H Association and Fanconi Anemia. Mol Syndromol (2013) 0.97
Sirenomelia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research, and literature review. Am J Med Genet C Semin Med Genet (2011) 0.96
Associations of anorectal malformations and related syndromes. Pediatr Surg Int (2013) 0.93
Considering the Embryopathogenesis of VACTERL Association. Mol Syndromol (2013) 0.91
Mitochondrial Factors and VACTERL Association-Related Congenital Malformations. Mol Syndromol (2013) 0.89
Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association. Eur J Med Genet (2011) 0.89
Modern imaging of the tracheo-bronchial tree. World J Radiol (2010) 0.88
VATER/VACTERL Association: Evidence for the Role of Genetic Factors. Mol Syndromol (2013) 0.88
Inheritance of the VATER/VACTERL association. Pediatr Surg Int (2012) 0.86
Preferential associated anomalies in 818 cases of microtia in South America. Am J Med Genet A (2013) 0.86
VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis. Clin Dysmorphol (2012) 0.86
Anorectal malformations associated with esophageal atresia in neonates. Pediatr Gastroenterol Hepatol Nutr (2013) 0.86
Long-term outcomes of adults with features of VACTERL association. Eur J Med Genet (2010) 0.84
Congenital pouch colon with prune belly syndrome and megalourethra. Pediatr Surg Int (2005) 0.84
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association. Eur J Hum Genet (2013) 0.84
Adriamycin produces a reproducible teratogenic model of gastrointestinal atresia in the mouse. Pediatr Surg Int (2008) 0.82
Spinal dysraphism: a neurosurgical review for the urologist. Rev Urol (2009) 0.82
Is urorectal septum malformation sequence a variant of the vertebral defects, anal atresia, tracheo-oesophageal fistula, renal defects and radial dysplasia association? Report of a case and a review of the literature. Eur J Pediatr (2005) 0.81
Growth failure and pituitary function in CHARGE and VATER associations. Arch Dis Child (1999) 0.81
Challenges in Studying Modifiable Risk Factors for Birth Defects. Curr Epidemiol Rep (2015) 0.80
Sacral nerve stimulation for faecal incontinence due to imperforate anus in VATER/VACTERL association. Int J Colorectal Dis (2015) 0.80
Consideration of VACTERL association in patients with trisomy 21. Clin Dysmorphol (2010) 0.80
Associated congenital anomalies between neonates with short-gap and long-gap esophageal atresia: a comparative study. Int J Gen Med (2011) 0.79
Adriamycin-Induced Models of VACTERL Association. Mol Syndromol (2013) 0.78
Analysis of renal anomalies in VACTERL association. Birth Defects Res A Clin Mol Teratol (2014) 0.78
The genetic landscape and clinical implications of vertebral anomalies in VACTERL association. J Med Genet (2016) 0.77
Surgical correction of tracheo-oesophageal fistula and oesophageal atresia in infants with VACTERL association: a retrospective case-control study. Pediatr Surg Int (2012) 0.76
Maternal hyperthyroidism increases the prevalence of foregut atresias in fetal rats exposed to adriamycin. Pediatr Surg Int (2014) 0.76
Posterior vertebral column resection for VATER/VACTERL associated spinal deformity: a case report. HSS J (2007) 0.76
Abnormalities of the vertebral column and ribs associated with anorectal malformations. Pediatr Surg Int (2004) 0.75
Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotype. Pediatr Nephrol (2016) 0.75
Role of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans. Curr Genomics (2015) 0.75
First Trimester Diagnosis of VACTERL Association. Clin Pract (2013) 0.75
Childhood cancer risk in those with chromosomal and non-chromosomal congenital anomalies in Washington State: 1984-2013. PLoS One (2017) 0.75
VACTERL association with double-chambered left ventricle: A rare occurrence. Ann Pediatr Cardiol (2013) 0.75
Medical predictors of psychological anxieties in VATER patients. Pediatr Surg Int (2011) 0.75
Omphalocele minor associated with complete absence of the large bowel. Pediatr Surg Int (2009) 0.75
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Can terathanasia explain the protective effect of folic-acid supplementation on birth defects? Lancet (1997) 3.93
Sudden unexplained infant death in 20 regions in Europe: case control study. Lancet (2004) 3.60
Perinatal death associated with planned home birth in Australia: population based study. BMJ (1998) 3.27
Stress doses of hydrocortisone reverse hyperdynamic septic shock: a prospective, randomized, double-blind, single-center study. Crit Care Med (1999) 3.20
Mortality associated with congenital heart defects in the United States: trends and racial disparities, 1979-1997. Circulation (2001) 2.92
Infant mortality and congenital anomalies from 1950 to 1994: an international perspective. J Epidemiol Community Health (2000) 2.89
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Health-related quality of life and posttraumatic stress disorder in survivors of the acute respiratory distress syndrome. Crit Care Med (1998) 2.85
Population-based study of congenital heart defects in Down syndrome. Am J Med Genet (1998) 2.74
Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. J Med Genet (2003) 2.72
Maternal obesity and excess of fetal growth in pre-eclampsia. BJOG (2014) 2.70
Retracted Outcome of pregnancy in diabetic women in northeast England and in Norway, 1994-7. BMJ (2000) 2.67
Familial risk of obstetric anal sphincter injuries: registry-based cohort study. BJOG (2013) 2.66
Public attitudes regarding the donation and storage of blood specimens for genetic research. Community Genet (2001) 2.66
The physiologic development of speech motor control: lip and jaw coordination. J Speech Lang Hear Res (2000) 2.64
Phenopedia and Genopedia: disease-centered and gene-centered views of the evolving knowledge of human genetic associations. Bioinformatics (2009) 2.59
Plasma total homocysteine, pregnancy complications, and adverse pregnancy outcomes: the Hordaland Homocysteine study. Am J Clin Nutr (2000) 2.53
Completeness of the discharge diagnoses as a measure of birth defects recorded in the hospital birth record. Am J Epidemiol (1991) 2.49
Fetal and maternal contributions to risk of pre-eclampsia: population based study. BMJ (1998) 2.48
Contribution of birth defects and genetic diseases to pediatric hospitalizations. A population-based study. Arch Pediatr Adolesc Med (1997) 2.42
The birth prevalence rates for the skeletal dysplasias. J Med Genet (1986) 2.40
Australian national birthweight percentiles by gestational age. Med J Aust (1999) 2.35
VATER non-random association of congenital malformations: study based on data from four malformation registers. Am J Med Genet (2001) 2.34
Prospective assessment of recurrence risk in sudden infant death syndrome siblings. J Pediatr (1984) 2.33
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Case-only design to measure gene-gene interaction. Epidemiology (1999) 2.30
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Prenatal diagnosis of severe structural congenital malformations in Europe. Ultrasound Obstet Gynecol (2005) 2.19
Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: report of three patients. Am J Med Genet (1997) 2.17
Transmission disequilibrium test (TDT) when only one parent is available: the 1-TDT. Am J Epidemiol (1999) 2.15
The association of Apgar score with subsequent death and cerebral palsy: A population-based study in term infants. J Pediatr (2001) 2.15
Congenital malformation and maternal occupational exposure to glycol ethers. Occupational Exposure and Congenital Malformations Working Group. Epidemiology (1997) 2.15
Pregnancy outcome following maternal exposure to statins: a multicentre prospective study. BJOG (2012) 2.14
Down syndrome is not increased in offspring of natural family planning users (case control analysis) Am J Med Genet (1995) 2.13
Evaluation of prenatal ultrasound diagnosis of fetal abdominal wall defects by 19 European registries. Ultrasound Obstet Gynecol (2001) 2.10
Birth prevalence study of the Apert syndrome. Am J Med Genet (1992) 2.10
Cell-type-specific calcium responses to drought, salt and cold in the Arabidopsis root. Plant J (2000) 2.09
A population study of the VACTERL association: evidence for its etiologic heterogeneity. Pediatrics (1983) 2.09
Dandy-Walker malformation and polydactyly: a possible expression of hydrolethalus syndrome. Clin Genet (1996) 2.07
Birth weight and perinatal mortality: the effect of gestational age. Am J Public Health (1992) 2.06
Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide. J Med Genet (2003) 2.03
Risk of stillbirth and infant deaths after assisted reproductive technology: a Nordic study from the CoNARTaS group. Hum Reprod (2014) 2.01
On the use of the term "syndrome" in clinical genetics and birth defects epidemiology. Am J Med Genet (1994) 1.98
Emergent applications of cardiopulmonary support: a multiinstitutional experience. Ann Thorac Surg (1992) 1.97
Valproic acid and spina bifida. Lancet (1982) 1.97
Philtrum length and intercommissural distance in newborn infants. J Med Genet (1983) 1.96
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Autosomal recessive acrorenal syndrome. Am J Med Genet (1992) 1.94
Chorionic villus sampling and transverse digital deficiencies: evidence for anatomic and gestational-age specificity of the digital deficiencies in two studies. Am J Med Genet (1996) 1.92
Commentary: facing the challenge of gene-environment interaction: the two-by-four table and beyond. Am J Epidemiol (2001) 1.87
Neuroectodermal tumours in children born after assisted conception. Lancet (1991) 1.87
Brief report: severe infectious mononucleosis-like syndrome and primary human herpesvirus 6 infection in an adult. N Engl J Med (1993) 1.84
Epidemiology of biliary atresia: a population-based study. Pediatrics (1997) 1.83
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VACTERL association, epidemiologic definition and delineation. Am J Med Genet (1996) 1.73
Hereditary hemochromatosis: gene discovery and its implications for population-based screening. JAMA (1998) 1.73
Periconceptional multivitamin use and the occurrence of conotruncal heart defects: results from a population-based, case-control study. Pediatrics (1996) 1.73
Two nonallelic insulin genes in Xenopus laevis are expressed differentially during neurulation in prepancreatic embryos. Proc Natl Acad Sci U S A (1991) 1.72
Birth defects among offspring of Norwegian farmers, 1967-1991. Epidemiology (1997) 1.72
Combined effects of sleeping position and prenatal risk factors in sudden infant death syndrome: the Nordic Epidemiological SIDS Study. Pediatrics (1997) 1.71
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Population screening for genetic disorders in the 21st century: evidence, economics, and ethics. Public Health Genomics (2009) 1.62
Paternal serum dioxin and reproductive outcomes among veterans of Operation Ranch Hand. Epidemiology (1995) 1.62
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Application of population screening principles to genetic screening for adult-onset conditions. Genet Test (2001) 1.60
Major congenital malformations in Down syndrome. Am J Med Genet (1996) 1.60
Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community. Am J Med Genet (1992) 1.59
Congenital eye malformations: clinical-epidemiological analysis of 1,124,654 consecutive births in Spain. Am J Med Genet (1998) 1.56
Short rib-polydactyly syndrome and pericentric inversion of chromosome 4. Am J Med Genet (1994) 1.56
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