Published in Birth Defects Orig Artic Ser on June 01, 1971
Choice of an estimate of genetic variance from twin data. Am J Hum Genet (1974) 3.36
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6. Clin Genet (1987) 3.14
Calcium supplementation and increases in bone mineral density in children. N Engl J Med (1992) 3.13
Salivary and pancreatic amylase: electrophoretic characterizations and genetic studies. Am J Hum Genet (1973) 3.12
Cleft lip+/-cleft palate: an overview of the literature and an analysis of Danish cases born between 1941 and 1968. Am J Med Genet (1980) 2.51
Genetic factors in determining bone mass. J Clin Invest (1973) 2.35
Segregation analysis of cleft lip with or without cleft palate: a comparison of Danish and Japanese data. Am J Hum Genet (1986) 2.23
A proposed classification for heritable human dentine defects with a description of a new entity. Arch Oral Biol (1973) 2.16
Improved outcome in Pierre Robin sequence: effect of multidisciplinary evaluation and management. Pediatrics (1990) 1.92
Genetic determinants of bone mass in adult women: a reevaluation of the twin model and the potential importance of gene interaction on heritability estimates. J Bone Miner Res (1991) 1.82
Familial variation of head size and adjustment for parental head circumference. J Pediatr (1980) 1.76
Multiple pterygium syndrome. Am J Dis Child (1978) 1.71
The NHLBI twin study of cardiovascular disease risk factors: methodology and summary of results. Am J Epidemiol (1977) 1.70
The ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome. Report of 2 cases and review of the literature. Clin Genet (1972) 1.63
Hereditary influences on cognitive functioning in older men. A study of 4000 twin pairs. Arch Neurol (1993) 1.62
Dermatoglyphic nomogram for the diagnosis of Down's syndrome. J Pediatr (1970) 1.56
Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus. J Clin Endocrinol Metab (1999) 1.45
Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis. J Clin Endocrinol Metab (2000) 1.43
Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers. Arch Neurol (1999) 1.41
Genetic analysis in families with van der Woude syndrome. J Craniofac Genet Dev Biol (1985) 1.37
Cognitive scores in carriers of Huntington's disease gene compared to noncarriers. Ann Neurol (1995) 1.36
Genetic predisposition to organ-specific endpoints of alcoholism. Alcohol Clin Exp Res (1996) 1.34
Human salivary amylase: genetics of electrophoretic variants. Am J Hum Genet (1971) 1.33
Subtle changes among presymptomatic carriers of the Huntington's disease gene. J Neurol Neurosurg Psychiatry (2000) 1.32
Influences on skeletal mineralization in children and adolescents: evidence for varying effects of sexual maturation and physical activity. J Pediatr (1994) 1.32
Congenital X-linked cataract, dental anomalies and brachymetacarpalia. Birth Defects Orig Artic Ser (1974) 1.30
Trapezoidocephaly, midfacial hypoplasia and cartilage abnormalities with multiple synostoses and skeletal fractures. Birth Defects Orig Artic Ser (1975) 1.29
Incidence of cleft lip and palate in the offspring of cleft parents. Clin Genet (1971) 1.29
Familial branchio-oto-renal dysplasia: a new addition to the branchial arch syndromes. Clin Genet (1976) 1.28
Simplified method for collection of pure submandibular saliva in large volumes. J Dent Res (1968) 1.28
TWINAN90: a FORTRAN program for conducting ANOVA-based and likelihood-based analyses of twin data. Comput Methods Programs Biomed (1992) 1.27
The Nance-Horan syndrome: a rare X-linked ocular-dental trait with expression in heterozygous females. Clin Genet (1984) 1.27
Effects of chorion type on variation in cord blood cholesterol of monozygotic twins. Am J Hum Genet (1976) 1.26
Urorectal septum malformation sequence. Report of six cases and embryological analysis. Am J Dis Child (1987) 1.26
Partial trisomy 1 due to a "shift" and probable location of the Duffy (Fy) locus. Am J Hum Genet (1977) 1.23
Phenotypic variation in the popliteal pterygium syndrome. Clin Genet (1973) 1.21
Cleft palate: a genetic and epidemiologic investigation. Clin Genet (1981) 1.20
Confirmation of subtle motor changes among presymptomatic carriers of the Huntington disease gene. Arch Neurol (2000) 1.19
Long-term bone loss in men: effects of genetic and environmental factors. Ann Intern Med (1992) 1.19
Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13. J Bone Miner Res (1998) 1.18
The acrocephalosyndactyly syndromes: a metacarpophalangeal pattern profile analysis. Clin Genet (1977) 1.18
Genome screen for quantitative trait loci underlying normal variation in femoral structure. J Bone Miner Res (2001) 1.16
Smoking and alcohol consumption in adult male twins: genetic heritability and shared environmental influences. J Subst Abuse (1990) 1.15
The NHLBI Twin Study: heritability of apolipoprotein A-I, B, and low density lipoprotein subclasses and concordance for lipoprotein(a). Atherosclerosis (1991) 1.15
On the classification of the acrocephalosyndactyly syndromes. Clin Genet (1977) 1.15
Familial resemblance in the blood pressure response to sodium restriction. Am J Epidemiol (1987) 1.14
Motor changes in presymptomatic Huntington disease gene carriers. Arch Neurol (1996) 1.14
Translocations of D chromosomes in two families: t(13q14q) and t(13q14q)+(13p14p). J Med Genet (1969) 1.13
Heritable features of the auditory oddball event-related potential: peaks, latencies, morphology and topography. Electroencephalogr Clin Neurophysiol (1994) 1.09
Diagnostic criteria for the whistling face syndrome. Birth Defects Orig Artic Ser (1975) 1.09
Periodontosis: a phenotypic and genetic analysis. Oral Surg Oral Med Oral Pathol (1976) 1.07
Hypertelorism, microtia, and facial clefting. A newly described inherited syndrome. Am J Dis Child (1969) 1.07
Maternal influence on plasma cholesterol variation. Am J Hum Genet (1977) 1.06
Twin study: relationship between birth weight, zygosity, placentation, and pathologic placental changes. Acta Genet Med Gemellol (Roma) (1988) 1.06
Dominance and environmental variances: their effect on heritabilities estimated from twin data. Hum Hered (1977) 1.05
Comparisons of dermatoglyphic patterns in monochorionic and dichorionic monozygotic twins. Am J Hum Genet (1978) 1.05
Salt sensitivity and resistance of blood pressure. Age and race as factors in physiological responses. Hypertension (1991) 1.04
Sampling variances in twin and sibling studies of man. Hum Hered (1974) 1.03
The genetics of proximal femur geometry, distribution of bone mass and bone mineral density. Osteoporos Int (1996) 1.02
Genetic analysis of dermatoglyphic patterns in twins. Hum Hered (1975) 1.02
Aggregation of blood pressure in the families of identical twins. Am J Epidemiol (1979) 1.02
Autosomal dominant branchiootorenal dysplasia. Birth Defects Orig Artic Ser (1975) 1.01
Multiclonal outbreak of methicillin-resistant Staphylococcus aureus infections on a collegiate football team. Epidemiol Infect (2008) 0.99
The effect of apolipoprotein E epsilon4 in the relationships of smoking and drinking to cognitive function. Neuroepidemiology (1999) 0.98
Possible localization of a major gene for cleft lip and palate to 4q. Clin Genet (1994) 0.98
Facial clefts in Danish twins. Cleft Palate J (1979) 0.97
The adducted thumbs syndrome. An autosomal recessive disease with arthrogryposis, dysmyelination, craniostenosis, and cleft palate. Clin Genet (1971) 0.97
Letters to the editor: Statistical analysis of genetic variance in twins. Am J Hum Genet (1975) 0.97
Genetic influences on age-related change in total cholesterol, low density lipoprotein-cholesterol, and triglyceride levels: longitudinal apolipoprotein E genotype effects. Genet Epidemiol (1994) 0.96
Blood pressure response to dietary sodium restriction in normotensive adults. Hypertension (1983) 0.96
Facial clefting: an alternative biologic explanation for its complex etiology. Birth Defects Orig Artic Ser (1977) 0.96
A proposed test of the difference between the means of monozygotic and dizygotic twins. Acta Genet Med Gemellol (Roma) (1977) 0.95
World War II-veteran male twins who are discordant for alcohol consumption: 24-year mortality. Am J Public Health (1995) 0.95
Genetics and clefting. Cleft Palate J (1981) 0.95
Testing twin means and estimating genetic variance: basic methodology for the analysis of quantitative twin data. Acta Genet Med Gemellol (Roma) (1979) 0.94
Genetics of plasma cholesterol and triglycerides: a study of adult male twins. Acta Genet Med Gemellol (Roma) (1976) 0.93
Concordance for dyslipidemic hypertension in male twins. JAMA (1991) 0.93
Effects of type of placentation on birthweight and its variability in monozygotic and dizygotic twins. Acta Genet Med Gemellol (Roma) (1979) 0.93
Clinical, laboratory, and genetic investigations of hypophosphatasia: support for autosomal dominant inheritance with homozygous lethality. J Craniofac Genet Dev Biol (1983) 0.93
Familial aortic dissection with iris anomalies--a new connective tissue disease syndrome? Birth Defects Orig Artic Ser (1976) 0.92
Determinants of plasma cholesterol in children--a family study. Am J Clin Nutr (1980) 0.91
Dominant microspherophakia. Arch Ophthalmol (1971) 0.91
Facial morphometrics in the identification of gene carriers of X-linked hypohidrotic ectodermal dysplasia. Am J Med Genet (1990) 0.91
Variance of plasma free and esterified cholesterol in adult twins. Am J Hum Genet (1976) 0.90
The use of twin registers in the study of birth defects. Birth Defects Orig Artic Ser (1978) 0.90
Genetic variability of human plasma and erythrocyte lipids. Lipids (1971) 0.90
Human parotid proline-rich proteins: correlation of genetic polymorphisms to dental caries. Genet Epidemiol (1986) 0.90
Linkage studies in Van der Woude syndrome. J Med Genet (1978) 0.89
Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family. Am J Med Genet (1983) 0.89
Maternal effects on fingertip dermatoglyphics. Am J Hum Genet (1979) 0.89
Dominant preaxial brachydactyly with hallux varus and thumb abduction. Am J Hum Genet (1972) 0.88
Unstable galactose-1-phosphate uridyl transferase: a new variant of galactosemia. J Pediatr (1971) 0.88
Studies of cleft lip and cleft palate in the population of Denmark. Prog Clin Biol Res (1980) 0.88
Efficiency of human monozygotic twins in studies of blood lipids. Metabolism (1972) 0.88
Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter. Hum Genet (1987) 0.87
The effects of changing caries prevalence and diagnostic criteria on clinical caries trials. Caries Res (1983) 0.87
Alcohol effects on the heritability of EEG spectral power. Alcohol Clin Exp Res (1996) 0.87
Fetal mortality in oral cleft families (IX): factors relating to the occurrence of sporadic clefts. Clin Genet (1984) 0.87