Published in Ala J Med Sci on October 01, 1966
Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity. Am J Hum Genet (1970) 1.23
Oral clefts in the American Indian. Public Health Rep (1967) 1.01
Consanguinity and blood group distribution in an Amish Isolate. Am J Hum Genet (1968) 0.84
Phenotype characterization and DSPP mutational analysis of three Brazilian dentinogenesis imperfecta type II families. Cells Tissues Organs (2008) 0.80
The dentin phosphoprotein repeat region and inherited defects of dentin. Mol Genet Genomic Med (2015) 0.75
Hereditary opalescent dentin. BMJ Case Rep (2013) 0.75
Analysis of family resemblance. 3. Complex segregation of quantitative traits. Am J Hum Genet (1974) 9.68
Undetectable intracellular free copper: the requirement of a copper chaperone for superoxide dismutase. Science (1999) 6.86
A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity. Nat Genet (1995) 5.87
Metal ion chaperone function of the soluble Cu(I) receptor Atx1. Science (1997) 4.55
Smoking and major depression. A causal analysis. Arch Gen Psychiatry (1993) 4.15
Multipoint linkage analysis. Am J Hum Genet (1986) 3.12
Dissociation in Pseudomonas aeruginosa. J Bacteriol (1964) 3.00
Effects of gonadal steroids in women with a history of postpartum depression. Am J Psychiatry (2000) 2.62
Opportunities of the "Now" generation. Q Natl Dent Assoc (1968) 2.51
Replication of linkage studies of complex traits: an examination of variation in location estimates. Am J Hum Genet (1999) 2.50
Modulation of cognition-specific cortical activity by gonadal steroids: a positron-emission tomography study in women. Proc Natl Acad Sci U S A (1997) 2.19
Effects of substance P on functionally identified units in cat spinal cord. Brain Res (1976) 1.90
Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families. Mol Psychiatry (1997) 1.87
Hereditary defects of dentin. Dent Clin North Am (1975) 1.77
Serum cholesterol and hemorrhagic stroke in the Honolulu Heart Program. Stroke (1989) 1.76
Visual system anomalies in human ocular albinos. Science (1978) 1.75
The incidence and prognosis of unrecognized myocardial infarction in the Honolulu, Hawaii, Heart Program. Arch Intern Med (1989) 1.74
The Saethre-Chotzen syndrome. Birth Defects Orig Artic Ser (1975) 1.72
Analysis of family resemblance. V. Height and weight in northeastern Brazil. Am J Hum Genet (1975) 1.67
Pulmonary function as a predictor of coronary heart disease. Am J Epidemiol (1989) 1.66
Asymmetric visually evoked potentials in human albinos: evidence for visual system anomalies. Invest Ophthalmol (1974) 1.66
Posttransfusion hepatitis after exclusion of commercial and hepatitis-B antigen-positive donors. Ann Intern Med (1972) 1.64
Dehydroepiandrosterone treatment of midlife dysthymia. Biol Psychiatry (1999) 1.57
Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes. Mol Psychiatry (2002) 1.56
A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). Am J Med Genet (1996) 1.55
Evidence for a schizophrenia vulnerability locus on chromosome 8p in the Irish Study of High-Density Schizophrenia Families. Am J Psychiatry (1996) 1.53
Relative impact of smoking and reduced pulmonary function on peptic ulcer risk. A prospective study of Japanese men in Hawaii. Gastroenterology (1989) 1.52
A proposal to standardize terminology for weak D antigen. Transfusion (1992) 1.52
A study of poliovaccination in infancy: excretion following challenge with live virus by children given killed or living poliovaccine. J Hyg (Lond) (1966) 1.51
A critical analysis of directive counselling as a component of tinnitus retraining therapy. Br J Audiol (1998) 1.51
Paw withdrawal threshold in the von Frey hair test is influenced by the surface on which the rat stands. J Neurosci Methods (1999) 1.50
Nerve constriction in the rat: model of neuropathic, surgical and central pain. Pain (1999) 1.48
Multilocus recombination frequencies. Genet Res (1984) 1.46
Predictors of sudden cardiac death among Hawaiian-Japanese men. Am J Epidemiol (1989) 1.46
Reported alcohol use in women with premenstrual syndrome. Am J Psychiatry (1994) 1.44
Posttransfusion hepatitis after open-heart operations. Incidence after the administration of blood from commercial and volunteer donor populations. JAMA (1970) 1.43
Combined analysis of genetic segregation and linkage under an oligogenic model. Comput Biomed Res (1984) 1.41
Albinism. Surv Ophthalmol (1986) 1.41
Estrogen-serotonin interactions: implications for affective regulation. Biol Psychiatry (1998) 1.40
Manifestations of genetic diseases in the human pulp. Oral Surg Oral Med Oral Pathol (1971) 1.40
Tests of hypotheses on recombination frequencies. Genet Res (1985) 1.39
Androgens, brain, and behavior. Am J Psychiatry (1996) 1.39
Irish study on high-density schizophrenia families: field methods and power to detect linkage. Am J Med Genet (1996) 1.35
Malformation syndromes. A selected miscellany. Birth Defects Orig Artic Ser (1975) 1.35
Neuropsychiatric effects of anabolic steroids in male normal volunteers. JAMA (1993) 1.34
Substance P and spinal neurones. Can J Physiol Pharmacol (1975) 1.34
Autosomal recessively inherited ocular albinism. A new form of ocular albinism affecting females as severely as males. Arch Ophthalmol (1978) 1.33
Estimation of myriad haplotype frequencies. Genet Epidemiol (1985) 1.29
Hermansky-Pudlak syndrome. Ophthalmic findings. Ophthalmology (1988) 1.26
Taurodontism, an isolated trait associated with syndromes and X-chromosomal aneuploidy. Am J Hum Genet (1980) 1.25
Trials of the beta model for complex inheritance. Proc Natl Acad Sci U S A (1996) 1.24
Albinism. Adv Hum Genet (1971) 1.23
Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity. Am J Hum Genet (1970) 1.23
Substance P-mediated slow excitatory postsynaptic potential elicited in dorsal horn neurons in vivo by noxious stimulation. Proc Natl Acad Sci U S A (1991) 1.23
Bridging the gap. J Dent Educ (1971) 1.21
Clinical features of schizophrenia and linkage to chromosomes 5q, 6p, 8p, and 10p in the Irish Study of High-Density Schizophrenia Families. Am J Psychiatry (2000) 1.21
Basal cell nevus syndrome. Combined clinical staff conference at the National Institutes of Health. Ann Intern Med (1966) 1.20
A method for the study of incest. Ann Hum Genet (1973) 1.20
Ophthalmologic, biochemical, platelet, and ultrastructural defects in the various types of oculocutaneous albinism. J Invest Dermatol (1973) 1.19
Metal transporters that contribute copper to metallochaperones in Saccharomyces cerevisiae. Mol Genet Genomics (2001) 1.18
Anti-i, a frequent cold agglutinin in infectious mononucleosis. Vox Sang (1966) 1.17
Menstrual cycle effects on cortical excitability. Neurology (1999) 1.17
Catecholaminergic depressant effects on bulbar respiratory mechanisms. Brain Res (1979) 1.16
Abnormal visual pathways in the brain of a human albino. Brain Res (1975) 1.14
Studies of platelets in a variant of the Hermansky-Pudlak syndrome. Am J Pathol (1971) 1.13
Study of subchondral bone adaptations in a rodent surgical model of OA using in vivo micro-computed tomography. Osteoarthritis Cartilage (2007) 1.12
Elevated urinary dolichol excretion in the Hermansky-Pudlak syndrome. Indicator of lysosomal dysfunction. Am J Med (1987) 1.12
A schizophrenia locus may be located in region 10p15-p11. Am J Med Genet (1998) 1.12
Aberrant U blood group accompanying Rh-null. Transfusion (1967) 1.11
A follow-up study of premenstrual syndrome. J Clin Psychiatry (1999) 1.11
Agenesis of succedaneous teeth: an expression of the homozygous state of the gene for the pegged or missing maxillary lateral incisor trait. Am J Med Genet (1987) 1.09
Genetic studies on hybrid populations. I. Individual estimates of ancestry and their relation to quantitative traits. Ann Hum Genet (1973) 1.09
Risk factors in middle age that predict early and late onset of coronary heart disease. J Clin Epidemiol (1989) 1.09
Partial expression of sex-linked recessive amelogenesis imperfecta in females compatible with the Lyon hypothesis. Oral Surg Oral Med Oral Pathol (1967) 1.08
The genetic susceptibility to insulin-dependent diabetes mellitus: combined segregation and linkage analysis. Genet Epidemiol (1985) 1.08
Hypoplastic enamel, onycholysis, and hypohidrosis inherited as an autosomal dominant trait. A review of ectodermal dysplasia syndromes. Oral Surg Oral Med Oral Pathol (1975) 1.08
Blacks in dentistry. J Am Dent Assoc (1974) 1.08
Where do we go from here. The plight of the Negro in dentistry. J Natl Med Assoc (1967) 1.07
The bicentennial of transfusion in America. Transfusion (1995) 1.07
The problems facing Negroes in dental education. J Am Coll Dent (1969) 1.07
Inherited defects in tooth structure. Birth Defects Orig Artic Ser (1971) 1.07
The determinants of parenting: an epidemiological, multi-informant, retrospective study. Psychol Med (1997) 1.06
Dental asymmetry as an indicator of genetic and environmental conditions in human populations. Hum Biol (1970) 1.06
Syndrome of amelogenesis imperfecta, nephrocalcinosis, impaired renal concentration, and possible abnormality of calcium metabolism. Am J Med Genet (1985) 1.05
Analyzing the relationship between age at onset and risk to relatives. Am J Hum Genet (1989) 1.05
Gamma-globulin in the prophylaxis of posttransfusion hepatitis. JAMA (1966) 1.05
Labile aggregation stimulating substance (LASS): the factor from storage pool deficient platelets correcting defective aggregation and release of aspirin treated normal platelets. Br J Haematol (1975) 1.05
Pathogenesis of pulmonary fibrosis: platelet-derived growth factor precedes structural alterations in the Hermansky-Pudlak syndrome. J Lab Clin Med (1994) 1.04
Effects of intrathecal administration of neuropeptides on a spinal nociceptive reflex in the rat: VIP, galanin, CGRP, TRH, somatostatin and angiotensin II. Neuropeptides (1988) 1.04
Resemblance of psychotic symptoms and syndromes in affected sibling pairs from the Irish Study of High-Density Schizophrenia Families: evidence for possible etiologic heterogeneity. Am J Psychiatry (1997) 1.03
Effects of morphine and naloxone on dorsal horn neurones in the cat. Can J Physiol Pharmacol (1974) 1.03
Parametric studies on electroacupuncture-like stimulation in a rat model: effects of intensity, frequency, and duration of stimulation on evoked antinociception. Brain Res Bull (1997) 1.02
Novel substance P antagonist, CP-96,345, blocks responses of cat spinal dorsal horn neurons to noxious cutaneous stimulation and to substance P. Neurosci Lett (1991) 1.02
A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico. Am J Hum Genet (1993) 1.01
A single base insertion in the putative transmembrane domain of the tyrosinase gene as a cause for tyrosinase-negative oculocutaneous albinism. Proc Natl Acad Sci U S A (1991) 1.01
Transmission of syphilis by fresh blood components. Transfusion (1969) 1.01
Likelihood ratio tests for linkage and linkage disequilibrium: asymptotic distribution and power. Am J Hum Genet (1996) 1.01
Hairbulb tyrosinase activity in oculocutaneous albinism. Nature (1976) 1.01
Heterogeneity in gingival fibromatosis. Birth Defects Orig Artic Ser (1971) 1.01
Sex ratio and cleft lip with or without cleft palate. Lancet (1972) 1.00