听力与言语-语言病理学

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医学伦理学

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  • Phenotypic effects of apolipoprotein structural variation on lipid profiles: II. Apolipoprotein A-IV and quantitative lipid measures in the healthy women study.

    abstract::Apolipoprotein A-IV (APO A-IV) is a major protein component of mesenteric lymph chylomicrons and very-low-density lipoproteins. It is found in plasma predominantly unassociated with major lipoprotein fractions and in high density lipoproteins. APO A-IV exhibits structural heterogeneity owing to two codominant alleles,...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370060404

    authors: Eichner JE,Kuller LH,Ferrell RE,Kamboh MI

    更新日期:1989-01-01 00:00:00

  • Segregation analysis of juvenile myoclonic epilepsy.

    abstract::We examined the inheritance of juvenile myoclonic epilepsy (JME). We looked at both the trait of "epilepsy" and the trait of "epilepsy-plus-EEG abnormalities," since EEG abnormalities are frequently found in the clinically unaffected sibs of JME patients. We tested several modes of inheritance including the fully pene...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370050204

    authors: Greenberg DA,Delgado-Escueta AV,Maldonado HM,Widelitz H

    更新日期:1988-01-01 00:00:00

  • Lifestyle and blood pressure levels in male twins in Utah.

    abstract::Healthy male monozygotic (MZ) and dizygotic (DZ) twin pairs (MZ pairs = 77; DZ pairs = 88) were studied to assess the effect of dietary intake, physical activity, physical fitness, body mass index (BMI), sum of the triceps and subscapular skinfold measurements, alcohol and caffeine consumption, and smoking patterns on...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370050409

    authors: Slattery ML,Bishop DT,French TK,Hunt SC,Meikle AW,Williams RR

    更新日期:1988-01-01 00:00:00

  • Major locus inheritance of apolipoprotein B in Utah pedigrees.

    abstract::A major locus that determines levels of apolipoprotein B (apoB) was revealed by likelihood analysis on 331 members of 36 pedigrees. The major locus explained 43.2% of the observed variance, with the remainder attributed to random environmental factors. Estimated mean apoB levels (mg/dl) were 110.5 +/- 2.5, 141.9 +/- 4...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370040202

    authors: Hasstedt SJ,Wu L,Williams RR

    更新日期:1987-01-01 00:00:00

  • Genetic epidemiology of cleft lip with or without cleft palate in the population of Hawaii.

    abstract::Orientals consisting of Japanese, Chinese, Koreans, and Filipinos are clearly at higher risk for cleft lip with or without cleft palate [CL(P)] than whites, Puerto Ricans, and Hawaiians/part-Hawaiians in Hawaii. Using the model of diallele cross, CL(P) incidences in incrosses and outcrosses involving 564,002 live birt...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370040603

    authors: Chung CS,Mi MP,Beechert AM

    更新日期:1987-01-01 00:00:00

  • Robust inference for variance components models in families ascertained through probands: I. Conditioning on proband's phenotype.

    abstract::A robust approach for estimating standard errors of variance components by using quantitative phenotypes from families ascertained through a proband with an extreme phenotypic value is presented. Estimators that use the multivariate normal distribution as a "working likelihood" are obtained by computing conditional ln...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370040305

    authors: Beaty TH,Liang KY

    更新日期:1987-01-01 00:00:00

  • The recurrence risks for isolated cases with incompletely penetrant X-linked conditions.

    abstract::The recurrence risks for an X-linked disease with incomplete penetrance are evaluated for a sib given that an isolated proband (male or female) is affected. The derived formulae are applied to the X-linked form of Alport and fragile X syndromes. ...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370030508

    authors: Rogatko A

    更新日期:1986-01-01 00:00:00

  • Familial resemblance of bone mass in adult women.

    abstract::Bone mass may be so reduced in some individuals as to be characterized as osteoporotic, with resulting fracture, particularly of the proximal femur, vertebrae, or wrist. We identified 34 mother-daughter sets (n = 70) and 29 sibling sets (n = 59) from a community study of bone mass correlates to assess the degree of re...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370030204

    authors: Sowers MR,Burns TL,Wallace RB

    更新日期:1986-01-01 00:00:00

  • Genetic epidemiology of Menkes disease.

    abstract::Copper incorporation studies were performed on individuals from 58 pedigrees, comprising 140 sibships. As previously reported, there is considerable overlap between heterozygotes and normal homozygotes. Segregation analysis supports recessive inheritance of disease, with residual heritability for 64Cu uptake in cultur...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370030403

    authors: Horn N,Morton NE

    更新日期:1986-01-01 00:00:00

  • The inheritance of pyloric stenosis explained by a multifactorial threshold model with sex dimorphism for liability.

    abstract::The inheritance of pyloric stenosis is explained by a multifactorial threshold model with an underlying assumption that the liability for the disease is distributed in males and females showing a sex dimorphism. From the available data on familial occurrences of pyloric stenosis, it is shown, that an extra maternal ef...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370030102

    authors: Chakraborty R

    更新日期:1986-01-01 00:00:00

  • Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group-specific loci: use of restriction fragment length polymorphisms extends exclusion region.

    abstract::In an earlier paper, positive but nonsignificant lod scores were found in pair-wise linkage tests between multiple endocrine neoplasia type 2A (MEN-2A) and both the haptoglobin (HP) locus on chromosome 16 and group-specific component (GC) locus on chromosome 4. Recently discovered restriction fragment length polymorph...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370030306

    authors: Kidd KK,Kidd JR,Castiglione CM,Pakstis AJ,Sparkes RS

    更新日期:1986-01-01 00:00:00

  • Genetic and environmental causes of variation in renal tubular handling of sodium and potassium: a twin study.

    abstract::We have conducted a study of renal sodium and potassium reabsorption in 205 pairs of twins on freely chosen diets; 89 of the subjects were studied on more than one occasion. Renal tubular sodium and potassium handling, as measured by the fractional excretions FENa and FEK, show repeatable differences between individua...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370020103

    authors: Whitfield JB,Martin NG

    更新日期:1985-01-01 00:00:00

  • Demonstration of a common major gene with pleiotropic effects on immunoglobulin E levels and allergy.

    abstract::Atopic disease is generally recognized to be familial, although specific genetic components have yet to be identified. High levels of a unique class of immunoglobulins, immunoglobulin E (IgE), have been shown to be associated with allergies. Several investigators have reported evidence indicating a recessive regulator...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370020402

    authors: Borecki IB,Rao DC,Lalouel JM,McGue M,Gerrard JW

    更新日期:1985-01-01 00:00:00

  • A general autosomal/X-linked model.

    abstract::This paper describes a general genetic model which encompasses both autosomal and X-linked inheritance as submodels. It allows one to test for X-linked inheritance of a trait by comparing the likelihood of X-linked inheritance to the likelihood of the general genetic model. The general model is formulated as two loci,...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370010105

    authors: Hasstedt SJ,Skolnick M

    更新日期:1984-01-01 00:00:00

  • Evaluation of path analysis through computer simulation: effect of incorrectly assuming independent distribution of familial correlations.

    abstract::Path analysis of family data has been widely applied to resolve genetic and environmental patterns of familial resemblance. A prevalent statistical approach in path analysis has been, first, to estimate the familial correlations and, second, by assuming these estimates to be independently distributed, define a likelih...

    journal_title:Genetic epidemiology

    pub_type: 杂志文章

    doi:10.1002/gepi.1370010305

    authors: McGue M,Wette R,Rao DC

    更新日期:1984-01-01 00:00:00

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