Search results for "heritability"

showing 10 items of 141 documents

Genetics of Perceived Family Interaction From 12 to 17 Years of Age

2019

We analyzed how the effects of genetic and environmental factors on the perceptions of family interaction change from early to late adolescence. The data were collected by postal surveys on Finnish twins (N = 4808) at 12, 14 and 17 years of age and analyzed using genetic twin modeling. Additive genetic factors explained a modest share of the variation in perceived relational support (a2 = 0.30 in boys and 0.18 in girls) and relational tensions (a2 = 0.13 and 0.14, respectively) at 12 years of age, with the proportions becoming larger through 17 years of age (a2 = 0.53 in boys and 0.49 in girls for relational support; a2 = 0.35 in boys and 0.33 in girls for relational tensions). Simultaneous…

MaleParents0301 basic medicineCHILDHOODTwinsADULTHOODsosiaalinen vuorovaikutusAdolescentsDevelopmental psychology0302 clinical medicinenuoretSurveys and QuestionnairesTwins DizygoticadolescentsChildFinlandGenetics (clinical)media_commonOriginal ResearchHERITABILITYAge Factors1184 Genetics developmental biology physiologyLate adolescence3142 Public health care science environmental and occupational healthETIOLOGYHealth psychologyVariation (linguistics)perhesuhteetADOLESCENCE5141 SociologyFemaleFamily Relationsgeneettiset tekijätPsychologymedicine.medical_specialtyAdolescentmedia_common.quotation_subjectEnvironmentBEHAVIORSFamily interactionENVIRONMENTAL-INFLUENCES03 medical and health sciencesSex FactorsPerceptionmedicineGeneticsHumansFamilyEcology Evolution Behavior and SystematicskaksostutkimusperinnöllisyystiedePublic healthCorrectionTwins MonozygoticHeritabilityfamily interactionkaksosetBODY-MASS INDEX030104 developmental biologyEtiologyGene-Environment InteractionPerceptionBody mass index030217 neurology & neurosurgeryBehavior Genetics
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Longitudinal heritability of childhood aggression

2016

The genetic and environmental contributions to the variation and longitudinal stability in childhood aggressive behavior were assessed in two large twin cohorts, the Netherlands Twin Register (NTR), and the Twins Early Development Study (TEDS; United Kingdom). In NTR, maternal ratings on aggression from the Child Behavior Checklist (CBCL) were available for 10,765 twin pairs at age 7, for 8,557 twin pairs at age 9/10, and for 7,176 twin pairs at age 12. In TEDS, parental ratings of conduct disorder from the Strength and Difficulty Questionnaire (SDQ) were available for 6,897 twin pairs at age 7, for 3,028 twin pairs at age 9 and for 5,716 twin pairs at age 12. In both studies, stability and…

MaleParentsNetherlands Twin Register (NTR)0301 basic medicinePersonality InventoryPoison controlCBCLheritability0302 clinical medicineLongitudinal StudiesChildChild Behavior Checklistta515Genetics (clinical)NetherlandsaggressionAge Factorsta3142Justice and Strong InstitutionsPsychiatry and Mental healthConduct disorderFemalePersonality Assessment Inventorymedicine.symptomPsychologyTwins Early Development StudySDG 16 - PeaceAdolescentlongitudinalEnvironment03 medical and health sciencesCellular and Molecular NeuroscienceSex FactorsDiseases in Twins/dk/atira/pure/keywords/cohort_studies/netherlands_twin_register_ntr_medicineHumansGenetic Association StudiesAggressionta1184SDG 16 - Peace Justice and Strong InstitutionsstabilityHeritabilitymedicine.diseasegenetic architecture/dk/atira/pure/sustainabledevelopmentgoals/peace_justice_and_strong_institutionsUnited Kingdomta3124030104 developmental biologyGene-Environment Interaction030217 neurology & neurosurgeryDemographyAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics
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Genetic and Environmental Influences on BMI From Late Childhood to Adolescence are Modified by Parental Education

2011

To investigate how parental education modifies genetic and environmental influences on variation in BMI during adolescence, self-reported BMI at 11-12, 14, and 17 years of age was collected from a population sample of 2,432 complete Finnish twin pairs born in 1983-1987. Based on parental report, twins were divided to those with high (both parents high school graduates), mixed level (one parent a graduate, the other not), and limited (neither parent a graduate) parental education. Genetic and environmental influences on variation in BMI in different education classes were modeled using twin analysis. Heritability of BMI among 11-12-year-olds with high parental education was 85-87% whereas it…

MaleParentsPediatricsmedicine.medical_specialtyAdolescentEndocrinology Diabetes and MetabolismTwinsMedicine (miscellaneous)Social EnvironmentAffect (psychology)Body Mass Index03 medical and health sciences0302 clinical medicineEndocrinologyParental educationGenetic variationmedicineHumansObesityProspective Studies030212 general & internal medicineChildSocioeconomic statusFinlandta515030304 developmental biology0303 health sciencesNutrition and DieteticsParentingGenetic VariationSocial environmentHeritabilityTwin studyEducational StatusFemaleSelf ReportPsychologyBody mass indexDemographyObesity
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Evaluation of the psychometric properties of “the Norwegian screening test for dyslexia”

2018

The aim of this study was to develop and investigate the psychometric properties of a screening protocol for Norwegian students in upper secondary school. The protocol was designed to assess skills that are at stake in dyslexia. It was administered to 232 students. In the absence of a “gold standard,” comparisons were made between students who reported normal literacy skills (n = 184) and literacy problems (n = 48). Significant group differences were found across all areas. Logistic regression and receiver operating characteristic curve analyses demonstrated good discriminatory power. The screening protocol met the standards for reliability and validity. It has the potential to be a useful …

MalePsychometricsiltalukiotheritabilityLogistic regressionNorjaspellingDevelopmental and Educational Psychologykeskiasteen koulutusReliability (statistics)ta515SchoolsNorway05 social sciences050301 educationGeneral MedicineperiytyvyyslanguageFemaleyläkouluPsychologyupper secondary050104 developmental & child psychologyClinical psychologyAdolescentPsychometricseducationExperimental and Cognitive PsychologyNorwegianbehavioral disciplines and activitiesEducationYoung AdultepäjärjestysdyslexiamedicineHumansdysleksia0501 psychology and cognitive sciencesStudentsUpper secondary general schools (evening classes)reading (activity)screening testProtocol (science)Receiver operating characteristicGold standardDyslexiaReproducibility of Resultslukeminen (toiminta)medicine.diseaselanguage.human_languageBehavior Rating Scalelukihäiriöt0503 educationDyslexia
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Genetic variation in neuromuscular performance.

1973

Using a simple cumulative model of heredity plus environment, based on intrapair differences observed in monozygous (MZ) and dizygous (DZ) twins, the relative contribution of heredity to the interindividual variance in several neuromuscular parameters was determined with 15 pairs of male (8 MZ and 7 DZ) and 14 pairs of female (7 MZ and 7 DZ) twins ranging in age from 10 to 14 years. The data disclosed that in boys the variability in maximal mechanical (anaerobic) power was 99.2% genetically determined under the environmental conditions of the study. The corresponding heritability estimate values for the patellar reflex time and reaction time were 97.5% and 85.7%, respectively. In girls the …

MaleReflex StretchAdolescentPhysiologyPhysical ExertionNeuromuscular JunctionTwinsPhysiologyBiologymedicine.disease_causePregnancyPhysiology (medical)Genetic variationHereditymedicineReaction TimeHumansOrthopedics and Sports MedicineGenetic variabilityChildGeneticsmedicine.diagnostic_testBody WeightPublic Health Environmental and Occupational HealthPatellar reflexGeneral MedicineHuman physiologyPatellaHeritabilityBody HeightGenetic TechniquesGenetic CodeFemaleInternationale Zeitschrift fur angewandte Physiologie, einschliesslich Arbeitsphysiologie
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Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM conso…

2015

To identify genetic variants associated with refractive astigmatism in the general population, meta-analyses of genome-wide association studies were performed for: White Europeans aged at least 25 years (20 cohorts, N = 31,968); Asian subjects aged at least 25 years (7 cohorts, N = 9,295); White Europeans aged <25 years (4 cohorts, N = 5,640); and all independent individuals from the above three samples combined with a sample of Chinese subjects aged <25 years (N = 45,931). Participants were classified as cases with refractive astigmatism if the average cylinder power in their two eyes was at least 1.00 diopter and as controls otherwise. Genome-wide association analysis was carried out for …

MaleRefractive errorBLUE MOUNTAINS EYECORNEAL ASTIGMATISMSpherical equivalentGenome-wide association studyastigmatism; gene; SNPDISEASECohort Studies0302 clinical medicineStatisticsGenetics(clinical)Neural Cell Adhesion MoleculesPOPULATIONGenetics (clinical)Original InvestigationGenetics0303 health scienceseducation.field_of_studyAge FactorsHigh Mobility Group ProteinsMiddle Aged3142 Public health care science environmental and occupational health3. Good healthFemaleOPEN-ANGLE GLAUCOMAAdultGenetic MarkersEXPERIMENTALLY-INDUCED MYOPIAKeratoconusSUSCEPTIBILITY LOCICell Adhesion Molecules NeuronaleducationPopulationNerve Tissue ProteinsAstigmatismBiologyWhite People03 medical and health sciencesAGEAsian PeopleMAJOR LOCUSmedicineGeneticsHumans3125 Otorhinolaryngology ophthalmologyeducation030304 developmental biologyGenetic associationCalcium-Binding ProteinsAstigmatismHeritabilitymedicine.diseaseNONCODING RNAS030221 ophthalmology & optometryGenome-Wide Association Study
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Genetic variants associated with human eye size are distinct from those conferring susceptibility to myopia

2021

Purpose: Emmetropization requires coordinated scaling of the major ocular components, corneal curvature and axial length. This coordination is achieved in part through a shared set of genetic variants that regulate eye size. Poorly coordinated scaling of corneal curvature and axial length results in refractive error. We tested the hypothesis that genetic variants regulating eye size in emmetropic eyes are distinct from those conferring susceptibility to refractive error.Methods: A genome-wide association study (GWAS) for corneal curvature in 22,180 adult emmetropic individuals was performed as a proxy for a GWAS for eye size. A polygenic score created using lead GWAS variants was tested for…

MaleRefractive errorLinkage disequilibriumgenetic structuresLOCIEmmetropiaGenome-wide association studyPRSS56AXIAL LENGTHLinkage Disequilibrium0302 clinical medicineCORNEAL CURVATURECorneaMyopiarefractive errorChild0303 health sciencesHERITABILITYMiddle Agedgenetic correlationAxial Length Eyemedicine.anatomical_structureeye sizeGROWTHFemaleAdultmedicine.medical_specialtyUK BiobankAdolescentBiologyRefraction OcularGenetic correlationPolymorphism Single NucleotideOCULAR COMPONENT DIMENSIONS03 medical and health sciencesYoung AdultOphthalmologymedicineGeneticsHumansGenetic Predisposition to Disease3125 Otorhinolaryngology ophthalmologyGENOME-WIDE ASSOCIATIONMETAANALYSIS030304 developmental biologyAgedmedicine.diseaseeye diseasesGenetic marker030221 ophthalmology & optometryHuman eyesense organsGenome-Wide Association StudyInvestigative Ophthalmology & Visual Science
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GeneticParameters for Milk Somatic Cell Score and Relationships with Production Traits in Primparous Dairy Sheep

2007

A total of 13,066 first-lactation test-day records of 2,277 Valle del Belice ewes from 17 flocks were used to estimate genetic parameters for somatic cell scores (SCS) and milk production traits, using a repeatability test-day animal model. Heritability estimates were low and ranged from 0.09 to 0.14 for milk, fat, and protein yields, and contents. For SCS, the heritability of 0.14 was relatively high. The repeatabilities were moderate and ranged from 0.29 to 0.47 for milk production traits. The repeatability for SCS was 0.36. Flock-test-day explained a large proportion of the variation for milk production traits, but it did not have a big effect on SCS. The genetic correlations of fat and …

MaleVeterinary medicineSomatic cellyieldsselectionBiologyAnimal Breeding and Genomicsheritabilitydairy sheepgenetic parameterAnimal scienceAnimal modelPregnancyfatGenetic variationGeneticsAnimalsLactationFokkerij en Genomicamilk productionlactation curvesSheepModels Geneticintegumentary systemsomatic cell countGenetic VariationewesHeritabilityMilk productionDairyingParityMilkPhenotypenervous systemcountprotein percentagemastitis resistanceTraitWIASAnimal Science and ZoologyFemaleFlockanimal-modelSomatic cell counttissuesFood Science
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Genetic and environmental influences on the fibrinolytic system: a twin study.

2004

SummaryThe determination of heritability is a key issue to assess the predictive power of polymorphisms for disease in clinical studies. The aim of this study was to determine the heritability of proteins and activation markers of the fibrinolytic system in a large cohort of healthy twins. Heritability was calculated as 0.76 for thrombin activatable fibrinolysis inhibitor (TAFI), 0.44 for plasminogen activator inhibitor-1 (PAI-1), and 0.43 for tissue plasminogen activator. No significant genetic influence was observed for α2-antiplasmin-plasmin-complex and D-dimer. Heritability explained by single gene polymorphisms was 25.2% for TAFI 505G&gt;A, 31.5% for 1542C&gt;G, and 50.0% for combinati…

Malemedicine.medical_specialtyCarboxypeptidase B2GenotypeArteriosclerosismedicine.medical_treatmentBiologyEnvironmentTissue plasminogen activatorCohort StudiesFibrin Fibrinogen Degradation ProductsInternal medicineFibrinolysisPlasminogen Activator Inhibitor 1medicineDiseases in TwinsHumansFibrinolysinGeneGeneticsalpha-2-AntiplasminPolymorphism GeneticActivator (genetics)FibrinolysisHematologyTwins MonozygoticHeritabilityTwin studyEndocrinologyPhenotypeHaplotypesHemostasisTwin Studies as TopicFemalePlasminogen activatormedicine.drugThrombosis and haemostasis
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The heritability of depressive symptoms: multiple informants and multiple measures

2002

Background: Earlier research suggests large rater differences in heritability estimates of children's depressive symptoms in the context of significant age and sex-limitation effects. Methods: With data from an ongoing, population-based twin-family study, we estimated genetic and environmental influences on children's depression with models allowing for sex-specific effects. Our assessments of twins included self-reports and ratings made by their classmate peers, their parents and their teachers, allowing estimates of genetic and environmental effects with data from different informants. Model-fitting used maximum likelihood estimation of log-transformed data from a sample of 1,366 11- and …

Malesex differencesMultivariate analysisCHILDHOODCHILDRENDevelopmental psychology0302 clinical medicineTwins DizygoticDevelopmental and Educational PsychologyANXIETYAdditive genetic effectsLongitudinal StudiesChildFinlandLikelihood Functionseducation.field_of_study05 social sciencesPSYCHOPATHOLOGYtwinsPsychiatry and Mental healthmultivariate analysisADOLESCENCEdepressionAnxietyFemalemedicine.symptomPsychologyBEHAVIOR050104 developmental & child psychologyPsychopathologyDISORDERSeducationPopulationTWINContext (language use)03 medical and health sciencesSex FactorsAGEGENETIC-ANALYSISDiseases in TwinsmedicineHumansGenetic Predisposition to Disease0501 psychology and cognitive scienceseducationModels GeneticSocial environmentTwins MonozygoticHeritabilityPediatrics Perinatology and Child Health030217 neurology & neurosurgeryJournal of Child Psychology and Psychiatry
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