Search results for "heritability"

showing 10 items of 141 documents

Effect of somatic cell count level on functional longevity in Valle del Belice dairy sheep assessed using survival analysis.

2009

The objectives of this study were to evaluate the effect of somatic cell count (SCC) on functional longevity and to estimate the heritability of functional longevity using survival analysis in Valle del Belice dairy sheep. A total of 4,880 lactations of 2,190 ewes from 11 flocks were used. In this study, SCC was considered as an indication of subclinical mastitis. In case of clinical cases, identified by the technicians at milking time, test-day weights and milk samples of those ewes were not considered. Somatic cells were analyzed as counts, without any transformation, and were grouped in 3 classes based on the observed SCC maximum (mxSCC). The mxSCC classes, expressed as 103 cells/mL, wer…

Veterinary medicinemedia_common.quotation_subjectLongevityselectionCell CountMastitisAnimal Breeding and GenomicsBiologygenetic-parametersModels BiologicalMilkingSettore AGR/17 - Zootecnica Generale E Miglioramento GeneticocowsAnimal scienceQuantitative Trait Heritabletraitsproductive lifeLactationsomatic cell count longevity survival analysis dairy sheepGeneticsmedicinescoreAnimalsFokkerij en Genomicasubclinical mastitisSurvival analysismedia_commonmilkSheepLongevityHeritabilitymedicine.diseaseSurvival AnalysisMastitisDairyingmedicine.anatomical_structureMilkcattleWIASholsteinAnimal Science and ZoologyFemaleFlockSomatic cell countFood ScienceJournal of dairy science
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Partial replication of a DRD4 association in ADHD individuals using a statistically derived quantitative trait for ADHD in a family-based association…

2007

Contains fulltext : 52515.pdf (Publisher’s version ) (Closed access) BACKGROUND: Previous research found an association between single nucleotide polymorphisms (SNPs) in the promoter region of DRD4 and statistically derived phenotypes generated from attention-deficit/hyperactivity disorder (ADHD) symptoms. We sought to replicate this finding by using the same methodology in an independent sample of ADHD individuals. METHODS: Four SNPs were genotyped in and around DRD4 in 2631 individuals in 642 families. We developed a quantitative phenotype at each SNP by weighting nine inattentive and nine hyperactive-impulsive symptoms. The weights were selected to maximize the heritability at each SNP. …

MaleLinkage disequilibriumGenetics and epigenetic pathways of disease [NCMLS 6]Databases FactualMedizinNeuroinformatics [DCN 3]Severity of Illness Index0302 clinical medicinePerception and Action [DCN 1]Determinants in Health and Disease [EBP 1]ChildPromoter Regions GeneticGenetics0303 health sciencesEuropePhenotypeChild PreschoolFemalemedicine.symptomPsychologyFunctional Neurogenomics [DCN 2]medicine.medical_specialtyAdolescentSingle-nucleotide polymorphismQuantitative trait locusImpulsivityMental health [NCEBP 9]Polymorphism Single NucleotideGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesQuantitative Trait HeritableCognitive neurosciences [UMCN 3.2]Genetic modelmental disordersmedicineAttention deficit hyperactivity disorderSNPHumansGenetic Predisposition to Diseaseddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersPsychiatryBiological Psychiatry030304 developmental biologyFamily HealthReceptors Dopamine D4Heritabilitymedicine.diseaseGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with Hyperactivity030217 neurology & neurosurgeryBiological psychiatry
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Estimation Of The Genetic Parameters Of Eight Soybean Varieties In The Wasegi Village At Prafi District Manokwari Regency

2020

This study aims to estimate genetic parameters including genetic diversity coefficient, phenotypic diversity coefficient, heritability value, and the correlation between the character of plants from eight soybean varieties. The research was conducted from August to December 2017, in the Wasafi Village of Prafi District, Manokwari Regency. The study was designed using Randomized Block Design (RBD) with 8 treatments of soybean varieties. Each treatment was repeated 4 times, to obtain 32 experimental units. The data obtained were analyzed using ANOVA and if it had a significant effect, it was further tested using the Duncan Multiple Range Test (DMRT) at the 95% level, through the Costat progra…

Genetic diversityVeterinary medicineRandomized block designNegative correlationHeritabilityPositive correlationSelection (genetic algorithm)MathematicsJERAMI Indonesian Journal of Crop Science
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Biological clocks and physical functioning in monozygotic female twins

2018

Background Biomarkers of biological aging – DNA methylation age (DNAm age) and leukocyte telomere length (LTL)– correlate strongly with chronological age across the life course. It is, however, unclear how these measures of cellular wear and tear are associated with muscle strength and functional capacity, which are known to decline with older age and are associated with mortality. We investigated if DNAm age and LTL were associated with body composition and physical functioning by examining 48 monozygotic twin sisters. Methods White blood cell DNAm age (predicted years) was calculated from Illumina 450 k BeadChip methylation data using an online calculator. DNAm age acceleration was define…

AgingEpigenetic clockTwin designfyysinen toimintakykybiomarkkeritWalkinglcsh:GeriatricsMethylationphysical functionAGEBiological ClocksPost-menopausalHumansMuscle Strengthpost-menopausalkaksostutkimusOLDERHERITABILITYHORMONE REPLACEMENT THERAPYMORTALITYTwins MonozygoticMiddle AgedBODY-MASS INDEXlcsh:RC952-954.6ikääntyminenTelomerestwin design3121 General medicine internal medicine and other clinical medicineTELOMERE LENGTHBody CompositionPhysical functionSKELETAL-MUSCLEFemaletelomeeritGRIP STRENGTHmethylationepigenetic clockResearch Article
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Genetic architecture of motives for leisure-time physical activity: a twin study

2017

The aim of this study was to estimate the contribution of genetic and environmental influences on motives for engaging in leisure‐time physical activity. The participants were obtained from the FinnTwin16 study. A modified version of the Recreational Exercise Motivation Measure was used to assess the motives for leisure‐time physical activity in 2542 twin individuals (mean age of 34.1 years). Linear structural equation modeling was used to investigate the genetic and environmental influences on motive dimensions. The highest heritability estimates were found for the motive dimensions of “enjoyment” [men 33% (95% CI 23–43%), women 53% (95% CI 45–60%)] and “affiliation” [men 39% (95% CI 0.28–…

AdultMaleLeisure timePhysical activityPhysical Therapy Sports Therapy and RehabilitationEnvironmentliikuntaheritabilityArticleExercise motivation03 medical and health sciencesLeisure ActivitiesQuantitative Trait Heritable0302 clinical medicinemotivationHumansOrthopedics and Sports Medicineta315ExerciseFinlandmotivaatioModels Statisticalta3141Mean agetwins030229 sport sciencesHeritabilityTwin studyGenetic architecturekaksosetperiytyvyysFemaleGene-Environment InteractionPsychology030217 neurology & neurosurgeryDemographyScandinavian Journal of Medicine & Science in Sports
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Characterisation of phenotypic plasticity in seedling stage of native and invasive populations in Ambrosia artemisiifolia L.

2012

Increased phenotypic plasticity has often been invoked as an hypothesis to explain the capacity of alien invasive plant species to colonize new environments, because it may enhance the ability of plants to cope with new biotic and abiotic conditions. Following this hypothesis, alien invasive populations should be represented by more plastic genotypes than populations in the native range. In annual species, the seedling stage is of crucial importance for population dynamics but surprisingly very few studies have investigated differences in phenotypic plasticity on seedling traits. Based on populations from the native range (North America) and the invasive range (France) of Ambrosia artemisii…

[SDV] Life Sciences [q-bio][SDE] Environmental Sciences[SDV]Life Sciences [q-bio][SDE]Environmental Sciencescommon ragweed[SDV.BV]Life Sciences [q-bio]/Vegetal Biologytemperaturenorm of reaction[SDV.BV] Life Sciences [q-bio]/Vegetal Biologyseedling traitheritabilityinvasive
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Insight into genetic susceptibility to male breast cancer by multigene panel testing: results from a multicenter study in Italy

2019

Breast cancer (BC) in men is rare and genetic predisposition is likely to play a relevant role in its etiology. Inherited mutations in BRCA1/2 account for about 13% of all cases and additional genes that may contribute to the missing heritability need to be investigated. In our study, a well-characterized series of 523 male BC (MBC) patients from the Italian multicenter study on MBC, enriched for non-BRCA1/2 MBC cases, was screened by a multigene custom panel of 50 cancer-associated genes. The main clinical-pathologic characteristics of MBC in pathogenic variant carriers and non-carriers were also compared. BRCA1/2 pathogenic variants were detected in twenty patients, thus, a total of 503 n…

OncologyAdultMaleCancer Researchmedicine.medical_specialtyPALB2Adenomatous Polyposis Coli Proteinmale breast cancerGene mutationBreast Neoplasms MaleDNA GlycosylasesBRCA1/2; cancer susceptibility genes; germline mutations; male breast cancer; multigene panel testing03 medical and health sciencesYoung Adult0302 clinical medicinemultigene panel testingMUTYHMissing heritability problemBRCA1/2Internal medicinemedicineGenetic predispositionHumansGenetic Predisposition to Diseasecancer susceptibility genecancer susceptibility genesskin and connective tissue diseasesCHEK2Genetic Association StudiesAgedAged 80 and overbusiness.industryCase-control studySequence Analysis DNAMiddle Agedmedicine.diseaseCheckpoint Kinase 2germline mutationOncologyItaly030220 oncology & carcinogenesisMale breast cancerCase-Control StudiesMutationgermline mutationsbusinessFanconi Anemia Complementation Group N Protein
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Contribution of genetic and environmental factors to variation in body compartments--a twin study in adults.

2004

This study aimed at analyzing the contribution of genetic and environmental factors on phenotypic variation of various traits of body composition. Subjects were 30 same-sexed pairs of twins including 20 monozygous (MZ) and 10 dizygous (DZ) pairs, aged 19-62 years. Zygosity was determined by DNA typing and morphological diagnosis. Body composition parameters (fat mass FM, lean body mass LBM, body cell mass BCM, extracellular mass ECM, total body water TBW, extracellular water ECW, and intracellular water ICW) were estimated by tetrapolar bioelectrical impedance analysis. Potential environmental factors influencing body composition (number of children, sporting activity and smoking behaviour)…

AdultMaleBody waterHealth BehaviorStatistics as TopicBiologySocial EnvironmentBody Mass IndexAnimal scienceQuantitative Trait HeritableGermanyTwins DizygoticHumansLife StyleEcology Evolution Behavior and SystematicsModels StatisticalBody WeightGeneral MedicineTwins MonozygoticStepwise regressionHeritabilityMiddle AgedTwin studyZygosityPhenotypeSocioeconomic FactorsAnthropologyLean body massBody CompositionAnimal Science and ZoologyFemaleBody mass indexBioelectrical impedance analysisDemographyAnthropologischer Anzeiger; Bericht uber die biologisch-anthropologische Literatur
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Polygenic Score for Physical Activity Is Associated with Multiple Common Diseases

2021

Supplemental digital content is available in the text.

MaleEpidemiologyPhysical fitnessType 2 diabetesDiseaseLogistic regressionTYPE 2 DIABETESOrthopedics and Sports Medicine315 Sport and fitness sciencesPREDICTORSChildkohorttitutkimusFinlandAged 80 and oversairastavuusHERITABILITYGenetic PleiotropyriskitekijätMiddle AgedCardiovascular DiseasesChild PreschoolCohortComputingMethodologies_DOCUMENTANDTEXTPROCESSINGFemaleSMOKINGgeneettiset tekijätfyysinen aktiivisuusAdultGenetic Markerskuolleisuusmedicine.medical_specialtyAdolescentGenotypePhysical Therapy Sports Therapy and RehabilitationEXERCISEpitkittäistutkimusLower riskRisk AssessmentYoung AdultMetabolic DiseasesInternal medicineClinical Decision RulesBENEFITSmedicineHumansAgedbusiness.industryRISK SCORESCardiometabolic Risk FactorsInfantOdds ratiomedicine.diseaseGENEBODY-MASS INDEXLogistic ModelsCase-Control StudiesLinear Modelssydän- ja verisuonitauditbusinessBody mass indexGenome-Wide Association Study
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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>A, 31.5% for 1542C>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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