Search results for "perinnöllisyystiede"

showing 10 items of 24 documents

Active hiding of social information from information-parasites

2014

Background: Coevolution between pairs of different kind of entities, such as providers and users of information, involves reciprocal selection pressures between them as a consequence of their ecological interaction. Pied flycatchers ( Ficedula hypoleuca ) have been shown to derive fitness benefits (larger clutches) when nesting in proximity to great tits ( Parus major ), presumably because they this way discover and obtain information about nesting sites. Tits suffer from the resulting association (smaller clutches). An arms race between the tits (information host) and the flycatchers (information parasite) could thus result . Great tits often cover eggs with nesting material before, but no…

0106 biological sciencesnestingfysiologiaevoluutioWaxwingZoologyParasitismBiology010603 evolutionary biology01 natural sciencesNesting BehaviorSongbirds03 medical and health sciencesNestAnimalsanimalPasseriformesFlycatcheroocyteEcology Evolution Behavior and SystematicsCoevolutionFinland030304 developmental biologyOvumParus0303 health sciencesperinnöllisyystiedeEcologyarticleFicedulabiology.organism_classificationsongbirdBiological Evolutionfemalecomic_booksembryonic structuresFemaleGarruluscomic_books.characterResearch ArticleBMC Evolutionary Biology
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A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol

2012

Serum lipid levels have been associated with cardiovascular diseases, metabolic syndrome and type II diabetes (Kannel et al., 1961; Miller & Miller, 1975; Pilia et al., 2006). Variation in lipids levels is highly influenced by heritable factors (Friedlander et al., 1997) and 95 loci have already been associated with levels of high density lipoprotein (HDL) cholesterol, low density lipoprotein (LDL) cholesterol, triglycerides (TG) and total cholesterol (TC) in numerous study samples and replicated in various populations using genome-wide approaches (Aulchenko et al., 2008; Kathiresan et al., 2008; Kooner et al., 2008; Teslovich et al., 2010; Willer et al., 2008). However, the genetic associa…

AdultNetherlands Twin Register (NTR)Candidate genegenetiikkaPopulationkolesteroliMonozygotic twinLocus (genetics)Genome-wide association studyBiologyPolymorphism Single NucleotideArticle03 medical and health sciences0302 clinical medicineGenetic variation/dk/atira/pure/keywords/cohort_studies/netherlands_twin_register_ntr_HumansAlleleGene–environment interactioneducationAllelesGenetics (clinical)Aged030304 developmental biologyAged 80 and overGenetics0303 health scienceseducation.field_of_studyperinnöllisyystiedeCholesterol HDLGTPase-Activating ProteinsObstetrics and Gynecologyta3141Twins MonozygoticMiddle AgedIntrons3. Good healthGenetic LociPediatrics Perinatology and Child HealthFemaleGene-Environment InteractionApolipoprotein A-II030217 neurology & neurosurgeryGenome-Wide Association Study
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Health endowment and later-life outcomes in the labour market : Evidence using genetic risk scores and reduced-form models

2019

This paper examines the relationship between health endowment and later-life outcomes in the labour market. The analysis is based on reduced-form models in which labour market outcomes are regressed on genetic variants related to the increased risk of cardiovascular diseases. We use linked Finnish data that have many strengths. Genetic risk scores constitute exogenous measures for health endowment, and accurate administrative tax records on earnings, employment and social income transfers provide a comprehensive account of an individual’s long-term performance in the labour market. The results show that although the direction of an effect is generally consistent with theoretical reasoning, …

EmploymentgenetiikkaKansanterveystiede ympäristö ja työterveys - Public health care science environmental and occupational healthtyömarkkinatArticlehealth endowmentReduced-form regressionGeneticssocial income transferslcsh:Social sciences (General)ansiotasoreduced-form regressionperinnöllisyystiedelcsh:Public aspects of medicineterveydentilatyöllistyminentyöllisyyslcsh:RA1-1270Health endowmentOikeuslääketiede ja muut lääketieteet - Forensic science and other medical sciencesEarningsSocial income transferslcsh:H1-99geneettiset tekijätterveysearnings
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The effect of weight on labor market outcomes: An application of genetic instrumental variables

2019

This paper contributes to the literature on the labor market consequences of obesity by using a novel instrument: genetic risk score, which reflects the predisposition to higher body mass index (BMI) across many genetic loci. We estimate instrumental variable models of the effect of BMI on labor market outcomes using Finnish data that have many strengths, for example, BMI that is measured rather than self‐reported, and data on earnings and social income transfers that are from administrative tax records and are thus free of the problems associated with nonresponse, reporting error or top coding. The empirical results are sensitive to whether we use a narrower or broader genetic risk score, …

EmploymentsosiaaliturvaobesitytulonsiirrotKansanterveystiede ympäristö ja työterveys - Public health care science environmental and occupational healthJ01J24Body Mass IndexI10502 economics and businessHumansoverweightgeneticssocial income transfers050207 economicsFinlandResearch Articlesansiotulot050208 financeperinnöllisyystiedeSalaries and Fringe BenefitsI12Body Weight05 social sciencestyöllisyysylipainogenetiset tekijätModels EconomicD62J78. Economic growthIncomeJ3lihavuusearningsResearch Article
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Objectively measured physical activity profile and cognition in Finnish elderly twins

2018

Introduction We studied whether objectively measured physical activity (PA) and sedentary behavior (SB) are associated with cognition in Finnish elderly twins. Methods This cross-sectional study comprised twins born in Finland from 1940 to 1944 in the Older Finnish Twin Cohort (mean age, 72.9 years; 726 persons). From 2014 to 2016, cognition was assessed with a validated telephonic interview, whereas PA was measured with a waist-worn accelerometer. Results In between-family models, SB and light physical activity had significant linear associations with cognition after adjusting for age, sex, wearing time, education level, body mass index, and living condition (SB: β-estimate, −0.21 [95% con…

GerontologykognitioTwinsphysical activityliikunta3124 Neurology and psychiatry0302 clinical medicineCognitionsedentary behaviorAccelerometryMedicine030212 general & internal medicine315 Sport and fitness sciences10. No inequalityta3152. Zero hungerexerciseCognitionta3141Sedentary behaviorta3142Psychiatry and Mental healthagedCohortikääntyneetfyysinen aktiivisuusgenetiikkaPhysical activityaktigrafiaistuminen03 medical and health sciencesGeneticsaccelerometryDementiaExerciseAgedperinnöllisyystiedebusiness.industryPhysical activityActigraphyFeatured Articlemedicine.diseaseActigraphyConfidence intervalta3124kaksosetSedentary behaviorDementiaNeurology (clinical)businessBody mass index030217 neurology & neurosurgerydementia
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FinnTwin12 Cohort: An Updated Review

2019

AbstractThis review offers an update on research conducted with FinnTwin12 (FT12), the youngest of the three Finnish Twin Cohorts. FT12 was designed as a two-stage study. In the first stage, we conducted multiwave questionnaire research enrolling all eligible twins born in Finland during 1983–1987 along with their biological parents. In stage 2, we intensively studied a subset of these twins with in-school assessments at age 12 and semistructured poly-diagnostic interviews at age 14. At baseline, parents of intensively studied twins were administered the adult version of the interview. Laboratory studies with repeat interviews, neuropsychological tests, and collection of DNA were made of in…

MaleGerontologyTwinsphysical activity030508 substance abuseruokavaliotLongitudinal twin-family studydiverse phenotypes0302 clinical medicinemielenterveysEarly adulthoodgeneticsChildkohorttitutkimusFinlandGenetics (clinical)alcoholNeuropsychologyObstetrics and GynecologytwinsmetabolomicsepigenetiikkaCohorttwo-stage designFemalealkoholinkäyttö0305 other medical sciencePsychologyfyysinen aktiivisuusmental healthAdultAdolescentSubstance-Related Disorderslongitudinal twin-family studyPhysical activitypitkittäistutkimusArticlesmoking03 medical and health sciencestupakointiHumanskaksostutkimusperinnöllisyystiedeepigeneticsMental healthPediatrics Perinatology and Child HealthfenotyyppiGene-Environment InteractionSubstance usedietterveysriskit030217 neurology & neurosurgeryFollow-Up StudiesTwin Research and Human Genetics
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Understanding developmental language disorder-The Helsinki longitudinal SLI study (HelSLI): A study protocol

2018

Background Developmental language disorder (DLD, also called specific language impairment, SLI) is a common developmental disorder comprising the largest disability group in pre-school-aged children. Approximately 7% of the population is expected to have developmental language difficulties. However, the specific etiological factors leading to DLD are not yet known and even the typical linguistic features appear to vary by language. We present here a project that investigates DLD at multiple levels of analysis and aims to make the reliable prediction and early identification of the difficulties possible. Following the multiple deficit model of developmental disorders, we investigate the DLD …

MaleLongitudinal studyRJ101kielelliset häiriötSpecific language impairmentArtificial grammar learningpreschool child3124 Neurology and psychiatryDevelopmental psychologytemperamenttiStudy Protocol0302 clinical medicinekielellinen kehitysClinical ProtocolsChild temperamentkielen omaksuminenEEGLongitudinal Studies10. No inequalitykielen oppiminenGeneral PsychologyFinlandpathophysiologyeducation.field_of_studychild4. Education05 social sciencesNeuropsychologylongitudinal studyCognitionGeneral MedicineLanguage acquisitionLanguage acquisitionpsychology ChildP1femaleSpecific language impairmentChild Preschoolgeneettiset tekijätPsychologyEvent-related potentialsChild behaviormultilingualism515 Psychology(Nonverbal) short-term memoryPopulationlcsh:BF1-990developmental language disorderlapset (ikäryhmät)050105 experimental psychology03 medical and health sciencesDevelopmental language disorderoppimisvaikeudetmedicineGeneticsHumans0501 psychology and cognitive sciencesLanguage Development Disorders6121 Languageshumaneducationkielellinen erityisvaikeusperinnöllisyystiedeSequential bilingualismmedicine.diseasetyömuistiDevelopmental disorderlcsh:PsychologySequential bilingualismClinical EEGclinical protocol030217 neurology & neurosurgery
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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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Recommendations for standardization and phenotype definitions in genetic studies of osteoarthritis: the TREAT-OA consortium

2011

Objective: To address the need for standardization of osteoarthritis (OA) phenotypes by examining the effect of heterogeneity among symptomatic (SOA) and radiographic osteoarthritis (ROA) phenotypes. Methods: Descriptions of OA phenotypes of the 28 studies involved in the TREAT-OA consortium were collected. We investigated whether different OA definitions result in different association results by creating various hip OA definitions in one large population based cohort (the Rotterdam Study I (RSI)) and testing those for association with gender, age and body mass index using one-way ANOVA. For ROA, we standardized the hip-, knee- and hand ROA definitions and calculated prevalence's of RO…

Malenivelrikkomedicine.medical_specialtygenetiikkaBiomedical EngineeringMEDLINEdiagnostiset kriteeritOsteoarthritisbehavioral disciplines and activitiesArticleCohort Studies03 medical and health sciencesRotterdam Study0302 clinical medicineRheumatologyInternal medicineTREATOAOsteoarthritismedicinePrevalenceGeneticsHumansOrthopedics and Sports Medicine030304 developmental biologyRheumatology and Autoimmunity2. Zero hunger030203 arthritis & rheumatology0303 health sciencesAnalysis of Varianceperinnöllisyystiedebusiness.industryCase-control studyDefinitionReference Standardsmedicine.diseaseGenetics Osteoarthritis Phenotype Definition TREATOA genome-wide association radiographic hip osteoarthritis bone-mineral density knee osteoarthritis hand osteoarthritis osteoporotic fractures general-population joint involvement risk-factors susceptibilityRheumatology3. Good healthPhenotypeCase-Control Studiesdiagnostic criteriaCohortPhysical therapyFemalebusinessBody mass indexCohort study
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Polymorphisms in DCDC2 and S100B associate with developmental dyslexia

2015

Genetic studies of complex traits have become increasingly successful as progress is made in next-generation sequencing. We aimed at discovering single nucleotide variation present in known and new candidate genes for developmental dyslexia: CYP19A1, DCDC2, DIP2A, DYX1C1, GCFC2 (also known as C2orf3), KIAA0319, MRPL19, PCNT, PRMT2, ROBO1 and S100B. We used next-generation sequencing to identify single-nucleotide polymorphisms in the exons of these 11 genes in pools of 100 DNA samples of Finnish individuals with developmental dyslexia. Subsequent individual genotyping of those 100 individuals, and additional cases and controls from the Finnish and German populations, validated 92 out of 111 …

Nonsynonymous substitutionCandidate genemedicine.medical_specialtyShort CommunicationGenomicsS100 Calcium Binding Protein beta SubunitBiologyPolymorphism Single NucleotideDyslexia03 medical and health sciences0302 clinical medicineDCDC2Molecular geneticssingle-nucleotide polymorphismsmedicineHumansGenetic Predisposition to DiseasegeneticsGenotypingGenetic Association StudiesGenetics (clinical)ta515030304 developmental biologyGenetics0303 health sciencesperinnöllisyystiedeta1184DyslexiaSequence Analysis DNAmedicine.diseasedevelopmental dyslexiata3124Genetic epidemiologyCase-Control Studiesindividual genotypingMicrotubule-Associated Proteins030217 neurology & neurosurgeryJournal of Human Genetics
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