Search results for " determinism"

showing 10 items of 54 documents

Genome-wide association scan of attention deficit hyperactivity disorder

2008

Contains fulltext : 70191.pdf (Publisher’s version ) (Closed access) Results of behavioral genetic and molecular genetic studies have converged to suggest that genes substantially contribute to the development of attention deficit/hyperactivity disorder (ADHD), a common disorder with an onset in childhood. Yet, despite numerous linkage and candidate gene studies, strongly consistent and replicable association has eluded detection. To search for ADHD susceptibility genes, we genotyped approximately 600,000 SNPs in 958 ADHD affected family trios. After cleaning the data, we analyzed 438,784 SNPs in 2,803 individuals comprising 909 complete trios using ADHD diagnosis as phenotype. We present t…

Candidate geneLinkage disequilibriumGenetics and epigenetic pathways of disease [NCMLS 6]Medizin2804 Cellular and Molecular NeuroscienceGenome-wide association studyNeuroinformatics [DCN 3]Linkage Disequilibrium2738 Psychiatry and Mental Health0302 clinical medicinePerception and Action [DCN 1]Genetics(clinical)ChildGenetics (clinical)Genetics0303 health sciencesHomozygote10058 Department of Child and Adolescent PsychiatrySNP genotypingPsychiatry and Mental healthChild PreschoolData Interpretation Statistical/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingFunctional Neurogenomics [DCN 2]Algorithms2716 Genetics (clinical)AdolescentSingle-nucleotide polymorphism610 Medicine & healthBiologyMental health [NCEBP 9]Polymorphism Single NucleotideGenetic determinismArticleGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular NeuroscienceCognitive neurosciences [UMCN 3.2]SDG 3 - Good Health and Well-beingmedicineSNPAttention deficit hyperactivity disorderHumansddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersAlleles030304 developmental biologyGenome Humanmedicine.diseaseGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with HyperactivityCase-Control Studies030217 neurology & neurosurgeryGenome-Wide Association Study
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The catechol o-methyltransferase (COMT) val158met polymorphism modulates the association of serious life events (SLE) and impulsive aggression in fem…

2009

Wagner S, Baskaya O, Anicker NJ, Dahmen N, Lieb K, Tadic A. The catechol o‐methyltransferase (COMT) val158met polymorphism modulates the association of serious life events (SLE) and impulsive aggression in female patients with borderline personality disorder (BPD). Objective: We analyzed i) the effects of serious life events (SLE) on impulsive aggression, and ii) modulating effects of the COMT Val158Met polymorphism on the association between SLEs and impulsive aggression in borderline personality disorder (BPD). Method: One hundred and twelve female BPD patients from Germany were included in this study. Impulsive aggression was assessed by the Buss‐Durkee‐Hostility Inventory (BDHI). Result…

Child abusemedicine.medical_specialtyCatechol-O-methyl transferaseAggressionPoison controlImpulsivitymedicine.diseasebehavioral disciplines and activitiesGenetic determinismPsychiatry and Mental healthSexual abusemental disordersmedicinemedicine.symptomPsychiatryPsychologyBorderline personality disorderActa Psychiatrica Scandinavica
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Beyond the Cultural Turn: A Critical Perspective on Culture-Discourse within Public Relations

2017

International audience; In 1992, Sriramesh and White (1992) pointed to the importance of culture for public relations. Two decades later, public relations scholars had answered their call in force (e.g., Bardhan & Weaver, 2011; Carayol & Frame, 2012; Edwards & Hodges, 2011; Sriramesh & Vercic, 2012). Sriramesh and other PR scholars have criticized much previous public relations research for its focus on the work of Hofstede and cultural characteristics that are apparently common across countries (Sriramesh, 2009), rather than approaches which present culture as a social phenomenon on the level of the social group (Frame, 2012), or as a communication resource or tool-kit (Swidler, 1986). Sri…

Cultural appropriationValue (ethics)stereotypesbusiness.industry[SHS.INFO]Humanities and Social Sciences/Library and information sciencesmedia_common.quotation_subjectculture discoursePublic relationsCultural turnSocial constructionism[SHS.INFO] Humanities and Social Sciences/Library and information sciencesculturePublic RelationsCritical intercultural theoryOriginalityCultural determinismcultural turnHofstede's cultural dimensions theorySociologyIdeologybusinesssocial discourseCultural determinismCultural appropriationmedia_common
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¿Es posible ser moralmente responsable? Notas para una nueva definición del concepto de sujeto

2006

The Strawson´s Basic Argument is the stronger against moral responsibility in Philosophy of action. One should be responsible of his identity to be moral responsible of his actions, but then nobody could be never responsible. In this article I criticize orthodox solutions to Strawson´s sceptical challenge and show how they share with the Argument the same theological notion of monadical agent. A new solution needs a new conception of agent..

DeterminismFilosofía de la acción; Responsabilidad moral; Agente; Compatibilismo; Incompatibilismo; Determinismo; Libre albedrío; Identidad socialIdentidad sociallcsh:AMoral ResponsibilityIncompatibilismResponsabilidad moralGeneral WorksAgentCompatibilismoFilosofía de la acciónSocial IdentityUNESCO::FILOSOFÍA:FILOSOFÍA [UNESCO]AgenteACompatibilismFree WillIncompatibilismoDeterminismoLibre albedríolcsh:General WorksPhilosophy of ActionArbor: Ciencia, Pensamiento y Cultura
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Unambiguous recognizable two-dimensional languages

2006

We consider the family UREC of unambiguous recognizable two-dimensional languages. We prove that there are recognizable languages that are inherently ambiguous, that is UREC family is a proper subclass of REC family. The result is obtained by showing a necessary condition for unambiguous recognizable languages. Further UREC family coincides with the class of picture languages defined by unambiguous 2OTA and it strictly contains its deterministic counterpart. Some closure and non-closure properties of UREC are presented. Finally we show that it is undecidable whether a given tiling system is unambiguous.

DeterminismSettore INF/01 - InformaticaDeterministic context-free languageGeneral MathematicsTwo-dimensional languagesAutomata and formal languages; Determinism; Two-dimensional languages; UnambiguityComputer Science::Computation and Language (Computational Linguistics and Natural Language and Speech Processing)Class (philosophy)Computer Science ApplicationsUndecidable problemAutomata and Formal Languages. ; Unambiguity ; Determinism. .; Two-dimensional languagesCombinatoricsClosure (mathematics)Computer Science::Programming LanguagesAutomata and formal languagesDeterminism.ArithmeticComputer Science::Formal Languages and Automata TheorySoftwareUnambiguityMathematics
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Over the Cuckoo’s Nest : Towards a Nordic Model of the Responsible University?

2019

AbstractThis concluding chapter takes stock of the major elements, both empirical and conceptual, that underpin the case chapters presented in the book. The chapter is organised in three distinct sections. First, addressing a largely scientific audience, the chapter attempts to make conceptual sense of the findings from an organisational theory perspective. Second, it shifts focus to the wider community of practitioners (policy makers, advisers, university managers and administrators, etc.) by shedding light on the practical implications of the volume’s core findings for both policy and practice. Third, the chapter once again addresses an academic audience by sketching out the road ahead re…

Future studiesbiologybusiness.industryStrategic ChoiceResponsibility accountability window-dressing resilience policyPublic relationsbiology.organism_classificationEnvironmental determinismVDP::Samfunnsvitenskap: 200SociologyNordic modelbusinessCuckooPractical implications
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Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families.

1999

Previously reported linkage of bipolar affective disorder to DNA markers on chromosome 18 was reexamined in a large sample of German bipolar families. Twenty-three short tandem repeat markers were investigated in 57 families containing 103 individuals with bipolar I disorder (BPI), 26 with bipolar II disorder (BPII), nine with schizoaffective disorder of the bipolar type (SA/BP), and 38 individuals with recurrent unipolar depression (UPR). Evidence for linkage was tested with parametric and non-parametric methods under two definitions of the affected phenotype. Analysis of all 57 families revealed no robust evidence for linkage. Following previous reports we performed separate analyses afte…

Genetic MarkersMaleBipolar I disorderBipolar DisorderGenetic LinkageSchizoaffective disorderGenes RecessiveGenetic determinismNuclear FamilyCellular and Molecular NeuroscienceBipolar II disorderGenomic ImprintingChromosome 18GermanymedicineHumansFamilyBipolar disorderMolecular BiologyGenes DominantLinkage (software)GeneticsRecombination GeneticSex CharacteristicsModels GeneticChromosome Mappingmedicine.diseasePsychiatry and Mental healthChromosomal regionFemaleLod ScorePsychologyChromosomes Human Pair 18Molecular psychiatry
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Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

2008

Contains fulltext : 69243.pdf (Publisher’s version ) (Closed access) Genetic contribution to the development of attention deficit hyperactivity disorder (ADHD) is well established. Seven independent genome-wide linkage scans have been performed to map loci that increase the risk for ADHD. Although significant linkage signals were identified in some of the studies, there has been limited replications between the various independent datasets. The current study gathered the results from all seven of the ADHD linkage scans and performed a Genome Scan Meta Analysis (GSMA) to identify the genomic region with most consistent linkage evidence across the studies. Genome-wide significant linkage (P(S…

Genetics and epigenetic pathways of disease [NCMLS 6]Genetic LinkageEuropean Continental Ancestry GroupMedizinGenome ScanBiologyNeuroinformatics [DCN 3]Mental health [NCEBP 9]Genetic determinismWhite PeopleArticleChromosomesGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicineGene mappingCognitive neurosciences [UMCN 3.2]Genetic linkageGenetic predispositionmedicinePerception and Action [DCN 1]Attention deficit hyperactivity disorderHumansddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersGenetics (clinical)030304 developmental biologyProbabilityLinkage (software)Genetics0303 health sciencesGenomeGenome HumanPair 16Chromosome Mappingmedicine.diseasePsychiatry and Mental healthGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with HyperactivityMeta-analysisLod ScoreFunctional Neurogenomics [DCN 2]030217 neurology & neurosurgeryChromosomes Human Pair 16HumanAmerican Journal of Medical Genetics. Part B: Neuropsychiatric Genetics
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Sexual selection for genetic quality: disentangling the roles of male and female behaviour

2009

According to the good genes model of sexual selection, females choose males of good heritable genetic quality to obtain offspring with high fitness. However, better mating success of high-quality males can also be brought about by direct interference competition between males, or simply through elevated activity of high-quality males. We examined the roles of different processes leading to sexual selection for genetic quality in Drosophila montana. We manipulated genetic quality of male flies by inducing mutations with ionizing radiation. We then recorded the effects of inherited heterozygous mutations on several aspects of mating behaviour of males and females in two experiments. We found …

GeneticsMutationOffspringmedia_common.quotation_subjectfungiBiologymedicine.disease_causeGenetic determinismCourtshipMate choiceSexual selectionmedicineAnimal Science and ZoologyMatingEcology Evolution Behavior and SystematicsSelection (genetic algorithm)media_commonAnimal Behaviour
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Genome search in celiac disease.

1998

SummaryCeliac disease (CD), a malabsorption disorder of the small intestine, results from ingestion of gluten. The HLA risk factors involved in CD are well known but do not explain the entire genetic susceptibility. To determine the localization of other genetic risk factors, a systematic screening of the genome has been undertaken. The typing information of 281 markers on 110 affected sib pairs and their parents was used to test linkage. Systematic linkage analysis was first performed on 39 pairs in which both sibs had a symptomatic form of CD. Replication of the regions of interest was then carried out on 71 pairs in which one sib had a symptomatic form and the other a silent form of CD. …

GenotypeGenetic LinkageHuman leukocyte antigenBiologyCoeliac diseaseGenetic determinismGenome screeningGene mappingGenetic linkageGeneticsGenetic predispositionmedicineHumansGenetics(clinical)Genetic TestingRisk factorGenetics (clinical)Genetic testingGeneticsmedicine.diagnostic_testLinkageGenome Humanmedicine.diseaseHLACeliac DiseaseResearch Article
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