Search results for "itä"
showing 10 items of 310 documents
Candidate genetic pathways for attention-deficit/hyperactivity disorder (ADHD) show association to hyperactive/impulsive symptoms in children with AD…
2013
Item does not contain fulltext OBJECTIVE: Because multiple genes with small effect sizes are assumed to play a role in attention-deficit/hyperactivity disorder (ADHD) etiology, considering multiple variants within the same analysis likely increases the total explained phenotypic variance, thereby boosting the power of genetic studies. This study investigated whether pathway-based analysis could bring scientists closer to unraveling the biology of ADHD. METHOD: The pathway was described as a predefined gene selection based on a well-established database or literature data. Common genetic variants in pathways involved in dopamine/norepinephrine and serotonin neurotransmission and genes involv…
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder
2010
Contains fulltext : 87688.pdf (Publisher’s version ) (Closed access) OBJECTIVE: Although twin and family studies have shown attention-deficit/hyperactivity disorder (ADHD) to be highly heritable, genetic variants influencing the trait at a genome-wide significant level have yet to be identified. As prior genome-wide association studies (GWAS) have not yielded significant results, we conducted a meta-analysis of existing studies to boost statistical power. METHOD: We used data from four projects: a) the Children's Hospital of Philadelphia (CHOP); b) phase I of the International Multicenter ADHD Genetics project (IMAGE); c) phase II of IMAGE (IMAGE II); and d) the Pfizer-funded study from the…
DSM-IV Combined Type ADHD Shows Familial Association With Sibling Trait Scores
2008
Contains fulltext : 69060.pdf (Publisher’s version ) (Closed access) Attention deficit hyperactivity disorder (ADHD) is a discrete clinical syndrome characterized by the triad of inattention, hyperactivity, and impulsivity in the context of marked impairments. Molecular genetic studies have been successful in identifying genetic variants associated with ADHD, particularly with DSM-IV inattentive and combined subtypes. Quantitative trait locus (QTL) approaches to linkage and association mapping have yet to be widely used in ADHD research, although twin studies investigating individual differences suggest that genetic liability for ADHD is continuously distributed throughout the population, u…
Construct validity of the anxiety sensitivity index-3 in clinical samples
2012
"Using two clinical samples of patients, the presented studies examined the construct validity of the recently revised Anxiety Sensitivity Index-3 (ASI-3). Confirmatory factor analyses established a clear three-factor structure that corresponds to the postulated subdivision of the construct into correlated somatic, social, and cognitive components. Participants with different primary clinical diagnoses differed from each other on the ASI-3 subscales in theoretically meaningful ways. Specifically, the ASI-3 successfully discriminated patients with anxiety disorders from patients with nonanxiety disorders. Moreover, patients with panic disorder or agoraphobia manifested more somatic concerns …
Tom Malmquist: Ilma joka meitä ympäröi
2020
Kirja-arvostelu teoksesta Tom Mamquist: Ilma joka meitä ympäröi (All den luft som omger oss). Suom. Outi Menna. S&S 2020. 347 sivua nonPeerReviewed
Intellectual engagements of accounting academics: The ‘forecasted losses' intervention
2022
This paper explores the social and political potential of accounting scholarship, presenting and discussing an intellectual intervention challenging a legislative reform that significantly affected Spanish industrial relations. In this reform, an accounting artifact (forecasted losses) played an unexpected role and was misrepresented, prompting a sizeable number of scholars to sign two manifestos in 2010 and 2012 against the use of forecasted losses made by the new legislation. As promoters of this manifesto, we perform in this paper a collaborative autoethnography to reflect on the context, events, reactions, and significance of this intervention for both the academic and the industrial re…
Die Förderung der Mehrsprachigkeit und der Transkulturalität in der gymnasialen Oberstufe über ein internationales und fremdsprachiges Projekt : Fal…
2010
Tässä laadullisessa tapaustutkimuksessa tutkittiin 2008 kevään aikana suomalaisen Jyväskylän Normaalikoulun lukion ja saksalaisen Görres-Gymnasiumin (Koblenz) toteuttamaa kansainvälistä yhteistyöprojektia. Tavoitteena oli selvittää, kuinka osallistujien transkulturaalinen identiteetti kehittyy sekä toteutuuko monikielisyys tässä kansainvälisessä projektissa. Lisäksi haluttiin selvittää opettajien ja oppilaiden motivaatioita projektiin osallistumiseen sekä kieltenkäyttöä eri tilanteissa. Tutkimus toteutettiin vuonna 2007 projektiin osallistuneiden suomalaisten oppilaiden sekä vuonna 2008 mukana olevien suomalaisten ja saksalaisten opettajien ryhmähaastattelujen ja oppilaiden kyselylomakkeide…
Guido Erwin Kolbenheyer und seine Rezeption des 16. Jahrhunderts am Beispiel der Trilogie des Paracelsus (1917-26).
2016
Der Beitrag fokussiert sich auf die Mystifizierung der paracelsisichen Gedanken, der Figur von Paracelsus selbst sowie des religiösen Diskurses und von manchen Debatten des 16. Jahrhunderst durch Guido Erwin Kolbenheyer. Im Mittelpunkt der Untersuchung steht die Herausbildung des "Andersartigen", der im Kontext einer nationalistischen und fremdenfeindlichen Gesinnug zum Inbegriff einer überlegenen pangermanischen Identität aufgefasst wird.
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
2013
AM Vicente - Cross-Disorder Group of the Psychiatric Genomics Consortium Most psychiatric disorders are moderately to highly heritable. The degree to which genetic variation is unique to individual disorders or shared across disorders is unclear. To examine shared genetic etiology, we use genome-wide genotype data from the Psychiatric Genomics Consortium (PGC) for cases and controls in schizophrenia, bipolar disorder, major depressive disorder, autism spectrum disorders (ASD) and attention-deficit/hyperactivity disorder (ADHD). We apply univariate and bivariate methods for the estimation of genetic variation within and covariation between disorders. SNPs explained 17-29% of the variance in …
Integration, Bewertung und Nutzung heterogener Datenquellen mittels semantischer Werkzeuge
2017
In diesem Artikel stellen wir unsere Forschung in der Integration von Geodaten in einen Semantic Web Kontext in unserem Projekt Semantic GIS vor. Zunächst möchten wir den Zweck und die Vorteile einer Integration und Interpretation von Daten in das Semantic Web beleuchten und anschließend unseren Integrationprozess bestehend aus Datengewin-nung, automatischer Interpretation, Qualitätssicherung und Provenance sowie den Datenzugriff erklären. Um die Anwendung unserer Forschung zu demonstrieren gehen wir auf zwei Anwendungsfälle in unserem Projekt ein: Die Bewertung von OpenStreetMap Daten und die Verbesserung des Katastrophenschutzes mittels semantischem Reasoning. Wir schließen den Artikel mi…