0000000001295619

AUTHOR

W. Maier

showing 11 related works from this author

Searches for lepton number violation and resonances in K± → πμμ decays

2017

The NA48/2 experiment at CERN collected a large sample of charged kaon decays to final states with multiple charged particles in 2003–2004. A new upper limit on the rate of the lepton number violating decay K±→π∓μ±μ± is reported: B(K±→π∓μ±μ±)<8.6×10−11 at 90% CL. Searches for two-body resonances X in K±→πμμ decays (such as heavy neutral leptons N4 and inflatons χ ) are also presented. In the absence of signals, upper limits are set on the products of branching fractions B(K±→μ±N4)B(N4→πμ) and B(K±→π±X)B(X→μ+μ−) for ranges of assumed resonance masses and lifetimes. The limits are in the (10−11,10−9) range for resonance lifetimes below 100 ps.

leptonBEAM01 natural sciences7. Clean energyPhysics Particles & FieldsHigh Energy Physics - ExperimentLIMITSkaon physicsCERNIntermediate statelepton number violation neutrinos dark matter kaon physicsPhysicsVMSMLarge Hadron ColliderPhysicsCharge KaonsneutrinosNuclear and High Energy Physics; CERN; leptonsHigh Energy Physics - Experiment; Charge Kaons; Lepton number violationNuclear & Particles PhysicsCharged particlelcsh:QC1-999NEUTRAL HEAVY-LEPTONSPhysics Nuclearlepton number violationPhysical SciencesParticle physicsNuclear and High Energy Physicsleptonskaon decays lepton number violationNuclear and High Energy Physics lepton kaon meson lepton number violation NA48Socio-culturaleAstronomy & AstrophysicsUPPER-BOUNDSdark matterNuclear physics0202 Atomic Molecular Nuclear Particle And Plasma Physics0103 physical sciencesDARK-MATTERPARTICLES010306 general physicsScience & Technologykaon decays010308 nuclear & particles physicsBranching fractionResonanceInflatonLepton numberkaon mesonNA48High Energy Physics::Experimentlcsh:PhysicsLepton
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Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene

1995

We report two novel polymorphisms and a rare deletion variant in the human dopaine D4 receptor gene. The two polymorphisms are characterized by single base pair substitutions, namely a G-->C transversion changing codon 11 from GGG (encoding Gly) to CGG (encoding Arg) and a C-->T transition in position -11 upstream from the start codon. The Arg11 variant occurs at a frequency of about 1% and the C-->T transition at a frequency of about 7% in German control subjects (n = 148). Allele frequencies observed in patients suffering from schizophrenia (n = 256) and bipolar affective disorder (n = 99) were similar. The deletion variant is characterized by a 21 bp deletion affecting codons 36 to 42 co…

AdultObsessive-Compulsive DisorderBipolar DisorderMolecular Sequence DataBiologymedicine.disease_causePolymerase Chain ReactionGene FrequencyStart codonReference ValuesLeukocytesGeneticsmedicineHumansPoint MutationAmino Acid SequenceAge of OnsetCodonTransversionGeneAllele frequencyBiological PsychiatryGenetics (clinical)DNA PrimersRepetitive Sequences Nucleic AcidSequence DeletionGeneticsMutationBase SequenceTransition (genetics)Receptors Dopamine D2Receptors Dopamine D4Genetic VariationDNAExonsMiddle Agedmedicine.diseasePsychiatry and Mental healthTransmembrane domainSchizophreniaSchizophreniaPanic DisorderPolymorphism Restriction Fragment Length
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Einfluss von multimodaler sportlicher Aktivität auf Kognition und Alltagskompetenzen bei früher Alzheimer-Demenz (SPORT&KOG)

2008

Der vorliegende Bericht beschreibt ein vom Bundesministerium für Gesundheit gefördertes Vorhaben zum «Leuchtturmprojekt Demenz» im Themenfeld 1 «Therapie und Pflegemaßnahmen: Wirksamkeit unter Alltagsbedingungen». Hierbei handelt es sich um eine multizentrische randomisierte Interventionsstudie, die den Einfluss von Sport (multimodale sportliche Aktivität) unter kontrollierten Bedingungen auf die kognitive Entwicklung von Alzheimer-Patienten im frühen Stadium prüft. In einem zweiarmigen Design werden je 150 Patienten mit früher AD unter Verum- bzw. Kontroll-Bedingungen untersucht. Die Verum-Gruppe erhält ein spezifisches sportliches Trainingsprogramm. In der Kontrollgruppe werden lediglich…

Gynecologymedicine.medical_specialtybusiness.industryPhysical activity3. Good health03 medical and health sciencesPsychiatry and Mental healthClinical Psychology0302 clinical medicineMedicine030212 general & internal medicineGeriatrics and GerontologybusinessGerontology030217 neurology & neurosurgeryAlzheimers dementiaZeitschrift für Gerontopsychologie & -psychiatrie
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The association between psychopathological aspects and CT measurements in affective disorders.

1988

AdultMalePsychiatric Status Rating Scalesbusiness.industryMood DisordersGeneral MedicineMiddle AgedPsychiatry and Mental healthMedicineHumansPharmacology (medical)FemalebusinessAssociation (psychology)PsychopathologyClinical psychologyCt measurementsTomography Emission-ComputedPharmacopsychiatry
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Asymmetrie des Planum temporale bei Zwillingen und Schizophrenen

1997

Anhand eines Zwillingskollektivs und einer Gruppe ersterkrankter Schizophrener (zehn eineiige und zehn zweieiige Zwillingspaare, 38 ersterkrankte Schizophrene, 15 Kontrollen) wird ein moglicher genetischer Einflus auf Grose und Windungsmuster des Planum temporale untersucht. MRT: FLASH-3D-T1-gewichtete Datensatze aus koronaren 3-mm-Schichten; 3D-Rekonstruktion mit ISG-Workstation Allegro. Gemessen wurden Lange und Flache des Planum temporale und Lange des Heschlschen Gyrus. Der Windungsverlauf wurde nach qualitativen Kriterien beurteilt. Schizophrene zeigen im Gegensatz zu gesunden Kontrollen, eineiigen und zweieiigen Zwillingen vor allem bei der Lanlge und weniger bei der Flache des Planum…

Gynecologymedicine.medical_specialtymedia_common.quotation_subjectmedicineRadiology Nuclear Medicine and imagingNeurology (clinical)Artmedia_commonKlinische Neuroradiologie
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Genetic Heterogeneity and Phenotype Variation of Schizophrenia

1995

It is well proven that the manifestation of schizophrenia is under genetic control (Kendler and Diehl 1993). It is however less clear: 1. How relevant environmental factors are, and how they operate and interact with genetic factors. 2. If the genetic susceptibility is identical across the total population of schizophrenics (or at least across all subjects with familial schizophrenia), or if the specific genetic components vary across families. 3. What is transmitted in families of schizophrenics and how co-familial traits are related to genetic and genetic risk factors; are only disorders and symptoms that belong to the schizophrenic sepctrum transmitted or are neurophysiological, neuropsy…

GeneticsGenetic heterogeneitySchizophreniaGenetic predispositionNeuropsychologymedicineHeritability of autismDiseaseBiologymedicine.diseasePhenotypeSchizotypal personality disorder
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Morbid risks for major disorders and frequencies of personality disorders among spouses of psychiatric inpatients and controls

1993

Three hundred fifty-three psychiatric inpatients and their 192 living spouses and 98 control subjects and their 54 living spouses were examined and interviewed for affective, schizoaffective, schizophrenic (Research Diagnostic Criteria [RDC]), and personality disorders (DSM-III-R) using the Lifetime Version of the Schedule for Affective Disorders and Schizophrenia (SADS-L) and the Structured Clinical Interview for DSM-III-Personality Disorders (SCID). The morbid risks of spouses for unipolar depression were between .15 and .25, and those for other major disorders were below .03. The morbid risks of spouses of bipolar patients for unipolar depression exceeded those of other spouses by 50% wi…

AdultMalemedicine.medical_specialtyBipolar DisorderPsychometricslcsh:RC435-571media_common.quotation_subjectResearch Diagnostic CriteriaPersonality AssessmentSocial EnvironmentPersonality DisordersRisk Factorslcsh:Psychiatrymental disordersmedicinePersonalityHumansMarriagePsychiatryDepression (differential diagnoses)media_commonAgedDepressive DisorderMental DisordersSchedule for Affective Disorders and SchizophreniaMiddle Agedmedicine.diseasePersonality disordersHospitalizationPsychiatry and Mental healthClinical PsychologyPsychotic DisordersSpouseSchizophreniaSchizophreniaFemaleSchizophrenic PsychologyPsychologyClinical psychologyComprehensive Psychiatry
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The genetic epidemiology of unipolar depression and panic disorder.

1993

medicine.medical_specialtyDepressive DisorderBipolar DisorderPanic disorderIncidenceComorbiditymedicine.diseasePsychiatry and Mental healthCross-Sectional StudiesGenetic epidemiologyGermanyAdoptionmedicineDiseases in TwinsHumansPanic DisorderPharmacology (medical)PsychiatryPsychologyDepression (differential diagnoses)International clinical psychopharmacology
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Neuropsychologische Charakterisierung des Phänotyps Schizophrenie

1993

Die Charakterisierung des Phanotyps im Rahmen genetischer Untersuchungen der Schizophrenie ist von entscheidender Bedeutung. Gleichwohl erweist sich die Validitat der klinischen Diagnose „Schizophrenie“zur alleinigen Charakterisierung des Phanotyps „Schizophrenie“als fraglich im Hinblick auf Sensitivitat (relativ geringes familiares Wiederholungsrisiko sowie relativ niedrige Konkordanzrate bei monozygoten Zwillingen) und Spezifitat (relativ hohe Anzahl sporadischer, nicht-familiarer Falle). Daraus ergibt sich die Frage, ob in den Familien Schizophrener lediglich die diagnostisch identifizierbaren psychopathologischen Syndrome oder auch andere, mit der Schizophrenie assoziierte Merkmale uber…

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What are depressive symptoms in acutely ill patients with schizophrenia spectrum disorder?

2014

AbstractBackground:Aim was to examine depressive symptoms in acutely ill schizophrenia patients on a single symptom basis and to evaluate their relationship with positive, negative and general psychopathological symptoms.Methods:Two hundred and seventy-eight patients suffering from a schizophrenia spectrum disorder were analysed within a naturalistic study by the German Research Network on Schizophrenia. Using the Calgary Depression Scale for Schizophrenia (CDSS) depressive symptoms were examined and the Positive and Negative Syndrome Scale (PANSS) was applied to assess positive, negative and general symptoms. Correlation and factor analyses were calculated to detect the underlying structur…

AdultMalemedicine.medical_specialtyDepression scaleMedizinSeverity of Illness Index03 medical and health sciences0302 clinical medicineGermanyPrevalencemedicineHumans030212 general & internal medicinePsychiatryDepression (differential diagnoses)Depressive symptomsPsychiatric Status Rating ScalesPositive and Negative Syndrome ScaleDepressionGeneral symptomsMiddle Agedmedicine.disease030227 psychiatry3. Good healthHospitalizationAffectPsychiatry and Mental healthResearch DesignSchizophreniaAcute DiseaseGuiltSchizophreniaFemaleSchizophrenic PsychologyFactor Analysis StatisticalPsychologyPsychopathologyClinical psychologySchizophrenia spectrumEuropean Psychiatry
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Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

2013

Eleven susceptibility loci for late-onset Alzheimer's disease (LOAD) were identified by previous studies; however, a large portion of the genetic risk for this disease remains unexplained. We conducted a large, two-stage meta-analysis of genome-wide association studies (GWAS) in individuals of European ancestry. In stage 1, we used genotyped and imputed data (7,055,881 SNPs) to perform meta-analysis on 4 previously published GWAS data sets consisting of 17,008 Alzheimer's disease cases and 37,154 controls. In stage 2, 11,632 SNPs were genotyped and tested for association in an independent set of 8,572 Alzheimer's disease cases and 11,312 controls. In addition to the APOE locu…

MaleApolipoprotein Eepidemiology [Alzheimer Disease]SORL1Medizingenetics [Alzheimer Disease]Genome-wide association studySingle-nucleotide polymorphismBiologyPolymorphism Single NucleotideArticlePICALMCohort StudiesAlzheimer Diseaseddc:570PSEN2GeneticsmedicineHumansGenetic Predisposition to DiseaseAge of OnsetBiologyAgedGenetic associationAged 80 and overGeneticsMiddle Agedmedicine.diseaseGenetic LociCase-Control StudiesFemaleHuman medicineAlzheimer's diseasestatistics & numerical data [Genome-Wide Association Study]Genome-Wide Association StudyNature Genetics
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