0000000000494084

AUTHOR

Stefan Nickels

showing 30 related works from this author

Prevalence of Strabismus and Its Impact on Vision-Related Quality of Life

2020

Purpose This study investigates the prevalence of manifest strabismus and its subtypes in adulthood and analyzes the risk factors and its impact on vision-related quality of life (VRQoL). Design The Gutenberg Health Study (GHS) is a population-based, observational cohort study. A cross-sectional analysis of the baseline examination was conducted. Participants Participants aged 35 to 74 years were included (n = 15  010). Methods All participants were examined with a comprehensive ophthalmologic and general examination including the Hirschberg corneal reflex test to detect manifest strabismus. The following risk factors were analyzed: age, sex, socioeconomic status, birth weight, maternal age…

Pediatricsmedicine.medical_specialtyVisual acuitygenetic structuresbusiness.industryCross-sectional studymedicine.diseaseeye diseasesOphthalmologyMedicinesense organsmedicine.symptombusinessStrabismusHirschberg testExotropiaEsotropiaAnisometropiaCohort studyOphthalmology
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New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics

2017

Item does not contain fulltext Primary open-angle glaucoma (POAG), the most common optic neuropathy, is a heritable disease. Siblings of POAG cases have a ten-fold increased risk of developing the disease. Intraocular pressure (IOP) and optic nerve head characteristics are used clinically to predict POAG risk. We conducted a genome-wide association meta-analysis of IOP and optic disc parameters and validated our findings in multiple sets of POAG cases and controls. Using imputation to the 1000 genomes (1000G) reference set, we identified 9 new genomic regions associated with vertical cup-disc ratio (VCDR) and 1 new region associated with IOP. Additionally, we found 5 novel loci for optic ne…

0301 basic medicineMaleIntraocular pressuregenetic structuresOptic diskGlaucomaPROTEINGenome-wide association studyIDENTIFIES 5Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12]Optic neuropathyOptic Nerve DiseasesPROSTATEGenetics (clinical)RISKAssociation Studies ArticlesCOMMON VARIANTSGeneral MedicineMiddle AgedCANCER3. Good healthmedicine.anatomical_structureOptic nerveFemaleGlaucoma Open-AngleOptic discCyclin-Dependent Kinase Inhibitor p21medicine.medical_specialtyOpen angle glaucomaSUSCEPTIBILITY LOCIOptic Disk610 Medicine & healthBiology03 medical and health sciencesTonometry OcularOphthalmologyGeneticsmedicineHumansGENOME-WIDE ASSOCIATIONMolecular BiologyIntraocular PressureHomeodomain ProteinsP53Genome HumanPOPULATION-BASED EPIDEMIOLOGYZebrafish Proteinsmedicine.diseaseeye diseases030104 developmental biologysense organsGenome-Wide Association StudyHuman Molecular Genetics
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Birthweight and its association with retinal vessel equivalents – Results from the population‐based German Gutenberg Health Study

2020

AdultMalemedicine.medical_specialtyAdolescentAssociation (object-oriented programming)610 MedizinBlood PressurePopulation basedGermanYoung Adult610 Medical sciencesEpidemiologymedicineBirth WeightHumansProspective StudiesChildAgedbusiness.industryInfant NewbornInfantRetinal VesselsGeneral MedicineMiddle Agedlanguage.human_languagePopulation based studyRetinal vesselOphthalmologyChild PreschoollanguageFemalebusinessDemographyActa Ophthalmologica
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Association of Low Birth Weight With Altered Corneal Geometry and Axial Length in Adulthood in the German Gutenberg Health Study

2019

IMPORTANCE: Low birth weight is associated with altered ocular organ development in childhood, including the morphology of the eye. However, no population-based data exist about this association in adulthood. OBJECTIVE: To evaluate whether low birth weight has a long-term association with anterior segment anatomy and axial length in adulthood. DESIGN, SETTING, AND PARTICIPANTS: The Gutenberg Health Study is a population-based, observational cohort study in Germany. All participants underwent ocular biometry. Among the participants with follow-up and self-reported birth weight available, associations were assessed between low birth weight and anterior segment anatomy and axial length using m…

AdultMaleBirth weightPopulationGeometry01 natural sciencesCohort StudiesCornea03 medical and health sciences0302 clinical medicineCorneaGermanymedicineHumansIn patient0101 mathematicseducationOriginal InvestigationAgedAged 80 and overeducation.field_of_studybusiness.industry010102 general mathematicsInfant NewbornRetinopathy of prematurityAxial lengthInfant Low Birth WeightMiddle Agedmedicine.diseaseOphthalmologyLow birth weightAxial Length Eyemedicine.anatomical_structure030221 ophthalmology & optometryFemalemedicine.symptombusinessCohort study
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ballaxy: web services for structural bioinformatics.

2014

Abstract Motivation: Web-based workflow systems have gained considerable momentum in sequence-oriented bioinformatics. In structural bioinformatics, however, such systems are still relatively rare; while commercial stand-alone workflow applications are common in the pharmaceutical industry, academic researchers often still rely on command-line scripting to glue individual tools together. Results: In this work, we address the problem of building a web-based system for workflows in structural bioinformatics. For the underlying molecular modelling engine, we opted for the BALL framework because of its extensive and well-tested functionality in the field of structural bioinformatics. The large …

Statistics and ProbabilityModels MolecularComputer sciencecomputer.software_genreBiochemistryWorkflowStructural bioinformaticsUser-Computer InterfaceHumansMolecular Biologybusiness.industryComputational BiologySequence Analysis DNAData structureComputer Science ApplicationsVisualizationSystems IntegrationComputational MathematicsWorkflowComputational Theory and MathematicsScripting languageWeb serviceSoftware engineeringbusinesscomputerAlgorithmsSoftwareBioinformatics (Oxford, England)
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Cardiovascular medication and intraocular pressure: results from the Gutenberg Health Study

2016

BACKGROUND Intraocular pressure (IOP) is well known to be associated with blood pressure and other cardiovascular risk factors. The influence of systemic cardiovascular, in particular antihypertensive, medication on IOP is still controversial. This study analyses the association between the use of cardiovascular medications and IOP in a large European cohort. METHODS The Gutenberg Health Study is a population-based, prospective,observational cohort study in mid-western Germany. IOP was measured using a non-contact tonometer. The medication classes examined were peripheral vasodilators, diuretics, β-blockers (overall, selective and non-selective), calcium channel blockers, renin-angiotensin …

AdultMaleIntraocular pressureTime Factorsgenetic structuresmedicine.drug_classHealth StatusBlood Pressure030204 cardiovascular system & hematologyRisk Assessment03 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicineRisk FactorsGermanyPrevalenceHumansMedicineProspective Studies610 Medicine & healthBeta blockerIntraocular PressureAgedAspirinbusiness.industryCARDIOVASCULAR MEDICATIONSCardiovascular AgentsMiddle AgedPrognosiseye diseasesSensory SystemsOphthalmologyBlood pressureCardiovascular DiseasesPopulation SurveillanceAnesthesiaCohort030221 ophthalmology & optometryFemaleOcular Hypertensionsense organsbusinessBody mass indexFollow-Up StudiesCohort studymedicine.drugBritish Journal of Ophthalmology
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The relationship of ocular geometry with refractive error in normal and low birth weight adults

2020

Purpose Low birth weight (BW) individuals have an increased risk for myopic refractive error. However, it is unclear which ocular geometric alterations lead to an increase in myopic refractive error. This study aims to evaluate the impact of ocular biometry in interaction with BW on refractive error. Methods Participants of the prospective, observational, population-based Gutenberg Health Study (GHS) with self-reported BW aged 40–80 years and objective refraction and optical biometry were included. Linear regression analyses were conducted to evaluate associations between spherical equivalent with corneal power, anterior chamber depth, lens thickness and axial length and its interaction wit…

AdultMalemedicine.medical_specialtyRefractive errorBiometrygenetic structuresEpidemiologyBirth weightPopulationRefraction OcularAxial lengthBirth weightOphthalmologyLinear regressionMyopiamedicineHumansProspective StudieseducationMathematicseducation.field_of_studyInfant NewbornContrast (statistics)Axial lengthInfant Low Birth WeightRefractive Errorsmedicine.diseaseRefractioneye diseasesRefractionLow birth weightFemaleOriginal Articlesense organsmedicine.symptomCorneal curvatureOptometryJournal of Optometry
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Association of low birth weight with myopic refractive error and lower visual acuity in adulthood: results from the population-based Gutenberg Health…

2017

PurposeLow birth weight (BW) is linked to impaired organ development in childhood, including altered ocular morphological and functional development. The aim of this study was to evaluate whether low BW has long-term effects on visual acuity and refraction in adulthood.MethodsThe Gutenberg Health Study is a population-based, observational cohort study in Germany, including 15 010 participants aged between 35 and 74 years. These participants were divided into three different BW groups (low: <2500 g; normal: between 2500 and 4000 g; and high: >4000 g). Best-corrected visual acuity and objective refraction were examined. We used multivariable linear regression models with adjustment for …

AdultMalemedicine.medical_specialtyRefractive errorVisual acuitygenetic structuresBirth weightVisual AcuityAstigmatismCohort Studies03 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicineOphthalmologyGermanymedicineMyopiaHumansProspective StudiesDioptreAgedbusiness.industryInfant NewbornMacular degenerationInfant Low Birth WeightMiddle Agedmedicine.diseaseRefractive ErrorsSensory SystemsOphthalmologyLow birth weightLogistic Models030221 ophthalmology & optometryFemalemedicine.symptombusiness030217 neurology & neurosurgeryCohort studyThe British journal of ophthalmology
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Epidemiologic Analysis of Asteroid Hyalosis and Associations: The Gutenberg Health Study

2021

AdultMalemedicine.medical_specialtyAsteroid hyalosisEye Diseasesbusiness.industryIncidenceVision DisordersMEDLINEMiddle AgedDermatologyVitreous BodyEpidemiologic StudiesOphthalmology/dk/atira/pure/subjectarea/asjc/2700/2731GermanyPrevalencemedicineHumansFemalebusinessAgedOphthalmology
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Distribution of Anterior Chamber Angle Width and Correlation With Age, Refraction, and Anterior Chamber Depth—The Gutenberg Health Study

2016

PURPOSE Scheimpflug imaging allows quantitative analysis of the width of the anterior chamber angle. We report the population-based distribution of the anterior chamber angle width using this noncontact imaging technique and investigate associated factors. METHODS A population-based cross-sectional study was carried out in Germany. A comprehensive ophthalmologic examination including refraction, biometry, and Scheimpflug imaging was performed. Automated measurement of the anterior chamber angle was performed in each anterior chamber quadrant. Exclusion criteria were previous ocular surgery or inadequate image quality. Association analyses were carried out to determine independently associat…

AdultMaleAnterior ChamberOcular surgeryScheimpflug principlePopulationGlaucoma610 Medicine & healthDiagnostic Techniques OphthalmologicalRefraction OcularAnterior chamber angleCornea03 medical and health sciences0302 clinical medicineRisk FactorsGermanyLens CrystallinemedicineHumans610 Medicine & healtheducationAgedSex Characteristicseducation.field_of_studybusiness.industryAge FactorsAstigmatismMiddle Agedmedicine.diseaseRefractionCross-Sectional StudiesOphthalmologic examination030221 ophthalmology & optometryFemaleGlaucoma Angle-ClosureNuclear medicinebusiness030217 neurology & neurosurgeryShallow anterior chamberInvestigative Opthalmology & Visual Science
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Birth Weight and Diabetic Retinopathy: Results From the Population-Based Gutenberg Health Study (GHS).

2020

Purpose: This study investigates the relationship between diabetic retinopathy (DR) and birth weight (BW) in diabetic subjects sampled from the general population. Methods: The Gutenberg Health Study (GHS) is a population-based, observational cohort study in participants aged from 35 to 74 years. Criteria for diabetes diagnosis were HbA1c ≥6.5% at study entry, a doctor-diagnosis of diabetes, or diabetes medication. The presence of DR was determined by evaluating fundus photographs. BW was assessed by self-reports. GHS participants were divided into three different BW groups (low: <2500 g; normal: 2500–4000 g; high:>4000 g). Logistic regression analysis was conducted as uni- and multiv…

medicine.medical_specialtyPediatricsEpidemiologyBirth weightPopulation basedCohort Studies03 medical and health sciences0302 clinical medicineSDG 3 - Good Health and Well-beingRisk FactorsDiabetes mellitusEpidemiologymedicinePrevalenceBirth WeightHumans030212 general & internal medicineGlycated HemoglobinDiabetic Retinopathybusiness.industryDiabetic retinopathymedicine.diseasePopulation based studyOphthalmologyCross-Sectional StudiesDiabetes Mellitus Type 2030221 ophthalmology & optometry/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingbusinesshormones hormone substitutes and hormone antagonistsOphthalmic epidemiology
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Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium.

2019

Purpose: To evaluate the roles of known myopia-associated genetic variants for development of myopic macular degeneration (MMD) in individuals with high myopia (HM), using case-control studies from the Consortium of Refractive Error and Myopia (CREAM). Methods: A candidate gene approach tested 50 myopia-associated loci for association with HM and MMD, using meta-analyses of case-control studies comprising subjects of European and Asian ancestry aged 30 to 80 years from 10 studies. Fifty loci with the strongest associations with myopia were chosen from a previous published GWAS study. Highly myopic (spherical equivalent [SE] ≤ -5.0 diopters [D]) cases with MMD (N = 348), and two sets of cont…

Refractive errorCandidate genegenetic structuresEmmetropiaGenome-wide association studySensory disorders Donders Center for Medical Neuroscience [Radboudumc 12]Macular DegenerationMathematical and Statistical TechniquesMedicine and Health SciencesMyopiaGeriatric OphthalmologyDioptreVisual ImpairmentsAged 80 and overMultidisciplinaryQRetinal DegenerationStatisticsRGenomicsMetaanalysisPhenotypeResearch DesignPhysical SciencesMedicineRetinal DisordersFemaleAnatomyResearch Articlemedicine.medical_specialtyScienceOcular AnatomySingle-nucleotide polymorphismResearch and Analysis MethodsRetinaOcular SystemOphthalmologyGeneticsGenome-Wide Association StudiesmedicineHumansStatistical Methodsbusiness.industryGene Expression ProfilingCase-control studyBiology and Life SciencesComputational BiologyGenetic VariationCorrectionHuman GeneticsMacular degenerationGenome Analysismedicine.diseaseeye diseasesOphthalmologyGenetic LociGeriatricsMacular DisordersCase-Control StudiesEyessense organsbusinessHeadMathematicsPloS one
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No evidence for an association of plasma homocysteine levels and refractive error – Results from the population-based Gutenberg Health Study (GHS)

2020

Purpose There is a strong association between severe hyperhomocysteinemia and myopia. Thus we studied the hypothesis that even moderately increased levels of homocysteine (Hcy) might be a potentially treatable risk factor for myopia. Methods The Gutenberg Health Study (GHS) is a population-based, prospective, observational cohort study in Germany, including 15,010 participants aged between 35 and 74 at recruitment. The baseline examination was conducted from 2007–2012. Refraction was measured using autorefraction (HARK 599, Carl Zeiss AG, Jena, Germany). Hcy was measured by an immunoassay. We included only phakic participants without a history of corneal surgery or corneal laser treatment. …

MaleRefractive errorHomocysteinegenetic structuresVisionVisual AcuitySocial SciencesCorneachemistry.chemical_compound0302 clinical medicineMathematical and Statistical TechniquesRisk FactorsGermanyMedicine and Health SciencesMyopiaMedicinePsychologyPublic and Occupational HealthProspective StudiesProspective cohort studyGeneralized estimating equationHomocysteineVisual ImpairmentsMultidisciplinaryEye LensQStatisticsRMiddle AgedRefractive ErrorsSocioeconomic Aspects of HealthPhysical SciencesMedicineRegression AnalysisSensory PerceptionFemaleAnatomyCohort studyResearch ArticleAdultHyperhomocysteinemiamedicine.medical_specialtyScienceOcular AnatomyHyperhomocysteinemiaSurgical and Invasive Medical ProceduresLinear Regression AnalysisResearch and Analysis Methods03 medical and health sciencesOcular SystemOphthalmologyLinear regressionHumansRisk factorStatistical MethodsAgedbusiness.industryBiology and Life Sciencesmedicine.diseaseeye diseasesHealth CareOphthalmologychemistry030221 ophthalmology & optometryEyessense organsbusinessHead030217 neurology & neurosurgeryMathematicsNeurosciencePLoS ONE
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Characteristics and pathologies of the vitreo‐macular interface—results from the Gutenberg Health Study

2019

Purpose We aimed to determine the prevalence of characteristics and pathologies of the vitreo-macular interface within the general population. Methods The Gutenberg Health Study is a population-based study in Germany, including an ophthalmological examination with refraction, biometry and optical coherence tomography (OCT) imaging. Characteristics of the vitreo-macular interface were graded on volume scans including visibility of an epiretinal membrane, full-thickness macular hole, lamellar hole and pseudohole. Overall and age-specific prevalences including 95% confidence intervals [95%-CI] were calculated. Association analyses were conducted to determine systemic and ocular factors that ar…

MaleRefractive errorIntraocular pressuremedicine.medical_specialtygenetic structuresmedicine.medical_treatmentPopulationVitreous Detachment03 medical and health scienceschemistry.chemical_compound0302 clinical medicineGermanyOphthalmologyMyopiaPrevalencemedicineHumansMacula LuteaProspective StudieseducationMacular holeAgededucation.field_of_studybusiness.industryAge FactorsEpiretinal MembraneRetinalGeneral MedicineMiddle AgedCataract surgerymedicine.diseaseeye diseasesConfidence intervalVitreous BodyOphthalmologyCross-Sectional Studieschemistry030221 ophthalmology & optometryFemalesense organsEpiretinal membranebusinessTomography Optical Coherence030217 neurology & neurosurgeryActa Ophthalmologica
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The Prevalence of Visual Impairment in the Adult Population

2019

Background The distribution of visual impairment is an indicator of the health status of the population and for the frequency of diseases of the eye. Methods The Gutenberg Health Study (GHS) is a population-based cohort study in Germany concerning adults aged 35 to 74. 15 010 subjects from the Mainz-Bingen region underwent general medical and ophthalmological examination, with measurement of the distance-corrected visual acuity in each eye separately. As per the World Health Organization criteria, visual impairment was defined as an acuity below 0.3 in the better eye, and blindness as an acuity below 0.05. All patients who were found to be visually impaired or blind underwent further indivi…

education.field_of_studyPediatricsmedicine.medical_specialtyVisual acuitygenetic structuresmedicine.diagnostic_testbusiness.industryCross-sectional studyVisual impairmentPopulationFundus photographyGeneral Medicineeye diseasesConfidence intervalmedicineEtiologymedicine.symptombusinesseducationCohort studyDeutsches Ärzteblatt international
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Schirmer test results: are they associated with topical or systemic medication?

2018

To test whether Schirmer test (ST) results are associated with topical or systemic medication and to evaluate the distribution of tear fluid quantity in a 3-min and 5-min ST.The Gutenberg Health Study is a population-based, prospective, observational cohort study in Germany. ST was assessed in a sub-cohort of 1,999 participants. ST was performed under topical anesthesia for 5 min (ST-5) or of 3 min (ST-3). Anthropometric factors, systemic diseases, use of systemic and eye medications were recorded. We used multivariable quantile regression analysis to assess the influence on ST measurements.The length of wetting of the Schirmer strips for ST-5 was 23.2 ± 9.31 mm for right and 22.9 ± 9.0 mm …

Malemedicine.medical_specialtyeducation.field_of_studybusiness.industryPopulationEye medicationsAnthropometryEyeLarge cohort03 medical and health sciencesOphthalmology0302 clinical medicineTopical anesthesiaInternal medicineTears030221 ophthalmology & optometrymedicineHumansSchirmer test030212 general & internal medicineProspective StudieseducationbusinessCohort studyThe ocular surface
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ProteinScanAR - An Augmented Reality Web Application for High School Education in Biomolecular Life Sciences

2012

Understanding protein structures is a crucial step in creating molecular insight for researchers as well as students and pupils. The enormous scaling gap between an atomic point of view and objects in daily life hampers developing an intuitive relation between them. Especially for high school students, it can be difficult to understand the spatial relations of a protein structure. Due to lack of direct imaging techniques, molecules can only be explored by studying abstract molecular models. Here, the use of Augmented reality (AR) techniques has proven to strongly improve structural perception. In this work we present ProteinScanAR, an augmented reality framework for biomolecular education t…

Structure (mathematical logic)Spatial relationHTML5Relation (database)business.industryHuman–computer interactionComputer scienceWeb applicationThe InternetAugmented realitybusinessLicense2012 16th International Conference on Information Visualisation
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When do myopia genes have their effect? Comparison of genetic risks between children and adults

2016

Item does not contain fulltext Previous studies have identified many genetic loci for refractive error and myopia. We aimed to investigate the effect of these loci on ocular biometry as a function of age in children, adolescents, and adults. The study population consisted of three age groups identified from the international CREAM consortium: 5,490 individuals aged 25 years. All participants had undergone standard ophthalmic examination including measurements of axial length (AL) and corneal radius (CR). We examined the lead SNP at all 39 currently known genetic loci for refractive error identified from genome-wide association studies (GWAS), as well as a combined genetic risk score (GRS). …

0301 basic medicineAdultMalemedicine.medical_specialtyBiometryAdolescentGenotypeEpidemiologySingle-nucleotide polymorphismGenome-wide association studyBiologyPolymorphism Single NucleotideConnexinsSensory disorders Donders Center for Medical Neuroscience [Radboudumc 12]03 medical and health sciencesYoung Adult0302 clinical medicineRisk FactorsInternal medicineGenotypemedicineMyopiaSNPHumansAlleleYoung adult610 Medicine & healthChildGenetics (clinical)AllelesGenetic associationGenetics030104 developmental biologyGenetic Loci030221 ophthalmology & optometryPopulation studyFemaleRELamininGenome-Wide Association Study
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Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

2013

Journal article TERT-locus SNPs and leukocyte telomere measures are reportedly associated with risks of multiple cancers. Using the Illumina custom genotyping array iCOGs, we analyzed ~480 SNPs at the TERT locus in breast (n = 103,991), ovarian (n = 39,774) and BRCA1 mutation carrier (n = 11,705) cancer cases and controls. Leukocyte telomere measurements were also available for 53,724 participants. Most associations cluster into three independent peaks. The minor allele at the peak 1 SNP rs2736108 associates with longer telomeres (P = 5.8 × 10!-7), lower risks for estrogen receptor (ER)-negative (P = 1.0 × 10!-8) and BRCA1 mutation carrier (P = 1.1 × 10!-5) breast cancers and altered promot…

TelomeraseMessengerCàncer d'ovariEstrogen receptorAetiology screening and detection [ONCOL 5]0302 clinical medicineBreast cancerRisk FactorsAlternative Splicing; Biomarkers Tumor; Breast Neoplasms; Case-Control Studies; Chromatin; DNA Methylation; Female; Gene Expression Profiling; Genetic Loci; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Humans; Luciferases; Oligonucleotide Array Sequence Analysis; Ovarian Neoplasms; Polymorphism Single Nucleotide; RNA Messenger; Real-Time Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; Risk Factors; Telomerase; Telomere; GeneticsGenotypeBUCCAL CELLSLuciferasesTelomeraseOligonucleotide Array Sequence AnalysisOvarian Neoplasms0303 health sciencesTumorTelòmerReverse Transcriptase Polymerase Chain ReactionGENETIC-VARIATIONCOMMON VARIANTSSingle Nucleotidetert-clptm1l locus; genome-wide association; genetic-variation; susceptibility loci; buccal cells; fibroblasts; common variants; carcinoma; reverse-transcriptase htert; metaanalysisTelomereAetiology screening and detection Immune Regulation [ONCOL 5]Chromatin3. Good healthTumor Markers Biological030220 oncology & carcinogenesisFemaleFIBROBLASTSGenotypeSUSCEPTIBILITY LOCICARCINOMASingle-nucleotide polymorphismBreast NeoplasmsBiologyReal-Time Polymerase Chain ReactionPolymorphism Single NucleotideArticleCàncer de mama03 medical and health sciencesBreast cancerSDG 3 - Good Health and Well-beingTranslational research [ONCOL 3]Ovarian cancermedicineGeneticsBiomarkers TumorHumansGenetic Predisposition to DiseaseRNA MessengerPolymorphismAlleleGENOME-WIDE ASSOCIATIONMETAANALYSIS030304 developmental biologyMolecular epidemiology Aetiology screening and detection [NCEBP 1]Breast cancer susceptibilityHereditary cancer and cancer-related syndromes [ONCOL 1]Translational research Genomic disorders and inherited multi-system disorders [ONCOL 3]Gene Expression ProfilingDNA Methylationmedicine.diseaseMolecular biologyTERT-CLPTM1L LOCUSTelomereMinor allele frequencyAlternative SplicingGenetic LociCase-Control StudiesRNABiomarkersREVERSE-TRANSCRIPTASE HTERTGenome-Wide Association StudyNature genetics
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Incidence of retinal artery occlusion in Germany

2020

Ophthalmologymedicine.medical_specialtyRetinal Artery Occlusionbusiness.industryOphthalmologyIncidence (epidemiology)610 Medical sciencesmedicine610 MedizinGeneral Medicinebusiness
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Incidence of Retinal Detachment in Germany: Results from the Gutenberg Health Study

2020

<b><i>Purpose:</i></b> To investigate the incidence of retinal detachment in the German population and to assess potential risk factors. <b><i>Methods:</i></b> The Gutenberg Health Study is a population-based cohort study in Mainz, Germany, including subjects (<i>n</i> = 15,010) with an age range from 35 to 74 years at baseline examination. Study participants underwent a comprehensive ophthalmological examination including distant-corrected visual acuity, refraction and slit-lamp examination at baseline examination. A computer-assisted telephone interview was conducted after 2.5 and 5 years, and health events were recorded. The 5-y…

AdultMalemedicine.medical_specialtyVisual acuityPopulationVisual AcuityCohort Studieschemistry.chemical_compoundGermanyOphthalmologymedicineHumansCumulative incidenceeducationAgededucation.field_of_studybusiness.industryIncidenceIncidence (epidemiology)Retinal DetachmentRetinal detachmentRetinalGeneral MedicineMiddle Agedmedicine.diseaseSensory SystemsOphthalmologychemistryFemalemedicine.symptombusinessPseudophakiaCohort studyOphthalmologica
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Relative Telomere Length and Cardiovascular Risk Factors

2019

(1) Background: Telomeres are repetitive DNA sequences located at the extremities of chromosomes that maintain genetic stability. Telomere biology is relevant to several human disorders and diseases, specifically cardiovascular disease. To better understand the link between cardiovascular disease and telomere length, we studied the effect of relative telomere length (RTL) on cardiovascular risk factors in a large population-based sample. (2) Methods: RTL was measured by a real-time quantitative polymerase chain reaction in subjects of the population-based Gutenberg Health Study (n = 4944). We then performed an association study of RTL with known cardiovascular risk factors of smoking status…

Malecardiovascular risk factorsmedicine.medical_specialtyCardiovascular risk factorsPopulationlcsh:QR1-502Disease030204 cardiovascular system & hematologyBiochemistryArticlelcsh:MicrobiologyBody Mass Index03 medical and health scienceschemistry.chemical_compound0302 clinical medicinecardiovascular diseaseInternal medicinetelomere lengthHumansMedicine030212 general & internal medicineeducationMolecular BiologyTriglyceridesAgededucation.field_of_studybusiness.industryCholesterolSmokingAge FactorsTelomere HomeostasisMiddle AgedtelomeresTelomereCholesterolEndocrinologyBlood pressurechemistryCardiovascular DiseasesageingAgeingFemalebusinessBody mass indexBiomolecules
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Quality of life and functional limitations after pulmonary embolism and its prognostic relevance

2019

Abstract Background While the importance of patients’ quality of life (QoL) in chronic cardiac or pulmonary disease is uncontroversial, the burden of an acute pulmonary embolism (PE) on QoL has received little attention thus far. Objectives We aimed to validate the German PEmb‐QoL questionnaire, identify associations between QoL and clinical/functional parameters, and investigate the prognostic relevance of QoL for long‐term survival in survivors of an acute PE episode. Patients/Methods Patients were invited for a clinical follow‐up visit including assessment of QoL using the German PEmb‐QoL questionnaire 6 months after an objectively confirmed PE at a single center. Internal consistency re…

Malemedicine.medical_specialtyTime FactorsPsychometricsPsychometricsHealth Status030204 cardiovascular system & hematologySingle Center03 medical and health sciences0302 clinical medicineCost of IllnessQuality of lifePredictive Value of TestsRisk FactorsInterquartile rangeGermanySurveys and QuestionnairesInternal medicinemedicineHumansProspective StudiesSurvivorsProspective cohort studyDepression (differential diagnoses)Agedbusiness.industryReproducibility of ResultsOriginal ArticlesHematologyMiddle AgedPrognosismedicine.diseasehumanities3. Good healthPulmonary embolismTHROMBOSISDyspneaPredictive value of testsQuality of LifeFemaleOriginal ArticleSymptom AssessmentPulmonary Embolismbusiness
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Genome-wide association studies identify four ER negative-specific breast cancer risk loci

2013

Estrogen receptor (ER)-negative tumors represent 20-30% of all breast cancers, with a higher proportion occurring in younger women and women of African ancestry. The etiology and clinical behavior of ER-negative tumors are different from those of tumors expressing ER (ER positive), including differences in genetic predisposition. To identify susceptibility loci specific to ER-negative disease, we combined in a metaanalysis 3 genome-wide association studies of 4,193 ER-negative breast cancer cases and 35,194 controls with a series of 40 follow-up studies (6,514 cases and 41,455 controls), genotyped using a custom Illumina array, iCOGS, developed by the Collaborative Oncological Gene-environm…

Oncologygenetic associationbody-mass indexEstrogen receptorGenome-wide association studycancer riskBioinformaticssusceptibilitychromosome 1q0302 clinical medicineRisk Factorssingle nucleotide polymorphismGenotypeestrogenCooperative Behaviorcomparative studyOligonucleotide Array Sequence Analysis0303 health scienceschromosome 16q3. Good healthReceptors Estrogenpriority journal030220 oncology & carcinogenesisFemalecancer invasionsignal transductionbreast cancer; cancer invasion; cancer risk; chromosome 1; chromosome 16q; chromosome 1q; chromosome 2p; comparative study; follow up; gene locus; genetic association; genetic susceptibility; human; nucleotide sequence; priority journal; signal transduction; single nucleotide polymorphismmedicine.medical_specialtyGenotypegene locusBreast NeoplasmsSingle-nucleotide polymorphismBiologyPolymorphism Single NucleotideArticle03 medical and health sciencesBreast cancerbreast cancerMeta-Analysis as TopicSDG 3 - Good Health and Well-beingInternal medicineexpressionGeneticsmedicineGenetic predispositionHumansfollow upGenetic Predisposition to Diseasehumanchromosome 1gene030304 developmental biologyCase-control studyCancernucleotide sequencemedicine.diseasechromosome 2pGenetic LociCase-Control Studiescommon variantGenome-Wide Association Studygenetic susceptibilityNature Genetics
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Prevalence of myopic maculopathy in the German population: results from the Gutenberg health study.

2019

AimsTo determine the prevalence of myopic maculopathy in the general population in Germany and to analyse potential associations with ocular and systemic factors.DesignThe Gutenberg Health Study is a population-based study, including 15 010 participants aged 35–74 years.MethodsMyopic maculopathy was graded in phakic eyes with spherical equivalent ≤−6 D by assessing fundus photographs according to a recent international photographic classification system (META-PM). 801 eyes of 519 participants (mean age 51.0±0.77 years) met the conditions and had gradable fundus photographs. Age-specific prevalence estimates were computed. Multivariable logistic regression analysis was used to assess associa…

AdultMalemedicine.medical_specialtyRefractive errorgenetic structuresPopulationVisual AcuityBlood PressureFundus (eye)Logistic regressionRefraction Ocular03 medical and health sciencesCellular and Molecular NeuroscienceMacular Degeneration0302 clinical medicineAtrophyGerman populationOphthalmologyGermanyEpidemiologymedicineMyopiaPhotographyPrevalenceHumanseducationTriglyceridesAgedRetrospective StudiesGlycated Hemoglobineducation.field_of_studybusiness.industryMiddle Agedmedicine.diseaseeye diseasesSensory SystemsLipoproteins LDLOphthalmology030221 ophthalmology & optometryMaculopathyFemalesense organsbusinessLipoproteins HDL030217 neurology & neurosurgeryThe British journal of ophthalmology
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Prevalence of pterygium and identification of associated factors in a German population - results from the Gutenberg Health Study.

2020

MaleRural Populationmedicine.medical_specialtybusiness.industry610 MedizinMEDLINEGeneral MedicineMiddle Agedmedicine.diseasePterygiumDermatologyPterygiumOphthalmologyGerman populationRisk Factors610 Medical sciencesOrganometallic CompoundsPrevalenceMedicineHumansIdentification (biology)FemalebusinessConjunctivaActa ophthalmologica
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Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive err…

2020

Corneal curvature, a highly heritable trait, is a key clinical endophenotype for myopia - a major cause of visual impairment and blindness in the world. Here we present a trans-ethnic meta-analysis of corneal curvature GWAS in 44,042 individuals of Caucasian and Asian with replication in 88,218 UK Biobank data. We identified 47 loci (of which 26 are novel), with population-specific signals as well as shared signals across ethnicities. Some identified variants showed precise scaling in corneal curvature and eye elongation (i.e. axial length) to maintain eyes in emmetropia (i.e. HDAC11/FBLN2 rs2630445, RBP3 rs11204213); others exhibited association with myopia with little pleiotropic effects …

genetic structureslikinäköisyyssense organsgeneettiset tekijäteye diseases
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Haplotype reference consortium panel: Practical implications of imputations with large reference panels.

2017

Contains fulltext : 177754.pdf (Publisher’s version ) (Open Access) Recently, the Haplotype Reference Consortium (HRC) released a large imputation panel that allows more accurate imputation of genetic variants. In this study, we compared a set of directly assayed common and rare variants from an exome array to imputed genotypes, that is, 1000 genomes project (1000GP) and HRC. We showed that imputation using the HRC panel improved the concordance between assayed and imputed genotypes at common, and especially, low-frequency variants. Furthermore, we performed a genome-wide association meta-analysis of vertical cup-disc ratio, a highly heritable endophenotype of glaucoma, in four cohorts usin…

0301 basic medicineGenotypeConcordanceGenome-wide association study610 Medicine & healthBiologyPolymorphism Single NucleotideSensory disorders Donders Center for Medical Neuroscience [Radboudumc 12]03 medical and health sciencesGene FrequencyGeneticsAssociation studies Imputation 1000 Genomes Project reference Panel Haplotype Reference Consortium Vertical cup-disc ratioHumansExome1000 Genomes Project610 Medicine & healthExomeAllele frequencyGenetics (clinical)Genetic associationGeneticsGenome HumanHaplotypeGenetic Variation030104 developmental biologyHaplotypesImputation (genetics)Genome-Wide Association Study
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A genome-wide association study of corneal astigmatism: The CREAM Consortium

2018

Contains fulltext : 191261.pdf (Publisher’s version ) (Open Access) Purpose: To identify genes and genetic markers associated with corneal astigmatism. Methods: A meta-analysis of genome-wide association studies (GWASs) of corneal astigmatism undertaken for 14 European ancestry (n=22,250) and 8 Asian ancestry (n=9,120) cohorts was performed by the Consortium for Refractive Error and Myopia. Cases were defined as having >0.75 diopters of corneal astigmatism. Subsequent gene-based and gene-set analyses of the meta-analyzed results of European ancestry cohorts were performed using VEGAS2 and MAGMA software. Additionally, estimates of single nucleotide polymorphism (SNP)-based heritability for …

0301 basic medicineReceptor Platelet-Derived Growth Factor alphaAcid PhosphataseGene Expression610 Medicine & healthbiomarkkeritPolymorphism Single NucleotideWhite PeopleSensory disorders Donders Center for Medical Neuroscience [Radboudumc 12]Corneal DiseasesCohort StudiesCornea03 medical and health sciences0302 clinical medicineAsian PeopleOdds RatioHumansGenetic Predisposition to Disease610 Medicine & healthsarveiskalvogeenitIntracellular Signaling Peptides and ProteinsAstigmatism030104 developmental biologysilmätauditClaudinsgenetic markers030221 ophthalmology & optometrycorneal astigmatismSoftwaresilmätResearch ArticleGenome-Wide Association Study
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Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

2023

Refractive error, measured here as mean spherical equivalent (SER), is a complex eye condition caused by both genetic and environmental factors. Individuals with strong positive or negative values of SER require spectacles or other approaches for vision correction. Common genetic risk factors have been identified by genome-wide association studies (GWAS), but a great part of the refractive error heritability is still missing. Some of this heritability may be explained by rare variants (minor allele frequency [MAF] ≤ 0.01.). We performed multiple gene-based association tests of mean Spherical Equivalent with rare variants in exome array data from the Consortium for Refractive Error and Myopi…

genetic predisposition to diseaseperinnölliset tauditympäristötekijättaittovirheetperinnöllisyyslääketiederiskitekijätquantitative traitperiytyvyysgenome-wide association studiesquantitative trait lociperimäsilmätauditmicroarraysperinnöllisyys
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