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0166-06161092024DecStudies in mycologyStud MycolKnown from trees and the tropics: new insights into the Fusarium lateritium species complex.403450403-45010.3114/sim.2024.109.06The Fusarium lateritium species complex (FLSC) currently comprises 11 phylogenetic species, including accepted names such as F. lateritium, F. sarcochroum, and F. stilboides, which have mostly been reported in association with citrus and coffee. Many varieties were documented by Wollenweber & Reinking (1935), which is indicative of a wider diversity of species within this group. The lack of type material in some cases, especially for the older names, means that definition by molecular phylogeny is very difficult. In the present study, we examined 179 strains related to F. lateritium from different countries and substrates. Historic reference material, including representative strains from the Wollenweber & Reinking (1935) varieties were included in this study, DNA sequences were generated for comparison, and the morphology correlated with original descriptions to enable the correct application of older names. Strains were characterized by multi-gene phylogenetic analyses based on fragments of the β-tubulin (tub2), calmodulin (CaM), RNA polymerase II second largest subunit (rpb2), and translation elongation factor 1-alpha (tef1) genes, evaluation of morphological characters and host-substrate preferences. The biological species concept was tested by crossings in vitro. Strains previously identified as F. lateritium, F. stilboides, or one of their varieties based on morphology, were found to belong to 16 species in the FLSC, but also to species from six other species complexes (SC), including the F. citricola SC, F. heterosporum SC, F. incarnatum-equiseti SC, F. redolens SC, F. sambucinum SC, and the F. tricinctum SC. Eleven new phylogenetic and two biological species are described in the FLSC, and emended descriptions are provided for four previously described species. An epitype is designated for F. lateritium, and F. lateritium var. longum, a former variety within the FLSC, is lecto- and epitypified, and elevated to species level with a replacement name. Taxonomic novelties: New species: F. aurantii M.M. Costa, Sand.-Den. & Crous, F. chlamydocopiosum M.M. Costa, Sand.-Den. & Crous, F. citri-sinensis L. Zhao & J.X. Deng, F. coffeibaccae M.M. Costa, L.H. Pfenning, Sand.-Den. & Crous, F. crocatum M.M. Costa, Sand.-Den. & Crous, F. malawiense M.M. Costa, Sand.-Den. & Crous, F. microcyclum M.M. Costa, Sand.-Den. & Crous, F. oliniae M.M. Costa, Sand.-Den. & Crous; F. rufum M.M. Costa, Sand.-Den. & Crous, F. stramineum M.M. Costa, Sand.-Den. & Crous, F. velutinum M.M. Costa, Sand.-Den. & Crous, F. verruculosum M.M. Costa, Sand.-Den. & Crous; Replacement name: F. hanswilhelmii M.M. Costa, Sand.-Den. & Crous; Epitype (basionym): F. lateritium Nees, F. lateritium var. longum Wollenw.; Lectotype (basionym): F. lateritium var. longum Wollenw. Citation: Costa MM, Sandoval-Denis M, Moreira GM, Kandemir H, Kermode A, Buddie AG, Ryan MJ, Becker Y, Yurkov A, Maier W, Groenewald JZ, Pfenning LH, Crous PW (2024). Known from trees and the tropics: new insights into the Fusarium lateritium species complex. Studies in Mycology 109: 403-450. doi: 10.3114/sim.2024.109.06.© 2024 Westerdijk Fungal Biodiversity Institute.CostaM MMMWesterdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.Sandoval-DenisMMWesterdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.MoreiraG MGMDepartment of Plant Pathology, Universidade Federal de Lavras, 37200-900, Lavras MG, Brazil.KandemirHHWesterdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.KermodeAACAB International (CABI), Bakeham Lane, TW20 9TY Egham, Surrey, United Kingdom.BuddieA GAGCAB International (CABI), Bakeham Lane, TW20 9TY Egham, Surrey, United Kingdom.RyanM JMJCAB International (CABI), Bakeham Lane, TW20 9TY Egham, Surrey, United Kingdom.BeckerYYInstitute for Epidemiology and Pathogen Diagnostics, Julius Kühn Institute (JKI), Federal Research Centre for Cultivated Plants, Messeweg 11-12, 38104 Braunschweig, Germany.YurkovAADepartment of Bioresources for Bioeconomy and Health Research, Leibniz Institute DSMZ - German Collection of Microorganisms and Cell Cultures GmbH, Inhoffenstraße 7B, 38124 Braunschweig, Germany.MaierWWInstitute for Epidemiology and Pathogen Diagnostics, Julius Kühn Institute (JKI), Federal Research Centre for Cultivated Plants, Messeweg 11-12, 38104 Braunschweig, Germany.GroenewaldJ ZJZWesterdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.PfenningL HLHDepartment of Plant Pathology, Universidade Federal de Lavras, 37200-900, Lavras MG, Brazil.CrousP WPWWesterdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.Department of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.Microbiology, Department of Biology, Utrecht University, Padualaan 8, Utrecht, 3584 CH, The Netherlands.engJournal Article20240926
NetherlandsStud Mycol84119840166-0616Biological species conceptfungal taxonomymultigene phylogenynew taxaThe authors declare that there is no conflict of interest.
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1520-688296472024Nov26Analytical chemistryAnal ChemValidated Multimethod Approach for Full Characterization of 2'-Fucosyl-d-lactose as an Industrially Produced Human Milk Oligosaccharide.186151862418615-1862410.1021/acs.analchem.4c01926Human milk oligosaccharides are of high interest as active ingredients in infant formulas and dietary food supplements. Full characterization of members of this compound class is challenging due to the intrinsic complexity of byproducts during synthesis by fermentation. Moreover, when method validation is targeted for a regulated environment, a robust chromatographic separation of the highly polar oligosaccharides needs to be addressed, including isomers and compounds relevant for potential product adulteration. We present a combined approach of validated chromatography and NMR spectroscopy, which allows for full mass balancing of industrially produced 2'-fucosyl-d-lactose. A combination of NMR spectroscopy, mass spectrometry, and action IR spectroscopy tackles structural elucidation of monoacetylated species as a new class of byproducts.NeuVolkerV0009-0009-7662-3152Analytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany.HoffmannWaldemarWAnalytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany.WeißThomas DTDAgricultural Solutions, BASF SE, Speyerer Strasse 2, Limburgerhof 67117, Germany.PuhlMichaelMChemicals and Catalysis Research, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany.AbikhodrAliAIsospec Analytics SA, Renens CH-1020, Switzerland.WarnkeStephanSIsospec Analytics SA, Renens CH-1020, Switzerland.Ben FalehAhmedAIsospec Analytics SA, Renens CH-1020, Switzerland.KlinckSandraSAnalytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany.PommerMariaMAnalytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany.KellnerSarahSAnalytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany.MaierWalterWAnalytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany.engJournal ArticleValidation Study20241114
United StatesAnal Chem03705360003-27000OligosaccharidesXO2533XO8R2'-fucosyllactose0TrisaccharidesJ2B2A4N98GLactoseIMMilk, HumanchemistryHumansOligosaccharideschemistryanalysisTrisaccharideschemistryMagnetic Resonance SpectroscopyLactosechemistryMass Spectrometry
2024112663420241114173820241114653ppublish3954046110.1021/acs.analchem.4c01926
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1552-485X2024Oct29American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric GeneticsAm J Med Genet B Neuropsychiatr GenetOptimizing the Prediction of Depression Remission: A Longitudinal Machine Learning Approach.e33014e3301410.1002/ajmg.b.33014Decisions about when to change antidepressant treatment are complex and benefit from accurate prediction of treatment outcome. Prognostic accuracy can be enhanced by incorporating repeated assessments of symptom severity collected during treatment. Participants (n = 714) from the Genome-Based Therapeutic Drugs for Depression study received escitalopram or nortriptyline over 12 weeks. Remission was defined as scoring ≤ 7 on the Hamilton Rating Scale. Predictors included demographic, clinical, and genetic variables (at 0 weeks) and measures of symptom severity (at 0, 2, 4, and 6 weeks). Longitudinal descriptors extracted with growth curves and topological data analysis were used to inform prediction of remission. Repeated assessments produced gradual and drug-specific improvements in predictive performance. By Week 4, models' discrimination in all samples reached levels that might usefully inform treatment decisions (area under the receiver operating curve (AUC) = 0.777 for nortriptyline; AUC = 0.807 for escitalopram; AUC = 0.794 for combined sample). Decisions around switching or modifying treatments for depression can be informed by repeated symptom assessments collected during treatment, but not until 4 weeks after the start of treatment.© 2024 The Author(s). American Journal of Medical Genetics Part B: Neuropsychiatric Genetics published by Wiley Periodicals LLC.CarrEwanEDepartment of Biostatistics & Health Informatics, Institute of Psychiatry, Psychology and Neuroscience (IoPPN), London, UK.RietschelMarcellaMDepartment of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.MorsOleOPsychosis Research Unit, Aarhus University Hospital-Psychiatry, Aarhus, Denmark.HenigsbergNevenNCroatian Institute for Brain Research, Medical School, University of Zagreb, Zagreb, Croatia.AitchisonKatherine JKJCollege of Health Sciences, Department of Psychiatry and Medical Genetics, University of Alberta, Edmonton, Alberta, Canada.Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.Women and Children's Health Research Institute, University of Alberta, Edmonton, Alberta, Canada.Northern Ontario School of Medicine, Thunder Bay, Ontario, Canada.MaierWolfgangWDepartment of Neurodegenerative Diseases and Geriatric Psychiatry, University Hospital Bonn, Bonn, Germany.German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.UherRudolfRDepartment of Psychiatry, Dalhousie University, Halifax, Nova Scotia, Canada.FarmerAnneASocial, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.McGuffinPeterPSocial, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.IniestaRaquelR0000-0003-1153-5417Department of Biostatistics & Health Informatics, Institute of Psychiatry, Psychology and Neuroscience (IoPPN), London, UK.King's Institute for Artificial Intelligence, King's College London, London, UK.engNIHR Maudsley Biomedical Research CentreBrain and Behavior Research FoundationSeventh Framework ProgrammeEuropean Federation of Pharmaceutical Industries and AssociationsEuropean CommissionJournal Article20241029
United StatesAm J Med Genet B Neuropsychiatr Genet1012357421552-4841IMdepression remissionmachine learningrepeated measurestopological data analysis
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1468-286910162024DecJournal of urban health : bulletin of the New York Academy of MedicineJ Urban HealthA Framework for Measuring Neighborhood Walkability for Older Adults-A Delphi Consensus Study.118811991188-119910.1007/s11524-024-00910-7While mobility in older age is of crucial importance for health and well-being, it is worth noting that currently, there is no German language framework for measuring walkability for older adults that also considers the functional status of a person. Therefore, we combined the results of an expert workshop, a literature review, and a Delphi consensus survey. Through this, we identified and rated indicators relevant for walkability for older adults, additionally focusing on their functional status. The expert workshop and the review led to an extensive list of potential indicators, which we hope will be useful in future research. Those indicators were then adapted and rated in a three-stage Delphi expert survey. A fourth additional Delphi round was conducted to assess the relevance of each indicator for the different frailty levels, namely "robust," "pre-frail," and "frail." Between 20 and 28 experts participated in each round of the Delphi survey. The Delphi process resulted in a list of 72 indicators deemed relevant for walkability in older age groups, grouped into three main categories: "Built environment and transport infrastructure," "Accessibility and meeting places," and "Attractiveness and sense of security." For 35 of those indicators, it was suggested that functional status should be additionally considered. This framework represents a significant step forward in comprehensively covering indicators for subjective and objective walkability in older age, while also incorporating aspects of functioning relevant to older adults. It would be beneficial to test and apply the indicator set in a community setting.© 2024. The Author(s).KollerDanielaD0000-0002-3203-7188Institute of Medical Information Processing, Biometry, and Epidemiology, Faculty of Medicine, LMU Munich, Munich, Germany. daniela.koller@med.uni-muenchen.de.BödekerMalteMFederal Centre for Health Education, Cologne, Germany.DappUlrikeU0000-0001-9497-2860Geriatrics Centre, Scientific Department at the University of Hamburg, Albertinen-Haus, Hamburg, Germany.GrillEvaE0000-0002-0273-7984Institute of Medical Information Processing, Biometry, and Epidemiology, Faculty of Medicine, LMU Munich, Munich, Germany.German Center for Vertigo and Balance Disorders, LMU University Hospital, Munich, Germany.FuchsJudithJ0000-0003-1594-2319Department of Epidemiology and Health Monitoring, Robert Koch Institute, Berlin, Germany.MaierWernerW0000-0003-4356-7296Institute of Medical Information Processing, Biometry, and Epidemiology, Faculty of Medicine, LMU Munich, Munich, Germany.StroblRalfR0000-0002-7719-948XInstitute of Medical Information Processing, Biometry, and Epidemiology, Faculty of Medicine, LMU Munich, Munich, Germany.German Center for Vertigo and Balance Disorders, LMU University Hospital, Munich, Germany.engJournal Article20240903
United StatesJ Urban Health98099091099-3460IMHumansDelphi TechniqueWalkingAgedResidence CharacteristicsConsensusEnvironment DesignFemaleMaleBuilt EnvironmentAged, 80 and overFunctional StatusAgeDelphiFunctioningNeighborhoodQualitative researchWalkability
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2158-31881412024Aug31Translational psychiatryTransl PsychiatryCorrection: Metabolic activity of CYP2C19 and CYP2D6 on antidepressant response from 13 clinical studies using genotype imputation: a meta-analysis.35035035010.1038/s41398-024-03064-xLiDanyangD0000-0001-7470-6645Social, Genetic and Developmental Psychiatry Centre, King's College London, London, GB, UK.Cancer Centre, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, CN, China.PainOliverO0000-0001-5680-3281Maurice Wohl Clinical Neuroscience Institute, Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, GB, UK.FabbriChiaraC0000-0003-0276-7865Social, Genetic and Developmental Psychiatry Centre, King's College London, London, GB, UK.Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.WongWin Lee EdwinWLE0000-0001-6905-6449Social, Genetic and Developmental Psychiatry Centre, King's College London, London, GB, UK.Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.LoChris Wai HangCWHSocial, Genetic and Developmental Psychiatry Centre, King's College London, London, GB, UK.RipkeStephanS0000-0003-3622-835XDepartment of Psychiatry and Psychotherapy, Universitätsmedizin Berlin Campus Charité Mitte, Berlin, DE, Germany.Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.CattaneoAnnamariaA0000-0002-9963-848XBiological Psychiatry Laboratory, IRCCS Fatebenefratelli, Brescia, Italy.Department of Pharmacological and Biomedical Sciences, University of Milan, Milan, Italy.SoueryDanielDLaboratoire de Psychologie Medicale, Universitè Libre de Bruxelles and Psy Pluriel, Centre Européen de Psychologie Medicale, Brussels, Italy.DernovsekMojca ZMZ0000-0001-5344-7007University Psychiatric Clinic, University of Ljubliana, Ljubljana, Slovenia.HenigsbergNevenN0000-0002-5303-1834Department of Psychiatry, Croatian Institute for Brain Research, University of Zagreb Medical School, Zagreb, HR, Croatia.HauserJoannaJ0000-0002-6621-3493Psychiatric Genetic Unit, Poznan University of Medical Sciences, Poznan, Poland.LewisGlynG0000-0001-5205-8245Division of Psychiatry, University College London, London, GB, UK.MorsOleOPsychosis Research Unit, Aarhus University Hospital - Psychiatry, Aarhus, Denmark.PerroudNaderNDepartment of Psychiatry, Geneva University Hospitals, Geneva, CH, Switzerland.RietschelMarcellaM0000-0002-5236-6149Department of Genetic Epidemiology in Psychiatry, Medical Faculty Mannheim, University of Heidelberg, Central Institute of Mental Health, Mannheim, Denmark.UherRudolfR0000-0002-2998-0546Department of Psychiatry, Dalhousie University, Halifax, NS, Canada.MaierWolfgangWDepartment of Psychiatry and Psychotherapy, University of Bonn, Bonn, Denmark.BauneBernhard TBTDepartment of Psychiatry, University of Münster, Münster, Denmark.Florey Institute for Neuroscience and Mental Health, University of Melbourne, Melbourne, Australia.Department of Psychiatry, Melbourne Medical School, University of Melbourne, Melbourne, Australia.BiernackaJoanna MJM0000-0001-9350-4440Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, USA.Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.BondolfiGuidoGDepartment of Psychiatry, Geneva University Hospitals, Geneva, CH, Switzerland.DomschkeKatharinaK0000-0002-2550-9132Department of Psychiatry and Psychotherapy, Medical Center, University of Freiburg, Freiburg, Denmark.KatoMasakiMDepartment of Neuropsychiatry, Kansai Medical University, Osaka, Japan.LiuYu-LiYL0000-0001-7519-2965Center for Neuropsychiatric Research, National Health Research Institutes, Miaoli, Taiwan.SerrettiAlessandroADepartment of Medicine and Surgery, Kore University of Enna, Enna, Italy.TsaiShih-JenSJ0000-0002-9987-022XDepartment of Psychiatry, Taipei Veterans General Hospital, Taipei, Taiwan.Division of Psychiatry, School of Medicine, National Yang-Ming University, Taipei, Taiwan.WeinshilboumRichardR0000-0002-4911-7985Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN, USA.GSRD Consortium, the Major Depressive Disorder Working Group of the Psychiatric Genomics ConsortiumMcIntoshAndrew MAM0000-0002-0198-4588Division of Psychiatry, University of Edinburgh, Edinburgh, GB, UK.LewisCathryn MCM0000-0002-8249-8476Social, Genetic and Developmental Psychiatry Centre, King's College London, London, GB, UK. cathryn.Lewis@kcl.ac.uk.Department of Medical & Molecular Genetics, King's College London, London, GB, UK. cathryn.Lewis@kcl.ac.uk.engPublished Erratum20240831
United StatesTransl Psychiatry1015626642158-3188IMTransl Psychiatry. 2024 Jul 19;14(1):296. doi: 10.1038/s41398-024-02981-139025838
20249116172024911616202483123132024831epublish39217139PMC1136601610.1038/s41398-024-03064-x10.1038/s41398-024-03064-x
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Publications by W Maier | LitMetric

Publications by authors named "W Maier"

The species complex (FLSC) currently comprises 11 phylogenetic species, including accepted names such as , , and , which have mostly been reported in association with citrus and coffee. Many varieties were documented by Wollenweber & Reinking (1935), which is indicative of a wider diversity of species within this group. The lack of type material in some cases, especially for the older names, means that definition by molecular phylogeny is very difficult.

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Human milk oligosaccharides are of high interest as active ingredients in infant formulas and dietary food supplements. Full characterization of members of this compound class is challenging due to the intrinsic complexity of byproducts during synthesis by fermentation. Moreover, when method validation is targeted for a regulated environment, a robust chromatographic separation of the highly polar oligosaccharides needs to be addressed, including isomers and compounds relevant for potential product adulteration.

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Decisions about when to change antidepressant treatment are complex and benefit from accurate prediction of treatment outcome. Prognostic accuracy can be enhanced by incorporating repeated assessments of symptom severity collected during treatment. Participants (n = 714) from the Genome-Based Therapeutic Drugs for Depression study received escitalopram or nortriptyline over 12 weeks.

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While mobility in older age is of crucial importance for health and well-being, it is worth noting that currently, there is no German language framework for measuring walkability for older adults that also considers the functional status of a person. Therefore, we combined the results of an expert workshop, a literature review, and a Delphi consensus survey. Through this, we identified and rated indicators relevant for walkability for older adults, additionally focusing on their functional status.

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