Search Results - "Fritsche, G"
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A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank
Published in American journal of human genetics (06-08-2020)“…With increasing biobanking efforts connecting electronic health records and national registries to germline genetics, the time-to-event data analysis has…”
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Evidence of a causal relationship between body mass index and psoriasis: A mendelian randomization study
Published in PLoS medicine (31-01-2019)“…Psoriasis is a common inflammatory skin disease that has been reported to be associated with obesity. We aimed to investigate a possible causal relationship…”
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Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies
Published in Nature genetics (01-09-2018)“…In genome-wide association studies (GWAS) for thousands of phenotypes in large biobanks, most binary traits have substantially fewer cases than controls. Both…”
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On cross-ancestry cancer polygenic risk scores
Published in PLoS genetics (16-09-2021)“…Polygenic risk scores (PRS) can provide useful information for personalized risk stratification and disease risk assessment, especially when combined with…”
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Exploring and visualizing large-scale genetic associations by using PheWeb
Published in Nature genetics (01-06-2020)“…The ability of investigators to explore their own data by alternating between these two view types, is an increasingly common feature of large-scale…”
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Age-Related Macular Degeneration: Genetics and Biology Coming Together
Published in Annual review of genomics and human genetics (01-01-2014)“…Genetic and genomic studies have enhanced our understanding of complex neurodegenerative diseases that exert a devastating impact on individuals and society…”
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Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative
Published in American journal of human genetics (07-06-2018)“…Health systems are stewards of patient electronic health record (EHR) data with extraordinarily rich depth and breadth, reflecting thousands of diagnoses and…”
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Interaction analysis under misspecification of main effects: Some common mistakes and simple solutions
Published in Statistics in medicine (20-05-2020)“…The statistical practice of modeling interaction with two linear main effects and a product term is ubiquitous in the statistical and epidemiological…”
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The emerging landscape of health research based on biobanks linked to electronic health records: Existing resources, statistical challenges, and potential opportunities
Published in Statistics in medicine (15-03-2020)“…Biobanks linked to electronic health records provide rich resources for health‐related research. With improvements in administrative and informatics…”
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Incorporating functional annotation with bilevel continuous shrinkage for polygenic risk prediction
Published in BMC bioinformatics (09-02-2024)“…Genetic variants can contribute differently to trait heritability by their functional categories, and recent studies have shown that incorporating functional…”
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Assessing the added value of linking electronic health records to improve the prediction of self-reported COVID-19 testing and diagnosis
Published in PloS one (25-07-2022)“…Since the beginning of the Coronavirus Disease 2019 (COVID-19) pandemic, a focus of research has been to identify risk factors associated with COVID-19-related…”
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Uncovering associations between pre-existing conditions and COVID-19 Severity: A polygenic risk score approach across three large biobanks
Published in PLoS genetics (01-12-2023)“…To overcome the limitations associated with the collection and curation of COVID-19 outcome data in biobanks, this study proposes the use of polygenic risk…”
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Systemic complement activation in age-related macular degeneration
Published in PloS one (02-07-2008)“…Dysregulation of the alternative pathway (AP) of complement cascade has been implicated in the pathogenesis of age-related macular degeneration (AMD), the…”
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Genome-wide analysis of disease progression in age-related macular degeneration
Published in Human molecular genetics (01-03-2018)“…Abstract Family- and population-based genetic studies have successfully identified multiple disease-susceptibility loci for Age-related macular degeneration…”
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Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk
Published in Human molecular genetics (01-11-2005)“…Age-related macular degeneration (AMD) is a multifactorial disease and a prevalent cause of visual impairment in developed countries. Risk factors include…”
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Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis
Published in Nature communications (23-04-2019)“…Chronic kidney disease (CKD) is a growing health burden currently affecting 10–15% of adults worldwide. Estimated glomerular filtration rate (eGFR) as a marker…”
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CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors
Published in Genome research (01-11-2010)“…Approximately 98% of mammalian DNA is noncoding, yet we understand relatively little about the function of this enigmatic portion of the genome. The…”
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An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD)
Published in Human molecular genetics (01-12-2010)“…A frequent deletion of complement factor H (CFH)-related genes CFHR3 and CFHR1 (ΔCFHR3/CFHR1) is considered to have a protective effect against age-related…”
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Assessment of a causal relationship between body mass index and atopic dermatitis
Published in Journal of allergy and clinical immunology (01-01-2021)Get full text
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Patterns of repeated diagnostic testing for COVID‐19 in relation to patient characteristics and outcomes
Published in Journal of internal medicine (01-05-2021)“…Background Whilst the COVID‐19 diagnostic test has a high false‐negative rate, not everyone initially negative is re‐tested. Michigan Medicine, a primary…”
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