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Author Details

Lars G Fritsche
2005
120
42
PMIDPaper TitleJournal TitlePublished Year
37890677Systematic review of prognostic factors associated with progression to late age-related macular degeneration: Pinnacle study report 2.Surv Ophthalmol2024
37934784Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration.Hum Mol Genet2024
37425863Design and Analysis Heterogeneity in Observational Studies of COVID-19 Booster Effectiveness: A Review and Case Study.medRxiv2023
35953562Correction: Developing and validating a multivariable prediction model which predicts progression of intermediate to late age-related macular degeneration-the PINNACLE trial protocol.Eye (Lond)2023
35614343Developing and validating a multivariable prediction model which predicts progression of intermediate to late age-related macular degeneration-the PINNACLE trial protocol.Eye (Lond)2023
37945903Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.Nat Genet2023
37910111Genetic Liability to Posttraumatic Stress Disorder Symptoms and Its Association With Cardiometabolic and Respiratory Outcomes.2023
38068365Using Multi-Modal Electronic Health Record Data for the Development and Validation of Risk Prediction Models for Long COVID Using the Super Learner Algorithm.2023
37624605Comparison of Novel Volumetric Microperimetry Metrics in Intermediate Age-Related Macular Degeneration: PINNACLE Study Report 3.Transl Vis Sci Technol2023
37090583Incorporating functional annotation with bilevel continuous shrinkage for polygenic risk prediction.2023
36835863Characterizing and Predicting Post-Acute Sequelae of SARS CoV-2 Infection (PASC) in a Large Academic Medical Center in the US.2023
36510710Identifying the prevalence of clinically actionable drug-gene interactions in a health system biorepository to guide pharmacogenetics implementation services.2023
36626383COVID-19 Outcomes by Cancer Status, Site, Treatment, and Vaccination.Cancer Epidemiol Biomarkers Prev2023
36739617A fast linkage method for population GWAS cohorts with related individuals.Genet Epidemiol2023
37113474Exploring Healthy Retinal Aging with Deep Learning.Ophthalmol Sci2023
34913882Unbiased immune profiling reveals a natural killer cell-peripheral nerve axis in fibromyalgia.Pain2022
35710628Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT.Commun Biol2022
36240765The construction of cross-population polygenic risk scores using transfer learning.American Journal of Human Genetics2022
35965108Polygenic Liability to Depression Is Associated With Multiple Medical Conditions in the Electronic Health Record: Phenome-wide Association Study of 46,782 Individuals.Biological Psychiatry2022
36283580A Case-Crossover Phenome-wide association study (PheWAS) for understanding Post-COVID-19 diagnosis patterns.Journal of Biomedical Informatics2022
36152628ExPRSweb: An online repository with polygenic risk scores for common health-related exposures.American Journal of Human Genetics2022
35877617Assessing the added value of linking electronic health records to improve the prediction of self-reported COVID-19 testing and diagnosis.PLoS ONE2022
35429399Global Prevalence of Post-Coronavirus Disease 2019 (COVID-19) Condition or Long COVID: A Meta-Analysis and Systematic Review.Journal of Infectious Diseases2022
35726068Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease.Nat Genet2022
36415469Characterizing and Predicting Post-Acute Sequelae of SARS CoV-2 infection (PASC) in a Large Academic Medical Center in the US.2022
36777998The HUNT study: A population-based cohort for genetic research.Cell Genom2022
36942016Estimating COVID-19 Vaccination and Booster Effectiveness Using Electronic Health Records From an Academic Medical Center in Michigan.2022
34529658On cross-ancestry cancer polygenic risk scores.PLoS Genetics2021
32433920Assessment of a causal relationship between body mass index and atopic dermatitis.J Allergy Clin Immunol2021
33805886A Phenome-Wide Association Study (PheWAS) of COVID-19 Outcomes by Race Using the Electronic Health Records Data in Michigan Medicine.J Clin Med2021
33961016Genome-wide association study of cardiac troponin I in the general population.Hum Mol Genet2021
33888516Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease.Gut2021
33730541A powerful subset-based method identifies gene set associations and improves interpretation in UK Biobank.Am J Hum Genet2021
34325054Cluster Analysis and Genotype-Phenotype Assessment of Geographic Atrophy in Age-Related Macular Degeneration: Age-Related Eye Disease Study 2 Report 25.Ophthalmol Retina2021
33253457Patterns of repeated diagnostic testing for COVID-19 in relation to patient characteristics and outcomes.Journal of Internal Medicine2021
32793923A phenome-wide association study (PheWAS) of COVID-19 outcomes by race using the electronic health records data in Michigan Medicine.medRxiv2021
33279681Phenotype risk scores (PheRS) for pancreatic cancer using time-stamped electronic health record data: Discovery and validation in two large biobanks.J Biomed Inform2021
34746691Type 2 diabetes sex-specific effects associated with E167K coding variant in .iScience2021
34916535Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer.Nat Commun2021
34773122Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease.Nat Genet2021
34640359Understanding the Patterns of Serological Testing for COVID-19 Pre- and Post-Vaccination Rollout in Michigan.Journal of Clinical Medicine2021
30936278Prediction of Ankylosing Spondylitis in the HUNT Study by a Genetic Risk Score Combining 110 Single-nucleotide Polymorphisms of Genome-wide Significance.Journal of Rheumatology2020
32198773An analytic framework for exploring sampling and observation process biases in genome and phenome-wide association studies using electronic health records.Statistics in Medicine2020
32424355Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts.Nat Genet2020
31736264Heritability of the Fibromyalgia Phenotype Varies by Age.Arthritis and Rheumatology2020
32056457Mitochondrial genome-wide association study of migraine - the HUNT Study.Cephalalgia2020
32341527Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.Nat Genet2020
31866045UK Biobank Whole-Exome Sequence Binary Phenome Analysis with Robust Region-Based Rare-Variant Test.American Journal of Human Genetics2020
31859414The emerging landscape of health research based on biobanks linked to electronic health records: Existing resources, statistical challenges, and potential opportunities.Stat Med2020
34317346A Novel Variant in Gene Causes Extremely Low LDL-C Without Known Adverse Effects.JACC: Case Reports2020
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