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Author Details

Krista Fischer
1999
129
49
PMIDPaper TitleJournal TitlePublished Year
37543033Genetic insights into the age-specific biological mechanisms governing human ovarian aging.Am J Hum Genet2023
36192438Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank.European Journal of Human Genetics2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37237050A retrospective cohort study of incidence and risk factors for severe SARS-CoV-2 breakthrough infection among fully vaccinated people.2023
37296919Polygenic Risk Score Predicts Modified Risk in Pathogenic Variant c.4035del and c.5266dup Carriers in Breast Cancer Patients.2023
35287021The 1<sup>st</sup> year of the COVID-19 epidemic in Estonia: a population-based nationwide sequential/consecutive cross-sectional study.Public Health2022
35653391Using genetic variation to disentangle the complex relationship between food intake and health outcomes.PLoS Genet2022
35966513Novel Early Pregnancy Multimarker Screening Test for Preeclampsia Risk Prediction.Frontiers in Cardiovascular Medicine2022
35505834Long-term mortality following SARS-CoV-2 infection: A national cohort study from Estonia.Lancet Regional Health - Europe, The2022
35504910DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases.Nat Commun2022
35938029Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting.Frontiers in Genetics2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
35923706A Principal Component Informed Approach to Address Polygenic Risk Score Transferability Across European Cohorts.Front Genet2022
36600884Effectiveness and feasibility of cardiovascular disease personalized prevention on high polygenic risk score subjects: a randomized controlled pilot study.2022
35073279A catalogue of omics biological ageing clocks reveals substantial commonality and associations with disease risk.Aging2022
34930164Evaluating the prognostic performance of a polygenic risk score for breast cancer risk stratification.BMC Cancer2021
32064741Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.Addict Biol2021
33594006Machine Learning Reveals Time-Varying Microbial Predictors with Complex Effects on Glucose Regulation.mSystems2021
33946982Advances in Genomic Discovery and Implications for Personalized Prevention and Medicine: Estonia as Example.J Pers Med2021
33879782Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis.Nat Commun2021
32893372Gallstones, Body Mass Index, C-Reactive Protein, and Gallbladder Cancer: Mendelian Randomization Analysis of Chilean and European Genotype Data.Hepatology2021
33268560Association of Circulating Metabolites in Plasma or Serum and Risk of Stroke: Meta-analysis From 7 Prospective Cohorts.Neurology2021
34790224Mendelian Randomization Identifies the Potential Causal Impact of Dietary Patterns on Circulating Blood Metabolites.Frontiers in Genetics2021
34670499Adherence to recommendations for secondary prevention medications after myocardial infarction in Estonia: comparison of real-world data from 2004 to 2005 and 2017 to 2018.BMC Cardiovascular Disorders2021
34358839Development of the Gastrointestinal Dysfunction Score (GIDS) for critically ill patients - A prospective multicenter observational study (iSOFA study).Clinical Nutrition2021
33011775Development and validation of two SCORE-based cardiovascular risk prediction models for Eastern Europe: a multicohort study.European Heart Journal2020
31846055Arsenic and gallbladder cancer risk: Mendelian randomization analysis of European prospective data.Int J Cancer2020
32128391Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases.Sci Adv2020
32242022Ancestry deconvolution and partial polygenic score can improve susceptibility predictions in recently admixed individuals.Nature Communications2020
32058310ABCB1/4 gallbladder cancer risk variants identified in India also show strong effects in Chileans.Cancer Epidemiol2020
32467615Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolome.Int J Obes (Lond)2020
32537749Validating the doubly weighted genetic risk score for the prediction of type 2 diabetes in the Lifelines and Estonian Biobank cohorts.Genet Epidemiol2020
31161197Food neophobia associates with poorer dietary quality, metabolic risk factors, and increased disease outcome risk in population-based cohorts in a metabolomics study.American Journal of Clinical Nutrition2019
31557729Circulating glucuronic acid predicts healthspan and longevity in humans and mice.Aging2019
30191727A meta-analysis of Italian and Estonian individuals shows an effect of common variants in on blood apoB levels.Biomarkers in Medicine2019
30640898PAIRUP-MS: Pathway analysis and imputation to relate unknowns in profiles from mass spectrometry-based metabolite data.PLoS Comput Biol2019
30635435Estimating the performance of three cardiovascular disease risk scores: the Estonian Biobank cohort study.Journal of Epidemiology and Community Health2019
31182048Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification.BMC Cancer2019
31080514Parents of early-maturing girls die younger.Evolutionary Applications2019
29316447Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies.Alzheimers Dement2018
29034571Association between subclinical thyroid dysfunction and change in bone mineral density in prospective cohorts.J Intern Med2018
30121176The risk-treatment paradox in non-ST-elevation myocardial infarction patients according to their estimated GRACE risk.International Journal of Cardiology2018
30442561Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults.EBioMedicine2018
30297969Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.Nat Genet2018
30388399Genome Analyses of &gt;200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.Am J Hum Genet2018
29519576Association of branched-chain amino acids and other circulating metabolites with risk of incident dementia and Alzheimer's disease: A prospective study in eight cohorts.Alzheimers Dement2018
29632382Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.Nat Genet2018
28209135MARV: a tool for genome-wide multi-phenotype analysis of rare variants.BMC Bioinformatics2017
28855160Education and coronary heart disease: mendelian randomisation study.BMJ2017
28724413Smoking-related general and cause-specific mortality in Estonia.BMC Public Health2017
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Erasmus University Medical Center
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University of Oxford
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Harvard T.H. Chan School of Public Health
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Ludwig-Maximilians-Universitat Munchen
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Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
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King's College London
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German Research Center for Cardiovascular Disease (DZHK)
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Stanford University School of Medicine
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University of Lausanne
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University of Iceland
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University of Iceland
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