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Life insurance

About: Life insurance is a research topic. Over the lifetime, 9950 publications have been published within this topic receiving 171487 citations. The topic is also known as: life assurance & NACE 65.11.


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Journal ArticleDOI
TL;DR: Acemoglu, Johnson, and Robinson as discussed by the authors used estimates of potential European settler mortality as an instrument for institutional variation in former European colonies today, and they followed the lead of Curtin who compiled data on the death rates faced by European soldiers in various overseas postings.
Abstract: In Acemoglu, Johnson, and Robinson, henceforth AJR, (2001), we advanced the hypothesis that the mortality rates faced by Europeans in different parts of the world after 1500 affected their willingness to establish settlements and choice of colonization strategy. Places that were relatively healthy (for Europeans) were—when they fell under European control—more likely to receive better economic and political institutions. In contrast, places where European settlers were less likely to go were more likely to have “extractive” institutions imposed. We also posited that this early pattern of institutions has persisted over time and influences the extent and nature of institutions in the modern world. On this basis, we proposed using estimates of potential European settler mortality as an instrument for institutional variation in former European colonies today. Data on settlers themselves are unfortunately patchy—particularly because not many went to places they believed, with good reason, to be most unhealthy. We therefore followed the lead of Curtin (1989 and 1998) who compiled data on the death rates faced by European soldiers in various overseas postings. 1 Curtin’s data were based on pathbreaking data collection and statistical work initiated by the British military in the mid-nineteenth century. These data became part of the foundation of both contemporary thinking about public health (for soldiers and for civilians) and the life insurance industry (as actuaries and executives considered the

6,495 citations

Journal ArticleDOI
TL;DR: It is a cause of rejoicing to be able to speak here today of World Health Statistics, not as one of the many desiderata still needed as a basis for a vigorous and wholesome international life, but as an accomplished fact.
Abstract: IT IS a cause of rejoicing to be able to speak here today of World Health Statistics, not as one of the many desiderata still needed as a basis for a vigorous and wholesome international life, but as an accomplished fact. When we are now primarily concerned with further extension, betterment of quality, and problems of comparability of world health statistics, our younger colleagues are apt to forget that the very creation of the system is of such a recent date that several of its pioneers are still with us. More than thirty years ago, while in the service of the Prudential Insurance Company of America, one of my daily tasks consisted of preparing ratings for extra life insurance premiums payable by Americans who were foolhardy enough to insist on travelling abroad. Our collection of mortality statistics and of information on health conditions in foreign countries was one of the very best existing at the time. Nevertheless, by far the most weighty ingredient of the brew was an arbitrary loading. Today there is a steady flow of valuable information from all parts of the world, and it is readily and promptly accessible to anyone who takes the trouble to ask for it. The history of health statistics as an international enterprise falls into three major periods. The first period, which lasted up to 1921, was characterized by private initiative. Then came the League of Nations period of a quarter of a century's duration. The third period, barely arising from our blueprints, is under the auspices of the United Nations and its specialized agencies, notably the World Health Organization. While inter-governmental organizations have taken the lead since 1921, private initiative is not dispensed with. Also, it should be remembered that no organization, however strategically placed, is better than the men who furnish the leadership and the daily work.

2,551 citations

Journal ArticleDOI
TL;DR: A revised Ghent nosology is established, which puts more weight on the cardiovascular manifestations and in which aortic root aneurysm and ectopia lentis are the cardinal clinical features and may delay a definitive diagnosis of MFS but will decrease the risk of premature or misdiagnosis.
Abstract: The diagnosis of Marfan syndrome (MFS) relies on defined clinical criteria (Ghent nosology), outlined by international expert opinion to facilitate accurate recognition of this genetic aneurysm syndrome and to improve patient management and counselling. These Ghent criteria, comprising a set of major and minor manifestations in different body systems, have proven to work well since with improving molecular techniques, confirmation of the diagnosis is possible in over 95% of patients. However, concerns with the current nosology are that some of the diagnostic criteria have not been sufficiently validated, are not applicable in children or necessitate expensive and specialised investigations. The recognition of variable clinical expression and the recently extended differential diagnosis further confound accurate diagnostic decision making. Moreover, the diagnosis of MFS—whether or not established correctly—can be stigmatising, hamper career aspirations, restrict life insurance opportunities, and cause psychosocial burden. An international expert panel has established a revised Ghent nosology, which puts more weight on the cardiovascular manifestations and in which aortic root aneurysm and ectopia lentis are the cardinal clinical features. In the absence of any family history, the presence of these two manifestations is sufficient for the unequivocal diagnosis of MFS. In absence of either of these two, the presence of a bonafide FBN1 mutation or a combination of systemic manifestations is required. For the latter a new scoring system has been designed. In this revised nosology, FBN1 testing, although not mandatory, has greater weight in the diagnostic assessment. Special considerations are given to the diagnosis of MFS in children and alternative diagnoses in adults. We anticipate that these new guidelines may delay a definitive diagnosis of MFS but will decrease the risk of premature or misdiagnosis and facilitate worldwide discussion of risk and follow-up/management guidelines.

1,663 citations

Book
05 Dec 2000
TL;DR: In this article, the authors present a risk analysis approach based on Monte-Carlo simulation, which is used to fit a first-order parametric distribution to observed data and then combine it with a second-order probability distribution.
Abstract: Preface. Part 1: Introduction. 1. Why do a risk analysis? 1.1. Moving on from "What If" Scenarios. 1.2. The Risk Analysis Process. 1.3. Risk Management Options. 1.4. Evaluating Risk Management Options. 1.5. Inefficiencies in Transferring Risks to Others. 1.6. Risk Registers. 2. Planning a risk analysis. 2.1. Questions and Motives. 2.2. Determine the Assumptions that are Acceptable or Required. 2.3. Time and Timing. 2.4. You'll Need a Good Risk Analyst or Team. 3. The quality of a risk analysis. 3.1. The Reasons Why a Risk Analysis can be Terrible. 3.2. Communicating the Quality of Data Used in a Risk Analysis. 3.3. Level of Criticality. 3.4. The Biggest Uncertainty in a Risk Analysis. 3.5. Iterate. 4. Choice of model structure. 4.1. Software Tools and the Models they Build. 4.2. Calculation Methods. 4.3. Uncertainty and Variability. 4.4. How Monte Carlo Simulation Works. 4.5. Simulation Modelling. 5. Understanding and using the results of a risk analysis. 5.1. Writing a Risk Analysis Report. 5.2. Explaining a Model's Assumptions. 5.3. Graphical Presentation of a Model's Results. 5.4. Statistical Methods of Analysing Results. Part 2: Introduction. 6. Probability mathematics and simulation. 6.1. Probability Distribution Equations. 6.2. The Definition of "Probability". 6.3. Probability Rules. 6.4. Statistical Measures. 7. Building and running a model. 7.1. Model Design and Scope. 7.2. Building Models that are Easy to Check and Modify. 7.3. Building Models that are Efficient. 7.4. Most Common Modelling Errors. 8. Some basic random processes. 8.1. Introduction. 8.2. The Binomial Process. 8.3. The Poisson Process. 8.4. The Hypergeometric Process. 8.5. Central Limit Theorem. 8.6. Renewal Processes. 8.7. Mixture Distributions. 8.8. Martingales. 8.9. Miscellaneous Example. 9. Data and statistics. 9.1. Classical Statistics. 9.2. Bayesian Inference. 9.3. The Bootstrap. 9.4. Maximum Entropy Principle. 9.5. Which Technique Should You Use? 9.6. Adding uncertainty in Simple Linear Least-Squares Regression Analysis. 10. Fitting distributions to data. 10.1. Analysing the Properties of the Observed Data. 10.2. Fitting a Non-Parametric Distribution to the Observed Data. 10.3. Fitting a First-Order Parametric Distribution to Observed Data. 10.4. Fitting a Second-Order Parametric Distribution to Observed Data. 11. Sums of random variables. 11.1. The Basic Problem. 11.2. Aggregate Distributions. 12. Forecasting with uncertainty. 12.1. The Properties of a Time Series Forecast. 12.2. Common Financial Time Series Models. 12.3. Autoregressive Models. 12.4. Markov Chain Models. 12.5. Birth and Death Models. 12.6. Time Series Projection of Events Occurring Randomly in Time. 12.7. Time Series Models with Leading Indicators. 12.8. Comparing Forecasting Fits for Different Models. 12.9. Long-Term Forecasting. 13. Modelling correlation and dependencies. 13.1. Introduction. 13.2. Rank Order Correlation. 13.3. Copulas. 13.4. The Envelope Method. 13.5. Multiple Correlation Using a Look-Up Table. 14. Eliciting from expert opinion. 14.1. Introduction. 14.2. Sources of Error in Subjective Estimation. 14.3. Modelling Techniques. 14.4. Calibrating Subject Matter Experts. 14.5. Conducting a Brainstorming Session. 14.6. Conducting the Interview. 15. Testing and modelling causal relationships. 15.1. Campylobacter Example. 15.2. Types of Model to Analyse Data. 15.3. From Risk Factors to Causes. 15.4. Evaluating Evidence. 15.5. The Limits of Causal Arguments. 15.6. An Example of a Qualitative Causal Analysis. 15.7. Is Causal Analysis Essential? 16. Optimisation in risk analysis. 16.1. Introduction. 16.2. Optimisation Methods. 16.3. Risk Analysis Modelling and Optimisation. 16.4. Working Example: Optimal Allocation of Mineral Pots. 17. Checking and validating a model. 17.1. Spreadsheet Model Errors. 17.2. Checking Model Behaviour. 17.3. Comparing Predictions Against Reality. 18. Discounted cashflow modelling. 18.1. Useful Time Series Models of Sales and Market Size. 18.2. Summing Random Variables. 18.3. Summing Variable Margins on Variable Revenues. 18.4. Financial Measures in Risk Analysis. 19. Project risk analysis. 19.1. Cost Risk Analysis. 19.2. Schedule Risk Analysis. 19.3. Portfolios of risks. 19.4. Cascading Risks. 20. Insurance and finance risk analysis modelling. 20.1. Operational Risk Modelling. 20.2. Credit Risk. 20.3. Credit Ratings and Markov Chain Models. 20.4. Other Areas of Financial Risk. 20.5. Measures of Risk. 20.6. Term Life Insurance. 20.7. Accident Insurance. 20.8. Modelling a Correlated Insurance Portfolio. 20.9. Modelling Extremes. 20.10. Premium Calculations. 21. Microbial food safety risk assessment. 21.1. Growth and Attenuation Models. 21.2. Dose-Response Models. 21.3. Is Monte Carlo Simulation the Right Approach? 21.4. Some Model Simplifications. 22. Animal import risk assessment. 22.1. Testing for an Infected Animal. 22.2. Estimating True Prevalence in a Population. 22.3. Importing Problems. 22.4. Confidence of Detecting an Infected Group. 22.5. Miscellaneous Animal Health and Food Safety Problems. I. Guide for lecturers. II. About ModelRisk. III. A compendium of distributions. III.1. Discrete and Continuous Distributions. III.2. Bounded and Unbounded Distributions. III.3. Parametric and Non-Parametric Distributions. III.4. Univariate and Multivariate Distributions. III.5. Lists of Applications and the Most Useful Distributions. III.6. How to Read Probability Distribution Equations. III.7. The Distributions. III.8. Introduction to Creating Your Own Distributions. III.9. Approximation of One Distribution with Another. III.10. Recursive Formulae for Discrete Distributions. III.11. A Visual Observation On The Behaviour Of Distributions. IV. Further reading. V. Vose Consulting. References. Index.

1,606 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023132
2022316
2021314
2020356
2019355
2018362