Does subjective life expectancy matter in purchasing life insurance among middle-aged and older adult? Evidence from China. [PDF]
Chen X, Guo Y, Lu C, Wang Y, Wen H.
europepmc +1 more source
A survey of U. S. state insurance commissioners concerning genetic testing and life insurance: Redux at 27. [PDF]
Golinghorst DR, Prince AER.
europepmc +1 more source
Do Variations in State Consultation Programs Affect Construction Fatality Rates?
ABSTRACT Background Along with its enforcement program, the Occupational Safety and Health Administration (OSHA) has a voluntary consultation program that responds to requests from firms to identify hazards at their workplaces. We studied the effects of this program on fatal work injuries in the construction industry.
Wayne B. Gray, John Mendeloff
wiley +1 more source
A Systematic Review and Meta‐Analysis of the Birth Prevalence of Turner Syndrome
ABSTRACT Turner syndrome, a chromosomal disorder, causes short stature, pubertal arrest, amenorrhea, and infertility in females. Prevalence estimates vary widely; however, reliable estimates are important for public health initiatives. Therefore, a meta‐analysis was undertaken.
David Hinds +5 more
wiley +1 more source
"Uninsurable because of a genetic test": a qualitative study of consumer views about the use of genetic test results in Australian life insurance. [PDF]
Muller C +12 more
europepmc +1 more source
Does Bancassurance Affect Performance of Non-life Insurance Sector – Case of EU Countries
Tomislava Pavić Kramarić +2 more
openalex +2 more sources
Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää +14 more
wiley +1 more source
ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes +3 more
wiley +1 more source
Denial of Inpatient Genetic Testing: A Study on Outpatient Yield and Outcomes
ABSTRACT Genetic conditions suspected in children often require genetic testing for accurate diagnoses, but testing remains costly. Case management teams review genetic test requests to improve access for patients while reducing the financial burden for medical institutions.
Cindy Y. Canales +6 more
wiley +1 more source

