Individual, personalized genetic information is increasingly available, leading to the possibility of greater adverse selection over time, particularly in individual-payer insurance markets. We use data on individuals at risk for Huntington disease (HD), a degenerative neurological disorder with significant effects on morbidity, to estimate adverse selection in long-term care insurance. We find strong evidence of adverse selection: individuals who carry the HD genetic mutation are up to 5 times as likely as the general population to own long-term care insurance. This finding is supported both by comparing individuals at risk for HD to those in the general population and by comparing across tested individuals in the HD-risk population with a...
BACKGROUND: Huntington's disease (HD) is an inherited neurodegenerative disorder caused by an expand...
The majority of individuals at risk for Huntington disease (HD) is afraid to learn more precisely ab...
Background: In addition to the effects on patients suffering from motor-manifest Hunting-ton’s dise...
Individual, personalized genetic information is increasingly available, leading to the possibility o...
We describe briefly a model of Huntington’s disease (HD), a highly penetrant, dominantly inherited, ...
We use novel data to study genetic testing among individuals at risk for Huntington disease (HD), a ...
Huntington disease (HD), the “Dancing Mania” of the Middle Ages, has always been a particular target...
Rapid advances in genetic epidemiology and the setting up of large-scale cohort studies have shifted...
We apply a model of Alzheimer’s Disease developed by Macdonald & Pritchard (1999) to the questio...
Huntington’s is a genetic neurodegenerative disease with dominant autosomal transmission, and high p...
The focus of genetics is shifting its contribution to common, complex disorders. New genetic risk fa...
Huntington disease (HD) is a late onset ultimately fatal neurodegenerative disorder caused by a cyto...
The dissertation can be viewed at as a contribution to the discussion about using genetic informatio...
As a Mendelian neurodegenerative disorder, the genetic risk of Huntington's disease (HD) is conferre...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN051862 / BLDSC - British Library D...
BACKGROUND: Huntington's disease (HD) is an inherited neurodegenerative disorder caused by an expand...
The majority of individuals at risk for Huntington disease (HD) is afraid to learn more precisely ab...
Background: In addition to the effects on patients suffering from motor-manifest Hunting-ton’s dise...
Individual, personalized genetic information is increasingly available, leading to the possibility o...
We describe briefly a model of Huntington’s disease (HD), a highly penetrant, dominantly inherited, ...
We use novel data to study genetic testing among individuals at risk for Huntington disease (HD), a ...
Huntington disease (HD), the “Dancing Mania” of the Middle Ages, has always been a particular target...
Rapid advances in genetic epidemiology and the setting up of large-scale cohort studies have shifted...
We apply a model of Alzheimer’s Disease developed by Macdonald & Pritchard (1999) to the questio...
Huntington’s is a genetic neurodegenerative disease with dominant autosomal transmission, and high p...
The focus of genetics is shifting its contribution to common, complex disorders. New genetic risk fa...
Huntington disease (HD) is a late onset ultimately fatal neurodegenerative disorder caused by a cyto...
The dissertation can be viewed at as a contribution to the discussion about using genetic informatio...
As a Mendelian neurodegenerative disorder, the genetic risk of Huntington's disease (HD) is conferre...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN051862 / BLDSC - British Library D...
BACKGROUND: Huntington's disease (HD) is an inherited neurodegenerative disorder caused by an expand...
The majority of individuals at risk for Huntington disease (HD) is afraid to learn more precisely ab...
Background: In addition to the effects on patients suffering from motor-manifest Hunting-ton’s dise...