[HTML][HTML] The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care …
Advances in genomics have led to mounting expectations in regard to their impact on health
care and disease prevention. In light of this fact, a comprehensive research agenda is …
care and disease prevention. In light of this fact, a comprehensive research agenda is …
Diagnosis and monitoring of hepatic injury. II. Recommendations for use of laboratory tests in screening, diagnosis, and monitoring
DR Dufour, JA Lott, FS Nolte, DR Gretch… - Clinical …, 2000 - academic.oup.com
Purpose: To review information on the use of laboratory tests in screening, diagnosis, and
monitoring of acute and chronic hepatic injury. Data Sources and Study Selection: A …
monitoring of acute and chronic hepatic injury. Data Sources and Study Selection: A …
Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank
Objective To compare prevalent and incident morbidity and mortality between those with the
HFE p. C282Y genetic variant (responsible for most hereditary haemochromatosis type 1) …
HFE p. C282Y genetic variant (responsible for most hereditary haemochromatosis type 1) …
Medical and societal consequences of the human genome project
FS Collins - New England Journal of Medicine, 1999 - Mass Medical Soc
The history of biology was forever altered a decade ago by the bold decision to launch a
research program that would characterize in ultimate detail the complete set of genetic …
research program that would characterize in ultimate detail the complete set of genetic …
HFE Gene and Hereditary Hemochromatosis: A HuGE Review
EH Hanson, G Imperatore… - American journal of …, 2001 - academic.oup.com
Hereditary hemochromatosis (HHC) is an autosomal recessive disorder of iron metabolism
characterized by increased iron absorption and deposition in the liver, pancreas, heart …
characterized by increased iron absorption and deposition in the liver, pancreas, heart …
A population-based study of the clinical expression of the hemochromatosis gene
JK Olynyk, DJ Cullen, S Aquilia, E Rossi… - … England Journal of …, 1999 - Mass Medical Soc
Background and Methods Hereditary hemochromatosis is associated with homozygosity for
the C282Y mutation in the hemochromatosis (HFE) gene on chromosome 6, elevated serum …
the C282Y mutation in the hemochromatosis (HFE) gene on chromosome 6, elevated serum …
Population screening in the age of genomic medicine
MJ Khoury, LL McCabe… - New England Journal of …, 2003 - Mass Medical Soc
Newborns are now routinely screened for the presence of a number of inherited diseases. In
these cases, early diagnosis allows treatment to be instituted before there are irreversible …
these cases, early diagnosis allows treatment to be instituted before there are irreversible …
[KSIĄŻKA][B] The Dependent Gene: The Fallacy of" nature Vs. Nurture"
DS Moore - 2003 - books.google.com
A masterful guide to human development that redefines the nature versus nurture debate A
much-needed antidote to genetic determinism, The Dependent Gene reveals how all traits …
much-needed antidote to genetic determinism, The Dependent Gene reveals how all traits …
Screening for hemochromatosis: high prevalence and low morbidity in an unselected population of 65,238 persons
Background: Hereditary hemochromatosis (HH) is a common genetic disease leading to
accumulation of iron in several organs, most notably the liver. The C282Y/C282Y mutation in …
accumulation of iron in several organs, most notably the liver. The C282Y/C282Y mutation in …
The complexities of predictive genetic testing
JP Evans, C Skrzynia, W Burke - Bmj, 2001 - bmj.com
Predictive genetic testing is the use of a genetic test in an asymptomatic person to predict
future risk of disease. These tests represent a new and growing class of medical tests …
future risk of disease. These tests represent a new and growing class of medical tests …