elsiatcase's Markel:H [6 articles] Export Sort

Recent papers posted to elsiatcase's library by the author Markel:H. You can also see everyone's Markel:H.

Hide details

	The stigma of disease: implications of genetic screening. [My Copy] Am J Med, Vol. 93, No. 2. (August 1992), pp. 209-215. by H. Markel posted to eugenics genetic-screening historical-perspective sickle-cell-anemia by elsiatcase on 2006-10-08 20:03:09 as
	Di Goldine Medina (The Golden Land): Historical Perspectives of Eugenics and the East European (Ashkenazi) Jewish-American Community, 1880-1925 [My Copy] Health Matrix, Vol. 7, No. 49., pp. 49-64. by Howard Markel posted to ashkenazi brac1-in-historical-cultural-context ethnicity-and-eugenics eugenics historical-perspective immigration jewish by elsiatcase on 2006-10-07 14:01:06 as
	"Knocking out the Cholera": Cholera, Class, and Quarantines in New York City, 1892 [My Copy] Bull. Hist. Med., Vol. 69 (1995), pp. 420-457. by Howard Markel posted to cholera class historical-perspective immigration public-health quarantine by elsiatcase on 2006-10-07 13:55:04 as
	Appendix 6 : Scientific Advances and Social Risks: Historical Perspectives of Genetic Screening Programs for Sickle Cell Disease, Tay-Sachs Disease, Neural Tube Defects and Down Syndrome, 1970-1997. [My Copy] pp. 161-176. by Howard Markel posted to african-american alpha-fetoprotein down-syndrome genetic-screening-programs historical-perspective importance-of-including-community-in-screening-programs jewish misinterpretation-of-test-results neural-tube-defects race-ethnicity-and-genetic-disease sickle-cell-disease tay-sachs-disease by elsiatcase on 2006-10-07 13:52:19 as
	Cholera, Quarantines, and Immigration Restriction: the View from Johns Hopkins, 1892 [My Copy] Bull. Hist. Med., Vol. 67 (1993), pp. 691-695. by Howard Markel posted to cholera history immigration-restriction public-health-policy quarantine by elsiatcase on 2006-10-07 02:52:46 as
	A Gate to the City: the Baltimore Quarantine Station, 1918-28 [My Copy] Public Health Reports, Vol. 110, No. 2. (March-April 1995), pp. 218-219. by Howard Markel posted to history public-health-policy quarantine stations by elsiatcase on 2006-10-07 02:49:50 as

Note: You may cite this page as: http://www.citeulike.org/user/elsiatcase/author/Markel:H

elsiatcase's tags

All tags in elsiatcase's library

Filter:

Only showing top 500 tags from 1730 total.

Privacy Statement | Terms & Conditions

Sort by:
Order:	Default Ascending Descending
Empty fields:	Default First Last

genetic-testing	105
genetics-and-law	80
genetic-counseling	55
policy	48
genetics	48
legal	48
ethics	43
attitudes	39
human-genome-project	39
genetic-discrimination	38
race	35
informed-consent	35
cystic-fibrosis	34
brca1	33
prenatal	33
privacy	32
genetic-research	29
breast-cancer	24
family-relations	23
amniocentesis	22
brca2	21
testing	20
behavioral-genetics	20
genetic-ancestry-tracing	20
genetics-and-media	20
genetic	19
confidentiality	19
pharmacogenomics	18
genetics-and-popular-culture	18
disclosure	18
diagnosis	18
medical-decision-making	17
ethnicity	16
health	16
screening	16
commercialization	15
predictive-genetic-testing-adult	14
reproductive	14
genetic-screening	14
genomics	13
health-insurance	13
prenatal-diagnosis	13
genetic-education	13
newborn-screening	13
race-and-genetics	13
predictive-genetic-testing	13
population-genetics	13
third-party-access	12
genetics-and-identity	12
intellectual-property	12
cancer	12
insurance	12
reproductive-health	12
prenatal-testing	11
medical	11
patents	11
family-history	10
identity	10
genetic-information	10
communication	10
african-american	10
employment	9
feminist	9
ethical	9
genetic-privacy	9
native-american	9
decision-making	9
of	9
gender-differences	9
genetic-exceptionalism	9
ethical-issues	9
eugenics	9
technology	8
african-americans	8
science-reporting	8
health-disparities	8
disability	8
carrier-screening	8
pregnant-women	8
historical-perspective	8
abortion	8
bioethics	8
discrimination	8
alzheimers-disease	8
community-engagement	8
jewish	8
biobanks	8
mexican-americans	8
latinas	7
cancer-genetics	7
primary-care-physicians	7
international	7
minors	7
dna-files	7
carrier-testing	7
gene-patenting	7
research-ethics	7
law	7
dna-and-identity	7
guidelines	7
physicians	7
genetic-determinism	7
reproduction	7
minorities	7
human-genetic-variation	7
human-genetics	7
prenatal-genetic-testing	7
research	6
autonomy	6
lemba	6
public-policy	6
at-risk-women	6
cultural-sensitivity	6
gender	6
family-dynamics	6
dna-samples	6
national-public-radio-transcript	6
family-studies	6
cost-effectiveness	6
primary-care	6
elsi	6
website	6
legislation	6
risk	6
recommendations	6
who-is-a-jew	6
cancer-susceptibility	6
focus-group	6
conference-proceedings	5
sociobiology	5
genome	5
care	5
recruitment	5
genetics-education	5
genetic-counselors	5
medicine	5
alpha-fetoprotein	5
family	5
patients	5
homosexuality	5
psychological-distress	5
biomedical-research	5
preimplantation-genetic-diagnosis	5
hereditary-nonpolyposis-colorectal-cancer	5
popular-culture	5
gene-therapy	5
biobanking	5
racism	5
biotechnology	5
dementia	5
genetic-privacy-act	5
educational-resource	5
survey	5
disabilities	5
down-syndrome	4
africa	4
knowledge	4
children	4
race-class-and-genetics	4
ashkenazi	4
policy-recommendations	4
emotions	4
public-health	4
human-genome	4
native-americans	4
wrongful-birth	4
insurance-discrimination	4
new-genetics	4
therapeutic-misconception	4
comparative	4
gene-transfer-research	4
gene-mapping	4
justice	4
family-communication	4
at-risk	4
rural	4
alzheimer-disease	4
brca1-2	4
history	4
results	4
congress	4
cancer-risk	4
human-subjects-research	4
social-implications	4
class-and-genetics	4
life-insurance	4
pharmacogenetics	4
genetic-engineering	4
benefit	4
quality-of-life	4
uncertainty	4
narratives	4
population-screening	4
anxiety	4
genetic-variation	4
experience	4
attitudes-toward-disability	4
preferences	4
women	4
dna	4
prenatal-screening	4
social	4
nursing	4
breast-cancer-susceptibility-testing	4
monitoring	4
developmental-disabilities	3
bidil	3
electronic-resource	3
genetic-identity	3
ovarian-cancer	3
heart-disease	3
human-genome-diversity-project	3
anti-aging	3
human-genome-research	3
clinical-trials	3
alcoholism	3
genetic-diversity	3
consent	3
breast-cancer-screening	3
pharos	3
colorectal-cancer	3
medical-education	3
quarantine	3
personalized-medicine	3
infertility	3
procreative-liberty	3
group-risk	3
pretest-education	3
bibliography	3
social-support	3
use-of-genetic-information	3
clinical-research	3
dna-banking	3
hereditable-cancer-syndromes	3
genomic-medicine	3
benefits	3
studies	3
toward	3
patient-education	3
adolescents	3
relations	3
neuroethics	3
gene-patents	3
genetics-and-public-health	3
genetic-susceptibility	3
public-opinion	3
populations	3
health-care	3
national-research-council	3
latinos	3
international-health-research	3
sickle-cell-disease	3
caucasian	3
scientific-racism	3
providers	3
race-and-medicine	3
medicalization	3
prenatal-care	3
follow-up	3
international-hapmap-project	3
biomedical	2
genetics-and-cancer	2
public-consultation	2
psychosocial-impact	2
patient-satisfaction	2
pku	2
families	2
interest	2
neurogenetics	2
coping	2
genetic-variation-research	2
bioinformatics	2
childhood	2
depression	2
indian	2
race-and-biomedical-research	2
compliance	2
family-members	2
incidental-findings	2
international-hap-map-project	2
informed-consent-process	2
project	2
in	2
bene-israel	2
professionals	2
maternal-alpha-fetoprotein-screening	2
diabetes	2
vulnerability	2
public-health-policy	2
lived-experience	2
genetic-reductionism	2
prenatal-genetic-screening	2
patenting-human-genetic-material	2
images	2
risks-and-benefits	2
oversight	2
psychosocial	2
breast-and-ovarian-cancer	2
genetic-screening-newborn	2
rights	2
symposium	2
cancer-and-genetics	2
genes	2
research-results	2
susceptibility-testing	2
ethnography	2
risk-communication	2
prenatal-genetic-counseling	2
forensic-genetics	2
managed-care	2
prenatal-counseling	2
adverse-selection	2
villus	2
academic	2
underclass	2
colon-cancer-gene-testing	2
american-indians	2
normalization	2
disclosure-research-results	2
commercial	2
medical-records-law	2
microbes	2
moral	2
human	2
impact-of-genetic-research-on-community	2
biomedicine	2
health-research	2
african	2
decison-making	2
anti-aging-research	2
open-source	2
conflict	2
movement	2
feminism	2
science-commons	2
american-	2
cancer-risk-assessment	2
epidemiology	2
mental-retardation	2
disability-rights-critique-of-prenatal-testing	2
human-genome-	2
adjudication	2
pregnancy	2
indian-country	2
risk-assessment	2
or	2
gender-selection	2
genome-research	2
stigmatization	2
genetic-testing-programs	2
sciences	2
mtdna	2
nondirective-counseling	2
trust	2
indian-jewish-community	2
gay-gene	2
genetics-and-culture	2
ethnographic-fieldwork	2
public-health-genetics	2
carriers	2
nurses	2
rac	2
cancer-susceptibility-testing	2
neuroscience	2
health-behavior	2
huntington-disease	2
internet	2
ethical-framework	2
recruitment-strategies	2
perfect-child	2
gender-and-genetics	2
data-access	2
embryo-screening	2
for-profit	2
patients-attitudes	2
computers	2
religion	2
altruism	2
genetic-explanations	2
named-populations	2
gender-equality	2
politics	2
genetic-outreach-services	2
plant-biotechnology	2
to	2
genetic-technologies	2
social-darwinism	2
genetic-disorders	2
raceethnicity	2
india	2
referrals	2
routinization	2
wrongful-life	2
chorionic	2
sickle-cell-anemia	2
genetic-patenting	2
anthropology	2
hereditary-colorectal-cancer	2
satisfaction	2
susceptibility	2
assisted-reproductive-technologies	2
cloning	2
breast-	2
science-education	2
genetic-counseling-training	2
for	2
pregnant	2
differential-impact-on-women	2
group-risks	2
patient-provider-communication	2
refusal	2
dna-databanks	2
analysis	2
-research	2
cultural-differences	2
cholera	2
hereditary-colon-cancer	2
parents	2
predictive	2
assisted-reproduction	2
academic-industry-relationships	2
maternal	2
marfan-syndrome	2
media	2
health-beliefs	2
patient-autonomy	2
communities	2
cross-cultural	2
ada	2
asia	2
human-enhancement	2
human-populations-and-genetic-variation	2
cancer-risk-counseling	2
human-genetic-diversity	2
family-issues	2
misattributed-paternity	2
kentucky	2
hncc	2
fetal	2
institutional-review-boards	2
mental-illness	2
dna-patenting-and-licensing	2
institutions	2
forensics	2
molecular-biology	2
philosophy	2
class	2
fetus	2
education	2
immigration	2
population-studies	2
social-stratification	2
social-policy	2
risks	2
clinical-practice	2
cystic-fibrosis-carrier-screening	2
policy-state-level	2
culture	2
patient	2
lay-understandings	2
cohanim	2
pharmacological-treatment	2
hiv-disclosure	2
ethical-legal-social-implications	2
smoking	2
industry-norms	2
genetic-testing-predictive	1
genotype-phenotype-studies	1
non-directive-counseling	1
cohort-study	1
employer-access	1
training	1
international-research	1
reproductive-genetics	1
genetic-knowledge	1
attitudes-toward-human-genome-project	1
collaborative-research	1
ethnicity-and-eugenics	1
research-standards	1
differential-impact-of-genetics-on-women	1
counseling	1
fetal-rights	1
individual-rights	1
gender-politics	1
assisted-reproduction-technologies	1
use	1
non-beneficial-medical-interventions	1
race-and-clinical-medicine	1
autism	1
product-development-incentives	1
sociodemographics	1
experts	1
hemochromatosis	1
colorectal-cancer-gene-testing	1
genetics-training-programs	1
sequence-tagged-site	1
genetic-databases	1
genetic-technology	1