Sara Chandros Hull - Concepedia

Author

Sara Chandros Hull

Also Known As

Henderson, Gail E., S Hull, S. C. Hull, S. Chandros Hull, S. Hull, S.C. Hull, SARA CHANDROS HULL, Sally Hull, Sara C. Hull, Sara Chandros Hull

Publications

3.6K

Citations

H-Index

115

Concepts

All Affiliations

National Institutes of Health National Human Genome Research Institute National Institutes of Health Clinical Center Harvard University University of Washington

About

Sara Chandros Hull is an author at National Institutes of Health specializing in medicine, research ethics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Education	3	3	141
2	Business	2	2	218
3	Health Sciences	2	2	135
4	Engineering	1	1	21
5	Language Studies	1	1	47

Sara Chandros Hull

Publications

Citations

H-Index

Page 1

	Year	Citations
Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between Gail P. Jarvik, Laura M. Amendola, Jonathan S. Berg, The American Journal of Human Genetics Genomic ResultsGenetic TestingResearch ParticipantsGeneticsStatistical Genetics	2014	368
Broad Consent for Research With Biological Samples: Workshop Conclusions Christine Grady, Lisa Eckstein, Ben Berkman, The American Journal of Bioethics Clinical SettingsMedical EthicsBiomedical EthicHealth PolicyBiobank	2015	320
Variability among institutional review boards’ decisions within the context of a multicenter trial Henry Silverman, Sara Chandros Hull, Jeremy Sugarman Critical Care Medicine	2001	188
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine Robert C. Green, Katrina A.B. Goddard, Gail P. Jarvik, The American Journal of Human Genetics EpidemiologySequencingMedicineNext-generation SequencingGenomics	2016	161
Direct-to-consumer sales of genetic services on the Internet Sarah E. Gollust, Benjamin S. Wilfond, Sara Chandros Hull Genetics in Medicine Genetic ServicesInteractive MarketingManagementConsumer ResearchBusiness	2003	140
Creating a global rare disease patient registry linked to a rare diseases biorepository database: Rare Disease-HUB (RD-HUB) Yaffa Rubinstein, Stephen C. Groft, Ronald Bartek, Contemporary Clinical Trials Health InformaticsClinical DataBiorepository DatabaseClinical DatabaseMedicine	2010	109
Patients' attitudes about the use of placebo treatments: telephone survey Sara Chandros Hull, Luana Colloca, Andrew L. Avins, BMJ	2013	104
Patients' Views on Identifiability of Samples and Informed Consent for Genetic Research Sara Chandros Hull, Richard R. Sharp, Jeffrey R. Botkin, The American Journal of Bioethics Family MedicineGenetic TestingGenetic EpidemiologyResearch EthicsClinical Genetics	2008	104
Consent Forms and the Therapeutic Misconception: The Example of Gene Transfer Research Nancy M. P. King, Gail E. Henderson, Larry R. Churchill, IRB Ethics and Human Research	2005	99
The Invisible Hand in Clinical Research: The Study Coordinator's Critical Role in Human Subjects Protection Arlene M. Davis, Sara Chandros Hull, Christine Grady, The Journal of Law Medicine & Ethics Humanity And MedicineClinical SpecialtiesResearch EthicsInvisible HandEthic Committee	2002	95

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