引用次数
引用: 13,140
H-指数: 52
I10-指数 : 113
出版物: 210
Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience
Sarah C Nelson , Stephanie M Gogarten , Stephanie M Fullerton , Carmen R Isasi
The American Journal of Human Genetics 109 ( 9) 1582 -1590
1
2022
Studying the impact of translational genomic research: Lessons from eMERGE
Ellen Wright Clayton , Maureen E Smith , Katherine C Anderson , Wendy K Chung
The American Journal of Human Genetics
2
2023
Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network
Anna CF Lewis , Rex L Chisholm , John J Connolly , Edward D Esplin
The American Journal of Human Genetics
2024
Advancing genomics to improve health equity
Ebony B Madden , Lucia A Hindorff , Vence L Bonham , Tabia Henry Akintobi
Nature genetics 1 -6
4
2024
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 , Kyle Brothers
American Journal of Human Genetics 94 ( 6) 818 -826
383
2014
Beyond inclusion: Enacting team equity in precision medicine research
Melanie Jeske , Emily Vasquez , Stephanie M Fullerton , Aliya Saperstein
PloS one 17 ( 2) e0263750 -e0263750
12
2022
Strategies of inclusion: The tradeoffs of pursuing “baked in” diversity through place-based recruitment
Janet K Shim , Michael Bentz , Emily Vasquez , Melanie Jeske
Social Science & Medicine 306 115132 -115132
7
2022
Conflating race and ancestry: Tracing decision points about population descriptors over the precision medicine research life course
Michael Bentz , Aliya Saperstein , Stephanie M Fullerton , Janet K Shim
Human Genetics and Genomics Advances 5 ( 1)
1
2024
A Proposed Approach for Implementing Genomics-Based Screening Programs for Healthy Adults
Michael F Murray , James P Evans , Misha Angrist , Kee Chan
NAM Perspectives
16
2018
Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience
Kathleen D Muenzen , Laura M Amendola , Tia L Kauffman , Kathleen F Mittendorf
Human Genetics and Genomics Advances 3 ( 3)
6
2022
Author/Subject Index
Victor B Penchaszadeh , Deborah J Bowen , Thuy Vu , Carol Kasten-Sportes
Public Health Genomics 11 ( 4) 250 -250
2008
Sequence Diversity and Large-Scale Typing of SNPs in the Human Apolipoprotein E Gene
Deborah A Nickerson , Scott L Taylor , Stephanie M Fullerton , Kenneth M Weiss
Genome Research 10 ( 10) 1532 -1545
167
2000
Risk perception and intended behavior change after uninformative genetic results for adult-onset hereditary conditions in unselected patients
Nandana D Rao , Kristine M King , Jailanie Kaganovsky , Sajida Hassan
European Journal of Human Genetics 32 ( 1) 77 -82
1
2024
MANAGING GENETIC RESEARCh DATA
Evette J Ludman , Stephanie M Fullerton , Leslie Spangler , Susan Brown Trinidad
2010
www. csueastbay. edu/JERHRE
Eleanor Singer , Mick P Couper , Evette J Ludman , Stephanie M Fullerton
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine
Robert C Green , Katrina AB Goddard , Gail P Jarvik , Laura M Amendola
American Journal of Human Genetics 98 ( 6) 1051 -1066
160
2016
Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network
Hana Zouk , Eric Venner , Niall J Lennon , Donna M Muzny
The American Journal of Human Genetics 105 ( 3) 588 -605
84
2019
Diagnostic yield of genetic screening in a diverse, community-ascertained cohort
Nandana D Rao , Jailanie Kaganovsky , Emily A Malouf , Sandy Coe
Genome Medicine 15 ( 1) 1 -12
6
2023
Factors influencing genetic screening enrollment among a diverse, community-ascertained cohort.
Nandana D Rao , Jailanie Kaganovsky , Stephanie M Fullerton , Annie T Chen
Public Health Genomics
2023
RECONTACTING PEOPLE WHO HAVE CONTRIBUTED GENETIC DATA
Laura M Beskow , Emily E Namey , R Jean Cadigan , Tracy Brazg