Stephanie Malia Fullerton
Stephanie Malia Fullerton
University of Washington School of Medicine
Verified email at - Homepage
Cited by
Cited by
Genomics is failing on diversity
AB Popejoy, SM Fullerton
Nature 538 (7624), 161-164, 2016
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
Archaic African and Asian lineages in the genetic ancestry of modern humans.
RM Harding, SM Fullerton, RC Griffiths, J Bond, MJ Cox, JA Schneider, ...
American journal of human genetics 60 (4), 772, 1997
Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism
SM Fullerton, AG Clark, KM Weiss, DA Nickerson, SL Taylor, JH Stengård, ...
The American journal of human genetics 67 (4), 881-900, 2000
Return of genomic results to research participants: the floor, the ceiling, and the choices in between
GP Jarvik, LM Amendola, JS Berg, K Brothers, EW Clayton, W Chung, ...
The American Journal of Human Genetics 94 (6), 818-826, 2014
Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group
RR Fabsitz, A McGuire, RR Sharp, M Puggal, LM Beskow, LG Biesecker, ...
Circulation: Cardiovascular Genetics 3 (6), 574-580, 2010
Actionable exomic incidental findings in 6503 participants: challenges of variant classification
LM Amendola, MO Dorschner, PD Robertson, JS Salama, R Hart, ...
Genome research 25 (3), 305-315, 2015
Local rates of recombination are positively correlated with GC content in the human genome
SM Fullerton, A Bernardo Carvalho, AG Clark
Molecular biology and evolution 18 (6), 1139-1142, 2001
From patients to partners: participant-centric initiatives in biomedical research
J Kaye, L Curren, N Anderson, K Edwards, SM Fullerton, N Kanellopoulou, ...
Nature Reviews Genetics 13 (5), 371-376, 2012
Inferring genetic ancestry: opportunities, challenges, and implications
CD Royal, J Novembre, SM Fullerton, DB Goldstein, JC Long, ...
The American Journal of Human Genetics 86 (5), 661-673, 2010
Broad consent for research with biological samples: workshop conclusions
C Grady, L Eckstein, B Berkman, D Brock, R Cook-Deegan, SM Fullerton, ...
The American Journal of Bioethics 15 (9), 34-42, 2015
Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene
DA Nickerson, SL Taylor, SM Fullerton, KM Weiss, AG Clark, JH Stengård, ...
Genome research 10 (10), 1532-1545, 2000
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ...
The American Journal of Human Genetics 94 (2), 233-245, 2014
Genomic research and wide data sharing: views of prospective participants
SB Trinidad, SM Fullerton, JM Bares, GP Jarvik, EB Larson, W Burke
Genetics in Medicine 12 (8), 486-495, 2010
Public attitudes toward consent and data sharing in biobank research: a large multi-site experimental survey in the US
SC Sanderson, KB Brothers, ND Mercaldo, EW Clayton, ...
The American Journal of Human Genetics 100 (3), 414-427, 2017
Eclipse of the gene and the return of divination
M Lock
Current anthropology 46 (S5), S47-S70, 2005
Phenogenetic drift and the evolution of genotype–phenotype relationships
KM Weiss, SM Fullerton
Theoretical population biology 57 (3), 187-195, 2000
Clinical sequencing exploratory research consortium: accelerating evidence-based practice of genomic medicine
RC Green, KAB Goddard, GP Jarvik, LM Amendola, PS Appelbaum, ...
The American Journal of Human Genetics 98 (6), 1051-1066, 2016
Glad you asked: participants' opinions of re-consent for dbGap data submission
EJ Ludman, SM Fullerton, L Spangler, SB Trinidad, MM Fujii, GP Jarvik, ...
Journal of Empirical Research on Human Research Ethics 5 (3), 9-16, 2010
Race and ancestry in biomedical research: exploring the challenges
T Caulfield, SM Fullerton, SE Ali-Khan, L Arbour, EG Burchard, ...
Genome medicine 1, 1-8, 2009
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