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Stephanie Hesselson
Stephanie Hesselson
Verified email at victorchang.edu.au
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Cited by
Year
Narcolepsy is strongly associated with the T-cell receptor alpha locus
J Hallmayer, J Faraco, L Lin, S Hesselson, J Winkelmann, M Kawashima, ...
Nature genetics 41 (6), 708-711, 2009
5592009
Characterizing race/ethnicity and genetic ancestry for 100,000 subjects in the genetic epidemiology research on adult health and aging (GERA) cohort
Y Banda, MN Kvale, TJ Hoffmann, SE Hesselson, D Ranatunga, H Tang, ...
Genetics 200 (4), 1285-1295, 2015
3452015
Common variants in P2RY11 are associated with narcolepsy
BR Kornum, M Kawashima, J Faraco, L Lin, TJ Rico, S Hesselson, ...
Nature genetics 43 (1), 66-71, 2011
2712011
Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array
TJ Hoffmann, MN Kvale, SE Hesselson, Y Zhan, C Aquino, Y Cao, ...
Genomics 98 (2), 79-89, 2011
2342011
Genotyping informatics and quality control for 100,000 subjects in the genetic epidemiology research on adult health and aging (GERA) cohort
MN Kvale, S Hesselson, TJ Hoffmann, Y Cao, D Chan, S Connell, ...
Genetics 200 (4), 1051-1060, 2015
2102015
Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel …
TJ Hoffmann, Y Zhan, MN Kvale, SE Hesselson, J Gollub, C Iribarren, ...
Genomics 98 (6), 422-430, 2011
1872011
A Common 5′‐UTR Variant in MATE2‐K Is Associated With Poor Response to Metformin
JH Choi, SW Yee, AH Ramirez, KM Morrissey, GH Jang, PJ Joski, ...
Clinical Pharmacology & Therapeutics 90 (5), 674-684, 2011
1702011
Automated assay of telomere length measurement and informatics for 100,000 subjects in the genetic epidemiology research on adult health and aging (GERA) cohort
K Lapham, MN Kvale, J Lin, S Connell, LA Croen, BP Dispensa, L Fang, ...
Genetics 200 (4), 1061-1072, 2015
1632015
Genetic variants in multidrug and toxic compound extrusion-1, hMATE1, alter transport function
Y Chen, K Teranishi, S Li, SW Yee, S Hesselson, D Stryke, SJ Johns, ...
The pharmacogenomics journal 9 (2), 127-136, 2009
1242009
Identification and characterization of novel polymorphisms in the basal promoter of the human transporter, MATE1
JH Choi, SW Yee, MJ Kim, L Nguyen, JH Lee, JO Kang, S Hesselson, ...
Pharmacogenetics and genomics 19 (10), 770-780, 2009
812009
Rat Mcs5a is a compound quantitative trait locus with orthologous human loci that associate with breast cancer risk
DJ Samuelson, SE Hesselson, BA Aperavich, Y Zan, JD Haag, ...
Proceedings of the National Academy of Sciences 104 (15), 6299-6304, 2007
712007
A case-control study of the HER2 Ile655Val polymorphism in relation to risk of invasive breast cancer
SE Nelson, MN Gould, JM Hampton, A Trentham-Dietz
Breast cancer research 7, 1-8, 2005
662005
Spontaneous coronary artery dissection: insights on rare genetic variation from genome sequencing
KJ Carss, AA Baranowska, J Armisen, TR Webb, SE Hamby, ...
Circulation: Genomic and Precision Medicine 13 (6), e003030, 2020
592020
Induction of mosquito hemolymph proteins in response to immune challenge and wounding
YS Han, J Chun, A Schwartz, S Nelson, SM Paskewitz
Developmental & Comparative Immunology 23 (7-8), 553-562, 1999
491999
Genetic variation in the proximal promoter of ABC and SLC superfamilies: liver and kidney specific expression and promoter activity predict variation
SE Hesselson, P Matsson, JE Shima, H Fukushima, SW Yee, ...
PloS one 4 (9), e6942, 2009
422009
Functional genetic variation in the basal promoter of the organic cation/carnitine transporters OCTN1 (SLC22A4) and OCTN2 (SLC22A5)
H Tahara, SW Yee, TJ Urban, S Hesselson, RA Castro, M Kawamoto, ...
Journal of Pharmacology and Experimental Therapeutics 329 (1), 262-271, 2009
402009
Functional characterization of liver enhancers that regulate drug‐associated transporters
MJ Kim, P Skewes‐Cox, H Fukushima, S Hesselson, SW Yee, LB Ramsey, ...
Clinical Pharmacology & Therapeutics 89 (4), 571-578, 2011
382011
Identification and characterization of proximal promoter polymorphisms in the human concentrative nucleoside transporter 2 (SLC28A2)
SW Yee, JE Shima, S Hesselson, L Nguyen, S De Val, RJ LaFond, ...
Journal of Pharmacology and Experimental Therapeutics 328 (3), 699-707, 2009
352009
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation
D Adlam, TE Berrandou, A Georges, CP Nelson, E Giannoulatou, J Henry, ...
Nature Genetics 55 (6), 964-972, 2023
332023
Exploring the genetic architecture of spontaneous coronary artery dissection using whole-genome sequencing
I Tarr, S Hesselson, SE Iismaa, E Rath, S Monger, M Troup, K Mishra, ...
Circulation: Genomic and Precision Medicine 15 (4), e003527, 2022
272022
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