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Scott Hebbring
Scott Hebbring
Marshfield Clinic
Verified email at marshfieldresearch.org
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Cited by
Year
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ...
Nature genetics 48 (2), 134-143, 2016
13852016
Comparison of RNA-seq and microarray-based models for clinical endpoint prediction
W Zhang, Y Yu, F Hertwig, J Thierry-Mieg, W Zhang, D Thierry-Mieg, ...
Genome biology 16, 1-12, 2015
3922015
The phenotypic legacy of admixture between modern humans and Neandertals
CN Simonti, B Vernot, L Bastarache, E Bottinger, DS Carrell, RL Chisholm, ...
Science 351 (6274), 737-741, 2016
3442016
A germline DNA polymorphism enhances alternative splicing of the KLF6 tumor suppressor gene and is associated with increased prostate cancer risk
G Narla, A DiFeo, HL Reeves, DJ Schaid, J Hirshfeld, E Hod, A Katz, ...
Cancer research 65 (4), 1213-1222, 2005
2672005
Phenotype risk scores identify patients with unrecognized Mendelian disease patterns
L Bastarache, JJ Hughey, S Hebbring, J Marlo, W Zhao, WT Ho, ...
Science 359 (6381), 1233-1239, 2018
1922018
The challenges, advantages and future of phenome‐wide association studies
SJ Hebbring
Immunology 141 (2), 157-165, 2014
1832014
Glycine and a Glycine Dehydrogenase (GLDC) SNP as Citalopram/Escitalopram Response Biomarkers in Depression: Pharmacometabolomics‐Informed …
Y Ji, S Hebbring, H Zhu, GD Jenkins, J Biernacka, K Snyder, M Drews, ...
Clinical Pharmacology & Therapeutics 89 (1), 97-104, 2011
1742011
A Combined Genomewide Linkage Scan of 1,233 Families for Prostate Cancer–Susceptibility Genes Conducted by the International Consortium for Prostate Cancer Genetics
J Xu, L Dimitrov, BL Chang, TS Adams, AR Turner, DA Meyers, RA Eeles, ...
The American Journal of Human Genetics 77 (2), 219-229, 2005
1692005
Comparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer–susceptibility loci
DJ Schaid, JC Guenther, GB Christensen, S Hebbring, C Rosenow, ...
The American Journal of Human Genetics 75 (6), 948-965, 2004
1642004
Nonparametric tests of association of multiple genes with human disease
DJ Schaid, SK McDonnell, SJ Hebbring, JM Cunningham, SN Thibodeau
The American Journal of Human Genetics 76 (5), 780-793, 2005
1592005
Opportunities for drug repositioning from phenome-wide association studies
M Rastegar-Mojarad, Z Ye, JM Kolesar, SJ Hebbring, SM Lin
Nature biotechnology 33 (4), 342-345, 2015
1252015
Evaluation of genetic variations in the androgen and estrogen metabolic pathways as risk factors for sporadic and familial prostate cancer
JM Cunningham, SJ Hebbring, SK McDonnell, MS Cicek, GB Christensen, ...
Cancer Epidemiology Biomarkers & Prevention 16 (5), 969-978, 2007
1252007
Human SULT1A1 gene: copy number differences and functional implications
SJ Hebbring, AA Adjei, JL Baer, GD Jenkins, J Zhang, JM Cunningham, ...
Human molecular genetics 16 (5), 463-470, 2007
1252007
Two common chromosome 8q24 variants are associated with increased risk for prostate cancer
L Wang, SK McDonnell, JP Slusser, SJ Hebbring, JM Cunningham, ...
Cancer research 67 (7), 2944-2950, 2007
1222007
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
C Tcheandjieu, X Zhu, AT Hilliard, SL Clarke, V Napolioni, S Ma, KM Lee, ...
Nature medicine 28 (8), 1679-1692, 2022
1172022
A PheWAS approach in studying HLA-DRB1* 1501
SJ Hebbring, SJ Schrodi, Z Ye, Z Zhou, D Page, MH Brilliant
Genes & Immunity 14 (3), 187-191, 2013
1062013
Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants
JH Karnes, L Bastarache, CM Shaffer, S Gaudieri, Y Xu, AM Glazer, ...
Science Translational Medicine 9 (389), eaai8708, 2017
972017
The gene for HMSN2C maps to 12q23-24: a region of neuromuscular disorders
CJ Klein, JM Cunningham, EJ Atkinson, DJ Schaid, SJ Hebbring, ...
Neurology 60 (7), 1151-1156, 2003
962003
The All of Us Research Program: data quality, utility, and diversity
AH Ramirez, L Sulieman, DJ Schlueter, A Halvorson, J Qian, ...
Patterns 3 (8), 2022
922022
Harmonizing clinical sequencing and interpretation for the eMERGE III network
H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ...
The American Journal of Human Genetics 105 (3), 588-605, 2019
922019
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