|Variance component model to account for sample structure in genome-wide association studies|
HM Kang, JH Sul, SK Service, NA Zaitlen, S Kong, NB Freimer, C Sabatti, ...
Nature genetics 42 (4), 348, 2010
|Genetic effects on gene expression across human tissues|
Nature 550 (7675), 204, 2017
|GWAS of 126,559 individuals identifies genetic variants associated with educational attainment|
CA Rietveld, SE Medland, J Derringer, J Yang, T Esko, NW Martin, ...
science 340 (6139), 1467-1471, 2013
|Colocalization of GWAS and eQTL signals detects target genes|
F Hormozdiari, M Van De Bunt, AV Segre, X Li, JWJ Joo, M Bilow, JH Sul, ...
The American Journal of Human Genetics 99 (6), 1245-1260, 2016
|Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease|
JL Stein, X Hua, JH Morra, S Lee, DP Hibar, AJ Ho, AD Leow, AW Toga, ...
Neuroimage 51 (2), 542-554, 2010
|Dynamic landscape and regulation of RNA editing in mammals|
MH Tan, Q Li, R Shanmugam, R Piskol, J Kohler, AN Young, KI Liu, ...
Nature 550 (7675), 249, 2017
|Effectively identifying eQTLs from multiple tissues by combining mixed model and meta-analytic approaches|
JH Sul, B Han, C Ye, T Choi, E Eskin
PLoS genetics 9 (6), e1003491, 2013
|The Minnesota Center for Twin and Family Research genome-wide association study|
MB Miller, S Basu, J Cunningham, E Eskin, SM Malone, WS Oetting, ...
Twin Research and Human Genetics 15 (6), 767-774, 2012
|Co-expression networks reveal the tissue-specific regulation of transcription and splicing|
A Saha, Y Kim, ADH Gewirtz, B Jo, C Gao, IC McDowell, BE Engelhardt, ...
Genome research 27 (11), 1843-1858, 2017
|Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome|
AY Huang, D Yu, LK Davis, JH Sul, F Tsetsos, V Ramensky, I Zelaya, ...
Neuron 94 (6), 1101-1111. e7, 2017
|Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid|
JJ Luykx, SC Bakker, E Lentjes, M Neeleman, E Strengman, L Mentink, ...
Molecular psychiatry 19 (2), 228, 2014
|De novo coding variants are strongly associated with Tourette disorder|
AJ Willsey, TV Fernandez, D Yu, RA King, A Dietrich, J Xing, SJ Sanders, ...
Neuron 94 (3), 486-499. e9, 2017
|An optimal weighted aggregated association test for identification of rare variants involved in common diseases|
JH Sul, B Han, D He, E Eskin
Genetics 188 (1), 181-188, 2011
|A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease|
JH Kim, HS Cheong, JH Sul, JM Seo, DY Kim, JT Oh, KW Park, HY Kim, ...
PloS one 9 (10), e110292, 2014
|Effectively identifying regulatory hotspots while capturing expression heterogeneity in gene expression studies|
JWJ Joo, JH Sul, B Han, C Ye, E Eskin
Genome biology 15 (4), r61, 2014
|Accounting for population structure in gene-by-environment interactions in genome-wide association studies using mixed models|
JH Sul, M Bilow, WY Yang, E Kostem, N Furlotte, D He, E Eskin
PLoS genetics 12 (3), e1005849, 2016
|Mapping subsets of scholarly information|
P Ginsparg, P Houle, T Joachims, JH Sul
Proceedings of the National Academy of Sciences 101 (suppl 1), 5236-5240, 2004
|Negative selection in humans and fruit flies involves synergistic epistasis|
M Sohail, OA Vakhrusheva, JH Sul, SL Pulit, LC Francioli, ...
Science 356 (6337), 539-542, 2017
|Mixed models can correct for population structure for genomic regions under selection|
JH Sul, E Eskin
Nature Reviews Genetics 14 (4), 300, 2013
|Identifying cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis|
F Yang, J Wang, BL Pierce, LS Chen, F Aguet, KG Ardlie, BB Cummings, ...
Genome research 27 (11), 1859-1871, 2017