Jae Hoon Sul
Jae Hoon Sul
Department of Psychiatry and Biobehavioral Sciences at UCLA
Verified email at mednet.ucla.edu - Homepage
TitleCited byYear
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
GTEx Consortium
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
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