Jae Hoon Sul
Jae Hoon Sul
Department of Psychiatry and Biobehavioral Sciences at UCLA
Verified email at mednet.ucla.edu - Homepage
Title
Cited by
Cited by
Year
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
13372010
Genetic effects on gene expression across human tissues
GTEx Consortium
Nature 550 (7675), 204-213, 2017
9902017
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
6822013
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
2012016
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), 249-254, 2017
1692017
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
1342010
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), 2013
722013
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
692017
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
682012
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
602017
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
582017
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), 228-234, 2014
492014
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
442011
Genetic effects on gene expression across human tissues
F Aguet, AV Segrč, BB Cummings, ET Gelfand, K Hadley, KH Huang, ...
Springer Science and Business Media, 2017
342017
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), 2014
322014
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
312014
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), 2016
292016
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
272017
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
262017
Interrogating the genetic determinants of Tourette’s syndrome and other tic disorders through genome-wide association studies
D Yu, JH Sul, F Tsetsos, MS Nawaz, AY Huang, I Zelaya, C Illmann, ...
American Journal of Psychiatry 176 (3), 217-227, 2019
252019
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