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), 348-354, 2010
15712010
Genetic effects on gene expression across human tissues
GTEx Consortium
Nature 550 (7675), 204, 2017
13402017
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
7622013
Landscape of X chromosome inactivation across human tissues
T Tukiainen, AC Villani, A Yen, MA Rivas, JL Marshall, R Satija, M Aguirre, ...
Nature 550 (7675), 244-248, 2017
3362017
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
3232016
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
2562017
The impact of rare variation on gene expression across tissues
X Li, Y Kim, EK Tsang, JR Davis, FN Damani, C Chiang, GT Hess, ...
Nature 550 (7675), 239-243, 2017
1712017
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
1472010
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
1042017
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 Genet 9 (6), e1003491, 2013
922013
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
892017
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
792017
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
732012
Population structure in genetic studies: Confounding factors and mixed models
JH Sul, LS Martin, E Eskin
PLoS genetics 14 (12), e1007309, 2018
622018
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
612019
Local genetic effects on gene expression across 44 human tissues
F Aguet, AA Brown, SE Castel, JR Davis, P Mohammadi, AV Segre, ...
BiorXiv, 074450, 2016
582016
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
552014
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
502011
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
452017
De novo sequence and copy number variants are strongly associated with tourette disorder and implicate cell polarity in pathogenesis
S Wang, JD Mandell, Y Kumar, N Sun, MT Morris, J Arbelaez, C Nasello, ...
Cell reports 24 (13), 3441-3454. e12, 2018
442018
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