| Genetic effects on gene expression across human tissues GTEx Consortium Lead analysts: Aguet François 1 Brown Andrew A. 2 3 4 Castel ... Nature 550 (7675), 204-213, 2017 | 3609 | 2017 |
| 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 | 2483 | 2010 |
| FinnGen provides genetic insights from a well-phenotyped isolated population MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, KM Donner, ... Nature 613 (7944), 508-518, 2023 | 2147 | 2023 |
| Service SK, Zaitlen NA, Kong SY, Freimer NB, et al. Variance component model to account for sample structure in genome-wide association studies HM Kang, JH Sul Nat Genet 42 (4), 348-54, 2010 | 1692 | 2010 |
| 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 | 1047 | 2013 |
| 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 | 1002 | 2017 |
| 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 | 780 | 2016 |
| 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 | 615 | 2017 |
| FinnGen: Unique genetic insights from combining isolated population and national health register data MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, K Donner, ... medrxiv, 2022.03. 03.22271360, 2022 | 449 | 2022 |
| Accurate estimation of cell composition in bulk expression through robust integration of single-cell information B Jew, M Alvarez, E Rahmani, Z Miao, A Ko, KM Garske, JH Sul, ... Nature communications 11 (1), 1971, 2020 | 366 | 2020 |
| 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 | 342 | 2019 |
| 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 | 283 | 2017 |
| Population structure in genetic studies: Confounding factors and mixed models JH Sul, LS Martin, E Eskin PLoS genetics 14 (12), e1007309, 2018 | 258 | 2018 |
| 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 | 200 | 2017 |
| 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 | 192 | 2017 |
| 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 | 185 | 2017 |
| 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 | 174 | 2010 |
| SK Service, NA Zaitlen, S.-y. Kong, NB Freimer, C. Sabatti, E. Eskin et al.,“Variance component model to account for sample structure in genome-wide association studies,” HM Kang, JH Sul Nat. Genet 42 (4), 348-354, 2010 | 166 | 2010 |
| 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 | 135 | 2018 |
| 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 | 128 | 2013 |
Eleazar EskinUniversity of California, Los AngelesBestätigte E-Mail-Adresse bei cs.ucla.edu
