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| The GTEx Consortium atlas of genetic regulatory effects across human tissues GTEx Consortium Science 369 (6509), 1318-1330, 2020 | 3276 | 2020 |
| The impact of sex on gene expression across human tissues M Oliva, M Muñoz-Aguirre, S Kim-Hellmuth, V Wucher, ADH Gewirtz, ... Science 369 (6509), eaba3066, 2020 | 865 | 2020 |
| A simple new approach to variable selection in regression, with application to genetic fine mapping G Wang, A Sarkar, P Carbonetto, M Stephens Journal of the Royal Statistical Society Series B: Statistical Methodology …, 2020 | 735 | 2020 |
| A quantitative proteome map of the human body L Jiang, M Wang, S Lin, R Jian, X Li, J Chan, G Dong, H Fang, ... Cell 183 (1), 269-283. e19, 2020 | 369 | 2020 |
| Flexible statistical methods for estimating and testing effects in genomic studies with multiple conditions SM Urbut, G Wang, P Carbonetto, M Stephens Nature genetics 51 (1), 187-195, 2019 | 359 | 2019 |
| Exploiting the GTEx resources to decipher the mechanisms at GWAS loci AN Barbeira, R Bonazzola, ER Gamazon, Y Liang, YS Park, ... Genome biology 22, 1-24, 2021 | 260 | 2021 |
| Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ... The American Journal of Human Genetics 94 (2), 233-245, 2014 | 246 | 2014 |
| Fine-mapping from summary data with the “Sum of Single Effects” model Y Zou, P Carbonetto, G Wang, M Stephens PLoS genetics 18 (7), e1010299, 2022 | 193 | 2022 |
| 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 | 184 | 2017 |
| RNF213 Rare Variants in an Ethnically Diverse Population With Moyamoya Disease AC Cecchi, D Guo, Z Ren, K Flynn, RLP Santos-Cortez, SM Leal, ... Stroke 45 (11), 3200-3207, 2014 | 165 | 2014 |
| Integrated annotation and analysis of genetic variants from next-generation sequencing studies with variant tools FA San Lucas, G Wang, P Scheet, B Peng Bioinformatics 28 (3), 421-422, 2012 | 159 | 2012 |
| Genetic analyses support the contribution of mRNA N6-methyladenosine (m6A) modification to human disease heritability Z Zhang, K Luo, Z Zou, M Qiu, J Tian, L Sieh, H Shi, Y Zou, G Wang, ... Nature genetics 52 (9), 939-949, 2020 | 157 | 2020 |
| De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay JX Chong, MJ McMillin, KM Shively, AE Beck, CT Marvin, JR Armenteros, ... The American Journal of Human Genetics 96 (3), 462-473, 2015 | 147 | 2015 |
| Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease OM de Goede, DC Nachun, NM Ferraro, MJ Gloudemans, AS Rao, ... Cell 184 (10), 2633-2648. e19, 2021 | 145 | 2021 |
| Transcriptomic signatures across human tissues identify functional rare genetic variation NM Ferraro, BJ Strober, J Einson, NS Abell, F Aguet, AN Barbeira, ... Science 369 (6509), eaaz5900, 2020 | 141 | 2020 |
| An atlas of alternative polyadenylation quantitative trait loci contributing to complex trait and disease heritability L Li, KL Huang, Y Gao, Y Cui, G Wang, ND Elrod, Y Li, YE Chen, P Ji, ... Nature genetics 53 (7), 994-1005, 2021 | 133 | 2021 |
| Guidelines for large-scale sequence-based complex trait association studies: lessons learned from the NHLBI exome sequencing project PL Auer, AP Reiner, G Wang, HM Kang, GR Abecasis, D Altshuler, ... The American Journal of Human Genetics 99 (4), 791-801, 2016 | 108 | 2016 |
| MECR mutations cause childhood-onset dystonia and optic atrophy, a mitochondrial fatty acid synthesis disorder G Heimer, JM Kerätär, LG Riley, S Balasubramaniam, E Eyal, ... The American Journal of Human Genetics 99 (6), 1229-1244, 2016 | 96 | 2016 |
| Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants S Zhang, H Zhang, Y Zhou, M Qiao, S Zhao, A Kozlova, J Shi, AR Sanders, ... Science 369 (6503), 561-565, 2020 | 94 | 2020 |
Matthew StephensUniversity of Chicago確認したメール アドレス: uchicago.edu
