| Next-generation genotype imputation service and methods S Das, L Forer, S Schönherr, C Sidore, AE Locke, A Kwong, SI Vrieze, ... Nature genetics 48 (10), 1284-1287, 2016 | 3337 | 2016 |
| A reference panel of 64,976 haplotypes for genotype imputation Nature genetics 48 (10), 1279-1283, 2016 | 2950 | 2016 |
| The GTEx Consortium atlas of genetic regulatory effects across human tissues GTEx Consortium Science 369 (6509), 1318-1330, 2020 | 2688 | 2020 |
| Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ... Nature 590 (7845), 290-299, 2021 | 1417 | 2021 |
| Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants LC Tsoi, PE Stuart, C Tian, JE Gudjonsson, S Das, M Zawistowski, ... Nature communications 8 (1), 15382, 2017 | 347 | 2017 |
| Genome-wide association analysis of psoriatic arthritis and cutaneous psoriasis reveals differences in their genetic architecture PE Stuart, RP Nair, LC Tsoi, T Tejasvi, S Das, HM Kang, E Ellinghaus, ... The American Journal of Human Genetics 97 (6), 816-836, 2015 | 329 | 2015 |
| 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 | 303 | 2020 |
| Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits LM Evans, R Tahmasbi, SI Vrieze, GR Abecasis, S Das, S Gazal, ... Nature genetics 50 (5), 737-745, 2018 | 277 | 2018 |
| Use of> 100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in … MH Kowalski, H Qian, Z Hou, JD Rosen, AL Tapia, Y Shan, D Jain, ... PLoS genetics 15 (12), e1008500, 2019 | 227 | 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 | 218 | 2021 |
| Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci LC Tsoi, SL Spain, E Ellinghaus, PE Stuart, F Capon, J Knight, T Tejasvi, ... Nature communications 6 (1), 7001, 2015 | 215 | 2015 |
| Genotype imputation from large reference panels S Das, GR Abecasis, BL Browning Annual review of genomics and human genetics 19 (1), 73-96, 2018 | 213 | 2018 |
| Genetic consequences of the transatlantic slave trade in the Americas SJ Micheletti, K Bryc, SGA Esselmann, WA Freyman, ME Moreno, ... The American Journal of Human Genetics 107 (2), 265-277, 2020 | 132 | 2020 |
| 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 | 122 | 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 | 113 | 2020 |
| Genetic signature to provide robust risk assessment of psoriatic arthritis development in psoriasis patients MT Patrick, PE Stuart, K Raja, JE Gudjonsson, T Tejasvi, J Yang, ... Nature communications 9 (1), 4178, 2018 | 111 | 2018 |
| PhenomeXcan: Mapping the genome to the phenome through the transcriptome M Pividori, PS Rajagopal, A Barbeira, Y Liang, O Melia, L Bastarache, ... Science advances 6 (37), eaba2083, 2020 | 99 | 2020 |
| De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population MD Kessler, DP Loesch, JA Perry, NL Heard-Costa, D Taliun, BE Cade, ... Proceedings of the National Academy of Sciences 117 (5), 2560-2569, 2020 | 68 | 2020 |
| A fully adjusted two‐stage procedure for rank‐normalization in genetic association studies T Sofer, X Zheng, SM Gogarten, CA Laurie, K Grinde, JR Shaffer, ... Genetic epidemiology 43 (3), 263-275, 2019 | 63 | 2019 |
| Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling N Dand, S Mucha, LC Tsoi, SK Mahil, PE Stuart, A Arnold, H Baurecht, ... Human molecular genetics 26 (21), 4301-4313, 2017 | 52 | 2017 |
Goncalo AbecasisUniversity of Michigan School of Public Health在 umich.edu 的电子邮件经过验证
