| A reference panel of 64,976 haplotypes for genotype imputation Nature genetics 48 (10), 1279-1283, 2016 | 3168 | 2016 |
| Discovery of common and rare genetic risk variants for colorectal cancer JR Huyghe, SA Bien, TA Harrison, HM Kang, S Chen, SL Schmit, ... Nature genetics 51 (1), 76-87, 2019 | 506 | 2019 |
| ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions E Dolzhenko, V Deshpande, F Schlesinger, P Krusche, R Petrovski, ... Bioinformatics 35 (22), 4754-4756, 2019 | 289 | 2019 |
| ExpansionHunter Denovo: a computational method for locating known and novel repeat expansions in short-read sequencing data E Dolzhenko, MF Bennett, PA Richmond, B Trost, S Chen, JJFA Van Vugt, ... Genome biology 21, 1-14, 2020 | 170 | 2020 |
| Paragraph: a graph-based structural variant genotyper for short-read sequence data S Chen, P Krusche, E Dolzhenko, RM Sherman, R Petrovski, ... Genome biology 20, 1-13, 2019 | 161 | 2019 |
| Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer SA Bien, YR Su, DV Conti, TA Harrison, C Qu, X Guo, Y Lu, D Albanes, ... Human genetics 138, 307-326, 2019 | 57 | 2019 |
| A mixed-effects model for powerful association tests in integrative functional genomics YR Su, C Di, S Bien, L Huang, X Dong, G Abecasis, S Berndt, S Bezieau, ... The American journal of human genetics 102 (5), 904-919, 2018 | 35 | 2018 |
| Proper conditional analysis in the presence of missing data: Application to large scale meta-analysis of tobacco use phenotypes Y Jiang, S Chen, D McGuire, F Chen, M Liu, WG Iacono, JK Hewitt, ... PLoS genetics 14 (7), e1007452, 2018 | 28 | 2018 |
| Optimal sequencing strategies for identifying disease-associated singletons S Rashkin, G Jun, S Chen, ... PLoS genetics 13 (6), e1006811, 2017 | 25 | 2017 |
| Tissue-specific alteration of metabolic pathways influences glycemic regulation NHJ Ng, SM Willems, J Fernandez, RS Fine, E Wheeler, J Wessel, ... BioRxiv, 790618, 2019 | 11 | 2019 |
| Improved score statistics for meta‐analysis in single‐variant and gene‐level association studies J Yang, S Chen, G Abecasis, IAMDGC Genetic epidemiology 42 (4), 333-343, 2018 | 11 | 2018 |
| Association analysis and meta-analysis of multi-allelic variants for large-scale sequence data Y Jiang, S Chen, X Wang, M Liu, WG Iacono, JK Hewitt, JE Hokanson, ... Genes 11 (5), 586, 2020 | 10 | 2020 |
| Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data SA Bien, PL Auer, TA Harrison, C Qu, CM Connolly, PG Greenside, ... PLoS One 12 (11), e0186518, 2017 | 8 | 2017 |
| A method for Quantifying circulating tumor DNA level and Molecular Response using Methylome Sequencing S Chen, K Chang, K Quinn, CY Lee, J Zhao, T Jiang, S Zhang, ... Cancer Res 83 (7_suppl), 3123, 2023 | 4 | 2023 |
| RFC1 repeat expansion analysis from whole genome sequencing data simplifies screening and increases diagnostic rates R Sullivan, S Chen, CT Saunders, WY Yau, YY Goh, E O’Connor, ... medRxiv, 2024.02. 28.24303510, 2024 | 3 | 2024 |
| Analytical validation of a robust integrated genomic and epigenomic liquid biopsy for biomarker discovery, therapy selection, and response monitoring T Jiang, I Wu, Y Kim, N Alla, G Tran, D Ma, F Shah, J Zhao, S Chen, ... Cancer Research 83 (7_Supplement), 6601-6601, 2023 | 3 | 2023 |
| BRCA1 promoter methylation in sporadic breast cancer patients detected by liquid biopsy J Yen, S Chen, C Jenkins, LM Drusbosky, B Overstreet, J Zhao, Y Fu, ... chemotherapy 1 (2), 3, 2023 | 2 | 2023 |
| Proper conditional analysis in the presence of missing data identified novel independently associated low frequency variants in nicotine dependence genes B Jiang, S Chen, Y Jiang, M Liu, WG Iacono, JK Hewitt, JE Hokanson, ... bioRxiv, 222695, 2017 | 2 | 2017 |
| Accurate epigenomic estimates of circulating tumor fraction in large-scale clinical data WWY Greenwald, Y He, S Chen, T Jiang, A Valouev, J Min, C Barbacioru, ... Lung 276, 203, 2022 | 1 | 2022 |
| The contribution of rare and low-frequency variants to colorectal cancer heritability JR Huyghe, S Chen, HM Kang, T Harrison, SI Berndt, S Bézieau, ... Cancer Research 77 (13_Supplement), 1304-1304, 2017 | 1 | 2017 |
Michael A EberlePacific BiosciencesPreverjeni e-poštni naslov na pacificbiosciences.com
