| Low-pass sequencing increases the power of GWAS and decreases measurement error of polygenic risk scores compared to genotyping arrays JH Li, CA Mazur, T Berisa, JK Pickrell Genome research 31 (4), 529-537, 2021 | 107 | 2021 |
| Validation of concurrent preimplantation genetic testing for polygenic and monogenic disorders, structural rearrangements, and whole and segmental chromosome aneuploidy with a … NR Treff, R Zimmerman, E Bechor, J Hsu, B Rana, J Jensen, J Li, ... European journal of medical genetics 62 (8), 103647, 2019 | 84 | 2019 |
| Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics K Wasik, T Berisa, JK Pickrell, JH Li, DJ Fraser, K King, C Cox BMC genomics 22, 1-7, 2021 | 71 | 2021 |
| Assessment of imputation from low-pass sequencing to predict merit of beef steers WM Snelling, JL Hoff, JH Li, LA Kuehn, BN Keel, AK Lindholm-Perry, ... Genes 11 (11), 1312, 2020 | 38 | 2020 |
| Time-dependent saddle–node bifurcation: Breaking time and the point of no return in a non-autonomous model of critical transitions JH Li, FXF Ye, H Qian, S Huang Physica D: Nonlinear Phenomena 395, 7-14, 2019 | 20 | 2019 |
| Low-pass sequencing plus imputation using avidity sequencing displays comparable imputation accuracy to sequencing by synthesis while reducing duplicates JH Li, K Findley, JK Pickrell, K Blease, J Zhao, S Kruglyak G3: Genes, Genomes, Genetics 14 (2), jkad276, 2024 | 6 | 2024 |
| Imputation of structural variants using a multi-ancestry long-read sequencing panel enables identification of disease associations B Noyvert, AM Erzurumluoglu, D Drichel, S Omland, TFM Andlauer, ... medRxiv, 2023.12. 20.23300308, 2023 | 5 | 2023 |
| Relative matching using low coverage sequencing E Petter, R Schweiger, B Shahino, T Shor, M Aker, L Almog, ... bioRxiv, 2020.09. 09.289322, 2020 | 5 | 2020 |
| Ancestry dynamics and trait selection in a designer cat breed CB Kaelin, KA McGowan, AD Hutcherson, JM Delay, JH Li, S Kiener, ... Current biology 34 (7), 1506-1518. e7, 2024 | 4 | 2024 |
| Validation of simultaneous preimplantation genetic testing (PGT) for aneuploidy, monogenic, and polygenic disorders NR Treff, R Zimmerman, J Li, E Bechor, B Rana, A Samoilenko, ... Fertility and Sterility 110 (4), e103-e104, 2018 | 3 | 2018 |
| Genotype inference from aggregated chromatin accessibility data reveals genetic regulatory mechanisms BM Wenz, Y He, NC Chen, JK Pickrell, JH Li, MF Dudek, T Li, R Keener, ... bioRxiv, 2024 | | 2024 |
| A comparison between low-cost library preparation kits for low coverage sequencing CM Stewart, MJS Gibson, JY Parsa, JH Li bioRxiv, 2024.01. 30.578044, 2024 | | 2024 |
| The effects of reference panel perturbations on the accuracy of genotype imputation JH Li, A Liu, CA Buerkle, W Palmer, GM Belbin, M Ahangari, MJS Gibson, ... bioRxiv, 2023.08. 10.552684, 2023 | | 2023 |
| Combined Low-pass Whole Genome and Targeted Sequencing Identifies Causative Mutations and Associated Genomic Scarring Indicative of Homologous Recombination Deficiency J An, GM Belbin, C Mazur, J Li, J Pickrell, D Metzger, S Gao, E Van Roey, ... JOURNAL OF MOLECULAR DIAGNOSTICS 24 (10), S109-S110, 2022 | | 2022 |