| Massively scaled-up testing for SARS-CoV-2 RNA via next-generation sequencing of pooled and barcoded nasal and saliva samples JS Bloom, L Sathe, C Munugala, EM Jones, M Gasperini, NB Lubock, ... Nature Biomedical Engineering 5 (7), 657-665, 2021 | 62 | 2021 |
| Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing JS Bloom, L Sathe, C Munugala, EM Jones, M Gasperini, NB Lubock, ... MedRxiv, 2020.08. 04.20167874, 2021 | 52 | 2021 |
| Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation I Lin, A Wei, Z Awamleh, M Singh, A Ning, A Herrera, BE Russell, ... JCI insight 8 (10), 2023 | 8 | 2023 |
| Central 22q11. 2 deletion (LCR22 B‐D) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL … I Lin, Y Afshar, J Goldstein, J Grossman, WW Grody, F Quintero‐Rivera American Journal of Medical Genetics Part A 185 (10), 3042-3047, 2021 | 5 | 2021 |
| Multi-omics on truncating ASXL1 mutations in Bohring Opitz syndrome identify dysregulation of canonical and non-canonical Wnt signaling I Lin, A Wei, Z Awamleh, M Singh, A Ning, A Herrera, B Russell, ... bioRxiv, 2022.12. 15.520167, 2022 | 2 | 2022 |
| ASXL1 truncating variants in BOS and myeloid leukemia drive shared disruption of Wnt-signaling pathways but have differential isoform usage of RUNX3 I Lin, Z Awamleh, M Sinvhal, A Wan, L Bondhus, A Wei, BE Russell, ... BMC Medical Genomics 17 (1), 282, 2024 | | 2024 |
| The evolution and functional significance of the programmed ribosomal frameshift in prfB CR Prince, IN Lin, HA Feaga bioRxiv, 2024 | | 2024 |
| Increased frequency of clonal hematopoiesis of indeterminate potential in Bloom syndrome probands and carriers I Lin, A Wei, TA Gebo, PC Boutros, M Flanagan, N Kucine, C Cunniff, ... Haematologica 110 (1), 187, 2024 | | 2024 |
| Development of Highly Efficient Universal Pneumocystis Primers and Their Application in Investigating the Prevalence and Genetic Diversity of Pneumocystis in … L Ma, I Lin, ST Hunter, B Blasi, P Danesi, C Weissenbacher-Lang, ... Journal of Fungi 10 (5), 355, 2024 | | 2024 |
| YebC2 resolves ribosome stalling at polyprolines independent of EF-P and the ABCF ATPase YfmR HR Hong, CR Prince, L Wu, I Lin, H Feaga bioRxiv, 2024.10. 18.618948, 2024 | | 2024 |
| From Germline to Somatic: ASXL1’s Multifaceted Role in Development and Disease I Lin UCLA, 2024 | | 2024 |
| P192: Deep neurologic phenotyping and biomarker development in Bohring-Opitz syndrome using EEGs, neurodevelopmental assessments, and DNA methylation signature B Russell, J Sloan, H Nariai, N Ludwig, A Dickinson, Z Awamleh, ... Genetics in Medicine Open 2, 2024 | | 2024 |
| Truncating ASXL1 mutations in Bohring-Opitz Syndrome cause epigenetically driven upregulation of Wnt signaling I Lin, A Wei, Z Awamleh, M Singh, A Ning, A Herrera, B Russell, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 38-39, 2024 | | 2024 |
| ASXL1 mutations that cause Bohring Opitz Syndrome (BOS) or acute myeloid leukemia share epigenomic and transcriptomic signatures I Lin, Z Awamleh, A Wei, B Russell, R Weksberg, VA Arboleda bioRxiv, 2022.12. 15.519823, 2022 | | 2022 |
| SwabSeq: A sequencing-based platform for high-throughput SARS-CoV-2 testing JS Bloom, L Sathe, C Munugala, EM Jones, M Gasperini, NB Lubock, ... Nature biomedical engineering 5 (7), 657, 2021 | | 2021 |
| Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing Joshua S. Bloom1, 2, 3, Laila Sathe4, Chetan Munugala1, 2, Eric M. Jones3, Molly Gasperini3 … L Guo, J Boocock, M Hochman, SW Simpkins, I Lin, N LaPierre, D Hong, ... | | |
