Parents
Sign in to add mentor| Jay Shendure | grad student | 2007-2012 | University of Washington | |
| (Next Generation Mendelian Genetics.) | ||||
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| Cheruba E, Viswanathan R, Wong PM, et al. (2022) Heat selection enables highly scalable methylome profiling in cell-free DNA for noninvasive monitoring of cancer patients. Science Advances. 8: eabn4030 |
| Herberts C, Annala M, Sipola J, et al. (2022) Deep whole-genome ctDNA chronology of treatment-resistant prostate cancer. Nature |
| Kleftogiannis D, Ho D, Liew JX, et al. (2020) Detection of genomic alterations in breast cancer with circulating tumour DNA sequencing. Scientific Reports. 10: 16774 |
| Bhatia NS, Lim JY, Bonnard C, et al. (2020) Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management. Archives of Disease in Childhood |
| Suzuki Y, Ng SB, Chua C, et al. (2017) Multiregion ultra-deep sequencing reveals early intermixing and variable levels of intratumoral heterogeneity in colorectal cancer. Molecular Oncology. 11: 124-139 |
| Ng SK, Hu T, Long X, et al. (2016) Feature co-localization landscape of the human genome. Scientific Reports. 6: 20650 |
| Kumar Y, Yang J, Hu T, et al. (2015) Massive interstitial copy-neutral loss-of-heterozygosity as evidence for cancer being a disease of the DNA-damage response. Bmc Medical Genomics. 8: 42 |
| Shinsky SA, Hu M, Vought VE, et al. (2014) A non-active-site SET domain surface crucial for the interaction of MLL1 and the RbBP5/Ash2L heterodimer within MLL family core complexes. Journal of Molecular Biology. 426: 2283-99 |
| Bernier FP, Caluseriu O, Ng S, et al. (2012) Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndrome. American Journal of Human Genetics. 90: 925-33 |
| O'Roak BJ, Deriziotis P, Lee C, et al. (2012) Corrigendum: Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (Nature Genetics (2011) 43, (585-589)) Nature Genetics. 44: 471 |