Seungtai Yoon, Ph.D.
Affiliations: | 2006 | Stony Brook University, Stony Brook, NY, United States |
Area:
StatisticsGoogle:
"Seungtai Yoon"Parents
Sign in to add mentor| Kenny Ye | grad student | 2006 | SUNY Stony Brook | |
| (Bayesian factor screening.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Wroten M, Yoon S, Andrews P, et al. (2023) Sharing parental genomes by siblings concordant or discordant for autism. Cell Genomics. 3: 100319 |
| Iossifov I, O'Roak BJ, Sanders SJ, et al. (2014) The contribution of de novo coding mutations to autism spectrum disorder. Nature. 515: 216-21 |
| McCarthy SE, Gillis J, Kramer M, et al. (2014) De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability. Molecular Psychiatry. 19: 652-8 |
| Ozomaro U, Cai G, Kajiwara Y, et al. (2013) Characterization of SLITRK1 variation in obsessive-compulsive disorder. Plos One. 8: e70376 |
| Schafer CM, Campbell NG, Cai G, et al. (2013) Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA. Genomics. 102: 270-7 |
| Scuoppo C, Miething C, Lindqvist L, et al. (2012) A tumour suppressor network relying on the polyamine-hypusine axis. Nature. 487: 244-8 |
| Neale BM, Kou Y, Liu L, et al. (2012) Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature. 485: 242-5 |
| Makarov V, O'Grady T, Cai G, et al. (2012) AnnTools: a comprehensive and versatile annotation toolkit for genomic variants. Bioinformatics (Oxford, England). 28: 724-5 |
| Marti-Masso JF, Ruiz-MartÃnez J, Makarov V, et al. (2012) Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia. Human Genetics. 131: 435-42 |
| Kato M, Yoon S, Hosono N, et al. (2011) Inferring haplotypes of copy number variations from high-throughput data with uncertainty. G3 (Bethesda, Md.). 1: 35-42 |