Author details

Full Name

Seungtai Yoon

Affiliation

ORCID

Career Start Year

2005

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37388917	Sharing parental genomes by siblings concordant or discordant for autism.		2023
34471188	Rates of contributory de novo mutation in high and low-risk autism families.	Commun Biol	2021
24776741	De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.	Mol Psychiatry	2014
25363768	The contribution of de novo coding mutations to autism spectrum disorder.	Nature	2014
23743231	Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.	Genomics	2013
23990902	Characterization of SLITRK1 variation in obsessive-compulsive disorder.	PLoS One	2013
21912879	Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia.	Hum Genet	2012
22495311	Patterns and rates of exonic de novo mutations in autism spectrum disorders.	Nature	2012
22722845	A tumour suppressor network relying on the polyamine-hypusine axis.	Nature	2012
22257670	AnnTools: a comprehensive and versatile annotation toolkit for genomic variants.	Bioinformatics	2012
22137099	Finding disease variants in Mendelian disorders by using sequence data: methods and applications.	Am J Hum Genet	2011
22384316	Inferring haplotypes of copy number variations from high-throughput data with uncertainty.	G3 (Bethesda)	2011
22373457	Principal components ancestry adjustment for Genetic Analysis Workshop 17 data.	BMC Proceedings	2011
22373183	Identification of genes and variants associated with quantitative traits using Bayesian factor screening.	BMC Proceedings	2011
21346763	Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia.	Nature	2011
21293372	Mapping copy number variation by population-scale genome sequencing.	Nature	2011
21321017	Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm.	Nucleic Acids Research	2011
22196331	High frequencies of de novo CNVs in bipolar disorder and schizophrenia.	Neuron	2011
21658582	Rare de novo and transmitted copy-number variation in autistic spectrum disorders.	Neuron	2011
19855392	Microduplications of 16p11.2 are associated with schizophrenia.	Nat Genet	2009
19657104	Sensitive and accurate detection of copy number variants using read depth of coverage.	Genome Res	2009
18466550	Mixture modeling of microarray gene expression data.	BMC Proceedings	2007
17363630	Strong association of de novo copy number mutations with autism.	Science	2007
17142309	Novel patterns of genome rearrangement and their association with survival in breast cancer.	Genome Res	2006
16451649	A Bayesian approach for applying Haseman-Elston methods.	BMC Genetics	2005