Publications by authors named "Seungtai Yoon"

22Publications

Characterization of SLITRK1 variation in obsessive-compulsive disorder.

PLoS One 2013 21;8(8):e70376. Epub 2013 Aug 21.

John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, United States of America ; Department of Neuroscience, University of Miami Miller School of Medicine, Miami, Florida, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0070376PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3749144PMC
April 2014

Principal components ancestry adjustment for Genetic Analysis Workshop 17 data.

BMC Proc 2011 Nov 29;5 Suppl 9:S66. Epub 2011 Nov 29.

Department of Applied Mathematics and Statistics, State University of New York at Stony Brook, Stony Brook, NY 11733, USA.

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http://dx.doi.org/10.1186/1753-6561-5-S9-S66DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287905PMC
November 2011

Identification of genes and variants associated with quantitative traits using Bayesian factor screening.

BMC Proc 2011 Nov 29;5 Suppl 9:S4. Epub 2011 Nov 29.

Department of Epidemiology and Population Health, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.

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http://dx.doi.org/10.1186/1753-6561-5-S9-S4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287876PMC
November 2011

AnnTools: a comprehensive and versatile annotation toolkit for genomic variants.

Bioinformatics 2012 Mar 18;28(5):724-5. Epub 2012 Jan 18.

The Seaver Autism Center for Research and Treatment, Department of Psychiatry, Levy Library, Mount Sinai School of Medicine, New York, NY 10029, USA.

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http://dx.doi.org/10.1093/bioinformatics/bts032DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3289923PMC
March 2012

Finding disease variants in Mendelian disorders by using sequence data: methods and applications.

Am J Hum Genet 2011 Dec 1;89(6):701-12. Epub 2011 Dec 1.

Department of Biostatistics, Columbia University, New York, NY 10032, USA.

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http://dx.doi.org/10.1016/j.ajhg.2011.11.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234377PMC
December 2011

Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm.

Nucleic Acids Res 2011 May 14;39(10):e65. Epub 2011 Feb 14.

Laboratory Department, Diagnostic Genetic Unit, Careggi Hospital, Florence 5014, Italy.

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https://academic.oup.com/nar/article-lookup/doi/10.1093/nar/
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http://dx.doi.org/10.1093/nar/gkr068DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105418PMC
May 2011

Sensitive and accurate detection of copy number variants using read depth of coverage.

Genome Res 2009 Sep 5;19(9):1586-92. Epub 2009 Aug 5.

Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA.

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http://genome.cshlp.org/cgi/doi/10.1101/gr.092981.109
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http://dx.doi.org/10.1101/gr.092981.109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752127PMC
September 2009

Mixture modeling of microarray gene expression data.

BMC Proc 2007 18;1 Suppl 1:S50. Epub 2007 Dec 18.

Department of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, New York 11790, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367561PMC
http://dx.doi.org/10.1186/1753-6561-1-s1-s50DOI Listing
December 2009

A Bayesian approach for applying Haseman-Elston methods.

BMC Genet 2005 Dec 30;6 Suppl 1:S39. Epub 2005 Dec 30.

Department of Applied Mathematics and Statistics, State University of New York at Stony Brook, Stony Brook, NY 11794, USA.

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http://dx.doi.org/10.1186/1471-2156-6-S1-S39DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866746PMC
December 2005