Yin Y Shugart

Yin Y Shugart

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Yin Y Shugart

Yin Y Shugart

Publications by authors named "Yin Y Shugart"

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19Publications

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A Novel Mixture Model to Estimate the Time to Drug Effect Onset and Its Association with Covariates.

Hum Hered 2015 16;80(2):90-9. Epub 2016 Jan 16.

Unit of Statistical Genomics, Intramural Research Program, National Institute of Mental Health, National Institutes of Health, Bethesda, Md., USA.

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http://dx.doi.org/10.1159/000440880DOI Listing
September 2016

Family-based tests applied to extended pedigrees identify rare variants related to hypertension.

BMC Proc 2014 17;8(Suppl 1):S31. Epub 2014 Jun 17.

Division of Intramural Research Program, National Institute of Mental Health, National Institutes of Health, Building 35, Room 3A 1000, 35 Convent Drive, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1186/1753-6561-8-S1-S31DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143699PMC
December 2014

Identification of genotype errors.

Methods Mol Biol 2012 ;850:11-24

Unit of Statistical Genomics, Intramural Research Program, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1007/978-1-61779-555-8_2DOI Listing
May 2012

The association between parental bonding and obsessive compulsive disorder in offspring at high familial risk.

J Affect Disord 2008 Nov 4;111(1):31-9. Epub 2008 Mar 4.

Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21287-7228, USA.

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http://dx.doi.org/10.1016/j.jad.2008.01.025DOI Listing
November 2008

Genetic association study of BDNF in depression: finding from two cohort studies and a meta-analysis.

Am J Med Genet B Neuropsychiatr Genet 2008 Sep;147B(6):814-21

Department of Social Medicine, University of Bristol, Bristol, United Kingdom.

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http://dx.doi.org/10.1002/ajmg.b.30686DOI Listing
September 2008

Dopaminergic polymorphisms in Tourette syndrome: association with the DAT gene (SLC6A3).

Am J Med Genet B Neuropsychiatr Genet 2007 Jul;144B(5):605-10

Department of Neurology, Johns Hopkins University School of Medicine, Harriet Lane Children's Health Building, Wolfe Street, Baltimore, Maryland 21205, USA.

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http://dx.doi.org/10.1002/ajmg.b.30466DOI Listing
July 2007

Covariate-based linkage analysis: application of a propensity score as the single covariate consistently improves power to detect linkage.

Eur J Hum Genet 2006 Sep 31;14(9):1018-26. Epub 2006 May 31.

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

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http://dx.doi.org/10.1038/sj.ejhg.5201650DOI Listing
September 2006

Application of the propensity score in a covariate-based linkage analysis of the Collaborative Study on the Genetics of Alcoholism.

BMC Genet 2005 Dec 30;6 Suppl 1:S33. Epub 2005 Dec 30.

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland 21205, USA.

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http://bmcgenet.biomedcentral.com/articles/10.1186/1471-2156
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http://dx.doi.org/10.1186/1471-2156-6-S1-S33DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866752PMC
December 2005

Application of family-based association testing to assess the genotype-phenotype association involved in complex traits using single-nucleotide polymorphisms.

BMC Genet 2005 Dec 30;6 Suppl 1:S68. Epub 2005 Dec 30.

Department of Epidemiology, Bloomberg School of Public Health, 615 North Work Street, Johns Hopkins University, Baltimore, Maryland 21205, USA.

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http://bmcgenet.biomedcentral.com/articles/10.1186/1471-2156
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http://dx.doi.org/10.1186/1471-2156-6-S1-S68DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866714PMC
December 2005

Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus.

Brain Dev 2004 Aug;26(5):326-34

Division of Neurogenetics and Howard Hughes Medical Institute, Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, HIM 816, 4 Blackfan Circle, Boston, MA 02115, USA.

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http://dx.doi.org/10.1016/j.braindev.2003.09.004DOI Listing
August 2004

The power and statistical behaviour of allele-sharing statistics when applied to models with two disease loci.

J Genet 2002 Dec;81(3):99-103

Epidemiology Department, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205, USA.

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December 2002

CGH-targeted linkage analysis reveals a possible BRCA1 modifier locus on chromosome 5q.

Hum Mol Genet 2002 May;11(11):1327-32

Department of Medicine, Abramson Family Cancer Research Institute, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

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http://dx.doi.org/10.1093/hmg/11.11.1327DOI Listing
May 2002

Mutations in the RPGR gene cause X-linked cone dystrophy.

Hum Mol Genet 2002 Mar;11(5):605-11

Cole Eye Institute, I-31, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA.

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http://dx.doi.org/10.1093/hmg/11.5.605DOI Listing
March 2002