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== Yoonhee Kim, M.P.H, Ph.D. ==
 
kimyoo@mail.nih.gov
 
  
Research fellow, Inherited Disease Research Branch
 
 
National Human Genome Research Institute (NHGRI)
 
 
National Institutes of Health (NIH)
 
 
333 Cassell Drive Suite 1200,
 
Baltimore, MD 21224
 
 
 
 
EDUCATION
 
 
----
 
2008      Ph.D. Biostatistics and Epidemiology, School of Public Health, Seoul National University
 
 
2005-2008  Pre-doctoral training at National Human Genome Research Institute, National Institutes of Health, USA
 
 
2003      M.P.H. Biostatistcs and Epidemiology, School of Public Health, Seoul National University
 
 
2001      B.S. in Statistics and B.S. in Biology, Ewha Womans University
 
 
 
 
RESEARCH INTERESTS
 
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Statistical Genetics, Genomics, Genometrics, Genetic Epidemiology, Bioinformatics, Next Generation Sequencing(NGS) data analysis, Human genetics in Autism, Cardiovascular diseases, Lung health (COPD, PAH), Oral cleft, Craniosynostosis, Behcet's disease.
 
 
 
 
 
HONOR AND AWARDS
 
 
----
 
 
 
2012 NHGRI Diversity and Community Outreach GREAT Award for teaching at University of District of Columbia, Washington D.C.
 
 
2012 Chief Judge for the Fellows Award for Research Excellence (FARE) 2013 in Genomics study section
 
 
2011 NIH FARE Award 2012
 
 
2007 Graduate Partnership Program Travel Award
 
 
2005    Pre-doctoral Training Fellowship supported by Korea Research Foundation of Korea Government
 
 
 
 
PUBLICATIONS
 
 
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(* co-first author).
 
 
K. C. Desch, A. B. Ozel, D. Siemieniak, Y. Kalish, C. Thornburg,  A. Sharathkumar, C. McHugh, C. Laurie, A. Crenshaw, D. Mirel, [[Y. Kim]], C. D. Cropp, A. M. Molloy,
 
P. N. Kirke, J. E. Bailey-Wilson, A. F. Wilson, J. L. Mills,  J. M. Scott, L. C. Brody, J. Z. Li and D. Ginsburg, “ Linkage Analysis Identifies a Novel Locus for Plasma von Willebrand
 
Factor Undetected by Genome Wide Association”, in press, PNAS, 2012.
 
 
C. M. Justice*, G. Yagnik*, [[Y. Kim]], I. Peter, E. W. Jabs, X. Ye, L. Shi, M.L. Cunningham, V. Kimonis, T. Roscioli, S. A. Wall, A. O.M. Wilkie, J. Stoler, J. T. Richtsmeier, Y. Heuze, P. A. Sanchez-Lara, M. F. Buckley, C. M. Druschel, J. L. Mills, M.Caggana, P. A. Romitti, D. M. Kay, C. Senders, P.J. Taub, O. D. Klein, J. Boggan, M. Zwienenberg-Lee, C. Naydenov, J. Kim,  A.F. Wilson, S. A. Boyadijiev, “A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9”, doi:10.1038/ng.2463 Nature Genetics, 2012.
 
 
Y. Kirino, G. Bertsias, Y. Ishigatsubo, N. Mizuki, I. Tugal-Tutkun, E. Seyahi, Y. Ozyazgan, F. S.Sacli, B. Erer, Z. Emrence, A. Cakar, D. Ustek, C. Satorius, A. Ueda, M. Takeno, [[Y. Kim]], M. J. Ombrello, A. Meguro, A. Gul, E.F. Remmers, D.L.Kastner, “A genome-wide association study identifies new susceptibility loci for Behcet’s disease and epistasis between HLA-B*51 and ERAP1”, in press Nature Genetics, 2012.
 
 
N. H. Miller, C. M. Justice, B. Marosy, K. Swindle,[[ Y. Kim]], MH. Roy-Gagnon, H. Sung, D. Behneman, K. F. Doheny, E. Pugh, A .F. Wilson “Fine-mapping and family-based association tests of idiopathic scoliosis on 9q31.3-134.3 and 16p12.3-q22.2,” Human Heredity, Vol 74, No. 1, 36-44, 2012.
 
 
N. N. Hansel, I. Ruczinski, N. Rafaels, D. D. Sin, D. Daley, A. Malinina, L. Huang, A. Sandford, M. Elliott, T. Murray, [[Y. Kim]], C. Vergara, S. R. Heckbert, B. M. Psaty, G. Li, F. Aminuddin, J. Dupuis, G. O’Connor, M. Boezen, D.S.Postma, J.Smolonska, R. Crystal, T. Toshiko, L. Ferruci, E. Silverman, E. Wan, J. Vestbo, D. Lomas, J. Connett, R. A. Wise, E.R. Neptune, R. Mathias, P.D. Pare, T. H. Beaty, K. C. Barnes “Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD,” Human Genetics, DOI: 10.1007/s00439-012-1219-6, 2012.
 
 
M. J. Emond, T. Louie, J. Emerson, W. Zhao, R. A. Mathias, M. R. Knowles, F. A. Wright, M. J. Rieder, H.K. Tabor, D.A. Nickerson, K.C. Barnes, NHLBI GO Exome Sequencing Project, Lung GO ([[Y. Kim]]), R.L. Gibson & M.J. Bamshad “Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis,” Nature Genetics, Vol 44: 886–889, 2012.
 
 
S. P. David, A. Hamidovic, G. K. Chen, A.W. Bergen, J. Wessel, J.L. Kasberger, W. M. Brown, S. Petruzella, E. L. Thacker, [[Y. Kim]], M.A. Nalls, G. J. Tranah, Y.J. Sung, AABC, AAPC, CHS, CARe, GeneSTAR, HANDLS, HealthABC, HyperGEN, WHI(SHARe), C.A. Haiman, H.Furberg, “Genome-wide meta-analyses of smoking behaviors in African Americans”, Translational Psychiatry, 2:e119; doi:10.1038/tp.2012.41, 2012.
 
 
[[Y. Kim]]*, Q. Li*, C.D. Cropp, H. Sung, J. Cai, C.L. Simpson, B.Perry, A.Dasgupta, J.D. Malley, A.F. Wilson, J.E. Bailey-Wilson “Performance of Random Forests and Logic Regression Methods Using Mini-Exome Sequence data,” BMC proceedings, Vol 5 (supp 9):S104, 2011.
 
 
J.E. Bailey-Wilson, J.S. Brennan, R. Culverhouse, [[Y. Kim]], Y. Jiang, J. Jung, Q. Li, C. Scholosberg, L. Wang, Y.E. Yilmaz, H. Zhang, Z. Zhan, “Regression and Data Mining Methods for Analyses of Multiple Rare Variants in GAW17 “ Mini-Exome” data,”  Genetic Epidemiology, Vol 35(supp 1):S92-S100, 2011.
 
 
H. Sung, [[Y. Kim]], J. Cai, C.D. Cropp, C.L. Simpson, Q. Li, B. C Perry,  A.J.M. Sorant, J.E. Bailey-Wilson, A.F. Wilson “A comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression,” BMC proceedings, Vol 5(supp 9):S15, 2011.
 
 
T.L. Assimes, H. Holm, ADVANCE, CATHGEN, GeneSTAR ([[Y. Kim]]), INTERHEART study groups, decode genetics, and T. Quertermous “Lack of association between the Trp719Arg polymorphism in kinesin-like protein 6 and coronary artery disease in 19 case-control studies,” Journal of the American College of Cardiology, Vol 56, No 19, 2010.
 
 
R.A. Mathias*, [[Y. Kim]]*, H. Sung, R.Y. Yanek, J.E. Hererra-Galeano, I. Ruczinski, A.F. Wilson, N. Faraday, L.C. Becker, D.M. Becker “A Combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in Caucasian and African American families with coronary artery disease,” BMC Medical Genomics, 3:22, 2010.
 
 
[[Y. Kim]], R. Wojciechowski, H. Sung, R.A. Mathias, L. Wang, A.P. Klein, R.K. Lenroot, J. Malley, J.E. Bailey-Wilson, “Evaluation of random forests performance for genome wide association studies in the presence of interaction effects,” BMC Proceedings, Vol3 (supp 7) s64, 2009.
 
 
[[Y. Kim]], P. Duggal, E.M. Gillanders, H. Kim, J.E. Bailey-Wilson, “Examining the effect of linkage disequilibrium between markers on the Type I error rate and power of nonparametric multipoint linkage analysis of two-generation and multigenerational pedigrees in the presence of missing genotype data,” Genetic Epidemiology; 32:41-51, 2008.
 
 
[[Y. Kim]], H. Kim. “Application of Random Forests to Association Studies Using Mitochondrial Single Nucleotide Polymorphisms,” Genomics & Informatics Vol. 5 (4) 168-173, 2007.
 
 
[[Y. Kim]], B. Doan, P. Duggal, J. E. Bailey-Wilson, “Normalization of microarray expression data using within-pedigree pool and its effect on linkage analysis,” BMC Genetics Proceedings, I (Supp 1) S152, 2007.
 
 
Sung J, Cho SI, Song YM, Lee K, Choi EY, Ha M, Kim J, Kim H, [[Kim Y]], Shin EK, Kim YH, Yoo KY, Park C, Kimm K, “Do we need more twin studies? The Healthy Twin Study, Korea,” Int J Epidemiology, 35(2):488-90, 2006.
 
 
S.H. Lee, J.M. Park, S.J. Kwon, H. Kim, [[Y.H. Kim]], J.K. Roh, and B.W. Yoon, “Left ventricular hypertrophy is associated with cerebral microbleeds in hypertensive patients,” Neurology, 63: 16-21, 2004.
 
 
S.H. Lee, H.J. Bae, S.J. Kwon, H. Kim, [[Y.H. Kim]], B.W. Yoon, and J.K. Roh, “Cerebral microbleeds are regionally associated with intra cerebral hemorrhage,”  Neurology, 62:72-76, 2004.
 
 
[[Y. Kim]], W. Park, H. Kim, “An iterative normalization algorithm from cDNA microarray medical data analysis,” Vol.2 (2) 94-100, Genomics & Informatics, 2004.
 

Revision as of 10:07, 29 November 2012