A gene-model-free method for linkage analysis of a disease-related-trait based on analysis of proband/sibling pairs

por Sung, Heejong, Finch, Stephen J, Ye, Kenny Q, Mendell, Nancy R
Publicado 2005

Craniopharyngiomas : Radiological Differentiation of Two Types

por Lee, In Ho, Zan, Elcin, Bell, W. Robert, Burger, Peter C., Sung, Heejong, Yousem, David M.
Publicado 2016

Type I error rates of rare single nucleotide variants are inflated in tests of association with non–normally distributed traits using simple linear regression methods

por Schwantes-An, Tae-Hwi, Sung, Heejong, Sabourin, Jeremy A., Justice, Cristina M., Sorant, Alexa J. M., Wilson, Alexander F.
Publicado 2016

Evaluation of random forests performance for genome-wide association studies in the presence of interaction effects

por Kim, Yoonhee, Wojciechowski, Robert, Sung, Heejong, Mathias, Rasika A, Wang, Li, Klein, Alison P, Lenroot, Rhoshel K, Malley, James, Bailey-Wilson, Joan E
Publicado 2009

Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression

por Sung, Heejong, Kim, Yoonhee, Cai, Juanliang, Cropp, Cheryl D, Simpson, Claire L, Li, Qing, Perry, Brian C, Sorant, Alexa JM, Bailey-Wilson, Joan E, Wilson, Alexander F
Publicado 2011

Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data

por Simpson, Claire L, Justice, Cristina M, Krishnan, Mera, Wojciechowski, Robert, Sung, Heejong, Cai, Jerry, Green, Tiffany, Lewis, Deyana, Behneman, Dana, Wilson, Alexander F, Bailey-Wilson, Joan E
Publicado 2011

Performance of random forests and logic regression methods using mini-exome sequence data

por Kim, Yoonhee, Li, Qing, Cropp, Cheryl D, Sung, Heejong, Cai, Juanliang, Simpson, Claire L, Perry, Brian, Dasgupta, Abhijit, Malley, James D, Wilson, Alexander F, Bailey-Wilson, Joan E
Publicado 2011

Genome‐wide association study of café‐au‐lait macule number in neurofibromatosis type 1

por Sung, Heejong, Hyland, Paula L., Pemov, Alexander, Sabourin, Jeremy A., Baldwin, Andrea M., Bass, Sara, Teshome, Kedest, Luo, Wen, Widemann, Brigitte C., Stewart, Douglas R., Wilson, Alexander F.
Publicado 2020

A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronar...

por Mathias, Rasika A, Kim, Yoonhee, Sung, Heejong, Yanek, Lisa R, Mantese, VJ, Hererra-Galeano, J Enrique, Ruczinski, Ingo, Wilson, Alexander F, Faraday, Nauder, Becker, Lewis C, Becker, Diane M
Publicado 2010

Strong Genetic Overlaps Between Dimensional and Categorical Models of Bipolar Disorders in a Family Sample

por Arbona-Lampaya, Alejandro, Sung, Heejong, D’Amico, Alexander, Knowles, Emma E. M., Besançon, Emily K., Freifeld, Ally, Lacbawan, Ley, Lopes, Fabiana, Kassem, Layla, Nardi, Antonio E., McMahon, Francis J.
Publicado 2023

Exome-wide association study of treatment-resistant depression suggests novel treatment targets

por Shah, Shrey B., Peddada, Teja N., Song, Christopher, Mensah, Maame, Sung, Heejong, Yavi, Mani, Yuan, Peixiong, Zarate, Carlos A., Mickey, Brian J., Burmeister, Margit, Akula, Nirmala, McMahon, Francis J.
Publicado 2023

Genetic Modifiers of Neurofibromatosis Type 1-Associated Café-au-Lait Macule Count Identified Using Multi-platform Analysis

por Pemov, Alexander, Sung, Heejong, Hyland, Paula L., Sloan, Jennifer L., Ruppert, Sarah L., Baldwin, Andrea M., Boland, Joseph F., Bass, Sara E., Lee, Hyo Jung, Jones, Kristine M., Zhang, Xijun, Mullikin, James C., Widemann, Brigitte C., Wilson, Alexander F., Stewart, Douglas R.
Publicado 2014