| 2012 | ||
|---|---|---|
| j5 | Mulin Jun Li, Panwen Wang, Xiaorong Liu, Ee Lyn Lim, Zhangyong Wang, Meredith Yeager, Maria P. Wong, Pak Chung Sham, Stephen J. Chanock, Junwen Wang: GWASdb: a database for human genetic variants identified by genome-wide association studies. Nucleic Acids Research 40(Database-Issue): 1047-1054 (2012) | |
| 2011 | ||
| j4 | Juan R. González, Benjamin Rodriguez-Santiago, Alejandro Cáceres, Roger Pique-Regi, Nathaniel Rothman, Stephen J. Chanock, Lluís Armengol, Luis A. Perez-Jurado: A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data. BMC Bioinformatics 12: 166 (2011) | |
| 2008 | ||
| j3 | Leah E. Mechanic, Brian T. Luke, Julie E. Goodman, Stephen J. Chanock, Curtis C. Harris: Polymorphism Interaction Analysis (PIA): a method for investigating complex gene-gene interactions. BMC Bioinformatics 9 (2008) | |
| 2006 | ||
| j2 | Bernice R. Packer, Meredith Yeager, Laura Burdett, Robert Welch, Michael Beerman, Liqun Qi, Hugues Sicotte, Brian Staats, Mekhala Acharya, Andrew Crenshaw, Andrew Eckert, Vinita Puri, Daniela S. Gerhard, Stephen J. Chanock: SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes. Nucleic Acids Research 34(Database-Issue): 617-621 (2006) | |
| 2004 | ||
| j1 | Bernice R. Packer, Meredith Yeager, Brian Staats, Robert Welch, Andrew Crenshaw, Maureen Kiley, Andrew Eckert, Michael Beerman, Edward Miller, Andrew Bergen, Nathaniel Rothman, Robert Strausberg, Stephen J. Chanock: SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes. Nucleic Acids Research 32(Database-Issue): 528-532 (2004) | |
Colors in the list of coauthors
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