Comparison of Statistical Tests for Association between Rare Variants and Binary Traits

by Bacanu, Silviu-Alin, Nelson, Matthew R., Whittaker, John C.
Published 2012

Multi-Population Classical HLA Type Imputation

by Dilthey, Alexander, Leslie, Stephen, Moutsianas, Loukas, Shen, Judong, Cox, Charles, Nelson, Matthew R., McVean, Gil
Published 2013

Improved genome inference in the MHC using a population reference graph

by Dilthey, Alexander, Cox, Charles, Iqbal, Zamin, Nelson, Matthew R., McVean, Gil
Published 2015

Association between a variation in the phosphodiesterase 4D gene and bone mineral density

by Reneland, Richard H, Mah, Steven, Kammerer, Stefan, Hoyal, Carolyn R, Marnellos, George, Wilson, Scott G, Sambrook, Philip N, Spector, Tim D, Nelson, Matthew R, Braun, Andreas
Published 2005

Comparing variant calling algorithms for target-exon sequencing in a large sample

by Lo, Yancy, Kang, Hyun M, Nelson, Matthew R, Othman, Mohammad I, Chissoe, Stephanie L, Ehm, Margaret G, Abecasis, Gonçalo R, Zöllner, Sebastian
Published 2015

Genetic polymorphisms in DPF3 associated with risk of breast cancer and lymph node metastases

by Hoyal, Carolyn R, Kammerer, Stefan, Roth, Richard B, Reneland, Richard, Marnellos, George, Kiechle, Marion, Schwarz-Boeger, Ulrike, Griffiths, Lyn R, Ebner, Florian, Rehbock, Joachim, Nelson, Matthew R, Braun, Andreas
Published 2005

Performance of Genotype Imputation for Rare Variants Identified in Exons and Flanking Regions of Genes

by Li, Li, Li, Yun, Browning, Sharon R., Browning, Brian L., Slater, Andrew J., Kong, Xiangyang, Aponte, Jennifer L., Mooser, Vincent E., Chissoe, Stephanie L., Whittaker, John C., Nelson, Matthew R., Ehm, Margaret Gelder
Published 2011

GWASdb v2: an update database for human genetic variants identified by genome-wide association studies

by Li, Mulin Jun, Liu, Zipeng, Wang, Panwen, Wong, Maria P., Nelson, Matthew R., Kocher, Jean-Pierre A., Yeager, Meredith, Sham, Pak Chung, Chanock, Stephen J., Xia, Zhengyuan, Wang, Junwen
Published 2016

Deep Resequencing Unveils Genetic Architecture of ADIPOQ and Identifies a Novel Low-Frequency Variant Strongly Associated With Adiponectin Variation

by Warren, Liling L., Li, Li, Nelson, Matthew R., Ehm, Margaret G., Shen, Judong, Fraser, Dana J., Aponte, Jennifer L., Nangle, Keith L., Slater, Andrew J., Woollard, Peter M., Hall, Matt D., Topp, Simon D., Yuan, Xin, Cardon, Lon R., Chissoe, Stephanie L., Mooser, Vincent, Morris, Andrew D., Palmer, Colin N.A., Perry, John R., Frayling, Timothy M., Whittaker, John C., Waterworth, Dawn M.
Published 2012

Association of liver injury from specific drugs, or groups of drugs, with polymorphisms in HLA and other genes in a genome-wide association study

by Nicoletti, Paola, Aithal, Guruprasad P., Bjornsson, Einar S., Andrade, Raul J., Sawle, Ashley, Arrese, Marco, Barnhart, Huiman X., Bondon-Guitton, Emmanuelle, Hayashi, Paul H., Bessone, Fernando, Carvajal, Alfonso, Cascorbi, Ingolf, Cirulli, Elizabeth T., Chalasani, Naga, Conforti, Anita, Coulthard, Sally A., Daly, Mark J., Day, Christopher P., Dillon, John F., Fontana, Robert J., Grove, Jane I., Hallberg, Pär, Hernández, Nelia, Ibáñez, Luisa, Kullak-Ublick, Gerd A., Laitinen, Tarja, Larrey, Dominique, Lucena, M. Isabel, Maitland-van der Zee, Anke H., Martin, Jennifer H., Molokhia, Mariam, Pirmohamed, Munir, Powell, Elizabeth E., Qin, Shengying, Serrano, Jose, Stephens, Camilla, Stolz, Andrew, Wadelius, Mia, Watkins, Paul B., Floratos, Aris, Shen, Yufeng, Nelson, Matthew R., Urban, Thomas J., Daly, Ann K.
Published 2016