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

Por Bacanu, Silviu-Alin, Nelson, Matthew R., Whittaker, John C.
Publicado em 2012

Improved genome inference in the MHC using a population reference graph

Por Dilthey, Alexander, Cox, Charles, Iqbal, Zamin, Nelson, Matthew R., McVean, Gil
Publicado no Nat Genet (2015)

Copy number variation in African Americans

Por McElroy, Joseph P, Nelson, Matthew R, Caillier, Stacy J, Oksenberg, Jorge R
Publicado em 2009

Noninvasive Measurement of Central Vascular Pressures With Arterial Tonometry: Clinical Revival of the Pulse Pressure Waveform?

Por Nelson, Matthew R., Stepanek, Jan, Cevette, Michael, Covalciuc, Michael, Hurst, R. Todd, Tajik, A. Jamil
Publicado em 2010

Multi-Population Classical HLA Type Imputation

Por Dilthey, Alexander, Leslie, Stephen, Moutsianas, Loukas, Shen, Judong, Cox, Charles, Nelson, Matthew R., McVean, Gil
Publicado em 2013

Large-Scale Validation of Single Nucleotide Polymorphisms in Gene Regions

Por Nelson, Matthew R., Marnellos, George, Kammerer, Stefan, Hoyal, Carolyn R., Shi, Michael M., Cantor, Charles R., Braun, Andreas
Publicado em 2004

Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests

Por Zawistowski, Matthew, Reppell, Mark, Wegmann, Daniel, St Jean, Pamela L, Ehm, Margaret G, Nelson, Matthew R, Novembre, John, Zöllner, Sebastian
Publicado em 2014

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

Por Lo, Yancy, Kang, Hyun M, Nelson, Matthew R, Othman, Mohammad I, Chissoe, Stephanie L, Ehm, Margaret G, Abecasis, Gonçalo R, Zöllner, Sebastian
Publicado no BMC Bioinformatics (2015)

Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometry

Por Ehrich, Mathias, Nelson, Matthew R., Stanssens, Patrick, Zabeau, Marc, Liloglou, Triantafillos, Xinarianos, George, Cantor, Charles R., Field, John K., van den Boom, Dirk
Publicado em 2005

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

Por 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
Publicado em 2005

Genes mirror geography within Europe

Por Novembre, John, Johnson, Toby, Bryc, Katarzyna, Kutalik, Zoltán, Boyko, Adam R., Auton, Adam, Indap, Amit, King, Karen S., Bergmann, Sven, Nelson, Matthew R., Stephens, Matthew, Bustamante, Carlos D.
Publicado em 2008

The influence of genomic context on mutation patterns in the human genome inferred from rare variants

Por Schaibley, Valerie M., Zawistowski, Matthew, Wegmann, Daniel, Ehm, Margaret G., Nelson, Matthew R., St. Jean, Pamela L., Abecasis, Gonçalo R., Novembre, John, Zöllner, Sebastian, Li, Jun Z.
Publicado em 2013

Genome-wide patterns of population structure and admixture in West Africans and African Americans

Por Bryc, Katarzyna, Auton, Adam, Nelson, Matthew R., Oksenberg, Jorge R., Hauser, Stephen L., Williams, Scott, Froment, Alain, Bodo, Jean-Marie, Wambebe, Charles, Tishkoff, Sarah A., Bustamante, Carlos D.
Publicado em 2009

Genetic polymorphisms in <it>DPF3 </it>associated with risk of breast cancer and lymph node metastases

Por 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
Publicado em 2005-08-01

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

Por 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
Publicado em 2005

Relationship between Genetic Variants in Myocardial Sodium and Potassium Channel Genes and QT Interval Duration in Diabetics: The Diabetes Heart Study

Por Lehtinen, Allison B., Daniel, Kurt R., Shah, Sidharth A., Nelson, Matthew R., Ziegler, Julie T., Freedman, Barry I., Carr, J. Jeffrey, Herrington, David M., Langefeld, Carl D., Bowden, Donald W.
Publicado em 2009

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

Por 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
Publicado no Nucleic Acids Res (2016)

Amino acid variant in the kinase binding domain of dual-specific A kinase-anchoring protein 2: A disease susceptibility polymorphism

Por Kammerer, Stefan, Burns-Hamuro, Lora L., Ma, Yuliang, Hamon, Sara C., Cànaves, Jaume M., Shi, Michael M., Nelson, Matthew R., Sing, Charles F., Cantor, Charles R., Taylor, Susan S., Braun, Andreas
Publicado em 2003

Association of the NuMA region on chromosome 11q13 with breast cancer susceptibility

Por Kammerer, Stefan, Roth, Richard B., Hoyal, Carolyn R., Reneland, Richard, Marnellos, George, Kiechle, Marion, Schwarz-Boeger, Ulrike, Griffiths, Lyn R., Ebner, Florian, Rehbock, Joachim, Cantor, Charles R., Nelson, Matthew R., Braun, Andreas
Publicado em 2005

Global distribution of genomic diversity underscores rich complex history of continental human populations

Por Auton, Adam, Bryc, Katarzyna, Boyko, Adam R., Lohmueller, Kirk E., Novembre, John, Reynolds, Andy, Indap, Amit, Wright, Mark H., Degenhardt, Jeremiah D., Gutenkunst, Ryan N., King, Karen S., Nelson, Matthew R., Bustamante, Carlos D.
Publicado em 2009