Resultats de la cerca - Matthew R. Nelson
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Future prospects for human genetics and genomics in drug discovery per Maya Ghoussaini, Matthew R. Nelson, Ian Dunham
Publicat 2023Revisão -
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Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometry per Mathias Ehrich, Matthew R. Nelson, Patrick Stanssens, Marc Zabeau, Triantafillos Liloglou, George Xinarianos, Charles R. Cantor, John K. Field, Dirk van den Boom
Publicat 2005Artigo -
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Amino acid variant in the kinase binding domain of dual-specific A kinase-anchoring protein 2: A disease susceptibility polymorphism per Stefan Kammerer, Lora Hamuro, Yuliang Ma, Sara Hamon, Jaume M. Cánaves, Michael Shi, Matthew R. Nelson, Charles F. Sing, Charles R. Cantor, Susan S. Taylor, Andreas Braun
Publicat 2003Artigo -
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The influence of genomic context on mutation patterns in the human genome inferred from rare variants per Valerie M. Schaibley, Matthew Zawistowski, Daniel Wegmann, Margaret G. Ehm, Matthew R. Nelson, Pamela L. St. Jean, Gonçalo R. Abecasis, John Novembre, Sebastian Zöllner, Jun Z. Li
Publicat 2013Artigo -
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GWASdb v2: an update database for human genetic variants identified by genome-wide association studies per Mulin Jun Li, Zipeng Liu, Panwen Wang, Maria Pik Wong, Matthew R. Nelson, Jean‐Pierre Kocher, Meredith Yeager, Pak C. Sham, Stephen J. Chanock, Zhengyuan Xia, Junwen Wang
Publicat 2015Artigo -
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Genome-wide patterns of population structure and admixture in West Africans and African Americans per Katarzyna Bryc, Adam Auton, Matthew R. Nelson, Jorge R. Oksenberg, Stephen L. Hauser, Scott M. Williams, Alain Froment, Jean-Marie Bodo, Charles Wambebe, Sarah A. Tishkoff, Carlos D. Bustamante
Publicat 2009Artigo -
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Performance of Genotype Imputation for Rare Variants Identified in Exons and Flanking Regions of Genes per Li Li, Yun Li, Sharon R. Browning, Brian L. Browning, Andrew J. Slater, Xiangyang Kong, Jennifer L. Aponte, Vincent Mooser, Stephanie L. Chissoe, John C. Whittaker, Matthew R. Nelson, Margaret G. Ehm
Publicat 2011Artigo -
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Comprehensive genome-wide evaluation of lapatinib-induced liver injury yields a single genetic signal centered on known risk allele HLA-DRB1*07:01 per Laura R. Parham, Linda P. Briley, L Li, Judong Shen, Paul J. Newcombe, Karen S. King, Andrew J. Slater, Alexander Dilthey, Zamin Iqbal, Gil McVean, Charles Cox, Matthew R. Nelson, Colin F. Spraggs
Publicat 2015Artigo -
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Global distribution of genomic diversity underscores rich complex history of continental human populations per Adam Auton, Katarzyna Bryc, Adam R. Boyko, Kirk E. Lohmueller, John Novembre, Andy Reynolds, Amit Indap, Mark H. Wright, Jeremiah D. Degenhardt, Ryan N. Gutenkunst, Karen S. King, Matthew R. Nelson, Carlos D. Bustamante
Publicat 2009Artigo -
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Association of the <i>PDCD5</i> Locus With Lung Cancer Risk and Prognosis in Smokers per Monica Spinola, Peter Meyer, Stefan Kammerer, Felicia Stefania Falvella, Melanie Barbara Boettger, Carolyn R. Hoyal, Carmen Pignatiello, R. Fischer, Richard B. Roth, Ugo Pastorino, Karl Haeußinger, Matthew R. Nelson, R Dierkesmann, Tommaso A. Dragani, Andreas Braun
Publicat 2006Artigo -
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Characterization of ADME gene variation in 21 populations by exome sequencing per Daniel H. Hovelson, Zhengyu Xue, Matthew Zawistowski, Margaret G. Ehm, E Clare Harris, Sophie L. Stocker, Annette S. Gross, In‐Jin Jang, Ichiro Ieiri, Jong Eun Lee, Lon R. Cardon, Stephanie L. Chissoe, Gonçalo R. Abecasis, Matthew R. Nelson
Publicat 2016Artigo
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Matèries relacionades
Biology
Gene
Genetics
Genotype
Medicine
Single-nucleotide polymorphism
Population
Computational biology
Allele
Antigen
Environmental health
Genome
Genome-wide association study
Internal medicine
Genetic association
Human leukocyte antigen
Genetic variation
Evolutionary biology
Computer science
Demography
Haplotype
Human genome
Immunology
Sociology
Bioinformatics
Genotyping
Pharmacology
Phenotype
SNP
1000 Genomes Project