Kết quả tìm kiếm - Joan E. Bailey‐Wilson
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Linkage Analysis in the Next-Generation Sequencing Era Bằng Joan E. Bailey‐Wilson, Alexander F. Wilson
Được phát hành 2011Revisão -
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Genes, environment and the value of prospective cohort studies Bằng Teri A. Manolio, Joan E. Bailey‐Wilson, Francis S. Collins
Được phát hành 2006Revisão -
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Functional Linear Models for Association Analysis of Quantitative Traits Bằng Ruzong Fan, Yifan Wang, James L. Mills, Alexander F. Wilson, Joan E. Bailey‐Wilson, Momiao Xiong
Được phát hành 2013Artigo -
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Evidence for a major gene influencing risk of pancreatic cancer Bằng Alison P. Klein, Terri H. Beaty, Joan E. Bailey‐Wilson, Kieran Brune, Ralph H. Hruban, Gloria M. Petersen
Được phát hành 2002Artigo -
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Genomewide Linkage Scan for Myopia Susceptibility Loci among Ashkenazi Jewish Families Shows Evidence of Linkage on Chromosome 22q12 Bằng Dwight Stambolian, Grace Ibay, Lauren Reider, Debra Dana, Chris Moy, Melissa Schlifka, Taura N. Holmes, Elise Ciner, Joan E. Bailey‐Wilson
Được phát hành 2004Artigo -
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r2VIM: A new variable selection method for random forests in genome-wide association studies Bằng Silke Szymczak, Emily Holzinger, Abhijit Dasgupta, James D. Malley, Anne M. Molloy, James L. Mills, Lawrence C. Brody, Dwight Stambolian, Joan E. Bailey‐Wilson
Được phát hành 2016Artigo -
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Attention-Deficit/Hyperactivity Disorder in a Population Isolate: Linkage to Loci at 4q13.2, 5q33.3, 11q22, and 17p11 Bằng Mauricio Arcos‐Burgos, F. Xavier Castellanos, David Pineda, Francisco Lopera, Juan David Palacio, Luis Palacio, Judith L. Rapoport, Kate Berg, Joan E. Bailey‐Wilson, Maximilian Muenke
Được phát hành 2004Artigo -
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Determination of the allelic frequency in Smith–Lemli–Opitz syndrome by analysis of massively parallel sequencing data sets Bằng Jennifer L. Cross, James Iben, Claire L. Simpson, Audrey Thurm, Susan E. Swedo, Elaine Tierney, Joan E. Bailey‐Wilson, Leslie G. Biesecker, Forbes D. Porter, Christopher A. Wassif
Được phát hành 2014Artigo -
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High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data sets Bằng Christopher A. Wassif, Joanna Cross, James Iben, Luis Sánchez‐Pulido, Antony Cougnoux, Frances M. Platt, Daniel S. Ory, Chris P. Ponting, Joan E. Bailey‐Wilson, Leslie G. Biesecker, Forbes D. Porter
Được phát hành 2015Artigo -
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Assessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization Study Bằng Gabriel Cuéllar-Partida, Yi Lu, Pik Fang Kho, Alex W. Hewitt, H.‐Erich Wichmann, Seyhan Yazar, Dwight Stambolian, Joan E. Bailey‐Wilson, Robert Wojciechowski, Jie Jin Wang, Paul Mitchell, David A. Mackey, Stuart MacGregor
Được phát hành 2015Artigo -
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A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1 Bằng Ying Chen, Melissa A. Gilbert, Christopher M. Grochowski, Deborah McEldrew, Jessica Llewellyn, Orith Waisbourd‐Zinman, Hákon Hákonarson, Joan E. Bailey‐Wilson, Pierre Russo, Rebecca G. Wells, Kathleen M. Loomes, Nancy B. Spinner, Marcella Devoto
Được phát hành 2018Artigo -
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Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). II. Biomarker studies Bằng Henry T. Lynch, Guy S. Schuelke, William J. Kimberling, William A. Albano, Jane F. Lynch, Karen A. Biscone, Martin Lipkin, Eleanor E. Deschner, Yves B. Mikol, Avery A. Sandberg, Robert C. Elston, Joan E. Bailey‐Wilson, B. Shannon Danes
Được phát hành 1985Artigo -
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Germline Alterations of the RNASEL Gene, a Candidate HPC1 Gene at 1q25, in Patients and Families with Prostate Cancer Bằng Annika Rökman, Tarja Ikonen, Eija H. Seppälä, Nina N. Nupponen, Ville Autio, Nina Mononen, Joan E. Bailey‐Wilson, Jeffrey M. Trent, John D. Carpten, Mika Matikainen, Pasi A. Koivisto, Teuvo L.J. Tammela, Olli Kallioniemi, Johanna Schleutker
Được phát hành 2002Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Gene
Genetics
Medicine
Genotype
Single-nucleotide polymorphism
Internal medicine
Allele
Genetic linkage
Genome-wide association study
Cancer
Locus (genetics)
Mutation
Genetic association
Oncology
Population
Environmental health
Computational biology
Lung cancer
Mathematics
Phenotype
Computer science
Disease
Haplotype
Pathology
Prostate cancer
Refractive error
Genome
Germline mutation
Linkage (software)