Resultados de procura - Joan E. Bailey‐Wilson
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Genomewide Linkage Scan for Myopia Susceptibility Loci among Ashkenazi Jewish Families Shows Evidence of Linkage on Chromosome 22q12 por Dwight Stambolian, Grace Ibay, Lauren Reider, Debra Dana, Chris Moy, Melissa Schlifka, Taura N. Holmes, Elise Ciner, Joan E. Bailey‐Wilson
Publicado 2004Artigo -
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r2VIM: A new variable selection method for random forests in genome-wide association studies por Silke Szymczak, Emily Holzinger, Abhijit Dasgupta, James D. Malley, Anne M. Molloy, James L. Mills, Lawrence C. Brody, Dwight Stambolian, Joan E. Bailey‐Wilson
Publicado 2016Artigo -
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Attention-Deficit/Hyperactivity Disorder in a Population Isolate: Linkage to Loci at 4q13.2, 5q33.3, 11q22, and 17p11 por 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
Publicado 2004Artigo -
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Determination of the allelic frequency in Smith–Lemli–Opitz syndrome by analysis of massively parallel sequencing data sets por 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
Publicado 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 por 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
Publicado 2015Artigo -
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Assessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization Study por 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
Publicado 2015Artigo -
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A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1 por 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
Publicado 2018Artigo -
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Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). II. Biomarker studies por 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
Publicado 1985Artigo -
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Germline Alterations of the RNASEL Gene, a Candidate HPC1 Gene at 1q25, in Patients and Families with Prostate Cancer por 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
Publicado 2002Artigo
Ferramentas de procura:
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Biology
Gene
Genetics
Medicine
Genotype
Single-nucleotide polymorphism
Internal medicine
Allele
Genetic linkage
Cancer
Genome-wide association study
Locus (genetics)
Mutation
Oncology
Genetic association
Population
Environmental health
Computational biology
Disease
Lung cancer
Mathematics
Phenotype
Prostate cancer
Computer science
Haplotype
Pathology
Refractive error
Exome sequencing
Genome
Germline mutation