نتائج البحث - Gary W. Beecham
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Integrated Whole Transcriptome and DNA Methylation Analysis Identifies Gene Networks Specific to Late-Onset Alzheimer's Disease حسب Crystal Humphries, Martin Kohli, Lubov Nathanson, Patrice L. Whitehead, Gary W. Beecham, Eden R. Martin, Deborah C. Mash, Margaret A. Pericak‐Vance, John R. Gilbert
منشور في 2015Artigo -
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Exome sequencing allows for rapid gene identification in a Charcot‐Marie‐Tooth family حسب Gladys Montenegro, Eric Powell, Jiaqiang Huang, Fiorella Speziani, Yvonne J. K. Edwards, Gary W. Beecham, William Hulme, Carly E. Siskind, Jeffery M. Vance, Michael E. Shy, Stephan Züchner
منشور في 2011Artigo -
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Whole exome sequencing of rare variants in <i>EIF4G1</i> and <i>VPS35</i> in Parkinson disease حسب Karen Nuytemans, Güney Bademci, Vanessa Inchausti, Amy Dressen, Daniel D. Kinnamon, Arpit Mehta, Liyong Wang, Stephan Züchner, Gary W. Beecham, Eden R. Martin, William K. Scott, Jeffery M. Vance
منشور في 2013Artigo -
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Vitamin D from different sources is inversely associated with Parkinson disease حسب Liyong Wang, Marian L. Evatt, Lizmarie Maldonado, William Perry, James Ritchie, Gary W. Beecham, Eden R. Martin, Jonathan L. Haines, Margaret A. Pericak‐Vance, Jeffery M. Vance, William K. Scott
منشور في 2014Artigo -
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Notch activation induces endothelial cell senescence and pro-inflammatory response: Implication of Notch signaling in atherosclerosis حسب Zhao‐Jun Liu, Yurong Tan, Gary W. Beecham, David Seo, Runxia Tian, Yan Li, Roberto I. Vázquez-Padrón, Margaret A. Pericak‐Vance, Jeffery M. Vance, Pascal J. Goldschmidt‐Clermont, Alan S. Livingstone, Omaida C. Velázquez
منشور في 2012Artigo -
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Local genetic covariance analysis with lipid traits identifies novel loci for early-onset Alzheimer’s Disease حسب Nicholas R. Ray, Joseph Bradley, Elanur Yılmaz, Çağhan Kızıl, Jiji T. Kurup, Eden R. Martin, Hans‐Ulrich Klein, Brian W. Kunkle, David A. Bennett, Philip L. De Jager, Gary W. Beecham, Carlos Cruchaga, Christiane Reitz
منشور في 2025Artigo -
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A rare missense variant of <i>CASP7</i> is associated with familial late‐onset Alzheimer's disease حسب Xiaoling Zhang, Congcong Zhu, Gary W. Beecham, Badri N. Vardarajan, Yiyi Ma, Daniel Lancour, John J. Farrell, Jaeyoon Chung, Richard Mayeux, Jonathan L. Haines, Gerard Schellenberg, Margaret Pericak‐Vance, Kathryn L. Lunetta, Lindsay A. Farrer
منشور في 2018Artigo -
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Identifying Consensus Disease Pathways in Parkinson's Disease Using an Integrative Systems Biology Approach حسب Yvonne J. K. Edwards, Gary W. Beecham, William K. Scott, Sawsan Khuri, Güney Bademci, Demet Tekin, Eden R. Martin, Zhijie Jiang, Deborah C. Mash, Jarlath M.H. ffrench‐Mullen, Margaret A. Pericak‐Vance, Nicholas F. Tsinoremas, Jeffery M. Vance
منشور في 2011Revisão -
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<i>C9ORF72</i> Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease حسب Karen Nuytemans, Güney Bademci, Martin M. Kohli, Gary W. Beecham, Liyong Wang, Juan I. Young, Fatta B. Nahab, Eden R. Martin, John R. Gilbert, Michael Benatar, Jonathan L. Haines, William K. Scott, Stephan Züchner, Margaret A. Pericak‐Vance, Jeffery M. Vance
منشور في 2013Artigo -
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Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform حسب Dale J. Hedges, Toumy Guettouche, Shan Yang, Güney Bademci, Ashley Diaz, Ashley Andersen, William Hulme, Sara B. Linker, Arpit Mehta, Yvonne J. K. Edwards, Gary W. Beecham, Eden R. Martin, Margaret A. Pericak‐Vance, Stephan Züchner, Jeffery M. Vance, John R. Gilbert
منشور في 2011Artigo -
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Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease حسب Juan I. Young, Sathesh K. Sivasankaran, Lily Wang, Aleena Ali, Arpit Mehta, David A. Davis, Derek M. Dykxhoorn, Carol K. Petito, Gary W. Beecham, Eden R. Martin, Deborah C. Mash, Margaret A. Pericak‐Vance, William K. Scott, Thomas J. Montine, Jeffery M. Vance
منشور في 2019Artigo -
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Genome‐Wide Association Study Confirms SNPs in <i>SNCA</i> and the <i>MAPT</i> Region as Common Risk Factors for Parkinson Disease حسب Todd L. Edwards, William K. Scott, Cherylyn Almonte, Amber Burt, Eric Powell, Gary W. Beecham, Liyong Wang, Stephan Züchner, Ioanna Konidari, Gaofeng Wang, Carlos Singer, Fatta B. Nahab, B.L. Scott, Jeffrey M. Stajich, Margaret A. Pericak‐Vance, Jonathan L. Haines, Jeffery M. Vance, Eden R. Martin
منشور في 2010Artigo -
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Dementia Revealed: Novel Chromosome 6 Locus for Late-Onset Alzheimer Disease Provides Genetic Evidence for Folate-Pathway Abnormalities حسب Adam C. Naj, Gary W. Beecham, Eden R. Martin, Paul J. Gallins, Eric Powell, Ioanna Konidari, Patrice L. Whitehead, Guiqing Cai, Vahram Haroutunian, William K. Scott, Jeffery M. Vance, Michael A. Slifer, Harry E. Gwirtsman, John R. Gilbert, Jonathan L. Haines, Joseph D. Buxbaum, Margaret A. Pericak‐Vance
منشور في 2010Artigo -
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Segregation of a rare <i>TTC3</i> variant in an extended family with late-onset Alzheimer disease حسب Martin Kohli, Holly N. Cukier, Kara L. Hamilton‐Nelson, Sophie Rolati, Brian W. Kunkle, Patrice L. Whitehead, Stephan Züchner, Lindsay A. Farrer, Eden R. Martin, Gary W. Beecham, Jonathan L. Haines, Jeffery M. Vance, Michael L. Cuccaro, John R. Gilbert, Gerard D. Schellenberg, Regina M. Carney, Margaret A. Pericak‐Vance
منشور في 2016Artigo -
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Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior حسب Andrea Ganna, Karin J. H. Verweij, Michel G. Nivard, Robert Maier, Robbee Wedow, Alexander S. Busch, Abdel Abdellaoui, Shengru Guo, J. Fah Sathirapongsasuti, Paul Lichtenstein, Sebastian Lundström, Niklas Långström, Adam Auton, Kathleen Mullan Harris, Gary W. Beecham, Eden R. Martin, Alan R. Sanders, John R. B. Perry, Benjamin M. Neale, Brendan P. Zietsch
منشور في 2019Artigo -
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Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport حسب Brian W. Kunkle, Badri N. Vardarajan, Adam C. Naj, Patrice L. Whitehead, Sophie Rolati, Susan Slifer, Regina M. Carney, Michael L. Cuccaro, Jeffery M. Vance, John R. Gilbert, Li-San Wang, Lindsay A. Farrer, Christiane Reitz, Jonathan L. Haines, Gary W. Beecham, Eden R. Martin, Gerard D. Schellenberg, Richard Mayeux, Margaret A. Pericak‐Vance
منشور في 2017Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Gene
Medicine
Disease
Genotype
Internal medicine
Single-nucleotide polymorphism
Genome-wide association study
Alzheimer's disease
Genetic association
Allele
Apolipoprotein E
Locus (genetics)
Pathology
Dementia
Population
Computational biology
Genome
Mutation
Psychology
Bioinformatics
Environmental health
Neuroscience
Phenotype
Exome
Exome sequencing
SNP
Genetic architecture
Oncology