检索结果 - Pericak‐Vance, Margaret

Beyond Proof of Principle: New Genes for Alzheimer Disease Through Collaboration 由 Pericak-Vance, Margaret A., Haines, Jonathan L.

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Bringing the genetics of macular degeneration into focus 由 Haines, Jonathan L., Spencer, Kylee M., Pericak-Vance, Margaret A.

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The Impact of the Human Genome Project on Complex Disease 由 Cooke Bailey, Jessica N., Pericak-Vance, Margaret A., Haines, Jonathan L.

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Genome-Wide Association Studies: Getting to Pathogenesis, the Role of Inflammation/Complement in Age-Related Macular Degeneration 由 Cooke Bailey, Jessica N., Pericak-Vance, Margaret A., Haines, Jonathan L.

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No Gene Is an Island: The Flip-Flop Phenomenon 由 Lin, Ping-I, Vance, Jeffery M., Pericak-Vance, Margaret A., Martin, Eden R.

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Response to Zaykin and Shibata 由 Lin, Ping-I, Vance, Jeffery M., Pericak-Vance, Margaret A., Martin, Eden R.

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A Second Leaky Splice-Site Mutation in the Spastin Gene 由 Svenson, Ingrid K., Ashley-Koch, Allison E., Pericak-Vance, Margaret A., Marchuk, Douglas A.

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Coding Variants in ARMS2 and the Risk of Age-Related Macular Degeneration 由 Wang, Gaofeng, Scott, William K., Agarwal, Anita, Haines, Jonathan L., Pericak-Vance, Margaret A.

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Genome-wide Linkage Scan in Fuchs Endothelial Corneal Dystrophy 由 Afshari, Natalie A., Li, Yi-Ju, Pericak-Vance, Margaret A., Gregory, Simon, Klintworth, Gordon K.

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Pathway-PDT: a flexible pathway analysis tool for nuclear families 由 Park, Yo Son, Schmidt, Michael, Martin, Eden R, Pericak-Vance, Margaret A, Chung, Ren-Hua

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An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3 由 Edwards, Todd L., Pericak-Vance, Margaret, Gilbert, Johnny, Haines, Jonathan L., Martin, Eden, Ritchie, Marylyn D.

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APOE is not associated with Alzheimer Disease: a cautionary tale of genotype imputation 由 Beecham, Gary W., Martin, Eden R., Gilbert, John R., Haines, Jonathan L., Pericak-Vance, Margaret A.

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Resolving the Relationship between Apolipoprotein E and Depression 由 Slifer, Michael A., Martin, Eden R., Gilbert, John R., Haines, Jonathan L., Pericak-Vance, Margaret A.

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Alzheimer disease (AD) specific transcription, DNA methylation and splicing in twenty AD associated loci 由 Humphries, Crystal, Kohli, Martin A., Whitehead, Patrice, Mash, Deborah C., Pericak-Vance, Margaret A., Gilbert, John

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Confronting Complexity in Late-Onset Alzheimer Disease: Application of Two-Stage Analysis Approach Addressing Heterogeneity and Epistasis 由 Thornton-Wells, Tricia A., Moore, Jason H., Martin, Eden R., Pericak-Vance, Margaret A., Haines, Jonathan L.

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PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility 由 Beecham, Gary W, Naj, Adam, Gilbert, John R, Haines, Jonathan L, Buxbaum, Joseph D, Pericak-Vance, Margaret A

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Coronary collateralization shows sex and racial-ethnic differences in obstructive artery disease patients 由 Liu, Zhi, Pericak-Vance, Margaret A., Goldschmidt-Clermont, Pascal, Seo, David, Wang, Liyong, Rundek, Tatjana, Beecham, Gary W.

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Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorder 由 Griswold, Anthony J., Van Booven, Derek, Cuccaro, Michael, Haines, Jonathan L., Gilbert, John R., Pericak-Vance, Margaret A.

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False Positive Rates in a Genomic Screen for Complex Quantitative Traits 由 Scott, William K., Speer, Marcy C., Pericak-Vance, Margaret A., Haynes, Carol S., Leal, Suzanne M., Brzustowicz, Linda M.

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Identification and Confirmation of an Exonic Splicing Enhancer Variation in Exon 5 of the Alzheimer Disease Associated PICALM Gene 由 Schnetz-Boutaud, Nathalie C., Hoffman, Joshua, Coe, Jared E., Murdock, Deborah G., Pericak-Vance, Margaret A., Haines, Jonathan L.

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