Výsledky vyhledávání - Slifer, Susan

DNA Methylation Variation Is Identified in Monozygotic Twins Discordant for Non-syndromic Cleft Lip and Palate Autor Young, Juan I., Slifer, Susan, Hecht, Jacqueline T., Blanton, Susan H.

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Properties of Global and Local Ancestry Adjustments in Genetic Association Tests in Admixed Populations Autor Martin, Eden R., Tunc, Ilker, Liu, Zhi, Slifer, Susan H., Beecham, Ashley H., Beecham, Gary W.

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Novel quantitative trait locus is mapped to chromosome 12p11 for left ventricular mass in Dominican families: the Family Study of Stroke Risk and Carotid Atherosclerosis Autor Wang, Liyong, Beecham, Ashley, Di Tullio, Marco R, Slifer, Susan, Blanton, Susan H, Rundek, Tatjana, Sacco, Ralph L

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Candidate gene study revealed sex specific association between the OLR1 gene and carotid plaque Autor Wang, Liyong, Yanuck, Danielle, Beecham, Ashley, Gardener, Hannah, Slifer, Susan, Blanton, Susan H., Sacco, Ralph L., Rundek, Tatjana

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Genomewide Linkage and Peakwide Association Analyses of Carotid Plaque in Caribbean Hispanics Autor Dong, Chuanhui, Beecham, Ashley, Slifer, Susan, Wang, Liyong, Blanton, Susan H., Wright, Clinton B., Rundek, Tatjana, Sacco, Ralph L.

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Genetic loci for blood lipid levels identified by linkage and association analyses in Caribbean Hispanics Autor Dong, Chuanhui, Beecham, Ashley, Wang, Liyong, Slifer, Susan, Wright, Clinton B., Blanton, Susan H., Rundek, Tatjana, Sacco, Ralph L.

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Genome-wide linkage and peak-wide association study of obesity-related quantitative traits in Caribbean Hispanics Autor Dong, Chuanhui, Beecham, Ashley, Slifer, Susan, Wang, Liyong, McClendon, Mark S., Blanton, Susan H., Rundek, Tatjana, Sacco, Ralph L.

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A comprehensive genetic study on left atrium size in Caribbean Hispanics identifies candidate genes in 17p10 Autor Wang, Liyong, Di Tullio, Marco R., Beecham, Ashley, Slifer, Susan, Rundek, Tatjana, Homma, Shunichi, Blanton, Susan H., Sacco, Ralph L.

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Heritability and Linkage Analysis for Carotid Intima-Media Thickness: The Family Study of Stroke Risk and Carotid Atherosclerosis Autor Sacco, Ralph L., Blanton, Susan H., Slifer, Susan, Beecham, Ashley, Glover, Khaleelah, Gardener, Hannah, Wang, Liyong, Sabala, Edison, Juo, Suh-Hang Hank, Rundek, Tatjana

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Carotid plaque and candidate genes related to inflammation and endothelial function in Hispanics from northern Manhattan Autor Gardener, Hannah, Beecham, Ashley, Cabral, Digna, Yanuck, Danielle, Slifer, Susan, Wang, Liyong, Blanton, Susan H., Sacco, Ralph L., Juo, Suh-Hang Hank, Rundek, Tatjana

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A follow-up study for left ventricular mass on chromosome 12p11 identifies potential candidate genes Autor Della-Morte, David, Beecham, Ashley, Rundek, Tatjana, Wang, Liyong, McClendon, Mark S, Slifer, Susan, Blanton, Susan H, Di Tullio, Marco R, Sacco, Ralph L

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Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study Autor Lee, Eunkyung, Takita, Cristiane, Wright, Jean L., Slifer, Susan H., Martin, Eden R., Urbanic, James J., Langefeld, Carl D., Lesser, Glenn J., Shaw, Edward G., Hu, Jennifer J.

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A modifier locus on chromosome 5 contributes to L1 cell adhesion molecule X-linked hydrocephalus in mice Autor Tapanes-Castillo, Alexis, Weaver, Eli J., Smith, Robin P., Kamei, Yoshimasa, Caspary, Tamara, Hamilton-Nelson, Kara L., Slifer, Susan H., Martin, Eden R., Bixby, John L., Lemmon, Vance P.

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Genetic Characterization and Influence on Inflammatory Bowel Disease Expression in a Diverse Hispanic South Florida Cohort Autor Damas, Oriana M, Gomez, Lissette, Quintero, Maria A, Rampersaud, Evadnie, Slifer, Susan, Beecham, Gary W, Kerman, David H, Deshpande, Amar R, Sussman, Daniel A, Abreu, Maria T, McCauley, Jacob L

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High Density SNP Screen in A Large Multiplex Neural Tube Defect Family Refines Linkage to Loci at 7p21-Pter And 2q33.1-35 Autor Stamm, Demetra S., Rampersaud, Evadnie, Slifer, Susan H., Mehltretter, Lorraine, Siegel, Deborah G., Xie, Jianzhen, Hu-Lince, Diane, Craig, David W., Stephan, Dietrich A., George, Timothy M., Gilbert, John R., Speer, Marcy C.

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Clinical and Pathologic Features of Familial Interstitial Pneumonia Autor Steele, Mark P., Speer, Marcy C., Loyd, James E., Brown, Kevin K., Herron, Aretha, Slifer, Susan H., Burch, Lauranell H., Wahidi, Momen M., Phillips, John A., Sporn, Thomas A., McAdams, H. Page, Schwarz, Marvin I., Schwartz, David A.

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Neural Tube Defects and Folate Pathway Genes: Family-Based Association Tests of Gene–Gene and Gene–Environment Interactions Autor Boyles, Abee L., Billups, Ashley V., Deak, Kristen L., Siegel, Deborah G., Mehltretter, Lorraine, Slifer, Susan H., Bassuk, Alexander G., Kessler, John A., Reed, Michael C., Nijhout, H. Frederik, George, Timothy M., Enterline, David S., Gilbert, John R., Speer, Marcy C.

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A genome-wide linkage analysis of dementia in the Amish Autor Hahs, Daniel W., McCauley, Jacob L., Crunk, Amy E., McFarland, Lynne L., Gaskell, Perry C., Jiang, Lan, Slifer, Susan H., Vance, Jeffery M., Scott, William K., Welsh-Bohmer, Kathleen A., Johnson, Stephanie R., Jackson, Charles E., Pericak-Vance, Margaret A., Haines, Jonathan L.

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SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects Autor Deak, Kristen L., Boyles, Abee L., Etchevers, Heather C., Melvin, Elizabeth C., Siegel, Deborah G., Graham, Felicia L., Slifer, Susan H., Enterline, David S., George, Timothy M., Vekemans, Michel, McClay, David, Bassuk, Alexander G., Kessler, John A., Linney, Elwood, Gilbert, John R., Speer, Marcy C.

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Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants Autor Griswold, Anthony J., Dueker, Nicole D., Van Booven, Derek, Rantus, Joseph A., Jaworski, James M., Slifer, Susan H., Schmidt, Michael A., Hulme, William, Konidari, Ioanna, Whitehead, Patrice L., Cuccaro, Michael L., Martin, Eden R., Haines, Jonathan L., Gilbert, John R., Hussman, John P., Pericak-Vance, Margaret A.

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