Search Results - Slifer, Susan

DNA Methylation Variation Is Identified in Monozygotic Twins Discordant for Non-syndromic Cleft Lip and Palate by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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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