Search Results - O’Connell, Jeffrey R.

An Optimal Algorithm for Automatic Genotype Elimination by O'Connell, Jeffrey R., Weeks, Daniel E.

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Fast imputation using medium or low-coverage sequence data by VanRaden, Paul M., Sun, Chuanyu, O’Connell, Jeffrey R.

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Improvement of Prediction Ability for Genomic Selection of Dairy Cattle by Including Dominance Effects by Sun, Chuanyu, VanRaden, Paul M., Cole, John B., O'Connell, Jeffrey R.

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Genomic evaluations with many more genotypes by VanRaden,, Paul M, O'Connell,, Jeffrey R, Wiggans, George R, Weigel, Kent A

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PedHunter 2.0 and its usage to characterize the founder structure of the Old Order Amish of Lancaster County by Lee, Woei-Jyh, Pollin, Toni I, O'Connell, Jeffrey R, Agarwala, Richa, Schäffer, Alejandro A

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Epigenetic Signature of Impaired Fasting Glucose in the Old Order Amish by Montasser, May E, Cheng, Yu-Ching, Tanner, Keith, Shuldiner, Alan R, O’Connell, Jeffrey R

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Sequence Variation in IGF1R is Associated with Differences in Insulin Levels in Nondiabetic Old Order Amish by Naj, Adam C., Kao, Wen-Hong L., O’Connell, Jeffrey R., Mitchell, Braxton D., Silver, Kristi D.

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Selecting sequence variants to improve genomic predictions for dairy cattle by VanRaden, Paul M., Tooker, Melvin E., O’Connell, Jeffrey R., Cole, John B., Bickhart, Derek M.

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Dissection of additive, dominance, and imprinting effects for production and reproduction traits in Holstein cattle by Jiang, Jicai, Shen, Botong, O’Connell, Jeffrey R., VanRaden, Paul M., Cole, John B., Ma, Li

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Exploiting gene × gene interaction in linkage analysis by Huang, Yungui, Bartlett, Christopher W, Segre, Alberto M, O'Connell, Jeffrey R, Mangin, LaVonne, Vieland, Veronica J

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Investigations of the Y Chromosome, Male Founder Structure and YSTR Mutation Rates in the Old Order Amish by Pollin, Toni I., McBride, Daniel J., Agarwala, Richa, Schäffer, Alejandro A., Shuldiner, Alan R., Mitchell, Braxton D., O'Connell, Jeffrey R.

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A FUNCTIONAL HAPLOTYPE IN EIF2AK3, AN ER STRESS SENSOR, IS ASSOCIATED WITH LOWER BONE MINERAL DENSITY by Liu, Jie, Hoppman, Nicole, O'Connell, Jeffrey R, Wang, Hong, Streeten, Elizabeth A, McLenithan, John C, Mitchell, Braxton D, Shuldiner, Alan R

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A Polymorphic 3’UTR Element in ATP1B1 Regulates Alternative Polyadenylation and Is Associated with Blood Pressure by Prasad, Megana K., Bhalla, Kavita, Pan, Zhen Hua, O’Connell, Jeffrey R., Weder, Alan B., Chakravarti, Aravinda, Tian, Bin, Chang, Yen-Pei C.

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Extent and Distribution of Linkage Disequilibrium in the Old Order Amish by Van Hout, Cristopher V, Levin, Albert M, Rampersaud, Evadnie, Shen, Haiqing, O'Connell, Jeffrey R, Mitchell, Braxton D, Shuldiner, Alan R, Douglas, Julie A

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Polymorphisms in the SOCS7 gene and glucose homeostasis traits by Capuano, Melissa M, Sorkin, John D, Chang, Yen-Pei C, Ling, Hua, O’Connell, Jeffrey R, Rothman, Paul B, Mitchell, Braxton D, Silver, Kristi D

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The Pharmacogenomics of Anti-Platelet Intervention (PAPI) Study: Variation in Platelet Response to Clopidogrel and Aspirin by Bozzi, Laura M., Mitchell, Braxton D., Lewis, Joshua P., Ryan, Kathy A., Herzog, William R., O’Connell, Jeffrey R., Horenstein, Richard B., Shuldiner, Alan R., Yerges-Armstrong, Laura M.

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FACTOR V LEIDEN AND ISCHEMIC STROKE RISK: THE GENETICS OF EARLY ONSET STROKE (GEOS) STUDY by Hamedani, Ali G., Cole, John W., Cheng, Yuching, Sparks, Mary J., O'Connell, Jeffrey R., Stine, Oscar C., Wozniak, Marcella A., Stern, Barney J., Mitchell, Braxton D., Kittner, Steven J.

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Genome-wide Association Scan Identifies Variants near Matrix Metalloproteinase (MMP) Genes on Chromosome 11q21-22 Strongly Associated with Serum MMP-1 Levels by Cheng, Yu-Ching, Kao, Wen-Hong L., Mitchell, Braxton D., O’Connell, Jeffrey R., Shen, Haiqing, McArdle, Patrick F, Gibson, Quince, Ryan, Kathleen A., Shuldiner, Alan R., Pollin, Toni I.

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A deletion mutation in bovine SLC4A2 is associated with osteopetrosis in Red Angus cattle by Meyers, Stacey N, McDaneld, Tara G, Swist, Shannon L, Marron, Brandy M, Steffen, David J, O'Toole, Donal, O'Connell, Jeffrey R, Beever, Jonathan E, Sonstegard, Tad S, Smith, Timothy PL

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From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases by Tise, Christina G., Perry, James A., Anforth, Leslie E., Pavlovich, Mary A., Backman, Joshua D., Ryan, Kathleen A., Lewis, Joshua P., O’Connell, Jeffrey R., Yerges-Armstrong, Laura M., Shuldiner, Alan R.

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