檢索結果 - O'Connell, Jeffrey R

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

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Fast imputation using medium or low-coverage sequence data 由 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 由 Sun, Chuanyu, VanRaden, Paul M., Cole, John B., O'Connell, Jeffrey R.

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Genomic evaluations with many more genotypes 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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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