Kết quả tìm kiếm - O’Connell, Jeffrey R.
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An Optimal Algorithm for Automatic Genotype Elimination Bằng O'Connell, Jeffrey R., Weeks, Daniel E.
Được phát hành 1999Text -
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Fast imputation using medium or low-coverage sequence data Bằng VanRaden, Paul M., Sun, Chuanyu, O’Connell, Jeffrey R.
Được phát hành 2015Text -
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Genomic evaluations with many more genotypes Bằng VanRaden,, Paul M, O'Connell,, Jeffrey R, Wiggans, George R, Weigel, Kent A
Được phát hành 2011Text -
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Investigations of the Y Chromosome, Male Founder Structure and YSTR Mutation Rates in the Old Order Amish Bằng Pollin, Toni I., McBride, Daniel J., Agarwala, Richa, Schäffer, Alejandro A., Shuldiner, Alan R., Mitchell, Braxton D., O'Connell, Jeffrey R.
Được phát hành 2007Text -
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A FUNCTIONAL HAPLOTYPE IN EIF2AK3, AN ER STRESS SENSOR, IS ASSOCIATED WITH LOWER BONE MINERAL DENSITY Bằng Liu, Jie, Hoppman, Nicole, O'Connell, Jeffrey R, Wang, Hong, Streeten, Elizabeth A, McLenithan, John C, Mitchell, Braxton D, Shuldiner, Alan R
Được phát hành 2012Text -
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A Polymorphic 3’UTR Element in ATP1B1 Regulates Alternative Polyadenylation and Is Associated with Blood Pressure Bằng Prasad, Megana K., Bhalla, Kavita, Pan, Zhen Hua, O’Connell, Jeffrey R., Weder, Alan B., Chakravarti, Aravinda, Tian, Bin, Chang, Yen-Pei C.
Được phát hành 2013Text -
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The Pharmacogenomics of Anti-Platelet Intervention (PAPI) Study: Variation in Platelet Response to Clopidogrel and Aspirin Bằng 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.
Được phát hành 2016Text -
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FACTOR V LEIDEN AND ISCHEMIC STROKE RISK: THE GENETICS OF EARLY ONSET STROKE (GEOS) STUDY Bằng 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.
Được phát hành 2011Text -
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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 Bằng 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.
Được phát hành 2009Text -
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A deletion mutation in bovine SLC4A2 is associated with osteopetrosis in Red Angus cattle Bằng 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
Được phát hành 2010Text -
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From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases Bằng 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.
Được phát hành 2016Text