An Optimal Algorithm for Automatic Genotype Elimination

par O'Connell, Jeffrey R., Weeks, Daniel E.
Publié 1999

Fast imputation using medium or low-coverage sequence data

par VanRaden, Paul M., Sun, Chuanyu, O’Connell, Jeffrey R.
Publié dans BMC Genet (2015)

Improvement of Prediction Ability for Genomic Selection of Dairy Cattle by Including Dominance Effects

par Sun, Chuanyu, VanRaden, Paul M., Cole, John B., O'Connell, Jeffrey R.
Publié 2014

Genomic evaluations with many more genotypes

par VanRaden,, Paul M, O'Connell,, Jeffrey R, Wiggans, George R, Weigel, Kent A
Publié 2011

PedHunter 2.0 and its usage to characterize the founder structure of the Old Order Amish of Lancaster County

par Lee, Woei-Jyh, Pollin, Toni I, O'Connell, Jeffrey R, Agarwala, Richa, Schäffer, Alejandro A
Publié 2010

Epigenetic Signature of Impaired Fasting Glucose in the Old Order Amish

par Montasser, May E, Cheng, Yu-Ching, Tanner, Keith, Shuldiner, Alan R, O’Connell, Jeffrey R
Publié dans J Clin Epigenet (2017)

Sequence Variation in IGF1R is Associated with Differences in Insulin Levels in Nondiabetic Old Order Amish

par Naj, Adam C., Kao, Wen-Hong L., O’Connell, Jeffrey R., Mitchell, Braxton D., Silver, Kristi D.
Publié 2009

Selecting sequence variants to improve genomic predictions for dairy cattle

par VanRaden, Paul M., Tooker, Melvin E., O’Connell, Jeffrey R., Cole, John B., Bickhart, Derek M.
Publié dans Genet Sel Evol (2017)

Dissection of additive, dominance, and imprinting effects for production and reproduction traits in Holstein cattle

par Jiang, Jicai, Shen, Botong, O’Connell, Jeffrey R., VanRaden, Paul M., Cole, John B., Ma, Li
Publié dans BMC Genomics (2017)

Exploiting gene × gene interaction in linkage analysis

par Huang, Yungui, Bartlett, Christopher W, Segre, Alberto M, O'Connell, Jeffrey R, Mangin, LaVonne, Vieland, Veronica J
Publié 2007

Investigations of the Y Chromosome, Male Founder Structure and YSTR Mutation Rates in the Old Order Amish

par Pollin, Toni I., McBride, Daniel J., Agarwala, Richa, Schäffer, Alejandro A., Shuldiner, Alan R., Mitchell, Braxton D., O'Connell, Jeffrey R.
Publié 2007

A FUNCTIONAL HAPLOTYPE IN EIF2AK3, AN ER STRESS SENSOR, IS ASSOCIATED WITH LOWER BONE MINERAL DENSITY

par Liu, Jie, Hoppman, Nicole, O'Connell, Jeffrey R, Wang, Hong, Streeten, Elizabeth A, McLenithan, John C, Mitchell, Braxton D, Shuldiner, Alan R
Publié 2012

A Polymorphic 3’UTR Element in ATP1B1 Regulates Alternative Polyadenylation and Is Associated with Blood Pressure

par Prasad, Megana K., Bhalla, Kavita, Pan, Zhen Hua, O’Connell, Jeffrey R., Weder, Alan B., Chakravarti, Aravinda, Tian, Bin, Chang, Yen-Pei C.
Publié 2013

Extent and Distribution of Linkage Disequilibrium in the Old Order Amish

par Van Hout, Cristopher V, Levin, Albert M, Rampersaud, Evadnie, Shen, Haiqing, O'Connell, Jeffrey R, Mitchell, Braxton D, Shuldiner, Alan R, Douglas, Julie A
Publié 2010

Polymorphisms in the SOCS7 gene and glucose homeostasis traits

par 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
Publié 2013

The Pharmacogenomics of Anti-Platelet Intervention (PAPI) Study: Variation in Platelet Response to Clopidogrel and Aspirin

par 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.
Publié dans Curr Vasc Pharmacol (2016)

FACTOR V LEIDEN AND ISCHEMIC STROKE RISK: THE GENETICS OF EARLY ONSET STROKE (GEOS) STUDY

par 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.
Publié 2011

Genome-wide Association Scan Identifies Variants near Matrix Metalloproteinase (MMP) Genes on Chromosome 11q21-22 Strongly Associated with Serum MMP-1 Levels

par 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.
Publié 2009

A deletion mutation in bovine SLC4A2 is associated with osteopetrosis in Red Angus cattle

par 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
Publié 2010

From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases

par 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.
Publié dans G3 (Bethesda) (2016)