Search Results - Haessler, Jeffrey

HNF1B and Endometrial Cancer Risk: Results from the PAGE study by Setiawan, Veronica Wendy, Haessler, Jeffrey, Schumacher, Fredrick, Cote, Michele L., Deelman, Ewa, Fesinmeyer, Megan D., Henderson, Brian E., Jackson, Rebecca D., Vöckler, Jens-S, Wilkens, Lynne R., Yasmeen, Shagufta, Haiman, Christopher A., Peters, Ulrike, Le Marchand, Loïc, Kooperberg, Charles

Get full text Get full text Get full text

Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure by He, Karen Y., Wang, Heming, Cade, Brian E., Nandakumar, Priyanka, Giri, Ayush, Ware, Erin B., Haessler, Jeffrey, Liang, Jingjing, Smith, Jennifer A., Franceschini, Nora, Le, Thu H., Kooperberg, Charles, Edwards, Todd L., Kardia, Sharon L. R., Lin, Xihong, Chakravarti, Aravinda, Redline, Susan, Zhu, Xiaofeng

Get full text Get full text Get full text

Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project by Johnsen, Jill M., Auer, Paul L., Morrison, Alanna C., Jiao, Shuo, Wei, Peng, Haessler, Jeffrey, Fox, Keolu, McGee, Sean R., Smith, Joshua D., Carlson, Christopher S., Smith, Nicholas, Boerwinkle, Eric, Kooperberg, Charles, Nickerson, Deborah A., Rich, Stephen S., Green, David, Peters, Ulrike, Cushman, Mary, Reiner, Alex P.

Get full text Get full text Get full text

Analyses of Biomarker Traits in Diverse UK Biobank Participants Identify Associations Missed by European-centric Analysis Strategies by Sun, Quan, Graff, Misa, Rowland, Bryce, Wen, Jia, Huang, Le, Miller-Fleming, Tyne W., Haessler, Jeffrey, Preuss, Michael H., Chai, Jin-Fang, Lee, Moa P., Avery, Christy L., Cheng, Ching-Yu, Franceschini, Nora, Sim, Xueling, Cox, Nancy J., Kooperberg, Charles, North, Kari E., Li, Yun, Raffield, Laura

Get full text Get full text Get full text

Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study by Hu, Yao, Bien, Stephanie A., Nishimura, Katherine K., Haessler, Jeffrey, Hodonsky, Chani J., Baldassari, Antoine R., Highland, Heather M., Wang, Zhe, Preuss, Michael, Sitlani, Colleen M., Wojcik, Genevieve L., Tao, Ran, Graff, Mariaelisa, Huckins, Laura M., Sun, Quan, Chen, Ming-Huei, Mousas, Abdou, Auer, Paul L., Lettre, Guillaume, Kooperberg, Charles

Get full text Get full text Get full text

Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans by Du, Mengmeng, Auer, Paul L., Jiao, Shuo, Haessler, Jeffrey, Altshuler, David, Boerwinkle, Eric, Carlson, Christopher S., Carty, Cara L., Chen, Yii-Der Ida, Curtis, Keith, Franceschini, Nora, Hsu, Li, Jackson, Rebecca, Lange, Leslie A., Lettre, Guillaume, Monda, Keri L., Nickerson, Deborah A., Reiner, Alex P., Rich, Stephen S., Rosse, Stephanie A., Rotter, Jerome I., Willer, Cristen J., Wilson, James G., North, Kari, Kooperberg, Charles, Heard-Costa, Nancy, Peters, Ulrike

Get full text Get full text Get full text

Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array by Bien, Stephanie A., Wojcik, Genevieve L., Zubair, Niha, Gignoux, Christopher R., Martin, Alicia R., Kocarnik, Jonathan M., Martin, Lisa W., Buyske, Steven, Haessler, Jeffrey, Walker, Ryan W., Cheng, Iona, Graff, Mariaelisa, Xia, Lucy, Franceschini, Nora, Matise, Tara, James, Regina, Hindorff, Lucia, Le Marchand, Loic, North, Kari E., Haiman, Christopher A., Peters, Ulrike, Loos, Ruth J. F., Kooperberg, Charles L., Bustamante, Carlos D., Kenny, Eimear E., Carlson, Christopher S.

Get full text Get full text Get full text

Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia by Setiawan, Veronica Wendy, Schumacher, Fredrick, Prescott, Jennifer, Haessler, Jeffrey, Malinowski, Jennifer, Wentzensen, Nicolas, Yang, Hannah, Chanock, Stephen, Brinton, Louise, Hartge, Patricia, Lissowska, Jolanta, Park, S.Lani, Cheng, Iona, Bush, William S., Crawford, Dana C., Ursin, Giske, Horn-Ross, Pamela, Bernstein, Leslie, Lu, Lingeng, Risch, Harvey, Yu, Herbert, Sakoda, Lori C., Doherty, Jennifer, Chen, Chu, Jackson, Rebecca, Yasmeen, Shagufta, Cote, Michele, Kocarnik, Jonathan M., Peters, Ulrike, Kraft, Peter, De Vivo, Immaculata, Haiman, Christopher A., Kooperberg, Charles, Le Marchand, Loic

Get full text Get full text Get full text

Epigenome-wide association study of mitochondrial genome copy number by Wang, Penglong, Castellani, Christina A, Yao, Jie, Huan, Tianxiao, Bielak, Lawrence F, Zhao, Wei, Haessler, Jeffrey, Joehanes, Roby, Sun, Xianbang, Guo, Xiuqing, Longchamps, Ryan J, Manson, JoAnn E, Grove, Megan L, Bressler, Jan, Taylor, Kent D, Lappalainen, Tuuli, Kasela, Silva, Van Den Berg, David J, Hou, Lifang, Reiner, Alexander, Liu, Yongmei, Boerwinkle, Eric, Smith, Jennifer A, Peyser, Patricia A, Fornage, Myriam, Rich, Stephen S, Rotter, Jerome I, Kooperberg, Charles, Arking, Dan E, Levy, Daniel, Liu, Chunyu

Get full text Get full text Get full text

Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemi... by Fesinmeyer, Megan D, Meigs, James B, North, Kari E, Schumacher, Fredrick R, Bůžková, Petra, Franceschini, Nora, Haessler, Jeffrey, Goodloe, Robert, Spencer, Kylee L, Voruganti, Venkata Saroja, Howard, Barbara V, Jackson, Rebecca, Kolonel, Laurence N, Liu, Simin, Manson, JoAnn E, Monroe, Kristine R, Mukamal, Kenneth, Dilks, Holli H, Pendergrass, Sarah A, Nato, Andrew, Wan, Peggy, Wilkens, Lynne R, Marchand, Loic Le, Ambite, José Luis, Buyske, Steven, Florez, Jose C, Crawford, Dana C, Hindorff, Lucia A, Haiman, Christopher A, Peters, Ulrike, Pankow, James S

Get full text Get full text Get full text

Clonal hematopoiesis is associated with higher risk of stroke by Bhattacharya, Romit, Zekavat, Seyedeh M., Haessler, Jeffrey, Fornage, Myriam, Raffield, Laura, Uddin, Md Mesbah, Bick, Alexander G., Niroula, Abhishek, Yu, Bing, Gibson, Christopher, Griffin, Gabriel, Morrison, Alanna C., Psaty, Bruce M., Longstreth, William T., Bis, Joshua C., Rich, Stephen S., Rotter, Jerome I., Tracy, Russell P., Correa, Adolfo, Seshadri, Sudha, Johnson, Andrew, Collins MPH, Jason M., Hayden, Kathleen M., Madsen, Tracy E., Ballantyne, Christie M., Jaiswal, Siddhartha, Ebert, Benjamin L., Kooperberg, Charles, Manson, JoAnn E., Whitsel, Eric A., Natarajan, Pradeep, Reiner, Alexander P.

Get full text Get full text Get full text

Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study by Buyske, Steven, Wu, Ying, Carty, Cara L., Cheng, Iona, Assimes, Themistocles L., Dumitrescu, Logan, Hindorff, Lucia A., Mitchell, Sabrina, Ambite, Jose Luis, Boerwinkle, Eric, Buzkova, Petra, Carlson, Chris S., Cochran, Barbara, Duggan, David, Eaton, Charles B., Fesinmeyer, Megan D., Franceschini, Nora, Haessler, Jeffrey, Jenny, Nancy, Kang, Hyun Min, Kooperberg, Charles, Lin, Yi, Le Marchand, Loic, Matise, Tara C., Robinson, Jennifer G., Rodriguez, Carlos, Schumacher, Fredrick R., Voight, Benjamin F., Young, Alicia, Manolio, Teri A., Mohlke, Karen L., Haiman, Christopher A., Peters, Ulrike, Crawford, Dana C., North, Kari E.

Get full text Get full text Get full text

Effects of smoking on the genetic risk of obesity: the population architecture using genomics and epidemiology study by Fesinmeyer, Megan D, North, Kari E, Lim, Unhee, Bůžková, Petra, Crawford, Dana C, Haessler, Jeffrey, Gross, Myron D, Fowke, Jay H, Goodloe, Robert, Love, Shelley-Ann, Graff, Misa, Carlson, Christopher S, Kuller, Lewis H, Matise, Tara C, Hong, Ching-Ping, Henderson, Brian E, Allen, Melissa, Rohde, Rebecca R, Mayo, Ping, Schnetz-Boutaud, Nathalie, Monroe, Kristine R, Ritchie, Marylyn D, Prentice, Ross L, Kolonel, Lawrence N, Manson, JoAnn E, Pankow, James, Hindorff, Lucia A, Franceschini, Nora, Wilkens, Lynne R, Haiman, Christopher A, Le Marchand, Loic, Peters, Ulrike

Get full text Get full text Get full text

Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium by Bien, Stephanie A., Pankow, James S., Haessler, Jeffrey, Lu, Yinchang N., Pankratz, Nathan, Rohde, Rebecca R., Tamuno, Alfred, Carlson, Christopher S., Schumacher, Fredrick R., Bůžková, Petra, Daviglus, Martha L., Lim, Unhee, Fornage, Myriam, Fernandez-Rhodes, Lindsay, Avilés-Santa, Larissa, Buyske, Steven, Gross, Myron D., Graff, Mariaelisa, Isasi, Carmen R., Kuller, Lewis H., Manson, JoAnn E., Matise, Tara C., Prentice, Ross L., Wilkens, Lynne R., Yoneyama, Sachiko, Loos, Ruth J. F., Hindorff, Lucia A., Le Marchand, Loic, North, Kari E., Haiman, Christopher A., Peters, Ulrike, Kooperberg, Charles

Get full text Get full text Get full text

Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium by Bien, Stephanie A., Pankow, James S., Haessler, Jeffrey, Lu, Yinchang, Pankratz, Nathan, Rohde, Rebecca R., Tamuno, Alfred, Carlson, Christopher S., Schumacher, Fredrick R., Bůžková, Petra, Daviglus, Martha L., Lim, Unhee, Fornage, Myriam, Fernandez-Rhodes, Lindsay, Avilés-Santa, Larissa, Buyske, Steven, Gross, Myron D., Graff, Mariaelisa, Isasi, Carmen R., Kuller, Lewis H., Manson, JoAnn E., Matise, Tara C., Prentice, Ross L., Wilkens, Lynne R., Yoneyama, Sachiko, Loos, Ruth J. F., Hindorff, Lucia A., Marchand, Loic Le, North, Kari E., Haiman, Christopher A., Peters, Ulrike, Kooperberg, Charles

Get full text Get full text Get full text

Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study by Hu, Yao, Bien, Stephanie A., Nishimura, Katherine K., Haessler, Jeffrey, Hodonsky, Chani J., Baldassari, Antoine R., Highland, Heather M., Wang, Zhe, Preuss, Michael, Sitlani, Colleen M., Wojcik, Genevieve L., Tao, Ran, Graff, Mariaelisa, Huckins, Laura M., Sun, Quan, Chen, Ming-Huei, Mousas, Abdou, Auer, Paul L., Lettre, Guillaume, Tang, Weihong, Qi, Lihong, Thyagarajan, Bharat, Buyske, Steve, Fornage, Myriam, Hindorff, Lucia A., Li, Yun, Lin, Danyu, Reiner, Alexander P., North, Kari E., Loos, Ruth J. F., Raffield, Laura M., Peters, Ulrike, Avery, Christy L., Kooperberg, Charles

Get full text Get full text Get full text

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project by Duan, Qing, Liu, Eric Yi, Auer, Paul L., Zhang, Guosheng, Lange, Ethan M., Jun, Goo, Bizon, Chris, Jiao, Shuo, Buyske, Steven, Franceschini, Nora, Carlson, Chris S., Hsu, Li, Reiner, Alex P., Peters, Ulrike, Haessler, Jeffrey, Curtis, Keith, Wassel, Christina L., Robinson, Jennifer G., Martin, Lisa W., Haiman, Christopher A., Le Marchand, Loic, Matise, Tara C., Hindorff, Lucia A., Crawford, Dana C., Assimes, Themistocles L., Kang, Hyun Min, Heiss, Gerardo, Jackson, Rebecca D., Kooperberg, Charles, Wilson, James G., Abecasis, Gonçalo R., North, Kari E., Nickerson, Deborah A., Lange, Leslie A., Li, Yun

Get full text Get full text Get full text

Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architect... by Kocarnik, Jonathan M, Richard, Melissa, Graff, Misa, Haessler, Jeffrey, Bien, Stephanie, Carlson, Chris, Carty, Cara L, Reiner, Alexander P, Avery, Christy L, Ballantyne, Christie M, LaCroix, Andrea Z, Assimes, Themistocles L, Barbalic, Maja, Pankratz, Nathan, Tang, Weihong, Tao, Ran, Chen, Dongquan, Talavera, Gregory A, Daviglus, Martha L, Chirinos-Medina, Diana A, Pereira, Rocio, Nishimura, Katie, Bůžková, Petra, Best, Lyle G, Ambite, José Luis, Cheng, Iona, Crawford, Dana C, Hindorff, Lucia A, Fornage, Myriam, Heiss, Gerardo, North, Kari E, Haiman, Christopher A, Peters, Ulrike, Le Marchand, Loic, Kooperberg, Charles

Get full text Get full text Get full text

BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion by Sofer, Tamar, Lee, Jiwon, Kurniansyah, Nuzulul, Jain, Deepti, Laurie, Cecelia A., Gogarten, Stephanie M., Conomos, Matthew P., Heavner, Ben, Hu, Yao, Kooperberg, Charles, Haessler, Jeffrey, Vasan, Ramachandran S., Cupples, L. Adrienne, Coombes, Brandon J., Seyerle, Amanda, Gharib, Sina A., Chen, Han, O’Connell, Jeffrey R., Zhang, Man, Gottlieb, Daniel J., Psaty, Bruce M., Longstreth, W.T., Rotter, Jerome I., Taylor, Kent D., Rich, Stephen S., Guo, Xiuqing, Boerwinkle, Eric, Morrison, Alanna C., Pankow, James S., Johnson, Andrew D., Pankratz, Nathan, Reiner, Alex P., Redline, Susan, Smith, Nicholas L., Rice, Kenneth M., Schifano, Elizabeth D.

Get full text Get full text Get full text

Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits by Highland, Heather M., Wojcik, Genevieve L., Graff, Mariaelisa, Nishimura, Katherine K., Hodonsky, Chani J., Baldassari, Antoine R., Cote, Alanna C., Cheng, Iona, Gignoux, Christopher R., Tao, Ran, Li, Yuqing, Boerwinkle, Eric, Fornage, Myriam, Haessler, Jeffrey, Hindorff, Lucia A., Hu, Yao, Justice, Anne E., Lin, Bridget M., Lin, Danyu, Stram, Daniel O., Haiman, Christopher A., Kooperberg, Charles, Le Marchand, Loic, Matise, Tara C., Kenny, Eimear E., Carlson, Christopher S., Stahl, Eli A., Avery, Christy L., North, Kari E., Ambite, Jose Luis, Buyske, Steven, Loos, Ruth J., Peters, Ulrike, Young, Kristin L., Bien, Stephanie A., Huckins, Laura M.

Get full text Get full text Get full text