检索结果 - Haessler, Jeffrey

HNF1B and Endometrial Cancer Risk: Results from the PAGE study 由 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

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Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure 由 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

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Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project 由 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.

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Analyses of Biomarker Traits in Diverse UK Biobank Participants Identify Associations Missed by European-centric Analysis Strategies 由 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

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Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study 由 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

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Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans 由 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

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Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array 由 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.

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Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia 由 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

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Epigenome-wide association study of mitochondrial genome copy number 由 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

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Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemi... 由 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

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Clonal hematopoiesis is associated with higher risk of stroke 由 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.

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Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study 由 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.

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Effects of smoking on the genetic risk of obesity: the population architecture using genomics and epidemiology study 由 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

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Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium 由 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

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Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium 由 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

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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 由 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

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Imputation of coding variants in African Americans: better performance using data from the exome sequencing project 由 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

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Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architect... 由 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

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BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion 由 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.

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Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits 由 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.

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