Výsledky vyhledávání - Haessler, Jeffrey

HNF1B and Endometrial Cancer Risk: Results from the PAGE study Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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... Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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... Autor 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 Autor 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 Autor 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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