Search Results - Polfus, Linda M.

Coronary Heart Disease and Genetic Variants with Low Phospholipase A(2) Activity by Polfus, Linda M., Gibbs, Richard A., Boerwinkle, Eric

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Genome-Wide Association Study of Gene by Smoking Interactions in Coronary Artery Calcification by Polfus, Linda M., Smith, Jennifer A., Shimmin, Lawrence C., Bielak, Lawrence F., Morrison, Alanna C., Kardia, Sharon L. R., Peyser, Patricia A., Hixson, James E.

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Lipoprotein-associated phospholipase A(2) and risk of incident peripheral arterial disease: Findings from The Atherosclerosis Risk in Communities study (ARIC) by Garg, Parveen K., Norby, Faye L., Polfus, Linda M., Boerwinkle, Eric, Gibbs, Richard A., Grove, Megan L., Folsom, Aaron R., Garimella, Pranav S., Matsushita, Kunihiro, Hoogeveen, Ron C., Ballantyne, Christie M.

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Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome by Polfus, Linda M., Boerwinkle, Eric, Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Grove, Megan, Shete, Sanjay, Wallace, Stephanie, Milewicz, Dianna, Hanchard, Neil, Lupski, James R., Hashmi, Syed Shahrukh, Gupta-Malhotra, Monesha

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Urinary phthalate exposures and risk of breast cancer: the Multiethnic Cohort study by Wu, Anna H., Franke, Adrian A., Wilkens, Lynne R., Tseng, Chiuchen, Conroy, Shannon M., Li, Yuqing, Polfus, Linda M., De Rouen, Mindy, Caberto, Christian, Haiman, Christopher, Stram, Daniel O., Le Marchand, Loïc, Cheng, Iona

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Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease by Li, Alexander H, Morrison, Alanna C, Kovar, Christie, Cupples, L Adrienne, Brody, Jennifer A, Polfus, Linda M, Yu, Bing, Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Liu, Xiaoming, Lumley, Thomas, Mosley, Thomas H, Gibbs, Richard A, Boerwinkle, Eric

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Risk of Breast Cancer and pre-diagnostic urinary excretion of bisphenol A, triclosan, and parabens: the Multiethnic Cohort Study by Wu, Anna H, Franke, Adrian A, Wilkens, Lynne R, Tseng, Chiuchen, Conroy, Shannon M, Li, Yuqing, Sangaramoorthy, Meera, Polfus, Linda M, DeRouen, Mindy C, Caberto, Christian, Haiman, Christopher, Stram, Daniel O, Le Marchand, Loïc, Cheng, Iona

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A common TCN1 loss-of-function variant is associated with lower vitamin B(12) concentration in African Americans by Hu, Yao, Raffield, Laura M., Polfus, Linda M., Moscati, Arden, Nadkarni, Girish, Preuss, Michael H., Zhong, Xue, Wei, Qiang, Rich, Stephen S., Li, Yun, Wilson, James G., Correa, Adolfo, Loos, Ruth J. F., Li, Bingshan, Auer, Paul L., Reiner, Alex P.

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Association of Exome Sequences With Cardiovascular Traits among Blacks in the Jackson Heart Study by Peloso, Gina M., Lange, Leslie A., Varga, Tibor V., Nickerson, Deborah A., Smith, Joshua D., Griswold, Michael E., Musani, Solomon, Polfus, Linda M., Mei, Hao, Gabriel, Stacey, Quarells, Rakale Collins, Altshuler, David, Boerwinkle, Eric, Daly, Mark J., Neale, Benjamin, Correa, Adolfo, Reiner, Alex P., Wilson, James G., Kathiresan, Sekar

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Genome-wide association study of pancreatic fat: The Multiethnic Cohort Adiposity Phenotype Study by Streicher, Samantha A., Lim, Unhee, Park, S. Lani, Li, Yuqing, Sheng, Xin, Hom, Victor, Xia, Lucy, Pooler, Loreall, Shepherd, John, Loo, Lenora W. M., Darst, Burcu F., Highland, Heather M., Polfus, Linda M., Bogumil, David, Ernst, Thomas, Buchthal, Steven, Franke, Adrian A., Setiawan, Veronica Wendy, Tiirikainen, Maarit, Wilkens, Lynne R., Haiman, Christopher A., Stram, Daniel O., Cheng, Iona, Le Marchand, Loïc

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Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African Americans by Polfus, Linda M, Raffield, Laura M, Wheeler, Marsha M, Tracy, Russell P, Lange, Leslie A, Lettre, Guillaume, Miller, Amanda, Correa, Adolfo, Bowler, Russell P, Bis, Joshua C, Salimi, Shabnam, Jenny, Nancy Swords, Pankratz, Nathan, Wang, Biqi, Preuss, Michael H, Zhou, Lisheng, Moscati, Arden, Nadkarni, Girish N, Loos, Ruth J F, Zhong, Xue, Li, Bingshan, Johnsen, Jill M, Nickerson, Deborah A, Reiner, Alex P, Auer, Paul L

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Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study by Downie, Carolina G., Dimos, Sofia F., Bien, Stephanie A., Hu, Yao, Darst, Burcu F., Polfus, Linda M., Wang, Yujie, Wojcik, Genevieve L., Tao, Ran, Raffield, Laura M., Armstrong, Nicole D., Polikowsky, Hannah G., Below, Jennifer E., Correa, Adolfo, Irvin, Marguerite R., Rasmussen-Torvik, Laura J. F., Carlson, Christopher S., Phillips, Lawrence S., Liu, Simin, Pankow, James S., Rich, Stephen S., Rotter, Jerome I., Buyske, Steven, Matise, Tara C., North, Kari E., Avery, Christy L., Haiman, Christopher A., Loos, Ruth J. F., Kooperberg, Charles, Graff, Mariaelisa, Highland, Heather M.

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Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts by Raffield, Laura M., Iyengar, Apoorva K., Wang, Biqi, Gaynor, Sheila M., Spracklen, Cassandra N., Zhong, Xue, Kowalski, Madeline H., Salimi, Shabnam, Polfus, Linda M., Benjamin, Emelia J., Bis, Joshua C., Bowler, Russell, Cade, Brian E., Choi, Won Jung, Comellas, Alejandro P., Correa, Adolfo, Cruz, Pedro, Doddapaneni, Harsha, Durda, Peter, Gogarten, Stephanie M., Jain, Deepti, Kim, Ryan W., Kral, Brian G., Lange, Leslie A., Larson, Martin G., Laurie, Cecelia, Lee, Jiwon, Lee, Seonwook, Lewis, Joshua P., Metcalf, Ginger A., Mitchell, Braxton D., Momin, Zeineen, Muzny, Donna M., Pankratz, Nathan, Park, Cheol Joo, Rich, Stephen S., Rotter, Jerome I., Ryan, Kathleen, Seo, Daekwan, Tracy, Russell P., Viaud-Martinez, Karine A., Yanek, Lisa R., Zhao, Lue Ping, Lin, Xihong, Li, Bingshan, Li, Yun, Dupuis, Josée, Reiner, Alexander P., Mohlke, Karen L., Auer, Paul L.

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Genetic discovery and risk characterization in type 2 diabetes across diverse populations by Polfus, Linda M., Darst, Burcu F., Highland, Heather, Sheng, Xin, Ng, Maggie C.Y., Below, Jennifer E., Petty, Lauren, Bien, Stephanie, Sim, Xueling, Wang, Wei, Fontanillas, Pierre, Patel, Yesha, Preuss, Michael, Schurmann, Claudia, Du, Zhaohui, Lu, Yingchang, Rhie, Suhn K., Mercader, Joseph M., Tusie-Luna, Teresa, González-Villalpando, Clicerio, Orozco, Lorena, Spracklen, Cassandra N., Cade, Brian E., Jensen, Richard A., Sun, Meng, Joo, Yoonjung Yoonie, An, Ping, Yanek, Lisa R., Bielak, Lawrence F., Tajuddin, Salman, Nicolas, Aude, Chen, Guanjie, Raffield, Laura, Guo, Xiuqing, Chen, Wei-Min, Nadkarni, Girish N., Graff, Mariaelisa, Tao, Ran, Pankow, James S., Daviglus, Martha, Qi, Qibin, Boerwinkle, Eric A., Liu, Simin, Phillips, Lawrence S., Peters, Ulrike, Carlson, Chris, Wikens, Lynne R., Le Marchand, Loic, North, Kari E., Buyske, Steven, Kooperberg, Charles, Loos, Ruth J.F., Stram, Daniel O., Haiman, Christopher A.

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Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis by Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Frank J.A., Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Walter, Klaudia, Chen, Lu, Yanek, Lisa, Becker, Lewis C., Peloso, Gina M., Wakabayashi, Aoi, Kals, Mart, Metspalu, Andres, Esko, Tõnu, Fox, Keolu, Wallace, Robert, Franceshini, Nora, Matijevic, Nena, Rice, Kenneth M., Bartz, Traci M., Lyytikäinen, Leo-Pekka, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T., Li-Gao, Ruifang, Mook-Kanamori, Dennis O., Lettre, Guillaume, van Duijn, Cornelia M., Franco, Oscar H., Rich, Stephen S., Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, André G., Wilson, James G., Psaty, Bruce M., Soranzo, Nicole, Dehghan, Abbas, Boerwinkle, Eric, Zhang, Xiaoling, Johnson, Andrew D., O’Donnell, Christopher J., Johnsen, Jill M., Reiner, Alexander P., Ganesh, Santhi K., Sankaran, Vijay G.

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Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis by Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Frank J.A., Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Walter, Klaudia, Chen, Lu, Yanek, Lisa, Becker, Lewis C., Peloso, Gina M., Wakabayashi, Aoi, Kals, Mart, Metspalu, Andres, Esko, Tõnu, Fox, Keolu, Wallace, Robert, Franceschini, Nora, Matijevic, Nena, Rice, Kenneth M., Bartz, Traci M., Lyytikäinen, Leo-Pekka, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T., Li-Gao, Ruifang, Mook-Kanamori, Dennis O., Lettre, Guillaume, van Duijn, Cornelia M., Franco, Oscar H., Rich, Stephen S., Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, André G., Wilson, James G., Psaty, Bruce M., Soranzo, Nicole, Dehghan, Abbas, Boerwinkle, Eric, Zhang, Xiaoling, Johnson, Andrew D., O’Donnell, Christopher J., Johnsen, Jill M., Reiner, Alexander P., Ganesh, Santhi K., Sankaran, Vijay G.

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Genetic invalidation of Lp-PLA(2) as a therapeutic target: Large-scale study of five functional Lp-PLA(2)-lowering alleles by Gregson, John M, Freitag, Daniel F, Surendran, Praveen, Stitziel, Nathan O, Chowdhury, Rajiv, Burgess, Stephen, Kaptoge, Stephen, Gao, Pei, Staley, James R, Willeit, Peter, Nielsen, Sune F, Caslake, Muriel, Trompet, Stella, Polfus, Linda M, Kuulasmaa, Kari, Kontto, Jukka, Perola, Markus, Blankenberg, Stefan, Veronesi, Giovanni, Gianfagna, Francesco, Männistö, Satu, Kimura, Akinori, Lin, Honghuang, Reilly, Dermot F, Gorski, Mathias, Mijatovic, Vladan, Munroe, Patricia B, Ehret, Georg B, Thompson, Alex, Uria-Nickelsen, Maria, Malarstig, Anders, Dehghan, Abbas, Vogt, Thomas F, Sasaoka, Taishi, Takeuchi, Fumihiko, Kato, Norihiro, Yamada, Yoshiji, Kee, Frank, Müller-Nurasyid, Martina, Ferrières, Jean, Arveiler, Dominique, Amouyel, Philippe, Salomaa, Veikko, Boerwinkle, Eric, Thompson, Simon G, Ford, Ian, Wouter Jukema, J, Sattar, Naveed, Packard, Chris J, Shafi Majumder, Abdulla al, Alam, Dewan S, Deloukas, Panos, Schunkert, Heribert, Samani, Nilesh J, Kathiresan, Sekar, Nordestgaard, Børge G, Saleheen, Danish, Howson, Joanna MM, Di Angelantonio, Emanuele, Butterworth, Adam S, Danesh, John

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Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program by Mikhaylova, Anna V., McHugh, Caitlin P., Polfus, Linda M., Raffield, Laura M., Boorgula, Meher Preethi, Blackwell, Thomas W., Brody, Jennifer A., Broome, Jai, Chami, Nathalie, Chen, Ming-Huei, Conomos, Matthew P., Cox, Corey, Curran, Joanne E., Daya, Michelle, Ekunwe, Lynette, Glahn, David C., Heard-Costa, Nancy, Highland, Heather M., Hobbs, Brian D., Ilboudo, Yann, Jain, Deepti, Lange, Leslie A., Miller-Fleming, Tyne W., Min, Nancy, Moon, Jee-Young, Preuss, Michael H., Rosen, Jonathon, Ryan, Kathleen, Smith, Albert V., Sun, Quan, Surendran, Praveen, de Vries, Paul S., Walter, Klaudia, Wang, Zhe, Wheeler, Marsha, Yanek, Lisa R., Zhong, Xue, Abecasis, Goncalo R., Almasy, Laura, Barnes, Kathleen C., Beaty, Terri H., Becker, Lewis C., Blangero, John, Boerwinkle, Eric, Butterworth, Adam S., Chavan, Sameer, Cho, Michael H., Choquet, Hélène, Correa, Adolfo, Cox, Nancy, DeMeo, Dawn L., Faraday, Nauder, Fornage, Myriam, Gerszten, Robert E., Hou, Lifang, Johnson, Andrew D., Jorgenson, Eric, Kaplan, Robert, Kooperberg, Charles, Kundu, Kousik, Laurie, Cecelia A., Lettre, Guillaume, Lewis, Joshua P., Li, Bingshan, Li, Yun, Lloyd-Jones, Donald M., Loos, Ruth J.F., Manichaikul, Ani, Meyers, Deborah A., Mitchell, Braxton D., Morrison, Alanna C., Ngo, Debby, Nickerson, Deborah A., Nongmaithem, Suraj, North, Kari E., O’Connell, Jeffrey R., Ortega, Victor E., Pankratz, Nathan, Perry, James A., Psaty, Bruce M., Rich, Stephen S., Soranzo, Nicole, Rotter, Jerome I., Silverman, Edwin K., Smith, Nicholas L., Tang, Hua, Tracy, Russell P., Thornton, Timothy A., Vasan, Ramachandran S., Zein, Joe, Mathias, Rasika A., Reiner, Alexander P., Auer, Paul L.

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Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases by Tajuddin, Salman M., Schick, Ursula M., Eicher, John D., Chami, Nathalie, Giri, Ayush, Brody, Jennifer A., Hill, W. David, Kacprowski, Tim, Li, Jin, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Mihailov, Evelin, O’Donoghue, Michelle L., Pankratz, Nathan, Pazoki, Raha, Polfus, Linda M., Smith, Albert Vernon, Schurmann, Claudia, Vacchi-Suzzi, Caterina, Waterworth, Dawn M., Evangelou, Evangelos, Yanek, Lisa R., Burt, Amber, Chen, Ming-Huei, van Rooij, Frank J.A., Floyd, James S., Greinacher, Andreas, Harris, Tamara B., Highland, Heather M., Lange, Leslie A., Liu, Yongmei, Mägi, Reedik, Nalls, Mike A., Mathias, Rasika A., Nickerson, Deborah A., Nikus, Kjell, Starr, John M., Tardif, Jean-Claude, Tzoulaki, Ioanna, Velez Edwards, Digna R., Wallentin, Lars, Bartz, Traci M., Becker, Lewis C., Denny, Joshua C., Raffield, Laura M., Rioux, John D., Friedrich, Nele, Fornage, Myriam, Gao, He, Hirschhorn, Joel N., Liewald, David C.M., Rich, Stephen S., Uitterlinden, Andre, Bastarache, Lisa, Becker, Diane M., Boerwinkle, Eric, de Denus, Simon, Bottinger, Erwin P., Hayward, Caroline, Hofman, Albert, Homuth, Georg, Lange, Ethan, Launer, Lenore J., Lehtimäki, Terho, Lu, Yingchang, Metspalu, Andres, O’Donnell, Chris J., Quarells, Rakale C., Richard, Melissa, Torstenson, Eric S., Taylor, Kent D., Vergnaud, Anne-Claire, Zonderman, Alan B., Crosslin, David R., Deary, Ian J., Dörr, Marcus, Elliott, Paul, Evans, Michele K., Gudnason, Vilmundur, Kähönen, Mika, Psaty, Bruce M., Rotter, Jerome I., Slater, Andrew J., Dehghan, Abbas, White, Harvey D., Ganesh, Santhi K., Loos, Ruth J.F., Esko, Tõnu, Faraday, Nauder, Wilson, James G., Cushman, Mary, Johnson, Andrew D., Edwards, Todd L., Zakai, Neil A., Lettre, Guillaume, Reiner, Alex P., Auer, Paul L.

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