Výsledky vyhledávání - Sarnowski, Chloé
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Genes Involved in Interleukin-1 Receptor Type II Activities Are Associated With Asthmatic Phenotypes Autor Madore, Anne-Marie, Vaillancourt, Vanessa T., Bouzigon, Emmanuelle, Sarnowski, Chloé, Monier, Florent, Dizier, Marie-Hélène, Demenais, Florence, Laprise, Catherine
Vydáno 2016Text -
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Genetic variants associated with earlier age at menopause increase the risk of cardiovascular events in women Autor Sarnowski, Chloé, Kavousi, Maryam, Isaacs, Steve, Demerath, Ellen W, Broer, Linda, Muka, Taulant, Franco, Oscar H., Ikram, M Arfan, Uitterlinden, André, Franceschini, Nora, Lunetta, Kathryn L, Murabito, Joanne M
Vydáno 2018Text -
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Whole genome sequence analyses of brain imaging measures in the Framingham Study Autor Sarnowski, Chloé, Satizabal, Claudia L., DeCarli, Charles, Pitsillides, Achilleas N., Cupples, L. Adrienne, Vasan, Ramachandran S., Wilson, James G., Bis, Joshua C., Fornage, Myriam, Beiser, Alexa S., DeStefano, Anita L., Dupuis, Josée, Seshadri, Sudha
Vydáno 2018Text -
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Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits Autor Merino, Jordi, Dashti, Hassan S., Sarnowski, Chloé, Lane, Jacqueline M., Todorov, Petar V., Udler, Miriam S., Song, Yanwei, Wang, Heming, Kim, Jaegil, Tucker, Chandler, Campbell, John, Tanaka, Toshiko, Chu, Audrey Y., Tsai, Linus, Pers, Tune H., Chasman, Daniel I., Rutter, Martin K., Dupuis, Josée, Florez, Jose C., Saxena, Richa
Vydáno 2022Text -
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A Common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults Autor Bouzigon, Emmanuelle, Nadif, Rachel, Thompson, Emma E., Concas, Maria Pina, Kuldanek, Susan, Du, Gaixin, Brossard, Myriam, Lavielle, Nolwenn, Sarnowski, Chloé, Vaysse, Amaury, Dessen, Philippe, van der Valk, Ralf JP, Duijts, Liesbeth, Henderson, A John, Jaddoe, Vincent WV, de Jongste, Johan C, Dizier, Marie-Hélène, Pin, Isabelle, Matran, Régis, Lathrop, Mark, Pirastu, Mario, Demenais, Florence, Ober, Carole
Vydáno 2015Text -
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Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program Autor Sarnowski, Chloé, Chen, Han, Biggs, Mary L., Wassertheil-Smoller, Sylvia, Bressler, Jan, Irvin, Marguerite R., Ryan, Kathleen A., Karasik, David, Arnett, Donna K., Cupples, L. Adrienne, Fardo, David W., Gogarten, Stephanie M., Heavner, Benjamin D., Jain, Deepti, Kang, Hyun Min, Kooperberg, Charles, Mainous, Arch G., Mitchell, Braxton D., Morrison, Alanna C., O’Connell, Jeffrey R., Psaty, Bruce M., Rice, Kenneth, Smith, Albert V., Vasan, Ramachandran S., Windham, B. Gwen, Kiel, Douglas P., Murabito, Joanne M., Lunetta, Kathryn L.
Vydáno 2021Text -
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Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels Autor Sarnowski, Chloé, Ghanbari, Mohsen, Bis, Joshua C., Logue, Mark, Fornage, Myriam, Mishra, Aniket, Ahmad, Shahzad, Beiser, Alexa S., Boerwinkle, Eric, Bouteloup, Vincent, Chouraki, Vincent, Cupples, L Adrienne, Damotte, Vincent, DeCarli, Charles S., DeStefano, Anita L., Djoussé, Luc, Fohner, Alison E., Franz, Carol E., Kautz, Tiffany F., Lambert, Jean-Charles, Lyons, Michael J., Mosley, Thomas H., Mukamal, Kenneth J., Pase, Matthew P., Portilla Fernandez, Eliana C., Rissman, Robert A., Satizabal, Claudia L., Vasan, Ramachandran S., Yaqub, Amber, Debette, Stephanie, Dufouil, Carole, Launer, Lenore J., Kremen, William S., Longstreth, William T., Ikram, M Arfan, Seshadri, Sudha
Vydáno 2022Text -
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Whole-genome sequencing association analyses of stroke and its subtypes in ancestrally-diverse populations from TOPMed Autor Hu, Yao, Haessler, Jeffrey W., Manansala, Regina, Wiggins, Kerri L., Moscati, Arden, Beiser, Alexa, Heard-Costa, Nancy L., Sarnowski, Chloe, Raffield, Laura M., Chung, Jaeyoon, Marini, Sandro, Anderson, Christopher D., Rosand, Jonathan, Xu, Huichun, Sun, Xiao, Kelly, Tanika N., Wong, Quenna, Lange, Leslie A., Rotter, Jerome I., Correa, Adolfo, Vasan, Ramachandran S., Seshadri, Sudha, Rich, Stephen S., Do, Ron, Loos, Ruth J.F., Longstreth, William T., Bis, Joshua C., Psaty, Bruce M., Tirschwell, David L., Assimes, Themistocles L., Silver, Brian, Liu, Simin, Jackson, Rebecca, Smoller, Sylvia, Mitchell, Braxton D., Fornage, Myriam, Auer, Paul L., Reiner, Alex P., Kooperberg, Charles
Vydáno 2022Text -
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Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program Autor Sarnowski, Chloé, Leong, Aaron, Raffield, Laura M., Wu, Peitao, de Vries, Paul S., DiCorpo, Daniel, Guo, Xiuqing, Xu, Huichun, Liu, Yongmei, Zheng, Xiuwen, Hu, Yao, Brody, Jennifer A., Goodarzi, Mark O., Hidalgo, Bertha A., Highland, Heather M., Jain, Deepti, Liu, Ching-Ti, Naik, Rakhi P., O’Connell, Jeffrey R., Perry, James A., Porneala, Bianca C., Selvin, Elizabeth, Wessel, Jennifer, Psaty, Bruce M., Curran, Joanne E., Peralta, Juan M., Blangero, John, Kooperberg, Charles, Mathias, Rasika, Johnson, Andrew D., Reiner, Alexander P., Mitchell, Braxton D., Cupples, L. Adrienne, Vasan, Ramachandran S., Correa, Adolfo, Morrison, Alanna C., Boerwinkle, Eric, Rotter, Jerome I., Rich, Stephen S., Manning, Alisa K., Dupuis, Josée, Meigs, James B.
Vydáno 2019Text -
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Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts Autor DiCorpo, Daniel, LeClair, Jessica, Cole, Joanne B., Sarnowski, Chloé, Ahmadizar, Fariba, Bielak, Lawrence F., Blokstra, Anneke, Bottinger, Erwin P., Chaker, Layal, Chen, Yii-Der I., Chen, Ye, de Vries, Paul S., Faquih, Tariq, Ghanbari, Mohsen, Gudmundsdottir, Valborg, Guo, Xiuqing, Hasbani, Natalie R., Ibi, Dorina, Ikram, M. Arfan, Kavousi, Maryam, Leonard, Hampton L., Leong, Aaron, Mercader, Josep M., Morrison, Alanna C., Nadkarni, Girish N., Nalls, Mike A., Noordam, Raymond, Preuss, Michael, Smith, Jennifer A., Trompet, Stella, Vissink, Petra, Yao, Jie, Zhao, Wei, Boerwinkle, Eric, Goodarzi, Mark O., Gudnason, Vilmundur, Jukema, J. Wouter, Kardia, Sharon L.R., Loos, Ruth J.F., Liu, Ching-Ti, Manning, Alisa K., Mook-Kanamori, Dennis, Pankow, James S., Picavet, H. Susan J., Sattar, Naveed, Simonsick, Eleanor M., Verschuren, W.M. Monique, Willems van Dijk, Ko, Florez, Jose C., Rotter, Jerome I., Meigs, James B., Dupuis, Josée, Udler, Miriam S.
Vydáno 2022Text -
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Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis Autor Merino, Jordi, Guasch-Ferré, Marta, Ellervik, Christina, Dashti, Hassan S, Sharp, Stephen J, Wu, Peitao, Overvad, Kim, Sarnowski, Chloé, Kuokkanen, Mikko, Lemaitre, Rozenn N, Justice, Anne E, Ericson, Ulrika, Braun, Kim V E, Mahendran, Yuvaraj, Frazier-Wood, Alexis C, Sun, Dianjianyi, Chu, Audrey Y, Tanaka, Toshiko, Luan, Jian’an, Hong, Jaeyoung, Tjønneland, Anne, Ding, Ming, Lundqvist, Annamari, Mukamal, Kenneth, Rohde, Rebecca, Schulz, Christina-Alexandra, Franco, Oscar H, Grarup, Niels, Chen, Yii-Der Ida, Bazzano, Lydia, Franks, Paul W, Buring, Julie E, Langenberg, Claudia, Liu, Ching-Ti, Hansen, Torben, Jensen, Majken K, Sääksjärvi, Katri, Psaty, Bruce M, Young, Kristin L, Hindy, George, Sandholt, Camilla Helene, Ridker, Paul M, Ordovas, Jose M, Meigs, James B, Pedersen, Oluf, Kraft, Peter, Perola, Markus, North, Kari E, Orho-Melander, Marju, Voortman, Trudy, Toft, Ulla, Rotter, Jerome I, Qi, Lu, Forouhi, Nita G, Mozaffarian, Dariush, Sørensen, Thorkild I A, Stampfer, Meir J, Männistö, Satu, Selvin, Elizabeth, Imamura, Fumiaki, Salomaa, Veikko, Hu, Frank B, Wareham, Nick J, Dupuis, Josée, Smith, Caren E, Kilpeläinen, Tuomas O, Chasman, Daniel I, Florez, Jose C
Vydáno 2019Text -
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Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women Autor Jones, Garan, Trajanoska, Katerina, Santanasto, Adam J., Stringa, Najada, Kuo, Chia-Ling, Atkins, Janice L., Lewis, Joshua R., Duong, ThuyVy, Hong, Shengjun, Biggs, Mary L., Luan, Jian’an, Sarnowski, Chloe, Lunetta, Kathryn L., Tanaka, Toshiko, Wojczynski, Mary K., Cvejkus, Ryan, Nethander, Maria, Ghasemi, Sahar, Yang, Jingyun, Zillikens, M. Carola, Walter, Stefan, Sicinski, Kamil, Kague, Erika, Ackert-Bicknell, Cheryl L., Arking, Dan E., Windham, B. Gwen, Boerwinkle, Eric, Grove, Megan L., Graff, Misa, Spira, Dominik, Demuth, Ilja, van der Velde, Nathalie, de Groot, Lisette C. P. G. M., Psaty, Bruce M., Odden, Michelle C., Fohner, Alison E., Langenberg, Claudia, Wareham, Nicholas J., Bandinelli, Stefania, van Schoor, Natasja M., Huisman, Martijn, Tan, Qihua, Zmuda, Joseph, Mellström, Dan, Karlsson, Magnus, Bennett, David A., Buchman, Aron S., De Jager, Philip L., Uitterlinden, Andre G., Völker, Uwe, Kocher, Thomas, Teumer, Alexander, Rodriguéz-Mañas, Leocadio, García, Francisco J., Carnicero, José A., Herd, Pamela, Bertram, Lars, Ohlsson, Claes, Murabito, Joanne M., Melzer, David, Kuchel, George A., Ferrucci, Luigi, Karasik, David, Rivadeneira, Fernando, Kiel, Douglas P., Pilling, Luke C.
Vydáno 2021Text -
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A meta-analysis of genome-wide association studies identifies multiple longevity genes Autor Deelen, Joris, Evans, Daniel S., Arking, Dan E., Tesi, Niccolò, Nygaard, Marianne, Liu, Xiaomin, Wojczynski, Mary K., Biggs, Mary L., van der Spek, Ashley, Atzmon, Gil, Ware, Erin B., Sarnowski, Chloé, Smith, Albert V., Seppälä, Ilkka, Cordell, Heather J., Dose, Janina, Amin, Najaf, Arnold, Alice M., Ayers, Kristin L., Barzilai, Nir, Becker, Elizabeth J., Beekman, Marian, Blanché, Hélène, Christensen, Kaare, Christiansen, Lene, Collerton, Joanna C., Cubaynes, Sarah, Cummings, Steven R., Davies, Karen, Debrabant, Birgit, Deleuze, Jean-François, Duncan, Rachel, Faul, Jessica D., Franceschi, Claudio, Galan, Pilar, Gudnason, Vilmundur, Harris, Tamara B., Huisman, Martijn, Hurme, Mikko A., Jagger, Carol, Jansen, Iris, Jylhä, Marja, Kähönen, Mika, Karasik, David, Kardia, Sharon L. R., Kingston, Andrew, Kirkwood, Thomas B. L., Launer, Lenore J., Lehtimäki, Terho, Lieb, Wolfgang, Lyytikäinen, Leo-Pekka, Martin-Ruiz, Carmen, Min, Junxia, Nebel, Almut, Newman, Anne B., Nie, Chao, Nohr, Ellen A., Orwoll, Eric S., Perls, Thomas T., Province, Michael A., Psaty, Bruce M., Raitakari, Olli T., Reinders, Marcel J. T., Robine, Jean-Marie, Rotter, Jerome I., Sebastiani, Paola, Smith, Jennifer, Sørensen, Thorkild I. A., Taylor, Kent D., Uitterlinden, André G., van der Flier, Wiesje, van der Lee, Sven J., van Duijn, Cornelia M., van Heemst, Diana, Vaupel, James W., Weir, David, Ye, Kenny, Zeng, Yi, Zheng, Wanlin, Holstege, Henne, Kiel, Douglas P., Lunetta, Kathryn L., Slagboom, P. Eline, Murabito, Joanne M.
Vydáno 2019Text -
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Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes Autor Deelen, Joris, Evans, Daniel S., Arking, Dan E., Tesi, Niccolò, Nygaard, Marianne, Liu, Xiaomin, Wojczynski, Mary K., Biggs, Mary L., van der Spek, Ashley, Atzmon, Gil, Ware, Erin B., Sarnowski, Chloé, Smith, Albert V., Seppälä, Ilkka, Cordell, Heather J., Dose, Janina, Amin, Najaf, Arnold, Alice M., Ayers, Kristin L., Barzilai, Nir, Becker, Elizabeth J., Beekman, Marian, Blanché, Hélène, Christensen, Kaare, Christiansen, Lene, Collerton, Joanna C., Cubaynes, Sarah, Cummings, Steven R., Davies, Karen, Debrabant, Birgit, Deleuze, Jean-François, Duncan, Rachel, Faul, Jessica D., Franceschi, Claudio, Galan, Pilar, Gudnason, Vilmundur, Harris, Tamara B., Huisman, Martijn, Hurme, Mikko A., Jagger, Carol, Jansen, Iris, Jylhä, Marja, Kähönen, Mika, Karasik, David, Kardia, Sharon L. R., Kingston, Andrew, Kirkwood, Thomas B. L., Launer, Lenore J., Lehtimäki, Terho, Lieb, Wolfgang, Lyytikäinen, Leo-Pekka, Martin-Ruiz, Carmen, Min, Junxia, Nebel, Almut, Newman, Anne B., Nie, Chao, Nohr, Ellen A., Orwoll, Eric S., Perls, Thomas T., Province, Michael A., Psaty, Bruce M., Raitakari, Olli T., Reinders, Marcel J. T., Robine, Jean-Marie, Rotter, Jerome I., Sebastiani, Paola, Smith, Jennifer, Sørensen, Thorkild I. A., Taylor, Kent D., Uitterlinden, André G., van der Flier, Wiesje, van der Lee, Sven J., van Duijn, Cornelia M., van Heemst, Diana, Vaupel, James W., Weir, David, Ye, Kenny, Zeng, Yi, Zheng, Wanlin, Holstege, Henne, Kiel, Douglas P., Lunetta, Kathryn L., Slagboom, P. Eline, Murabito, Joanne M.
Vydáno 2021Text -
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Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation Autor Bis, Joshua C., Jian, Xueqiu, Kunkle, Brian W., Chen, Yuning, Hamilton-Nelson, Kara L., Bush, William S., Salerno, William J., Lancour, Daniel, Ma, Yiyi, Renton, Alan E., Marcora, Edoardo, Farrell, John J., Zhao, Yi, Qu, Liming, Ahmad, Shahzad, Amin, Najaf, Amouyel, Philippe, Beecham, Gary W., Below, Jennifer E., Campion, Dominique, Cantwell, Laura, Charbonnier, Camille, Chung, Jaeyoon, Crane, Paul K., Cruchaga, Carlos, Cupples, L. Adrienne, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Fulton, Lucinda, Gabriel, Stacey B., Genin, Emmanuelle, Gibbs, Richard A., Goate, Alison, Grenier-Boley, Benjamin, Gupta, Namrata, Haines, Jonathan L., Havulinna, Aki S., Helisalmi, Seppo, Hiltunen, Mikko, Howrigan, Daniel P., Ikram, M. Arfan, Kaprio, Jaakko, Konrad, Jan, Kuzma, Amanda, Lander, Eric S., Lathrop, Mark, Lehtimäki, Terho, Lin, Honghuang, Mattila, Kari, Mayeux, Richard, Muzny, Donna M., Nasser, Waleed, Neale, Benjamin, Nho, Kwangsik, Nicolas, Gaël, Patel, Devanshi, Pericak-Vance, Margaret A., Perola, Markus, Psaty, Bruce M., Quenez, Olivier, Rajabli, Farid, Redon, Richard, Reitz, Christiane, Remes, Anne M., Salomaa, Veikko, Sarnowski, Chloe, Schmidt, Helena, Schmidt, Michael, Schmidt, Reinhold, Soininen, Hilkka, Thornton, Timothy A., Tosto, Giuseppe, Tzourio, Christophe, van der Lee, Sven J., van Duijn, Cornelia M., Valladares, Otto, Vardarajan, Badri, Wang, Li-San, Wang, Weixin, Wijsman, Ellen, Wilson, Richard K., Witten, Daniela, Worley, Kim C., Zhang, Xiaoling, Bellenguez, Celine, Lambert, Jean-Charles, Kurki, Mitja I., Palotie, Aarno, Daly, Mark, Boerwinkle, Eric, Lunetta, Kathryn L., Destefano, Anita L., Dupuis, Josée, Martin, Eden R., Schellenberg, Gerard D., Seshadri, Sudha, Naj, Adam C., Fornage, Myriam, Farrer, Lindsay A.
Vydáno 2018Text