Treffer 1 - 20 von 42 für Suche 'C., Curran Jerome', Suchdauer: 1,63s Treffer weiter einschränken
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    Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program von Hu, Yao, Stilp, Adrienne M., McHugh, Caitlin P., Rao, Shuquan, Jain, Deepti, Zheng, Xiuwen, Lane, John, Méric de Bellefon, Sébastian, Raffield, Laura M., Chen, Ming-Huei, Yanek, Lisa R., Wheeler, Marsha, Yao, Yao, Ren, Chunyan, Broome, Jai, Moon, Jee-Young, de Vries, Paul S., Hobbs, Brian D., Sun, Quan, Surendran, Praveen, Brody, Jennifer A., Blackwell, Thomas W., Choquet, Hélène, Ryan, Kathleen, Duggirala, Ravindranath, Heard-Costa, Nancy, Wang, Zhe, Chami, Nathalie, Preuss, Michael H., Min, Nancy, Ekunwe, Lynette, Lange, Leslie A., Cushman, Mary, Faraday, Nauder, Curran, Joanne E., Almasy, Laura, Kundu, Kousik, Smith, Albert V., Gabriel, Stacey, Rotter, Jerome I., Fornage, Myriam, Lloyd-Jones, Donald M., Vasan, Ramachandran S., Smith, Nicholas L., North, Kari E., Boerwinkle, Eric, Becker, Lewis C., Lewis, Joshua P., Abecasis, Goncalo R., Hou, Lifang, O’Connell, Jeffrey R., Morrison, Alanna C., Beaty, Terri H., Kaplan, Robert, Correa, Adolfo, Blangero, John, Jorgenson, Eric, Psaty, Bruce M., Kooperberg, Charles, Walton, Russell T., Kleinstiver, Benjamin P., Tang, Hua, Loos, Ruth J.F., Soranzo, Nicole, Butterworth, Adam S., Nickerson, Debbie, Rich, Stephen S., Mitchell, Braxton D., Johnson, Andrew D., Auer, Paul L., Li, Yun, Mathias, Rasika A., Lettre, Guillaume, Pankratz, Nathan, Laurie, Cathy C., Laurie, Cecelia A., Bauer, Daniel E., Conomos, Matthew P., Reiner, Alexander P.


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    Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program von 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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    Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension von Kelly, Tanika N., Sun, Xiao, He, Karen Y., Brown, Michael R., Taliun, Sarah A. Gagliano, Hellwege, Jacklyn N., Irvin, Marguerite R., Mi, Xuenan, Brody, Jennifer A., Franceschini, Nora, Guo, Xiuqing, Hwang, Shih-Jen, de Vries, Paul S., Gao, Yan, Moscati, Arden, Nadkarni, Girish N., Yanek, Lisa R., Elfassy, Tali, Smith, Jennifer A., Chung, Ren-Hua, Beitelshees, Amber L., Patki, Amit, Aslibekyan, Stella, Blobner, Brandon M., Peralta, Juan M., Assimes, Themistocles L., Palmas, Walter R., Liu, Chunyu, Bress, Adam P., Huang, Zhijie, Hwa, Chii-Min, O’Connell, Jeffrey R., Carlson, Jenna C., Warren, Helen R., Das, Sayantan, Giri, Ayush, Martin, Lisa W., Craig Johnson, W., Fox, Ervin R., Bottinger, Erwin P., Razavi, Alexander C., Vaidya, Dhananjay, Chuang, Lee-Ming, Chang, Yen-Pei C., Jain, Deepti, Kang, Hyun Min, Hung, Adriana M., Srinivasasainagendra, Vinodh, Snively, Beverly M., Gu, Dongfeng, Montasser, May E., Reupena, Muagututi‘a Sefuiva, Heavner, Benjamin D., LeFaive, Jonathon, Hixson, James E., Rice, Kenneth M., Wang, Fei Fei, Nielsen, Jonas B., Huang, Jianfeng, Khan, Alyna T., Zhou, Wei, Nierenberg, Jovia L., Laurie, Cathy C., Armstrong, Nicole D., Shi, Mengyao, Pan, Yang, Stilp, Adrienne M., Emery, Leslie, Wong, Quenna, Minster, Ryan L., Curran, Joanne E., Munroe, Patricia B., Weeks, Daniel E., North, Kari E., Tracy, Russell P., Kenny, Eimear E., Shimbo, Daichi, Chakravarti, Aravinda, Rich, Stephen S., Blangero, John, Redline, Susan, Mitchell, Braxton D., Ida Chen, Yii-Der, Kardia, Sharon L.R., Kaplan, Robert C., Mathias, Rasika A., He, Jiang, Psaty, Bruce M., Fornage, Myriam, Loos, Ruth J.F., Correa, Adolfo, Boerwinkle, Eric, Rotter, Jerome I., Kooperberg, Charles, Edwards, Todd L., Abecasis, Gonçalo R., Zhu, Xiaofeng, Levy, Daniel, Arnett, Donna K., Morrison, Alanna C.


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    Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing von Chen, Fang, Wang, Xingyan, Jang, Seon-Kyeong, Quach, Bryan C., Weissenkampen, J. Dylan, Khunsriraksakul, Chachrit, Yang, Lina, Sauteraud, Renan, Albert, Christine M., Allred, Nicholette D. D., Arnett, Donna K., Ashley-Koch, Allison E., Barnes, Kathleen C., Barr, R. Graham, Becker, Diane M., Bielak, Lawrence F., Bis, Joshua C., Blangero, John, Boorgula, Meher Preethi, Chasman, Daniel I., Chavan, Sameer, Chen, Yii-Der I., Chuang, Lee-Ming, Correa, Adolfo, Curran, Joanne E., David, Sean P., Fuentes, Lisa de las, Deka, Ranjan, Duggirala, Ravindranath, Faul, Jessica D., Garrett, Melanie E., Gharib, Sina A., Guo, Xiuqing, Hall, Michael E., Hawley, Nicola L., He, Jiang, Hobbs, Brian D., Hokanson, John E., Hsiung, Chao A., Hwang, Shih-Jen, Hyde, Thomas M., Irvin, Marguerite R., Jaffe, Andrew E., Johnson, Eric O., Kaplan, Robert, Kardia, Sharon L. R., Kaufman, Joel D., Kelly, Tanika N., Kleinman, Joel E., Kooperberg, Charles, Lee, I-Te, Levy, Daniel, Lutz, Sharon M., Manichaikul, Ani W., Martin, Lisa W., Marx, Olivia, McGarvey, Stephen T., Minster, Ryan L., Moll, Matthew, Moussa, Karine A., Naseri, Take, North, Kari E., Oelsner, Elizabeth C., Peralta, Juan M., Peyser, Patricia A., Psaty, Bruce M., Rafaels, Nicholas, Raffield, Laura M., Reupena, Muagututi’a Sefuiva, Rich, Stephen S., Rotter, Jerome I., Schwartz, David A., Shadyab, Aladdin H., Sheu, Wayne H-H., Sims, Mario, Smith, Jennifer A., Sun, Xiao, Taylor, Kent D., Telen, Marilyn J., Watson, Harold, Weeks, Daniel E., Weir, David R., Yanek, Lisa R., Young, Kendra A., Young, Kristin L., Zhao, Wei, Hancock, Dana B., Jiang, Bibo, Vrieze, Scott, Liu, Dajiang J.

    Veröffentlicht in Nature genetics

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    Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study von Wang, Yuxuan, Selvaraj, Margaret Sunitha, Li, Xihao, Li, Zilin, Holdcraft, Jacob A., Arnett, Donna K., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Cade, Brian E., Carlson, Jenna C., Carson, April P., Chen, Yii-Der Ida, Curran, Joanne E., de Vries, Paul S., Dutcher, Susan K., Ellinor, Patrick T., Floyd, James S., Fornage, Myriam, Freedman, Barry I., Gabriel, Stacey, Germer, Soren, Gibbs, Richard A., Guo, Xiuqing, He, Jiang, Heard-Costa, Nancy, Hildalgo, Bertha, Hou, Lifang, Irvin, Marguerite R., Joehanes, Roby, Kaplan, Robert C., Kardia, Sharon LR, Kelly, Tanika N., Kim, Ryan, Kooperberg, Charles, Kral, Brian G., Levy, Daniel, Li, Changwei, Liu, Chunyu, Lloyd-Jone, Don, Loos, Ruth JF, Mahaney, Michael C., Martin, Lisa W., Mathias, Rasika A., Minster, Ryan L., Mitchell, Braxton D., Montasser, May E., Morrison, Alanna C., Murabito, Joanne M., Naseri, Take, O'Connell, Jeffrey R., Palmer, Nicholette D., Preuss, Michael H., Psaty, Bruce M., Raffield, Laura M., Rao, Dabeeru C., Redline, Susan, Reiner, Alexander P., Rich, Stephen S., Ruepena, Muagututi’a Sefuiva, Sheu, Wayne H.-H., Smith, Jennifer A., Smith, Albert, Tiwari, Hemant K., Tsai, Michael Y., Viaud-Martinez, Karine A., Wang, Zhe, Yanek, Lisa R., Zhao, Wei, Rotter, Jerome I., Lin, Xihong, Natarajan, Pradeep, Peloso, Gina M.


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    Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed von Taub, Margaret A, Conomos, Matthew P, Keener, Rebecca, Iyer, Kruthika R, Weinstock, Joshua S, Yanek, Lisa R, Lane, John, Miller-Fleming, Tyne W, Brody, Jennifer A, Raffield, Laura M, McHugh, Caitlin P, Jain, Deepti, Gogarten, Stephanie M, Laurie, Cecelia A, Keramati, Ali, Arvanitis, Marios, Smith, Albert V, Heavner, Benjamin, Barwick, Lucas, Becker, Lewis C, Bis, Joshua C, Blangero, John, Bleecker, Eugene R, Burchard, Esteban G, Celedón, Juan C, Chang, Yen Pei C, Custer, Brian, Darbar, Dawood, de Las Fuentes, Lisa, DeMeo, Dawn L, Freedman, Barry I, Garrett, Melanie E, Gladwin, Mark T, Heckbert, Susan R, Hidalgo, Bertha A, Irvin, Marguerite R, Islam, Talat, Johnson, W Craig, Kaab, Stefan, Launer, Lenore, Lee, Jiwon, Liu, Simin, Moscati, Arden, North, Kari E, Peyser, Patricia A, Rafaels, Nicholas, Seidman, Christine, Weeks, Daniel E, Wen, Fayun, Wheeler, Marsha M, Williams, L Keoki, Yang, Ivana V, Zhao, Wei, Aslibekyan, Stella, Auer, Paul L, Bowden, Donald W, Cade, Brian E, Chen, Zhanghua, Cho, Michael H, Cupples, L Adrienne, Curran, Joanne E, Daya, Michelle, Deka, Ranjan, Eng, Celeste, Fingerlin, Tasha E, Guo, Xiuqing, Hou, Lifang, Hwang, Shih-Jen, Johnsen, Jill M, Kenny, Eimear E, Levin, Albert M, Liu, Chunyu, Minster, Ryan L, Naseri, Take, Nouraie, Mehdi, Reupena, Muagututi'a Sefuiva, Sabino, Ester C, Smith, Jennifer A, Smith, Nicholas L, Lasky-Su, Jessica, Taylor, 6th, James G, Telen, Marilyn J, Tiwari, Hemant K, Tracy, Russell P, White, Marquitta J, Zhang, Yingze, Wiggins, Kerri L, Weiss, Scott T, Vasan, Ramachandran S, Taylor, Kent D, Sinner, Moritz F, Silverman, Edwin K, Shoemaker, M Benjamin, Sheu, Wayne H-H, Sciurba, Frank, Schwartz, David A, Rotter, Jerome I, Roden, Daniel, Redline, Susan, Raby, Benjamin A

    Veröffentlicht in Cell genomics

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