Treffer 1 - 20 von 102 für Suche 'DONALD H. DE VRIES', Suchdauer: 1,14s Treffer weiter einschränken
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    Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixe... von Kowalski, Madeline H, Qian, Huijun, Hou, Ziyi, Rosen, Jonathan D, Tapia, Amanda L, Shan, Yue, Jain, Deepti, Argos, Maria, Arnett, Donna K, Avery, Christy, Barnes, Kathleen C, Becker, Lewis C, Bien, Stephanie A, Bis, Joshua C, Blangero, John, Boerwinkle, Eric, Bowden, Donald W, Buyske, Steve, Cai, Jianwen, Cho, Michael H, Choi, Seung Hoan, Choquet, Hélène, Cupples, L Adrienne, Cushman, Mary, Daya, Michelle, de Vries, Paul S, Ellinor, Patrick T, Faraday, Nauder, Fornage, Myriam, Gabriel, Stacey, Ganesh, Santhi K, Graff, Misa, Gupta, Namrata, He, Jiang, Heckbert, Susan R, Hidalgo, Bertha, Hodonsky, Chani J, Irvin, Marguerite R, Johnson, Andrew D, Jorgenson, Eric, Kaplan, Robert, Kardia, Sharon L R, Kelly, Tanika N, Kooperberg, Charles, Lasky-Su, Jessica A, Loos, Ruth J F, Lubitz, Steven A, Mathias, Rasika A, McHugh, Caitlin P, Montgomery, Courtney, Moon, Jee-Young, Morrison, Alanna C, Palmer, Nicholette D, Pankratz, Nathan, Papanicolaou, George J, Peralta, Juan M, Peyser, Patricia A, Rich, Stephen S, Rotter, Jerome I, Silverman, Edwin K, Smith, Jennifer A, Smith, Nicholas L, Taylor, Kent D, Thornton, Timothy A, Tiwari, Hemant K, Tracy, Russell P, Wang, Tao, Weiss, Scott T, Weng, Lu-Chen, Wiggins, Kerri L, Wilson, James G, Yanek, Lisa R, Zöllner, Sebastian, North, Kari E, Auer, Paul L, Raffield, Laura M, Reiner, Alexander P, Li, Yun

    Veröffentlicht in PLoS genetics

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    SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function von Li, Man, Li, Yong, Weeks, Olivia, Mijatovic, Vladan, Teumer, Alexander, Huffman, Jennifer E, Tromp, Gerard, Fuchsberger, Christian, Gorski, Mathias, Lyytikäinen, Leo-Pekka, Nutile, Teresa, Sedaghat, Sanaz, Sorice, Rossella, Tin, Adrienne, Yang, Qiong, Ahluwalia, Tarunveer S, Arking, Dan E, Bihlmeyer, Nathan A, Böger, Carsten A, Carroll, Robert J, Chasman, Daniel I, Cornelis, Marilyn C, Dehghan, Abbas, Faul, Jessica D, Feitosa, Mary F, Gambaro, Giovanni, Gasparini, Paolo, Giulianini, Franco, Heid, Iris, Huang, Jinyan, Imboden, Medea, Jackson, Anne U, Jeff, Janina, Jhun, Min A, Katz, Ronit, Kifley, Annette, Kilpeläinen, Tuomas O, Kumar, Ashish, Laakso, Markku, Li-Gao, Ruifang, Lohman, Kurt, Lu, Yingchang, Mägi, Reedik, Malerba, Giovanni, Mihailov, Evelin, Mohlke, Karen L, Mook-Kanamori, Dennis O, Robino, Antonietta, Ruderfer, Douglas, Salvi, Erika, Schick, Ursula M, Schulz, Christina-Alexandra, Smith, Albert V, Smith, Jennifer A, Traglia, Michela, Yerges-Armstrong, Laura M, Zhao, Wei, Goodarzi, Mark O, Kraja, Aldi T, Liu, Chunyu, Wessel, Jennifer, Boerwinkle, Eric, Borecki, Ingrid B, Bork-Jensen, Jette, Bottinger, Erwin P, Braga, Daniele, Brandslund, Ivan, Brody, Jennifer A, Campbell, Archie, Carey, David J, Christensen, Cramer, Coresh, Josef, Crook, Errol, Curhan, Gary C, Cusi, Daniele, de Boer, Ian H, de Vries, Aiko P J, Denny, Joshua C, Devuyst, Olivier, Dreisbach, Albert W, Endlich, Karlhans, Esko, Tõnu, Franco, Oscar H, Fulop, Tibor, Gerhard, Glenn S, Glümer, Charlotte, Gottesman, Omri, Grarup, Niels, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B, Hayward, Caroline, Hocking, Lynne, Hofman, Albert, Hu, Frank B, Husemoen, Lise Lotte N, Jackson, Rebecca D, Jørgensen, Torben, Jørgensen, Marit E, Kähönen, Mika


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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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    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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