Search Results - Chami, Myriam

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    Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis by Weinstock, Joshua S., Gopakumar, Jayakrishnan, Burugula, Bala Bharathi, Jahn, Nikolaus, Belk, Julia A., Bouzid, Hind, Daniel, Bence, Miao, Zhuang, Ly, Nghi, Mack, Taralynn M., Luna, Sofia E., Prothro, Katherine P., Mitchell, Shaneice R., Laurie, Cecelia A., Broome, Jai G., Taylor, Kent D., Guo, Xiuqing, Sinner, Moritz F., von Falkenhausen, Aenne S., Shuldiner, Alan R., O’Connell, Jeffrey R., Lewis, Joshua P., Boerwinkle, Eric, Chami, Nathalie, Kenny, Eimear E., Loos, Ruth J. F., Fornage, Myriam, Hou, Lifang, Lloyd-Jones, Donald M., Redline, Susan, Cade, Brian E., Psaty, Bruce M., Bis, Joshua C., Brody, Jennifer A., Yun, Jeong H., Qiao, Dandi, Palmer, Nicholette D., Freedman, Barry I., Bowden, Donald W., Cho, Michael H., Vasan, Ramachandran S., Yanek, Lisa R., Becker, Lewis C., Kardia, Sharon L. R., Peyser, Patricia A., He, Jiang, Rienstra, Michiel, Van der Harst, Pim, Kaplan, Robert, Heckbert, Susan R., Smith, Nicholas L., Wiggins, Kerri L., Arnett, Donna K., Irvin, Marguerite R., Tiwari, Hemant, Cutler, Michael J., Knight, Stacey, Muhlestein, J. Brent, Correa, Adolfo, Raffield, Laura M., Gao, Yan, de Andrade, Mariza, Rotter, Jerome I., Rich, Stephen S., Konkle, Barbara A., Johnsen, Jill M., Wheeler, Marsha M., Smith, J. Gustav, Melander, Olle, Nilsson, Peter M., Custer, Brian S., Duggirala, Ravindranath, Curran, Joanne E., Blangero, John, Xiao, Shujie, Yang, Mao, Gu, C. Charles, Chen, Yii-Der Ida, Lee, Wen-Jane, Marcus, Gregory M., Kane, John P., Pullinger, Clive R., Shoemaker, M. Benjamin, Darbar, Dawood, Roden, Dan M., Kooperberg, Charles, Zhou, Ying, Manson, JoAnn E., Desai, Pinkal, Johnson, Andrew D., Mathias, Rasika A., Abecasis, Goncalo R., Kang, Hyun M., Satpathy, Ansuman T., Natarajan, Pradeep, Kitzman, Jacob O., Whitsel, Eric A., Reiner, Alexander P., Bick, Alexander G., Jaiswal, Siddhartha

    Published in Nature (London)
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    Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program by 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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    Aberrant activation of TCL1A promotes stem cell expansion in clonal hematopoiesis by Weinstock, Joshua S., Gopakumar, Jayakrishnan, Burugula, Bala Bharathi, Uddin, Md Mesbah, Jahn, Nikolaus, Belk, Julia A., Bouzid, Hind, Daniel, Bence, Miao, Zhuang, Ly, Nghi, Mack, Taralyn M., Luna, Sofia E., Prothro, Katherine P., Mitchell, Shaneice R., Laurie, Cecelia A., Broome, Jai G., Taylor, Kent D., Guo, Xiuqing, Sinner, Moritz F., von Falkenhausen, Aenne S., Kääb, Stefan, Shuldiner, Alan R., O'Connell, Jeffrey R., Lewis, Joshua P., Boerwinkle, Eric, Barnes, Kathleen C., Chami, Nathalie, Kenny, Eimear E., Loos, Ruth J., Fornage, Myriam, Hou, Lifang, Lloyd-Jones, Donald M., Redline, Susan, Cade, Brian E., Psaty, Bruce M., Bis, Joshua C., Brody, Jennifer A., Silverman, Edwin K., Yun, Jeong H., Qiao, Dandi, Palmer, Nicholette D., Freedman, Barry I., Bowden, Donald W., Cho, Michael H., DeMeo, Dawn L., Vasan, Ramachandran S., Yanek, Lisa R., Becker, Lewis C., Kardia, Sharon, Peyser, Patricia A., He, Jiang, Rienstra, Michiel, Van der Harst, Pim, Kaplan, Robert, Heckbert, Susan R., Smith, Nicholas L., Wiggins, Kerri L., Arnett, Donna K., Irvin, Marguerite R., Tiwari, Hemant, Cutler, Michael J., Knight, Stacey, Muhlestein, J Brent, Correa, Adolfo, Raffield, Laura M., Gao, Yan, de Andrade, Mariza, Rotter, Jerome I., Rich, Stephen S., Tracy, Russell P., Konkle, Barbara A., Johnsen, Jill M., Wheeler, Marsha M., Smith, J. Gustav, Melander, Olle, Nilsson, Peter M., Custer, Brian S., Duggirala, Ravindranath, Curran, Joanne E., Blangero, John, McGarvey, Stephen, Williams, L. Keoki, Xiao, Shujie, Yang, Mao, Gu, C. Charles, Chen, Yii-Der Ida, Lee, Wen-Jane, Marcus, Gregory M., Kane, John P., Pullinger, Clive R., Shoemaker, M. Benjamin, Darbar, Dawood, Roden, Dan, Albert, Christine, Kooperberg, Charles, Zhou, Ying, Manson, JoAnn E., Desai, Pinkal, Johnson, Andrew D., Mathias, Rasika A.

    Published in Nature (London)
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    Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits by Chami, Nathalie, Chen, Ming-Huei, Slater, Andrew J., Eicher, John D., Evangelou, Evangelos, Tajuddin, Salman M., Love-Gregory, Latisha, Schick, Ursula M., Nomura, Akihiro, Giri, Ayush, Lessard, Samuel, Brody, Jennifer A., Schurmann, Claudia, Pankratz, Nathan, Yanek, Lisa R., Manichaikul, Ani, Mihailov, Evelin, Hill, W. David, Raffield, Laura M., Burt, Amber, Bartz, Traci M., Becker, Diane M., Becker, Lewis C., Boerwinkle, Eric, Bork-Jensen, Jette, Bottinger, Erwin P., O’Donoghue, Michelle L., Crosslin, David R., de Denus, Simon, Dubé, Marie-Pierre, Engström, Gunnar, Evans, Michele K., Floyd, James S., Gao, He, Greinacher, Andreas, Gudnason, Vilmundur, Hansen, Torben, Hayward, Caroline, Hernesniemi, Jussi, Highland, Heather M., Hirschhorn, Joel N., Hofman, Albert, Irvin, Marguerite R., Kähönen, Mika, Lange, Ethan, Launer, Lenore J., Lehtimäki, Terho, Li, Jin, Liewald, David C.M., Liu, Yongmei, Lu, Yingchang, Lyytikäinen, Leo-Pekka, Mägi, Reedik, Mathias, Rasika A., Melander, Olle, Mononen, Nina, Nalls, Mike A., Nickerson, Deborah A., Nikus, Kjell, O’Donnell, Chris J., Orho-Melander, Marju, Polfus, Linda, Psaty, Bruce M., Raitoharju, Emma, Richard, Melissa, Rice, Kenneth M., Rivadeneira, Fernando, Rotter, Jerome I., Schmidt, Frank, Smith, Albert Vernon, Starr, John M., Taylor, Kent D., Teumer, Alexander, Thuesen, Betina H., Torstenson, Eric S., Tzoulaki, Ioanna, Zakai, Neil A., Vacchi-Suzzi, Caterina, van Duijn, Cornelia M., van Rooij, Frank J.A., Cushman, Mary, Deary, Ian J., Velez Edwards, Digna R., Vergnaud, Anne-Claire, Wallentin, Lars, Waterworth, Dawn M., White, Harvey D., Wilson, James G., Zonderman, Alan B., Kathiresan, Sekar, Grarup, Niels, Esko, Tõnu, Loos, Ruth J.F., Lange, Leslie A., Faraday, Nauder, Abumrad, Nada A., Edwards, Todd L., Ganesh, Santhi K., Johnson, Andrew D., Reiner, Alexander P.

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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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    Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin by Liu, Ching-Ti, Raghavan, Sridharan, Maruthur, Nisa, Kabagambe, Edmond Kato, Hong, Jaeyoung, Hivert, Marie-France, Lu, Yingchang, Bentley, Amy R., Drolet, Anne M., Gaulton, Kyle J., Guo, Xiuqing, Armstrong, Loren L., Irvin, Marguerite R., Li, Man, Rybin, Denis V., Agyemang, Charles, Palmer, Nicholette D., Cade, Brian E., Chen, Wei-Min, Dauriz, Marco, Delaney, Joseph A.C., Edwards, Todd L., Lange, Leslie A., Leong, Aaron, Liu, Jingmin, Liu, Yongmei, Nayak, Uma, Patel, Sanjay R., Rasmussen-Torvik, Laura J., Snijder, Marieke B., Stallings, Sarah C., Tanaka, Toshiko, Yanek, Lisa R., Becker, Diane M., Bielak, Lawrence F., Biggs, Mary L., Chen, Guanjie, Correa, Adolfo, Couper, David J., Crawford, Dana C., Cushman, Mary, Eicher, John D., Fornage, Myriam, Franceschini, Nora, Fu, Yi-Ping, Goodarzi, Mark O., Gottesman, Omri, Harris, Tamara B., Jensen, Richard A., Jhun, Min A., Karter, Andrew J., Keller, Margaux F., Kho, Abel N., Kizer, Jorge R., Krauss, Ronald M., Langefeld, Carl D., Li, Xiaohui, Liang, Jingling, Liu, Simin, Lowe, William L., Mosley, Thomas H., North, Kari E., Pacheco, Jennifer A., Peyser, Patricia A., Patrick, Alan L., Rice, Kenneth M., Selvin, Elizabeth, Sims, Mario, Tajuddin, Salman M., Vaidya, Dhananjay, Wren, Mary P., Yao, Jie, Ziegler, Julie T., Zmuda, Joseph M., Zonderman, Alan B., Zwinderman, Aeilko H., Adeyemo, Adebowale, Boerwinkle, Eric, Ferrucci, Luigi, Hayes, M. Geoffrey, Kardia, Sharon L.R., Miljkovic, Iva, Pankow, James S., Rotimi, Charles N., Sale, Michele M., Wagenknecht, Lynne E., Arnett, Donna K., Chen, Yii-Der Ida, Province, Michael A., Kao, W.H. Linda, Siscovick, David S., Psaty, Bruce M., Wilson, James G., Loos, Ruth J.F., Dupuis, Josée, Rich, Stephen S., Florez, Jose C., Rotter, Jerome I., Morris, Andrew P., Meigs, James B.

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    Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program by 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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    The genetic determinants of recurrent somatic mutations in 43,693 blood genomes by Weinstock, Joshua S, Laurie, Cecelia A, Broome, Jai G, Taylor, Kent D, Guo, Xiuqing, Shuldiner, Alan R, O'Connell, Jeffrey R, Lewis, Joshua P, Boerwinkle, Eric, Barnes, Kathleen C, Chami, Nathalie, Kenny, Eimear E, Loos, Ruth J F, Fornage, Myriam, Redline, Susan, Cade, Brian E, Gilliland, Frank D, Chen, Zhanghua, Gauderman, W James, Kumar, Rajesh, Grammer, Leslie, Schleimer, Robert P, Psaty, Bruce M, Bis, Joshua C, Brody, Jennifer A, Silverman, Edwin K, Yun, Jeong H, Qiao, Dandi, Weiss, Scott T, Lasky-Su, Jessica, DeMeo, Dawn L, Palmer, Nicholette D, Freedman, Barry I, Bowden, Donald W, Cho, Michael H, Vasan, Ramachandran S, Johnson, Andrew D, Yanek, Lisa R, Becker, Lewis C, Kardia, Sharon, He, Jiang, Kaplan, Robert, Heckbert, Susan R, Smith, Nicholas L, Wiggins, Kerri L, Arnett, Donna K, Irvin, Marguerite R, Tiwari, Hemant, Correa, Adolfo, Raffield, Laura M, Gao, Yan, de Andrade, Mariza, Rotter, Jerome I, Rich, Stephen S, Manichaikul, Ani W, Konkle, Barbara A, Johnsen, Jill M, Wheeler, Marsha M, Custer, Brian S, Duggirala, Ravindranath, Curran, Joanne E, Blangero, John, Gui, Hongsheng, Xiao, Shujie, Williams, L Keoki, Meyers, Deborah A, Li, Xingnan, Ortega, Victor, McGarvey, Stephen, Gu, C Charles, Chen, Yii-Der Ida, Lee, Wen-Jane, Shoemaker, M Benjamin, Darbar, Dawood, Roden, Dan, Albert, Christine, Kooperberg, Charles, Desai, Pinkal, Blackwell, Thomas W, Abecasis, Goncalo R, Smith, Albert V, Kang, Hyun M, Mathias, Rasika, Natarajan, Pradeep, Jaiswal, Siddhartha, Reiner, Alexander P, Bick, Alexander G

    Published in Science advances
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