Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Lewis, Joshua P."'
Autor:
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 JF, 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, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Publikováno v:
Science advances, vol 9, iss 17
Nononcogenic somatic mutations are thought to be uncommon and inconsequential. To test this, we analyzed 43,693 National Heart, Lung and Blood Institute Trans-Omics for Precision Medicine blood whole genomes from 37 cohorts and identified 7131 non-mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::9065bc0faf2d3ecc58a098ed4c436645
https://escholarship.org/uc/item/1496g128
https://escholarship.org/uc/item/1496g128
Autor:
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 JF, 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, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Reiner, Alexander P, Auer, Paul L
Publikováno v:
American journal of human genetics, vol 108, iss 10
Many common and rare variants associated with hematologic traits have been discovered through imputation on large-scale reference panels. However, the majority of genome-wide association studies (GWASs) have been conducted in Europeans, and determini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::1f3a94426432e7d8d437082d4c6c39d7
https://escholarship.org/uc/item/6432c6xx
https://escholarship.org/uc/item/6432c6xx
Autor:
Keramati, Ali R, Chen, Ming-Huei, Rodriguez, Benjamin AT, Yanek, Lisa R, Bhan, Arunoday, Gaynor, Brady J, Ryan, Kathleen, Brody, Jennifer A, Zhong, Xue, Wei, Qiang, NHLBI Trans-Omics for Precision (TOPMed) Consortium, Kammers, Kai, Kanchan, Kanika, Iyer, Kruthika, Kowalski, Madeline H, Pitsillides, Achilleas N, Cupples, L Adrienne, Li, Bingshan, Schlaeger, Thorsten M, Shuldiner, Alan R, O'Connell, Jeffrey R, Ruczinski, Ingo, Mitchell, Braxton D, Faraday, Nauder, Taub, Margaret A, Becker, Lewis C, Lewis, Joshua P, Mathias, Rasika A, Johnson, Andrew D
Publikováno v:
Nature communications, vol 12, iss 1
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-13 (2021)
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-13 (2021)
Platelet aggregation at the site of atherosclerotic vascular injury is the underlying pathophysiology of myocardial infarction and stroke. To build upon prior GWAS, here we report on 16 loci identified through a whole genome sequencing (WGS) approach
Autor:
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 JF, 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, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Publikováno v:
American journal of human genetics, vol 108, iss 5
Whole-genome sequencing (WGS), a powerful tool for detecting novel coding and non-coding disease-causing variants, has largely been applied to clinical diagnosis of inherited disorders. Here we leveraged WGS data in up to 62,653 ethnically diverse pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::445eb02b1c412ec0c77798d591b7420a
https://escholarship.org/uc/item/24j6v92r
https://escholarship.org/uc/item/24j6v92r
Autor:
Chen, Han, Huffman, Jennifer E, Brody, Jennifer A, Wang, Chaolong, Lee, Seunggeun, Li, Zilin, Gogarten, Stephanie M, Sofer, Tamar, Bielak, Lawrence F, Bis, Joshua C, Blangero, John, Bowler, Russell P, Cade, Brian E, Cho, Michael H, Correa, Adolfo, Curran, Joanne E, de Vries, Paul S, Glahn, David C, Guo, Xiuqing, Johnson, Andrew D, Kardia, Sharon, Kooperberg, Charles, Lewis, Joshua P, Liu, Xiaoming, Mathias, Rasika A, Mitchell, Braxton D, O'Connell, Jeffrey R, Peyser, Patricia A, Post, Wendy S, Reiner, Alex P, Rich, Stephen S, Rotter, Jerome I, Silverman, Edwin K, Smith, Jennifer A, Vasan, Ramachandran S, Wilson, James G, Yanek, Lisa R, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Hematology and Hemostasis Working Group, Redline, Susan, Smith, Nicholas L, Boerwinkle, Eric, Borecki, Ingrid B, Cupples, L Adrienne, Laurie, Cathy C, Morrison, Alanna C, Rice, Kenneth M, Lin, Xihong
Publikováno v:
American journal of human genetics, vol 104, iss 2
With advances in whole-genome sequencing (WGS) technology, more advanced statistical methods for testing genetic association with rare variants are being developed. Methods in which variants are grouped for analysis are also known as variant-set, gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::e04981594ad18439135805d7f8a27f68
https://escholarship.org/uc/item/1918z4zr
https://escholarship.org/uc/item/1918z4zr
Publikováno v:
BMC Genomics, Vol 13, Iss 1, p 246 (2012)
Abstract Background Gene duplication has had a major impact on genome evolution. Localized (or tandem) duplication resulting from unequal crossing over and whole genome duplication are believed to be the two dominant mechanisms contributing to verteb
Externí odkaz:
https://doaj.org/article/df794d2c622c48a1821469910ec9b3ba
Autor:
Wang Jenny Z, Deogan Mandeep S, Lewis Joshua R, Chew Shelby, Mullin Ben H, McNab Tegan J, Wilson Scott G, Ingley Evan, Prince Richard L
Publikováno v:
BMC Medical Genetics, Vol 12, Iss 1, p 165 (2011)
Abstract Background The biosynthesis of estrogens from androgens is catalyzed by aromatase P450 enzyme, coded by the CYP19A1 gene on chromosome 15q21.2. Genetic variation within the CYP19A1 gene sequence has been shown to alter the function of the en
Externí odkaz:
https://doaj.org/article/24b0b9ed00c94f6cbc23cb759fb321d7
Autor:
Walford, Geoffrey A, Gustafsson, Stefan, Rybin, Denis, Stančáková, Alena, Chen, Han, Liu, Ching-Ti, Hong, Jaeyoung, Jensen, Richard A, Rice, Ken, Morris, Andrew P, Mägi, Reedik, Tönjes, Anke, Prokopenko, Inga, Kleber, Marcus E, Delgado, Graciela, Silbernagel, Günther, Jackson, Anne U, Appel, Emil V, Grarup, Niels, Lewis, Joshua P, Montasser, May E, Landenvall, Claes, Staiger, Harald, Luan, Jian'an, Frayling, Timothy M, Weedon, Michael N, Xie, Weijia, Morcillo, Sonsoles, Martínez-Larrad, María Teresa, Biggs, Mary L, Chen, Yii-Der Ida, Corbaton-Anchuelo, Arturo, Færch, Kristine, Gómez-Zumaquero, Juan Miguel, Goodarzi, Mark O, Kizer, Jorge R, Koistinen, Heikki A, Leong, Aaron, Lind, Lars, Lindgren, Cecilia, Machicao, Fausto, Manning, Alisa K, Martín-Núñez, Gracia María, Rojo-Martínez, Gemma, Rotter, Jerome I, Siscovick, David S, Zmuda, Joseph M, Zhang, Zhongyang, Serrano-Rios, Manuel, Smith, Ulf, Soriguer, Federico, Hansen, Torben, Jørgensen, Torben J, Linnenberg, Allan, Pedersen, Oluf, Walker, Mark, Langenberg, Claudia, Scott, Robert A, Wareham, Nicholas J, Fritsche, Andreas, Häring, Hans-Ulrich, Stefan, Norbert, Groop, Leif, O'Connell, Jeff R, Boehnke, Michael, Bergman, Richard N, Collins, Francis S, Mohlke, Karen L, Tuomilehto, Jaakko, März, Winfried, Kovacs, Peter, Stumvoll, Michael, Psaty, Bruce M, Kuusisto, Johanna, Laakso, Markku, Meigs, James B, Dupuis, Josée, Ingelsson, Erik, Florez, Jose C
Publikováno v:
Diabetes, vol 65, iss 10
Genome-wide association studies (GWAS) have found few common variants that influence fasting measures of insulin sensitivity. We hypothesized that a GWAS of an integrated assessment of fasting and dynamic measures of insulin sensitivity would detect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::a50262ea3920341ede502a7f2e98d6a4
https://escholarship.org/uc/item/8x18q019
https://escholarship.org/uc/item/8x18q019
Akademický článek
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Autor:
Palmer, Nicholette D, McDonough, Caitrin W, Hicks, Pamela J, Roh, Bong H, Wing, Maria R, An, S Sandy, Hester, Jessica M, Cooke, Jessica N, Bostrom, Meredith A, Rudock, Megan E, Talbert, Matthew E, Lewis, Joshua P, DIAGRAM Consortium, MAGIC Investigators, Ferrara, Assiamira, Lu, Lingyi, Ziegler, Julie T, Sale, Michele M, Divers, Jasmin, Shriner, Daniel, Adeyemo, Adebowale, Rotimi, Charles N, Ng, Maggie CY, Langefeld, Carl D, Freedman, Barry I, Bowden, Donald W, Voight, Benjamin F, Scott, Laura J, Steinthorsdottir, Valgerdur, Morris, Andrew P, Dina, Christian, Welch, Ryan P, Zeggini, Eleftheria, Huth, Cornelia, Aulchenko, Yurii S, Thorleifsson, Gudmar, McCulloch, Laura J, Ferreira, Teresa, Grallert, Harald, Amin, Najaf, Wu, Guanming, Willer, Cristen J, Raychaudhuri, Soumya, McCarroll, Steve A, Langenberg, Claudia, Hofmann, Oliver M, Dupuis, Josée, Qi, Lu, Segrè, Ayellet V, Van Hoek, Mandy, Navarro, Pau, Ardlie, Kristin, Balkau, Beverley, Benediktsson, Rafn, Bennett, Amanda J, Blagieva, Roza, Boerwinkle, Eric, Bonnycastle, Lori L, Boström, Kristina Bengtsson, Bravenboer, Bert, Bumpstead, Suzannah, Burtt, Noël P, Charpentier, Guillaume, Chines, Peter S, Cornelis, Marilyn, Couper, David J, Crawford, Gabe, Doney, Alex SF, Elliott, Katherine S, Elliott, Amanda L, Erdos, Michael R, Fox, Caroline S, Franklin, Christopher S, Ganser, Martha, Gieger, Christian, Grarup, Niels, Green, Todd, Griffin, Simon, Groves, Christopher J, Guiducci, Candace, Hadjadj, Samy, Hassanali, Neelam, Herder, Christian, Isomaa, Bo, Jackson, Anne U, Johnson, Paul RV, Jørgensen, Torben, Kao, Wen HL, Klopp, Norman, Kong, Augustine, Kraft, Peter, Kuusisto, Johanna, Lauritzen, Torsten, Li, Man, Lieverse, Aloysius, Lindgren, Cecilia M, Lyssenko, Valeriya, Marre, Michel, Meitinger, Thomas, Midthjell, Kristian, Morken, Mario A, Narisu, Narisu, Nilsson, Peter, Owen, Katharine R, Payne, Felicity, Perry, John RB, Petersen, Ann-Kristin, Platou, Carl, Proença, Christine, Prokopenko, Inga, Rathmann, Wolfgang, Rayner, N William, Robertson, Neil R, Rocheleau, Ghislain, Roden, Michael, Sampson, Michael J, Saxena, Richa, Shields, Beverley M, Shrader, Peter, Sigurdsson, Gunnar, Sparsø, Thomas, Strassburger, Klaus, Stringham, Heather M, Sun, Qi, Swift, Amy J, Thorand, Barbara, Tichet, Jean, Tuomi, Tiinamaija, Van Dam, Rob M, Van Haeften, Timon W, Van Herpt, Thijs, Van Vliet-Ostaptchouk, Jana V, Walters, G Bragi, Weedon, Michael N, Wijmenga, Cisca, Witteman, Jacqueline, Bergman, Richard N, Cauchi, Stephane, Collins, Francis S, Gloyn, Anna L, Gyllensten, Ulf, Hansen, Torben, Hide, Winston A, Hitman, Graham A, Hofman, Albert, Hunter, David J, Hveem, Kristian, Laakso, Markku, Mohlke, Karen L, Morris, Andrew D, Palmer, Colin NA, Pramstaller, Peter P, Rudan, Igor, Sijbrands, Eric, Stein, Lincoln D, Tuomilehto, Jaakko, Uitterlinden, Andre, Walker, Mark, Wareham, Nicholas J, Watanabe, Richard M, Abecasis, Goncalo R, Boehm, Bernhard O, Campbell, Harry, Daly, Mark J, Hattersley, Andrew T, Hu, Frank B, Meigs, James B, Pankow, James S, Pedersen, Oluf, Wichmann, H-Erich, Barroso, Inês, Florez, Jose C, Frayling, Timothy M, Groop, Leif, Sladek, Rob, Thorsteinsdottir, Unnur, Wilson, James F, Illig, Thomas, Froguel, Philippe, Van Duijn, Cornelia M, Stefansson, Kari, Altshuler, David, Boehnke, Michael, McCarthy, Mark I, Soranzo, Nicole, Wheeler, Eleanor, Glazer, Nicole L, Bouatia-Naji, Nabila, Mägi, Reedik, Randall, Joshua, Johnson, Toby, Elliott, Paul, Rybin, Denis, Henneman, Peter, Dehghan, Abbas, Hottenga, Jouke Jan, Song, Kijoung, Goel, Anuj, Egan, Josephine M, Lajunen, Taina, Doney, Alex, Kanoni, Stavroula, Cavalcanti-Proença, Christine, Kumari, Meena, Timpson, Nicholas J, Zabena, Carina, Ingelsson, Erik, An, Ping, O'Connell, Jeffrey, Luan, Jian'an, Elliott, Amanda, McCarroll, Steven A, Roccasecca, Rosa Maria, Pattou, François, Sethupathy, Praveen, Ariyurek, Yavuz, Barter, Philip, Beilby, John P, Ben-Shlomo, Yoav, Bergmann, Sven, Bochud, Murielle, Bonnefond, Amélie, Borch-Johnsen, Knut, Böttcher, Yvonne, Brunner, Eric, Bumpstead, Suzannah J, Chen, Yii-Der Ida, Chines, Peter, Clarke, Robert, Coin, Lachlan JM, Cooper, Matthew N, Crisponi, Laura, Day, Ian NM, De Geus, Eco JC, Delplanque, Jerome, Fedson, Annette C, Fischer-Rosinsky, Antje, Forouhi, Nita G, Frants, Rune, Franzosi, Maria Grazia, Galan, Pilar, Goodarzi, Mark O, Graessler, Jürgen, Grundy, Scott, Gwilliam, Rhian, Hallmans, Göran, Hammond, Naomi, Han, Xijing, Hartikainen, Anna-Liisa, Hayward, Caroline, Heath, Simon C, Hercberg, Serge, Hicks, Andrew A, Hillman, David R, Hingorani, Aroon D, Hui, Jennie, Hung, Joe, Jula, Antti, Kaakinen, Marika, Kaprio, Jaakko, Kesaniemi, Y Antero, Kivimaki, Mika, Knight, Beatrice, Koskinen, Seppo, Kovacs, Peter, Kyvik, Kirsten Ohm, Lathrop, G Mark, Lawlor, Debbie A, Le Bacquer, Olivier, Lecoeur, Cécile, Li, Yun, Mahley, Robert, Mangino, Massimo, Manning, Alisa K, Martínez-Larrad, María Teresa, McAteer, Jarred B, McPherson, Ruth, Meisinger, Christa, Melzer, David, Meyre, David, Mitchell, Braxton D, Mukherjee, Sutapa, Naitza, Silvia, Neville, Matthew J, Oostra, Ben A, Orrù, Marco, Pakyz, Ruth, Paolisso, Giuseppe, Pattaro, Cristian, Pearson, Daniel, Peden, John F, Pedersen, Nancy L, Perola, Markus, Pfeiffer, Andreas FH, Pichler, Irene, Polasek, Ozren, Posthuma, Danielle, Potter, Simon C, Pouta, Anneli, Province, Michael A, Psaty, Bruce M, Rayner, Nigel W, Rice, Kenneth, Ripatti, Samuli, Rivadeneira, Fernando, Rolandsson, Olov, Sandbaek, Annelli, Sandhu, Manjinder, Sanna, Serena, Sayer, Avan Aihie, Scheet, Paul, Seedorf, Udo, Sharp, Stephen J, Shields, Beverley, Sijbrands, Eric JG, Silveira, Angela, Simpson, Laila, Singleton, Andrew, Smith, Nicholas L, Sovio, Ulla, Swift, Amy, Syddall, Holly, Syvänen, Ann-Christine, Tanaka, Toshiko, Tönjes, Anke, Uitterlinden, André G, Van Dijk, Ko Willems, Varma, Dhiraj, Visvikis-Siest, Sophie, Vitart, Veronique, Vogelzangs, Nicole, Waeber, Gérard, Wagner, Peter J, Walley, Andrew, Ward, Kim L, Watkins, Hugh, Wild, Sarah H, Willemsen, Gonneke, Witteman, Jaqueline CM, Yarnell, John WG, Zelenika, Diana, Zethelius, Björn, Zhai, Guangju, Zhao, Jing Hua, Zillikens, M Carola, Borecki, Ingrid B, Loos, Ruth JF, Meneton, Pierre, Magnusson, Patrik KE, Nathan, David M, Williams, Gordon H, Silander, Kaisa, Salomaa, Veikko, Smith, George Davey, Bornstein, Stefan R, Schwarz, Peter, Spranger, Joachim, Karpe, Fredrik, Shuldiner, Alan R, Cooper, Cyrus, Dedoussis, George V, Serrano-Ríos, Manuel, Lind, Lars, Palmer, Lyle J, Franks, Paul W, Ebrahim, Shah, Marmot, Michael, Kao, WH Linda, Pramstaller, Peter Paul, Wright, Alan F, Stumvoll, Michael, Hamsten, Anders, Buchanan, Thomas A, Valle, Timo T, Rotter, Jerome I, Siscovick, David S, Penninx, Brenda WJH, Boomsma, Dorret I, Deloukas, Panos, Spector, Timothy D, Ferrucci, Luigi, Cao, Antonio, Scuteri, Angelo, Schlessinger, David, Uda, Manuela, Ruokonen, Aimo, Jarvelin, Marjo-Riitta, Waterworth, Dawn M, Vollenweider, Peter, Peltonen, Leena, Mooser, Vincent, Sladek, Robert
Publikováno v:
PLoS ONE, 7(1):e29202. PUBLIC LIBRARY SCIENCE
Palmer, N D, McDonough, C W, Hicks, P J, Roh, B H, Wing, M R, Sandy An, S, Hester, J M, Cooke, J N, Bostrom, M A, Rudock, M E, Talbert, M E, Lewis, J P, Hottenga, J J, de Geus, E J C, Willemsen, G, Boomsma, D I, Ferrara, A, Lu, L, Ziegler, J T, Sale, M M, Divers, J, Shriner, D, Adeyemo, A, Rotimi, C N, Ng, M C Y, Langefeld, C D, Freedman, B I, Bowden, D W, Posthuma, D, Penninx, B W J H & Sladek, R 2012, ' A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans ', PLoS ONE, vol. 7, no. 1, e29202, pp. e29202 . https://doi.org/10.1371/journal.pone.0029202
PLoS ONE, Vol 7, Iss 1, p e29202 (2012)
PLoS ONE, 7(1)
PLoS ONE
PLoS ONE, 7(1):e29202. Public Library of Science
PLoS ONE 7:e29202 (2012)
DIAGRAM Consortium & MAGIC Investigators 2012, ' A genome-wide association search for type 2 diabetes genes in African Americans ', P L o S One, vol. 7, no. 1, pp. e29202 . https://doi.org/10.1371/journal.pone.0029202
Palmer, N D, McDonough, C W, Hicks, P J, Roh, B H, Wing, M R, An, S S, Hester, J M, Cooke, J N, Bostrom, M A, Rudock, M E, Talbert, M E, Lewis, J P, Ferrara, A, Lu, L, Ziegler, J T, Sale, M M, Divers, J, Shriner, D, Adeyemo, A, Rotimi, C N, Ng, M C Y, Langefeld, C D, Freedman, B I, Bowden, D W, Voight, B F, Scott, L J, Steinthorsdottir, V, Morris, A P, Dina, C, Welch, R P, Zeggini, E, Huth, C, Aulchenko, Y S, Thorleifsson, G, McCulloch, L J, Ferreira, T, Grallert, H, Amin, N, Wu, G, Willer, C J, Raychaudhuri, S, McCarroll, S A, Navarro, P, Rudan, I, Campbell, H, Wilson, J F, Hayward, C, Vitart, V & Wild, S H & Wright, A F 2012, ' A genome-wide association search for type 2 diabetes genes in African Americans ', PLoS ONE, vol. 7, no. 1, e29202, pp. 1-14 . https://doi.org/10.1371/journal.pone.0029202
Palmer, N D, McDonough, C W, Hicks, P J, Roh, B H, Wing, M R, An, S S, Hester, J M, Cooke, J N, Bostrom, M A, Rudock, M E, Talbert, M E, Lewis, J P, Ferrara, A, Lu, L, Ziegler, J T, Sale, M M, Divers, J, Shriner, D, Adeyemo, A, Rotimi, C N, Ng, M C Y, Langefeld, C D, Freedman, B I, Bowden, D W, Voight, B F, Scott, L J, Steinthorsdottir, V, Morris, A P, Dina, C, Welch, R P, Zeggini, E, Huth, C, Aulchenko, Y S, Thorleifsson, G, McCulloch, L J, Ferreira, T, Grallert, H, Amin, N, Wu, G, Willer, C J, Raychaudhuri, S, McCarroll, S A, Langenberg, C, Hofmann, O M, Dupuis, J, Qi, L, Segrè, A V, van Hoek, M, Borch-Johnsen, K, Kyvik, K O & DIAGRAM Consortium 2012, ' A genome-wide association search for type 2 diabetes genes in African Americans ', P L o S One, vol. 7, no. 1, pp. e29202 . https://doi.org/10.1371/journal.pone.0029202
PLOS ONE
Plos One, vol. 7, no. 1, pp. e29202
PLoS ONE; Vol 7
Yarnell, J & Palmer, N D 2012, ' A Genome-wide association search for Type 2 Diabetes genes in African Americans ', PLoS ONE, vol. 7, no. 1, e29202 . https://doi.org/10.1371/journal.pone.0029202
Palmer, N D, McDonough, C W, Hicks, P J, Roh, B H, Wing, M R, Sandy An, S, Hester, J M, Cooke, J N, Bostrom, M A, Rudock, M E, Talbert, M E, Lewis, J P, Hottenga, J J, de Geus, E J C, Willemsen, G, Boomsma, D I, Ferrara, A, Lu, L, Ziegler, J T, Sale, M M, Divers, J, Shriner, D, Adeyemo, A, Rotimi, C N, Ng, M C Y, Langefeld, C D, Freedman, B I, Bowden, D W, Posthuma, D, Penninx, B W J H & Sladek, R 2012, ' A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans ', PLoS ONE, vol. 7, no. 1, e29202, pp. e29202 . https://doi.org/10.1371/journal.pone.0029202
PLoS ONE, Vol 7, Iss 1, p e29202 (2012)
PLoS ONE, 7(1)
PLoS ONE
PLoS ONE, 7(1):e29202. Public Library of Science
PLoS ONE 7:e29202 (2012)
DIAGRAM Consortium & MAGIC Investigators 2012, ' A genome-wide association search for type 2 diabetes genes in African Americans ', P L o S One, vol. 7, no. 1, pp. e29202 . https://doi.org/10.1371/journal.pone.0029202
Palmer, N D, McDonough, C W, Hicks, P J, Roh, B H, Wing, M R, An, S S, Hester, J M, Cooke, J N, Bostrom, M A, Rudock, M E, Talbert, M E, Lewis, J P, Ferrara, A, Lu, L, Ziegler, J T, Sale, M M, Divers, J, Shriner, D, Adeyemo, A, Rotimi, C N, Ng, M C Y, Langefeld, C D, Freedman, B I, Bowden, D W, Voight, B F, Scott, L J, Steinthorsdottir, V, Morris, A P, Dina, C, Welch, R P, Zeggini, E, Huth, C, Aulchenko, Y S, Thorleifsson, G, McCulloch, L J, Ferreira, T, Grallert, H, Amin, N, Wu, G, Willer, C J, Raychaudhuri, S, McCarroll, S A, Navarro, P, Rudan, I, Campbell, H, Wilson, J F, Hayward, C, Vitart, V & Wild, S H & Wright, A F 2012, ' A genome-wide association search for type 2 diabetes genes in African Americans ', PLoS ONE, vol. 7, no. 1, e29202, pp. 1-14 . https://doi.org/10.1371/journal.pone.0029202
Palmer, N D, McDonough, C W, Hicks, P J, Roh, B H, Wing, M R, An, S S, Hester, J M, Cooke, J N, Bostrom, M A, Rudock, M E, Talbert, M E, Lewis, J P, Ferrara, A, Lu, L, Ziegler, J T, Sale, M M, Divers, J, Shriner, D, Adeyemo, A, Rotimi, C N, Ng, M C Y, Langefeld, C D, Freedman, B I, Bowden, D W, Voight, B F, Scott, L J, Steinthorsdottir, V, Morris, A P, Dina, C, Welch, R P, Zeggini, E, Huth, C, Aulchenko, Y S, Thorleifsson, G, McCulloch, L J, Ferreira, T, Grallert, H, Amin, N, Wu, G, Willer, C J, Raychaudhuri, S, McCarroll, S A, Langenberg, C, Hofmann, O M, Dupuis, J, Qi, L, Segrè, A V, van Hoek, M, Borch-Johnsen, K, Kyvik, K O & DIAGRAM Consortium 2012, ' A genome-wide association search for type 2 diabetes genes in African Americans ', P L o S One, vol. 7, no. 1, pp. e29202 . https://doi.org/10.1371/journal.pone.0029202
PLOS ONE
Plos One, vol. 7, no. 1, pp. e29202
PLoS ONE; Vol 7
Yarnell, J & Palmer, N D 2012, ' A Genome-wide association search for Type 2 Diabetes genes in African Americans ', PLoS ONE, vol. 7, no. 1, e29202 . https://doi.org/10.1371/journal.pone.0029202
African Americans are disproportionately affected by type 2 diabetes (T2DM) yet few studies have examined T2DM using genome-wide association approaches in this ethnicity. The aim of this study was to identify genes associated with T2DM in the African
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::373ffe21cfe482b2e100586455896d9e
https://research.rug.nl/en/publications/4fbcdf97-a239-44a7-9038-6f4d3c2df849
https://research.rug.nl/en/publications/4fbcdf97-a239-44a7-9038-6f4d3c2df849