Zobrazeno 1 - 10
of 67
pro vyhledávání: '"O'Connell Jeffery R"'
Autor:
Wozniak Marcella A, O'Connell Jeffery R, Stine Oscar C, MacClellan Leah R, Howard Timothy D, Cole John W, Mez Jesse B, Stern Barney J, Sorkin John D, Mitchell Braxton D, Kittner Steven J
Publikováno v:
BMC Research Notes, Vol 2, Iss 1, p 260 (2009)
Abstract Background Population-based association studies are used to identify common susceptibility variants for complex genetic traits. These studies are susceptible to confounding from unknown population substructure. Here we apply a model-based cl
Externí odkaz:
https://doaj.org/article/54464691a30f4772aadc8f6038da3841
Autor:
McArdle Patrick F, Dytch Harvey, O'Connell Jeffery R, Shuldiner Alan R, Mitchell Braxton D, Abney Mark
Publikováno v:
BMC Genetics, Vol 8, Iss 1, p 66 (2007)
Abstract Background High blood pressure is a well established risk factor for morbidity and mortality acting through heart disease, stroke and cardiovascular disease. Genome wide scans have linked regions of nearly every human chromosome to blood pre
Externí odkaz:
https://doaj.org/article/5ea6f0cf37184c4fa9b453eddf9baf53
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Akademický článek
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Akademický článek
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Autor:
Karasik, David, Zillikens, M Carola, Hsu, Yi-Hsiang, Aghdassi, Ali, Akesson, Kristina, Amin, Najaf, Barroso, Inês, Bennett, David A, Bertram, Lars, Bochud, Murielle, Borecki, Ingrid B, Broer, Linda, Buchman, Aron S, Byberg, Liisa, Campbell, Harry, Campos-Obando, Natalia, Cauley, Jane A, Cawthon, Peggy M, Chambers, John C, Chen, Zhao, Cho, Nam H, Choi, Hyung Jin, Chou, Wen-Chi, Cummings, Steven R, de Groot, Lisette CPGM, De Jager, Phillip L, Demuth, Ilja, Diatchenko, Luda, Econs, Michael J, Eiriksdottir, Gudny, Enneman, Anke W, Eriksson, Joel, Eriksson, Johan G, Estrada, Karol, Evans, Daniel S, Feitosa, Mary F, Fu, Mao, Gieger, Christian, Grallert, Harald, Gudnason, Vilmundur, Lenore, Launer J, Hayward, Caroline, Hofman, Albert, Homuth, Georg, Huffman, Kim M, Husted, Lise B, Illig, Thomas, Ingelsson, Erik, Ittermann, Till, Jansson, John-Olov, Johnson, Toby, Biffar, Reiner, Jordan, Joanne M, Jula, Antti, Karlsson, Magnus, Khaw, Kay-Tee, Kilpeläinen, Tuomas O, Klopp, Norman, Kloth, Jacqueline SL, Koller, Daniel L, Kooner, Jaspal S, Kraus, William E, Kritchevsky, Stephen, Kutalik, Zoltán, Kuulasmaa, Teemu, Kuusisto, Johanna, Laakso, Markku, Lahti, Jari, Lang, Thomas, Langdahl, Bente L, Lerch, Markus M, Lewis, Joshua R, Lill, Christina, Lind, Lars, Lindgren, Cecilia, Liu, Yongmei, Livshits, Gregory, Ljunggren, Östen, Loos, Ruth JF, Lorentzon, Mattias, Luan, Jian'an, Luben, Robert N, Malkin, Ida, McGuigan, Fiona E, Medina-Gomez, Carolina, Meitinger, Thomas, Melhus, Håkan, Mellström, Dan, Michaëlsson, Karl, Mitchell, Braxton D, Morris, Andrew P, Mosekilde, Leif, Nethander, Maria, Newman, Anne B, O'Connell, Jeffery R, Oostra, Ben A, Orwoll, Eric S, Palotie, Aarno, Peacock, Munro, Perola, Markus
Publikováno v:
The American journal of clinical nutrition, vol 109, iss 2
BackgroundLean body mass (LM) plays an important role in mobility and metabolic function. We previously identified five loci associated with LM adjusted for fat mass in kilograms. Such an adjustment may reduce the power to identify genetic signals ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0675f64e1d2bf51f0bf21ab553dfc4c2
https://escholarship.org/uc/item/8sb0856c
https://escholarship.org/uc/item/8sb0856c
Autor:
Ganesh, Santhi K, Tragante, Vinicius, Guo, Wei, Guo, Yiran, Lanktree, Matthew B, Smith, Erin N, Johnson, Toby, Castillo, Berta Almoguera, Barnard, John, Baumert, Jens, Chang, Yen-Pei Christy, Elbers, Clara C, Farrall, Martin, Fischer, Mary E, Franceschini, Nora, Gaunt, Tom R, Gho, Johannes MIH, Gieger, Christian, Gong, Yan, Isaacs, Aaron, Kleber, Marcus E, Mateo Leach, Irene, McDonough, Caitrin W, Meijs, Matthijs FL, Mellander, Olle, Molony, Cliona M, Nolte, Ilja M, Padmanabhan, Sandosh, Price, Tom S, Rajagopalan, Ramakrishnan, Shaffer, Jonathan, Shah, Sonia, Shen, Haiqing, Soranzo, Nicole, van der Most, Peter J, Van Iperen, Erik PA, Van Setten, Jessica, Vonk, Judith M, Zhang, Li, Beitelshees, Amber L, Berenson, Gerald S, Bhatt, Deepak L, Boer, Jolanda MA, Boerwinkle, Eric, Burkley, Ben, Burt, Amber, Chakravarti, Aravinda, Chen, Wei, Cooper-Dehoff, Rhonda M, Curtis, Sean P, Dreisbach, Albert, Duggan, David, Ehret, Georg B, Fabsitz, Richard R, Fornage, Myriam, Fox, Ervin, Furlong, Clement E, Gansevoort, Ron T, Hofker, Marten H, Hovingh, G Kees, Kirkland, Susan A, Kottke-Marchant, Kandice, Kutlar, Abdullah, Lacroix, Andrea Z, Langaee, Taimour Y, Li, Yun R, Lin, Honghuang, Liu, Kiang, Maiwald, Steffi, Malik, Rainer, CARDIOGRAM, METASTROKE, Murugesan, Gurunathan, Newton-Cheh, Christopher, O'Connell, Jeffery R, Onland-Moret, N Charlotte, Ouwehand, Willem H, Palmas, Walter, Penninx, Brenda W, Pepine, Carl J, Pettinger, Mary, Polak, Joseph F, Ramachandran, Vasan S, Ranchalis, Jane, Redline, Susan, Ridker, Paul M, Rose, Lynda M, Scharnag, Hubert, Schork, Nicholas J, Shimbo, Daichi, Shuldiner, Alan R, Srinivasan, Sathanur R, Stolk, Ronald P, Taylor, Herman A, Thorand, Barbara, Trip, Mieke D, van Duijn, Cornelia M, Verschuren, W Monique, Wijmenga, Cisca, Winkelmann, Bernhard R, Wyatt, Sharon
Publikováno v:
Human molecular genetics, vol 22, iss 8
Blood pressure (BP) is a heritable determinant of risk for cardiovascular disease (CVD). To investigate genetic associations with systolic BP (SBP), diastolic BP (DBP), mean arterial pressure (MAP) and pulse pressure (PP), we genotyped ∼50 000 sing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1273710eb6287dcc440e8c23006a5ea2
https://escholarship.org/uc/item/16d246b2
https://escholarship.org/uc/item/16d246b2
Autor:
Padmanabhan, Sandosh, Li, Yun R., Meijs, Matthijs F.L., Guo, Yiran, Beitelshees, Amber L., Kleber, Marcus E., van Iperen, Erik P.A., Chen, Yii-Der Ida, Li, Mingyao, Liu, Kiang, Appelman, Yolande E., Gong, Yan, Gaunt, Tom R., McDonough, Caitrin W., Langaee, Taimour Y., Asselbergs, Folkert W., Barnard, John, Almoguera, Berta, Nelson, Christopher P., Pankratz, Nathan, Bhangale, Tushar R., O’Connell, Jeffery R., Tragante, Vinicius, Sivapalaratnam, Suthesh, Baumert, Jens, Lange, Leslie A., Pankow, James S., Middelberg, Rita P.S., Lanktree, Matthew B., Hopewell, Jemma C., Musunuru, Kiran, Johnson, Toby
Genome-wide association studies (GWASs) have identified many SNPs underlying variations in plasma-lipid levels. We explore whether additional loci associated with plasma-lipid phenotypes, such as high-density lipoprotein cholesterol (HDL-C), low-dens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7664a9aa9a3539dccea989339836b03c
Autor:
Yerges-Armstrong, Laura M., Sumbul Chai, O'Connell, Jeffery R., Curran, Joanne E., Blangero, John, Mitchell, Braxton D., Shuldiner, Alan R., Damcott, Coleen M., Chai, Sumbul
Publikováno v:
Journals of Gerontology Series A: Biological Sciences & Medical Sciences; Oct2016, Vol. 71 Issue 10, p1295-1299, 5p, 1 Diagram, 2 Charts, 1 Graph