Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Jane E. Ranchalis"'
Autor:
Daniel Seung Kim, Amber A. Burt, Jane E. Ranchalis, Simona Vuletic, Tomas Vaisar, Wan-Fen Li, Elisabeth A. Rosenthal, Weijiang Dong, Jason F. Eintracht, Arno G. Motulsky, John D. Brunzell, John J. Albers, Clement E. Furlong, Gail P. Jarvik
Publikováno v:
Journal of Lipid Research, Vol 56, Iss 7, Pp 1351-1362 (2015)
Recent studies have failed to demonstrate a causal cardioprotective effect of HDL cholesterol levels, shifting focus to the functional aspects of HDL. Phospholipid transfer protein (PLTP) is an HDL-associated protein involved in reverse cholesterol t
Externí odkaz:
https://doaj.org/article/50a74900d86049efa0ff06e02c7afed0
Autor:
Daniel S. Kim, Amber A. Burt, Jane E. Ranchalis, Ella R. Jarvik, Elisabeth A. Rosenthal, Thomas S. Hatsukami, Clement E. Furlong, Gail P. Jarvik
Publikováno v:
Journal of Lipid Research, Vol 54, Iss 5, Pp 1512-1520 (2013)
Cardiovascular disease (CVD) is the leading cause of death in developed countries. Plasma cholesterol level is a key risk factor in CVD pathogenesis. Genetic and dietary variation both influence plasma cholesterol; however, little is known about diet
Externí odkaz:
https://doaj.org/article/3045810c21fd47a9aafb8063fcc3a7bf
Autor:
Daniel S. Kim, Amber A. Burt, David R. Crosslin, Peggy D. Robertson, Jane E. Ranchalis, Edward J. Boyko, Deborah A. Nickerson, Clement E. Furlong, Gail P. Jarvik
Publikováno v:
Journal of Lipid Research, Vol 54, Iss 2, Pp 552-560 (2013)
HDL-associated paraoxonase 1 (PON1) activity is associated with cardiovascular and other human diseases. As the role of genetic variants outside of the PON gene cluster on PON1 activity is unknown, we sought to identify common and rare variants in su
Externí odkaz:
https://doaj.org/article/555b9bb6a93540c5850c4ff38f6297f9
Autor:
Daniel S. Kim, Amber A. Burt, Jane E. Ranchalis, Rebecca J. Richter, Julieann K. Marshall, Karen S. Nakayama, Ella R. Jarvik, Jason F. Eintracht, Elisabeth A. Rosenthal, Clement E. Furlong, Gail P. Jarvik
Publikováno v:
Journal of Lipid Research, Vol 53, Iss 11, Pp 2450-2458 (2012)
HDL-associated paraoxonase 1 (PON1) activity has been consistently associated with cardiovascular and other diseases. Vitamins C and E intake have previously been positively associated with PON1 in a subset of the Carotid Lesion Epidemiology and Risk
Externí odkaz:
https://doaj.org/article/035a84a8aa654da4b77a15603f51e4f4
Autor:
Daniel S. Kim, Amber A. Burt, Jane E. Ranchalis, Rebecca J. Richter, Julieann K. Marshall, Jason F. Eintracht, Elisabeth A. Rosenthal, Clement E. Furlong, Gail P. Jarvik
Publikováno v:
Journal of Lipids, Vol 2012 (2012)
Background. Paraoxonase 1 (PON1) enzymatic activity has been consistently predictive of cardiovascular disease, while the genotypes at the four functional polymorphisms at PON1 have not. The goal of this study was to identify additional variation at
Externí odkaz:
https://doaj.org/article/b94e4efa3f9d49b186aa8ebeb2b36ab1
Autor:
Bradley P. Coe, Yatong K. Li, Karynne E. Patterson, Amber A. Burt, Deborah A. Nickerson, Michael J. Bamshad, James M. Swanson, Joel T. Nigg, Jane E. Ranchalis, Evan E. Eichler, Molly A. Nikolas, Beth Wilmot, Joshua D. Smith, Daniel Seung Kim, Gail P. Jarvik
Attention-Deficit Hyperactivity Disorder (ADHD) has high heritability; however, studies of common variation account for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74350aeb24dcd5e95450b4835297a44a
https://europepmc.org/articles/PMC5467442/
https://europepmc.org/articles/PMC5467442/
Autor:
Nora Franceschini, Yen Pei C. Chang, Susan Kirkland, Aravinda Chakravarti, Alice Stanton, Erik P A Van Iperen, Ilja M. Nolte, Jonathan A. Shaffer, Christopher P. Nelson, Aeilko H. Zwinderman, G. Kees Hovingh, Paul I.W. de Bakker, Christian Gieger, Shen Haiqing, John M. C. Connell, Xiaofeng Zhu, Patricia B. Munroe, Thomas S. Price, Eric Boerwinkle, Deepak L. Bhatt, Santhi K. Ganesh, Anna F. Dominiczak, Caitrin W. McDonough, Harold Snieder, Vinicius Tragante, Albertine J. Oldehinkel, Eoin O'Brien, Barbara E.K. Klein, Alexander P. Reiner, Mary E. Fischer, N. Charlotte Onland-Moret, Kate Witkowska, Christopher Newton-Cheh, Andrew D. Johnson, Laura Steele, Lynda M. Rose, Li Zhang, Erin N. Smith, Mark J. Caulfield, Sharon B. Wyatt, Morris Brown, Martin D. Tobin, Christian Delles, Gail P. Jarvik, Tom R. Gaunt, Hans L. Hillege, Steffi Maiwald, Nilesh J. Samani, Wolfgang Koenig, Konrad J. Karczewski, Julie A. Johnson, Brenda W.J.H. Penninx, Matthijs F.L. Meijs, Judith M. Vonk, Yvonne T. van der Schouw, Daniel I. Chasman, John Barnard, J. Hunter Young, Paul M. Ridker, Sean P. Curtis, Marten H. Hofker, Yan Gong, Jeffrey R. O'Connell, Barbara Thorand, Garret A. FitzGerald, Daichi Shimbo, Sonia Shah, Martin Farrall, Ronald P. Stolk, John G. Gums, Amber L. Beitelshees, Juan P. Casas, Pim van der Harst, Daniel Seung Kim, Peter S. Sever, André G. Uitterlinden, Michael Snyder, Brendan J. Keating, Susan Redline, Muredach P. Reilly, Michael V. Holmes, Maciej Tomaszewski, Daniel J. Rader, Sarah S. Murray, Myriam Fornage, Walter Palmas, Karina W. Davidson, Connie R. Bezzina, Gerald S. Berenson, Toby Johnson, Afshin Parsa, Cornelia M. van Duijn, Kandice Kottke-Marchant, Winfried März, Thomas Illig, W M Monique Verschuren, Aaron Isaacs, Matthew B. Lanktree, Amber A. Burt, Hugh Watkins, Daniel Levy, Hakon Hakonarson, Ramachandran S. Vasan, Johannes M.I.H. Gho, Nathan Pankratz, Sandosh Padmanabhan, Michael R. Barnes, Anuj Goel, Berta Almoguera, Xiuqing Guo, Peter J. van der Most, Ronald Klein, Mieke D. Trip, James S. Pankow, George Davey-Smith, Eric E. Schadt, Indrani Halder, Irene Mateo Leach, Meena Kumari, Claire E. Hastie, John J.P. Kastelein, Caroline O. L. Wong, Clara C. Elbers, Folkert W. Asselbergs, Wei Guo, Marcus E. Kleber, Karen J. Cruickshanks, Pieter A. Doevendans, Jane E. Ranchalis, Yun Li, Olle Melander, Jens Baumert, Ron T. Gansevoort, Rhonda M. Cooper-DeHoff, Mary Pettinger, Cisca Wijmenga
Publikováno v:
American Journal of Human Genetics, 94(3), 349-360. Cell Press
Tragante, V, Barnes, M R, Ganesh, S K, Lanktree, M B, Guo, W, Franceschini, N, Smith, E N, Johnson, T, Holmes, M V, Padmanabhan, S, Karczewski, K J, Almoguera, B, Barnard, J, Baumert, J, Chang, Y P C, Elbers, C C, Farrall, M, Fischer, M E, Gaunt, T R, Gho, J M I H, Gieger, C, Goel, A, Gong, Y, Isaacs, A, Kleber, M E, Leach, I M, McDonough, C W, Meijs, M F L, Melander, O, Nelson, C P, Nolte, I M, Pankratz, N, Price, T S, Shaffer, J, Shah, S, Tomaszewski, M, van der Most, P J, van Iperen, E P A, Vonk, J M, Witkowska, K, Wong, C O L, Zhang, L, Beitelshees, A L, Berenson, G S, Bhatt, D L, Brown, M, Burt, A, Cooper-DeHoff, R M, Connell, J M, Cruickshanks, K J, Curtis, S P, Davey-Smith, G, Delles, C, Gansevoort, R T, Guo, X Q, Haiqing, S, Hastie, C E, Hofker, M H, Hovingh, G K, Kim, D S, Kirkland, S A, Klein, B E, Klein, R, Li, Y R, Maiwald, S, Newton-Cheh, C, O'Brien, E T, Onland-Moret, N C, Palmas, W, Parsa, A, Penninx, B W, Pettinger, M, Vasan, R S, Ranchalis, J E, Ridker, P M, Rose, L M, Sever, P, Shimbo, D, Steele, L, Stolk, R P, Thorand, B, Trip, M D, van Duijn, C M, Verschuren, W M, Wijmenga, C, Wyatt, S, Young, J H, Zwinderman, A H, Bezzina, C R, Boerwinkle, E, Casas, J P, Caulfield, M J, Chakravarti, A, Chasman, D I, Davidson, K W, Doevendans, P A, Dominiczak, A F, FitzGerald, G A, Gums, J G, Munroe, P B & Keating, B J 2014, ' Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci ', American journal of human genetics, vol. 94, no. 3, pp. 349-360 . https://doi.org/10.1016/j.ajhg.2013.12.016
Tragante, V, Barnes, M R, Ganesh, S K, Lanktree, M B, Guo, W, Franceschini, N, Smith, E N, Johnson, T, Holmes, M V, Padmanabhan, S, Karczewski, K J, Almoguera, B, Barnard, J, Baumert, J, Chang, Y P C, Elbers, C C, Farrall, M, Fischer, M E, Gaunt, T R, Gho, J M I H, Gieger, C, Goel, A, Gong, Y, Isaacs, A, Kleber, M E, Leach, I M, McDonough, C W, Meijs, M F L, Melander, O, Nelson, C P, Nolte, I M, Pankratz, N, Price, T S, Shaffer, J, Shah, S, Tomaszewski, M, van der Most, P J, van Iperen, E P A, Vonk, J M, Witkowska, K, Wong, C O L, Zhang, L, Beitelshees, A L, Berenson, G S, Bhatt, D L, Brown, M, Burt, A, Cooper-DeHoff, R M, Connell, J M, Cruickshanks, K J, Curtis, S P, Davey-Smith, G, Delles, C, Gansevoort, R T, Guo, X Q, Haiqing, S, Hastie, C E, Hofker, M H, Hovingh, G K, Kim, D S, Kirkland, S A, Klein, B E, Klein, R, Li, Y R, Maiwald, S, Newton-Cheh, C, O'Brien, E T, Onland-Moret, N C, Palmas, W, Parsa, A, Penninx, B W, Pettinger, M, Vasan, R S, Ranchalis, J E, Ridker, P M, Rose, L M, Sever, P, Shimbo, D, Steele, L, Stolk, R P, Thorand, B, Trip, M D, van Duijn, C M, Verschuren, W M, Wijmenga, C, Wyatt, S, Young, J H, Zwinderman, A H, Bezzina, C R, Boerwinkle, E, Casas, J P, Caulfield, M J, Chakravarti, A, Chasman, D I, Davidson, K W, Doevendans, P A, Dominiczak, A F, FitzGerald, G A, Gums, J G, Munroe, P B & Keating, B J 2014, ' Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci ', American Journal of Human Genetics, vol. 94, no. 3, pp. 349-360 . https://doi.org/10.1016/j.ajhg.2013.12.016
Europe PubMed Central
American journal of human genetics, 94(3), 349-360. Cell Press
American Journal of Human Genetics, 94(3), 349-60. Cell Press
American Journal of Human Genetics, 94(3), 349-360. CELL PRESS
Tragante, V, Barnes, M R, Ganesh, S K, Lanktree, M B, Guo, W, Franceschini, N, Smith, E N, Johnson, T, Holmes, M V, Padmanabhan, S, Karczewski, K J, Almoguera, B, Barnard, J, Baumert, J, Chang, Y P C, Elbers, C C, Farrall, M, Fischer, M E, Gaunt, T R, Gho, J M I H, Gieger, C, Goel, A, Gong, Y, Isaacs, A, Kleber, M E, Leach, I M, McDonough, C W, Meijs, M F L, Melander, O, Nelson, C P, Nolte, I M, Pankratz, N, Price, T S, Shaffer, J, Shah, S, Tomaszewski, M, van der Most, P J, van Iperen, E P A, Vonk, J M, Witkowska, K, Wong, C O L, Zhang, L, Beitelshees, A L, Berenson, G S, Bhatt, D L, Brown, M, Burt, A, Cooper-DeHoff, R M, Connell, J M, Cruickshanks, K J, Curtis, S P, Davey-Smith, G, Delles, C, Gansevoort, R T, Guo, X Q, Haiqing, S, Hastie, C E, Hofker, M H, Hovingh, G K, Kim, D S, Kirkland, S A, Klein, B E, Klein, R, Li, Y R, Maiwald, S, Newton-Cheh, C, O'Brien, E T, Onland-Moret, N C, Palmas, W, Parsa, A, Penninx, B W, Pettinger, M, Vasan, R S, Ranchalis, J E, Ridker, P M, Rose, L M, Sever, P, Shimbo, D, Steele, L, Stolk, R P, Thorand, B, Trip, M D, van Duijn, C M, Verschuren, W M, Wijmenga, C, Wyatt, S, Young, J H, Zwinderman, A H, Bezzina, C R, Boerwinkle, E, Casas, J P, Caulfield, M J, Chakravarti, A, Chasman, D I, Davidson, K W, Doevendans, P A, Dominiczak, A F, FitzGerald, G A, Gums, J G, Munroe, P B & Keating, B J 2014, ' Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci ', American journal of human genetics, vol. 94, no. 3, pp. 349-360 . https://doi.org/10.1016/j.ajhg.2013.12.016
Tragante, V, Barnes, M R, Ganesh, S K, Lanktree, M B, Guo, W, Franceschini, N, Smith, E N, Johnson, T, Holmes, M V, Padmanabhan, S, Karczewski, K J, Almoguera, B, Barnard, J, Baumert, J, Chang, Y P C, Elbers, C C, Farrall, M, Fischer, M E, Gaunt, T R, Gho, J M I H, Gieger, C, Goel, A, Gong, Y, Isaacs, A, Kleber, M E, Leach, I M, McDonough, C W, Meijs, M F L, Melander, O, Nelson, C P, Nolte, I M, Pankratz, N, Price, T S, Shaffer, J, Shah, S, Tomaszewski, M, van der Most, P J, van Iperen, E P A, Vonk, J M, Witkowska, K, Wong, C O L, Zhang, L, Beitelshees, A L, Berenson, G S, Bhatt, D L, Brown, M, Burt, A, Cooper-DeHoff, R M, Connell, J M, Cruickshanks, K J, Curtis, S P, Davey-Smith, G, Delles, C, Gansevoort, R T, Guo, X Q, Haiqing, S, Hastie, C E, Hofker, M H, Hovingh, G K, Kim, D S, Kirkland, S A, Klein, B E, Klein, R, Li, Y R, Maiwald, S, Newton-Cheh, C, O'Brien, E T, Onland-Moret, N C, Palmas, W, Parsa, A, Penninx, B W, Pettinger, M, Vasan, R S, Ranchalis, J E, Ridker, P M, Rose, L M, Sever, P, Shimbo, D, Steele, L, Stolk, R P, Thorand, B, Trip, M D, van Duijn, C M, Verschuren, W M, Wijmenga, C, Wyatt, S, Young, J H, Zwinderman, A H, Bezzina, C R, Boerwinkle, E, Casas, J P, Caulfield, M J, Chakravarti, A, Chasman, D I, Davidson, K W, Doevendans, P A, Dominiczak, A F, FitzGerald, G A, Gums, J G, Munroe, P B & Keating, B J 2014, ' Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci ', American Journal of Human Genetics, vol. 94, no. 3, pp. 349-360 . https://doi.org/10.1016/j.ajhg.2013.12.016
Europe PubMed Central
American journal of human genetics, 94(3), 349-360. Cell Press
American Journal of Human Genetics, 94(3), 349-60. Cell Press
American Journal of Human Genetics, 94(3), 349-360. CELL PRESS
Blood pressure (BP) is a heritable risk factor for cardiovascular disease. To investigate genetic associations with systolic BP (SBP), diastolic BP (DBP), mean arterial pressure (MAP), and pulse pressure (PP), we genotyped ∼50,000 SNPs in up to 87,
Autor:
Braxton D. Mitchell, Wei Chen, Wei Guo, Joseph F. Polak, Wolfgang Koenig, Jonathan A. Shaffer, Christian Gieger, Thomas Illig, Abdullah Kutlar, Jessica van Setten, Matthew B. Lanktree, Pieter A. Doevendans, Nicholas J. Schork, Cisca Wijmenga, G. Kees Hovingh, Christopher Newton-Cheh, Daniel Levy, Marten H. Hofker, Eric E. Schadt, Folkert W. Asselbergs, Nicole Soranzo, Sathanur R. Srinivasan, Olle Mellander, Daniel J. Rader, Roy L. Silverstein, David Duggan, Lynda M. Rose, Ron T. Gansevoort, Cliona Molony, André G. Uitterlinden, Li Zhang, Gerald S. Berenson, John Barnard, Vasan S. Ramachandran, Paul M. Ridker, Toby Johnson, Cornelia M. van Duijn, J. Hunter Young, Martin Farrall, Willem H. Ouwehand, Muredach P. Reilly, Tom S. Price, Sean P. Curtis, Brendan J. Keating, John G. Gums, Deepak L. Bhatt, Ilja M. Nolte, Barbara Thorand, Georg Ehret, Hans L. Hillege, Julie A. Johnson, Bernhard R. Winkelmann, Andrea Z. LaCroix, Patricia B. Munroe, Vinicius Tragante, Alan R. Shuldiner, Mieke D. Trip, Karina W. Davidson, Kandice Kottke-Marchant, Hubert Scharnag, Andrew D. Johnson, Ben Burkley, Clement E. Furlong, Winfried März, Yvonne T. van der Schouw, Yen Pei C. Chang, Hakon Hakonarson, Erin N. Smith, Aaron Isaacs, Eric Boerwinkle, Albertine J. Oldehinkel, Haiqing Shen, Richard R. Fabsitz, Alice Stanton, Steffi Maiwald, Matthijs F.L. Meijs, Johannes M.I.H. Gho, Yan Gong, Herman A. Taylor, Mary E. Fischer, Jeffery R. O'Connell, Santhi K. Ganesh, Rhonda M. Cooper-DeHoff, Ervin R. Fox, Albert W. Dreisbach, Brenda W.J.H. Penninx, Susan Kirkland, Caitrin W. McDonough, Nora Franceschini, Daniel I. Chasman, Amber L. Beitelshees, Carl J. Pepine, Tom R. Gaunt, Gurunathan Murugesan, Pim van der Harst, Irene Mateo Leach, Aravinda Chakravarti, Mary Pettinger, Gail P. Jarvik, Marcus E. Kleber, Paul I.W. de Bakker, Myriam Fornage, Mark J. Caulfield, Amber A. Burt, Judith M. Vonk, Sandosh Padmanabhan, Jane E. Ranchalis, Sonia Shah, Berta Almoguera Castillo, Erik P A Van Iperen, Jolanda M. A. Boer, Kiang Liu, Ronald P. Stolk, Garret A. FitzGerald, Yun Li, Rainer Malik, Jens Baumert, Peter J. van der Most, W. M. Monique Verschuren, Bernhard O. Boehm, Clara C. Elbers, Xiaofeng Zhu, Harold Snieder, N. Charlotte Onland-Moret, Honghuang Lin, Taimour Y. Langaee, Ramakrishnan Rajagopalan, John J.P. Kastelein, Nilesh J. Samani, Daichi Shimbo, Susan Redline, Sarah S. Murray, Alexander P. Reiner, Sharon B. Wyatt, Walter Palmas, Yiran Guo
Publikováno v:
Human Molecular Genetics; Vol 22
Ganesh, S K, Tragante, V, Guo, W, Guo, Y R, Lanktree, M B, Smith, E N, Johnson, T, Castillo, B A, Barnard, J, Baumert, J, Chang, Y P C, Elbers, C C, Farrall, M, Fischer, M E, Franceschini, N, Gaunt, T R, Gho, J M I H, Gieger, C, Gong, Y, Isaacs, A, Kleber, M E, Leach, I M, McDonough, C W, Meijs, M F L, Mellander, O, Molony, C M, Nolte, I M, Padmanabhan, S, Price, T S, Rajagopalan, R, Shaffer, J, Shah, S, Shen, H Q, Soranzo, N, van der Most, P J, van Iperen, E P A, Van Setten, J A, Vonk, J M, Zhang, L, Beitelshees, A L, Berenson, G S, Bhatt, D L, Boer, J M A, Boerwinkle, E, Burkley, B, Burt, A, Chakravarti, A, Chen, W, Cooper-DeHoff, R M, Curtis, S P, Dreisbach, A, Duggan, D, Ehret, G B, Fabsitz, R R, Fornage, M, Fox, E, Furlong, C E, Gansevoort, R T, Hofker, M H, Hovingh, G K, Kirkland, S A, Kottke-Marchant, K, Kutlar, A, LaCroix, A Z, Langaee, T Y, Li, Y R, Lin, H H, Liu, K, Maiwald, S, Malik, R, Murugesan, G, Newton-Cheh, C, OConnell, J R, Onland-Moret, N C, Ouwehand, W H, Palmas, W, Penninx, B W J H, Pepine, C J, Pettinger, M, Polak, J F, Ramachandran, V S, Ranchalis, J, Redline, S, Ridker, P M, Rose, L M, Scharnag, H, Schork, N J, Shimbo, D, Shuldiner, A R, Srinivasan, S R, Stolk, R P, Taylor, H A, Thorand, B, Trip, M D, van Duijn, C M, Verschuren, W M, Wijmenga, C, Winkelmann, B R, Wyatt, S, Keating, B J & Asselbergs, F W 2013, ' Loci influencing blood pressure identified using a cardiovascular gene-centric array ', Human Molecular Genetics, vol. 22, no. 8, pp. 1663-1678 . https://doi.org/10.1093/hmg/dds555
Europe PubMed Central
Human Molecular Genetics, 22(8), 1663-78. Oxford University Press
Human Molecular Genetics, 22(8), 1663-1678. Oxford University Press
Human Molecular Genetics, Vol. 22, No 8 (2013) pp. 1663-78
Human molecular genetics, 22(8), 1663-1678. Oxford University Press
Human Molecular Genetics
Ganesh, S K, Tragante, V, Guo, W, Guo, Y R, Lanktree, M B, Smith, E N, Johnson, T, Castillo, B A, Barnard, J, Baumert, J, Chang, Y P C, Elbers, C C, Farrall, M, Fischer, M E, Franceschini, N, Gaunt, T R, Gho, J M I H, Gieger, C, Gong, Y, Isaacs, A, Kleber, M E, Leach, I M, McDonough, C W, Meijs, M F L, Mellander, O, Molony, C M, Nolte, I M, Padmanabhan, S, Price, T S, Rajagopalan, R, Shaffer, J, Shah, S, Shen, H Q, Soranzo, N, van der Most, P J, van Iperen, E P A, Van Setten, J A, Vonk, J M, Zhang, L, Beitelshees, A L, Berenson, G S, Bhatt, D L, Boer, J M A, Boerwinkle, E, Burkley, B, Burt, A, Chakravarti, A, Chen, W, Cooper-DeHoff, R M, Curtis, S P, Dreisbach, A, Duggan, D, Ehret, G B, Fabsitz, R R, Fornage, M, Fox, E, Furlong, C E, Gansevoort, R T, Hofker, M H, Hovingh, G K, Kirkland, S A, Kottke-Marchant, K, Kutlar, A, LaCroix, A Z, Langaee, T Y, Li, Y R, Lin, H H, Liu, K, Maiwald, S, Malik, R, Murugesan, G, Newton-Cheh, C, OConnell, J R, Onland-Moret, N C, Ouwehand, W H, Palmas, W, Penninx, B W J H, Pepine, C J, Pettinger, M, Polak, J F, Ramachandran, V S, Ranchalis, J, Redline, S, Ridker, P M, Rose, L M, Scharnag, H, Schork, N J, Shimbo, D, Shuldiner, A R, Srinivasan, S R, Stolk, R P, Taylor, H A, Thorand, B, Trip, M D, van Duijn, C M, Verschuren, W M, Wijmenga, C, Winkelmann, B R, Wyatt, S, Keating, B J & Asselbergs, F W 2013, ' Loci influencing blood pressure identified using a cardiovascular gene-centric array ', Human Molecular Genetics, vol. 22, no. 8, pp. 1663-1678 . https://doi.org/10.1093/hmg/dds555
Europe PubMed Central
Human Molecular Genetics, 22(8), 1663-78. Oxford University Press
Human Molecular Genetics, 22(8), 1663-1678. Oxford University Press
Human Molecular Genetics, Vol. 22, No 8 (2013) pp. 1663-78
Human molecular genetics, 22(8), 1663-1678. Oxford University Press
Human Molecular Genetics
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
Autor:
Gail P. Jarvik, Julieann K Marshall, Rebecca J. Richter, Daniel Seung Kim, Ella R. Jarvik, Elisabeth A. Rosenthal, Amber A. Burt, Karen S. Nakayama, Jason F. Eintracht, Clement E. Furlong, Jane E. Ranchalis
Publikováno v:
Journal of Lipid Research, Vol 53, Iss 11, Pp 2450-2458 (2012)
HDL-associated paraoxonase 1 (PON1) activity has been consistently associated with cardiovascular and other diseases. Vitamins C and E intake have previously been positively associated with PON1 in a subset of the Carotid Lesion Epidemiology and Risk
Autor:
Mark J. Rieder, Magdalena Ahearn, Deborah A. Nickerson, Jane E. Ranchalis, Michelle Wong, Cynthia Shephard, Gerard D. Schellenberg, Michael D. Badzioch, Ellen M. Wijsman, Dana C. Crawford, Laura A. McKinstry, Alexander Nord, Patrick J. Heagerty, Caterina Bertucci, Gail P. Jarvik
Publikováno v:
Journal of Lipid Research, Vol 49, Iss 3, Pp 588-596 (2008)
The genetic factors associated with carotid artery disease (CAAD) are not fully known. Because of its role in lipid metabolism, we hypothesized that common genetic variation in the very low density lipoprotein receptor (VLDLR) gene is associated with