Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Andrew P Boright"'
Autor:
Thomas Donner, P. Rezaeian, John I. Malone, Sharon B. Schwartz, Xiaoyu Gao, Szilard Kiss, Matthew J. Budoff, David R. Sell, A. Dwoskin, Ronald J. Prineas, C. Pittman, M. Reid, C. McDonald, S. Caulder, M. Szpiech, Oscar B. Crofford, Rachel G. Miller, Louis A. Lobes, M. Patronas, C. Canny, M. E. Lackaye, Sandra R. Montezuma, Richard M. Bergenstal, Patricia Gatcomb, Julie A. Stoner, H. Pan, James L. Kinyoun, J. Mortenson, Osama Hamdy, Connie Fountain, David D. Moore, Kusiel Perlman, R. Trail, David A. Lee, J. Sheindlin, Samuel Dagogo-Jack, Jeffrey L. Mahon, Jill P. Crandall, L. Gill, T. Thompson, Lee M. Jampol, K. Koushan, David S. Schade, J. Brown-Friday, M. Basco, S. Dunnigan, J. Bylsma, R. Birk, L. H. Ketai, J. Hotaling, Stephen W. Scherer, W. Mestrezat, Stephan Villavicencio, R. Lyon, M. Carney, John Kramer, Sunder Mudaliar, David M. Nathan, M. Moran, F. Leandre, James W. Albers, L. Survant, Joseph F. Polak, Manjot K. Gill, Anton Orlin, M. Prince, Pamela A. Silver, Amy K. Saenger, John D. Brunzell, Kathleen E. Bainbridge, L. Babbione, Amisha Wallia, J. Vaccaro-Kish, Bradley D. Jones, M. Hebdon, L. McKenzie, Richard M. Hoffman, S. Chang, C. Siebert, George S. Sharuk, D. Counts, A. Lucas, P. Ramos, N. Burkhart, N. Bakshi, N. Flaherty, D. Kenny, M. Driscoll, Harjit Chahal, Ronald K. Mayfield, S. Hensley, E. Weimann, M. Franz, Martin J. Stevens, N. S. Gregory, Christopher J. O'Donnell, J. Laechelt, Pamela Ossorio, Jerry P. Palmer, Rama Natarajan, G. Ziegler, K. Martin, R. Beaser, C. Beck, L. Zhang, T. J. Declue, David M. Kendall, H. Solc, A. Vella, H. Martinez, Cormac T. Taylor, S. Neill, Douglas A. Greene, P. Lee, D. Norman, Andrew J. Barkmeier, Dean P. Hainsworth, Alka Jain, Sapna Gangaputra, N. Thangthaeng, Lorraine Thomas, Michael H. Brent, M. Bracey, Philip Raskin, Q. Clemens, Barbara H. Braffett, Mark S. Mandelcorn, Lloyd Paul Aiello, John E. Godine, T. Speigelberg, R. Chan, R. Hanna, Shelley B. Bull, William I. Sivitz, R. Sussman, C. Kwong, S. Cercone, P. Hollander, N. Leloudes, Joseph M. Terry, J. Wesche, E. A. Tanaka, D. Rosenberg, Wanjie Sun, L. Sun, Tom Clark, Deborah K. Schlossman, Louis M. Luttrell, R. Dunn, A. Farr, K. McVary, Gayle M. Lorenzi, A. Joseph, Catherine C. Cowie, M. Barr, D. Zimbler, S. Mendley, S. Schussler, N. Grove, Matthew D. Davis, Jong Mu Sun, Sophie Rogers, John P. Bantle, Brandy N. Rutledge, Senda Ajroud-Driss, Vincent M. Monnier, Cladd E. Stevens, Y. G. He, M. Phillips, C. Williams, J. MacIndoe, Kaleigh Farrell, Helen Lambeth, Ayad A. Jaffa, J. Quin, Morey W. Haymond, R. Kirby, D. Steinberg, William H. Herman, M. Mech, Arup Das, Robert Detrano, J. Brown, D. McMillan, Linda Snetselaar, Mark W. Johnson, R. Zeitler, T. Taylor, Peter R. Pavan, Michael H. Goldbaum, Bruce A. Perkins, R. G. Campbell, David A. Nicolle, R. J. van der Geest, Irene Hramiak, D. Freking, Lucy A. Levandoski, S. Colson, Charles Campbell, Victoria R. Trapani, Lawrence J. Singerman, D. Meyer, W. Tang, J. Soule, Anita Harrington, Julie A. Nelson, John A. Colwell, Naji Younes, P. Salemi, K. Hansen, Trevor J. Orchard, S. Huddleston, L. Steranchak, C. Sommer, G. Castle, J. Ginsberg, Paula McGee, V. Gama, John Dupre, Z. Strugula, M. Swenson, N. Wong, David A. Bluemke, M. Nutaitis, Anita Agarwal, M. Lin, K. Nickander, Elsayed Z. Soliman, Joao A. Lima, M. L. Schluter, Fred W. Whitehouse, Lisa Diminick, C. Cornish, M. Spencer, Daniel T. Lackland, Ionut Bebu, Hunter Wessells, S. Yacoub-Wasef, A. Determan, L. Van Ottingham, Howard Wolpert, R. Ehrlich, A. Blevins, L. Jovanovic, D. Finegold, Davida F. Kruger, Jye-Yu C. Backlund, K. Chan, Timothy J. Murtha, R. K. Mayfield, Robert W. Cavicchi, Maria F. Lopes-Virella, Thomas A. Weingeist, K. Lee, Mary E. Larkin, B. Blodi, J. Gott, Timothy J. Lyons, J. Selby, Chris Ryan, J. Harth, P. Pugsley, L. Keasler, John D. Maynard, Paul G. Arrigg, Amy B. Karger, P. Colby, J. Farquhar, Mark H. Schutta, Murk-Hein Heinemann, Kathie L. Hermayer, B. Bosco, C. Lovell, A. Bhan, A. Galprin, M. Cayford, M. Schumer, John E. Chapin, D. Rubinstein, F. Miao, V. Asuquo, Catherine L. Martin, Rodney A. Lorenz, Samuel S. Engel, L. Funk, Cyndi F. Liu, Barbara J. Maschak-Carey, Stephen S. Feman, P. Lindsey, M. Giotta, Philip A. Low, S. Kwon, R. Fahlstrom, A. Iannacone, B. French, H. Remtema, L. Cimino, S. Barron, J. McConnell, Jane L. Lynch, L. Kim, T. Williams, A. Degillio, Blanche M. Chavers, M. Novak, Julio V. Santiago, Ronald P. Danis, P. Gaston, Tae Sup Lee, T. Woodfill, R. Cuddihy, Scott M. Steidl, Alanna C. Morrison, E. Ryan, D. Lawrence, D. Cros, T. Adkins, D. Adelman, L. Dews, Patricia A. Cleary, J. Parker, L. Olmos De Koo, C. Kim, Mark R. Palmert, P. Astelford, Stefan Fritz, B. Olson, Kelvin C. Fong, Alan M. Jacobson, Stanley L. Hazen, D. Hornbeck, K. Folino, M. L. Bernal, Gabriel Virella, William V. Tamborlane, Neil H. White, Daniel L. McGee, Denis Daneman, H. Shamoon, William Dahms, S. Elsing, S. Brink, J. Ahern, Delnaz Roshandel, John M. Pach, N. W. Rodger, E. Cupelli, Dara D. Koozekanani, Abbas E. Kitabchi, K. Stoessel, B. Petty, Jamie R. Wood, J. Seegmiller, T. Strand, Y. Li, Eva L. Feldman, Larry Rand, Robert C. Colligan, T. Smith, A. Carlson, David J. Brillon, Margaret L. Bayless, M. Ong, S. Darabian, W. Hsu, Janet E. Olson, B. Rogness, N. Silvers, M. Pfiefer, B. Schaefer, E. Mendelson, S. Braunstein, Maren Nowicki, R. Reed, James S. Floyd, Z. M. Zhang, T. Sandford, R. B. Avery, A. Pratt, Paolo S. Silva, H. Bode, Alexander J. Brucker, Nikhil D. Patel, Alexander R. Lyon, M. Jenner, N. Wimmergren, L. Tuason, J. Rosenzwieg, D. J. Becker, C. Gauthier-Kelly, M. Richardson, Richard S. Crow, Andrew D. Paterson, Mark E. Molitch, Suzanne M. Strowig, S. Pendegast, M. Burger, Ramzi K. Hemady, J. Dingledine, I. H. de Boer, L. Mayer, F. Perdikaris, Om P. Ganda, F. Thoma, Karen J. Cruickshanks, Abraham Thomas, K. Klumpp, Jerry D. Cavallerano, D. Zheng, Annette Barnie, J. L. Canady, C. Wigley, David G. Miller, Sheila Smith-Brewer, D. Ostrowski, P. Crawford, K. Kelly, Robert G. Devenyi, B. Zimmerman, Susan M. Hitt, C. Johnson, L. Gurry, R. Jarboe, E. Angus, David E. Goldstein, A. Killeen, H. Schrott, Orville G. Kolterman, Mark R. Burge, Michael Rubin, J. Lipps Hagan, Alicia J. Jenkins, Hugh D. Wabers, R. Warhol, Edward Chaum, Karen L. Jones, L. Spillers, C. Miao, J. K. Jones, Angelo J. Canty, Rickey E. Carter, Evrim B. Turkbey, B. Burzuk, R. Woodwick, Evica Simjanoski, Michael W. Steffes, S. Crowell, Suresh D. Shah, H. Ricks, J. D. Carey, Paul A. Edwards, S. Holt, W. F. Schwenk, Ronald J. Oudiz, E. Brown, J. Heier, R. L. Ufret-Vincenty, L. M. Aiello, Robert A. Rizza, Karen L. Anderson, Valerie L. Arends, J. Giangiacomo, R. Liss, Aruna V. Sarma, B. Levy, Ellen J. Anderson, S. Catton, P. Callahan, Rodica Pop-Busui, S. Debrabandere, S. Moser, Bernard H. Doft, A. Malayeri, C. Johannes, R. Ramker, J. Rich, M. Fox, Rukhsana G. Mirza, Katherine A. Morgan, Thomas J. Songer, C. Shah, H. Engel, Saul M. Genuth, S. Ferguson, Anushka Patel, C. Haggan, P. Lou, J. Gordon, M. B. Murphy, D. Sandstrom, Dawn M. Ryan, Daniel H. O'Leary, B. Gloeb, Lois E. Schmidt, H. Zegarra, D. Dalton, W. Brown, Tom G. Sheidow, Margaret E. Stockman, Shyam M. Thomas, Charles McKitrick, Jyotika K. Fernandes, P. A. Bourne, L. Baker, G. Friedenberg, Allan Gordon, Allan L. Drash, S. Yoser, D. Wood, S. Johnsonbaugh, A. De Manbey, L. Kaminski, M. May, L. Bestourous, A. Kowarski, M. Geckle, M. Hartmuller, Michael Bryer-Ash, S. List, F. Goetz, V. Reppucci, D. Etzwiler, Rose A. Gubitosi-Klug, M. Brabham, E. Golden, A. Nayate, J. Hu, M. McLellan, Ronald Klein, N. Rude, B. Vittetoe, John M. Lachin, M. Christofi, Zhuo Chen, Isaac Boniuk, C. Strauch, K. Gunyou, L. Delahanty, W. T. Garvey, Andrew P. Boright, Larry D. Hubbard, D. Weiss, Igor Grant, Jonathan Q. Purnell, Jean M. Bucksa, N. Olson, B. Zinman
Publikováno v:
Clinical Epigenetics
Background Many CpGs become hyper or hypo-methylated with age. Multiple methods have been developed by Horvath et al. to estimate DNA methylation (DNAm) age including Pan-tissue, Skin & Blood, PhenoAge, and GrimAge. Pan-tissue and Skin & Blood try to
Autor:
Niina Sandholm, Rany M Salem, Amy Jayne McKnight, Eoin P Brennan, Carol Forsblom, Tamara Isakova, Gareth J McKay, Winfred W Williams, Denise M Sadlier, Ville-Petteri Mäkinen, Elizabeth J Swan, Cameron Palmer, Andrew P Boright, Emma Ahlqvist, Harshal A Deshmukh, Benjamin J Keller, Huateng Huang, Aila J Ahola, Emma Fagerholm, Daniel Gordin, Valma Harjutsalo, Bing He, Outi Heikkilä, Kustaa Hietala, Janne Kytö, Päivi Lahermo, Markku Lehto, Raija Lithovius, Anne-May Osterholm, Maija Parkkonen, Janne Pitkäniemi, Milla Rosengård-Bärlund, Markku Saraheimo, Cinzia Sarti, Jenny Söderlund, Aino Soro-Paavonen, Anna Syreeni, Lena M Thorn, Heikki Tikkanen, Nina Tolonen, Karl Tryggvason, Jaakko Tuomilehto, Johan Wadén, Geoffrey V Gill, Sarah Prior, Candace Guiducci, Daniel B Mirel, Andrew Taylor, S Mohsen Hosseini, DCCT/EDIC Research Group, Hans-Henrik Parving, Peter Rossing, Lise Tarnow, Claes Ladenvall, François Alhenc-Gelas, Pierre Lefebvre, Vincent Rigalleau, Ronan Roussel, David-Alexandre Tregouet, Anna Maestroni, Silvia Maestroni, Henrik Falhammar, Tianwei Gu, Anna Möllsten, Danut Cimponeriu, Mihai Ioana, Maria Mota, Eugen Mota, Cristian Serafinceanu, Monica Stavarachi, Robert L Hanson, Robert G Nelson, Matthias Kretzler, Helen M Colhoun, Nicolae Mircea Panduru, Harvest F Gu, Kerstin Brismar, Gianpaolo Zerbini, Samy Hadjadj, Michel Marre, Leif Groop, Maria Lajer, Shelley B Bull, Daryl Waggott, Andrew D Paterson, David A Savage, Stephen C Bain, Finian Martin, Joel N Hirschhorn, Catherine Godson, Jose C Florez, Per-Henrik Groop, Alexander P Maxwell
Publikováno v:
PLoS Genetics, Vol 8, Iss 9, p e1002921 (2012)
Diabetic kidney disease, or diabetic nephropathy (DN), is a major complication of diabetes and the leading cause of end-stage renal disease (ESRD) that requires dialysis treatment or kidney transplantation. In addition to the decrease in the quality
Externí odkaz:
https://doaj.org/article/818e5a61debb4667aafbe14358bd9b2a
Autor:
Emma Ahlqvist, Catherine Godson, Darrell Andrews, Per-Henrik Groop, Raimund Weitgasser, Andrzej S. Krolewski, Kristine E. Lee, Lina Radzeviciene, Stuart J. McGurnaghan, Colin N. A. Palmer, Joanne B. Cole, Shelley B. Bull, Andrew P. Boright, Lars Stechemesser, Katalin Susztak, Barbara E.K. Klein, Wei-Min Chen, Kerstin Brismar, Carol Forsblom, Jani K. Haukka, Beata Gyorgy, Adam M. Smiles, Jose C. Florez, Harvest F. Gu, Niina Sandholm, Leif Groop, Gareth J. McKay, Maria Hughes, Mark I. McCarthy, Joel N. Hirschhorn, Athina Spiliopoulou, Michael Mauer, Samy Hadjadj, Nicolae Mircea Panduru, Helen M. Colhoun, Jingchuan Guo, Robert G. Nelson, Matthias Kretzler, Valdis Pīrāgs, Marcus G. Pezzolesi, Tarunveer S. Ahluwalia, Rasa Verkauskiene, Michel Marre, Linda T. Hiraki, Janet K. Snell-Bergeon, Bernhard Paulweber, Stephen S. Rich, Erkka Valo, Chen Di Liao, David M. Maahs, Vita Rovīte, Rachel G. Miller, Eoin P. Brennan, Peter Rossing, Natalie R. van Zuydam, Maria Luiza Caramori, Jan Skupien, Rany M. Salem, A. Peter Maxwell, Paul M. McKeigue, Maria Lajer, Gianpaolo Zerbini, Chengxiang Qiu, David-Alexandre Trégouët, Henrik Falhammar, Jennifer Todd, Rajasree Menon, Jelizaveta Sokolovska, Valma Harjutsalo, Anna Möllsten, Ronald Klein, Xiaoyu Gao, Viji Nair, Jihwan Park, Amy Jayne McKnight, Jing Jing Cao, Silvia Maestroni, Edita Prakapiene, Ian H. de Boer, Finian Martin, Andrew D. Paterson, Suna Onengut-Gumuscu, Ross Doyle, Hyun Min Kang, Angelo J. Canty, Andrew C. Liu, Tina Costacou, Carine M. Boustany-Kari
Publikováno v:
Salem, R M, Todd, J N, Sandholm, N, Rossing, P, Rich, S S, Hirschhorn, J N, Florez, J C & SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium 2019, ' Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen ', Journal of the American Society of Nephrology, vol. 30, no. 10, pp. 2000-2016 . https://doi.org/10.1681/ASN.2019030218
2019, ' Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen ', Journal of the American Society of Nephrology . https://doi.org/10.1681/ASN.2019030218
SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium, Kretzler, M, Susztak, K, Colhoun, H M, Krolewski, A S, Paterson, A D, Groop, P-H, Rich, S S, Hirschhorn, J N & Florez, J C 2019, ' Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen ', Journal of the American Society of Nephrology, vol. 30, no. 10, pp. 2000-2016 . https://doi.org/10.1681/ASN.2019030218
J Am Soc Nephrol
2019, ' Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen ', Journal of the American Society of Nephrology . https://doi.org/10.1681/ASN.2019030218
SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium, Kretzler, M, Susztak, K, Colhoun, H M, Krolewski, A S, Paterson, A D, Groop, P-H, Rich, S S, Hirschhorn, J N & Florez, J C 2019, ' Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen ', Journal of the American Society of Nephrology, vol. 30, no. 10, pp. 2000-2016 . https://doi.org/10.1681/ASN.2019030218
J Am Soc Nephrol
BACKGROUND: Although diabetic kidney disease demonstrates both familial clustering and single nucleotide polymorphism heritability, the specific genetic factors influencing risk remain largely unknown.METHODS: To identify genetic variants predisposin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7c5428acfac62f36ff4056292157371
https://curis.ku.dk/portal/da/publications/genomewide-association-study-of-diabetic-kidney-disease-highlights-biology-involved-in-glomerular-basement-membrane-collagen(b30453e6-4f70-4b36-83fd-2afa1bcee756).html
https://curis.ku.dk/portal/da/publications/genomewide-association-study-of-diabetic-kidney-disease-highlights-biology-involved-in-glomerular-basement-membrane-collagen(b30453e6-4f70-4b36-83fd-2afa1bcee756).html
Autor:
Jihwan Park, Angelo J. Canty, Robert G. Nelson, Vita Rovīte, Anna Möllsten, Peter Rossing, Linda T Hiraki, Katalin Susztak, Ronald Klein, Shelley B. Bull, Jan Skupien, Jani K. Haukka, Andrew D. Paterson, Niina Sandholm, Catherine Godson, Athina Spiliopoulou, A. Peter Maxwell, Suna Onengut-Gumuscu, Tina Costacou, Harvest F. Gu, Andrew P. Boright, Barbara E.K. Klein, Rany M. Salem, David-Alexandre Trégouët, Carine M. Boustany-Kari, Lina Radzeviciene, Ross Doyle, Valma Harjutsalo, Hyun Min Kang, Gareth J. McKay, Rachel G. Miller, Jose C. Florez, Jennifer N. Todd, Maria Luiza Caramori, Leif Groop, Eoin P. Brennan, Andrzej Krolewski, Maria Lajer, Rajasree Menon, Jelizaveta Sokolovska, Michel Marre, Darrel Andrews, Dcct, Wei-Min Chen, Emma Ahlqvist, Maria Hughes, Raimund Weitgasser, Andrew S.K. Liu, Jingchuan Guo, Edita Prakapiene, Viji Nair, Matthias Kretzler, Bernhard Paulweber, Chen Di Liao, Ian H. de Boer, Jing Jing Cao, Valdis Pīrāgs, Gianpaolo Zerbini, Mark I. McCarthy, Stephen S. Rich, Tarunveer S. Ahluwalia, Janet K. Snell-Bergeon, Joel N. Hirschhorn, Colin N. A. Palmer, F Martin, Kerstin Brismar, Beata Gyorgy, Adam M. Smiles, David M. Maahs, Michael Mauer, Kristine E. Lee, Joanne B. Cole, Per-Henrik Groop, Rasa Verkauskiene, Marcus G. Pezzolesi, Xiaoyu Gao, Paul M. McKeigue, Henrik Falhammar, Stuart J. McGurnaghan, Erkka Valo, Silvia Maeastroni, Lars Stechemesser, Helen M. Colhoun, Natalie R. van Zuydam, Amy J. McKnight, Chengxiang Qiu, Carol Forsblom, Nicolae Mircea Panduru, Samy Hadjadj
Diabetic kidney disease (DKD) is a heritable but poorly understood complication of diabetes. To identify genetic variants predisposing to DKD, we performed genome-wide association analyses in 19,406 individuals with type 1 diabetes (T1D) using a spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::237f22af230d972819585a6a36b1f76c
https://doi.org/10.1101/499616
https://doi.org/10.1101/499616
Autor:
N. Silvers, Patricia A. Cleary, Gail Musen, Christopher M. Ryan, Alan M. Jacobson, William Dahms, J. Harth, Barbara H. Waberski, Andrew D. Paterson, Meg Bayless, Katie Weinger, Andrew P. Boright
Publikováno v:
Diabetic Medicine. 27:15-22
Diabet. Med. 27, 15–22 (2010) Abstract Aims Specific polymorphisms of the apolipoprotein E (APOE) and angiotensin-converting enzyme (ACE) genes appear to increase risk for Alzheimer’s disease and cognitive dysfunction in the general population, y
Autor:
Maria F. Lopes-Virella, Andrew D. Paterson, Lei Sun, Andrew P. Boright, Daryl Waggott, Lucia Mirea, Shelley B. Bull, Rickey E. Carter, S. Mohsen Hosseini, Bhupinder Bharaj, Enqing Shen
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 29:1958-1967
Background— Elevated serum soluble E-selectin levels have been associated with a number of diseases. Although E-selectin levels are heritable, little is known about the specific genetic factors involved. E-selectin levels have been associated with
Autor:
John M. Lachin, Isidro Wong, Bhupinder Bharaj, Enqing Shen, Angelo J. Canty, Patricia A. Cleary, Nancy J. Cox, Dan L. Nicolae, Daryl Waggott, Jennifer E. Below, Lei Sun, Shelley B. Bull, S. Mohsen Hosseini, Marie-Pierre Sylvestre, Andrew D. Paterson, Andrew P. Boright
Publikováno v:
Diabetes. 59:539-549
OBJECTIVE Glycemia is a major risk factor for the development of long-term complications in type 1 diabetes; however, no specific genetic loci have been identified for glycemic control in individuals with type 1 diabetes. To identify such loci in typ
Autor:
Daryl Waggott, Masahiko Kure, Pisut Katavetin, Michael L. Merchant, James H. Warram, Jonathon Dunn, Andrew D. Paterson, Alessandro Doria, Krzysztof Wanic, Jacek Bochenski, Shelley B. Bull, John J. Rogus, G. David Poznik, William H. Walker, Paweł Wołkow, Daniel P.K. Ng, Jon B. Klein, Adam M. Smiles, Stephen S. Rich, Marcus G. Pezzolesi, Michelle T. Barati, Luis Henrique Santos Canani, Andrew P. Boright, Lucia Mirea, Grzegorz Placha, Bozena Krolewski, Josyf C. Mychaleckyj, Andrzej S. Krolewski
Publikováno v:
Diabetes
OBJECTIVE Despite extensive evidence for genetic susceptibility to diabetic nephropathy, the identification of susceptibility genes and their variants has had limited success. To search for genes that contribute to diabetic nephropathy, a genome-wide
Autor:
Michael Ho, Alireza Mowjoodi, Michael W. Steffes, Rinku Sutradhar, Bhupinder Bharaj, A. Peter Maxwell, Amy Jayne McKnight, William C. Speed, Lei Sun, Judith R. Kidd, Patricia A. Cleary, Paul S. Thorner, Jean M. Bucksa, Michelle Liu, Trevor J. Orchard, Xinlei Xie, Wanjie Sun, Hussam Al-Kateb, Rachel G. Miller, David A. Savage, Valerie L. Arends, Shelley B. Bull, Andrew D. Paterson, Andrew P. Boright, Kenneth K. Kidd, Lucia Mirea, John M. Lachin
Publikováno v:
Diabetes. 57:218-228
BACKGROUND— Despite familial clustering of nephropathy and retinopathy severity in type 1 diabetes, few gene variants have been consistently associated with these outcomes. RESEARCH DESIGN AND METHODS— We performed an individual-based genetic ass
Autor:
Xinlei Xie, Shelley B. Bull, Lei Sun, Lucia Mirea, Andrew D. Paterson, Hongtao Chen, Andrew P. Boright, Hussam Al-Kateb, Michelle Liu
Publikováno v:
Diabetes. 56:2161-2168
OBJECTIVE—We sought to determine if any common variants in the gene for vascular endothelial growth factor (VEGFA) are associated with long-term renal and retinal complications in type 1 diabetes. RESEARCH DESIGN AND METHODS—A total of 1,369 Cauc