Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Adrienne, Tin"'
Autor:
Elena V. Feofanova, Pascal Schlosser, Bing Yu, Anna Köttgen, Josef Coresh, Morgan E. Grams, Shengyuan Luo, Adrienne Tin, Dan E. Arking, Sarah Tung, Aditya Surapaneni, Yong Li, Eugene P. Rhee
Publikováno v:
Kidney Int
The genome-wide association study (GWAS) is a powerful means to study genetic determinants of disease traits and generate insights into disease pathophysiology. To date, few GWAS of circulating metabolite levels have been performed in African America
Autor:
Eric Boerwinkle, Josef Coresh, Nilanjan Chatterjee, Zhi Yu, Alexander Teumer, Morgan E. Grams, Anna Köttgen, Guanghao Qi, Cristian Pattaro, Harold Snieder, Adrienne Tin
Publikováno v:
Kidney International, 98(3), 708-716. ELSEVIER SCIENCE INC
Kidney Int
Kidney Int
Blood pressure and kidney function have a bidirectional relation. Hypertension has long been considered as a risk factor for kidney function decline. However, whether intensive blood pressure control could promote kidney health has been uncertain. Th
Autor:
Mallory D. Witt, Joseph B. Margolick, Alison G. Abraham, Adrienne Tin, Long Zhang, Lisa P. Jacobson, Todd T. Brown, Frank J. Palella, Lawrence A. Kingsley, Andrew N. Hoofnagle
Publikováno v:
AIDS Research and Human Retroviruses. 34:1067-1074
The inflammatory context of HIV infection has been posited to contribute to the higher comorbidity risk noted in HIV-infected populations. One possible pathway may involve 1,25-dihydroxyvitamin D [1,25(OH)(2)D], which plays a wide biologic role in ma
Autor:
Lukas Habegger, Charumathi Sabanayagam, Michael Preuss, Laura M. Raffield, Mary F. Feitosa, Bamidele O. Tayo, Kevin Ho, Leo-Pekka Lyytikäinen, Florian Kronenberg, Valencia Hui Xian Foo, Adrienne Tin, Michael Cantor, Nisha Bansal, Tarunveer S. Ahluwalia, Melanie Waldenberger, Sarah A. Pendergrass, Behrooz Z. Alizadeh, Wolfgang Koenig, Qiong Yang, Xiaodong Bai, Christoph Wanner, Ben Schöttker, Giovanni Coppola, A. R. Shuldiner, Leslie A. Lange, Piyush Gampawar, Markus Scholz, Tien Yin Wong, Mary L. Biggs, Morris Swertz, Alicia Hawes, Girish N. Nadkarni, Christina-Alexandra Schulz, Chiea Chuen Khor, Ricardo H. Ulloa, Jeffrey C. Staples, Miao-Li Chee, Laura M. Yerges-Armstrong, Andrew Blumenfeld, Karlhans Endlich, Bernhard Banas, Bruce H.R. Wolffenbuttel, Kai-Uwe Eckardt, Pavel Hamet, Carsten A. Böger, Harold Snieder, Marcus B. Jones, Judy Wang, Shih-Jen Hwang, Mathias Gorski, Anselm Hoppmann, Josyf C. Mychaleckyj, Bernd Holleczek, Pamela R. Matias-Garcia, Rainer Rettig, Karsten B. Sieber, Manasi Pradhan, Pashupati P. Mishra, Peter Rossing, Matthias Wuttke, Miao-Ling Chee, H. Marike Boezen, Yong Li, M. Arfan Ikram, Jeffrey G. Reid, Teresa Nutile, Maria Sotiropoulos Padilla, Lude Franke, Robert J. Carroll, Luca A. Lotta, Bernhard K. Krämer, Kjell Nikus, Jerome I. Rotter, Thomas Meitinger, Lars Wallentin, Cisca Wijmenga, Kent D. Taylor, Holly Kramer, Louis Widom, Olli T. Raitakari, Marcus E. Kleber, Man Li, Nina Hutri-Kähönen, Massimiliano Cocca, Reinhold Schmidt, John D. Overton, Cristian Pattaro, Michael Lattari, Sarah E. Wolf, Jin-Fang Chai, Karina Toledo, Brigitte Kühnel, Zhenhua Gu, Peter Almgren, Caitlin Forsythe, Yuri Milaneschi, Stephan J. L. Bakker, Layal Chaker, Dawn M. Waterworth, Silke Szymczak, James G. Wilson, Peter J. van der Most, Michelle L. O'Donoghue, William Salerno, Masayuki Yasuda, Sahar Ghasemi, Eric Boerwinkle, Josef Coresh, Ilja M. Nolte, Kia Manoochehri, Konstantin Strauch, Thomas D. Schleicher, Myriam Rheinberger, Audrey Y. Chu, Sanaz Sedaghat, Sandra Freitag-Wolf, Boting Ning, Matthias Nauck, Christina Beechert, Helena Schmidt, Harvey D. White, Nina Mononen, Johanne Tremblay, Navya Shilpa Josyula, Mika Kähönen, Katrin Horn, Andre Franke, Marianne Rots, Bettina Jung, Alexander R. Rosenkranz, Christian M. Shaffer, Mary Ann Lukas, Gerjan Navis, Christian Gieger, John Chalmers, Shareef Khalid, Uwe Völker, Marju Orho-Melander, Iris M. Heid, Brenda W.J.H. Penninx, A. Baras, Alexander Lopez, Evan Maxwell, Ruth J. F. Loos, Erin D. Fuller, Christa Meisinger, Gonçalo R. Abecasis, Suganthi Balasubramanian, Chris H. L. Thio, Martin H. de Borst, Stefan Coassin, Ching-Yu Cheng, Wolfgang Lieb, Kenneth Rice, Alexander Teumer, Mark Woodward, Gisu Eom, Hermann Brenner, Thomas W. Winkler, Anna Köttgen, Edith Hofer, Aris Economides, Ron T. Gansevoort, Pim van der Harst, Lyndon J. Mitnaul, Bruce M. Psaty, Erwin P. Bottinger, Olle Melander, Niek Verweij, Frauke Degenhardt, Yan Zhang, Mohsen Ghanbari, Veronika Wanner, Terho Lehtimäki, Leland Barnard
Publikováno v:
Gorski, M, Jung, B, Li, Y, Matias-Garcia, P R, Wuttke, M, Coassin, S, Thio, C H L, Kleber, M E, Winkler, T W, Wanner, V, Chai, J-F, Chu, A Y, Cocca, M, Feitosa, M F, Ghasemi, S, Hoppmann, A, Horn, K, Li, M, Nutile, T, Scholz, M, Sieber, K B, Teumer, A, Tin, A, Wang, J, Tayo, B O, Ahluwalia, T S, Almgren, P, Bakker, S J L, Banas, B, Bansal, N, Biggs, M L, Boerwinkle, E, Bottinger, E P, Brenner, H, Carroll, R J, Chalmers, J, Chee, M-L, Chee, M-L, Cheng, C-Y, Coresh, J, de Borst, M H, Degenhardt, F, Eckardt, K-U, Endlich, K, Franke, A, Freitag-Wolf, S, Gampawar, P, Gansevoort, R T, Loos, R J F, Rossing, P & LifeLines Cohort Study 2021, ' Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline ', Kidney International, vol. 99, no. 4, pp. 926-939 . https://doi.org/10.1016/j.kint.2020.09.030
Kidney international (2020). doi:10.1016/j.kint.2020.09.030
info:cnr-pdr/source/autori:Mathias Gorski et al/titolo:Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline/doi:10.1016%2Fj.kint.2020.09.030/rivista:Kidney international/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume
Kidney International
Lifelines Cohort Study & Regeneron Genetics Center 2021, ' Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline ', Kidney International, vol. 99, no. 4, pp. 926-939 . https://doi.org/10.1016/j.kint.2020.09.030
Kidney International, 99(4), 926-939. ELSEVIER SCIENCE INC
Kidney International, 99(4), 926-939. Elsevier Inc.
Kidney International, 99(4), 926-939. Nature Publishing Group
Kidney international (2020). doi:10.1016/j.kint.2020.09.030
info:cnr-pdr/source/autori:Mathias Gorski et al/titolo:Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline/doi:10.1016%2Fj.kint.2020.09.030/rivista:Kidney international/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume
Kidney International
Lifelines Cohort Study & Regeneron Genetics Center 2021, ' Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline ', Kidney International, vol. 99, no. 4, pp. 926-939 . https://doi.org/10.1016/j.kint.2020.09.030
Kidney International, 99(4), 926-939. ELSEVIER SCIENCE INC
Kidney International, 99(4), 926-939. Elsevier Inc.
Kidney International, 99(4), 926-939. Nature Publishing Group
Rapid decline of glomerular filtration rate estimated from creatinine (eGFRcrea) is associated with severe clinical endpoints. In contrast to cross-sectionally assessed eGFRcrea, the genetic basis for rapid eGFRcrea decline is largely unknown. To hel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfe030174e9e300043a2bda6960bc9c1
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-430992
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-430992
Autor:
Stefan Haug, Pascal Schlosser, Matthias Wuttke, Alexander Teumer, Cristian Pattaro, Yong Li, Anna Köttgen, Adrienne Tin
Publikováno v:
J Am Soc Nephrol
Background Genetic variants identified in genome-wide association studies (GWAS) are often not specific enough to reveal complex underlying physiology. By integrating RNA-seq data and GWAS summary statistics, novel computational methods allow unbiase
Autor:
Jingsha Chen, Casey M. Rebholz, Jiun-Ruey Hu, Morgan E. Grams, Lawrence J. Appel, Andrew S. Levey, Mark J. Sarnak, Josef Coresh, Zihe Zheng, Adrienne Tin, Lesley A. Inker
Publikováno v:
Kidney International. 94:381-389
Chronic kidney disease (CKD) involves significant metabolic abnormalities and has a high mortality rate. Because the levels of serum metabolites in patients with CKD might provide insight into subclinical disease states and risk for future mortality,
Autor:
James S. Pankow, Chen Yao, Pascal Schlosser, Daniel Levy, Shih-Jen Hwang, Qiong Yang, Eric Boerwinkle, Caroline Gluck, Morgan E. Grams, Josef Coresh, Myriam Fornage, Anna Köttgen, Audrey Y. Chu, Yi-An Ko, Chengxiang Qiu, Roby Joehanes, Adrienne Tin, Chunyu Liu, Liming Liang, Caroline S. Fox, Katalin Susztak
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-12 (2017)
Chronic kidney disease (CKD) is defined by reduced estimated glomerular filtration rate (eGFR). Previous genetic studies have implicated regulatory mechanisms contributing to CKD. Here we present epigenome-wide association studies of eGFR and CKD usi
Autor:
Jeffery Hunter Young, Adrienne Tin, Jeremy K. Nicholson, Queenie Chan, Gonçalo D S Correia, Paul Elliott, Elaine Holmes, Anisha Wijeyesekera, Elena Chekmeneva
Publikováno v:
Journal of Proteome Research
Large-scale metabolic profiling requires the development of novel economical high-throughput analytical methods to facilitate characterization of systemic metabolic variation in population phenotypes. We report a fit-for-purpose direct infusion nanoe
Autor:
Alex R. Chang, Yanfei Zhang, Adrienne Tin, Ming Ta Michael Lee, Waleed Zafar, Dustin N. Hartzel, Marc S. Williams
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Frontiers in Genetics
Frontiers in Genetics
Deletion of glutathione S-transferase µ1 (GSTM1) is common in populations and has been asserted to associate with chronic kidney disease progression in some research studies. The association needs to be validated. We estimated GSTM1 copy number usin
Autor:
Elizabeth Selvin, Priya Duggal, Josef Coresh, Eric Boerwinkle, Richard A. Gibbs, Adrienne Tin, Stephanie J. Loomis, Donna M. Muzny, Man Li, Anna Köttgen, James S. Pankow
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Serum 1,5-anhydroglucitol (1,5-AG) is an emerging biomarker used to monitor glycemic control in persons with diabetes. We performed whole-exome sequencing, examining the association between rare, coding genetic variants and 1,5-AG among European ance