Zobrazeno 1 - 10
of 352
pro vyhledávání: '"Sudha K Iyengar"'
Autor:
Radhika Krishnan, Astha Jain, Siddhita Nare, Rajkumar Sankaranarayanan, Jacquelaine Bartlett, Sudha K Iyengar, Scott M Williams, Natarajan Sundaram
Publikováno v:
PLOS Global Public Health, Vol 3, Iss 4, p e0000351 (2023)
Diabetes onset precedes diabetic retinopathy (DR) by 5-10 years, but many people with diabetes remain free of this microvascular complication. Our aim was to identify risk factors for DR progression in a unique and diverse population, the slums of Mu
Externí odkaz:
https://doaj.org/article/3d054c9e8e544ce1badbecee2eae2c73
Autor:
Anurag Verma, Noah L Tsao, Lauren O Thomann, Yuk-Lam Ho, Sudha K Iyengar, Shiuh-Wen Luoh, Rotonya Carr, Dana C Crawford, Jimmy T Efird, Jennifer E Huffman, Adriana Hung, Kerry L Ivey, Michael G Levin, Julie Lynch, Pradeep Natarajan, Saiju Pyarajan, Alexander G Bick, Lauren Costa, Giulio Genovese, Richard Hauger, Ravi Madduri, Gita A Pathak, Renato Polimanti, Benjamin Voight, Marijana Vujkovic, Seyedeh Maryam Zekavat, Hongyu Zhao, Marylyn D Ritchie, VA Million Veteran Program COVID-19 Science Initiative, Kyong-Mi Chang, Kelly Cho, Juan P Casas, Philip S Tsao, J Michael Gaziano, Christopher O'Donnell, Scott M Damrauer, Katherine P Liao
Publikováno v:
PLoS Genetics, Vol 18, Iss 4, p e1010113 (2022)
The study aims to determine the shared genetic architecture between COVID-19 severity with existing medical conditions using electronic health record (EHR) data. We conducted a Phenome-Wide Association Study (PheWAS) of genetic variants associated wi
Externí odkaz:
https://doaj.org/article/ffdb9e4bf94d4c729a4428cb28eaf0c9
Autor:
E. Ricky Chan, Penelope Benchek, Gabrielle Miller, Kim Brustoski, Ashleigh Schaffer, Barbara Truitt, Jessica Tag, Lisa Freebairn, Barbara A. Lewis, Catherine M. Stein, Sudha K. Iyengar
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-13 (2024)
Abstract Childhood apraxia of speech (CAS) is a severe and rare form of speech sound disorder (SSD). CAS is typically sporadic, but may segregate in families with broader speech and language deficits. We hypothesize that genetic changes may be involv
Externí odkaz:
https://doaj.org/article/400fb69bb6e74c66b15212f4f8ec8dbd
Autor:
Theru A Sivakumaran, Robert P Igo, Jeffrey M Kidd, Andy Itsara, Laura J Kopplin, Wei Chen, Stephanie A Hagstrom, Neal S Peachey, Peter J Francis, Michael L Klein, Emily Y Chew, Vedam L Ramprasad, Wan-Ting Tay, Paul Mitchell, Mark Seielstad, Dwight E Stambolian, Albert O Edwards, Kristine E Lee, Dmitry V Leontiev, Gyungah Jun, Yang Wang, Liping Tian, Feiyou Qiu, Alice K Henning, Thomas LaFramboise, Parveen Sen, Manoharan Aarthi, Ronnie George, Rajiv Raman, Manmath Kumar Das, Lingam Vijaya, Govindasamy Kumaramanickavel, Tien Y Wong, Anand Swaroop, Goncalo R Abecasis, Ronald Klein, Barbara E K Klein, Deborah A Nickerson, Evan E Eichler, Sudha K Iyengar
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0209943 (2018)
[This corrects the article DOI: 10.1371/journal.pone.0025598.].
Externí odkaz:
https://doaj.org/article/3f840f4e244c4d6187538a538daff490
Autor:
Sudha K Iyengar, John R Sedor, Barry I Freedman, W H Linda Kao, Matthias Kretzler, Benjamin J Keller, Hanna E Abboud, Sharon G Adler, Lyle G Best, Donald W Bowden, Allison Burlock, Yii-Der Ida Chen, Shelley A Cole, Mary E Comeau, Jeffrey M Curtis, Jasmin Divers, Christiane Drechsler, Ravi Duggirala, Robert C Elston, Xiuqing Guo, Huateng Huang, Michael Marcus Hoffmann, Barbara V Howard, Eli Ipp, Paul L Kimmel, Michael J Klag, William C Knowler, Orly F Kohn, Tennille S Leak, David J Leehey, Man Li, Alka Malhotra, Winfried März, Viji Nair, Robert G Nelson, Susanne B Nicholas, Stephen J O'Brien, Madeleine V Pahl, Rulan S Parekh, Marcus G Pezzolesi, Rebekah S Rasooly, Charles N Rotimi, Jerome I Rotter, Jeffrey R Schelling, Michael F Seldin, Vallabh O Shah, Adam M Smiles, Michael W Smith, Kent D Taylor, Farook Thameem, Denyse P Thornley-Brown, Barbara J Truitt, Christoph Wanner, E Jennifer Weil, Cheryl A Winkler, Philip G Zager, Robert P Igo, Robert L Hanson, Carl D Langefeld, Family Investigation of Nephropathy and Diabetes (FIND)
Publikováno v:
PLoS Genetics, Vol 11, Iss 8, p e1005352 (2015)
Diabetic kidney disease (DKD) is the most common etiology of chronic kidney disease (CKD) in the industrialized world and accounts for much of the excess mortality in patients with diabetes mellitus. Approximately 45% of U.S. patients with incident e
Externí odkaz:
https://doaj.org/article/60f7e3700dd5412789cd4b99b548f387
Autor:
Maggie C Y Ng, Daniel Shriner, Brian H Chen, Jiang Li, Wei-Min Chen, Xiuqing Guo, Jiankang Liu, Suzette J Bielinski, Lisa R Yanek, Michael A Nalls, Mary E Comeau, Laura J Rasmussen-Torvik, Richard A Jensen, Daniel S Evans, Yan V Sun, Ping An, Sanjay R Patel, Yingchang Lu, Jirong Long, Loren L Armstrong, Lynne Wagenknecht, Lingyao Yang, Beverly M Snively, Nicholette D Palmer, Poorva Mudgal, Carl D Langefeld, Keith L Keene, Barry I Freedman, Josyf C Mychaleckyj, Uma Nayak, Leslie J Raffel, Mark O Goodarzi, Y-D Ida Chen, Herman A Taylor, Adolfo Correa, Mario Sims, David Couper, James S Pankow, Eric Boerwinkle, Adebowale Adeyemo, Ayo Doumatey, Guanjie Chen, Rasika A Mathias, Dhananjay Vaidya, Andrew B Singleton, Alan B Zonderman, Robert P Igo, John R Sedor, FIND Consortium, Edmond K Kabagambe, David S Siscovick, Barbara McKnight, Kenneth Rice, Yongmei Liu, Wen-Chi Hsueh, Wei Zhao, Lawrence F Bielak, Aldi Kraja, Michael A Province, Erwin P Bottinger, Omri Gottesman, Qiuyin Cai, Wei Zheng, William J Blot, William L Lowe, Jennifer A Pacheco, Dana C Crawford, eMERGE Consortium, DIAGRAM Consortium, Elin Grundberg, MuTHER Consortium, Stephen S Rich, M Geoffrey Hayes, Xiao-Ou Shu, Ruth J F Loos, Ingrid B Borecki, Patricia A Peyser, Steven R Cummings, Bruce M Psaty, Myriam Fornage, Sudha K Iyengar, Michele K Evans, Diane M Becker, W H Linda Kao, James G Wilson, Jerome I Rotter, Michèle M Sale, Simin Liu, Charles N Rotimi, Donald W Bowden, MEta-analysis of type 2 DIabetes in African Americans Consortium
Publikováno v:
PLoS Genetics, Vol 10, Iss 8, p e1004517 (2014)
Type 2 diabetes (T2D) is more prevalent in African Americans than in Europeans. However, little is known about the genetic risk in African Americans despite the recent identification of more than 70 T2D loci primarily by genome-wide association studi
Externí odkaz:
https://doaj.org/article/56bb7be103094e20a1ebafe269f259c2
Autor:
Farook Thameem, Robert P Igo, Barry I Freedman, Carl Langefeld, Robert L Hanson, Jeffrey R Schelling, Robert C Elston, Ravindranath Duggirala, Susanne B Nicholas, Katrina A B Goddard, Jasmin Divers, Xiuqing Guo, Eli Ipp, Paul L Kimmel, Lucy A Meoni, Vallabh O Shah, Michael W Smith, Cheryl A Winkler, Philip G Zager, William C Knowler, Robert G Nelson, Madeline V Pahl, Rulan S Parekh, W H Linda Kao, Rebekah S Rasooly, Sharon G Adler, Hanna E Abboud, Sudha K Iyengar, John R Sedor, Family Investigation of Nephropathy and Diabetes Research Group
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e81888 (2013)
Estimated glomerular filtration rate (eGFR), a measure of kidney function, is heritable, suggesting that genes influence renal function. Genes that influence eGFR have been identified through genome-wide association studies. However, family-based lin
Externí odkaz:
https://doaj.org/article/918ae96f77ff4b0ead41503b95daf6bf
Autor:
Robert P Igo, Laura J Kopplin, Peronne Joseph, Barbara Truitt, Jeremy Fondran, David Bardenstein, Anthony J Aldave, Christopher R Croasdale, Marianne O Price, Miriam Rosenwasser, Jonathan H Lass, Sudha K Iyengar, FECD Genetics Multi-center Study Group
Publikováno v:
PLoS ONE, Vol 7, Iss 10, p e46742 (2012)
Fuchs endothelial corneal dystrophy (FECD) is the most common late-onset, vision-threatening corneal dystrophy in the United States, affecting about 4% of the population. Advanced FECD involves a thickening of the cornea from stromal edema and change
Externí odkaz:
https://doaj.org/article/70f3b8eeefee4eff94c5c8752ca8c5bf
Autor:
Theru A Sivakumaran, Robert P Igo, Jeffrey M Kidd, Andy Itsara, Laura J Kopplin, Wei Chen, Stephanie A Hagstrom, Neal S Peachey, Peter J Francis, Michael L Klein, Emily Y Chew, Vedam L Ramprasad, Wan-Ting Tay, Paul Mitchell, Mark Seielstad, Dwight E Stambolian, Albert O Edwards, Kristine E Lee, Dmitry V Leontiev, Gyungah Jun, Yang Wang, Liping Tian, Feiyou Qiu, Alice K Henning, Thomas LaFramboise, Parveen Sen, Manoharan Aarthi, Ronnie George, Rajiv Raman, Manmath Kumar Das, Lingam Vijaya, Govindasamy Kumaramanickavel, Tien Y Wong, Anand Swaroop, Goncalo R Abecasis, Ronald Klein, Barbara E K Klein, Deborah A Nickerson, Evan E Eichler, Sudha K Iyengar
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e25598 (2011)
Complement factor H shows very strong association with Age-related Macular Degeneration (AMD), and recent data suggest that multiple causal variants are associated with disease. To refine the location of the disease associated variants, we characteri
Externí odkaz:
https://doaj.org/article/850e56f68fac421fb62b9945cb62ab2c
Autor:
M Kamran Ikram, Xueling Sim, Richard A Jensen, Mary Frances Cotch, Alex W Hewitt, M Arfan Ikram, Jie Jin Wang, Ronald Klein, Barbara E K Klein, Monique M B Breteler, Ning Cheung, Gerald Liew, Paul Mitchell, Andre G Uitterlinden, Fernando Rivadeneira, Albert Hofman, Paulus T V M de Jong, Cornelia M van Duijn, Linda Kao, Ching-Yu Cheng, Albert Vernon Smith, Nicole L Glazer, Thomas Lumley, Barbara McKnight, Bruce M Psaty, Fridbert Jonasson, Gudny Eiriksdottir, Thor Aspelund, Global BPgen Consortium, Tamara B Harris, Lenore J Launer, Kent D Taylor, Xiaohui Li, Sudha K Iyengar, Quansheng Xi, Theru A Sivakumaran, David A Mackey, Stuart Macgregor, Nicholas G Martin, Terri L Young, Josh C Bis, Kerri L Wiggins, Susan R Heckbert, Christopher J Hammond, Toby Andrew, Samantha Fahy, John Attia, Elizabeth G Holliday, Rodney J Scott, F M Amirul Islam, Jerome I Rotter, Annie K McAuley, Eric Boerwinkle, E Shyong Tai, Vilmundur Gudnason, David S Siscovick, Johannes R Vingerling, Tien Y Wong
Publikováno v:
PLoS Genetics, Vol 6, Iss 10, p e1001184 (2010)
There is increasing evidence that the microcirculation plays an important role in the pathogenesis of cardiovascular diseases. Changes in retinal vascular caliber reflect early microvascular disease and predict incident cardiovascular events. We perf
Externí odkaz:
https://doaj.org/article/4bf4067a29b347a382d33d4accfb1e43