Zobrazeno 1 - 10
of 119
pro vyhledávání: '"Yi-Ping Fu"'
Autor:
Russell H. Knutsen, Leah M. Gober, Elise K. Kronquist, Maninder Kaur, Danielle R. Donahue, Danielle Springer, Zu Xi Yu, Marcus Y. Chen, Yi-Ping Fu, Feri Choobdar, My-Le Nguyen, Sharon Osgood, Joy L. Freeman, Neelam Raja, Mark D. Levin, Beth A. Kozel
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
BackgroundWilliams Beuren syndrome (WBS) is a recurrent microdeletion disorder that removes one copy of elastin (ELN), resulting in large artery vasculopathy. Early stenosis of the pulmonary vascular tree is common, but few data are available on long
Externí odkaz:
https://doaj.org/article/c78ace6652984ae09c04d4d5b7428a7c
Autor:
Elise K. Kronquist, Maninder Kaur, Leah M. Gober, Russell H. Knutsen, Yi-Ping Fu, Zu-Xi Yu, Danielle R. Donahue, Marcus Y. Chen, Sharon Osgood, Neelam Raja, Mark D. Levin, Amisha Barochia, Beth A. Kozel
Publikováno v:
Diagnostics, Vol 12, Iss 6, p 1438 (2022)
Williams–Beuren syndrome (WS) results from the deletion of 25–27 coding genes, including elastin (ELN), on human chromosome 7q11.23. Elastin provides recoil to tissues; emphysema and chronic obstructive pulmonary disease have been linked to its d
Externí odkaz:
https://doaj.org/article/22bc546de50a497e9af62410db397f9c
Autor:
Julie Hahn, Yi-Ping Fu, Michael R Brown, Joshua C Bis, Paul S de Vries, Mary F Feitosa, Lisa R Yanek, Stefan Weiss, Franco Giulianini, Albert Vernon Smith, Xiuqing Guo, Traci M Bartz, Diane M Becker, Lewis C Becker, Eric Boerwinkle, Jennifer A Brody, Yii-Der Ida Chen, Oscar H Franco, Megan Grove, Tamara B Harris, Albert Hofman, Shih-Jen Hwang, Brian G Kral, Lenore J Launer, Marcello R P Markus, Kenneth M Rice, Stephen S Rich, Paul M Ridker, Fernando Rivadeneira, Jerome I Rotter, Nona Sotoodehnia, Kent D Taylor, André G Uitterlinden, Uwe Völker, Henry Völzke, Jie Yao, Daniel I Chasman, Marcus Dörr, Vilmundur Gudnason, Rasika A Mathias, Wendy Post, Bruce M Psaty, Abbas Dehghan, Christopher J O'Donnell, Alanna C Morrison
Publikováno v:
PLoS ONE, Vol 15, Iss 11, p e0230035 (2020)
BackgroundGenome-wide association studies have identified multiple genomic loci associated with coronary artery disease, but most are common variants in non-coding regions that provide limited information on causal genes and etiology of the disease.
Externí odkaz:
https://doaj.org/article/9d94d892f87c4153a189fd83c7b58f38
Autor:
Cavin K Ward-Caviness, Paul S de Vries, Kerri L Wiggins, Jennifer E Huffman, Lisa R Yanek, Lawrence F Bielak, Franco Giulianini, Xiuqing Guo, Marcus E Kleber, Tim Kacprowski, Stefan Groß, Astrid Petersman, George Davey Smith, Fernando P Hartwig, Jack Bowden, Gibran Hemani, Martina Müller-Nuraysid, Konstantin Strauch, Wolfgang Koenig, Melanie Waldenberger, Thomas Meitinger, Nathan Pankratz, Eric Boerwinkle, Weihong Tang, Yi-Ping Fu, Andrew D Johnson, Ci Song, Moniek P M de Maat, André G Uitterlinden, Oscar H Franco, Jennifer A Brody, Barbara McKnight, Yii-Der Ida Chen, Bruce M Psaty, Rasika A Mathias, Diane M Becker, Patricia A Peyser, Jennifer A Smith, Suzette J Bielinski, Paul M Ridker, Kent D Taylor, Jie Yao, Russell Tracy, Graciela Delgado, Stella Trompet, Naveed Sattar, J Wouter Jukema, Lewis C Becker, Sharon L R Kardia, Jerome I Rotter, Winfried März, Marcus Dörr, Daniel I Chasman, Abbas Dehghan, Christopher J O'Donnell, Nicholas L Smith, Annette Peters, Alanna C Morrison
Publikováno v:
PLoS ONE, Vol 14, Iss 5, p e0216222 (2019)
BackgroundFibrinogen is an essential hemostatic factor and cardiovascular disease risk factor. Early attempts at evaluating the causal effect of fibrinogen on coronary heart disease (CHD) and myocardial infraction (MI) using Mendelian randomization (
Externí odkaz:
https://doaj.org/article/138107b510a249878e58480e248bba04
Autor:
Idan Menashe, Jonine D Figueroa, Montserrat Garcia-Closas, Nilanjan Chatterjee, Nuria Malats, Antoni Picornell, Dennis Maeder, Qi Yang, Ludmila Prokunina-Olsson, Zhaoming Wang, Francisco X Real, Kevin B Jacobs, Dalsu Baris, Michael Thun, Demetrius Albanes, Mark P Purdue, Manolis Kogevinas, Amy Hutchinson, Yi-Ping Fu, Wei Tang, Laurie Burdette, Adonina Tardón, Consol Serra, Alfredo Carrato, Reina García-Closas, Josep Lloreta, Alison Johnson, Molly Schwenn, Alan Schned, Gerald Andriole, Amanda Black, Eric J Jacobs, Ryan W Diver, Susan M Gapstur, Stephanie J Weinstein, Jarmo Virtamo, Neil E Caporaso, Maria Teresa Landi, Joseph F Fraumeni, Stephen J Chanock, Debra T Silverman, Nathaniel Rothman
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e29396 (2012)
Pathway analysis of genome-wide association studies (GWAS) offer a unique opportunity to collectively evaluate genetic variants with effects that are too small to be detected individually. We applied a pathway analysis to a bladder cancer GWAS contai
Externí odkaz:
https://doaj.org/article/83ba9e6c0bd540c49b4769911fdfbdeb
Autor:
Yi-Ping Fu, D. Michael Hallman, Victor H. Gonzalez, Barbara E. K. Klein, Ronald Klein, M. Geoffrey Hayes, Nancy J. Cox, Graeme I. Bell, Craig L. Hanis
Publikováno v:
Journal of Ophthalmology, Vol 2010 (2010)
To identify genetic loci for severe diabetic retinopathy, 286 Mexican-Americans with type 2 diabetes from Starr County, Texas, completed physical examinations including fundus photography for diabetic retinopathy grading. Individuals with moderate-to
Externí odkaz:
https://doaj.org/article/791d0e2412e5453788c06588e2c372c2
Autor:
Brenden S. Ingraham, Michael E. Farkouh, Ryan J. Lennon, Derek So, Shaun G. Goodman, Nancy Geller, Jang-Ho Bae, Myung Ho Jeong, Linnea M. Baudhuin, Verghese Mathew, Malcolm R. Bell, Amir Lerman, Yi-Ping Fu, Ahmed Hasan, Erin Iturriaga, Jean-Francois Tanguay, Robert C. Welsh, Yves Rosenberg, Kent Bailey, Charanjit Rihal, Naveen L. Pereira
Publikováno v:
JACC: Cardiovascular Interventions. 16:816-825
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba2a5ed06d9b9a7eaeeb4ecc6ec3d5c9
https://doi.org/10.1016/j.jcin.2023.01.356
https://doi.org/10.1016/j.jcin.2023.01.356
Autor:
Mark D. Levin, Brianna M. Cathey, Kevin Smith, Sharon Osgood, Neelam Raja, Yi-Ping Fu, Beth A. Kozel
Publikováno v:
JACC: Clinical Electrophysiology. 9:359-370
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73dae3d559bd74e421ee4a68558235a7
https://doi.org/10.1016/j.jacep.2022.10.010
https://doi.org/10.1016/j.jacep.2022.10.010
Autor:
Ananth V. Charya, Ileana L. Ponor, Adam Cochrane, Deborah Levine, Mary Philogene, Yi-Ping Fu, Moon K. Jang, Hyesik Kong, Pali Shah, Ann Mary Bon, Aravind Krishnan, Joby Mathew, Helen Luikart, Kiran K. Khush, Gerald Berry, Charles Marboe, Aldo Iacono, Jonathan B. Orens, Steven D. Nathan, Sean Agbor-Enoh
Publikováno v:
The Journal of Heart and Lung Transplantation. 42:226-235
Pulmonary antibody-mediated rejection (AMR) consensus criteria categorize AMR by diagnostic certainty. This study aims to define the clinical features and associated outcomes of these recently defined AMR categories.Adjudication committees reviewed c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03e7cc712a0fd63ff37a19f79dac9ff1
https://doi.org/10.1016/j.healun.2022.09.012
https://doi.org/10.1016/j.healun.2022.09.012
Autor:
Yifan Pang, Ananth V. Charya, Michael B. Keller, Arlene Sirajuddin, Yi-Ping Fu, Noa G. Holtzman, Steven Z. Pavletic, Sean Agbor-Enoh
Publikováno v:
Blood Advances. 6:4196-4207
Pulmonary chronic graft-versus-host disease (PcGVHD) is a devastating complication of allogeneic hematopoietic stem cell transplant (HCT). The 2014 National Institutes of Health cGVHD consensus criteria (NIH criteria) only captures bronchiolitis obli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3796b735d668427fcd78231942902ab2
https://doi.org/10.1182/bloodadvances.2021006885
https://doi.org/10.1182/bloodadvances.2021006885