Zobrazeno 1 - 10
of 296
pro vyhledávání: '"Ewa Deelman"'
Autor:
Sarah A Pendergrass, Steven Buyske, Janina M Jeff, Alex Frase, Scott Dudek, Yuki Bradford, Jose-Luis Ambite, Christy L Avery, Petra Buzkova, Ewa Deelman, Megan D Fesinmeyer, Christopher Haiman, Gerardo Heiss, Lucia A Hindorff, Chun-Nan Hsu, Rebecca D Jackson, Yi Lin, Loic Le Marchand, Tara C Matise, Kristine R Monroe, Larry Moreland, Kari E North, Sungshim L Park, Alex Reiner, Robert Wallace, Lynne R Wilkens, Charles Kooperberg, Marylyn D Ritchie, Dana C Crawford
Publikováno v:
PLoS ONE, Vol 14, Iss 12, p e0226771 (2019)
We performed a hypothesis-generating phenome-wide association study (PheWAS) to identify and characterize cross-phenotype associations, where one SNP is associated with two or more phenotypes, between thousands of genetic variants assayed on the Meta
Externí odkaz:
https://doaj.org/article/d1011295931b4e4fb3037f3c735bbbb4
Autor:
Unhee Lim, Jonathan M Kocarnik, William S Bush, Tara C Matise, Christian Caberto, Sungshim Lani Park, Christopher S Carlson, Ewa Deelman, David Duggan, Megan Fesinmeyer, Christopher A Haiman, Brian E Henderson, Lucia A Hindorff, Laurence N Kolonel, Ulrike Peters, Daniel O Stram, Maarit Tiirikainen, Lynne R Wilkens, Chunyuan Wu, Charles Kooperberg, Loïc Le Marchand
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e89791 (2014)
Risk of non-Hodgkin lymphoma (NHL) is higher among individuals with a family history or a prior diagnosis of other cancers. Genome-wide association studies (GWAS) have suggested that some genetic susceptibility variants are associated with multiple c
Externí odkaz:
https://doaj.org/article/53e5c007be0f4ae58066a720fecbce12
Autor:
Sarah A Pendergrass, Kristin Brown-Gentry, Scott Dudek, Alex Frase, Eric S Torstenson, Robert Goodloe, Jose Luis Ambite, Christy L Avery, Steve Buyske, Petra Bůžková, Ewa Deelman, Megan D Fesinmeyer, Christopher A Haiman, Gerardo Heiss, Lucia A Hindorff, Chu-Nan Hsu, Rebecca D Jackson, Charles Kooperberg, Loic Le Marchand, Yi Lin, Tara C Matise, Kristine R Monroe, Larry Moreland, Sungshim L Park, Alex Reiner, Robert Wallace, Lynn R Wilkens, Dana C Crawford, Marylyn D Ritchie
Publikováno v:
PLoS Genetics, Vol 9, Iss 1, p e1003087 (2013)
Using a phenome-wide association study (PheWAS) approach, we comprehensively tested genetic variants for association with phenotypes available for 70,061 study participants in the Population Architecture using Genomics and Epidemiology (PAGE) network
Externí odkaz:
https://doaj.org/article/c6158d1a2b2546dfaf4fd8c71d1e4d61
Autor:
Veronica Wendy Setiawan, Jeffrey Haessler, Fredrick Schumacher, Michele L Cote, Ewa Deelman, Megan D Fesinmeyer, Brian E Henderson, Rebecca D Jackson, Jens-S Vöckler, Lynne R Wilkens, Shagufta Yasmeen, Christopher A Haiman, Ulrike Peters, Loïc Le Marchand, Charles Kooperberg
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e30390 (2012)
We examined the association between HNF1B variants identified in a recent genome-wide association study and endometrial cancer in two large case-control studies nested in prospective cohorts: the Multiethnic Cohort Study (MEC) and the Women's Health
Externí odkaz:
https://doaj.org/article/5bdf54c8c3b040f08cfe9297481e716a
Autor:
Alicia Esquivel Morel, Chengyi Qu, Prasad Calyam, Cong Wang, Komal Thareja, Anirban Mandal, Eric Lyons, Michael Zink, George Papadimitriou, Ewa Deelman
Publikováno v:
IEEE Internet Computing. 27:35-43
Autor:
Sandra Gesing, Ewa Deelman, Michael Hildreth, Ramandeep Makhija, Mary Ann McDowell, Natalie K. Meyers, Douglas Thain
Publikováno v:
Computing in Science & Engineering. :1-5
Autor:
Shelley L. Knuth, Julie Ma, Joel C. Adams, Alan Chalker, Ewa Deelman, Layla Freeborn, Vikram Gazula, John Goodhue, James Griffioen, David Hudak, Andrew Pasquale, Dylan Perkins, Alana Romanella, Mats Rynge
Publikováno v:
The Journal of Computational Science Education. 13:17-20
Autor:
Ria Patel, Brandan Roachell, Silvina Caíno-Lores, Ross Ketron, Jacob Leonard, Nigel Tan, Karan Vahi, Duncan A. Brown, Ewa Deelman, Michela Taufer
Publikováno v:
Computing in Science & Engineering. 24:42-52
Autor:
Loïc Le Marchand, Iona Cheng, Charles Kooperberg, William S. Bush, Lynne R. Wilkens, Christopher A. Haiman, Dana C. Crawford, Gerardo Heiss, Kari E. North, Ulrike Peters, Ying Han, Ewa Deelman, Fridtjof Thomas, Lifang Hou, Chu Chen, Jennifer Beebe-Dimmer, Fredrick R. Schumacher, Jay H. Fowke, Lucia A. Hindorff, Tara C. Matise, Shelly-Ann Love, Logan Dumitrescu, Robert J. Goodloe, Yi Lin, Christian P. Caberto, S. Lani Park
Background: Multiple primary cancers account for approximately 16% of all incident cancers in the United States. Although genome-wide association studies (GWAS) have identified many common genetic variants associated with various cancer sites, no stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1228c60acc931c314f844ca39083ff
https://doi.org/10.1158/1055-9965.c.6514956
https://doi.org/10.1158/1055-9965.c.6514956
Autor:
Loïc Le Marchand, Iona Cheng, Charles Kooperberg, William S. Bush, Lynne R. Wilkens, Christopher A. Haiman, Dana C. Crawford, Gerardo Heiss, Kari E. North, Ulrike Peters, Ying Han, Ewa Deelman, Fridtjof Thomas, Lifang Hou, Chu Chen, Jennifer Beebe-Dimmer, Fredrick R. Schumacher, Jay H. Fowke, Lucia A. Hindorff, Tara C. Matise, Shelly-Ann Love, Logan Dumitrescu, Robert J. Goodloe, Yi Lin, Christian P. Caberto, S. Lani Park
Supplementary Table 1. Summary of Study Design and Case/Control Definitions for participating studies. Supplementary Table 2. Distribution of the incident index and second cancer site among incident multiple primary cancer cases, stratified by study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57ee0fdc6ed071ef55bea319957dc662
https://doi.org/10.1158/1055-9965.22435488
https://doi.org/10.1158/1055-9965.22435488