Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Lana M. Olson"'
Autor:
Stephanie J. Loomis, Lana M. Olson, Louis R. Pasquale, Janey Wiggs, Daniel Mirel, Andrew Crenshaw, Melissa Parkin, Brandon Rahhal, Stephanie Tetreault, Peter Kraft, Shelley S. Tworoger, Jonathan L. Haines, Jae H. Kang
Publikováno v:
Biomarker Insights, Vol 2010, Iss 5, Pp 49-55 (2010)
It is unclear if buccal cell samples contain sufficient human DNA with adequately sized fragments for high throughput genetic bioassays. Yet buccal cell sample collection is an attractive alternative to gathering blood samples for genetic epidemiolog
Externí odkaz:
https://doaj.org/article/cd0710c23b6c466d925baefd987cad01
Autor:
Janey L Wiggs, Brian L Yaspan, Michael A Hauser, Jae H Kang, R Rand Allingham, Lana M Olson, Wael Abdrabou, Bao J Fan, Dan Y Wang, Wendy Brodeur, Donald L Budenz, Joseph Caprioli, Andrew Crenshaw, Kristy Crooks, Elizabeth Delbono, Kimberly F Doheny, David S Friedman, Douglas Gaasterland, Terry Gaasterland, Cathy Laurie, Richard K Lee, Paul R Lichter, Stephanie Loomis, Yutao Liu, Felipe A Medeiros, Cathy McCarty, Daniel Mirel, Sayoko E Moroi, David C Musch, Anthony Realini, Frank W Rozsa, Joel S Schuman, Kathleen Scott, Kuldev Singh, Joshua D Stein, Edward H Trager, Paul Vanveldhuisen, Douglas Vollrath, Gadi Wollstein, Sachiko Yoneyama, Kang Zhang, Robert N Weinreb, Jason Ernst, Manolis Kellis, Tomohiro Masuda, Don Zack, Julia E Richards, Margaret Pericak-Vance, Louis R Pasquale, Jonathan L Haines
Publikováno v:
PLoS Genetics, Vol 8, Iss 4, p e1002654 (2012)
Optic nerve degeneration caused by glaucoma is a leading cause of blindness worldwide. Patients affected by the normal-pressure form of glaucoma are more likely to harbor risk alleles for glaucoma-related optic nerve disease. We have performed a meta
Externí odkaz:
https://doaj.org/article/c0f601961fb1441ea4c7117937edd651
Autor:
Paul Leger, Lana M. Olson, David W. Haas, Husamettin Erdem, Danielle M. Richardson, Paxton Baker, Michael Leonard, Jacinta N. Nwogu, Sanika Chirwa, Megan Turner
Publikováno v:
Pharmacogenetics and Genomics
Background Atazanavir causes plasma indirect bilirubin to increase. We evaluated associations between Gilbert's polymorphism and bilirubin-related atazanavir discontinuation stratified by race/ethnicity. Patients and methods Patients had initiated at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1872425ee28f0ab51d070b2ec26b0c8f
https://doi.org/10.1097/fpc.0000000000000316
https://doi.org/10.1097/fpc.0000000000000316
Autor:
Jeffrey A. Canter, Carol Lyons, Amy Saupe, Yuki Bradford, Nicole Comstock, Katie Garman, Timothy F. Jones, Rajal K. Mody, Sarah L. Lathrop, Lana M. Olson, Asha R. Kallianpur, Amanda Palmer, Katie Wymore
Publikováno v:
The Journal of Infectious Diseases. 217:1000-1010
Background Postdiarrheal hemolytic-uremic syndrome (D+HUS) following Shiga toxin-producing Escherichia coli (STEC) infection is a serious condition lacking specific treatment. Host immune dysregulation and genetic susceptibility to complement hyperac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c9b14477345a145e43c63cd2099742f
https://doi.org/10.1093/infdis/jix633
https://doi.org/10.1093/infdis/jix633
Publikováno v:
International Forum of Allergy & Rhinology. 7:467-473
Background The clinical association between cystic fibrosis (CF) and chronic rhinosinusitis (CRS) is well known. Studies have identified several non-CF transmembrane conductance regulator single nucleotide polymorphisms (SNPs) associated with disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3710e984998a3d7c6f31c05b7c787564
https://doi.org/10.1002/alr.21926
https://doi.org/10.1002/alr.21926
Autor:
Megan Turner, Sanika Chirwa, Lana M. Olson, Michael Leonard, Danielle M. Richardson, Paxton Baker, Paul Leger, David W. Haas, Husamettin Erdem
Publikováno v:
Pharmacogenetics and Genomics. 26:473-480
Efavirenz frequently causes central nervous system (CNS) symptoms. We evaluated genetic associations with efavirenz discontinuation for CNS symptoms within 12 months of treatment initiation.Patients had initiated efavirenz-containing regimens at an H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d62271abad0e43b0490eb8d71fad749d
https://doi.org/10.1097/fpc.0000000000000238
https://doi.org/10.1097/fpc.0000000000000238
Autor:
Lindsay A. Farrer, Chi-Chao Chan, Lana M. Olson, Barbara E.K. Klein, Andrew J. Lotery, Jacqueline Ramke, Kyu Hyung Park, Yuri V. Sergeev, Felix Grassmann, John C. Merriam, Debra A. Schaumberg, Gonçalo R. Abecasis, Evangelia E. Tsironi, Anand Swaroop, Tammy M. Martin, Kari Branham, Naushin Waseem, Mohammad Othman, Donald J. Zack, Albert O. Edwards, Hendrik P. N. Scholl, Xiaowei Zhan, David Zipprer, Margaret A. Pericak-Vance, Harsha Rajasimha, Bingshan Li, José Sahel, Ronald Klein, Matthew P. Johnson, Michael B. Gorin, Thierry Léveillard, Denise J. Morgan, Stephanie A. Hagstrom, Mark Lathrop, Giuliana Silvestri, Ivana K. Kim, Robert N. Fariss, Barbara Truitt, Dwight Stambolian, James S. Friedman, Jonathan L. Haines, Arvydas Maminishkis, Yoichiro Kamatani, Robert P. Igo, Rinki Ratnapriya, Yvette P. Conley, Margaux A. Morrison, Rando Allikmets, Robert V. Baron, Jingsheng Tuo, Christina Chakarova, Bernhard H. F. Weber, Matthew Brooks, Gerald A. Fishman, Michael L. Klein, Shomi S. Bhattacharya, Joanna E. Merriam, Eric H Souied, Samuel G. Jacobson, Daniel E. Weeks, John R. Heckenlively, Emily Y. Chew, Neal S. Peachey, Margaret M. DeAngelis, Maria M Campos, Sudha K. Iyengar, Yingda Jiang
Publikováno v:
Human molecular genetics, vol 23, iss 21
Neurodegenerative diseases affecting the macula constitute a major cause of incurable vision loss and exhibit considerable clinical and genetic heterogeneity, from early-onset monogenic disease to multifactorial late-onset age-related macular degener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4e429a2040b8b7575ed0b3e9d1e48d2
https://doi.org/10.1093/hmg/ddu276
https://doi.org/10.1093/hmg/ddu276
Autor:
Russell A. Wilke, Lana M. Olson, Hua Ling, Elizabeth W. Pugh, Teri A. Manolio, Yuki Bradford, Rongling Li, Loren L. Armstrong, Justin Paschall, Marylyn D. Ritchie, Lan Jiang, Christopher S. Carlson, Catherine A. McCarty, Gail P. Jarvik, Stephen D. Turner, Kimberly F. Doheny, Iftikhar J. Kullo, Andrew Crenshaw, Martha E. Matsumoto, M. Geoffrey Hayes, Daniel B. Mirel, Laura J. Rasmussen-Torvik, Andrew McDavid, Jonathan L. Haines, Rebecca L. Zuvich, Dana C. Crawford, Mariza de Andrade, Luke V. Rasmussen, Suzette J. Bielinski
Publikováno v:
Genetic Epidemiology. 35:887-898
Genome-wide association studies (GWAS) are a useful approach in the study of the genetic components of complex phenotypes. Aside from large cohorts, GWAS have generally been limited to the study of one or a few diseases or traits. The emergence of bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25741459932fe9416235b5a9bdb0eead
https://doi.org/10.1002/gepi.20639
https://doi.org/10.1002/gepi.20639
Autor:
Michael A. Hauser, William K. Scott, Lana M. Olson, Anita Agarwal, Silke Schmidt, Kylee L. Spencer, Eric A. Postel, Paul Gallins, Jonathan L. Haines, Margaret A. Pericak-Vance
Publikováno v:
Human Molecular Genetics. 17:971-977
Age-related macular degeneration (AMD) impairs vision for approximately 7.5 million Americans. Both susceptibility variants and protective haplotypes in the complement factor H (CFH) gene modulate risk for AMD. Recently, deletion of the 'CFH-related'
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dbb1f83af51b93d752ea0f41a770ed6
https://doi.org/10.1093/hmg/ddm369
https://doi.org/10.1093/hmg/ddm369
Autor:
Ighovwerha Ofotokun, Raphael J. Landovitz, David W. Haas, Judith S. Currier, Lana M. Olson, Saran Vardhanabhuti, Jeffrey L. Lennox, Heather J. Ribaudo
Publikováno v:
Open forum infectious diseases, vol 2, iss 3
Vardhanabhuti, S; Ribaudo, HJ; Landovitz, RJ; Ofotokun, I; Lennox, JL; Currier, JS; et al.(2015). Screening for UGT1A1 Genotype in Study A5257 Would Have Markedly Reduced Premature Discontinuation of Atazanavir for Hyperbilirubinemia. OPEN FORUM INFECTIOUS DISEASES, 2(3). doi: 10.1093/ofid/ofv085. UCLA: Retrieved from: http://www.escholarship.org/uc/item/4w49n9tm
Open Forum Infectious Diseases
Vardhanabhuti, S; Ribaudo, HJ; Landovitz, RJ; Ofotokun, I; Lennox, JL; Currier, JS; et al.(2015). Screening for UGT1A1 Genotype in Study A5257 Would Have Markedly Reduced Premature Discontinuation of Atazanavir for Hyperbilirubinemia. OPEN FORUM INFECTIOUS DISEASES, 2(3). doi: 10.1093/ofid/ofv085. UCLA: Retrieved from: http://www.escholarship.org/uc/item/4w49n9tm
Open Forum Infectious Diseases
Background. Some patients are not prescribed atazanavir because of concern about possible jaundice. Atazanavir-associated hyperbilirubinemia correlates with UGT1A1 rs887829 genotype. We examined bilirubin-related discontinuation of atazanavir in part
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21340603a814ae8d390aecc616adf1f7
https://escholarship.org/uc/item/4w49n9tm
https://escholarship.org/uc/item/4w49n9tm
