Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Shiow J. Lin"'
Autor:
E. Warwick Daw, James Hicks, Petra Lenzini, Shiow J. Lin, Judy Wang, Christine Williams, Ping An, Michael A. Province, Aldi T. Kraja
Publikováno v:
BMC Proceedings, Vol 12, Iss S9, Pp 169-173 (2018)
Abstract To examine whether single-nucleotide polymorphism (SNP) by methylation interactions can be detected, we analyzed GAW20 simulated triglycerides at visits 3 and 4 against baseline (visits 1 and 2) under 4 general linear models and 2 tree-based
Externí odkaz:
https://doaj.org/article/d3f0337fa6fd4b76b76bfeabe8fba3c5
Autor:
Nitin B. Jain, Elizabeth L. Yanik, Bradley A. Evanoff, Rick W. Wright, Jay D. Keener, Shiow J Lin, Nancy L. Saccone, Graham A. Colditz
Publikováno v:
J Bone Joint Surg Am
BACKGROUND While evidence indicates that familial predisposition influences the risk of developing degenerative rotator cuff disease (RCD), knowledge of specific genetic markers is limited. We conducted a genome-wide association study of RCD surgery
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::149e5698a38e9c3f6f9e88ffec08f6cd
https://doi.org/10.2106/jbjs.20.01474
https://doi.org/10.2106/jbjs.20.01474
Autor:
Joanne M. Murabito, Aldi T. Kraja, Sandra Barral, E. Warwick Daw, Thomas T. Perls, Giuseppe Tosto, Kathryn L. Lunetta, Paola Sebastiani, Lihua Wang, Michael A. Province, Anatoly I. Yashin, Shiow J. Lin, Alan Wells, Christine A. Williams, Petra A. Lenzini, Ryan L. Minster
Publikováno v:
International Journal of Bioinformatics Research and Applications. 16:59
This study compares methods of imputing genetic markers, given a typed GWAS scaffold from the Long Life Family Study (LLFS) and latest reference panel of 1000-Genomes. We examined two programs for ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f310cc5c00c6a043837e7dcb02678be
https://doi.org/10.1504/ijbra.2020.104855
https://doi.org/10.1504/ijbra.2020.104855
Autor:
Ping An, Judy Wang, Petra A. Lenzini, Shiow J. Lin, Christine Williams, Aldi T. Kraja, E. Warwick Daw, Michael A. Province, James E. Hicks
Publikováno v:
BMC Proceedings, Vol 12, Iss S9, Pp 169-173 (2018)
To examine whether single-nucleotide polymorphism (SNP) by methylation interactions can be detected, we analyzed GAW20 simulated triglycerides at visits 3 and 4 against baseline (visits 1 and 2) under 4 general linear models and 2 tree-based models i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95efb93e44abfeeacfac9f66504bacdc
https://doi.org/10.1186/s12919-018-0140-y
https://doi.org/10.1186/s12919-018-0140-y
Autor:
Lihua Wang, Kaare Christensen, Shiow J. Lin, Qunyuan Zhang, E. Warwick Daw, Joseph H. Lee, Benjamin T. Levinson, Michael A. Province, Anne B. Newman, Richard Mayeux, Bharat Thyagarajan, Enrique Ramos, Haley J. Abel, Sara E. Chasnoff, Todd E. Druley
Publikováno v:
Druley, T E, Wang, L, Lin, S J, Lee, J H, Zhang, Q, Daw, E W, Abel, H J, Chasnoff, S E, Ramos, E I, Levinson, B T, Thyagarajan, B, Newman, A B, Christensen, K, Mayeux, R & Province, M A 2016, ' Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study ', BMC Geriatrics, vol. 16, no. 1, 80, pp. 1-12 . https://doi.org/10.1186/s12877-016-0253-y
BMC Geriatrics
BMC Geriatrics
BACKGROUND: The Long Life Family Study (LLFS) is an international study to identify the genetic components of various healthy aging phenotypes. We hypothesized that pedigree-specific rare variants at longevity-associated genes could have a similar fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad52aec1e74bd67834759ac8b83a4890
https://doi.org/10.1186/s12877-016-0253-y
https://doi.org/10.1186/s12877-016-0253-y
Autor:
Nauder Faraday, Lewis C. Becker, Lisa R. Yanek, Shiow J. Lin, Diane M. Becker, Michael A. Province, Qiong Yang, Ming-Huei Chen, Geoffrey H. Tofler, Christopher J. O'Donnell, Andrew D. Johnson, Martin G. Larson, Aldi T. Kraja
Publikováno v:
Nature Genetics. 42:608-613
Platelet function mediates both beneficial and harmful effects on human health, but few genes are known to contribute to variability in this process. We tested association of 2.5 million SNPs with platelet aggregation responses to three agonists (ADP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f78f6bf363beb4d3b1b7d1619acf686
https://doi.org/10.1038/ng.604
https://doi.org/10.1038/ng.604
Autor:
Jane L Yen-Revollo, Shiow J. Lin, Michael A. Province, Aldi T. Kraja, Eric Peters, Howard L. McLeod, Sharon Marsh
Publikováno v:
Pharmacogenetics and genomics. 19(5)
Identifying relevant cytotoxicity genes using an ex-vivo lymphoblastoid cell line (LCLs) model has distinct advantages for pharmacogenomic discovery studies of cancer chemotherapy, including standardized treatment conditions, availability of large nu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2170421f3ee2706a19dc32dd415ca7d
https://pubmed.ncbi.nlm.nih.gov/19339911
https://pubmed.ncbi.nlm.nih.gov/19339911