Zobrazeno 1 - 10 of 29 pro vyhledávání: '"Holli H. Dilks"'
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Akademický článek
Population stratification in the context of diverse epidemiologic surveys sans genome-wide data
Autor: Matthew T. Oetjens, Kristin eBrown-Gentry, Robert eGoodloe, Holli H. Dilks, Dana C. Crawford
Publikováno v: Frontiers in Genetics, Vol 7 (2016)
Population stratification or confounding by genetic ancestry is a potential cause of false associations in genetic association studies. Estimation of and adjustment for genetic ancestry has become common practice thanks in part to the availability of
Externí odkaz: https://doaj.org/article/260e8c20680c42f69f82397ac0511e2a
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2
Should next-generation sequencing tests be performed on all cancer patients?
Autor: Andrew J. McKenzie, Suzanne F. Jones, Holli H. Dilks, Howard A. Burris
Publikováno v: Expert review of molecular diagnostics. 19(2)
Oncologists require as much data as possible in order to develop and execute the optimal treatment plan for their patients. Next-Generation Sequencing (NGS) provides rich data informing possible ta...
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f487facef81d176a613b3c36e184d6b
https://pubmed.ncbi.nlm.nih.gov/30618301
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6
Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia
Autor: Edward Giovannucci, Chris S. Carlson, Christopher A. Haiman, Holli H. Dilks, Charles Kooperberg, Mathieu Lemire, Steven Gallinger, David Duggan, Noralane M. Lindor, Lynne R. Wilkens, Gowri Kumaraguruparan, Robert W. Haile, Michael Hoffmeister, Andrew T. Chan, Lucia A. Hindorff, Thomas J. Hudson, Richard B. Hayes, Fredrick R. Schumacher, José Luis Ambite, Cara L. Carty, Loic Le Marchand, Sonja I. Berndt, Gerardo Heiss, Ulrike Peters, Sue L. Mann, Stéphane Bézieau, Danielle M. Richardson, Paxton Baker, John L. Hopper, Polly A. Newcomb, Stephen J. Chanock, Martha L. Slattery, Sungshim L. Park, John D. Potter, Shuo Jiao, Yi Lin, Bette J. Caan, Jenny Chang-Claude, Dana C. Crawford, Christy L. Avery, Daniela Seminara, Tabitha A. Harrison, Carolyn M. Hutter, David V. Conti, Logan Dumitrescu, Iona Cheng, Robert Goodloe, Li Hsu, Emily White, Peter T. Campbell, Kristine R. Monroe, Robert E. Schoen, Anne M. Butler, Peter Kraft, Graham Casey, Hermann Brenner, Christian Caberto, Sébastien Küry, Brent W. Zanke, Charles S. Fuchs, William S. Bush, John A. Baron, Mark A. Jenkins, Jing Ma, Shelly Ann Love, Lifang Hou, Jonathan M. Kocarnik
Publikováno v: Gut. 63:800-807
Objective Genome-wide association studies have identified a large number of single nucleotide polymorphisms (SNPs) associated with a wide array of cancer sites. Several of these variants demonstrate associations with multiple cancers, suggesting plei
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddf487b68d8a8b973cb2a6cc8d0f6cdb
https://doi.org/10.1136/gutjnl-2013-305189
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7
Assessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical records
Autor: Joshua C. Denny, Russell A. Wilke, Erica Bowton, Dan M. Roden, Niloufar B. Gillani, Marylyn D. Ritchie, Nicole A. Restrepo, Matthew T. Oetjens, Holli H. Dilks, Jill M. Pulley, Daniel R. Masys, Melissa A. Basford, Dana C. Crawford, Danielle M. Richardson
Publikováno v: Pharmacogenomics. 14:735-744
Background: The ADME Core Panel assays 184 variants across 34 pharmacogenes, many of which are difficult to accurately genotype with standard multiplexing methods. Methods: We genotyped 326 frequently medicated individuals of European descent in Vand
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e94c26b3eb0430a3328ac1300f770480
https://doi.org/10.2217/pgs.13.64
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8
Evidence for extensive pleiotropy among pharmacogenes
Autor: Nuri Kodaman, Anurag Verma, Joshua C. Denny, Holli H. Dilks, Marylyn D. Ritchie, William S. Bush, Sarah A. Pendergrass, Matthew T. Oetjens, Kelly A. Birdwell, Dana C. Crawford
Aim: We sought to identify potential pleiotropy involving pharmacogenes. Methods: We tested 184 functional variants in 34 pharmacogenes for associations using a custom grouping of International Classification and Disease, Ninth Revision billing codes
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc25edf8db9fbb967b2487e4a8aabab1
https://europepmc.org/articles/PMC5352965/
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9
Population Stratification in the Context of Diverse Epidemiologic Surveys Sans Genome-Wide Data
Autor: Dana C. Crawford, Robert Goodloe, Kristin Brown-Gentry, Holli H. Dilks, Matthew T. Oetjens
Publikováno v: Frontiers in Genetics
Frontiers in Genetics, Vol 7 (2016)
Population stratification or confounding by genetic ancestry is a potential cause of false associations in genetic association studies. Estimation of and adjustment for genetic ancestry has become common practice thanks in part to the availability of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cb22010cdb46aad99da378ce1530679
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