Mayer J - Search Results

1

Multisite evaluation of prediction models for emergency department crowding before and during the COVID-19 pandemic.

Smith AJ, Patterson BW, Pulia MS, Mayer J, Schwei RJ, Nagarajan R, Liao F, Shah MN, Boutilier JJ. Smith AJ, et al. Among authors: mayer j. J Am Med Inform Assoc. 2023 Jan 18;30(2):292-300. doi: 10.1093/jamia/ocac214. J Am Med Inform Assoc. 2023. PMID: 36308445 Free PMC article.

2

Machine learning for phenotyping opioid overdose events.

Badger J, LaRose E, Mayer J, Bashiri F, Page D, Peissig P. Badger J, et al. Among authors: mayer j. J Biomed Inform. 2019 Jun;94:103185. doi: 10.1016/j.jbi.2019.103185. Epub 2019 Apr 25. J Biomed Inform. 2019. PMID: 31028874 Free PMC article.

3

Adverse Drug Event Discovery Using Biomedical Literature: A Big Data Neural Network Adventure.

P Tafti A, Badger J, LaRose E, Shirzadi E, Mahnke A, Mayer J, Ye Z, Page D, Peissig P. P Tafti A, et al. Among authors: mayer j. JMIR Med Inform. 2017 Dec 8;5(4):e51. doi: 10.2196/medinform.9170. JMIR Med Inform. 2017. PMID: 29222076 Free PMC article.

4

Estimating the efficacy of pharmacogenomics over a lifetime.

Ye Z, Mayer J, Leary EJ, Kitchner T, Dart RA, Brilliant MH, Hebbring SJ. Ye Z, et al. Among authors: mayer j. Front Med (Lausanne). 2023 Oct 31;10:1006743. doi: 10.3389/fmed.2023.1006743. eCollection 2023. Front Med (Lausanne). 2023. PMID: 38020121 Free PMC article.

5

E-Pedigrees: a large-scale automatic family pedigree prediction application.

Huang X, Tatonetti N, LaRow K, Delgoffee B, Mayer J, Page D, Hebbring SJ. Huang X, et al. Among authors: mayer j. Bioinformatics. 2021 Nov 5;37(21):3966-3968. doi: 10.1093/bioinformatics/btab419. Bioinformatics. 2021. PMID: 34086863 Free PMC article.

6

Identifying genetically driven clinical phenotypes using linear mixed models.

Mosley JD, Witte JS, Larkin EK, Bastarache L, Shaffer CM, Karnes JH, Stein CM, Phillips E, Hebbring SJ, Brilliant MH, Mayer J, Ye Z, Roden DM, Denny JC. Mosley JD, et al. Among authors: mayer j. Nat Commun. 2016 Apr 25;7:11433. doi: 10.1038/ncomms11433. Nat Commun. 2016. PMID: 27109359 Free PMC article.

7

Applying family analyses to electronic health records to facilitate genetic research.

Huang X, Elston RC, Rosa GJ, Mayer J, Ye Z, Kitchner T, Brilliant MH, Page D, Hebbring SJ. Huang X, et al. Among authors: mayer j. Bioinformatics. 2018 Feb 15;34(4):635-642. doi: 10.1093/bioinformatics/btx569. Bioinformatics. 2018. PMID: 28968884 Free PMC article.

8

Genetic risk score in multiple sclerosis is associated with unique gut microbiome.

Elsayed NS, Valenzuela RK, Kitchner T, Le T, Mayer J, Tang ZZ, Bayanagari VR, Lu Q, Aston P, Anantharaman K, Shukla SK. Elsayed NS, et al. Among authors: mayer j. Sci Rep. 2023 Sep 27;13(1):16269. doi: 10.1038/s41598-023-43217-4. Sci Rep. 2023. PMID: 37758833 Free PMC article.

9

Use of an electronic medical record to create the marshfield clinic twin/multiple birth cohort.

Mayer J, Kitchner T, Ye Z, Zhou Z, He M, Schrodi SJ, Hebbring SJ. Mayer J, et al. Genet Epidemiol. 2014 Dec;38(8):692-8. doi: 10.1002/gepi.21855. Epub 2014 Sep 22. Genet Epidemiol. 2014. PMID: 25250975 Free PMC article.

10

Application of clinical text data for phenome-wide association studies (PheWASs).

Hebbring SJ, Rastegar-Mojarad M, Ye Z, Mayer J, Jacobson C, Lin S. Hebbring SJ, et al. Among authors: mayer j. Bioinformatics. 2015 Jun 15;31(12):1981-7. doi: 10.1093/bioinformatics/btv076. Epub 2015 Feb 4. Bioinformatics. 2015. PMID: 25657332 Free PMC article.

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