Page D - Search Results

1

Phenome-wide association studies (PheWASs) for functional variants.

Ye Z, Mayer J, Ivacic L, Zhou Z, He M, Schrodi SJ, Page D, Brilliant MH, Hebbring SJ. Ye Z, et al. Among authors: page d. Eur J Hum Genet. 2015 Apr;23(4):523-9. doi: 10.1038/ejhg.2014.123. Epub 2014 Jul 30. Eur J Hum Genet. 2015. PMID: 25074467 Free PMC article.

2

Genetic variants improve breast cancer risk prediction on mammograms.

Liu J, Page D, Nassif H, Shavlik J, Peissig P, McCarty C, Onitilo AA, Burnside E. Liu J, et al. Among authors: page d. AMIA Annu Symp Proc. 2013 Nov 16;2013:876-85. eCollection 2013. AMIA Annu Symp Proc. 2013. PMID: 24551380 Free PMC article.

3

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: page d. Bioinformatics. 2018 Feb 15;34(4):635-642. doi: 10.1093/bioinformatics/btx569. Bioinformatics. 2018. PMID: 28968884 Free PMC article.

4

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: page d. JMIR Med Inform. 2017 Dec 8;5(4):e51. doi: 10.2196/medinform.9170. JMIR Med Inform. 2017. PMID: 29222076 Free PMC article.

5

Using machine learning to identify patterns of lifetime health problems in decedents with autism spectrum disorder.

Bishop-Fitzpatrick L, Movaghar A, Greenberg JS, Page D, DaWalt LS, Brilliant MH, Mailick MR. Bishop-Fitzpatrick L, et al. Among authors: page d. Autism Res. 2018 Aug;11(8):1120-1128. doi: 10.1002/aur.1960. Epub 2018 May 7. Autism Res. 2018. PMID: 29734508 Free PMC article.

6

Health Profiles of Mosaic Versus Non-mosaic FMR1 Premutation Carrier Mothers of Children With Fragile X Syndrome.

Mailick MR, Movaghar A, Hong J, Greenberg JS, DaWalt LS, Zhou L, Jackson J, Rathouz PJ, Baker MW, Brilliant M, Page D, Berry-Kravis E. Mailick MR, et al. Among authors: page d. Front Genet. 2018 May 16;9:173. doi: 10.3389/fgene.2018.00173. eCollection 2018. Front Genet. 2018. PMID: 29868121 Free PMC article.

7

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: page d. 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.

8

Data-driven phenotype discovery of FMR1 premutation carriers in a population-based sample.

Movaghar A, Page D, Brilliant M, Baker MW, Greenberg J, Hong J, DaWalt LS, Saha K, Kuusisto F, Stewart R, Berry-Kravis E, Mailick MR. Movaghar A, et al. Among authors: page d. Sci Adv. 2019 Aug 21;5(8):eaaw7195. doi: 10.1126/sciadv.aaw7195. eCollection 2019 Aug. Sci Adv. 2019. PMID: 31457090 Free PMC article.

9

Artificial intelligence-assisted phenotype discovery of fragile X syndrome in a population-based sample.

Movaghar A, Page D, Scholze D, Hong J, DaWalt LS, Kuusisto F, Stewart R, Brilliant M, Mailick M. Movaghar A, et al. Among authors: page d. Genet Med. 2021 Jul;23(7):1273-1280. doi: 10.1038/s41436-021-01144-7. Epub 2021 Mar 26. Genet Med. 2021. PMID: 33772223 Free PMC article.

10

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: page d. Bioinformatics. 2021 Nov 5;37(21):3966-3968. doi: 10.1093/bioinformatics/btab419. Bioinformatics. 2021. PMID: 34086863 Free PMC article.

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