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Jason E. Miller - Publications

Affiliations: 
Geisinger Health System 
Area:
Data Integration and Biomedical Informatics
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24 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Graham SE, Clarke SL, Wu KH, Kanoni S, Zajac GJM, Ramdas S, Surakka I, Ntalla I, Vedantam S, Winkler TW, Locke AE, Marouli E, Hwang MY, Han S, Narita A, ... ... Miller JE, et al. Author Correction: The power of genetic diversity in genome-wide association studies of lipids. Nature. PMID 37237109 DOI: 10.1038/s41586-023-06194-2  0.763
2022 Kanoni S, Graham SE, Wang Y, Surakka I, Ramdas S, Zhu X, Clarke SL, Bhatti KF, Vedantam S, Winkler TW, Locke AE, Marouli E, Zajac GJM, Wu KH, Ntalla I, ... ... Miller JE, et al. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Genome Biology. 23: 268. PMID 36575460 DOI: 10.1186/s13059-022-02837-1  0.712
2022 Park J, MacLean MT, Lucas AM, Torigian DA, Schneider CV, Cherlin T, Xiao B, Miller JE, Bradford Y, Judy RL, Verma A, Damrauer SM, Ritchie MD, Witschey WR, Rader DJ. Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Cell Reports. Medicine. 100855. PMID 36513072 DOI: 10.1016/j.xcrm.2022.100855  0.705
2022 Yengo L, Vedantam S, Marouli E, Sidorenko J, Bartell E, Sakaue S, Graff M, Eliasen AU, Jiang Y, Raghavan S, Miao J, Arias JD, Graham SE, Mukamel RE, Spracklen CN, ... ... Miller JE, et al. A saturated map of common genetic variants associated with human height. Nature. PMID 36224396 DOI: 10.1038/s41586-022-05275-y  0.76
2022 Ramdas S, Judd J, Graham SE, Kanoni S, Wang Y, Surakka I, Wenz B, Clarke SL, Chesi A, Wells A, Bhatti KF, Vedantam S, Winkler TW, Locke AE, Marouli E, ... ... Miller JE, et al. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids. American Journal of Human Genetics. 109: 1366-1387. PMID 35931049 DOI: 10.1016/j.ajhg.2022.06.012  0.726
2021 Graham SE, Clarke SL, Wu KH, Kanoni S, Zajac GJM, Ramdas S, Surakka I, Ntalla I, Vedantam S, Winkler TW, Locke AE, Marouli E, Hwang MY, Han S, Narita A, ... ... Miller JE, et al. The power of genetic diversity in genome-wide association studies of lipids. Nature. PMID 34887591 DOI: 10.1038/s41586-021-04064-3  0.783
2021 Shivakumar M, Miller JE, Dasari VR, Zhang Y, Lee MTM, Carey DJ, Gogoi R, Kim D. Genetic analysis of functional rare germline variants across 9 cancer types from an electronic health record linked biobank. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 34244158 DOI: 10.1158/1055-9965.EPI-21-0082  0.702
2021 Veturi Y, Lucas A, Bradford Y, Hui D, Dudek S, Theusch E, Verma A, Miller JE, Kullo I, Hakonarson H, Sleiman P, Schaid D, Stein CM, Edwards DRV, Feng Q, et al. A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. Nature Genetics. PMID 34140684 DOI: 10.1038/s41588-021-00879-y  0.728
2020 Oh JJ, Shivakumar M, Miller J, Verma S, Lee H, Hong SK, Lee SE, Lee Y, Lee SJ, Sung J, Kim D, Byun SS. Author Correction: An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer. Scientific Reports. 10: 2481. PMID 32034279 DOI: 10.1038/S41598-020-59361-0  0.753
2019 Oh JJ, Shivakumar M, Miller J, Verma S, Lee H, Hong SK, Lee SE, Lee Y, Lee SJ, Sung J, Kim D, Byun SS. An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer. Scientific Reports. 9: 17173. PMID 31748686 DOI: 10.1038/S41598-019-53445-2  0.767
2019 Shivakumar M, Miller JE, Dasari VR, Gogoi R, Kim D. Exome-Wide Rare Variant Analysis From the DiscovEHR Study Identifies Novel Candidate Predisposition Genes for Endometrial Cancer. Frontiers in Oncology. 9: 574. PMID 31338326 DOI: 10.3389/Fonc.2019.00574  0.741
2019 Miller JE, Metpally RP, Person TN, Krishnamurthy S, Dasari VR, Shivakumar M, Lavage DR, Cook AM, Carey DJ, Ritchie MD, Kim D, Gogoi R. Correction to: Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population. Bmc Medical Genomics. 12: 65. PMID 31118041 DOI: 10.1186/S12920-019-0523-6  0.714
2019 Miller JE, Veturi Y, Ritchie MD. Innovative strategies for annotating the "relationSNP" between variants and molecular phenotypes. Biodata Mining. 12: 10. PMID 31114635 DOI: 10.1186/S13040-019-0197-9  0.658
2019 Miller JE, Metpally RP, Person TN, Krishnamurthy S, Dasari VR, Shivakumar M, Lavage DR, Cook AM, Carey DJ, Ritchie MD, Kim D, Gogoi R. Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population. Bmc Medical Genomics. 12: 59. PMID 31053132 DOI: 10.1186/S12920-019-0504-9  0.771
2019 Han S, Miller JE, Byun S, Kim D, Risacher SL, Saykin AJ, Lee Y, Nho K. Identification of exon skipping events associated with Alzheimer's disease in the human hippocampus. Bmc Medical Genomics. 12: 13. PMID 30704480 DOI: 10.1186/S12920-018-0453-8  0.699
2019 Miller JE, Dudek SM, Frase AT, Ritchie MD. P4-486: EXPLORING RARE VARIATIONS THAT IMPACT REGIONS OF PROTEINS ASSOCIATED WITH ALZHEIMER'S DISEASE Alzheimer's & Dementia. 15: P1498-P1498. DOI: 10.1016/J.Jalz.2019.08.032  0.627
2018 Verma A, Bang L, Miller JE, Zhang Y, Lee MTM, Zhang Y, Byrska-Bishop M, Carey DJ, Ritchie MD, Pendergrass SA, Kim D. Human-Disease Phenotype Map Derived from PheWAS across 38,682 Individuals. American Journal of Human Genetics. PMID 30598166 DOI: 10.1016/J.Ajhg.2018.11.006  0.726
2018 Miller JE, Shivakumar MK, Lee Y, Han S, Horgousluoglu E, Risacher SL, Saykin AJ, Nho K, Kim D. Rare variants in the splicing regulatory elements of EXOC3L4 are associated with brain glucose metabolism in Alzheimer's disease. Bmc Medical Genomics. 11: 76. PMID 30255815 DOI: 10.1186/S12920-018-0390-6  0.723
2018 Han S, Kim D, Kim Y, Choi K, Miller JE, Kim D, Lee Y. CAS-viewer: web-based tool for splicing-guided integrative analysis of multi-omics cancer data. Bmc Medical Genomics. 11: 25. PMID 29697367 DOI: 10.1186/S12920-018-0348-8  0.7
2018 Han S, Kim D, Shivakumar M, Lee YJ, Garg T, Miller JE, Kim JH, Kim D, Lee Y. The effects of alternative splicing on miRNA binding sites in bladder cancer. Plos One. 13: e0190708. PMID 29300757 DOI: 10.1371/Journal.Pone.0190708  0.654
2018 Miller JE, Shivakumar MK, Risacher SL, Saykin AJ, Lee S, Nho K, Kim D. Codon bias among synonymous rare variants is associated with Alzheimer's disease imaging biomarker. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 23: 365-376. PMID 29218897  0.726
2018 Dasari VR, Bang L, Miller JE, Kim D, Gogoi R. Verteporfin sensitizes endometrial cancer cells to radiation or chemo treatment Gynecologic Oncology. 149: 66. DOI: 10.1016/J.Ygyno.2018.04.148  0.643
2011 Miller W, Hayes VM, Ratan A, Petersen DC, Wittekindt NE, Miller J, Walenz B, Knight J, Qi J, Zhao F, Wang Q, Bedoya-Reina OC, Katiyar N, Tomsho LP, Kasson LM, et al. Genetic diversity and population structure of the endangered marsupial Sarcophilus harrisii (Tasmanian devil). Proceedings of the National Academy of Sciences of the United States of America. 108: 12348-53. PMID 21709235 DOI: 10.1073/Pnas.1102838108  0.31
2006 Miller JE, Shivakumar MK, Risacher SL, Saykin AJ, Ritchie MD, Nho K, Kim D. P4-238: PATHWAY LEVEL CODON BIAS AMONG SYNONYMOUS RARE VARIANTS IS ASSOCIATED WITH ALZHEIMER'S DISEASE IMAGING BIOMARKER Alzheimer's & Dementia. 14: P1534-P1534. DOI: 10.1016/J.Jalz.2018.07.059  0.755
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