| Year |
Citation |
Score |
| 2024 |
Woerner J, Sriram V, Nam Y, Verma A, Kim D. Uncovering genetic associations in the human diseasome using an endophenotype-augmented disease network. Bioinformatics (Oxford, England). 40. PMID 38527901 DOI: 10.1093/bioinformatics/btae126 |
0.593 |
|
| 2023 |
Lee BN, Wang J, Hall MA, Kim D, Stites SD, Shen L. Sex modifies effects of imaging and CSF biomarkers on cognitive and functional outcomes: a study of Alzheimer's disease. Neurobiology of Aging. 133: 67-77. PMID 37913627 DOI: 10.1016/j.neurobiolaging.2023.10.002 |
0.659 |
|
| 2023 |
Nam Y, Lucas A, Yun JS, Lee SM, Park JW, Chen Z, Lee B, Ning X, Shen L, Verma A, Kim D. Development of complemented comprehensive networks for rapid screening of repurposable drugs applicable to new emerging disease outbreaks. Journal of Translational Medicine. 21: 415. PMID 37365631 DOI: 10.1186/s12967-023-04223-2 |
0.537 |
|
| 2023 |
Singhal P, Guare L, Morse C, Lucas A, Byrska-Bishop M, Guerraty MA, Kim D, Ritchie MD, Verma A. DETECT: Feature extraction method for disease trajectory modeling in electronic health records. Amia Joint Summits On Translational Science Proceedings. Amia Joint Summits On Translational Science. 2023: 487-496. PMID 37350926 |
0.781 |
|
| 2023 |
Woerner J, Sriram V, Nam Y, Verma A, Kim D. Uncovering genetic associations in the human diseasome using an endophenotype-augmented disease network. Medrxiv : the Preprint Server For Health Sciences. PMID 37293013 DOI: 10.1101/2023.05.11.23289852 |
0.609 |
|
| 2023 |
Xiao B, Velez Edwards DR, Lucas A, Drivas T, Gray K, Keating B, Weng C, Jarvik GP, Hakonarson H, Kottyan L, Elhadad N, Wei WQ, Luo Y, Kim D, Ritchie M, et al. Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions. Journal of the American Heart Association. e026561. PMID 36846987 DOI: 10.1161/JAHA.121.026561 |
0.732 |
|
| 2022 |
Nam Y, Jung SH, Yun JS, Sriram V, Singhal P, Byrska-Bishop M, Verma A, Shin H, Park WY, Won HH, Kim D. Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data. Bioinformatics (Oxford, England). PMID 36571484 DOI: 10.1093/bioinformatics/btac822 |
0.791 |
|
| 2022 |
Hui D, Xiao B, Dikilitas O, Freimuth RR, Irvin MR, Jarvik GP, Kottyan L, Kullo I, Limdi NA, Liu C, Luo Y, Namjou B, Puckelwartz MJ, Schaid D, Tiwari H, ... ... Kim D, et al. Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 28: 437-448. PMID 36540998 |
0.723 |
|
| 2022 |
Choe EK, Shivakumar M, Lee SM, Verma A, Kim D. Dissecting the clinical relevance of polygenic risk score for obesity-a cross-sectional, longitudinal analysis. International Journal of Obesity (2005). PMID 35752651 DOI: 10.1038/s41366-022-01168-2 |
0.493 |
|
| 2022 |
Zarzar TG, Lee B, Coughlin R, Kim D, Shen L, Hall MA. Sex Differences in the Metabolome of Alzheimer's Disease Progression. Frontiers in Radiology. 2. PMID 35445209 DOI: 10.3389/fradi.2022.782864 |
0.662 |
|
| 2022 |
Sriram V, Shivakumar M, Jung SH, Nam Y, Bang L, Verma A, Lee S, Choe EK, Kim D. NETMAGE: A human disease phenotype map generator for the network-based visualization of phenome-wide association study results. Gigascience. 11. PMID 35166337 DOI: 10.1093/gigascience/giac002 |
0.606 |
|
| 2022 |
Choe EK, Shivakumar M, Verma A, Verma SS, Choi SH, Kim JS, Kim D. Leveraging deep phenotyping from health check-up cohort with 10,000 Korean individuals for phenome-wide association study of 136 traits. Scientific Reports. 12: 1930. PMID 35121771 DOI: 10.1038/s41598-021-04580-2 |
0.734 |
|
| 2022 |
Nam Y, Jung SH, Verma A, Sriram V, Won HH, Yun JS, Kim D. netCRS: Network-based comorbidity risk score for prediction of myocardial infarction using biobank-scaled PheWAS data. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 27: 325-336. PMID 34890160 |
0.588 |
|
| 2021 |
Sriram V, Nam Y, Shivakumar M, Verma A, Jung SH, Lee SM, Kim D. A Network-Based Analysis of Disease Complication Associations for Obstetric Disorders in the UK Biobank. Journal of Personalized Medicine. 11. PMID 34945853 DOI: 10.3390/jpm11121382 |
0.568 |
|
| 2021 |
Holmes JH, Beinlich J, Boland MR, Bowles KH, Chen Y, Cook TS, Demiris G, Draugelis M, Fluharty L, Gabriel PE, Grundmeier R, Hanson CW, Herman DS, Himes BE, Hubbard RA, ... ... Kim D, et al. Why Is the Electronic Health Record So Challenging for Research and Clinical Care? Methods of Information in Medicine. PMID 34282602 DOI: 10.1055/s-0041-1731784 |
0.619 |
|
| 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 |
0.742 |
|
| 2021 |
Bang L, Shivakumar M, Garg T, Kim D. Genetic Analysis Reveals Rare Variants in T-Cell Response Gene MR1 Associated with Poor Overall Survival after Urothelial Cancer Diagnosis. Cancers. 13. PMID 33919687 DOI: 10.3390/cancers13081864 |
0.307 |
|
| 2021 |
Kim D, Kim JH, Moore JH. Translational Bioinformatics: Integrating Electronic Health Record and Omics Data. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 26: 356-359. PMID 33691034 |
0.407 |
|
| 2021 |
Beaulieu-Jones B, Darabos C, Kim D, Verma A, Kobren SN. Innovative methodological approaches for data integration to derive patterns across diverse, large-scale biomedical datasets. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 26: 256-260. PMID 33691022 |
0.522 |
|
| 2020 |
Lee S, Choe EK, Kim SY, Kim HS, Park KJ, Kim D. Liver imaging features by convolutional neural network to predict the metachronous liver metastasis in stage I-III colorectal cancer patients based on preoperative abdominal CT scan. Bmc Bioinformatics. 21: 382. PMID 32938394 DOI: 10.1186/S12859-020-03686-0 |
0.302 |
|
| 2020 |
Moore JH, Barnett I, Boland MR, Chen Y, Demiris G, Gonzalez-Hernandez G, Herman DS, Himes BE, Hubbard RA, Kim D, Morris JS, Mowery DL, Ritchie MD, Shen L, Urbanowicz R, et al. Ideas for how informaticians can get involved with COVID-19 research. Biodata Mining. 13: 3. PMID 32419848 DOI: 10.1186/S13040-020-00213-Y |
0.644 |
|
| 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 |
0.779 |
|
| 2020 |
Kobren SN, Beaulieu-Jones B, Darabos C, Kim D, Verma A. Ongoing challenges and innovative approaches for recognizing patterns across large-scale, integrative biomedical datasets. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 25: 286-294. PMID 31797604 |
0.518 |
|
| 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 |
0.789 |
|
| 2019 |
Glessner JT, Li J, Desai A, Palmer M, Kim D, Lucas AM, Chang X, Connolly JJ, Almoguera B, Harley JB, Jarvik GP, Ritchie MD, Sleiman PMA, Roden DM, Crosslin D, et al. CNV Association of Diverse Clinical Phenotypes from eMERGE reveals novel disease biology underlying cardiovascular disease. International Journal of Cardiology. PMID 31447229 DOI: 10.1016/J.Ijcard.2019.07.058 |
0.637 |
|
| 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 |
0.777 |
|
| 2019 |
Lee G, Kang B, Nho K, Sohn KA, Kim D. MildInt: Deep Learning-Based Multimodal Longitudinal Data Integration Framework. Frontiers in Genetics. 10: 617. PMID 31316553 DOI: 10.3389/Fgene.2019.00617 |
0.309 |
|
| 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 |
0.753 |
|
| 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 |
0.801 |
|
| 2019 |
Verma SS, Verma A, Kim D, Darabos C. Session Introduction - Pattern Recognition in Biomedical Data: Challenges in putting big data to work. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 24: 1-7. PMID 30864305 |
0.677 |
|
| 2019 |
Bang LG, Dasari VR, Kim D, Gogoi RP. Differential gene expression induced by Verteporfin in endometrial cancer cells. Scientific Reports. 9: 3839. PMID 30846786 DOI: 10.1038/S41598-019-40495-9 |
0.318 |
|
| 2019 |
Moore JH, Boland MR, Camara PG, Chervitz H, Gonzalez G, Himes BE, Kim D, Mowery DL, Ritchie MD, Shen L, Urbanowicz RJ, Holmes JH. Preparing next-generation scientists for biomedical big data: artificial intelligence approaches. Personalized Medicine. PMID 30760118 DOI: 10.2217/Pme-2018-0145 |
0.667 |
|
| 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 |
0.737 |
|
| 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 |
0.79 |
|
| 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 |
0.757 |
|
| 2018 |
El-Manzalawy Y, Hsieh TY, Shivakumar M, Kim D, Honavar V. Min-redundancy and max-relevance multi-view feature selection for predicting ovarian cancer survival using multi-omics data. Bmc Medical Genomics. 11: 71. PMID 30255801 DOI: 10.1186/S12920-018-0388-0 |
0.412 |
|
| 2018 |
Li R, Kim D, Wheeler HE, Dudek SM, Dolan ME, Ritchie MD. Integration of genetic and functional genomics data to uncover chemotherapeutic induced cytotoxicity. The Pharmacogenomics Journal. PMID 29795408 DOI: 10.1038/S41397-018-0024-6 |
0.81 |
|
| 2018 |
Verma SS, Lucas A, Zhang X, Veturi Y, Dudek S, Li B, Li R, Urbanowicz R, Moore JH, Kim D, Ritchie MD. Collective feature selection to identify crucial epistatic variants. Biodata Mining. 11: 5. PMID 29713383 DOI: 10.1186/S13040-018-0168-6 |
0.754 |
|
| 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 |
0.771 |
|
| 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 |
0.715 |
|
| 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 |
0.755 |
|
| 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 |
0.706 |
|
| 2017 |
Hall MA, Wallace J, Lucas A, Kim D, Basile AO, Verma SS, McCarty CA, Brilliant MH, Peissig PL, Kitchner TE, Verma A, Pendergrass SA, Dudek SM, Moore JH, Ritchie MD. PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies. Nature Communications. 8: 1167. PMID 29079728 DOI: 10.1038/S41467-017-00802-2 |
0.787 |
|
| 2017 |
Li R, Kim D, Ritchie MD. Methods to analyze big data in pharmacogenomics research. Pharmacogenomics. PMID 28612644 DOI: 10.2217/Pgs-2016-0152 |
0.793 |
|
| 2017 |
Wang S, Jeong HH, Kim D, Wee K, Park HS, Kim SH, Sohn KA. Integrative information theoretic network analysis for genome-wide association study of aspirin exacerbated respiratory disease in Korean population. Bmc Medical Genomics. 10: 31. PMID 28589859 DOI: 10.1186/S12920-017-0266-1 |
0.404 |
|
| 2017 |
Shivakumar M, Lee Y, Bang L, Garg T, Sohn KA, Kim D. Identification of epigenetic interactions between miRNA and DNA methylation associated with gene expression as potential prognostic markers in bladder cancer. Bmc Medical Genomics. 10: 30. PMID 28589857 DOI: 10.1186/S12920-017-0269-Y |
0.317 |
|
| 2017 |
Nho K, Kim S, Horgusluoglu E, Risacher SL, Shen L, Kim D, Lee S, Foroud T, Shaw LM, Trojanowski JQ, Aisen PS, Petersen RC, Jack CR, Weiner MW, Green RC, et al. Association analysis of rare variants near the APOE region with CSF and neuroimaging biomarkers of Alzheimer's disease. Bmc Medical Genomics. 10: 29. PMID 28589856 DOI: 10.1186/S12920-017-0267-0 |
0.353 |
|
| 2017 |
Lee G, Bang L, Kim SY, Kim D, Sohn KA. Identifying subtype-specific associations between gene expression and DNA methylation profiles in breast cancer. Bmc Medical Genomics. 10: 28. PMID 28589855 DOI: 10.1186/S12920-017-0268-Z |
0.329 |
|
| 2017 |
Kim D, Basile AO, Bang L, Horgusluoglu E, Lee S, Ritchie MD, Saykin AJ, Nho K. Knowledge-driven binning approach for rare variant association analysis: application to neuroimaging biomarkers in Alzheimer's disease. Bmc Medical Informatics and Decision Making. 17: 61. PMID 28539126 DOI: 10.1186/S12911-017-0454-0 |
0.8 |
|
| 2017 |
Kim D, Volk H, Girirajan S, Pendergrass S, Hall MA, Verma SS, Schmidt RJ, Hansen RL, Ghosh D, Ludena-Rodriguez Y, Kim K, Ritchie MD, Hertz-Picciotto I, Selleck SB. The joint effect of air pollution exposure and copy number variation on risk for autism. Autism Research : Official Journal of the International Society For Autism Research. PMID 28448694 DOI: 10.1002/Aur.1799 |
0.767 |
|
| 2017 |
Oh JJ, Lee SJ, Hwang JY, Kim D, Lee SE, Hong SK, Ho JN, Yoon S, Sung J, Kim WJ, Byun SS. Exome-based genome-wide association study and risk assessment using genetic risk score to prostate cancer in the Korean population. Oncotarget. PMID 28380453 DOI: 10.18632/Oncotarget.16540 |
0.381 |
|
| 2016 |
Kim D, Li R, Lucas A, Verma SS, Dudek SM, Ritchie MD. Using knowledge-driven genomic interactions for multi-omics data analysis: metadimensional models for predicting clinical outcomes in ovarian carcinoma. Journal of the American Medical Informatics Association : Jamia. PMID 28040685 DOI: 10.1093/Jamia/Ocw165 |
0.803 |
|
| 2016 |
Nho K, Horgusluoglu E, Kim S, Risacher SL, Kim D, Foroud T, Aisen PS, Petersen RC, Jack CR, Shaw LM, Trojanowski JQ, Weiner MW, Green RC, Toga AW, Saykin AJ, et al. Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer's disease. Bmc Medical Genomics. 9: 30. PMID 27535542 DOI: 10.1186/S12920-016-0190-9 |
0.371 |
|
| 2016 |
Li R, Dudek SM, Kim D, Hall MA, Bradford Y, Peissig PL, Brilliant MH, Linneman JG, McCarty CA, Bao L, Ritchie MD. Identification of genetic interaction networks via an evolutionary algorithm evolved Bayesian network. Biodata Mining. 9: 18. PMID 27168765 DOI: 10.1186/S13040-016-0094-4 |
0.806 |
|
| 2016 |
Kim D, Lucas A, Glessner J, Verma SS, Bradford Y, Li R, Frase AT, Hakonarson H, Peissig P, Brilliant M, Ritchie MD. BIOFILTER AS A FUNCTIONAL ANNOTATION PIPELINE FOR COMMON AND RARE COPY NUMBER BURDEN. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 21: 357-68. PMID 26776200 |
0.813 |
|
| 2015 |
Kim D, Li R, Dudek SM, Ritchie MD. Predicting censored survival data based on the interactions between meta-dimensional omics data in breast cancer. Journal of Biomedical Informatics. PMID 26048077 DOI: 10.1016/J.Jbi.2015.05.019 |
0.805 |
|
| 2015 |
Kim D, Li R, Dudek SM, Wallace JR, Ritchie MD. Binning somatic mutations based on biological knowledge for predicting survival: an application in renal cell carcinoma. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 96-107. PMID 25592572 |
0.776 |
|
| 2015 |
Ritchie MD, Holzinger ER, Li R, Pendergrass SA, Kim D. Methods of integrating data to uncover genotype-phenotype interactions. Nature Reviews. Genetics. 16: 85-97. PMID 25582081 DOI: 10.1038/nrg3868 |
0.805 |
|
| 2015 |
Kim D, Joung JG, Sohn KA, Shin H, Park YR, Ritchie MD, Kim JH. Knowledge boosting: a graph-based integration approach with multi-omics data and genomic knowledge for cancer clinical outcome prediction. Journal of the American Medical Informatics Association : Jamia. 22: 109-20. PMID 25002459 DOI: 10.1136/Amiajnl-2013-002481 |
0.68 |
|
| 2014 |
Kim D, Li R, Dudek SM, Frase AT, Pendergrass SA, Ritchie MD. Knowledge-driven genomic interactions: an application in ovarian cancer. Biodata Mining. 7: 20. PMID 25214892 DOI: 10.1186/1756-0381-7-20 |
0.794 |
|
| 2014 |
Joung JG, Kim D, Lee SY, Kang HJ, Kim JH. Integrated analysis of microRNA-target interactions with clinical outcomes for cancers. Bmc Medical Genomics. 7: S10. PMID 25079112 DOI: 10.1186/1755-8794-7-S1-S10 |
0.344 |
|
| 2014 |
Kim D, Shin H, Sohn KA, Verma A, Ritchie MD, Kim JH. Incorporating inter-relationships between different levels of genomic data into cancer clinical outcome prediction. Methods (San Diego, Calif.). 67: 344-53. PMID 24561168 DOI: 10.1016/J.Ymeth.2014.02.003 |
0.755 |
|
| 2014 |
Oh JJ, Byun SS, Lee SE, Hong SK, Jeong CW, Kim D, Kim HJ, Myung SC. Genetic variations in VDR associated with prostate cancer risk and progression in a Korean population Gene. 533: 86-93. PMID 24120391 DOI: 10.1016/J.Gene.2013.09.119 |
0.314 |
|
| 2014 |
Kim D, Ritchie MD. Data Integration for Cancer Clinical Outcome Prediction Journal of Health and Medical Informatics. 5: 1-2. DOI: 10.4172/2157-7420.1000E122 |
0.613 |
|
| 2014 |
Li R, Kim D, Dudek SM, Ritchie MD. An integrated analysis of genome-wide DNA Methylation and genetic variants underlying etoposide-induced cytotoxicity in European and African populations Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 8602: 928-938. DOI: 10.1007/978-3-662-45523-4_75 |
0.716 |
|
| 2013 |
Kim D, Kim S, Risacher SL, Shen L, Ritchie MD, Weiner MW, Saykin AJ, Nho K. A Graph-Based Integration of Multimodal Brain Imaging Data for the Detection of Early Mild Cognitive Impairment (E-MCI). Multimodal Brain Image Analysis : Third International Workshop, Mbia 2013, Held in Conjunction With Miccai 2013, Nagoya, Japan, September 22, 2013 : Proceedings / Li Shen, Tianming Liu, Pew-Thian Yap, Heng Huang, Dinggang Shen, Carl-Fre.... 8159: 159-169. PMID 25383392 DOI: 10.1007/978-3-319-02126-3_16 |
0.553 |
|
| 2013 |
Sohn KA, Kim D, Lim J, Kim JH. Relative impact of multi-layered genomic data on gene expression phenotypes in serous ovarian tumors. Bmc Systems Biology. 7: S9. PMID 24521303 DOI: 10.1186/1752-0509-7-S6-S9 |
0.388 |
|
| 2013 |
Kim D, Shin H, Joung JG, Lee SY, Kim JH. Intra-relation reconstruction from inter-relation: miRNA to gene expression. Bmc Systems Biology. 7: S8. PMID 24521265 DOI: 10.1186/1752-0509-7-S3-S8 |
0.345 |
|
| 2013 |
Kim D, Li R, Dudek SM, Ritchie MD. ATHENA: Identifying interactions between different levels of genomic data associated with cancer clinical outcomes using grammatical evolution neural network. Biodata Mining. 6: 23. PMID 24359638 DOI: 10.1186/1756-0381-6-23 |
0.807 |
|
| 2012 |
Seo H, Kim D, Chae JH, Kang HG, Lim BC, Cheong HI, Kim JH. Development of korean rare disease knowledge base. Healthcare Informatics Research. 18: 272-8. PMID 23346478 DOI: 10.4258/Hir.2012.18.4.272 |
0.349 |
|
| 2012 |
Kim D, Shin H, Song YS, Kim JH. Synergistic effect of different levels of genomic data for cancer clinical outcome prediction. Journal of Biomedical Informatics. 45: 1191-8. PMID 22910106 DOI: 10.1016/J.Jbi.2012.07.008 |
0.43 |
|
| 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 |
0.78 |
|
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