نتائج البحث - Shivakumar, Manu
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Exome-Wide Rare Variant Analysis From the DiscovEHR Study Identifies Novel Candidate Predisposition Genes for Endometrial Cancer حسب Shivakumar, Manu, Miller, Jason E., Dasari, Venkata Ramesh, Gogoi, Radhika, Kim, Dokyoon
منشور في 2019نص -
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Identification of epigenetic interactions between miRNA and DNA methylation associated with gene expression as potential prognostic markers in bladder cancer حسب Shivakumar, Manu, Lee, Younghee, Bang, Lisa, Garg, Tullika, Sohn, Kyung-Ah, Kim, Dokyoon
منشور في 2017نص -
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Reliability of microarray analysis for studying periodontitis: low consistency in 2 periodontitis cohort data sets from different platforms and an integrative meta-analysis حسب Jeon, Yoon-Seon, Shivakumar, Manu, Kim, Dokyoon, Kim, Chang-Sung, Lee, Jung-Seok
منشور في 2020نص -
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Multi-layered network-based pathway activity inference using directed random walks: application to predicting clinical outcomes in urologic cancer حسب Kim, So Yeon, Choe, Eun Kyung, Shivakumar, Manu, Kim, Dokyoon, Sohn, Kyung-Ah
منشور في 2021نص -
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Leveraging deep phenotyping from health check-up cohort with 10,000 Korean individuals for phenome-wide association study of 136 traits حسب Choe, Eun Kyung, Shivakumar, Manu, Verma, Anurag, Verma, Shefali Setia, Choi, Seung Ho, Kim, Joo Sung, Kim, Dokyoon
منشور في 2022نص -
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Polygenic risk for type 2 diabetes, lifestyle, metabolic health, and cardiovascular disease: a prospective UK Biobank study حسب Yun, Jae-Seung, Jung, Sang-Hyuk, Shivakumar, Manu, Xiao, Brenda, Khera, Amit V., Won, Hong-Hee, Kim, Dokyoon
منشور في 2022نص -
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Population-dependent Intron Retention and DNA Methylation in Breast Cancer حسب Kim, Dongwook, Shivakumar, Manu, Han, Seonggyun, Sinclair, Michael S, Lee, Young-ji, Zheng, Yonglan, Olopade, Olufunmilayo I, Kim, Dokyoon, Lee, Younghee
منشور في 2018نص -
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Genetic analysis of functional rare germline variants across 9 cancer types from an electronic health record linked biobank حسب Shivakumar, Manu, Miller, Jason E., Dasari, Venkata Ramesh, Zhang, Yanfei, Michael Lee, Ming Ta, Carey, David, Gogoi, Radhika, Kim, Dokyoon
منشور في 2021نص -
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NETMAGE: A human disease phenotype map generator for the network-based visualization of phenome-wide association study results حسب Sriram, Vivek, Shivakumar, Manu, Jung, Sang-Hyuk, Nam, Yonghyun, Bang, Lisa, Verma, Anurag, Lee, Seunggeun, Choe, Eun Kyung, Kim, Dokyoon
منشور في 2022نص -
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Rare variants in the splicing regulatory elements of EXOC3L4 are associated with brain glucose metabolism in Alzheimer’s disease حسب Miller, Jason E., Shivakumar, Manu K., Lee, Younghee, Han, Seonggyun, Horgousluoglu, Emrin, Risacher, Shannon L., Saykin, Andrew J., Nho, Kwangsik, Kim, Dokyoon
منشور في 2018نص -
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An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer حسب Oh, Jong Jin, Shivakumar, Manu, Miller, Jason, Verma, Shefali, Lee, Hakmin, Hong, Sung Kyu, Lee, Sang Eun, Lee, Younghee, Lee, Soo Ji, Sung, Joohon, Kim, Dokyoon, Byun, Seok-Soo
منشور في 2019نص -
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Author Correction: An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer حسب Oh, Jong Jin, Shivakumar, Manu, Miller, Jason, Verma, Shefali, Lee, Hakmin, Hong, Sung Kyu, Lee, Sang Eun, Lee, Younghee, Lee, Soo Ji, Sung, Joohon, Kim, Dokyoon, Byun, Seok-Soo
منشور في 2020نص -
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Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population حسب Miller, Jason E., Metpally, Raghu P., Person, Thomas N., Krishnamurthy, Sarathbabu, Dasari, Venkata Ramesh, Shivakumar, Manu, Lavage, Daniel R., Cook, Adam M., Carey, David J., Ritchie, Marylyn D., Kim, Dokyoon, Gogoi, Radhika
منشور في 2019نص