Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 33 Records) |
| Query Trace: Big data[original query] |
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| [Genetic risk factors for rheumatoid arthritis]. Nihon rinsho. Japanese journal of clinical medicine 2016 Jun 74 (6): 897-901. Ikari Katsuno |
| Genetic Testing in Pediatric Cardiomyopathy. Pediatric cardiology 2018 Mar 39 (3): 491-500. Ellepola Chalani D, Knight Linda M, Fischbach Peter, Deshpande Shriprasad |
Genome-wide Association Study of Idiopathic Osteonecrosis of the Femoral Head.
Scientific reports 2017 Nov 7 (1): 15035. Sakamoto Yuma, Yamamoto Takuaki, Sugano Nobuhiko, Takahashi Daisuke, Watanabe Toshiyuki, Atsumi Takashi, Nakamura Junichi, Hasegawa Yukiharu, Akashi Koichi, Narita Ichiei, Miyamoto Takeshi, Takeuchi Tsutomu, Ikari Katsunori, Amano Koichi, Fujie Atsuhiro, Kubo Toshikazu, Tada Yoshifumi, Kaneuji Ayumi, Nakamura Hiroaki, Miyamura Tomoya, Kabata Tamon, Yamaji Ken, Okawa Takahiro, Sudo Akihiro, Ohzono Kenji, Tanaka Yoshiya, Yasunaga Yuji, Matsuda Shuichi, Imai Yuuki, , Akiyama Masato, Kubo Michiaki, Kamatani Yoichiro, Iwamoto Yukihide, Ikegawa Shi |
| Meta-Prediction of the Effect of Methylenetetrahydrofolate Reductase Polymorphisms and Air Pollution on Alzheimer's Disease Risk. International journal of environmental research and public health 2017 1 14 (1): . Wu Suh-Mian, Chen Zhao-Feng, Young Lufei, Shiao S Pamela |
| Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer's disease. Scientific reports 2018 5 8 (1): 7102. Grace Christopher, Clarke Robert, Goel Anuj, Farrall Martin, Watkins Hugh, Hopewell Jemma |
| Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs. PLoS genetics 2018 5 14 (4): e1007361. Donner Jonas, Anderson Heidi, Davison Stephen, Hughes Angela M, Bouirmane Julia, Lindqvist Johan, Lytle Katherine M, Ganesan Balasubramanian, Ottka Claudia, Ruotanen Päivi, Kaukonen Maria, Forman Oliver P, Fretwell Neale, Cole Cynthia A, Lohi Hann |
| Clinical and research uses of genetic risk scores in type 1 diabetes. Current opinion in genetics & development 2018 4 50 96-102. Sharp Seth A, Weedon Michael N, Hagopian William A, Oram Richard |
| Use of Big Data to Estimate Prevalence of Defective DNA Repair Variants in the US Population. JAMA dermatology 2019 Jan 155 (1): 72-78. Pugh Jennifer, Khan Sikandar G, Tamura Deborah, Goldstein Alisa M, Landi Maria Teresa, DiGiovanna John J, Kraemer Kenneth |
| Multi-faceted computational assessment of risk and progression in oligodendroglioma implicates NOTCH and PI3K pathways. NPJ precision oncology 2018 11 2 24. Halani Sameer H, Yousefi Safoora, Velazquez Vega Jose, Rossi Michael R, Zhao Zheng, Amrollahi Fatemeh, Holder Chad A, Baxter-Stoltzfus Amelia, Eschbacher Jennifer, Griffith Brent, Olson Jeffrey J, Jiang Tao, Yates Joseph R, Eberhart Charles G, Poisson Laila M, Cooper Lee A D, Brat Daniel |
| Toward personalized cognitive diagnostics of at-genetic-risk Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America 2019 4 116 (19): 9285-9292. Coughlan Gillian, Coutrot Antoine, Khondoker Mizanur, Minihane Anne-Marie, Spiers Hugo, Hornberger Micha |
| Studying the effects of haplotype partitioning methods on the RA-associated genomic results from the North American Rheumatoid Arthritis Consortium (NARAC) dataset.
Journal of advanced research 2019 Jul 18 113-126. Saad Mohamed N, Mabrouk Mai S, Eldeib Ayman M, Shaker Olfat |
| Towards precision medicine: interrogating the human genome to identify drug pathways associated with potentially functional, population-differentiated polymorphisms. The pharmacogenomics journal 2019 10 19 (6): 516-527. Bachtiar Maulana, Ooi Brandon Nick Sern, Wang Jingbo, Jin Yu, Tan Tin Wee, Chong Samuel S, Lee Caroline G |
| RETRACTED: CGVD: a genomic variation database for Chinese populations. Nucleic acids research 2019 10 48 (D1): D1174-D1180. Zeng Jingyao, Yuan Na, Zhu Junwei, Pan Mengyu, Zhang Hao, Wang Qi, Shi Shuo, Du Zhenglin, Xiao Jing |
| Neuroimaging PheWAS (Phenome-Wide Association Study): A Free Cloud-Computing Platform for Big-Data, Brain-Wide Imaging Association Studies. Neuroinformatics 2020 8 19 (2): 285-303. Zhao Lu, Batta Ishaan, Matloff William, O'Driscoll Caroline, Hobel Samuel, Toga Arthur |
| The effect of ALDH2 rs671 gene mutation on clustering of cardiovascular risk factors in a big data study of Chinese population: associations differ between the sexes. BMC cardiovascular disorders 2020 Dec 20 (1): 509. Wang Danchen, Zou Yutong, Yu Songlin, Lin Songbai, Li Honglei, Yin Yicong, Qiu Ling, Xu Tengda, Wu J |
| Using machine learning and big data to explore the drug resistance landscape in HIV. PLoS computational biology 2021 8 17 (8): e1008873. Blassel Luc, Tostevin Anna, Villabona-Arenas Christian Julian, Peeters Martine, Hué Stéphane, Gascuel Olivier, |
| Utilizing Publicly Available Cancer Clinicogenomic Data on CBioPortal to Compare Epidermal Growth Factor Receptor Mutant and Wildtype Non-Small Cell Lung Cancer. Cureus 2021 5 13 (4): e14683. Dhar Chir |
| Identifying Clinical and Genomic Features Associated With Chronic Kidney Disease. Frontiers in big data 2020 3 528828. Moreno M Megan, Bain Travaughn C, Moreno Melissa S, Carroll Katherine C, Cunningham Emily R, Ashton Zoe, Poteau Roby, Subasi Ersoy, Lipkowitz Michael, Subasi Munevver Mi |
| Using big data of genetics, health claims, and brain imaging to challenge the categorical classification in mental illness. Journal of the Chinese Medical Association : JCMA 2021 12 85 (2): 139-144. Su Tung-Ping, Chen Mu-Hong, Tu Pei-C |
| Impact of age-related macular degeneration on diabetic retinopathy: An electronic health record based big data analysis from a tertiary eye centre in South India. Indian journal of ophthalmology 2021 10 69 (11): 3184-3188. Sahoo Niroj K, Mehta Mehul C, Rani Padmaja K, Khanna Rohit C, Raman Rajiv, Bhattacharya Jayanta, Das Anthony V, Murthy Gudlavalleti V S, Narayanan Ra |
| GWASinspector: comprehensive quality control of genome-wide association study results. Bioinformatics (Oxford, England) 2021 1 37 (1): 129-30. Ani Alireza, van der Most Peter J, Snieder Harold, Vaez Ahmad, Nolte Ilja |
| Discovering Innate Driver Variants for Risk Assessment of Early Colorectal Cancer Metastasis. Frontiers in oncology 2022 7 12 898117. Ding Ruo-Fan, Zhang Yun, Wu Lv-Ying, You Pan, Fang Zan-Xi, Li Zhi-Yuan, Zhang Zhong-Ying, Ji Zhi-Lia |
| The prevalence and real-world therapeutic analysis of Chinese patients with KRAS-Mutant Non-Small Cell lung cancer. Cancer medicine 2022 4 11 (19): 3581-3592. Chen Hanxiao, Huang Dingzhi, Lin Gen, Yang Xue, Zhuo Minglei, Chi Yujia, Zhai Xiaoyu, Jia Bo, Wang Jingjing, Wang Yuyan, Li Jianjie, An Tongtong, Wu Meina, Wang Ziping, Zhao J |
| Frequency of actionable secondary findings in 7472 Korean genomes derived from the National Project of Bio Big Data pilot study. Human genetics 2023 9 . Youngjun Kim, Jeong-Min Kim, Hye-Won Cho, Hyun-Young Park, Mi-Hyun Pa |
| A novel missense compound heterozygous variant in TLR1 gene is associated with susceptibility to rheumatoid arthritis - structural perspective and functional annotations. Clinical rheumatology 2023 7 . Usman Pasha, Kiran Hanif, Haseeb Nisar, Rizwan Abid, Muhammad Usman Mirza, Bilal Wajid, Saima Sad |
| Minor alleles in the FTO SNPs contributed to the increased risk of obesity among Korean adults: meta-analysis from nationwide big data-based studies. Nutrition research and practice 2023 2 17 (1): 62-72. Kim Oh Yoen, Park Jihyun, Lee Jounghee, Sohn Cheongmin, Yoon Mi Ock, Lee Myoungso |
| Whole genome sequencing for inherited retinal diseases in the Korean National Project of Bio Big Data. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2023 11 . Richul Oh, Se Joon Woo, Kwangsic J |
| Exploring novel MYH7 gene variants using in silico analyses in Korean patients with cardiomyopathy. BMC medical genomics 2024 9 17 (1): 225. Oc-Hee Kim, Jihyun Kim, Youngjun Kim, Soyoung Lee, Beom Hee Lee, Bong-Jo Kim, Hyun-Young Park, Mi-Hyun Pa |
| Family history of cancer and lung cancer: Utility of big data and artificial intelligence for exploring the role of genetic risk. Lung cancer (Amsterdam, Netherlands) 2024 8 195 107920. Virginia Calvo, Emetis Niazmand, Enric Carcereny, Delvys Rodriguez-Abreu, Manuel Cobo, Rafael López-Castro, María Guirado, Carlos Camps, Ana Laura Ortega, Reyes Bernabé, Bartomeu Massutí, Rosario Garcia-Campelo, Edel Del Barco, José Luis González-Larriba, Joaquim Bosch-Barrera, Marta Martínez, María Torrente, María-Esther Vidal, Mariano Provenc |
| Secondary findings in genes related to cancer phenotypes in Turkish exome sequencing data from 2020 individuals. American journal of medical genetics. Part A 2024 6 e63806. Oguzhan Demir, Kubra Adanur Saglam, Mustafa Yilmaz, Tuna Apuhan, Alper Han Cebi, Ayberk Turkyilm |
- Page last reviewed:Feb 1, 2024
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