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Year | Number of Results |
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2020 | 1 |
2022 | 4 |
2023 | 1 |
2024 | 0 |
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Page 1
Identification of Genetic Variants Associated with Severe Myocardial Bridging through Whole-Exome Sequencing.
J Pers Med. 2023 Oct 18;13(10):1509. doi: 10.3390/jpm13101509.
J Pers Med. 2023.
PMID: 37888120
Free PMC article.
Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population.
Wong HS, Tsai SY, Chu HW, Lin MR, Lin GH, Tai YT, Shen CY, Chang WC.
Wong HS, et al. Among authors: lin mr.
PLoS Genet. 2022 Jan 20;18(1):e1009952. doi: 10.1371/journal.pgen.1009952. eCollection 2022 Jan.
PLoS Genet. 2022.
PMID: 35051171
Free PMC article.
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Identification of Druggable Genes for Asthma by Integrated Genomic Network Analysis.
Adikusuma W, Chou WH, Lin MR, Ting J, Irham LM, Perwitasari DA, Chang WP, Chang WC.
Adikusuma W, et al. Among authors: lin mr.
Biomedicines. 2022 Jan 6;10(1):113. doi: 10.3390/biomedicines10010113.
Biomedicines. 2022.
PMID: 35052792
Free PMC article.
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Whole-Exome Sequencing Identifies Genetic Variants for Severe Adolescent Idiopathic Scoliosis in a Taiwanese Population.
Lin MR, Chou PH, Huang KJ, Ting J, Liu CY, Chou WH, Lin GH, Chang JG, Ikegawa S, Wang ST, Chang WC.
Lin MR, et al.
J Pers Med. 2022 Dec 23;13(1):32. doi: 10.3390/jpm13010032.
J Pers Med. 2022.
PMID: 36675693
Free PMC article.
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Application of Whole Exome Sequencing and Functional Annotations to Identify Genetic Variants Associated with Marfan Syndrome.
Lin MR, Chang CM, Ting J, Chang JG, Chou WH, Huang KJ, Cheng G, Chang HH, Chang WC.
Lin MR, et al.
J Pers Med. 2022 Feb 1;12(2):198. doi: 10.3390/jpm12020198.
J Pers Med. 2022.
PMID: 35207686
Free PMC article.
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Germline Genetic Association between Stromal Interaction Molecule 1 (STIM1) and Clinical Outcomes in Breast Cancer Patients.
Huang CC, Lin MR, Yang YC, Hsu YW, Wong HS, Chang WC.
Huang CC, et al. Among authors: lin mr.
J Pers Med. 2020 Dec 17;10(4):287. doi: 10.3390/jpm10040287.
J Pers Med. 2020.
PMID: 33348924
Free PMC article.
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