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    Last Update: 2024-12-01 10:58


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    Showing items 26-50 of 72. (3 Page(s) Totally)
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    DateTitleRelation
    2022-08-01 Insights from a large-scale whole-genome sequencing study of systolic blood pressure, diastolic blood pressure, and hypertension Hypertension. 2022 Aug 1;79(8):1656-1667.
    2022-05 Association of the D-amino acid oxidase gene with methadone dose in heroin dependent patients under methadone maintenance treatment Journal of Human Genetics. 2022 May;67(5):273-278.
    2022-03-07 Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data Nature Genetics. 2022 Mar 07;54(3):263-273.
    2022-01 Increase in plasma CCL11 (Eotaxin-1) in patients with alcohol dependence and changes during detoxification Brain, Behavior, and Immunity. 2022 Jan;99:83-90.
    2021-11-02 A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response[Erratum:Nature Genetics. 202 Oct 05;53(10):1504-1516.] Nature Genetics. 2021 Nov 02;53(12):1722.
    2021-10-05 A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response Nature Genetics. 2021 Oct 05;53(10):1504-1516.
    2021-07 Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose Diabetologia. 2021 Jul;64(7):1613-1625.
    2021-06-15 Genome sequencing unveils a regulatory landscape of platelet reactivity Nature Communications. 2021 Jun 15;12:Article number 3626.
    2021-06-09 Variant-specific inflation factors for assessing population stratification at the phenotypic variance level Nature Communications. 2021 Jun 9;12:Article number 3506.
    2021-03-11 Inherited causes of clonal haematopoiesis in 97,691 whole genomes[Erratum:Nature. 2020 Oct;586(7831):763-768.] Nature. 2021 Mar 11;591:Article number E27.
    2021-02-10 Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program Nature. 2021 Feb 10;590(7845):290-299.
    2020-12-18 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease Nature Communications. 2020 Dec 18;11:Article number 6417.
    2020-10-22 CUX2, BRAP and ALDH2 are associated with metabolic traits in people with excessive alcohol consumption Scientific Reports. 2020 Oct 22;10:Article number 18118.
    2020-10 Inherited causes of clonal haematopoiesis in 97,691 whole genomes Nature. 2020 Oct;586(7831):763-768.
    2020-09 Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale Nature Genetics. 2020 Sep;52(9):969-983.
    2020-06-18 Genetic variants in NECTIN4 encoding an adhesion molecule are associated with continued opioid use PLoS ONE. 2020 Jun 18;15(6):Article number e0234549.
    2020-04 Genetic polymorphisms in the opioid receptor delta 1 (OPRD1) gene are associated with methadone dose in methadone maintenance treatment for heroin dependence Journal of Human Genetics. 2020 Apr;65:381-386.
    2020-02 pWGBSSimla: A profile-based whole-genome bisulfite sequencing data simulator incorporating methylation QTLs, allele-specific methylations and differentially methylated regions Bioinformatics. 2020 Feb;36(3):660-665.
    2020-02 Predicting lung cancer occurrence in never-smoking females in Asia: TNSF-SQ, a prediction model Cancer Epidemiology, Biomarkers and Prevention. 2020 Feb;29(2):452-459.
    2019-05-01 A multi-omics data simulator for complex disease studies and its application to evaluate multi-omics data analysis methods for disease classification GigaScience. 2019 May 1;8(5):Article number giz045.
    2019-03 Genetic loci determining total immunoglobulin E levels from birth through adulthood Allergy. 2019 Mar;74(3):621-625.
    2018-10 GRK5 is associated with the regulation of methadone dosage in heroin dependence International Journal of Neuropsychopharmacology. 2018 Oct;21(10):910-917.
    2018-06 IGF1 gene is associated with triglyceride levels in subjects with family history of hypertension from the SAPPHIRe and TWB projects International Journal of Medical Sciences. 2018 Jun;15(10):1035-1042.
    2018-01 A powerful gene-based test accommodating common and low-frequency variants to detect both main effects and gene-gene interaction effects in case-control studies Frontiers in Genetics. 2018 Jan;8:Article number 228.
    2017-11-16 Missense mutation at CLDN8 associated with a high plasma interferon gamma-inducible protein 10 level in methadone-maintained patients with urine test positive for morphine PLoS ONE. 2017 Nov 16;12(11):Article number e0187639.

    Showing items 26-50 of 72. (3 Page(s) Totally)
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