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    MARK LAWRENCE WAHLQVIST(2008-2012) [138/140]
    吳易謙 [54/55]
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    林肇堂 [35/35]
    梁賡義 [15/15]
    江博煌 [72/78]
    溫啟邦(2001-2010) [177/188]
    潘文涵 [110/115]
    熊昭 [369/379]
    莊淑鈞 [43/44]
    莊紹源 [162/168]
    蔡慧如 [162/165]
    蔡憶文(1999-2010) [34/34]
    蕭金福 [188/197]
    藍祚運(2003-2011) [22/23]
    許志成 [385/393]
    邱亞文(2005-2013) [63/99]
    邱弘毅 [49/49]
    邱燕楓 [82/82]
    郭耿南(2003-2010) [89/105]
    鄒小蕙 [101/105]
    陳主智 [61/61]
    陳慶餘(2006-2010) [70/70]
    陳美惠 [32/32]
    陳豐奇 [53/55]
    陳麗光 [106/106]
    黃國晉 [15/15]
    丘政民(2000-2004) [8/8]
    其他 [238/244]
    劉仁沛(1998-2002) [64/65]
    姚姿君(1999-2002) [3/3]
    戴東原(2003-2005) [21/22]
    李明亮(2003-2007) [6/6]
    林仲彥(1999-2005) [31/33]
    林錦瑜(2002-2003) [5/5]
    涂醒哲(2003-2004) [4/4]
    石曜堂(1999-2006) [20/24]
    蔡碧紋(2004-2006) [3/4]
    陳淑媛(2001-2004) [3/3]

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    最後更新時間: 2024-12-01 03:17

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    Showing items 26-50 of 86. (4 Page(s) Totally)
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    DateTitleRelation
    2022-10-27 A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies Nature Methods. 2022 Oct 27;19:1599-1611.
    2022-10-12 A saturated map of common genetic variants associated with human height Nature. 2022 Oct 12;610(7933):704-712.
    2022-10-11 Whole genome sequence analysis of blood lipid levels in >66,000 individuals Nature Communications. 2022 Oct 11;13:Article number 5995.
    2022-08-22 Whole genome association study of the plasma metabolome identifies metabolites linked to cardiometabolic disease in black individuals Nature Communications. 2022 Aug 22;13:Article number 4923.
    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.
    2022-06 Pulse pressure associated with physical function decline and frailty syndrome progression Journal of Hypertension. 2022 Jun;40(Suppl. 1):e1.
    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.
    2021-10-29 Linkage disequilibrium and association analysis Genetic Analysis of Complex Diseases: Third Edition. 2021 Oct 29:182-204.
    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.

    Showing items 26-50 of 86. (4 Page(s) Totally)
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