子類別 圖書 [1/2] 會議論文/會議摘要 [12/12] 期刊論文 [72/72] 鄰近社群 MARK LAWRENCE WAHLQVIST(2008-2012) [138/140] 吳易謙 [54/55] 吳秀英 [10/10] 廖本揚 [39/39] 廖玉潔 [63/65] 張新儀 [245/268] 李孟智 [51/54] 李蘭 [28/28] 林培生 [25/25] 林煜軒 [47/47] 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] 社群統計 近3年內發表的文件:34(39.53%) 含全文筆數:85(98.84%) 文件下載次數統計 下載大於0次:85(100.00%) 下載大於100次:63(74.12%) 檔案下載總次數:21310(0.40%) 最後更新時間: 2024-11-28 12:12 上傳排行 資料載入中..... 下載排行 資料載入中..... 最近上傳 Association of bone turnover marker... Latent space representation of elec... Rare variant contribution to the he... Clustering-based risk stratificatio... Using large language model (LLM) to... Alcohol drinking may modify the ass... A linear relationship of ankle-brac... Understanding and alleviating infor... Machine learning models for predict... Pulse pressure is associated with d...

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顯示項目26-50 / 86. (共4頁) << < 1 2 3 4 > >> 每頁顯示[10|25|50]項目

日期	題名	關聯
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.

顯示項目26-50 / 86. (共4頁) << < 1 2 3 4 > >> 每頁顯示[10|25|50]項目