日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Research on the degradation mechanism, product effects and optimization strategy of the tributyl phosphate solvent system in the PUREX process

对PUREX工艺中磷酸三丁酯溶剂体系的降解机理、产物效应及优化策略的研究

Arnett, D; Spraker, T E; Lan, Tian; Liu, Jiaxin; Liu, Yi

Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry

针对欧洲和非洲血统人群,对变异与利尿剂相互作用作为脂质性状调节因子的全基因组荟萃分析

de las Fuentes, Lisa; Sung, Y J; Sitlani, C M; Avery, C L; Bartz, T M; Keyser, C de; Evans, D S; Li, X; Musani, S K; Ruiter, R; Smith, A V; Sun, F; Trompet, S; Xu, H; Arnett, D K; Bis, J C; Broeckel, U; Busch, E L; Chen, Y-D I; Correa, A; Cummings, S R; Floyd, J S; Ford, I; Guo, X; Harris, T B; Ikram, M A; Lange, L; Launer, L J; Reiner, A P; Schwander, K; Smith, N L; Sotoodehnia, N; Stewart, J D; Stott, D J; Stürmer, T; Taylor, K D; Uitterlinden, A; Vasan, R S; Wiggins, K L; Cupples, L A; Gudnason, V; Heckbert, S R; Jukema, J W; Liu, Y; Psaty, B M; Rao, D C; Rotter, J I; Stricker, B; Wilson, J G; Whitsel, E A

Corrigendum: Identification and validation of seven new loci showing differential DNA methylation related to serum lipid profile: an epigenome-wide approach. The REGICOR study

更正:鉴定和验证七个与血脂谱相关的差异性DNA甲基化新位点:一种全表观基因组方法。REGICOR研究

Sayols-Baixeras, S; Subirana, I; Lluis-Ganella, C; Civeira, F; Roquer, J; Do, A N; Absher, D; Cenarro, A; Muñoz, D; Soriano-Tárraga, C; Jiménez-Conde, J; Ordovas, J M; Senti, M; Aslibekyan, S; Marrugat, J; Arnett, D K; Elosua, R

A DNA methylation biomarker of alcohol consumption

酒精摄入的DNA甲基化生物标志物

Liu, C; Marioni, R E; Hedman, Å K; Pfeiffer, L; Tsai, P-C; Reynolds, L M; Just, A C; Duan, Q; Boer, C G; Tanaka, T; Elks, C E; Aslibekyan, S; Brody, J A; Kühnel, B; Herder, C; Almli, L M; Zhi, D; Wang, Y; Huan, T; Yao, C; Mendelson, M M; Joehanes, R; Liang, L; Love, S-A; Guan, W; Shah, S; McRae, A F; Kretschmer, A; Prokisch, H; Strauch, K; Peters, A; Visscher, P M; Wray, N R; Guo, X; Wiggins, K L; Smith, A K; Binder, E B; Ressler, K J; Irvin, M R; Absher, D M; Hernandez, D; Ferrucci, L; Bandinelli, S; Lohman, K; Ding, J; Trevisi, L; Gustafsson, S; Sandling, J H; Stolk, L; Uitterlinden, A G; Yet, I; Castillo-Fernandez, J E; Spector, T D; Schwartz, J D; Vokonas, P; Lind, L; Li, Y; Fornage, M; Arnett, D K; Wareham, N J; Sotoodehnia, N; Ong, K K; van Meurs, J B J; Conneely, K N; Baccarelli, A A; Deary, I J; Bell, J T; North, K E; Liu, Y; Waldenberger, M; London, S J; Ingelsson, E; Levy, D

APOL1, CDKN2A/CDKN2B, and HDAC9 polymorphisms and small vessel ischemic stroke

APOL1、CDKN2A/CDKN2B 和 HDAC9 多态性与小血管缺血性卒中

Akinyemi, R; Tiwari, H K; Arnett, D K; Ovbiagele, B; Irvin, M R; Wahab, K; Sarfo, F; Srinivasasainagendra, V; Adeoye, A; Perry, R T; Akpalu, A; Jenkins, C; Arulogun, O; Gebregziabher, M; Owolabi, L; Obiako, R; Sanya, E; Komolafe, M; Fawale, M; Adebayo, P; Osaigbovo, G; Sunmonu, T; Olowoyo, P; Chukwuonye, I; Obiabo, Y; Onoja, A; Akinyemi, J; Ogbole, G; Melikam, S; Saulson, R; Owolabi, M

CPT1A methylation is associated with plasma adiponectin

CPT1A甲基化与血浆脂联素相关

Aslibekyan, S; Do, A N; Xu, H; Li, S; Irvin, M R; Zhi, D; Tiwari, H K; Absher, D M; Shuldiner, A R; Zhang, T; Chen, W; Tanner, K; Hong, C; Mitchell, B D; Berenson, G; Arnett, D K

Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans

CHRNA5基因中罕见、低频和常见编码变异及其对欧洲裔和非裔美国人尼古丁依赖的影响

Olfson, E; Saccone, N L; Johnson, E O; Chen, L-S; Culverhouse, R; Doheny, K; Foltz, S M; Fox, L; Gogarten, S M; Hartz, S; Hetrick, K; Laurie, C C; Marosy, B; Amin, N; Arnett, D; Barr, R G; Bartz, T M; Bertelsen, S; Borecki, I B; Brown, M R; Chasman, D I; van Duijn, C M; Feitosa, M F; Fox, E R; Franceschini, N; Franco, O H; Grove, M L; Guo, X; Hofman, A; Kardia, S L R; Morrison, A C; Musani, S K; Psaty, B M; Rao, D C; Reiner, A P; Rice, K; Ridker, P M; Rose, L M; Schick, U M; Schwander, K; Uitterlinden, A G; Vojinovic, D; Wang, J-C; Ware, E B; Wilson, G; Yao, J; Zhao, W; Breslau, N; Hatsukami, D; Stitzel, J A; Rice, J; Goate, A; Bierut, L J

The effects of genes implicated in cardiovascular disease on blood pressure response to treatment among treatment-naive hypertensive African Americans in the GenHAT study

GenHAT 研究中,与心血管疾病相关的基因对未经治疗的高血压非裔美国人血压治疗反应的影响

Do, A N; Lynch, A I; Claas, S A; Boerwinkle, E; Davis, B R; Ford, C E; Eckfeldt, J H; Tiwari, H K; Arnett, D K; Irvin, M R

Identification and validation of seven new loci showing differential DNA methylation related to serum lipid profile: an epigenome-wide approach. The REGICOR study

鉴定和验证七个与血脂谱相关的差异性DNA甲基化新位点:一种全表观基因组方法。REGICOR研究

Sayols-Baixeras, S; Subirana, I; Lluis-Ganella, C; Civeira, F; Roquer, J; Do, A N; Absher, D; Cenarro, A; Muñoz, D; Soriano-Tárraga, C; Jiménez-Conde, J; Ordovas, J M; Senti, M; Aslibekyan, S; Marrugat, J; Arnett, D K; Elosua, R

The role of genetic variants in CRP in radiographic severity in African Americans with early and established rheumatoid arthritis

CRP基因变异在早期和确诊类风湿性关节炎的非裔美国人放射学严重程度中的作用

Danila, M I; Westfall, A O; Raman, K; Chen, L; Reynolds, R J; Hughes, L B; Arnett, D K; McGwin, G; Szalai, A J; van der Heijde, D M; Conn, D; Callahan, L F; Moreland, L W; Bridges, S L Jr