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

Circulating thyroid hormones and metabolites in children with autism spectrum disorder

自闭症谱系障碍儿童体内循环甲状腺激素及其代谢物

Hancock, Michael; Zhang, Rui; Brown, Suzanne J; Boyder, Conchita; Mullin, Shelby; Campbell, Purdey J; Wilson, Scott G; Lim, Ee Mun; Whitehouse, Andrew J O; Walsh, John P

Plasma Metabolite Profiles of Children with Autism Spectrum Disorder

自闭症谱系障碍儿童的血浆代谢物谱

Mullin, Benjamin H; Stuckey, Madeleine; Brown, Suzanne J; Mullin, Shelby; Campbell, Purdey J; Dudbridge, Frank; Menni, Cristina; Walsh, John P; Whitehouse, Andrew J O; Wilson, Scott G

Genome topology analysis and transcriptomics of human osteoclasts reveals enhancer-promoter interactions at loci for bone traits and diseases

人类破骨细胞的基因组拓扑分析和转录组学揭示了骨骼性状和疾病相关基因位点的增强子-启动子相互作用

Wilson, Scott G; Campbell, Purdey J; Sooraj, Dhanya; Leatherbarrow, Kassandra; Mullin, Benjamin H; Brown, Suzanne J; Zhu, Kun; Mullin, Shelby; Ward, Bryan K; Zhang, Jordan; Torchia, Jonathon; Dudbridge, Frank; Xu, Jiake; Pavlos, Nathan J; Chandler, David; Walsh, John P

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

多性状分析能够阐明甲状腺功能的遗传特征,并识别与临床意义相关的因果关系。

Sterenborg, Rosalie B T M; Steinbrenner, Inga; Li, Yong; Bujnis, Melissa N; Naito, Tatsuhiko; Marouli, Eirini; Galesloot, Tessel E; Babajide, Oladapo; Andreasen, Laura; Astrup, Arne; Åsvold, Bjørn Olav; Bandinelli, Stefania; Beekman, Marian; Beilby, John P; Bork-Jensen, Jette; Boutin, Thibaud; Brody, Jennifer A; Brown, Suzanne J; Brumpton, Ben; Campbell, Purdey J; Cappola, Anne R; Ceresini, Graziano; Chaker, Layal; Chasman, Daniel I; Concas, Maria Pina; Coutinho de Almeida, Rodrigo; Cross, Simone M; Cucca, Francesco; Deary, Ian J; Kjaergaard, Alisa Devedzic; Echouffo Tcheugui, Justin B; Ellervik, Christina; Eriksson, Johan G; Ferrucci, Luigi; Freudenberg, Jan; Fuchsberger, Christian; Gieger, Christian; Giulianini, Franco; Gögele, Martin; Graham, Sarah E; Grarup, Niels; Gunjača, Ivana; Hansen, Torben; Harding, Barbara N; Harris, Sarah E; Haunsø, Stig; Hayward, Caroline; Hui, Jennie; Ittermann, Till; Jukema, J Wouter; Kajantie, Eero; Kanters, Jørgen K; Kårhus, Line L; Kiemeney, Lambertus A L M; Kloppenburg, Margreet; Kühnel, Brigitte; Lahti, Jari; Langenberg, Claudia; Lapauw, Bruno; Leese, Graham; Li, Shuo; Liewald, David C M; Linneberg, Allan; Lominchar, Jesus V T; Luan, Jian'an; Martin, Nicholas G; Matana, Antonela; Meima, Marcel E; Meitinger, Thomas; Meulenbelt, Ingrid; Mitchell, Braxton D; Møllehave, Line T; Mora, Samia; Naitza, Silvia; Nauck, Matthias; Netea-Maier, Romana T; Noordam, Raymond; Nursyifa, Casia; Okada, Yukinori; Onano, Stefano; Papadopoulou, Areti; Palmer, Colin N A; Pattaro, Cristian; Pedersen, Oluf; Peters, Annette; Pietzner, Maik; Polašek, Ozren; Pramstaller, Peter P; Psaty, Bruce M; Punda, Ante; Ray, Debashree; Redmond, Paul; Richards, J Brent; Ridker, Paul M; Russ, Tom C; Ryan, Kathleen A; Olesen, Morten Salling; Schultheiss, Ulla T; Selvin, Elizabeth; Siddiqui, Moneeza K; Sidore, Carlo; Slagboom, P Eline; Sørensen, Thorkild I A; Soto-Pedre, Enrique; Spector, Tim D; Spedicati, Beatrice; Srinivasan, Sundararajan; Starr, John M; Stott, David J; Tanaka, Toshiko; Torlak, Vesela; Trompet, Stella; Tuhkanen, Johanna; Uitterlinden, André G; van den Akker, Erik B; van den Eynde, Tibbert; van der Klauw, Melanie M; van Heemst, Diana; Verroken, Charlotte; Visser, W Edward; Vojinovic, Dina; Völzke, Henry; Waldenberger, Melanie; Walsh, John P; Wareham, Nicholas J; Weiss, Stefan; Willer, Cristen J; Wilson, Scott G; Wolffenbuttel, Bruce H R; Wouters, Hanneke J C M; Wright, Margaret J; Yang, Qiong; Zemunik, Tatijana; Zhou, Wei; Zhu, Gu; Zöllner, Sebastian; Smit, Johannes W A; Peeters, Robin P; Köttgen, Anna; Teumer, Alexander; Medici, Marco

Enhanced resolution profiling in twins reveals differential methylation signatures of type 2 diabetes with links to its complications

双胞胎高分辨率分析揭示了2型糖尿病的差异甲基化特征及其与并发症的关联

Christiansen, Colette; Potier, Louis; Martin, Tiphaine C; Villicaña, Sergio; Castillo-Fernandez, Juan E; Mangino, Massimo; Menni, Cristina; Tsai, Pei-Chien; Campbell, Purdey J; Mullin, Shelby; Ordoñana, Juan R; Monteagudo, Olga; Sachdev, Perminder S; Mather, Karen A; Trollor, Julian N; Pietilainen, Kirsi H; Ollikainen, Miina; Dalgård, Christine; Kyvik, Kirsten; Christensen, Kaare; van Dongen, Jenny; Willemsen, Gonneke; Boomsma, Dorret I; Magnusson, Patrik K E; Pedersen, Nancy L; Wilson, Scott G; Grundberg, Elin; Spector, Tim D; Bell, Jordana T

Epigenome-wide Association Study Shows Differential DNA Methylation of MDC1, KLF9, and CUTA in Autoimmune Thyroid Disease

全基因组关联研究显示自身免疫性甲状腺疾病中MDC1、KLF9和CUTA的DNA甲基化存在差异

Lafontaine, Nicole; Shore, Christopher J; Campbell, Purdey J; Mullin, Benjamin H; Brown, Suzanne J; Panicker, Vijay; Dudbridge, Frank; Brix, Thomas H; Hegedüs, Laszlo; Wilson, Scott G; Bell, Jordana T; Walsh, John P

Identification and field testing of sex-attractant semiochemicals produced by male deer mice, Peromyscus maniculatus

对雄性鹿鼠(Peromyscus maniculatus)产生的性引诱半化学物质进行鉴定和野外试验

Varner, Elana; Gries, Regine; Takács, Stephen; Jackson, Hanna; Purdey, Leah; Gofredo, Daniella; Bibal, Alishba; Gries, Gerhard

Epigenome-Wide Association Study Reveals CpG Sites Associated with Thyroid Function and Regulatory Effects on KLF9

全基因组表观遗传关联研究揭示与甲状腺功能相关的 CpG 位点及其对 KLF9 的调控作用

Weihs, Antoine; Chaker, Layal; Martin, Tiphaine C; Braun, Kim V E; Campbell, Purdey J; Cox, Simon R; Fornage, Myriam; Gieger, Christian; Grabe, Hans J; Grallert, Harald; Harris, Sarah E; Kühnel, Brigitte; Marioni, Riccardo E; Martin, Nicholas G; McCartney, Daniel L; McRae, Allan F; Meisinger, Christa; van Meurs, Joyce B J; Nano, Jana; Nauck, Matthias; Peters, Annette; Prokisch, Holger; Roden, Michael; Selvin, Elizabeth; Beekman, Marian; van Heemst, Diana; Slagboom, Eline P; Swenson, Brenton R; Tin, Adrienne; Tsai, Pei-Chien; Uitterlinden, Andre; Visser, W Edward; Völzke, Henry; Waldenberger, Melanie; Walsh, John P; Köttgen, Anna; Wilson, Scott G; Peeters, Robin P; Bell, Jordana T; Medici, Marco; Teumer, Alexander

Genetic determinants of thyroid function in children

儿童甲状腺功能的遗传决定因素

Mulder, Tessa A; Campbell, Purdey J; Taylor, Peter N; Peeters, Robin P; Wilson, Scott G; Medici, Marco; Dayan, Colin; Jaddoe, Vincent V W; Walsh, John P; Martin, Nicholas G; Tiemeier, Henning; Korevaar, Tim I M

Epigenome-Wide Association Study of Thyroid Function Traits Identifies Novel Associations of fT3 With KLF9 and DOT1L

全基因组关联研究揭示了甲状腺功能性状中游离三碘甲状腺原氨酸(fT3)与KLF9和DOT1L基因的新关联

Lafontaine, Nicole; Campbell, Purdey J; Castillo-Fernandez, Juan E; Mullin, Shelby; Lim, Ee Mun; Kendrew, Phillip; Lewer, Michelle; Brown, Suzanne J; Huang, Rae-Chi; Melton, Phillip E; Mori, Trevor A; Beilin, Lawrence J; Dudbridge, Frank; Spector, Tim D; Wright, Margaret J; Martin, Nicholas G; McRae, Allan F; Panicker, Vijay; Zhu, Gu; Walsh, John P; Bell, Jordana T; Wilson, Scott G