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

Relationship between genetically determined telomere length and childhood glioma risk

遗传决定的端粒长度与儿童神经胶质瘤风险之间的关系

Zhou, Naying; Li, Shaobo; Foss-Skiftesvik, Jon; Dahlin, Anna M; Bybjerg-Grauholm, Jonas; Melin, Beatrice; de Smith, Adam J; Walsh, Kyle M; Wiemels, Joseph L

The impact of Indigenous American-like ancestry on the risk of acute lymphoblastic leukemia in Hispanic/Latino children

具有美洲原住民血统对西班牙裔/拉丁裔儿童急性淋巴细胞白血病风险的影响

Langie, Jalen; Chan, Tsz Fung; Yang, Wenjian; Kang, Alice Y; Morimoto, Libby; Stram, Daniel O; Mancuso, Nicholas; Ma, Xiaomei; Metayer, Catherine; Lupo, Philip J; Rabin, Karen R; Scheurer, Michael E; Wiemels, Joseph L; Yang, Jun J; de Smith, Adam J; Chiang, Charleston W K

Genome-wide association study of childhood B-cell acute lymphoblastic leukemia reveals novel African ancestry-specific susceptibility loci

儿童B细胞急性淋巴细胞白血病的全基因组关联研究揭示了新的非洲血统特异性易感基因位点

Im, Cindy; Raduski, Andrew R; Mills, Lauren J; Bhattarai, Kashi Raj; Mobley, Robert J; Barnett, Kelly R; Lu, Zhanni; Liao, Kenneth; Anderson, Nathan; Johnson, Rebecca A; Langer, Erica; Hooten, Anthony J; Seif, Alix E; Bernt, Kathrin M; Tsang, Matthew; Mamou, Brandon A; Gil-de-Gómez, Luis; Wolfson, Julie A; Friedman, Danielle N; Shukla, Neerav; Klesse, Laura J; Marcotte, Erin L; Ji, Lingyun; Dang, Alice; Luo, Minjie; Zhong, Yiming; Langie, Jalen; Chiang, Charleston W K; de Smith, Adam; Wiemels, Joseph L; DeWan, Andrew; Ma, Xiaomei; Metayer, Catherine; Wang, Zhaoming; Nelson, Heather H; Pankratz, Nathan; Yang, Tianzhong; Basu, Saonli; Turcotte, Lucie M; Yang, Jun J; Savic, Daniel; Scheurer, Michael E; Spector, Logan G

Toward Equitable Risk Classification for All Patients with T-ALL

为所有T细胞急性淋巴细胞白血病(T-ALL)患者实现公平的风险分类

de Smith, Adam J

Lower Antemortem [(18)F]flortaucipir PET retention in Males and Older Individuals is Explained by Lower Postmortem Tau Tangle Density

男性和老年人死前[(18)F]flortaucipir PET滞留量较低可由死后tau蛋白缠结密度较低来解释。

Okonechnikov, Konstantin; Schrimpf, Daniel; Koster, Jan; Sievers, Philipp; Milde, Till; Sahm, Felix; Jones, David T W; von Deimling, Andreas; Pfister, Stefan M; Kool, Marcel; Korshunov, Andrey; Behjat, Harry H; Vogel, Jacob W; Strandberg, Olof; Spotorno, Nicola; Rittmo, Jonathan; Collij, Lyduine E; Binette, Alexa Pichet; Xiao, Yu; van Westen, Danielle; Stomrud, Erik; Palmqvist, Sebastian; Mattsson‐Carlgren, Niklas; Ville, Dimitri Van De; Smith, Ruben; Hansson, Oskar; Ossenkoppele, Rik; Cumplido‐Mayoral, Irene; Hristovska, Ines; Binette, Alexa Pichet; Kumar, Atul; Strandberg, Olof; Janelidze, Shorena; Stomrud, Erik; Palmqvist, Sebastian; Ossenkoppele, Rik; Vogel, Jacob W; Mattsson‐Carlgren, Niklas; Hansson, Oskar; Bali, Divya; Janelidze, Shorena; Salvadó, Gemma; Ashton, Nicholas J; Palmqvist, Sebastian; Rodriguez, Juan Lantero; Stomrud, Erik; Mattsson‐Carlgren, Niklas; Hansson, Oskar; Coomans, Emma M; van Tol, Bastaan; Groot, Colin; Smith, Ruben; Palmqvist, Sebastian; Stomrud, Erik; Pontecorvo, Michael; Shcherbinin, Sergey; Kennedy, Ian A; Kotari, Vikas; van der Flier, Wiesje M; Pijnenburg, Yolande AL; Mattsson‐Carlgren, Niklas; Hansson, Oskar; van de Giessen, Elsmarieke; Ossenkoppele, Rik; Coomans, Emma M; Smith, Ruben; Pawlik, Daria; Hauer, Kevin Oliveira; Palmqvist, Sebastian; Pontecorvo, Michael; Shcherbinin, Sergey; Kotari, Vikas; Serrano, Geidy E; Beach, Thomas G; Stomrud, Erik; Mattsson‐Carlgren, Niklas; Rozemuller, Annemieke JM; van der Flier, Wiesje M; Pijnenburg, Yolande AL; van de Giessen, Elsmarieke; Hansson, Oskar; Ossenkoppele, Rik

Genome-wide association study of somatic GATA1s mutations in newborns with Down syndrome

唐氏综合征新生儿体细胞GATA1s突变的全基因组关联研究

Li, Yunqi; Elliott, Natalina; Lein, Patricia; Vyas, Paresh; Roberts, Irene; de Smith, Adam J

Individual functional connectivity constraints on spatial progression of tau pathology in Alzheimer's disease

阿尔茨海默病中tau蛋白病理空间进展的个体功能连接限制

Mabbott, N A; Brown, K L; Manson, J; Bruce, M E; Behjat, Harry H; Vogel, Jacob W; Strandberg, Olof; Spotorno, Nicola; Rittmo, Jonathan; Collij, Lyduine E; Binette, Alexa Pichet; Xiao, Yu; van Westen, Danielle; Stomrud, Erik; Palmqvist, Sebastian; Mattsson‐Carlgren, Niklas; Ville, Dimitri Van De; Smith, Ruben; Hansson, Oskar; Ossenkoppele, Rik

EFFECTS OF BEHAVIORAL THERAPY ON MOUSE MODEL OF ASD ASSOCIATED WITH TUBEROUS SCLEROSIS COMPLEX AND DNA METHYLATION ANALYSIS

行为疗法对伴有结节性硬化症的自闭症谱系障碍小鼠模型的影响及DNA甲基化分析

Mouat, Julia S; Li, Shaobo; Myint, Swe Swe; Laufer, Benjamin I; Lupo, Philip J; Schraw, Jeremy M; Woodhouse, John P; de Smith, Adam J; LaSalle, Janine M; Kotajima, *Hiroko; Sato, Atsushi; Kasai, Shinya; Hagino, Yoko; Tanaka, Miho; Takamatsu, Yukio; Nishito, Yoshimasa; Uchino, Shigeo; Ikeda, Kazutaka

Genome-Wide Association Studies of Down Syndrome Associated Congenital Heart Defects Suggests a Genetically Heterogeneous Risk for CHD in DS

全基因组关联研究表明,唐氏综合征患者发生先天性心脏缺陷的风险存在遗传异质性。

Feldman, Elizabeth R; Li, Yunqi; Cutler, David J; Rosser, Tracie C; Wechsler, Stephanie B; Sanclemente, Lauren; Rachubinski, Angela L; Elliott, Natalina; Vyas, Paresh; Roberts, Irene; Rabin, Karen R; Wagner, Michael; Gelb, Bruce D; Espinosa, Joaquin M; Lupo, Philip J; de Smith, Adam J; Sherman, Stephanie L; Leslie-Clarkson, Elizabeth J

Identifying independent causal cell types for human diseases and risk variants

识别人类疾病和风险变异的独立致病细胞类型

Kim, Artem; Zhang, Zixuan Eleanor; Legros, Come; Lu, Zeyun; de Smith, Adam J; Moore, Jill E; Durvasula, Arun; Mancuso, Nicholas; Gazal, Steven