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

Rare genetic variants confer a high risk of ADHD and implicate neuronal biology

罕见基因变异会增加患注意力缺陷多动障碍(ADHD)的风险,并与神经元生物学有关。

Demontis, Ditte; Duan, Jinjie; Hsu, Yu-Han H; Pintacuda, Greta; Grove, Jakob; Nielsen, Trine Tollerup; Thirstrup, Janne; Martorana, Makayla; Botts, Travis; Satterstrom, F Kyle; Bybjerg-Grauholm, Jonas; Tsai, Jason H Y; Glerup, Simon; Hoogman, Martine; Buitelaar, Jan; Klein, Marieke; Ziegler, Georg C; Jacob, Christian; Grimm, Oliver; Bayas, Maximilian; Kobayashi, Nene F; Kittel-Schneider, Sarah; Lesch, Klaus-Peter; Franke, Barbara; Reif, Andreas; Agerbo, Esben; Werge, Thomas; Nordentoft, Merete; Mors, Ole; Mortensen, Preben Bo; Lage, Kasper; Daly, Mark J; Neale, Benjamin M; Børglum, Anders D

Precision functional neuroimaging reveals individually specific auditory responses in infants

精准的功能性神经影像学揭示了婴儿个体特异性的听觉反应

Moser, Julia; Labonte, Alyssa K; Madison, Thomas J; Hantzsch, Lana; Pham, Han H N; Weldon, Kimberly B; Camacho, M Catalina; Schwarzlose, Rebecca F; Koirala, Sanju; Lundquist, Jacob T; Sung, Sooyeon; Morales Carrasco, Cristian; Hermosillo, Robert J M; Nelson, Steven M; Elison, Jed T; Fair, Damien A; Sylvester, Chad M

CRISPR/Cas9 editing of β-Conglycinin subunits reduces IgE binding in soybean [Glycine max (L.) Merr.]

利用 CRISPR/Cas9 对 β-伴球蛋白亚基进行编辑可降低大豆 [Glycine max (L.) Merr.] 中的 IgE 结合。

Park, Hye Rang; Park, Sewon; Jun, Joo-Mi; Shin, Yoon Ji; Hwang, Yeojin; Jeong, Kyoung Yong; Kim, Min Young; Kim, Sun Tae; Park, Sangjun; Yoo, Yo-Han H; Lee, Eunsoo; Park, Girim; Kim, Sang-Gyu; Park, Soo-Kwon

Deep learning-based stratification of Schizophrenia Spectrum Disorder from real-world data reveals distinct profiles of common and rare variant genetic signal

基于深度学习的真实世界数据对精神分裂症谱系障碍进行分层,揭示了常见和罕见变异基因信号的不同特征。

Cobuccio, Leonardo; Avellí, Marc Pielies; Webel, Henry; Medina, Ricardo Hernandez; Vaez, Morteza; Hellberg, Kajsa-Lotta Georgii; Hsu, Yu-Han H; Pintacuda, Greta; Rosengren, Anders; Werge, Thomas; Lage, Kasper; Rasmussen, Simon

Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition.

同步长读长基因组、甲基化组、表观基因组和转录组分析揭示了孟德尔遗传病的成因

Vollger Mitchell R, Korlach Jonas, Eldred Kiara C, Swanson Elliott, Underwood Jason G, Bohaczuk Stephanie C, Mao Yizi, Cheng Yong-Han H, Ranchalis Jane, Blue Elizabeth E, Schwarze Ulrike, Munson Katherine M, Saunders Christopher T, Wenger Aaron M, Allworth Aimee, Chanprasert Sirisak, Duerden Brittney L, Glass Ian, Horike-Pyne Martha, Kim Michelle, Leppig Kathleen A, McLaughlin Ian J, Ogawa Jessica, Rosenthal Elisabeth A, Sheppeard Sam, Sherman Stephanie M, Strohbehn Samuel, Yuen Amy L, Stacey Andrew W, Reh Thomas A, Byers Peter H, Bamshad Michael J, Hisama Fuki M, Jarvik Gail P, Sancak Yasemin, Dipple Katrina M, Stergachis Andrew B

Polygenic Score for the Prediction of Postoperative Nausea and Vomiting: A Retrospective Derivation and Validation Cohort Study

多基因评分预测术后恶心呕吐:一项回顾性推导和验证队列研究

Douville, Nicholas J; Bastarache, Lisa; He, Jing; Wu, Kuan-Han H; Vanderwerff, Brett; Bertucci-Richter, Emily; Hornsby, Whitney E; Lewis, Adam; Jewell, Elizabeth S; Kheterpal, Sachin; Shah, Nirav; Mathis, Michael; Engoren, Milo C; Douville, Christopher B; Surakka, Ida; Willer, Cristen; Kertai, Miklos D

Early detection of renal cell carcinoma: a novel cell-free DNA fragmentomics-based liquid biopsy assay

肾细胞癌的早期检测:一种新型的基于无细胞DNA片段组学的液体活检检测方法

Peng, Y L; Yu, B; Huang, T X; Zhou, Z H; Zhang, H; Tang, W X F; Xu, X X; Zhu, D Q; Yang, R W; Bao, H; Wu, X; Han, H; Zhang, Zh L; He, L R; Dong, P; Wei, W S

Multipopulation GWAS for venous thromboembolism identifies novel loci followed by experimental validation in zebrafish

针对静脉血栓栓塞的多群体全基因组关联研究(GWAS)鉴定出新的基因位点,随后在斑马鱼中进行了实验验证。

Wolford, Brooke N; Zhao, Queena Yakun; Wu, Kuan-Han H; Yu, Xinge; Richter, Catherine E; Bhatta, Laxmi; Brumpton, Ben M; Desch, Karl C; Thibord, Florian; Klarin, Derek; Johnson, Andrew D; Trégouët, David-Alexandre; Damrauer, Scott M; Smith, Nicholas L; Lo Faro, Valeria; Tsuo, Kristin; Daly, Mark J; Neale, Benjamin M; Zhou, Wei; Willer, Cristen J; Shavit, Jordan A; Surakka, Ida

A foundational neuronal protein network model unifying multimodal genetic, transcriptional, and proteomic perturbations in schizophrenia

一个基础性的神经元蛋白网络模型,统一了精神分裂症中多模态的遗传、转录和蛋白质组扰动

Pintacuda, Greta; Hsu, Yu-Han H; Páleníková, Petra; Dubonyte, Ugne; Fornelos, Nadine; Chen, Miao; Mena, Daya; Biagini, Julia C; Botts, Travis; Martorana, Makayla; Rebelo, Danzel; Ching, Joshua K T; Crouse, Ethan; Gebre, Hilena; Adiconis, Xian; Haywood, Nathan; Simmons, Sean; Weïwer, Michel; Hawes, Derek; Pietilainen, Olli; Werge, Thomas; Li, Ka Wan; Smit, August B; Kirkeby, Agnete; Levin, Joshua Z; Nehme, Ralda; Lage, Kasper

Precision Functional Neuroimaging Reveals Individually Specific Auditory Responses in Infants

精准功能性神经影像学揭示婴儿个体特异性听觉反应

Moser, Julia; Labonte, Alyssa K; Madison, Thomas J; Hantzsch, Lana; Pham, Han H N; Weldon, Kimberly B; Camacho, M Catalina; Schwarzlose, Rebecca F; Koirala, Sanju; Lundquist, Jacob T; Sung, Sooyeon; Carrasco, Cristian Morales; Hermosillo, Robert J M; Nelson, Steven M; Elison, Jed T; Fair, Damien A; Sylvester, Chad M