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

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

非编码RNA基因RNU4-2的双等位基因变异会导致一种隐性遗传的神经发育综合征,并伴有明显的白质改变。

Rius, Rocio; Blakes, Alexander J M; Chen, Yuyang; De Jonghe, Joachim; Lecoquierre, François; Dawes, Ruebena; Cogne, Benjamin; Kim, Hyung Chul; Alvi, Javeria R; Amblard, Florence; Ansari, Morad; Arlt, Annabelle; Austin-Tse, Christina; Baer, Sarah; Balasubramanian, Meena; Balton, Elsa V; Barcia, Giulia; Beleza-Meireles, Ana; Bernstein, Jonathan A; Beygo, Jasmin; Blanc, Pierre; Bramswig, Nuria C; Braun, Frederik; Buchzik, Daniel; Calame, Daniel G; Campbell, Jamie; Coutton, Charles; Cunningham, Chloe A; Dargie, Nitsuh; Depienne, Christel; Dipple, Katrina M; Dieux, Anne; Dixit, Abhijit; Dreyer, Lauren; Du, Haowei; El Chehadeh, Salima; Field, Michael; Ewans, Lisa J; Geiger, Vanessa; Gibbs, Richard A; Glass, Ian; Grunewald, Olivier; Gueguen, Paul; Haack, Tobias B; Hadj Abdallah, Hamza; Harbuz, Radu; Helbig, Ingo; Horvath, Judit; Hustinx, Alexander; Isidor, Bertrand; Jacquemont, Marie-Line; Jamie, Fraser; Jeanne, Médéric; Kessler, Riley; Klinkhammer, Hannah; Korenke, G Christoph; Kotzaeridou, Urania; Krawitz, Peter; Laurie, Steven; Leventer, Richard J; Levy, Rebecca J; Lupski, James R; Marijon, Pierre; McGinnis, Kaitlin E; Mendez, Rodrigo; Messaoud, Olfa; Nava, Caroline; Nizard, Mevyn; O'Donnell-Luria, Anne; O'Leary, Melanie C; Olivieri, Simone; Parida, Amitav; Pehlivan, Davut; Prentice, Anna Jenne; Posey, Jennifer E; Reuter, Chloe M; Satre, Véronique; Schluth-Bolard, Caroline; Smol, Thomas; Sultan, Tipu; Taylor, John; Thauvin-Robinetvin, Christel; Thevenon, Julien; Uebergang, Eloise; Ueberberg, Sandra; Vincent-Delorme, Catherine; Wassmer, Evangeline; Westwood, Emma; Wheeler, Matthew T; Gulec, Elif Yilmaz; Vanderver, Adeline; Vossough, Arastoo; Sanders, Stephan J; Banka, Siddharth; Findlay, Gregory M; MacArthur, Daniel G; Simons, Cas; Whiffin, Nicola

Targeted BDNF upregulation via upstream open reading frame disruption

通过上游开放阅读框破坏靶向上调BDNF

Feng, Ning; Goedert, Thomas; Svrzikapa, Nenad; Yan, Dongnan; Friedrichsen, Hans J; Hanson, Britt; Ljungdahl, Alicia; Dafinca, Ruxandra; Talbot, Kevin; Sanders, Stephan J; Gupta, Dhanu; Wood, Mathew J A; Roberts, Thomas C

Crossing the finish line towards a disease-modifying treatment for Angelman syndrome

距离研发出安格曼综合征的疾病改善疗法又近了一步

Judson, Matthew C; de Almeida, Luis Pereira; Burdine, Rebecca D; Chamberlain, Stormy J; Deverman, Benjamin E; Distel, Ben; Ehlers, Michael D; Jalazo, Elizabeth; Kushner, Steven A; Nespeca, Mark; Sanders, Stephan J; Scheffner, Martin; Yi, Jason J; Zylka, Mark J; Elgersma, Ype; Philpot, Benjamin D

Genome-scale functional mapping of the mammalian whole brain with in vivo Perturb-seq

利用体内Perturb-seq技术对哺乳动物全脑进行基因组规模的功能图谱绘制

Shi, Tuo; Korshunova, Maria; Kim, Seoyeon; DeTomaso, David; Zheng, Xinhe; Vishvanath, Lavanya; Nyasulu, Thokozile; Huynh, Nhan; Sun, Alexander; Thompson, Patrick C; Zhang, Yifan; Wigdor, Emilie M; Rohani, Narjes; Ali, Salma; Qiu, Huixian; Geralt, Michael; Zhao, Ziyan; Rabhi, Sara; Yao, Zizhen; van Velthoven, Cindy Tj; Nery, Joseph R; Castanon, Rosa Gomez; Dicks, Severin; Chen, Tiffany J; Ecker, Joseph R; Zeng, Hongkui; Zheng, Grace Xy; Sanders, Stephan J; Sundaram, Laksshman; Jin, Xin

Molecular dynamics of Brodmann Area 22 in development and autism

发育和自闭症中布罗德曼22区的分子动力学

Suresh, Varun; Wigdor, Emilie M; Hao, Yuhan; Leonard, Rachel; Asfouri, Joseph; Griffiths, Michael; Evans, Clements; Yuan, Guohua; Rohani, Narjes; Weiss, Jakob; Dema, Chimmi; Mukthar, Tanzila; Lassen, Frederik H; Schafer, Nicole; Dong, Shan; Palmer, Duncan S; Chang, Edward F; Sanders, Stephan J; Nowakowski, Tomasz J

CRISPR activation for SCN2A-related neurodevelopmental disorders

CRISPR激活治疗SCN2A相关神经发育障碍

Tamura, Serena; Nelson, Andrew D; Spratt, Perry W E; Hamada, Elizabeth C; Zhou, Xujia; Kyoung, Henry; Li, Zizheng; Arnould, Coline; Barskyi, Vladyslav; Krupkin, Beniamin; Young, Kiana; Zhao, Jingjing; Holden, Stephanie S; Sahagun, Atehsa; Keeshen, Caroline M; Lu, Congyi; Ben-Shalom, Roy; Taloma, Sunrae E; Schamiloglu, Selin; Li, Ying C; Min, Lia; Jenkins, Paul M; Pan, Jen Q; Paz, Jeanne T; Sanders, Stephan J; Matharu, Navneet; Ahituv, Nadav; Bender, Kevin J

Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry

对超过7万名欧洲血统婴儿开始行走年龄的全基因组关联荟萃分析

Gui, Anna; Hollowell, Anja; Wigdor, Emilie M; Morgan, Morgan J; Hannigan, Laurie J; Corfield, Elizabeth C; Odintsova, Veronika; Hottenga, Jouke-Jan; Wong, Andrew; Pool, René; Cullen, Harriet; Wilson, Siân; Warrier, Varun; Eilertsen, Espen M; Andreassen, Ole A; Middeldorp, Christel M; St Pourcain, Beate; Bartels, Meike; Boomsma, Dorret I; Hartman, Catharina A; Robinson, Elise B; Arichi, Tomoki; Edwards, Anthony D; Johnson, Mark H; Dudbridge, Frank; Sanders, Stephan J; Havdahl, Alexandra; Ronald, Angelica

Massively parallel reporter assays and mouse transgenic assays provide correlated and complementary information about neuronal enhancer activity.

大规模平行报告基因检测和转基因小鼠检测提供了关于神经元增强子活性的相关和互补信息

Kosicki Michael, Laboy Cintrón Dianne, Keukeleire Pia, Schubach Max, Page Nicholas F, Georgakopoulos-Soares Ilias, Akiyama Jennifer A, Plajzer-Frick Ingrid, Novak Catherine S, Kato Momoe, Hunter Riana D, von Maydell Kianna, Barton Sarah, Godfrey Patrick, Beckman Erik, Sanders Stephan J, Kircher Martin, Pennacchio Len A, Ahituv Nadav

Publisher Correction: Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism

出版商更正:评估家族表型偏差以衡量自闭症中新发突变的影响

Kim, Soo-Whee; Lee, Hyeji; Song, Da Yea; Lee, Gang-Hee; Han, Jae Hyun; Lee, Jee Won; Byun, Hee Jung; Son, Ji Hyun; Kim, Ye Rim; Lee, Yoojeong; Kim, Eunjoon; Werling, Donna M; Kim, So Hyun; Sanders, Stephan J; Yoo, Hee Jeong; An, Joon-Yong

Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism

评估家族表型偏差以衡量自闭症中新发突变的影响

Kim, Soo-Whee; Lee, Hyeji; Song, Da Yea; Lee, Gang-Hee; Han, Jae Hyun; Lee, Jee Won; Byun, Hee Jung; Son, Ji Hyun; Kim, Ye Rim; Lee, Yoojeong; Kim, Eunjoon; Werling, Donna M; Kim, So Hyun; Sanders, Stephan J; Yoo, Hee Jeong; An, Joon-Yong