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

NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke

NOTCH3 p.Arg1231Cys 突变在南亚人群中显著富集,且与中风相关。

Rodriguez-Flores, Juan Lorenzo; Khalid, Shareef; Parikshak, Neelroop; Rasheed, Asif; Ye, Bin; Kapoor, Manav; Backman, Joshua; Sepehrband, Farshid; Gioia, Silvio Alessandro Di; Gelfman, Sahar; De, Tanima; Banerjee, Nilanjana; Sharma, Deepika; Martinez, Hector; Castaneda, Sofia; D'Ambrosio, David; Zhang, Xingmin A; Xun, Pengcheng; Tsai, Ellen; Tsai, I-Chun; Khan, Maleeha Zaman; Jahanzaib, Muhammad; Mian, Muhammad Rehan; Liaqat, Muhammad Bilal; Mahmood, Khalid; Salam, Tanvir Us; Hussain, Muhammad; Iqbal, Javed; Aslam, Faizan; Cantor, Michael N; Tzoneva, Gannie; Overton, John; Marchini, Jonathan; Reid, Jeffrey G; Baras, Aris; Verweij, Niek; Lotta, Luca A; Coppola, Giovanni; Karalis, Katia; Economides, Aris; Fazio, Sergio; Liedtke, Wolfgang; Danesh, John; Kamal, Ayeesha; Frossard, Philippe; Coleman, Thomas; Shuldiner, Alan R; Saleheen, Danish

Transcriptional profiling in microglia across physiological and pathological states identifies a transcriptional module associated with neurodegeneration

对生理和病理状态下小胶质细胞的转录组分析,鉴定出一个与神经退行性变相关的转录模块。

Guvenek, Aysegul; Parikshak, Neelroop; Zamolodchikov, Daria; Gelfman, Sahar; Moscati, Arden; Dobbyn, Lee; Stahl, Eli; Shuldiner, Alan; Coppola, Giovanni

Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes

作者更正:常见和罕见变异与克隆性造血表型的关联

Kessler, Michael D; Damask, Amy; O'Keeffe, Sean; Banerjee, Nilanjana; Li, Dadong; Watanabe, Kyoko; Marketta, Anthony; Van Meter, Michael; Semrau, Stefan; Horowitz, Julie; Tang, Jing; Kosmicki, Jack A; Rajagopal, Veera M; Zou, Yuxin; Houvras, Yariv; Ghosh, Arkopravo; Gillies, Christopher; Mbatchou, Joelle; White, Ryan R; Verweij, Niek; Bovijn, Jonas; Parikshak, Neelroop N; LeBlanc, Michelle G; Jones, Marcus; Glass, David J; Lotta, Luca A; Cantor, Michael N; Atwal, Gurinder S; Locke, Adam E; Ferreira, Manuel A R; Deering, Raquel; Paulding, Charles; Shuldiner, Alan R; Thurston, Gavin; Ferrando, Adolfo A; Salerno, Will; Reid, Jeffrey G; Overton, John D; Marchini, Jonathan; Kang, Hyun M; Baras, Aris; Abecasis, Gonçalo R; Jorgenson, Eric

Rare coding variants in CHRNB2 reduce the likelihood of smoking

CHRNB2基因的罕见编码变异会降低吸烟的可能性

Rajagopal, Veera M; Watanabe, Kyoko; Mbatchou, Joelle; Ayer, Ariane; Quon, Peter; Sharma, Deepika; Kessler, Michael D; Praveen, Kavita; Gelfman, Sahar; Parikshak, Neelroop; Otto, Jacqueline M; Bao, Suying; Chim, Shek Man; Pavlopoulos, Elias; Avbersek, Andreja; Kapoor, Manav; Chen, Esteban; Jones, Marcus B; Leblanc, Michelle; Emberson, Jonathan; Collins, Rory; Torres, Jason; Morales, Pablo Kuri; Tapia-Conyer, Roberto; Alegre, Jesus; Berumen, Jaime; Shuldiner, Alan R; Balasubramanian, Suganthi; Abecasis, Gonçalo R; Kang, Hyun M; Marchini, Jonathan; Stahl, Eli A; Jorgenson, Eric; Sanchez, Robert; Liedtke, Wolfgang; Anderson, Matthew; Cantor, Michael; Lederer, David; Baras, Aris; Coppola, Giovanni

LIF signaling regulates outer radial glial to interneuron fate during human cortical development

LIF信号通路调控人类皮层发育过程中外放射状胶质细胞向中间神经元的分化命运

Madeline G Andrews ,Clara Siebert ,Li Wang ,Matthew L White ,Jayden Ross ,Raul Morales ,Megan Donnay ,Gradi Bamfonga ,Tanzila Mukhtar ,Arpana Arjun McKinney ,Kaila Gemenes ,Shaohui Wang ,Qiuli Bi ,Elizabeth E Crouch ,Neelroop Parikshak ,Georgia Panagiotakos ,Eric Huang ,Aparna Bhaduri ,Arnold R Kriegstein

A large meta-analysis identifies genes associated with anterior uveitis

一项大型荟萃分析确定了与前葡萄膜炎相关的基因

Gelfman, Sahar; Moscati, Arden; Huergo, Santiago Mendez; Wang, Rujin; Rajagopal, Veera; Parikshak, Neelroop; Pounraja, Vijay Kumar; Chen, Esteban; Leblanc, Michelle; Hazlewood, Ralph; Freudenberg, Jan; Cooper, Blerta; Ligocki, Ann J; Miller, Charles G; Van Zyl, Tavé; Weyne, Jonathan; Romano, Carmelo; Sagdullaev, Botir; Melander, Olle; Baras, Aris; Stahl, Eli A; Coppola, Giovanni

Common and rare variant associations with clonal haematopoiesis phenotypes

常见和罕见变异与克隆性造血表型的关联

Kessler, Michael D; Damask, Amy; O'Keeffe, Sean; Banerjee, Nilanjana; Li, Dadong; Watanabe, Kyoko; Marketta, Anthony; Van Meter, Michael; Semrau, Stefan; Horowitz, Julie; Tang, Jing; Kosmicki, Jack A; Rajagopal, Veera M; Zou, Yuxin; Houvras, Yariv; Ghosh, Arkopravo; Gillies, Christopher; Mbatchou, Joelle; White, Ryan R; Verweij, Niek; Bovijn, Jonas; Parikshak, Neelroop N; LeBlanc, Michelle G; Jones, Marcus; Glass, David J; Lotta, Luca A; Cantor, Michael N; Atwal, Gurinder S; Locke, Adam E; Ferreira, Manuel A R; Deering, Raquel; Paulding, Charles; Shuldiner, Alan R; Thurston, Gavin; Ferrando, Adolfo A; Salerno, Will; Reid, Jeffrey G; Overton, John D; Marchini, Jonathan; Kang, Hyun M; Baras, Aris; Abecasis, Gonçalo R; Jorgenson, Eric

Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD

自闭症谱系障碍患者的大脑皮层存在广泛的转录组失调。

Gandal, Michael J; Haney, Jillian R; Wamsley, Brie; Yap, Chloe X; Parhami, Sepideh; Emani, Prashant S; Chang, Nathan; Chen, George T; Hoftman, Gil D; de Alba, Diego; Ramaswami, Gokul; Hartl, Christopher L; Bhattacharya, Arjun; Luo, Chongyuan; Jin, Ting; Wang, Daifeng; Kawaguchi, Riki; Quintero, Diana; Ou, Jing; Wu, Ye Emily; Parikshak, Neelroop N; Swarup, Vivek; Belgard, T Grant; Gerstein, Mark; Pasaniuc, Bogdan; Geschwind, Daniel H

Tropism of SARS-CoV-2 for human cortical astrocytes

SARS-CoV-2 对人类皮质星形胶质细胞的嗜性

Andrews, Madeline G; Mukhtar, Tanzila; Eze, Ugomma C; Simoneau, Camille R; Ross, Jayden; Parikshak, Neelroop; Wang, Shaohui; Zhou, Li; Koontz, Mark; Velmeshev, Dmitry; Siebert, Clara-Vita; Gemenes, Kaila M; Tabata, Takako; Perez, Yonatan; Wang, Li; Mostajo-Radji, Mohammed A; de Majo, Martina; Donohue, Kevin C; Shin, David; Salma, Jahan; Pollen, Alex A; Nowakowski, Tomasz J; Ullian, Erik; Kumar, G Renuka; Winkler, Ethan A; Crouch, Elizabeth E; Ott, Melanie; Kriegstein, Arnold R

Case Report: A False Negative Case of Anti-Yo Paraneoplastic Myelopathy

病例报告:一例抗Yo副肿瘤性脊髓病假阴性病例

Bartley, Christopher M; Parikshak, Neelroop N; Ngo, Thomas T; Alexander, Jessa A; Zorn, Kelsey C; Alvarenga, Bonny A; Kang, Min K; Pedriali, Massimo; Pleasure, Samuel J; Wilson, Michael R