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

The oligogenic inheritance test GCOD detects risk genes and their interactions in congenital heart defects

寡基因遗传检测 GCOD 可检测先天性心脏缺陷的风险基因及其相互作用。

Pittman, Maureen; Lee, Kihyun; Felix, Franco; Huang, Yu; Lam, Adrienne; Costa, Mauro W; Srivastava, Deepak; Pollard, Katherine S

Electrophysiological development and functional plasticity in dissociated human cerebral organoids across multiple cell lines

多种细胞系中分离的人类脑类器官的电生理发育和功能可塑性

Pavlinek, Adam; Guerrisi, Sara; O'Driscoll, Kara; Polit, Lucia Dutan; Nagy, Roland; Lancaster, Madeline A; Vernon, Anthony C; Srivastava, Deepak P

Genome-wide CRISPRi screen identifies basigin loss as protective in cardiac hypoxia

全基因组CRISPRi筛选发现basigin缺失在心脏缺氧中具有保护作用

Flanigan, Will R; Midha, Ayush D; Blume, Skyler Y; Marti-Mateos, Yolanda; Costa, Mauro W; Huang, Yu; Baik, Alan H; Huynh, Helen; Susarla, Gautam; Bennett, Neal K; Nowak, Romana A; Srivastava, Deepak; Nakamura, Ken; Jain, Isha H

Author Correction: Myocardial reprogramming by HMGN1 underlies heart defects in trisomy 21

作者更正:HMGN1介导的心肌重编程是21三体综合征心脏缺陷的根本原因

Ranade, Sanjeev S; Li, Feiya; Whalen, Sean; Pelonero, Angelo; Ye, Lin; Huang, Yu; Brand, Abigail; Nishino, Tomohiro; Mital, Rahul; Boileau, Ryan M; Koback, Frances; Padmanabhan, Arun; Yu, Victoria; Cimarosti, Bastien; Presas-Ramos, Diana; Merriman, Alexander F; Wallace, Langley Grace; Nguyen, Annie; Poulis, Nikolaos; Costa, Mauro W; Gifford, Casey A; Pollard, Katherine S; Srivastava, Deepak

Myocardial reprogramming by HMGN1 underlies heart defects in trisomy 21.

HMGN1介导的心肌重编程是21三体综合征心脏缺陷的根本原因。

Ranade Sanjeev S, Li Feiya, Whalen Sean, Pelonero Angelo, Ye Lin, Huang Yu, Brand Abigail, Nishino Tomohiro, Mital Rahul, Boileau Ryan M, Koback Frances, Padmanabhan Arun, Yu Victoria, Cimarosti Bastien, Presas-Ramos Diana, Merriman Alexander F, Wallace Langley Grace, Nguyen Annie, Poulis Nikolaos, Costa Mauro W, Gifford Casey A, Pollard Katherine S, Srivastava Deepak

The maternal X chromosome affects cognition and brain ageing in female mice.

母系 X 染色体影响雌性小鼠的认知能力和大脑衰老

Abdulai-Saiku Samira, Gupta Shweta, Wang Dan, Marino Francesca, Moreno Arturo J, Huang Yu, Srivastava Deepak, Panning Barbara, Dubal Dena B

Recessive genetic contribution to congenital heart disease in 5,424 probands

5424例先证者中隐性遗传因素对先天性心脏病的影响

Dong, Weilai; Jin, Sheng Chih; Sierant, Michael C; Lu, Ziyu; Li, Boyang; Lu, Qiongshi; Morton, Sarah U; Zhang, Junhui; López-Giráldez, Francesc; Nelson-Williams, Carol; Knight, James R; Zhao, Hongyu; Cao, Junyue; Mane, Shrikant; Gruber, Peter J; Lek, Monkol; Goldmuntz, Elizabeth; Deanfield, John; Giardini, Alessandro; Mital, Seema; Russell, Mark; Gaynor, J William; Cnota, James F; Wagner, Michael; Srivastava, Deepak; Bernstein, Daniel; Porter, George A Jr; Newburger, Jane; Roberts, Amy E; Yandell, Mark; Yost, H Joseph; Tristani-Firouzi, Martin; Kim, Richard; Seidman, Jonathan; Chung, Wendy K; Gelb, Bruce D; Seidman, Christine E; Lifton, Richard P; Brueckner, Martina

Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genes

对 11,555 名先证者的基因组分析鉴定出 60 个显性先天性心脏病基因

Sierant, Michael C; Jin, Sheng Chih; Bilguvar, Kaya; Morton, Sarah U; Dong, Weilai; Jiang, Wei; Lu, Ziyu; Li, Boyang; López-Giráldez, Francesc; Tikhonova, Irina; Zeng, Xue; Lu, Qiongshi; Choi, Jungmin; Zhang, Junhui; Nelson-Williams, Carol; Knight, James R; Zhao, Hongyu; Cao, Junyue; Mane, Shrikant; Sedore, Stanley C; Gruber, Peter J; Lek, Monkol; Goldmuntz, Elizabeth; Deanfield, John; Giardini, Alessandro; Mital, Seema; Russell, Mark; Gaynor, J William; King, Eileen; Wagner, Michael; Srivastava, Deepak; Shen, Yufeng; Bernstein, Daniel; Porter, George A Jr; Newburger, Jane W; Seidman, Jonathan G; Roberts, Amy E; Yandell, Mark; Yost, H Joseph; Tristani-Firouzi, Martin; Kim, Richard; Chung, Wendy K; Gelb, Bruce D; Seidman, Christine E; Brueckner, Martina; Lifton, Richard P

Uncovering Developmental Origins of Aortic Valve Disease: A Clinically Relevant Genetic Model of Aortic Stenosis

揭示主动脉瓣疾病的发育起源:主动脉瓣狭窄的临床相关遗传模型

Srivastava, Deepak

Coffee intake is associated with telomere length in severe mental disorders

咖啡摄入量与严重精神障碍患者的端粒长度有关

Mlakar, Vid; Di Forti, Marta; Halff, Els F; Srivastava, Deepak P; Akkouh, Ibrahim; Djurovic, Srdjan; Martin-Ruiz, Carmen; Quintana, Daniel S; Birkenæs, Viktoria; Steen, Nils Eiel; Ormerod, Monica Beg; Andreassen, Ole A; Aas, Monica