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

Human organoids for rapid validation of gene variants linked to cochlear malformations.

利用人类类器官快速验证与耳蜗畸形相关的基因变异

Zafeer Mohammad Faraz, Ramzan Memoona, Duman Duygu, Mutlu Ahmet, Seyhan Serhat, Kalcioglu M Tayyar, Fitoz Suat, DeRosa Brooke A, Guo Shengru, Dykxhoorn Derek M, Tekin Mustafa

Pharmacogenomics of steroid-induced ocular hypertension: relationship to high-tension glaucomas and new pathophysiologic insight

类固醇诱发性眼高压的药物基因组学:与高眼压性青光眼的关系及新的病理生理学见解

Song, Zeyuan; Pany, Satyabrata; Guo, Shengru; Mazumder, Arpan G; Itakura, Tatsuo; Huang, Jonathan; Magarychoff, Evan; Gurinovich, Anastasia; Benchek, Penelope H; Stamer, W Daniel; Price, Francis W Jr; Willoughby, Colin E; Senthilkumari, Srinivasan; George, Ronnie J; Chitipothu, Srujana; Lass, Jonathan H; Iyengar, Sudha K; Schwartz, Stephen G; Griswold, Anthony J; Sebastiani, Paola; Price, Marianne O; Fini, M Elizabeth

Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2.

遗传性听力损失的遗传异质性:纤毛运动蛋白 TOGARAM2 的潜在作用

Ramzan Memoona, Zafeer Mohammad Faraz, Abad Clemer, Guo Shengru, Owrang Daniel, Alper Ozgul, Mutlu Ahmet, Atik Tahir, Duman Duygu, Bademci Guney, Vona Barbara, Kalcioglu Mahmut Tayyar, Walz Katherina, Tekin Mustafa

Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss

在常染色体显性遗传性感觉神经性听力损失家族中鉴定出新的MYH14变异

Duman, Duygu; Ramzan, Memoona; Subasioglu, Asli; Mutlu, Ahmet; Peart, LéShon; Seyhan, Serhat; Guo, Shengru; Ila, Kadri; Balta, Burhan; Kalcioglu, Mahmut Tayyar; Bademci, Guney; Tekin, Mustafa

H4C5 missense variant leads to a neurodevelopmental phenotype overlapping with Angelman syndrome

H4C5错义变异导致一种与安格曼综合征重叠的神经发育表型。

Borja, Nicholas; Borjas-Mendoza, Paulo; Bivona, Stephanie; Peart, LéShon; Gonzalez, Joanna; Johnson, Brittney Keira; Guo, Shengru; Yusupov, Roman; Bademci, Guney; Tekin, Mustafa

Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice

MINAR2基因(编码膜整合型NOTCH2相关受体2)的突变会导致人类和小鼠耳聋。

Bademci, Guney; Lachgar-Ruiz, María; Deokar, Mangesh; Zafeer, Mohammad Faraz; Abad, Clemer; Yildirim Baylan, Muzeyyen; Ingham, Neil J; Chen, Jing; Sineni, Claire J; Vadgama, Nirmal; Karakikes, Ioannis; Guo, Shengru; Duman, Duygu; Singh, Nitu; Harlalka, Gaurav; Jain, Shirish P; Chioza, Barry A; Walz, Katherina; Steel, Karen P; Nasir, Jamal; Tekin, Mustafa

Specific depletion of resident microglia in the early stage of stroke reduces cerebral ischemic damage

在卒中早期阶段特异性地清除驻留小胶质细胞可减少脑缺血损伤。

Ting Li ,Jin Zhao ,Wenguang Xie ,Wanru Yuan ,Jing Guo ,Shengru Pang ,Wen-Biao Gan ,Diego Gómez-Nicola ,Shengxiang Zhang

Genome-Wide Linkage Study Meta-Analysis of Male Sexual Orientation

男性性取向的全基因组连锁研究荟萃分析

Sanders, Alan R; Beecham, Gary W; Guo, Shengru; Badner, Judith A; Bocklandt, Sven; Mustanski, Brian S; Hamer, Dean H; Martin, Eden R

Genome-Wide Linkage and Association Study of Childhood Gender Nonconformity in Males

男性儿童性别不符的全基因组连锁和关联研究

Sanders, Alan R; Beecham, Gary W; Guo, Shengru; Dawood, Khytam; Rieger, Gerulf; Krishnappa, Ritesha S; Kolundzija, Alana B; Bailey, J Michael; Martin, Eden R

Outreach and recruitment of African Americans for Alzheimer’s disease studies during the COVID‐19 pandemic

在新冠疫情期间,开展针对非裔美国人的阿尔茨海默病研究的宣传和招募工作

Borja, Nicholas; Bivona, Stephanie; Peart, Lé Shon; Johnson, Brittany; Gonzalez, Joanna; Barbouth, Deborah; Moore, Henry; Guo, Shengru; Bademci, Guney; Tekin, Mustafa; Johnson, Francelethia S; Lacroix, Faina C; Contreras, Maricarmen; Baez, Penelope; Ayodele, Temitope; Martinez, Izri; Fonseca, Sandra; Adams, Larry D; Welch, Jacob; Jean‐Francois, Melissa N; Mena, Pedro Ramon; Reitz, Christiane; Vance, Jeffery M; Pericak‐Vance, Margaret A; Cuccaro, Michael L; Beecham, Gary W; Starks, Takiyah D; Caban‐Holt, Allison M; Williams, Kelvin; Adams, Larry D; Haines, Johnathan L; Beecham, Gary W; Reitz, Christiane; Cuccaro, Michael L; Vance, Jeffery M; Pericak‐Vance, Margaret A; Byrd, Goldie S