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

Advanced technologies in InGaN micro-LED fabrication to mitigate the sidewall effect

采用先进技术制造InGaN微型LED器件以减轻侧壁效应

Liu, Zhiyuan; Cao, Haicheng; Tang, Xiao; Liu, Tingang; Lu, Yi; Jiang, Zixian; Xiao, Na; Li, Xiaohang

Bi-Allelic MARVELD2 Variant Identified with Exome Sequencing in a Consanguineous Multiplex Ghanaian Family Segregating Non-Syndromic Hearing Loss.

通过外显子组测序在加纳近亲多重家族中鉴定出双等位基因 MARVELD2 变异,该家族表现出非综合征性听力损失

Twumasi Aboagye Elvis, Adadey Samuel Mawuli, Alves de Souza Rios Leonardo, Esoh Kevin K, Wonkam-Tingang Edmond, Xhakaza Lettilia, De Kock Carmen, Schrauwen Isabelle, Amenga-Etego Lucas, Lang Dirk, Awandare Gordon A, Leal Suzanne M, Mowla Shaheen, Wonkam Ambroise

Etching-free pixel definition in InGaN green micro-LEDs

InGaN绿色微型LED的无蚀刻像素定义

Liu, Zhiyuan; Lu, Yi; Cao, Haicheng; Maciel Garcia, Glen Isaac; Liu, Tingang; Tang, Xiao; Xiao, Na; Aguileta Vazquez, Raul; Nong, Mingtao; Li, Xiaohang

Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension

外显子组测序表明 SYNE1 基因的祖先相关孟德尔变异与儿童期原发性高血压有关

Ian Copeland, Edmond Wonkam-Tingang, Monesha Gupta-Malhotra, S Shahrukh Hashmi, Yixing Han, Aarti Jajoo, Nancy J Hall, Paula P Hernandez, Natasha Lie, Dan Liu, Jun Xu, Jill Rosenfeld, Aparna Haldipur, Zelene Desire, Zeynep H Coban-Akdemir, Daryl A Scott, Qing Li, Hsiao-Tuan Chao, Ana M Zaske, James

Study on the Powder-Spreading Process of Walnut Shell/Co-PES Biomass Composite Powder in Additive Manufacturing

核桃壳/Co-PES生物质复合粉末在增材制造中的粉末铺展工艺研究

Yu, Yueqiang; Ma, Tingang; Wang, Suling; Jiang, Minzheng; Gao, Sheng; Guo, Yanling; Jiang, Ting; Doumbia, Bakary S; Yan, Bo; Shen, Shaorui

Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment

与非综合征性听力障碍相关的创始人变异体的全球分布

Aboagye, Elvis Twumasi; Adadey, Samuel Mawuli; Wonkam-Tingang, Edmond; Amenga-Etego, Lucas; Awandare, Gordon A; Wonkam, Ambroise

Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes

对加纳家族进行外显子组测序,揭示了已知的和候选的听力障碍基因

Wonkam, Ambroise; Adadey, Samuel Mawuli; Schrauwen, Isabelle; Aboagye, Elvis Twumasi; Wonkam-Tingang, Edmond; Esoh, Kevin; Popel, Kalinka; Manyisa, Noluthando; Jonas, Mario; deKock, Carmen; Nembaware, Victoria; Cornejo Sanchez, Diana M; Bharadwaj, Thashi; Nasir, Abdul; Everard, Jenna L; Kadlubowska, Magda K; Nouel-Saied, Liz M; Acharya, Anushree; Quaye, Osbourne; Amedofu, Geoffrey K; Awandare, Gordon A; Leal, Suzanne M

Hearing loss in Africa: current genetic profile

非洲听力损失:当前基因谱

Adadey, Samuel Mawuli; Wonkam-Tingang, Edmond; Aboagye, Elvis Twumasi; Quaye, Osbourne; Awandare, Gordon A; Wonkam, Ambroise

Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families

基于细胞的 CLIC5A 和 SLC12A2 变异与两个非洲家庭的听力障碍相关分析

Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Leonardo Alves de Souza Rios, Elvis Twumasi Aboagye, Kevin Esoh, Noluthando Manyisa, Carmen De Kock, Gordon A Awandare, Shaheen Mowla, Ambroise Wonkam

Hearing Impairment in South Africa and the Lessons Learned for Planetary Health Genomics: A Systematic Review

南非听力障碍及其对地球健康基因组学的启示:系统性综述

Manyisa, Noluthando; Adadey, Samuel Mawuli; Wonkam-Tingang, Edmond; Yalcouye, Abdoulaye; Wonkam, Ambroise