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

The Diverse Genetic Landscape of Hearing Impairment in South African Families

南非家庭听力障碍的多样化遗传图谱

Bharadwaj, Thashi; Acharya, Anushree; Manyisa, Noluthando Rearabetswe; Aboagye, Elvis Twumasi; Peigou Wonkam, Ramses; Xhakaza, Lettilia; Popel, Kalinka; de Kock, Carmen; Schrauwen, Isabelle; Wonkam, Ambroise; Leal, Suzanne M

Trauma team members' perceptions of the effectiveness of the current trauma care system in Addis Ababa, Ethiopia: a phenomenological study

埃塞俄比亚亚的斯亚贝巴创伤团队成员对当前创伤护理系统有效性的看法:一项现象学研究

Goshu, Eyayalem Melese; Manyisa, Zodwa Margaret

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

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

Factors influencing the preparedness for the implementation of the national health insurance scheme at a selected hospital in Gauteng Province, South Africa

影响南非豪登省某医院实施国家医疗保险计划准备情况的因素

Mukwena, Ntsibeng Valerie; Manyisa, Zodwa Margaret

Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon

全外显子组测序揭示了喀麦隆个体中 MYO3A、MYO15A 和 COL9A3 的致病变异以及听力障碍基因祖先等位基因的差异频率

Wonkam, Ambroise; Manyisa, Noluthando; Bope, Christian D; Dandara, Collet; Chimusa, Emile R

Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment

全外显子组测序在被诊断为非综合征性听力障碍的非洲个体中,发现了新的人类-小鼠同源基因中的罕见编码变异

Oluwole, Oluwafemi G; Esoh, Kevin K; Wonkam-Tingang, Edmond; Manyisa, Noluthando; Noubiap, Jean Jacques; Chimusa, Emile R; Wonkam, Ambroise

A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family

REST 中的单等位基因变异与南非家庭中的无综合征常染色体显性听力障碍有关

Noluthando Manyisa, Isabelle Schrauwen, Leonardo Alves de Souza Rios, Shaheen Mowla, Cedrik Tekendo-Ngongang, Kalinka Popel, Kevin Esoh, Thashi Bharadwaj, Liz M Nouel-Saied, Anushree Acharya, Abdul Nasir, Edmond Wonkam-Tingang, Carmen de Kock, Collet Dandara, Suzanne M Leal, Ambroise Wonkam

The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research

听力障碍本体:一种统一听力障碍知识以促进合作研究的工具

Hotchkiss, Jade; Manyisa, Noluthando; Adadey, Samuel Mawuli; Oluwole, Oluwafemi Gabriel; Wonkam, Edmond; Mnika, Khuthala; Yalcouye, Abdoulaye; Nembaware, Victoria; Haendel, Melissa; Vasilevsky, Nicole; Mulder, Nicola J; Jupp, Simon; Wonkam, Ambroise; Mazandu, Gaston K