Muhammad Umair
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Muhammad Umair has a total of 11 co-authors. Here are the top co-authors by number of shared publications:
- Alberto M. Parra-Perez
Otology and Neurotology Group CTS495 Division of Otolaryngology Department of Surgery Instituto De Investigación Biosanitaria ibs.GRANADA Universidad De Granada Granada Spain
1 shared publication - Daniel Burn
Department of Information and Communication Technology, Faculty of Medicine & Health, NSW, The University of Sydney
1 shared publication - Giselle Bianco-Bortoletto
Meniere Disease Neuroscience Research Program, Faculty of Medicine & Health, School of Medical Sciences, The Kolling Institute, University of Sydney
1 shared publication - Jose Antonio López Escámez
The Kolling Institute, University of Sydney
1 shared publication - Kiana Bagheri-Loftabad
Meniere Disease Neuroscience Research Program, Faculty of Medicine & Health, School of Medical Sciences, The Kolling Institute, University of Sydney
1 shared publication - Mai T. Pham
Meniere Disease Neuroscience Research Program, Faculty of Medicine & Health, School of Medical Sciences, The Kolling Institute, University of Sydney
1 shared publication
Latest Publications
- Open Access
MDAtlas: A Multiomics Meniere Disease Database of Genes and Cells
The MDAtlas is a crowdsourcing initiative to provide an open access resource with multiomic dataset about Meniere Disease (MD) -a debilitating audiovestibular disorder- to the scientific/medical community. The platform ( https://multiomic-md.sydney.edu.au ) integrates anonymised genomic, transcriptomic and epigenomic datasets from several MD cohorts with diverse ancestry through the MD multiomic Agreggation Consortium (MD-MAC), helping users investigate common and rare genomic variability, immune cell gene expression, and DNA methylation patterns involved in these conditions. MDAtlas supports secure data upload, advanced filtering, and easy downloading, allowing researchers to compare datasets across populations and discover new disease mechanisms or biomarkers for diagnosis and therapy. By providing interactive tools and harmonized data, MDAtlas accelerates scientific progress and collaboration in hearing and vestibular research.
Open AccessMDAtlas: A Multiomics Meniere Disease Database of Genes and Cells
The MDAtlas is a crowdsourcing initiative to provide an open access resource with multiomic dataset about Meniere Disease (MD) -a debilitating audiovestibular disorder- to the scientific/medical community. The platform ( https://multiomic-md.sydney.edu.au ) integrates anonymised genomic, transcriptomic and epigenomic datasets from several MD cohorts with diverse ancestry through the MD multiomic Agreggation Consortium (MD-MAC), helping users investigate common and rare genomic variability, immune cell gene expression, and DNA methylation patterns involved in these conditions. MDAtlas supports secure data upload, advanced filtering, and easy downloading, allowing researchers to compare datasets across populations and discover new disease mechanisms or biomarkers for diagnosis and therapy. By providing interactive tools and harmonized data, MDAtlas accelerates scientific progress and collaboration in hearing and vestibular research.