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Qi Ma

Affiliation : University of Miami

• 4Publications (affiliation in the United States)
• 72Total publications
• 1830Citations
• 27h-index

ORCIDOpenAlex

Research areas

• Angiogenesis and VEGF in Cancer
• Viral-associated cancers and disorders
• MicroRNA in disease regulation
• Herpesvirus Infections and Treatments
• Telomeres, Telomerase, and Senescence

Publications (4)

• A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60
  2016 · Human Genetics · cited 40 times
• MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform
  2016 · Human Mutation · cited 38 times
• A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation
  2015 · Human Molecular Genetics · cited 91 times
• Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53
  2015 · Molecular Genetics and Genomics · cited 28 times

Co-authors

• Xue Zhong Liu
• M’hamed Grati
• Denise Lu Shun Yan
• Rahul Mittal
• Mustafa Tekin
• Zhongmin Lu
• Amjad Farooq
• Susan Halloran Blanton
• Xiao Shi
• Qi Yao
• Manmeet H. Raval
• Tom Walsh

Bibliographic data from OpenAlex (open database).