Rizwan Yousaf

机构：Revvity (United States) · ORCID：0000-0003-2323-0004

发表论文 39 篇 · 总被引 874 次 · h-index 13

代表论文

• Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48 (2012 · Nature Genetics · 被引 257)
• Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74 (2010 · The American Journal of Human Genetics · 被引 122)
• Tricellulin deficiency affects tight junction architecture and cochlear hair cells (2013 · Journal of Clinical Investigation · 被引 104)
• Identification of micro-RNAs in cotton (2008 · Plant Physiology and Biochemistry · 被引 72)
• Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse (2018 · PLoS Genetics · 被引 51)
• Modifier variant of METTL13 suppresses human GAB1–associated profound deafness (2018 · Journal of Clinical Investigation · 被引 44)