Wasim Ahmad
Quaid-i-Azam University(PK)University of Engineering and Technology Taxila(PK)Petronas (Malaysia)(MY)Ernst Abbe University of Applied Sciences Jena(DE)Amplyx Pharmaceuticals (United States)(US)Friedrich Schiller University Jena(DE)
Publications by Year
Research Areas
Skin and Cellular Biology Research, Hair Growth and Disorders, Wnt/β-catenin signaling in development and cancer, Hearing, Cochlea, Tinnitus, Genetics, Congenital limb and hand anomalies
Most-Cited Works
- → Alopecia Universalis Associated with a Mutation in the Human hairless Gene(1998)413 cited
- → WDR62 is associated with the spindle pole and is mutated in human microcephaly(2010)288 cited
- → Exposing the human nude phenotype(1999)271 cited
- → Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48(2012)247 cited
- → Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease(2013)238 cited
- → Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse(1998)212 cited