Jean‐Pierre Hardelin
Centre National de la Recherche Scientifique(FR)Inserm(FR)Sorbonne Université(FR)Institut de Biologie Paris-Seine(FR)Neurosciences Paris-Seine(FR)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Hypothalamic control of reproductive hormones, Vestibular and auditory disorders, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Biochemical Analysis and Sensing Techniques
Most-Cited Works
- → Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome(2003)827 cited
- → The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules(1991)683 cited
- → KCNQ4, a K + channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway(2000)403 cited
- → Molecular Genetics of Hearing Loss(2001)321 cited
- → Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model(2019)284 cited
- → Kallmann syndrome(2008)213 cited