Standout Papers
- Defective myosin VIIA gene responsible for Usher syndrome type IB (1995)
- KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness (1999)
- A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome (1997)
- A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family (1997)
Immediate Impact
13 by Nobel laureates 42 from Science/Nature 68 standout
Citing Papers
Hearing Loss in Adults
2017 Standout
Chemotherapy drugs induce pyroptosis through caspase-3 cleavage of a gasdermin
2017 StandoutNature
Works of Christine Petit being referenced
How the Genetics of Deafness Illuminates Auditory Physiology
2011
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy
2006
Author Peers
| Author | Last Decade | Papers | Cites | |||
|---|---|---|---|---|---|---|
| Christine Petit | 11608 | 9977 | 3055 | 332 | 19.6k | |
| Cynthia C. Morton | 8600 | 2996 | 1332 | 277 | 18.6k | |
| Bechara Kachar | 6283 | 5679 | 3071 | 209 | 14.0k | |
| Klaus Willecke | 23099 | 1744 | 1875 | 351 | 28.3k | |
| Xavier Estivill | 10516 | 2179 | 916 | 507 | 21.8k | |
| Karen P. Steel | 6598 | 5793 | 1517 | 179 | 11.0k | |
| David P. Corey | 8856 | 9194 | 2354 | 148 | 19.4k | |
| Val C. Sheffield | 16912 | 1700 | 1228 | 310 | 27.1k | |
| Shigeyoshi Itohara | 10081 | 894 | 2795 | 276 | 25.0k | |
| Guy Van Camp | 6123 | 7043 | 3068 | 377 | 13.8k | |
| Liqun Luo | 15353 | 2248 | 1798 | 239 | 35.4k |
All Works
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