C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
2007 · Nature Genetics · 444 citations
https://doi.org/10.1038/ng2082
R
Robert W. Baloh
Claim or correct this author profile
Claim this profile or suggest corrections to the name, affiliation, bio, photo, or paper titles. Approved changes appear as verified CitedEvidence overlays.
482
Papers
24.3K
Citations
89
h-index
269
i10-index
Robert W. Baloh is an academic researcher from University of California, Los Angeles. The author has contributed to research in topics: Vestibular and auditory disorders & Ophthalmology and Eye Disorders & Genetic Neurodegenerative Diseases. The author has an h-index of 89, co-authored 410 publications.
Papers by this author
worksMigraine and Benign Positional Vertigo
2000 · Annals of Otology Rhinology & Laryngology · 264 citations
https://doi.org/10.1177/000348940010900407
Voluntary Control of the Human Vestibulo-Ocular Reflex
1984 · Acta Oto-Laryngologica · 191 citations
https://doi.org/10.3109/00016488409130958
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
2016 · Brain · 167 citations
https://doi.org/10.1093/brain/aww217
Familial Clustering of Migraine, Episodic Vertigo, and Ménière's Disease
2008 · Otology & Neurotology · 108 citations
https://doi.org/10.1097/mao.0b013e31815c2abb
Dejerine–Sottas syndrome and vestibular loss due to a point mutation in the PMP22 gene
2005 · Journal of the Neurological Sciences · 20 citations
https://doi.org/10.1016/j.jns.2005.05.003
Research topics
topicsChat about Author
Papers
Chat
Click to start Chat