Joseph J. Higgins
Center for Human Genetics and Child Neurology
Mid-Hudson Family Health Institute
279 Main Street
Suite 203A
USA
Name/email consistency: high
- HS1-BP3 gene variant is common in familial essential tremor. Higgins, J.J., Lombardi, R.Q., Pucilowska, J., Jankovic, J., Golbe, L.I., Verhagen, L. Mov. Disord. (2006)
- A variant in the HS1-BP3 gene is associated with familial essential tremor. Higgins, J.J., Lombardi, R.Q., Pucilowska, J., Jankovic, J., Tan, E.K., Rooney, J.P. Neurology (2005)
- Integrated physical map of the human essential tremor gene region (ETM2) on chromosome 2p24.3-p24.2. Higgins, J.J., Lombardi, R.Q., Pucilowska, J., Ruszczyk, M.U. Am. J. Med. Genet. B Neuropsychiatr. Genet. (2004)
- Candidate genes for recessive non-syndromic mental retardation on chromosome 3p (MRT2A). Higgins, J.J., Pucilowska, J., Lombardi, R.Q., Rooney, J.P. Clin. Genet. (2004)
- Haplotype analysis at the ETM2 locus in a Singaporean sample with familial essential tremor. Higgins, J.J., Lombardi, R.Q., Tan, E.K., Jankovic, J., Pucilowska, J., Rooney, J.P. Clin. Genet. (2004)
- A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation. Higgins, J.J., Pucilowska, J., Lombardi, R.Q., Rooney, J.P. Neurology (2004)
- Haplotype analysis of the ETM2 locus in familial essential tremor. Higgins, J.J., Jankovic, J., Lombardi, R.Q., Pucilowska, J., Tan, E.K., Ashizawa, T., Ruszczyk, M.U. Neurogenetics (2003)
- An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia. Higgins, J.J., Loveless, J.M., Goswami, S., Nee, L.E., Cozzo, C., De Biase, A., Rosen, D.R. Neurology (2001)
