Joseph J Higgins, MD, PhD
Affiliations: | 2006-2018 | Neurology | Weill Cornell Medical College, New York, NY, United States |
2012-2018 | Neurology | Quest Diagnostics | |
2018-2019 | Clinical Development | uniQure | |
2020- | SalioGen Therapeutics |
Area:
NeurogeneticsGoogle:
"Joseph Higgins"Mean distance: (not calculated yet) | S | N | B | C | P |
Parents
Sign in to add mentorNorman W Barton | post-doc | 1990-1993 | National Institutes of Health-NINDS |
Roscoe O. Brady | post-doc | 1990-1993 | National Institutes of Health-NINDS |
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Publications
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Higgins JJ, Lombardi RQ, Pucilowska J, et al. (2005) A variant in the HS1-BP3 gene is associated with familial essential tremor Neurology. 64: 417-421 |
Higgins JJ, Lombardi RQ, Tan EK, et al. (2004) Haplotype analysis at the ETM2 locus in a Singaporean sample with familial essential tremor Clinical Genetics. 66: 353-357 |
Gasser T, Bressman S, Dürr A, et al. (2003) State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis. Movement Disorders : Official Journal of the Movement Disorder Society. 18: 3-18 |
Higgins JJ, Loveless JM, Goswami S, et al. (2001) An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia. Neurology. 56: 1482-1485 |
Higgins JJ, Golbe LI, De Biase A, et al. (2000) An extended 5'-tau susceptibility haplotype in progressive supranuclear palsy Neurology. 55: 1364-1367 |
Higgins JJ, Rosen DR, Loveless JM, et al. (2000) A gene for nonsyndromic mental retardation maps to chromosome 3p25-pter. Neurology. 55: 335-340 |
Higgins JJ, Kluetzman K, Berciano J, et al. (2000) Posterior column ataxia and retinitis pigmentosa: a distinct clinical and genetic disorder. Movement Disorders : Official Journal of the Movement Disorder Society. 15: 575-8 |
Higgins JJ, Adler RL, Loveless JM. (1999) Mutational analysis of the tau gene in progressive supranuclear palsy. Neurology. 53: 1421-1421 |
Higgins JJ, Litvan I, Nee LE, et al. (1999) A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration Neurology. 52: 404-406 |
Higgins JJ, Morton DH, Loveless JM. (1999) Posterior column ataxia with retinitis pigmentosa (AXPC1) maps to chromosome 1q31-q32. Neurology. 52: 146-146 |