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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:
Neurogenetics
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"Joseph Higgins"
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Parents

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Norman 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
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