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James (Jim) F. Gusella, PhD

Genetics Harvard Medical School, Boston, MA, United States 
Huntington's Disease
"James (Jim) Gusella"

Cross-listing: Neurotree

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Long JD, Lee JM, Aylward EH, et al. (2018) Genetic Modification of Huntington Disease Acts Early in the Prediagnosis Phase. American Journal of Human Genetics
Lee JM, Chao MJ, Harold D, et al. (2017) A modifier of Huntington's disease onset at the MLH1 locus. Human Molecular Genetics. 26: 3859-3867
Chao MJ, Gillis T, Atwal RS, et al. (2017) Haplotype-based stratification of Huntington's disease. European Journal of Human Genetics : Ejhg
Maussion G, Cruceanu C, Rosenfeld JA, et al. (2016) Implication of LRRC4C and DPP6 in neurodevelopmental disorders. American Journal of Medical Genetics. Part A
Rodan LH, Cohen J, Fatemi A, et al. (2016) A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene. European Journal of Human Genetics : Ejhg
Ramos EM, Gillis T, Mysore JS, et al. (2015) Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 168: 135-43
Quintero-Rivera F, Xi QJ, Keppler-Noreuil KM, et al. (2015) MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus. Human Molecular Genetics. 24: 2375-89
Lee JM, Wheeler VC, Chao MJ, et al. (2015) Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease Cell. 162: 516-526
Jones L, Gusella J, MacDonald M, et al. (2014) A03 Genetic Modifiers Affecting The Age At Motor Onset In Huntington’s Disease Journal of Neurology, Neurosurgery, and Psychiatry. 85
Talkowski ME, Maussion G, Crapper L, et al. (2012) Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities. American Journal of Human Genetics. 91: 1128-34
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