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Nature Reviews. Genetics|February 2, 2002
No post-genetics era in human disease researchJames Gusella, Marcy MacDonald
The Journal of Neuroscience Nursing : Journal of the American Association of Neuroscience Nurses|January 28, 2009
Patient and physician attitudes regarding clinical trials in neurofibromatosis 1Mary McQueen, Mia MacCollin, James Gusella, et al.
European Journal of Human Genetics : EJHG|June 23, 2016
A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin geneLance H Rodan, Julie Cohen, Ali Fatemi, et al.
Cancer Genetics and Cytogenetics|October 11, 2005
Inactivation patterns of NF2 and DAL-1/4.1B (EPB41L3) in sporadic meningiomaFabio Nunes, Yiping Shen, Yo Niida, et al.
Plos One|November 19, 2010
Screening for familial APP mutations in sporadic cerebral amyloid angiopathyAlessandro Biffi, Anna Plourde, Yiping Shen, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2019
A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal RegulatorMaria Stamou, Shi-Yan Ng, Harrison Brand, et al.
Nature Neuroscience|April 3, 2012
An evolutionary recent neuroepithelial cell adhesion function of huntingtin implicates ADAM10-NcadherinValentina Lo Sardo, Chiara Zuccato, Germano Gaudenzi, et al.
The American Journal of Psychiatry|April 3, 2010
Prevalence of incompletely penetrant Huntington's disease alleles among individuals with major depressive disorderRoy H Perlis, Jordan W Smoller, Jayalakshmi Mysore, et al.
Archives of General Psychiatry|August 6, 2008
Association of a polymorphism near CREB1 with differential aversion processing in the insula of healthy participantsRoy H Perlis, Daphne J Holt, Jordan W Smoller, et al.
Somatic Cell and Molecular Genetics|January 1, 1994
Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeatChristine M Ambrose, Mabel P Duyao, Glenn Barnes, et al.
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