Browsing HMS Scholarly Articles by Author "9e09e2e30bcff8b488d319a6bb833514"

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Browsing HMS Scholarly Articles by Author "9e09e2e30bcff8b488d319a6bb833514"

Now showing items 1-12 of 12

Complex Reorganization and Predominant Non-Homologous Repair Following Chromosomal Breakage in Karyotypically Balanced Germline Rearrangements and Transgenic Integration

Chiang, Colby; Jacobsen, Jessie C.; Ernst, Carl; Hanscom, Carrie; Heilbut, Adrian; Blumenthal, Ian; Mills, Ryan E. et al. (Nature Genetics, 2012) Link to Published Version
Genome-wide Significance for a Modifier of Age at Neurological Onset in Huntington's Disease at 6q23-24: The HD MAPS Study

Li, Jian-Liang; Hayden, Michael R; Warby, Simon C; Durr, Alexandra; Morrison, Patrick J; Nance, Martha; Ross, Christopher A et al. (BMC Medical Genetics, 2006) Link to Published Version
Genomewide Association Study for Onset Age in Parkinson Disease

Latourelle, Jeanne C; Pankratz, Nathan; Dumitriu, Alexandra; Wilk, Jemma B; Goldwurm, Stefano; Pezzoli, Gianni; Mariani, Claudio B et al. (BMC Medical Genetics, 2009) Link to Published Version
Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas

Engler, David A; Roy, Jennifer; Shen, Yiping; Nunes, Fabio Pereira; Stemmer-Rachamimov, Anat; James, Marianne F.; Mohapatra, Gayatry et al. (BMC Medical Genomics, 2009) Link to Published Version
The Gly2019Ser Mutation in LRRK2 is not Fully Penetrant in Familial Parkinson's Disease: The GenePD Study

Latourelle, Jeanne C; Lew, Mark F; Suchowersky, Oksana; Klein, Christine; Golbe, Lawrence I; Mark, Margery H; Wooten, G Frederick et al. (BMC Medicine, 2008) Link to Published Version
Huntingtin Facilitates Polycomb Repressive Complex 2

Woda, Juliana M.; Song, Ji-Joon; Lloret, Alejandro; Abeyrathne, Priyanka D.; Gregory, Gillian; Lee, Jong-Min; Conlon, Ronald A. et al. (Human Molecular Genetics, 2009) Link to Published Version
KCTD13 is a Major Driver of Mirrored Neuroanatomical Phenotypes Associated with the 16p11.2 CNV

Golzio, Christelle; Willer, Jason; Oh, Edwin C; Taniguchi, Yu; Jacquemont, Sébastien; Reymond, Alexandre; Sun, Mei et al. (Nature, 2012) Link to Published Version
Lack of Association of Rare Functional Variants in TSC1/TSC2 Genes with Autism Spectrum Disorder

Chiang, Colby; Beauchamp, Roberta L; Bahl, Samira; Neale, Benjamin Michael; Daly, Mark Joseph; Gusella, James Francis; Talkowski, Michael Edward et al. (Molecular Autism, 2013) Link to Published Version
Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset

Ramos, Eliana Marisa; Latourelle, Jeanne C.; Lee, Ji-Hyun; Gillis, Tammy; Mysore, Jayalakshmi S.; Squitieri, Ferdinando; Di Pardo, Alba et al. (Human Genetics, 2012) Link to Published Version
The Predominantly HEAT-Like Motif Structure of Huntingtin and its Association and Coincident Nuclear Entry with Dorsal, an NF-kB/Rel/Dorsal Family Transcription Factor

Takano, Hiroki; Gusella, James Francis (BMC Neuroscience, 2002) Link to Published Version
Reversal of a Full-length Mutant Huntingtin Neuronal Cell Phenotype by Chemical Inhibitors of Polyglutamine-mediated Aggregation

Gines, Silvia; Wang, Jin; MacDonald, Marcy Elizabeth; Gusella, James Francis (BMC Neuroscience, 2005) Link to Published Version
Screening for Familial APP Mutations in Sporadic Cerebral Amyloid Angiopathy

Plourde, Anna; Onofrio, Robert; Prada, Claudia M.; Biffi, Alessandro; Shen, Yiping; Smith, Eric E.; Frosch, Matthew P. et al. (PLoS ONE, 2010) Link to Published Version

Now showing items 1-12 of 12

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