TETSUO ASHIZAWA to Polymorphism, Single Nucleotide
This is a "connection" page, showing publications TETSUO ASHIZAWA has written about Polymorphism, Single Nucleotide.
Connection Strength
0.507
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How much expansion to be diseased?: toward repeat size and myotonic dystrophy type 2. Neurology. 2009 Feb 10; 72(6):484-5.
Score: 0.168
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Extended haplotype with rs41524547-G defines the ancestral origin of SCA10. Hum Mol Genet. 2024 09 03; 33(18):1567-1574.
Score: 0.124
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Two novel SNPs in ATXN3 3' UTR may decrease age at onset of SCA3/MJD in Chinese patients. PLoS One. 2015; 10(2):e0117488.
Score: 0.064
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Population stratification may bias analysis of PGC-1a as a modifier of age at Huntington disease motor onset. Hum Genet. 2012 Dec; 131(12):1833-40.
Score: 0.053
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A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample. Arch Neurol. 2005 Jan; 62(1):74-8.
Score: 0.032
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Intron retention induced by microsatellite expansions as a disease biomarker. Proc Natl Acad Sci U S A. 2018 04 17; 115(16):4234-4239.
Score: 0.020
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Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph disease. Brain. 2017 04 01; 140(4):e25.
Score: 0.018
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Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry. PLoS One. 2013; 8(11):e81342.
Score: 0.015
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Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. Am J Hum Genet. 2012 Mar 09; 90(3):434-44.
Score: 0.013