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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1960 1
1961 1
1963 3
1964 1
1968 1
1976 2
1983 1
1987 1
1989 2
1994 1
1999 3
2000 1
2001 2
2002 4
2003 2
2004 7
2005 7
2006 8
2007 7
2008 12
2009 22
2010 20
2011 11
2012 18
2013 34
2014 19
2015 16
2016 14
2017 16
2018 15
2019 29
2020 3
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244 results
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Page 1
LRP10 in α-synucleinopathies
Kia DA, et al. Lancet Neurol 2018. PMID 30507383
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
Moss DJH, et al. Lancet Neurol 2017 - Clinical Trial. PMID 28642124
The meta-analysis of progression in TRACK-HD and REGISTRY gave a genome-wide significant signal (p=1·12 × 10(-10)) on chromosome 5 spanning three genes: MSH3, DHFR, and MTRNR2L2. The genes in this locus were associated with progression in TRACK-HD (MSH3 p=2·94 × 10(-8)DHFR p=8·37 × 10(-7) MTRNR2L2 p=2·15 × 10(-9)) and to a lesser extent in REGISTRY (MSH3 p=9·36 × 10(-4)DHFR p=8·45 × 10(-4)MTRNR2L2 p=1·20 × 10(-3)). ...
The meta-analysis of progression in TRACK-HD and REGISTRY gave a genome-wide significant signal (p=1·12 × 10(-10)) on chromosome 5 sp …
De Novo Coding Variants Are Strongly Associated with Tourette Disorder
Willsey AJ, et al. Neuron 2017. PMID 28472652 Free PMC article.
We observe strong and consistent evidence for the contribution of de novo likely gene-disrupting (LGD) variants (rate ratio [RR] 2.32, p = 0.002). Additionally, de novo damaging variants (LGD and probably damaging missense) are overrepresented in probands (RR 1.37, p = 0.003). ...
We observe strong and consistent evidence for the contribution of de novo likely gene-disrupting (LGD) variants (rate ratio [RR] 2.32, p
244 results
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