Biblio
Found 13 results
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HAMR: high-throughput annotation of modified ribonucleotides.. RNA. 19(12):1684-92.
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2013. Using machine learning and high-throughput RNA sequencing to classify the precursors of small non-coding RNAs.. Methods. 67(1):28-35.
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2014. Heritability of the shape of subcortical brain structures in the general population.. Nat Commun. 7:13738.
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2016. Next-generation gene discovery for variants of large impact on lipid traits.. Curr Opin Lipidol. 26(2):114-9.
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2015. Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop.. Neurology. 43(2):250-60.
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1993. Alzheimer's disease: analyzing the missing heritability.. PLoS One. 8(11):e79771.
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2013. A survey of ABCA1 sequence variation confirms association with dementia.. Hum Mutat. 30(9):1348-54.
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2009. Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk.. Hum Mol Genet. 19(10):2068-78.
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2010. Genetic diagnosis and prognosis of Alzheimer's disease: challenges and opportunities.. Expert Rev Mol Diagn. 15(3):339-48.
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2015. Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP).. Transl Psychiatry. 3:e256.
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2013. Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.. JAMA. 309(14):1483-92.
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2013. GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.. Neuron. 54(5):713-20.
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2007. Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer's disease.. Ann Clin Transl Neurol. 5(7):832-842.
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2018.