Biblio

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Ryvkin P, Leung YYee, Silverman IM, Childress M, Valladares O, Dragomir I, Gregory BD, San Wang L-. 2013. HAMR: high-throughput annotation of modified ribonucleotides.. RNA. 19(12):1684-92.

Ryvkin P, Leung YYee, Ungar LH, Gregory BD, San Wang L-. 2014. Using machine learning and high-throughput RNA sequencing to classify the precursors of small non-coding RNAs.. Methods. 67(1):28-35.

Roshchupkin GV, Gutman BA, Vernooij MW, Jahanshad N, Martin NG, Hofman A, McMahon KL, van der Lee SJ, van Duijn CM, de Zubicaray GI et al.. 2016. Heritability of the shape of subcortical brain structures in the general population.. Nat Commun. 7:13738.

Rosenthal E, Blue E, Jarvik GP. 2015. Next-generation gene discovery for variants of large impact on lipid traits.. Curr Opin Lipidol. 26(2):114-9.

Román GC, Tatemichi TK, Erkinjuntti T, Cummings JL, Masdeu JC, Garcia JH, Amaducci L, Orgogozo JM, Brun A, Hofman A. 1993. Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop.. Neurology. 43(2):250-60.

Ridge PG, Mukherjee S, Crane PK, Kauwe JSK. 2013. Alzheimer's disease: analyzing the missing heritability.. PLoS One. 8(11):e79771.

Reynolds CA, Hong M-G, Eriksson UK, Blennow K, Bennet AM, Johansson B, Malmberg B, Berg S, Wiklund F, Gatz M et al.. 2009. A survey of ABCA1 sequence variation confirms association with dementia.. Hum Mutat. 30(9):1348-54.

Reynolds CA, Hong M-G, Eriksson UK, Blennow K, Wiklund F, Johansson B, Malmberg B, Berg S, Alexeyenko A, Grönberg H et al.. 2010. Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk.. Hum Mol Genet. 19(10):2068-78.

Reitz C. 2015. Genetic diagnosis and prognosis of Alzheimer's disease: challenges and opportunities.. Expert Rev Mol Diagn. 15(3):339-48.

Reitz C, Tosto G, Vardarajan B, Rogaeva E, Ghani M, Rogers RS, Conrad C, Haines JL, Pericak-Vance MA, Fallin MD et al.. 2013. 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.

Reitz C, Jun G, Naj A, Rajbhandary R, Vardarajan BNarayan, San Wang L-, Valladares O, Lin C-F, Larson EB, Graff-Radford NR et al.. 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.

Reiman EM, Webster JA, Myers AJ, Hardy J, Dunckley T, Zismann VL, Joshipura KD, Pearson JV, Hu-Lince D, Huentelman MJ et al.. 2007. GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.. Neuron. 54(5):713-20.

Raghavan NS, Brickman AM, Andrews H, Manly JJ, Schupf N, Lantigua R, Wolock CJ, Kamalakaran S, Petrovski S, Tosto G et al.. 2018. Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer's disease.. Ann Clin Transl Neurol. 5(7):832-842.