Nickerson DA - Search Results

1

Comparable specimen collection from both ends of at-home mid-turbinate swabs.

Truong M, Pfau B, McDermot E, Han PD, Brandstetter E, Richardson M, Kim AE, Rieder MJ, Chu HY, Englund JA, Nickerson DA, Shendure J, Lockwood CM, Konnick EQ, Starita LM. Truong M, et al. Among authors: nickerson da. medRxiv [Preprint]. 2020 Dec 8:2020.12.05.20244632. doi: 10.1101/2020.12.05.20244632. medRxiv. 2020. PMID: 33330895 Free PMC article. Updated. Preprint.

2

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome.

Rieder MJ, Taylor SL, Tobe VO, Nickerson DA. Rieder MJ, et al. Among authors: nickerson da. Nucleic Acids Res. 1998 Feb 15;26(4):967-73. doi: 10.1093/nar/26.4.967. Nucleic Acids Res. 1998. PMID: 9461455 Free PMC article.

3

Sequence variation in the human angiotensin converting enzyme.

Rieder MJ, Taylor SL, Clark AG, Nickerson DA. Rieder MJ, et al. Among authors: nickerson da. Nat Genet. 1999 May;22(1):59-62. doi: 10.1038/8760. Nat Genet. 1999. PMID: 10319862

4

Hypertension and single nucleotide polymorphisms.

Rieder MJ, Nickerson DA. Rieder MJ, et al. Among authors: nickerson da. Curr Hypertens Rep. 2000 Feb;2(1):44-9. doi: 10.1007/s11906-000-0057-4. Curr Hypertens Rep. 2000. PMID: 10981126 Review.

5

Sequence-based detection of single nucleotide polymorphisms.

Nickerson DA, Kolker N, Taylor SL, Rieder MJ. Nickerson DA, et al. Methods Mol Biol. 2001;175:29-35. doi: 10.1385/1-59259-235-X:029. Methods Mol Biol. 2001. PMID: 11462842 Review. No abstract available.

6

Mitochondrial genetic variants and Alzheimer disease: a case-control study of the T4336C and G5460A variants.

Edland SD, Tobe VO, Rieder MJ, Bowen JD, McCormick W, Teri L, Schellenberg GD, Larson EB, Nickerson DA, Kukull WA. Edland SD, et al. Among authors: nickerson da. Alzheimer Dis Assoc Disord. 2002 Jan-Mar;16(1):1-7. doi: 10.1097/00002093-200201000-00001. Alzheimer Dis Assoc Disord. 2002. PMID: 11882743

7

Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans.

Carlson CS, Eberle MA, Rieder MJ, Smith JD, Kruglyak L, Nickerson DA. Carlson CS, et al. Among authors: nickerson da. Nat Genet. 2003 Apr;33(4):518-21. doi: 10.1038/ng1128. Epub 2003 Mar 24. Nat Genet. 2003. PMID: 12652300

8

Novel paraoxonase (PON1) nonsense and missense mutations predicted by functional genomic assay of PON1 status.

Jarvik GP, Jampsa R, Richter RJ, Carlson CS, Rieder MJ, Nickerson DA, Furlong CE. Jarvik GP, et al. Among authors: nickerson da. Pharmacogenetics. 2003 May;13(5):291-5. doi: 10.1097/00008571-200305000-00009. Pharmacogenetics. 2003. PMID: 12724622

9

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium.

Carlson CS, Eberle MA, Rieder MJ, Yi Q, Kruglyak L, Nickerson DA. Carlson CS, et al. Among authors: nickerson da. Am J Hum Genet. 2004 Jan;74(1):106-20. doi: 10.1086/381000. Epub 2003 Dec 15. Am J Hum Genet. 2004. PMID: 14681826 Free PMC article.

10

Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations.

Crawford DC, Carlson CS, Rieder MJ, Carrington DP, Yi Q, Smith JD, Eberle MA, Kruglyak L, Nickerson DA. Crawford DC, et al. Among authors: nickerson da. Am J Hum Genet. 2004 Apr;74(4):610-22. doi: 10.1086/382227. Epub 2004 Mar 10. Am J Hum Genet. 2004. PMID: 15015130 Free PMC article.

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