Nickerson DA - Search Results

1

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome.

Ng SB, Bigham AW, Buckingham KJ, Hannibal MC, McMillin MJ, Gildersleeve HI, Beck AE, Tabor HK, Cooper GM, Mefford HC, Lee C, Turner EH, Smith JD, Rieder MJ, Yoshiura K, Matsumoto N, Ohta T, Niikawa N, Nickerson DA, Bamshad MJ, Shendure J. Ng SB, et al. Among authors: nickerson da. Nat Genet. 2010 Sep;42(9):790-3. doi: 10.1038/ng.646. Epub 2010 Aug 15. Nat Genet. 2010. PMID: 20711175 Free PMC article.

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

DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene.

Nickerson DA, Taylor SL, Weiss KM, Clark AG, Hutchinson RG, Stengård J, Salomaa V, Vartiainen E, Boerwinkle E, Sing CF. Nickerson DA, et al. Nat Genet. 1998 Jul;19(3):233-40. doi: 10.1038/907. Nat Genet. 1998. PMID: 9662394

4

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

5

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.

6

Localization of a small genomic region associated with elevated ACE.

Zhu X, McKenzie CA, Forrester T, Nickerson DA, Broeckel U, Schunkert H, Doering A, Jacob HJ, Cooper RS, Rieder MJ. Zhu X, et al. Among authors: nickerson da. Am J Hum Genet. 2000 Nov;67(5):1144-53. doi: 10.1016/S0002-9297(07)62945-0. Epub 2000 Sep 19. Am J Hum Genet. 2000. PMID: 11001581 Free PMC article.

7

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.

8

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

9

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

10

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

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