Rieder MJ - Search Results

1

Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes.

Ramirez AH, Shaffer CM, Delaney JT, Sexton DP, Levy SE, Rieder MJ, Nickerson DA, George AL Jr, Roden DM. Ramirez AH, et al. Among authors: rieder mj. Pharmacogenomics J. 2013 Aug;13(4):325-9. doi: 10.1038/tpj.2012.14. Epub 2012 May 15. Pharmacogenomics J. 2013. PMID: 22584458 Free PMC article.

2

An excess of rare genetic variation in ABCE1 among Yorubans and African-American individuals with HIV-1.

Crawford DC, Zheng N, Speelmon EC, Stanaway I, Rieder MJ, Nickerson DA, McElrath MJ, Lingappa J. Crawford DC, et al. Among authors: rieder mj. Genes Immun. 2009 Dec;10(8):715-21. doi: 10.1038/gene.2009.57. Epub 2009 Aug 6. Genes Immun. 2009. PMID: 19657357 Free PMC article.

3

Hypertension and single nucleotide polymorphisms.

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

4

Sequence-based detection of single nucleotide polymorphisms.

Nickerson DA, Kolker N, Taylor SL, Rieder MJ. Nickerson DA, et al. Among authors: rieder mj. 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.

5

Sequence variation in the human angiotensin converting enzyme.

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

6

Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5.

Chen YZ, Matsushita MM, Robertson P, Rieder M, Girirajan S, Antonacci F, Lipe H, Eichler EE, Nickerson DA, Bird TD, Raskind WH. Chen YZ, et al. Arch Neurol. 2012 May;69(5):630-5. doi: 10.1001/archneurol.2012.54. Arch Neurol. 2012. PMID: 22782511 Free PMC article.

7

Association between patterns of nucleotide variation across the three fibrinogen genes and plasma fibrinogen levels: the Coronary Artery Risk Development in Young Adults (CARDIA) study.

Reiner AP, Carty CL, Carlson CS, Wan JY, Rieder MJ, Smith JD, Rice K, Fornage M, Jaquish CE, Williams OD, Tracy RP, Lewis CE, Siscovick DS, Boerwinkle E, Nickerson DA. Reiner AP, et al. Among authors: rieder mj. J Thromb Haemost. 2006 Jun;4(6):1279-87. doi: 10.1111/j.1538-7836.2006.01907.x. J Thromb Haemost. 2006. PMID: 16706972 Free article.

8

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants.

Fu W, O'Connor TD, Jun G, Kang HM, Abecasis G, Leal SM, Gabriel S, Rieder MJ, Altshuler D, Shendure J, Nickerson DA, Bamshad MJ; NHLBI Exome Sequencing Project; Akey JM. Fu W, et al. Among authors: rieder mj. Nature. 2013 Jan 10;493(7431):216-20. doi: 10.1038/nature11690. Epub 2012 Nov 28. Nature. 2013. PMID: 23201682 Free PMC article.

9

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. 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.

10

Coagulation factor VII gene haplotypes, obesity-related traits, and cardiovascular risk in young women.

Reiner AP, Carlson CS, Rieder MJ, Siscovick DS, Liu K, Chandler WL, Green D, Schwartz SM, Nickerson DA. Reiner AP, et al. Among authors: rieder mj. J Thromb Haemost. 2007 Jan;5(1):42-9. doi: 10.1111/j.1538-7836.2006.02279.x. Epub 2006 Oct 16. J Thromb Haemost. 2007. PMID: 17059418 Free article.

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