HL66642/HL/NHLBI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2002	1
2003	2
2004	4
2005	2
2006	3
2008	2
2009	4
2010	2
2011	1
2024	0

1

Targeted interrogation of copy number variation using SCIMMkit.

Zerr T, Cooper GM, Eichler EE, Nickerson DA. Zerr T, et al. Bioinformatics. 2010 Jan 1;26(1):120-2. doi: 10.1093/bioinformatics/btp606. Epub 2009 Oct 21. Bioinformatics. 2010. PMID: 19846438 Free PMC article.

2

Sequence-based linkage analysis.

Furman I, Rieder MJ, Da Ponte S, Carrington DP, Nickerson DA, Kruglyak L, Markianos K. Furman I, et al. Am J Hum Genet. 2004 Oct;75(4):647-53. doi: 10.1086/424888. Epub 2004 Aug 25. Am J Hum Genet. 2004. PMID: 15329798 Free PMC article.

3

Sequence variation in the human T-cell receptor loci.

Mackelprang R, Carlson CS, Subrahmanyan L, Livingston RJ, Eberle MA, Nickerson DA. Mackelprang R, et al. Immunol Rev. 2002 Dec;190:26-39. doi: 10.1034/j.1600-065x.2002.19003.x. Immunol Rev. 2002. PMID: 12493004 Review.

4

Paraoxonase activity, but not haplotype utilizing the linkage disequilibrium structure, predicts vascular disease.

Jarvik GP, Hatsukami TS, Carlson C, Richter RJ, Jampsa R, Brophy VH, Margolin S, Rieder M, Nickerson D, Schellenberg GD, Heagerty PJ, Furlong CE. Jarvik GP, et al. Arterioscler Thromb Vasc Biol. 2003 Aug 1;23(8):1465-71. doi: 10.1161/01.ATV.0000081635.96290.D3. Epub 2003 Jun 12. Arterioscler Thromb Vasc Biol. 2003. PMID: 12805074

5

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. 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.

6

Population history and natural selection shape patterns of genetic variation in 132 genes.

Akey JM, Eberle MA, Rieder MJ, Carlson CS, Shriver MD, Nickerson DA, Kruglyak L. Akey JM, et al. PLoS Biol. 2004 Oct;2(10):e286. doi: 10.1371/journal.pbio.0020286. Epub 2004 Sep 7. PLoS Biol. 2004. PMID: 15361935 Free PMC article.

7

Estimating coverage and power for genetic association studies using near-complete variation data.

Bhangale TR, Rieder MJ, Nickerson DA. Bhangale TR, et al. Nat Genet. 2008 Jul;40(7):841-3. doi: 10.1038/ng.180. Epub 2008 Jun 22. Nat Genet. 2008. PMID: 18568023

8

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease.

Mefford HC, Cooper GM, Zerr T, Smith JD, Baker C, Shafer N, Thorland EC, Skinner C, Schwartz CE, Nickerson DA, Eichler EE. Mefford HC, et al. Genome Res. 2009 Sep;19(9):1579-85. doi: 10.1101/gr.094987.109. Epub 2009 Jun 8. Genome Res. 2009. PMID: 19506092 Free PMC article.

9

Direct detection of null alleles in SNP genotyping data.

Carlson CS, Smith JD, Stanaway IB, Rieder MJ, Nickerson DA. Carlson CS, et al. Hum Mol Genet. 2006 Jun 15;15(12):1931-7. doi: 10.1093/hmg/ddl115. Epub 2006 Apr 27. Hum Mol Genet. 2006. PMID: 16644863

10

Genomic regions exhibiting positive selection identified from dense genotype data.

Carlson CS, Thomas DJ, Eberle MA, Swanson JE, Livingston RJ, Rieder MJ, Nickerson DA. Carlson CS, et al. Genome Res. 2005 Nov;15(11):1553-65. doi: 10.1101/gr.4326505. Genome Res. 2005. PMID: 16251465 Free PMC article.

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