Devlin B - Search Results

1

Testing for an unusual distribution of rare variants.

Neale BM, Rivas MA, Voight BF, Altshuler D, Devlin B, Orho-Melander M, Kathiresan S, Purcell SM, Roeder K, Daly MJ. Neale BM, et al. Among authors: devlin b. PLoS Genet. 2011 Mar;7(3):e1001322. doi: 10.1371/journal.pgen.1001322. Epub 2011 Mar 3. PLoS Genet. 2011. PMID: 21408211 Free PMC article.

2

Mixture models for linkage analysis of affected sibling pairs and covariates.

Devlin B, Jones BL, Bacanu SA, Roeder K. Devlin B, et al. Genet Epidemiol. 2002 Jan;22(1):52-65. doi: 10.1002/gepi.1043. Genet Epidemiol. 2002. PMID: 11754473

3

Association studies for quantitative traits in structured populations.

Bacanu SA, Devlin B, Roeder K. Bacanu SA, et al. Among authors: devlin b. Genet Epidemiol. 2002 Jan;22(1):78-93. doi: 10.1002/gepi.1045. Genet Epidemiol. 2002. PMID: 11754475

4

Integration of association statistics over genomic regions using Bayesian adaptive regression splines.

Zhang X, Roeder K, Wallstrom G, Devlin B. Zhang X, et al. Among authors: devlin b. Hum Genomics. 2003 Nov;1(1):20-9. doi: 10.1186/1479-7364-1-1-20. Hum Genomics. 2003. PMID: 15601530 Free PMC article.

5

On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants.

Luca D, Ringquist S, Klei L, Lee AB, Gieger C, Wichmann HE, Schreiber S, Krawczak M, Lu Y, Styche A, Devlin B, Roeder K, Trucco M. Luca D, et al. Among authors: devlin b. Am J Hum Genet. 2008 Feb;82(2):453-63. doi: 10.1016/j.ajhg.2007.11.003. Epub 2008 Jan 24. Am J Hum Genet. 2008. PMID: 18252225 Free PMC article.

6

Linkage disequilibrium mapping of the chromosome 6q21-22.31 bipolar I disorder susceptibility locus.

Fan J, Ionita-Laza I, McQueen MB, Devlin B, Purcell S, Faraone SV, Allen MH, Bowden CL, Calabrese JR, Fossey MD, Friedman ES, Gyulai L, Hauser P, Ketter TB, Marangell LB, Miklowitz DJ, Nierenberg AA, Patel JK, Sachs GS, Thase ME, Molay FB, Escamilla MA, Nimgaonkar VL, Sklar P, Laird NM, Smoller JW. Fan J, et al. Among authors: devlin b. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):29-37. doi: 10.1002/ajmg.b.30942. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19308960 Free PMC article.

7

Discovering genetic ancestry using spectral graph theory.

Lee AB, Luca D, Klei L, Devlin B, Roeder K. Lee AB, et al. Among authors: devlin b. Genet Epidemiol. 2010 Jan;34(1):51-9. doi: 10.1002/gepi.20434. Genet Epidemiol. 2010. PMID: 19455578 Free PMC article.

8

A genome-wide linkage and association scan reveals novel loci for autism.

Weiss LA, Arking DE; Gene Discovery Project of Johns Hopkins & the Autism Consortium; Daly MJ, Chakravarti A. Weiss LA, et al. Nature. 2009 Oct 8;461(7265):802-8. doi: 10.1038/nature08490. Nature. 2009. PMID: 19812673 Free PMC article.

9

Screen and clean: a tool for identifying interactions in genome-wide association studies.

Wu J, Devlin B, Ringquist S, Trucco M, Roeder K. Wu J, et al. Among authors: devlin b. Genet Epidemiol. 2010 Apr;34(3):275-85. doi: 10.1002/gepi.20459. Genet Epidemiol. 2010. PMID: 20088021 Free PMC article.

10

Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies.

Crossett A, Kent BP, Klei L, Ringquist S, Trucco M, Roeder K, Devlin B. Crossett A, et al. Among authors: devlin b. Stat Med. 2010 Dec 10;29(28):2932-45. doi: 10.1002/sim.4057. Stat Med. 2010. PMID: 20862653 Free PMC article.

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