1. 1.Shi G, Boerwinkle E, Morrison AC, Gu CC, Chakravarti A, Rao DC: Mining gold dust under the genome-wide significance level: A two stage approach to analysis of GWAS.  Genetic Epidemiology 35:111-118, 2011. PMID: 21197625


  1. 2.Lettre G, Palmer CD, Young T, et al. (includes Chakravarti A): Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: The NHLBI CARe Project. PLoS Genetics 7:e1001300, 2011. PMID: 21347282


  1. 3.Mills RE, Walter K, Stewart C, et al. (includes Chakravarti A): Mapping copy number variation by population-scale genome sequencing. Nature 471:59-65, 2011. PMID: 21293372


  1. 4.Kraja A, Vaidya D, Pankow JS et al. (includes Chakravarti A): A bivariate genome-wide approach to metabolic syndrome: STAMPEED Consortium.  Diabetes 60:1329- 1339, 2011. PMID: 21386085


  1. 5.Johnson AD, Newton-Cheh C, Chasman DI, Ehret GB, Johnson T, Rose L, Rice K, Verwoert GC, Launer LJ, Gudnason V, Larson MG, Chakravarti A, Psaty BM, Caulfield M, van Duijn CM, Ridker P, Munroe PB, Levy D on Behalf of the CHARGE Consortium, Global BPgen Consortium, Women’s Genome Health Study: Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals. Hypertension 57:903-910, 2011. PMID: 21444836


  1. 6.Chakravarti A: Genomic contributions to Mendelian disease. Genome Research 21:643-644, 2011. PMID: 21536725


  1. 7.Fox E, Young JH, Li Y et al. (includes Chakravarti A): Association of Genetic Variation with Systolic and Diastolic Blood Pressure among African Americans: the Candidate Gene Association Resource (CARe) Study. Human Molecular Genetics April 1 [Epub ahead of print], 2011. PMID: 21378095


  1. 8.Zhu X, Young JH, Fox E et al. (includes Chakravarti A): Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium. Human Molecular Genetics April 5 [Epub ahead of print], 2011. PMID: 21422096


  1. 9.Burns K, Chakravarti A: Massively parallel rare disease genetics. Genome Medicine 3:29-31, 2011. PMID: 21635711


  1. 10.Arking DE, Juntilla MJ, Goyette P, et al. (includes Chakravarti A): Identification of a sudden cardiac death locus at 2q24.2 using genome-wide association in European-ancestry individuals. PLoS Genetics 7:e1002158, 2011. PMID: 21738491


  1. 11.Ho Y-Y, Matteini AM, Beamer B, Fried L, Xue Q-L, Arking DE, Chakravarti A, Walston J, Fallin D: Exploring biologically relevant pathways in frailty. Journal of Gerontology A: Biological Science & Medical Science 66:975-979, 2011. PMID: 21743092


  1. 12.Jiang Q, Ho Y-Y, Hao L, Nichols Berrios C, Chakravarti A: Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease.  PLoS One 6:a21219, 2011.


  1. 13.Nalls MA, Couper DJ, Tanaka T, van Rooij FJA, Chen M-H, et al. (includes Chakravarti A): Multiple loci are associated with white blood cell phenotypes. PLoS Genetics 7:e1002113, 2011. PMID: 21738480


  1. 14.Gravel S, Henn BM, Gutenkunst RN, Indap AR, Marth GT, Clark AG, Yu F, Gibbs RA; The 1000 Genomes Project, Bustamante CD: Demographic history and rare allele sharing among human populations. Proceedings of the National Academy of Science (USA) 108:11983-11988, 2011. PMID: 21730125


  1. 15.Conrad DF, Keebler JE, DePristo MA, Lindsay SJ, Zhang Y, Casals F, Idaghdour Y, Hartl CL, Torroja C, Garimella KV, Zilversmit M, Cartwright R, Rouleau GA, Daly M, Stone EA, Hurles ME, Awadalla P; 1000 Genomes Project: Variation in genome-wide mutation rates within and between human families. Nature Genetics 2011 43:712-714, 2011. PMID: 21666693


  1. 16.Danecek P, Auton A, Abecasis G, Albers CA, Banks E, DePristo MA, Handsaker RE, Lunter G, Marth GT, Sherry ST, McVean G, Durbin R; 1000 Genomes Project Analysis Group: The variant call format and VCFtools. Bioinformatics 27:2156-2158, 2011. PMID: 21653522


  1. 17.Jiang Q, Turner T, Sosa M, Rakha A, Arnold S, Chakravarti A: Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer. Human Mutation Sep 6. doi: 10.1002/humu.21602. [Epub ahead of print], 2011. PMID: 21898659


  1. 18.Ehret GB, Monroe PB, Rice KM et al. (includes Chakravarti A): Common polymorphisms impacting blood pressure and cardiovascular disease in diverse populations highlight novel biological pathways. Nature 478:103-109, 2011.


  1. 19.Wain LV, Verwoert GC, O’Reilly PF et al. (includes Chakravarti A): Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure Nature Genetics 43:1005-1011, 2011. PMID: 21909110


  1. 20.Turner T, Pihur V, Chakravarti A: Quantifying and modeling birth order effects in autism. PLoS One 6:e26418, 2011. PMID: 22039484


  1. 21.Chakravarti A: Genomics is not enough. Science 334:15, 2011. PMID: 21980079


  1. 22.Chakravarti A: Widespread promiscuous genetic information transfer from DNA to RNA. Circulation Research 109:1202-1203, 2011. PMID: 22076505


  1. 23.Benke KS, Carlson MC, Doan BQ, Walston JD, Xue QL, Reiner AP, Fried LP, Arking DE, Chakravarti A, Fallin MD: The association of genetic variants in interleukin-1 genes with cognition: Findings from the cardiovascular health study. Experimental Gerontology 46:1010-1019, 2011. PMID: 21968104


  1. 24.Amin N, Byrne E, Johnson J, Chenevix-Trench G, Walter S, Nolte IM; kConFab Investigators, Vink JM, Rawal R, Mangino M, Teumer A, Keers JC, Verwoert G, Baumeister S, Biffar R, Petersmann A, Dahmen N, Doering A, Isaacs A, Broer L, Wray NR, Montgomery GW, Levy D, Psaty BM, Gudnason V, Chakravarti A, Sulem P, Gudbjartsson DF, Kiemeney LA, Thorsteinsdottir U, Stefansson K, van Rooij FJ, Aulchenko YS, Hottenga JJ, Rivadeneira FR, Hofman A, Uitterlinden AG, Hammond CJ, Shin SY, Ikram A, Witteman JC, Janssens AC, Snieder H, Tiemeier H, Wolfenbuttel BH, Oostra BA, Heath AC, Wichmann E, Spector TD, Grabe HJ, Boomsma DI, Martin NG, van Duijn CM: Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Molecular Psychiatry Aug 30. doi: 10.1038/mp.2011.101. [Epub ahead of print], 2011. PMID: 21876539


  1. 25.Won J-H, Ehret G, Chakravarti A, Olshen RA:  SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of quantitative phenotypes for hypertension. PLoS One (in the press), 2011. PMID: 22140480

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