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2016
Testing the Role of Predicted Gene Knockouts in Human Anthropometric Trait Variation.Lessard, S., Manning AK, Low-Kam C., Auer PL, Giri A., Graff M., Schurmann C., Yaghootkar H., Luan J., Esko T., Karaderi T., NHLBI GO Exome Sequence Project, GOT2D, T2D-GENES, GIANT Consortium, Bottinger EP, Lu Y., Carlson C., Caulfield M., Dubé MP, et al. Human molecular genetics, 2016/02/21, (2016) Read More / View Supplemental Materials
Abstract
Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project.Kan, M., Auer PL, Wang GT, Bucasas KL, Hooker S., Rodriguez A., Li B., Ellis J., Adrienne Cupples L., Ida Chen YD, Dupuis J., Fox CS, Gross MD, Smith JD, Heard-Costa N., Meigs JB, Pankow JS, Rotter JI, Siscovick D., Wilson JG, et al. European journal of human genetics : EJHG, 2016/01/13, (2016) Read More / View Supplemental Materials
Abstract
2015
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.Zheng, HF, Forgetta V., Hsu YH, Estrada K., Rosello-Diez A., Leo PJ, Dahia CL, Park-Min KH, Tobias JH, Kooperberg C., Kleinman A., Styrkarsdottir U., Liu CT, Uggla C., Evans DS, Nielson CM, Walter K., Pettersson-Kymmer U., McCarthy S., Eriksson J., et al. Nature, 2015/09/14, (2015) Read More / View Supplemental Materials
Abstract
2014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.Peloso, GM, Auer PL, Bis JC, Voorman A., Morrison AC, Stitziel NO, Brody JA, Khetarpal SA, Crosby JR, Fornage M., Isaacs A., Jakobsdottir J., Feitosa MF, Davies G., Huffman JE, Manichaikul A., Davis B., Lohman K., Joon AY, Smith AV, et al. American journal of human genetics, 2014/02/06, Volume 94, Issue 2, p.223-32, (2014) Read More / View Supplemental Materials
Abstract
  • Showing 1-4 of 4 Results