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  • Showing 1-10 of 10 Results
2016
Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes.Harel, T., Yoon WH, Garone C., Gu S., Coban-Akdemir Z., Eldomery MK, Posey JE, Jhangiani SN, Rosenfeld JA, Cho MT, Fox S., Withers M., Brooks SM, Chiang T., Duraine L., Erdin S., Yuan B., Shao Y., Moussallem E., Lamperti C., et al. American journal of human genetics, 2016/09/07, (2016) Read More / View Supplemental Materials
Abstract
Fine-mapping, Novel Loci Identification, and SNP Association Transferability in a Genome-Wide Association Study of QRS Duration in African Americans.Evans, DS, Avery CL, Nalls MA, Li G., Barnard J., Smith EN, Tanaka T., Butler AM, Buxbaum SG, Alonso A., Arking DE, Berenson GS, Bis JC, Buyske S., Carty CL, Chen W., Chung MK, Cummings SR, Deo R., Eaton CB, et al. Human molecular genetics, 2016/08/29, (2016) Read More / View Supplemental Materials
Abstract
Association of Exome Sequences with Cardiovascular Traits among African Americans in the Jackson Heart Study.Peloso, GM, Lange LA, Varga TV, Nickerson DA, Smith JD, Griswold ME, Musani S., Polfus LM, Mei H., Gabriel S., Quarells RC, Altshuler D., Boerwinkle E., Daly M. J., Neale B., Correa A., Reiner AP, Wilson JG, and Kathiresan S. Circulation. Cardiovascular genetics, 2016/07/15, (2016) Read More / View Supplemental Materials
Abstract
The genetic architecture of type 2 diabetes.Fuchsberger, C., Flannick J., Teslovich TM, Mahajan A., Agarwala V., Gaulton KJ, Ma C., Fontanillas P., Moutsianas L., McCarthy DJ, Rivas MA, Perry JR, Sim X., Blackwell TW, Robertson NR, Rayner NW, Cingolani P., Locke AE, Tajes JF, Highland HM, et al. Nature, 2016/07/11, (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
2014
Association of Sickle Cell Trait With Chronic Kidney Disease and Albuminuria in African Americans.Naik, RP, Derebail VK, Grams ME, Franceschini N., Auer PL, Peloso GM, Young BA, Lettre G., Peralta CA, Katz R., Hyacinth HI, Quarells RC, Grove ML, Bick AG, Fontanillas P., Rich SS, Smith JD, Boerwinkle E., Rosamond WD, Ito K., et al. JAMA, 2014/11/26, Volume 312, Issue 20, p.2115-2125, (2014) Read More / View Supplemental Materials
Abstract
Integrating Genetic, Transcriptional, and Functional Analyses to Identify Five Novel Genes for Atrial Fibrillation.Sinner, MF, Tucker NR, Lunetta KL, Ozaki K., Smith JG, Trompet S., Bis JC, Lin H., Chung MK, Nielsen JB, Lubitz SA, Krijthe BP, Magnani JW, Ye J., Gollob MH, Tsunoda T., Müller-Nurasyid M., Lichtner P., Peters A., Dolmatova E., et al. Circulation, 2014/08/14, (2014) Read More / View Supplemental Materials
Abstract
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.Lange, LA, Hu Y., Zhang H., Xue C., Schmidt EM, Tang ZZ, Bizon C., Lange EM, Smith JD, Turner EH, Jun G., Kang HM, Peloso G., Auer P., Li KP, Flannick J., Zhang J., Fuchsberger C., Gaulton K., Lindgren C., et al. American journal of human genetics, 2014/02/06, Volume 94, Issue 2, p.233-45, (2014) Read More / View Supplemental Materials
Abstract
2011
The genome of the green anole lizard and a comparative analysis with birds and mammals.Alföldi, J., Di Palma F., Grabherr M., Williams C., Kong L., Mauceli E., Russell P., Lowe CB, Glor RE, Jaffe JD, Ray DA, Boissinot S., Shedlock AM, Botka C., Castoe TA, Colbourne JK, Fujita MK, Moreno RG, ten Hallers BF, Haussler D., et al. Nature, 2011/08/31, Volume 477, Issue 7366, p.587-91, (2011) Read More / View Supplemental Materials
Abstract
2008
Mapping and sequencing of structural variation from eight human genomes.Kidd, JM, Cooper GM, Donahue WF, Hayden HS, Sampas N., Graves T., Hansen N., Teague B., Alkan C., Antonacci F., Haugen E., Zerr T., Yamada NA, Tsang P., Newman TL, Tüzün E., Cheng Z., Ebling HM, Tusneem N., David R., et al. Nature, 2008/05/01, Volume 453, Issue 7191, p.56-64, (2008) Read More / View Supplemental Materials
Abstract
  • Showing 1-10 of 10 Results