Center-Authored Papers

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Chami N, Chen M-H, Slater AJ, Eicher JD, Evangelou E, Tajuddin SM, Love-Gregory L, Kacprowski T, Schick UM, Nomura A et al..  2016.  Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.. American journal of human genetics. Abstract
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Fuchsberger C, Flannick J, Teslovich TM, Mahajan A, Agarwala V, Gaulton KJ, Ma C, Fontanillas P, Moutsianas L, McCarthy DJ et al..  2016.  The genetic architecture of type 2 diabetes.. Nature. 536(7614):41-7. Abstract
Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang S-J et al..  2011.  Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.. Nature. 478(7367):103-9. Abstract
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Tajuddin SM, Schick UM, Eicher JD, Chami N, Giri A, Brody JA, Hill DW, Kacprowski T, Li J, Lyytikäinen L-P et al..  2016.  Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.. American journal of human genetics. Abstract
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Marouli E, Graff M, Medina-Gomez C, Lo KS, Wood AR, Kjaer TR, Fine RS, Lu Y, Schurmann C, Highland HM et al..  2017.  Rare and low-frequency coding variants alter human adult height.. Nature. 542(7640):186-190. Abstract
Mousas A, Ntritsos G, Chen M-H, Song C, Huffman JE, Tzoulaki I, Elliott P, Psaty BM, Auer PL, Johnson AD et al..  2017.  Rare coding variants pinpoint genes that control human hematological traits.. PLoS genetics. 13(8):e1006925. Abstract