Evidence for two independent associations with type 1 diabetes at the 12q13 locus
Keene, K L, Quinlan, A R, Hou, X, Hall, I M, Mychaleckyj, J C, Onengut-Gumuscu, S, Concannon, P
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Published in Genes and immunity (01.01.2012)
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Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes
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Published in Nature genetics (01.10.2018)
Published in Nature genetics (01.10.2018)
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Single-nucleus chromatin accessibility profiling highlights regulatory mechanisms of coronary artery disease risk
Turner, Adam W., Hu, Shengen Shawn, Mosquera, Jose Verdezoto, Ma, Wei Feng, Hodonsky, Chani J., Wong, Doris, Auguste, Gaëlle, Song, Yipei, Sol-Church, Katia, Farber, Emily, Kundu, Soumya, Kundaje, Anshul, Lopez, Nicolas G., Ma, Lijiang, Ghosh, Saikat Kumar B., Onengut-Gumuscu, Suna, Ashley, Euan A., Quertermous, Thomas, Finn, Aloke V., Leeper, Nicholas J., Kovacic, Jason C., Björkegren, Johan L. M., Zang, Chongzhi, Miller, Clint L.
Published in Nature genetics (01.06.2022)
Published in Nature genetics (01.06.2022)
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A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases
Han, Buhm, Pouget, Jennie G, Slowikowski, Kamil, Stahl, Eli, Lee, Cue Hyunkyu, Diogo, Dorothee, Hu, Xinli, Park, Yu Rang, Kim, Eunji, Gregersen, Peter K, Dahlqvist, Solbritt Rantapää, Worthington, Jane, Martin, Javier, Eyre, Steve, Klareskog, Lars, Huizinga, Tom, Chen, Wei-Min, Onengut-Gumuscu, Suna, Rich, Stephen S, Wray, Naomi R, Raychaudhuri, Soumya
Published in Nature genetics (01.07.2016)
Published in Nature genetics (01.07.2016)
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Author Correction: Single-nucleus chromatin accessibility profiling highlights regulatory mechanisms of coronary artery disease risk
Turner, Adam W., Hu, Shengen Shawn, Mosquera, Jose Verdezoto, Ma, Wei Feng, Hodonsky, Chani J., Wong, Doris, Auguste, Gaëlle, Song, Yipei, Sol-Church, Katia, Farber, Emily, Kundu, Soumya, Kundaje, Anshul, Lopez, Nicolas G., Ma, Lijiang, Ghosh, Saikat Kumar B., Onengut-Gumuscu, Suna, Ashley, Euan A., Quertermous, Thomas, Finn, Aloke V., Leeper, Nicholas J., Kovacic, Jason C., Björkegren, Johan L. M., Zang, Chongzhi, Miller, Clint L.
Published in Nature genetics (01.08.2022)
Published in Nature genetics (01.08.2022)
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Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen: J Am Soc Nephrol
Salem, R. M., Todd, J. N., Sandholm, N., Cole, J. B., Chen, W. M., Andrews, D., Pezzolesi, M. G., Mckeigue, P. M., Hiraki, L. T., Qiu, C., Nair, V., Di Liao, C., Cao, J. J., Valo, E., Onengut-Gumuscu, S., Smiles, A. M., Mcgurnaghan, S. J., Haukka, J. K., Harjutsalo, V., Brennan, E. P., van Zuydam, N., Ahlqvist, E., Doyle, R., Ahluwalia, T. S., Lajer, M., Hughes, M. F., Park, J., Skupien, J., Spiliopoulou, A., Liu, A., Menon, R., Boustany-Kari, C. M., Kang, H. M., Nelson, R. G., Klein, R., Klein, B. E., Lee, K. E., Gao, X., Mauer, M., Maestroni, S., Caramori, M. L., de Boer, I. H., Miller, R. G., Guo, J., Boright, A. P., Tregouet, D., Gyorgy, B., Snell-Bergeon, J. K., Maahs, D. M., Bull, S. B., Canty, A. J., Palmer, C. N. A., Stechemesser, L., Paulweber, B., Weitgasser, R., Sokolovska, J., Rovite, V., Pirags, V., Prakapiene, E., Radzeviciene, L., Verkauskiene, R., Panduru, N. M., Groop, L. C., Mccarthy, M. I., Gu, H. F., Mollsten, A., Falhammar, H., Brismar, K., Martin, F., Rossing, P., Costacou, T., Zerbini, G., Marre, M., Hadjadj, S., Mcknight, A. J., Forsblom, C., Mckay, G., Godson, C., Maxwell, A. P., Kretzler, M., Susztak, K., Colhoun, H. M., Krolewski, A., Paterson, A. D., Groop, P. H., Rich, S. S., Hirschhorn, J. N., Florez, J. C.
Published in Journal of the American Society of Nephrology (01.10.2019)
Published in Journal of the American Society of Nephrology (01.10.2019)
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Multi-ancestry genetic analysis of gene regulation in coronary arteries prioritizes disease risk loci
Hodonsky, Chani J., Turner, Adam W., Khan, Mohammad Daud, Barrientos, Nelson B., Methorst, Ruben, Ma, Lijiang, Lopez, Nicolas G., Mosquera, Jose Verdezoto, Auguste, Gaëlle, Farber, Emily, Ma, Wei Feng, Wong, Doris, Onengut-Gumuscu, Suna, Kavousi, Maryam, Peyser, Patricia A., van der Laan, Sander W., Leeper, Nicholas J., Kovacic, Jason C., Björkegren, Johan L.M., Miller, Clint L.
Published in Cell genomics (10.01.2024)
Published in Cell genomics (10.01.2024)
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Genetic Regulation of Atherosclerosis-relevant Phenotypes in Human Vascular Smooth Muscle Cells
Aherrahrou, R, Guo, L, Nagraj, V, Aguhob, AA, Hinkle, J, Chen, L, Soh, JY, Lue, D, Alencar, G, Boltjes, A, van der Laan, SW, Farber, E, Fuller, D, Wae, RA, Akingbesote, N, Ma, LJ, Bjorkegren, J, Onengut-Gumuscu, S, Pasterkamp, G, Miller, C, Owens, GK, Finn, A, Navab, M, Civelek, M
Published in ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2020)
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Published in ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2020)
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The genetics of type 1 diabetes: Lessons learned and future challenges
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Decrease in Memory B Cell Frequency and Activation is Associated with PTPN22 1858T Variant in Healthy Subjects
Rieck, Mary, Research Technician II, Benaroya Research Institute, Seattle, WA, Concannon, Patric, Professor, Center for Public Health Genomic, University of Virginia, Charlotte, SC, Arechiga, Adrian, Research Associate, Benaroya Research Institute, Seattle, WA, Buckner, Jane, Associate Member, Benaroya Research Institute, Seattle, WA, Onengut-Gumuscu, Suna, Research Associate, Center for Health Genomics, Charlotte, SC
Published in Clinical immunology (Orlando, Fla.) (01.01.2007)
Published in Clinical immunology (Orlando, Fla.) (01.01.2007)
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