Prospective economic evaluation alongside the non-invasive ventilation trial von Mowitz, M E, Zupancic, J A F, Millar, D, Kirpalani, H, Gaulton, J S, Roberts, R S, Mao, W, Dukhovny, D

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Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos von Sofer, Tamar, Wong, Quenna, Hartwig, Fernando P., Taylor, Kent, Warren, Helen R., Evangelou, Evangelos, Cabrera, Claudia P., Levy, Daniel, Kramer, Holly, Lange, Leslie A., Horta, Bernardo L., Kerr, Kathleen F., Reiner, Alex P., Franceschini, Nora

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Characterizing cis-regulatory elements using single-cell epigenomics von Preissl, Sebastian, Gaulton, Kyle J., Ren, Bing

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A single-cell atlas of chromatin accessibility in the human genome von Zhang, Kai, Hocker, James D., Miller, Michael, Hou, Xiaomeng, Chiou, Joshua, Poirion, Olivier B., Qiu, Yunjiang, Li, Yang E., Gaulton, Kyle J., Wang, Allen, Preissl, Sebastian, Ren, Bing

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The miRNA profile of human pancreatic islets and beta-cells and relationship to type 2 diabetes pathogenesis von van de Bunt, Martijn, Gaulton, Kyle J, Parts, Leopold, Moran, Ignasi, Johnson, Paul R, Lindgren, Cecilia M, Ferrer, Jorge, Gloyn, Anna L, McCarthy, Mark I

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The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease von Moutsianas, Loukas, Agarwala, Vineeta, Fuchsberger, Christian, Flannick, Jason, Rivas, Manuel A, Gaulton, Kyle J, Albers, Patrick K, McVean, Gil, Boehnke, Michael, Altshuler, David, McCarthy, Mark I

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Interpreting non-coding disease-associated human variants using single-cell epigenomics von Gaulton, Kyle J., Preissl, Sebastian, Ren, Bing

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Detection of human adaptation during the past 2000 years von Field, Yair, Boyle, Evan A, Telis, Natalie, Gao, Ziyue, Gaulton, Kyle J., Golan, David, Yengo, Loic, Rocheleau, Ghislain, Froguel, Philippe, McCarthy, Mark I., Pritchard, Jonathan K.

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Transcript Expression Data from Human Islets Links Regulatory Signals from Genome-Wide Association Studies for Type 2 Diabetes and Glycemic Traits to Their Downstream Effectors von van de Bunt, Martijn, Manning Fox, Jocelyn E, Dai, Xiaoqing, Barrett, Amy, Grey, Caleb, Li, Lei, Bennett, Amanda J, Johnson, Paul R, Rajotte, Raymond V, Gaulton, Kyle J, Dermitzakis, Emmanouil T, MacDonald, Patrick E, McCarthy, Mark I, Gloyn, Anna L

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Leveraging type 1 diabetes human genetic and genomic data in the T1D knowledge portal von Kudtarkar, Parul, Costanzo, Maria C, Sun, Ying, Jang, Dongkeun, Koesterer, Ryan, Mychaleckyj, Josyf C, Nayak, Uma, Onengut-Gumuscu, Suna, Rich, Stephen S, Flannick, Jason A, Gaulton, Kyle J, Burtt, Noël P

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Single-cell chromatin accessibility identifies pancreatic islet cell type– and state-specific regulatory programs of diabetes risk von Chiou, Joshua, Zeng, Chun, Cheng, Zhang, Han, Jee Yun, Schlichting, Michael, Miller, Michael, Mendez, Robert, Huang, Serina, Wang, Jinzhao, Sui, Yinghui, Deogaygay, Allison, Okino, Mei-Lin, Qiu, Yunjiang, Sun, Ying, Kudtarkar, Parul, Fang, Rongxin, Preissl, Sebastian, Sander, Maike, Gorkin, David U., Gaulton, Kyle J.

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138-OR: Characterization and Prediction of Genetic Risk of T1D in Individuals without HLA-DR3 or HLA-DR4 von MCGRAIL, CAROLYN, GAULTON, KYLE J.

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Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants von Pasquali, Lorenzo, Gaulton, Kyle J, Rodríguez-Seguí, Santiago A, Mularoni, Loris, Miguel-Escalada, Irene, Akerman, İldem, Tena, Juan J, Morán, Ignasi, Gómez-Marín, Carlos, van de Bunt, Martijn, Ponsa-Cobas, Joan, Castro, Natalia, Nammo, Takao, Cebola, Inês, García-Hurtado, Javier, Maestro, Miguel Angel, Pattou, François, Piemonti, Lorenzo, Berney, Thierry, Gloyn, Anna L, Ravassard, Philippe, Skarmeta, José Luis Gómez, Müller, Ferenc, McCarthy, Mark I, Ferrer, Jorge

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Interpreting type 1 diabetes risk with genetics and single-cell epigenomics von Chiou, Joshua, Geusz, Ryan J., Okino, Mei-Lin, Han, Jee Yun, Miller, Michael, Melton, Rebecca, Beebe, Elisha, Benaglio, Paola, Huang, Serina, Korgaonkar, Katha, Heller, Sandra, Kleger, Alexander, Preissl, Sebastian, Gorkin, David U., Sander, Maike, Gaulton, Kyle J.

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Mechanisms of Type 2 Diabetes Risk Loci von Gaulton, Kyle J.

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Single-cell multiomic profiling of human lungs reveals cell-type-specific and age-dynamic control of SARS-CoV2 host genes von Wang, Allen, Chiou, Joshua, Poirion, Olivier B, Buchanan, Justin, Valdez, Michael J, Verheyden, Jamie M, Hou, Xiaomeng, Kudtarkar, Parul, Narendra, Sharvari, Newsome, Jacklyn M, Guo, Minzhe, Faddah, Dina A, Zhang, Kai, Young, Randee E, Barr, Justinn, Sajti, Eniko, Misra, Ravi, Huyck, Heidie, Rogers, Lisa, Poole, Cory, Whitsett, Jeffery A, Pryhuber, Gloria, Xu, Yan, Gaulton, Kyle J, Preissl, Sebastian, Sun, Xin

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Glucocorticoid signaling in pancreatic islets modulates gene regulatory programs and genetic risk of type 2 diabetes von Aylward, Anthony, Okino, Mei-Lin, Benaglio, Paola, Chiou, Joshua, Beebe, Elisha, Padilla, Jose Andres, Diep, Sharlene, Gaulton, Kyle J

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Identification of a regulatory variant that binds FOXA1 and FOXA2 at the CDC123/CAMK1D type 2 diabetes GWAS locus von Fogarty, Marie P, Cannon, Maren E, Vadlamudi, Swarooparani, Gaulton, Kyle J, Mohlke, Karen L

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Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies von Morris, Andrew P., Le, Thu H., Wu, Haojia, Akbarov, Artur, van der Most, Peter J., Hemani, Gibran, Smith, George Davey, Mahajan, Anubha, Gaulton, Kyle J., Nadkarni, Girish N., Valladares-Salgado, Adan, Wacher-Rodarte, Niels, Mychaleckyj, Josyf C., Dueker, Nicole D., Guo, Xiuqing, Hai, Yang, Haessler, Jeffrey, Kamatani, Yoichiro, Stilp, Adrienne M., Zhu, Gu, Cook, James P., Ärnlöv, Johan, Blanton, Susan H., de Borst, Martin H., Bottinger, Erwin P., Buchanan, Thomas A., Cechova, Sylvia, Charchar, Fadi J., Chu, Pei-Lun, Damman, Jeffrey, Eales, James, Gharavi, Ali G., Giedraitis, Vilmantas, Heath, Andrew C., Ipp, Eli, Kiryluk, Krzysztof, Kramer, Holly J., Kubo, Michiaki, Larsson, Anders, Lindgren, Cecilia M., Lu, Yingchang, Madden, Pamela A. F., Montgomery, Grant W., Papanicolaou, George J., Raffel, Leslie J., Sacco, Ralph L., Sanchez, Elena, Stark, Holger, Sundstrom, Johan, Taylor, Kent D., Xiang, Anny H., Zivkovic, Aleksandra, Lind, Lars, Ingelsson, Erik, Martin, Nicholas G., Whitfield, John B., Cai, Jianwen, Laurie, Cathy C., Okada, Yukinori, Matsuda, Koichi, Kooperberg, Charles, Chen, Yii-Der Ida, Rundek, Tatjana, Rich, Stephen S., Loos, Ruth J. F., Parra, Esteban J., Cruz, Miguel, Rotter, Jerome I., Snieder, Harold, Tomaszewski, Maciej, Humphreys, Benjamin D., Franceschini, Nora

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Lipid-induced epigenomic changes in human macrophages identify a coronary artery disease-associated variant that regulates PPAP2B Expression through Altered C/EBP-beta binding von Reschen, Michael E, Gaulton, Kyle J, Lin, Da, Soilleux, Elizabeth J, Morris, Andrew J, Smyth, Susan S, O'Callaghan, Christopher A

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