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2023
Mark Genetic modification of inflammation- and clonal hematopoiesis-associated cardiovascular risk
Yu, Zhi ; Fidler, Trevor P. ; Ruan, Yunfeng ; Vlasschaert, Caitlyn ; Nakao, Tetsushi ; Uddin, Md Mesbah ; Mack, Taralynn ; Niroula, Abhishek ^LU ; Brett Heimlich, J. and Zekavat, Seyedeh M. , et al. (2023) In Journal of Clinical Investigation 133(18).
- Contribution to journal › Article
2021
Mark Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19
Klaric, Lucija ; Gisby, Jack S ; Papadaki, Artemis ; Muckian, Marisa D ; Macdonald-Dunlop, Erin ; Zhao, Jing Hua ; Tokolyi, Alex ; Persyn, Elodie ; Pairo-Castineira, Erola and Morris, Andrew P , et al. (2021)
- Working paper/Preprint › Preprint in preprint archive
2019
Mark Epigenome-wide association study of incident type 2 diabetes in a British population : EPIC-Norfolk study
Cardona, Alexia ; Day, Felix R. ; Perry, John R.B. ; Loh, Marie ; Chu, Audrey Y. ; Lehne, Benjamin ; Paul, Dirk S. ; Lotta, Luca A. ; Stewart, Isobel D. and Kerrison, Nicola D. , et al. (2019) In Diabetes 68(12). p.2315-2326
- Contribution to journal › Article
2018
Mark Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
Feitosa, Mary F. ; Kraja, Aldi T. ; Chasman, Daniel I. ; Sung, Yun J. ; Winkler, Thomas W. ; Ntalla, Ioanna ; Guo, Xiuqing ; Franceschini, Nora ; Cheng, Ching Yu and Sim, Xueling , et al. (2018) In PLoS ONE 13(6).
- Contribution to journal › Article
2017
Mark New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
Kraja, Aldi T. ; Cook, James P. ; Warren, Helen R. ; Surendran, Praveen ; Liu, Chunyu ; Evangelou, Evangelos ; Manning, Alisa K. ; Grarup, Niels ; Drenos, Fotios and Sim, Xueling , et al. (2017) In Circulation: Cardiovascular Genetics 10(5).
- Contribution to journal › Article
2016
Mark Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease
Jakobsdottir, Johanna ; van der Lee, Sven J. ; Bis, Joshua C. ; Chouraki, Vincent ; Li-Kroeger, David ; Yamamoto, Shinya ; Grove, Megan L. ; Naj, Adam ; Vronskaya, Maria and Salazar, Jose L. , et al. (2016) In PLoS Genetics 12(10).
- Contribution to journal › Article
Mark Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure
Smith, Gustav ^LU ; Felix, Janine F. ; Morrison, Alanna C. ; Kalogeropoulos, Andreas ; Trompet, Stella ; Wilk, Jemma B. ; Gidlöf, Olof ^LU ; Wang, Xinchen ; Morley, Michael and Mendelson, Michael , et al. (2016) In PLoS Genetics 12(5).
- Contribution to journal › Article
Mark The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
Ehret, Georg B. ; Ferreira, Teresa ; Chasman, Daniel I. ; Jackson, Anne U. ; Schmidt, Ellen M. ; Johnson, Toby ; Thorleifsson, Gudmar ; Luan, Jian'An ; Donnelly, Louise A. and Kanoni, Stavroula , et al. (2016) In Nature Genetics 48(10). p.1171-1184
- Contribution to journal › Article
2015
Mark Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
Wessel, Jennifer ; Chu, Audrey Y ; Willems, Sara M ; Wang, Shuai ; Yaghootkar, Hanieh ; Brody, Jennifer A ; Dauriz, Marco ; Hivert, Marie-France ; Raghavan, Sridharan and Lipovich, Leonard , et al. (2015) In Nature Communications 6.
- Contribution to journal › Article
2014
Mark Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
Lange, Leslie A ; Hu, Youna ; Zhang, He ; Xue, Chenyi ; Schmidt, Ellen M ; Tang, Zheng-Zheng ; Bizon, Chris ; Lange, Ethan M ; Smith, Joshua D and Turner, Emily H , et al. (2014) In American Journal of Human Genetics 94(2). p.233-245
- Contribution to journal › Article

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