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Ball, Amy L, Bloch, Katarzyna M, Rainbow, Lucille ORCID: 0000-0003-0447-6885, Liu, Xuan, Kenny, John, Lyon, Jonathan J, Gregory, Richard, Alfirevic, Ana ORCID: 0000-0002-2801-9817 and Chadwick, Amy E ORCID: 0000-0002-7399-8655 (2021) Assessment of the impact of mitochondrial genotype upon drug-induced mitochondrial dysfunction in platelets derived from healthy volunteers. Archives of Toxicology, 95 (4). pp. 1335-1347.

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Maroteau, Cyrielle, Siddiqui, Moneeza Kalhan, Veluchamy, Abirami, Carr, Fiona, White, Myra, Cassidy, Andrew J, Baranova, Ekaterina V, Rasmussen, Eva R, Eriksson, Niclas, Bloch, Katarzyna M et al (show 13 more authors) , Brown, Nancy J, Bygum, Anette, Hallberg, Par, Karawajczyk, Malgorzata, Magnusson, Patrik KE, Yue, QunYing, Syvnen, AnnChristine, Buchwald, Christian, Alfirevic, Ana ORCID: 0000-0002-2801-9817, Maitland-van der Zee, Anke H, Wadelius, Mia, Palmer, Colin NA and PREDICTION-ADR, (2020) Exome Sequencing Reveals Common and Rare Variants in F5 Associated With ACE Inhibitor and Angiotensin Receptor Blocker–Induced Angioedema. CLINICAL PHARMACOLOGY & THERAPEUTICS, 108 (6). pp. 1195-1202.

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Floyd, James S, Bloch, Katarzyna M, Brody, Jennifer A, Maroteau, Cyrielle, Siddiqui, Moneeza K, Gregory, Richard, Carr, Daniel F, Molokhia, Mariam, Liu, Xiaoming, Bis, Joshua C et al (show 32 more authors) , Ahmed, Ammar, Liu, Xuan, Hallberg, Pär, Yue, Qun-Ying, Magnusson, Patrik KE, Brisson, Diane, Wiggins, Kerri L, Morrison, Alanna C, Khoury, Etienne, McKeigue, Paul, Stricker, Bruno H, Lapeyre-Mestre, Maryse, Heckbert, Susan R, Gallagher, Arlene M, Chinoy, Hector, Gibbs, Richard A, Bondon-Guitton, Emmanuelle, Tracy, Russell, Boerwinkle, Eric, Gaudet, Daniel, Conforti, Anita, van Staa, Tjeerd, Sitlani, Colleen M, Rice, Kenneth M, Maitland-van der Zee, Anke-Hilse, Wadelius, Mia, Morris, Andrew P, Pirmohamed, Munir ORCID: 0000-0002-7534-7266, Palmer, Colin AN, Psaty, Bruce M, Alfirevic, Ana ORCID: 0000-0002-2801-9817 and PREDICTION-ADR Consortium and EUDRAGENE, (2019) Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing. PLoS One, 14 (6). e0218115-.