Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study

Autor: Hawcutt, Daniel B, Francis, Ben, Carr, Daniel F, Jorgensen, Andrea L, Yin, Peng, Wallin, Naomi, O'Hara, Natalie, Zhang, Eunice J, Bloch, Katarzyna M, Ganguli, Amitava, Thompson, Ben, McEvoy, Laurence, Peak, Matthew, Crawford, Andrew A, Walker, Brian R, Blair, Joanne C, Couriel, Jonathan, Smyth, Rosalind L, Pirmohamed, Munir

Publikováno v: In The Lancet Respiratory Medicine June 2018 6(6):442-450

Developing and Validating a Clinical Warfarin Dose-Initiation Model for Black-African Patients in South Africa and Uganda (vol 109, pg 1564, 2021)

Autor: Asiimwe, Innocent G, Waitt, Catriona, Sekaggya-Wiltshire, Christine, Hutchinson, Claire, Okello, Emmy, Zhang, Eunice J, Semakula, Jerome R, Mouton, Johannes P, Cohen, Karen, Blockman, Marc, Lamorde, Mohammed, Jorgensen, Andrea L, Pirmohamed, Munir

Publikováno v: CLINICAL PHARMACOLOGY & THERAPEUTICS

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::313f715bfb96873eeb744d8b05be0863

Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients

Autor: McCormack, Mark, Gui, Hongsheng, Ingason, Andrés, Speed, Doug, Wright, Galen E B, Zhang, Eunice J., Secolin, Rodrigo, Yasuda, Clarissa, Kwok, Maxwell, Wolking, Stefan, Becker, Felicitas, Rau, Sarah, Avbersek, Andreja, Heggeli, Kristin, Leu, Costin, Depondt, Chantal, Sills, Graeme J., Marson, Anthony G., Auce, Pauls, Brodie, Martin J., Francis, Ben, Johnson, Michael R., Koeleman, Bobby P C, Striano, Pasquale, Coppola, Antonietta, Zara, Federico, Kunz, Wolfram S., Sander, Josemir W., Lerche, Holger, Klein, Karl Martin, Weckhuysen, Sarah, Krenn, Martin, Gudmundsson, Lárus J, Stefánsson, Kári, Krause, Roland, Shear, Neil, Ross, Colin J D, Delanty, Norman, Pirmohamed, Munir, Carleton, Bruce C., Cendes, Fernando, Lopes-Cendes, Iscia, Liao, Wei-Ping, O'Brien, Terence J., Sisodiya, Sanjay M., Cherny, Stacey, Kwan, Patrick, Baum, Larry, Cavalleri, Gianpiero L., International League Against Epilepsy Consortium on Complex Epilepsies, Bisulli, Francesca

Publikováno v: Neurology
Neurology, 91 (16
Møller, R S & EPIGEN Consortium; 2018, ' Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients ', Neurology, vol. 90, no. 4, pp. e332-e341 . https://doi.org/10.1212/WNL.0000000000004853
Neurology. United States (2017).
E341
E332

Publisher's version (útgefin grein)
Objective To characterize, among European and Han Chinese populations, the genetic predictors of maculopapular exanthema (MPE), a cutaneous adverse drug reaction common to antiepileptic drugs. Methods We cond

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11a6f66cf05d199b6df8b570ce06c15d
http://livrepository.liverpool.ac.uk/3009749/1/e332.full.pdf

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