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BMC Public Health|January 21, 2011
Trial Protocol: Communicating DNA-based risk assessments for Crohn's disease: a randomised controlled trial assessing impact upon stopping smokingSophia C L Whitwell, Christopher G Mathew, Cathryn M Lewis, et al.
International Journal of Cancer|February 2, 2023
Kaposi sarcoma-associated herpesvirus, HIV-1 and Kaposi sarcoma risk in black South Africans diagnosed with cancer during antiretroviral treatment rolloutMelitah Motlhale, Mazvita Muchengeti, Debbie Bradshaw, et al.
Brain : a Journal of Neurology|October 9, 2021
Whole-exome sequencing reveals a role of HTRA1 and EGFL8 in brain white matter hyperintensitiesRainer Malik, Nathalie Beaufort, Simon Frerich, et al.
Pharmacogenetics|February 4, 2003
Genetic determinants of the thiopurine methyltransferase intermediate activity phenotype in British Asians and CaucasiansAnthony M Marinaki, Monica Arenas, Zubair H Khan, et al.
Plos One|December 8, 2021
Ranking lifestyle risk factors for cervical cancer among Black women: A case-control study from Johannesburg, South AfricaMwiza Gideon Singini, Freddy Sitas, Debbie Bradshaw, et al.
Gastroenterology|March 23, 2002
The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel diseaseAndrew P Cuthbert, Sheila A Fisher, Muddassar M Mirza, et al.
The British Journal of Psychiatry : the Journal of Mental Science|November 24, 2018
Genome-wide association study of treatment-resistance in depression and meta-analysis of three independent samplesChiara Fabbri, Siegfried Kasper, Alexander Kautzky, et al.
American Journal of Human Genetics|March 6, 2003
Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn diseaseMuddassar M Mirza, Sheila A Fisher, Kathy King, et al.
JAMA Dermatology|June 6, 2019
Prevalence of Advanced Liver Fibrosis in Patients With Severe PsoriasisCatriona M Maybury, Heather F Porter, Ewa Kloczko, et al.
Human Mutation|July 13, 2006
Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn diseaseSheila A Fisher, Jochen Hampe, Clive M Onnie, et al.
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