Search

Home
Staff
Sarah Al Ashmori Theophile Bigirumurame Andy Bryant Thomas Chadwick Svetlana Cherlin Mike Cole Holly Fisher Tony Fouweather Shaun Hiu Dorcas Kareithi Ann Breeze Konkoth Nan Lin Jingky Lozano-Kuehne Helen Mossop Ellen Moss Jérémie Nsengimana Vicky Ryan Marzieh Shahmandi Moha Shojaei Dawn Teare James Wason Faye Williamson Nina Wilson Sylvia Zhang
PhD students
Ruqayya Azher Nicole Cizauskas Laura Etfer Niamh Fitzgerald Raiann Hamshaw Aritra Mukherjee Pela Okorie Samuel Sarkodie Lou Whitehead
Methodology research
Overview Adaptive designs Master protocols Transforming IMID trials
Projects
Publications
News
Courses
Adaptive Designs and Multiple Testing Procedures Leveraging External Information Precision Medicine Clinical Trials
Contact

Goodship JA

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease
Increased power for detection of parent-of-origin effects via the use of haplotype estimation
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of fallot
Aetiological role of folate deficiency in congenital cardiovascular malformation: Evidence from 'mendelian randomisation' and meta-analysis
A common variant in the PTPN11 gene contributes to the risk of tetralogy of fallot

Published with Wowchemy — the free, open source website builder that empowers creators.