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Browsing publications by Dr Thahira Rahman

Newcastle AuthorsTitleYearFull text
Dr Sarra Ryan
Elizabeth Matheson
Dr Paul Sinclair
Dr Matthew Bashton
Claire Schwab
et al.		The role of the RAS pathway in iAMP21-ALL2016
Darren Houniet
Dr Thahira Rahman
Dr Yaobo Xu
Professor Judith Goodship
Professor Bernard Keavney
Using population data for assessing next-generation sequencing performance2015
Dr Ana Topf
Dr Helen Griffin
Dr Elise Glen
Rachel Soemedi
Dr Danielle Brown
et al.		Functionally Significant, Rare Transcription Factor Variants in Tetralogy of Fallot2014
Matthieu Miossec
Raf Hussain
Dr Thahira Rahman
Dr Ana Topf
Dr Mauro Santibanez Koref
et al.		Investigating the cause of transposition of great arteries; exome sequencing analysis2014
Valentina Mamasoula
Dr Tomasz Pierscionek
Dr Darroch Hall
Dr Ana Topf
Dr Danielle Brown
et al.		Association between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7,697 Cases and 13,125 Controls2013
Dr Thahira Rahman
Valentina Mamasoula
Dr Peter Avery
Professor Bernard Keavney
Common Variation Neighbouring Micro-RNA 22 Is Associated with Increased Left Ventricular Mass2013
Dr Thahira Rahman
Professor Bernard Keavney
Professor Judith Goodship
Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH72013
Professor Heather Cordell
Dr Ana Topf
Valentina Mamasoula
Dr Rebecca Darlay
Rachel Soemedi
et al.		Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot2013
Professor Heather Cordell
Dr Ana Topf
Valentina Mamasoula
Rachel Soemedi
Dr Ruairidh Martin
et al.		Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p162013
Darren Houniet
Dr Thahira Rahman
Dr Mauro Santibanez Koref
Professor Bernard Keavney
Mutations in FAM111B Cause Hereditary Fibrosing Poikiloderma with Tendon Contracture, Myopathy, and Pulmonary Fibrosis2013
Professor Judith Goodship
Dr Darroch Hall
Dr Ana Topf
Valentina Mamasoula
Dr Helen Griffin
et al.		A Common Variant in the PTPN11 Gene Contributes to the Risk of Tetralogy of Fallot2012
Professor Rita Horvath
Vivienne Neeve
Dr Angela Pyle
Dr Helen Griffin
Deepthi Ashok
et al.		A new phenotype of brain iron accumulation with dystonia, optic atrophy, and peripheral neuropathy2012
Valentina Mamasoula
Dr Tomasz Pierscionek
Dr Ana Topf
Dr Thahira Rahman
Dr John O'Sullivan
et al.		Aetiological Role Of Folate Deficiency In Congenital Cardiovascular Malformation: Evidence From "Mendelian Randomisation" And Meta-Analysis2012
Rachel Soemedi
Dr Ian Wilson
Dr Rebecca Darlay
Dr Ana Topf
Dr Simon Zwolinski
et al.		Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease2012
Rachel Soemedi
Dr Ana Topf
Dr Ian Wilson
Dr Rebecca Darlay
Dr Thahira Rahman
et al.		Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls2012
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