Publications by Valentina Mamasoula - ePrints

Browsing publications by Valentina Mamasoula.

Newcastle Authors	Title	Year
Valentina Mamasoula Professor Heather Cordell Professor Bernard Keavney	Marked variation in heritability estimates of left ventricular mass depending on modality of measurement	2019
Dr Kristin Ayers Professor Heather Cordell Valentina Mamasoula	Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits	2018
Professor Bernard Keavney Dr Kristin Ayers Professor Heather Cordell Dr Lenore Launer Valentina Mamasoula et al.	Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk	2017
Professor Heather Cordell Valentina Mamasoula	Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets from Blood and the Kidney	2017
Professor Andrew Fisher Anders Andreasson Alexandros Chrysos Dr Joanne Lally Valentina Mamasoula et al.	An observational study of Donor Ex Vivo Lung Perfusion in UK Lung Transplantation : DEVELOP-UK	2016
Professor Hamish McAllister-Williams Dr Andreas Finkelmeyer Dr Peter Gallagher Professor Heinz Grunze Dr Adrian Lloyd et al.	Antidepressant augmentation with metyrapone for treatment-resistant depression (the ADD study): a double-blind, randomised, placebo-controlled trial	2016
Dr Kristin Ayers Professor Heather Cordell Valentina Mamasoula Professor Bernard Keavney	Genome-wide analysis identifies 12 loci influencing human reproductive behavior	2016
Dr Richard Howey Valentina Mamasoula Dr Ana Topf Professor Judith Goodship Professor Bernard Keavney et al.	Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation	2015
Dr Richard Howey Valentina Mamasoula Dr Ana Topf Professor Judith Goodship Professor Bernard Keavney et al.	Increased power for detection of parent-of-origin effects via the use of haplotype estimation	2015
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 Controls	2013
Dr Thahira Rahman Valentina Mamasoula Dr Peter Avery Professor Bernard Keavney	Common Variation Neighbouring Micro-RNA 22 Is Associated with Increased Left Ventricular Mass	2013
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 Fallot	2013
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 4p16	2013
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 Fallot	2012
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-Analysis	2012
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 Disease	2012
Valentina Mamasoula Dr Tomasz Pierscionek Addison Palomino Doza Dr Ana Topf Dr Thahira Rahman et al.	Aetiological role of folate deficiency in congenital heart disease: evidence from Mendelian randomisation and meta-analysis	2011
Valentina Mamasoula	Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data	2011