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Browsing publications by Valentina Mamasoula.

Newcastle AuthorsTitleYearFull text
Valentina Mamasoula
Professor Heather Cordell
Professor Bernard Keavney
Marked variation in heritability estimates of left ventricular mass depending on modality of measurement2019
Dr Kristin Ayers
Professor Heather Cordell
Valentina Mamasoula
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits2018
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 risk2017
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 Kidney2017
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-UK2016
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 trial2016
Dr Kristin Ayers
Professor Heather Cordell
Valentina Mamasoula
Professor Bernard Keavney
Genome-wide analysis identifies 12 loci influencing human reproductive behavior2016
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 Estimation2015
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 estimation2015
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
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
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
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
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-analysis2011
Valentina Mamasoula
Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data2011