Valentina Mamasoula
Professor Heather Cordell
Professor Bernard Keavney
| Marked variation in heritability estimates of left ventricular mass depending on modality of measurement | 2019 |
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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 |
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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 |
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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 |
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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 |
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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 |
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Dr Kristin Ayers
Professor Heather Cordell
Valentina Mamasoula
Professor Bernard Keavney
| Genome-wide analysis identifies 12 loci influencing human reproductive behavior | 2016 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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Valentina Mamasoula
| Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data | 2011 |
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