Chrysovalanto Mamasoula

发表

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.

Marc Gewillig, Rachel Soemedi, Koenraad Devriendt, 2012, American journal of human genetics.

An observational study of Donor Ex Vivo Lung Perfusion in UK lung transplantation: DEVELOP-UK.

J. Lally, M. Pearce, E. McColl, 2016, Health technology assessment.

Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data

H. Cordell, K. Ayers, Chrysovalanto Mamasoula, 2011, BMC proceedings.

Randomised controlled trial of Antiglucocorticoid augmentation (metyrapone) of antiDepressants in Depression (ADD Study)

A. House, I. Anderson, H. Grunze, 2015 .

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Christian Gieger, Gonçalo Abecasis, He Gao, 2018, Nature Genetics.

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Christian Gieger, Gonçalo Abecasis, He Gao, 2017, bioRxiv.

Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation

H. Cordell, B. Keavney, J. Goodship, 2015, American journal of human genetics.

A Common Variant in the PTPN11 Gene Contributes to the Risk of Tetralogy of Fallot

H. Cordell, S. Bhattacharya, B. Keavney, 2012, Circulation. Cardiovascular genetics.

Prevalence of congenital heart defects in Europe, 2008–2015: A registry‐based study

M. Haeusler, A. Neville, A. Pierini, 2022, Birth defects research.

Common Variation Neighbouring Micro-RNA 22 Is Associated with Increased Left Ventricular Mass

Antony Rodriguez, A. Harper, B. Keavney, 2013, PloS one.

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

Andrew D. Johnson, Lorna M. Lopez, P. O’Reilly, 2017, Hypertension.

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

He Gao, Andres Metspalu, Fotios Drenos, 2017, Nature Genetics.

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

S. Heath, G. Lathrop, M. Farrall, 2013, Nature Genetics.

Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot

S. Heath, G. Lathrop, A. Moorman, 2013, Human molecular genetics.

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Andrew D. Johnson, Yan V. Sun, Sara M. Willems, 2018, Nature Genetics.

Association Between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7697 Cases and 13 125 Controls

G. Lathrop, M. Farrall, A. Moorman, 2013, Circulation. Cardiovascular genetics.

Association between C 677 T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease : Meta-Analysis of 7 , 697 Cases and 13 , 125 Controls Running title : Mamasoula : MTHFR C 677 T polymorphism and congenital heart disease

Faith, G. Lathrop, D. Zélénika, 2013 .

Antidepressant augmentation with metyrapone for treatment-resistant depression (the ADD study): a double-blind, randomised, placebo-controlled trial.

I. Anderson, A. Finkelmeyer, H. Grunze, 2016, The lancet. Psychiatry.

Maternal age and the prevalence of congenital heart defects in Europe, 1995–2015: A register‐based study

M. Haeusler, A. Neville, A. Pierini, 2023, Birth defects research.

Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

Andrew D. Johnson, Lorna M. Lopez, Aude Saint Pierre, 2017, bioRxiv.

Association Between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7697 Cases and 13 125 Controls

M. Farrall, K. Devriendt, D. Zélénika, 2013, Circulation. Cardiovascular genetics.

Antidepressant augmentation with metyrapone for treatment-resistant depression (the ADD study): a double-blind, randomised, placebo-controlled trial.

I. Anderson, E. McColl, S. Pearce, 2016, The lancet. Psychiatry.

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Andrew D. Johnson, Peter K. Joshi, Sara M. Willems, 2018, Nature Genetics.

A systematic review and meta‐analysis of school and cognitive function domains of health‐related quality of life measures for children and young adults with congenital heart disease

Chrysovalanto Mamasoula, A. Adesanya, Lindsay Pennington, 2023, Birth defects research.

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Andrew D. Johnson, Sara M. Willems, Lorna M. Lopez, 2018, Nature Genetics.

Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation

H. Cordell, B. Keavney, J. Goodship, 2015, American Journal of Human Genetics.

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

M. P. Concas, Jacob M. Keaton, Loren R. Risch, 2024, Nature genetics.

Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

Andrew D. Johnson, Lorna M. Lopez, P. O’Reilly, 2017 .

Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

Sara M. Willems, Lorna M. Lopez, Loren R. Risch, 2024, Kidney international reports.