J. P. Doza

Molecular Analysis of BMPR 2 , TBX 4 , and KCNK 3 and Genotype-Phenotype Correlations in Spanish Patients and Families With Idiopathic and Hereditary Pulmonary Arterial Hypertension

P. Lapunzina, A. Santos-Lozano, P. E. Subías, 2019 .

Variable Expressivity of a Founder Mutation in the EIF2AK4 Gene in Hereditary Pulmonary Veno-occlusive Disease and Its Impact on Survival.

P. Tejedor, Amaya Martínez Meñaca, J. P. Doza, 2017 .

An homozygous mutation in KCNK3 is associated with an aggressive form of hereditary pulmonary arterial hypertension

P. Tejedor, J. P. Doza, P. Lajara, 2017 .

Association between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7,697 Cases and 13,125 Controls Running title: Mamasoula: MTHFR C677T polymorphism and congenital heart disease

G. Lathrop, M. Farrall, D. Zélénika, 2017 .

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 .

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.