List of works - Javier T Granados-Riveron

A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.

scientific article published on 13 April 2012

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

scientific article published on 22 July 2013

Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations

scientific article published on 20 October 2011

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

scientific article

Formation, contraction, and mechanotransduction of myofribrils in cardiac development: clues from genetics

scientific article published on 10 June 2012

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation

scientific article

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

scientific journal article

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

scientific article published on 26 May 2013

High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic dystrophy cell lines

scientific article

Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot

scientific article

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

scientific article

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

scientific article published in July 2014

Rare variants in NR2F2 cause congenital heart defects in humans

scientific article published on April 2014

The Impact of Mechanical Forces in Heart Morphogenesis ⬇️

scientific article published on February 1, 2012

α-cardiac actin mutations produce atrial septal defects

October 2007 scholarly article in Human Molecular Genetics

α-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

scientific article

List of works by Javier T Granados-Riveron

A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations

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

Formation, contraction, and mechanotransduction of myofribrils in cardiac development: clues from genetics

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation

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

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

High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic dystrophy cell lines

Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

Rare variants in NR2F2 cause congenital heart defects in humans

The Impact of Mechanical Forces in Heart Morphogenesis ⬇️

α-cardiac actin mutations produce atrial septal defects

α-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects