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Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Published in:
Nature Genetics, 2013, v. 45, n. 7, p. 822, doi. 10.1038/ng.2637
By:
- Cordell, Heather J;
- Bentham, Jamie;
- Topf, Ana;
- Zelenika, Diana;
- Heath, Simon;
- Mamasoula, Chrysovalanto;
- Cosgrove, Catherine;
- Blue, Gillian;
- Granados-Riveron, Javier;
- Setchfield, Kerry;
- Thornborough, Chris;
- Breckpot, Jeroen;
- Soemedi, Rachel;
- Martin, Ruairidh;
- Rahman, Thahira J;
- Hall, Darroch;
- van Engelen, Klaartje;
- Moorman, Antoon F M;
- Zwinderman, Aelko H;
- Barnett, Phil
Publication type:
Article
Functionally Significant, Rare Transcription Factor Variants in Tetralogy of Fallot.
Published in:
PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0095453
By:
- Töpf, Ana;
- Griffin, Helen R.;
- Glen, Elise;
- Soemedi, Rachel;
- Brown, Danielle L.;
- Hall, Darroch;
- Rahman, Thahira J.;
- Eloranta, Jyrki J.;
- Jüngst, Christoph;
- Stuart, A. Graham;
- O'Sullivan, John;
- Keavney, Bernard D.;
- Goodship, Judith A.
Publication type:
Article
Common Variation Neighbouring Micro-RNA 22 Is Associated with Increased Left Ventricular Mass.
Published in:
PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0055061
By:
- Harper, Andrew R.;
- Mayosi, Bongani M.;
- Rodriguez, Antony;
- Rahman, Thahira;
- Hall, Darroch;
- Mamasoula, Chrysovalanto;
- Avery, Peter J.;
- Keavney, Bernard D.
Publication type:
Article
Genotype at the P554L Variant of the Hexose-6 Phosphate Dehydrogenase Gene Is Associated with Carotid Intima-Medial Thickness.
Published in:
PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023248
By:
- Rahman, Thahira J.;
- Walker, Elizabeth A.;
- Mayosi, Bongani M.;
- Hall, Darroch H.;
- Avery, Peter J.;
- Connell, John M. C.;
- Watkins, Hugh;
- Stewart, Paul M.;
- Keavney, Bernard
Publication type:
Article
Genetic Variation in VEGF Does Not Contribute Significantly to the Risk of Congenital Cardiovascular Malformation.
Published in:
PLoS ONE, 2009, v. 4, n. 3, p. 1, doi. 10.1371/journal.pone.0004978
By:
- Griffin, Helen R.;
- Hall, Darroch H.;
- Topf, Ana;
- Eden, James;
- Stuart, A. Graham;
- Parsons, Jonathan;
- Peart, Ian;
- Deanfield, John E.;
- O'Sullivan, John;
- Babu-Narayan, Sonya V.;
- Gatzoulis, Michael A.;
- Bu'Lock, Frances A.;
- Bhattacharya, Shoumo;
- Bentham, Jamie;
- Farrall, Martin;
- Riveron, Javier Granados;
- Brook, J. David;
- Burn, John;
- Cordell, Heather J.;
- Goodship, Judith A.
Publication type:
Article
Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 7, p. 1473, doi. 10.1093/hmg/dds552
By:
- Cordell, Heather J.;
- Töpf, Ana;
- Mamasoula, Chrysovalanto;
- Postma, Alex V.;
- Bentham, Jamie;
- Zelenika, Diana;
- Heath, Simon;
- Blue, Gillian;
- Cosgrove, Catherine;
- Granados Riveron, Javier;
- Darlay, Rebecca;
- Soemedi, Rachel;
- Wilson, Ian J.;
- Ayers, Kristin L.;
- Rahman, Thahira J.;
- Hall, Darroch;
- Mulder, Barbara J.M.;
- Zwinderman, Aelko H.;
- van Engelen, Klaartje;
- Brook, J. David
Publication type:
Article
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
Published in:
Human Molecular Genetics, 2012, v. 21, n. 7, p. 1513, doi. 10.1093/hmg/ddr589
By:
- Soemedi, Rachel;
- Topf, Ana;
- Wilson, Ian J.;
- Darlay, Rebecca;
- Rahman, Thahira;
- Glen, Elise;
- Hall, Darroch;
- Huang, Ni;
- Bentham, Jamie;
- Bhattacharya, Shoumo;
- Cosgrove, Catherine;
- Brook, J. David;
- Granados-Riveron, Javier;
- Setchfield, Kerry;
- Bu'Lock, Frances;
- Thornborough, Chris;
- Devriendt, Koenraad;
- Breckpot, Jeroen;
- Hofbeck, Michael;
- Lathrop, Mark
Publication type:
Article
Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation.
Published in:
Human Mutation, 2012, v. 33, n. 4, p. 720, doi. 10.1002/humu.22030
By:
- Tan, Huay L.;
- Glen, Elise;
- Töpf, Ana;
- Hall, Darroch;
- O'Sullivan, John J;
- Sneddon, Linda;
- Wren, Christopher;
- Avery, Peter;
- Lewis, Richard J.;
- ten Dijke, Peter;
- Arthur, Helen M.;
- Goodship, Judith A.;
- Keavney, Bernard D.
Publication type:
Article
The C-532T polymorphism of the angiotensinogen gene is associated with pulse pressure: A possible explanation for heterogeneity in genetic association studies of AGT and hypertension.
Published in:
International Journal of Epidemiology, 2007, v. 36, n. 6, p. 1356, doi. 10.1093/ije/dym213
By:
- Michelle Baker;
- Thahira Rahman;
- Darroch Hall;
- Peter J Avery;
- Bongani M Mayosi;
- John M C Connell;
- Martin Farrall;
- Hugh Watkins;
- Bernard Keavney
Publication type:
Article
INSIG-2 promoter polymorphism and obesity related phenotypes: association study in 1428 members of 248 families.
Published in:
BMC Medical Genetics, 2006, v. 7, p. 83, doi. 10.1186/1471-2350-7-83
By:
- Hall, Darroch H;
- Rahman, Thahira;
- Avery, Peter J;
- Bernard Keavney
Publication type:
Article

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