Browsing by Author Bhattacharya, Shoumo

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 3 of 3
Issue DateTitleAuthor(s)Citation
2013Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13125 controlsWinlaw, David; Bentham, Jamie; Bhattacharya, Shoumo; Brown, Danielle L; Cosgrove, Catherine; Druschel, Charlotte; et al, Various; Granados-Riveron, Javier; Hall, Darroch; Mamasoula, Chrysovalanto; Mills, James; Pangilinan, Faith; Pass, Kenneth; Pierscionek, Tomasz; Prentice, R Reid; Russel, Mark W; Topf, Ana; Zelenika, Diana; Children's Hospital Westmead: Paediatrics & Child HealthAssociation between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13125 controls, Circulation Cardiovascular Genetics, vol.6, 4, 2013,pp 347-353
2015NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targetsWaardenberg, Ashley; Bhattacharya, Shoumo; Blanpain, Cedric; Bondue, Antoine; Bouveret, Romaric; Chapman, G.; Chen, Chiann-mun; de Jong, Danielle; Doan, Tram; Dunwoodie, Sally; Fonoudi, Hananeh; Harvey, R; Kaur, Gurpreet; Mohamed, Stephanie; Plachta, Nicolas; Ramialison, Mirana; Schonrock, Nicole; Wouters, Merridee A.; Childrens Medical Research Institute (CMRI)NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets, eLife, vol.4, N/A, 2015,pp 1-30
2012Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controlsWinlaw, David; Bentham, Jamie; Bhattacharya, Shoumo; Darlay, Rebecca; et al, Various; Glan, Elise; Hall, Darroch; Huang, Ni; Rahman, Thahira; Soemedi, Rachel; Topf, Ana; Wilson, Ian J; Children's Hospital Westmead: Paediatrics & Child HealthPhenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls, Human Molecular Genetics, vol.21, 7, 2012,pp 1513-1520