Genetics of congenital heart disease: BEYOND half-measures

Trends in Cardiovascular Medicine

Volumn 25, Issue 4, 2015, Pages 302-304

  Barnett, Phil ^a   Postma, Alex V ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR;

CHROMOSOME ABERRATION; CONGENITAL HEART DISEASE; CONSANGUINITY; EDITORIAL; GENE LOCUS; GENE MUTATION; GENETICS; HEART DEVELOPMENT; HUMAN; HUMAN GENOME; INHERITANCE; PRIORITY JOURNAL; CONGENITAL HEART MALFORMATION; DOWN SYNDROME; MUTATION;

DOWN SYNDROME; HEART DEFECTS, CONGENITAL; HUMANS; MUTATION;

EID: 84928760846     PISSN: 10501738     EISSN: 18732615     Source Type: Journal    
DOI: 10.1016/j.tcm.2014.11.012     Document Type: Editorial

References (14)

1. Fahed A.C., Gelb B.D., Seidman J.G., Seidman C.E. Genetics of congenital heart disease: the glass half empty. Circ Res 2013, 112:707-720.
2. Van der Bom T., Zomer A.C., Zwinderman A.H., Meijboom F.J., Bouma B.J., Mulder B.J.M. The changing epidemiology of congenital heart disease. Nat Rev Cardiol 2011, 8:50-60.
3. Gilboa S.M., Salemi J.L., Nembhard W.N., Fixler D.E., Correa A. Mortality resulting from congenital heart disease among children and adults in the United States, 1999 to 2006. Circulation 2010, 122:2254-2263.
4. Zaidi S., Choi M., Wakimoto H., Ma L., Jiang J., Overton J.D., et al. De novo mutations in histone-modifying genes in congenital heart disease. Nature 2013, 498:220-223.
5. Al Turki S., Manickaraj A.K., Mercer C.L., Gerety S.S., Hitz M.P., Lindsay S., et al. Rare variants in NR2F2 cause congenital heart defects in humans. Am J Hum Genet 2014, 94:574-585.
6. Shieh J.T.C., Bittles A.H., Hudgins L. Consanguinity and the risk of congenital heart disease. Am J Med Genet A 2012, 158A:1236-1241.
7. Aburawi E., Aburawi H., Bagnall K., Bhuiyan Z.A. Molecular insight into heart development and congenital heart disases: an update review from the Arab countries. Trends Cardiovasc Med 2014, [this issue].
8. Al-Mesned A., Al Akhfash A.A., Sayed M. Incidence of severe congenital heart disease at the province of Al-Qassim, Saudi Arabia. Congenit Heart Dis 2012, 7:277-282.
9. Bernstein B.E., Birney E., Dunham I., Green E.D., Gunter C., Snyder M. An integrated encyclopedia of DNA elements in the human genome. Nature 2012, 489:57-74.
10. Smemo S., Campos L.C., Moskowitz I.P., Krieger J.E., Pereira A.C., Nobrega M.A. Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease. Hum Mol Genet 2012, 21:3255-3263.
11. Robertson G., Hirst M., Bainbridge M., Bilenky M., Zhao Y., Zeng T., et al. Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing. Nat Methods 2007, 4:651-657.
12. Arnold C.D., Gerlach D., Stelzer C., Boryń Ł.M., Rath M., Stark A. Genome-wide quantitative enhancer activity maps identified by STARR-seq. Science 2013, 339:1074-1077.
13. De Wit E., de Laat W. A decade of 3C technologies: insights into nuclear organization. Genes Dev 2012, 26:11-24.
14. Tian Y., Yuan L., Goss A.M., Wang T., Yang J., Lepore J.J., et al. Characterization and in vivo pharmacological rescue of a Wnt2-Gata6 pathway required for cardiac inflow tract development. Dev Cell 2010, 18:275-287.