Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans-Reference-Cited by-同舟云学术

Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans

Published:2010-06 Issue:6 Volume:86 Page:839-849
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Thienpont Bernard,Zhang Litu,Postma Alex V.,Breckpot Jeroen,Tranchevent Léon-Charles,Van Loo Peter,Møllgård Kjeld,Tommerup Niels,Bache Iben,Tümer Zeynep,van Engelen Klaartje,Menten Björn,Mortier Geert,Waggoner Darrel,Gewillig Marc,Moreau Yves,Devriendt Koen,Larsen Lars Allan

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference40 articles.

1. The incidence of congenital heart disease;Hoffman;J. Am. Coll. Cardiol.,2002

2. Heart disease and stroke statistics—2006 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee;Thom;Circulation,2006

3. Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics;Jenkins;Circulation,2007

4. Familial recurrence of congenital heart disease: an overview and review of the literature;Calcagni;Eur. J. Pediatr.,2007

5. A study to determine the incidence of structural congenital heart disease in monochorionic twins;Manning;Prenat. Diagn.,2006

Cited by 91 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. TAK1 operates at the primary cilium in non-canonical TGFB/BMP signaling to control heart development;2024-05-08

2. Generation of a TAB2 knockout hESC line (WAe009-A-Z) derived from H9 using CRISPR/Cas9;Stem Cell Research;2024-02

3. Myxomatous degeneration of cardiac valves in a fetus with 6q25.1 (TAB2) deletion;Cardiology in the Young;2024-01-03

4. Genetics of Common Birth Defects in Newborns;Principles of Neonatology;2024

5. Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome study;2023-12-28