Literature DB >> 15857420

Analysis of CRELD1 as a candidate 3p25 atrioventicular septal defect locus (AVSD2).

M Zatyka, M Priestley, E J Ladusans, A E Fryer, J Mason, F Latif, E R Maher.   

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Year:  2005        PMID： 15857420     DOI： 10.1111/j.1399-0004.2005.00435.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  16 in total

Review 1.  Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

Authors:  Mary Ella Pierpont; Martina Brueckner; Wendy K Chung; Vidu Garg; Ronald V Lacro; Amy L McGuire; Seema Mital; James R Priest; William T Pu; Amy Roberts; Stephanie M Ware; Bruce D Gelb; Mark W Russell
Journal:  Circulation       Date:  2018-11-20       Impact factor: 29.690

Review 2.  Echocardiography in children with Down syndrome.

Authors:  Mohammed A Al-Biltagi
Journal:  World J Clin Pediatr       Date:  2013-11-08

3.  Specific association of missense mutations in CRELD1 with cardiac atrioventricular septal defects in heterotaxy syndrome.

Authors:  Samaneh Zhian; John Belmont; Cheryl L Maslen
Journal:  Am J Med Genet A       Date:  2012-06-27       Impact factor: 2.802

4.  The matricellular protein CCN1 is essential for cardiac development.

Authors:  Fan-E Mo; Lester F Lau
Journal:  Circ Res       Date:  2006-10-05       Impact factor: 17.367

Review 5.  The pathogenesis of atrial and atrioventricular septal defects with special emphasis on the role of the dorsal mesenchymal protrusion.

Authors:  Laura E Briggs; Jayant Kakarla; Andy Wessels
Journal:  Differentiation       Date:  2012-06-17       Impact factor: 3.880

6.  Unintended diagnosis of Von Hippel Lindau syndrome using Array Comparative Genomic Hybridization (CGH): counseling challenges arising from unexpected information.

Authors:  Jennifer Hogan; A Turner; K Tucker; L Warwick
Journal:  J Genet Couns       Date:  2012-08-16       Impact factor: 2.537

7.  Novel CRELD1 gene mutations in patients with atrioventricular septal defect.

Authors:  Ying Guo; Jie Shen; Lang Yuan; Fen Li; Jian Wang; Kun Sun
Journal:  World J Pediatr       Date:  2010-11-16       Impact factor: 2.764

8.  Genetic modifiers predisposing to congenital heart disease in the sensitized Down syndrome population.

Authors:  Huiqing Li; Sheila Cherry; Donna Klinedinst; Valerie DeLeon; Jennifer Redig; Benjamin Reshey; Michael T Chin; Stephanie L Sherman; Cheryl L Maslen; Roger H Reeves
Journal:  Circ Cardiovasc Genet       Date:  2012-04-20

Review 9.  Familial recurrence of congenital heart disease: an overview and review of the literature.

Authors:  Giulio Calcagni; M Cristina Digilio; Anna Sarkozy; Bruno Dallapiccola; Bruno Marino
Journal:  Eur J Pediatr       Date:  2006-11-08       Impact factor: 3.183

10.  An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects.

Authors:  Christine Ackerman; Adam E Locke; Eleanor Feingold; Benjamin Reshey; Karina Espana; Janita Thusberg; Sean Mooney; Lora J H Bean; Kenneth J Dooley; Clifford L Cua; Roger H Reeves; Stephanie L Sherman; Cheryl L Maslen
Journal:  Am J Hum Genet       Date:  2012-10-05       Impact factor: 11.025
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