Literature DB >> 21706508

Refining the critical region for congenital diaphragmatic hernia on chromosome 15q26 from the study of four fetuses.

A L Mosca, L Pinson, J Andrieux, H Copin, N Bigi, J Puechberty, P Sarda, A Receveur, H Sevestre, S Pigeonnat, N Marle, M Payet, C Ragon, T Rousseau, C Thauvin-Robinet, A Masurel-Paulet, A Schneider, N Laurent, P Sagot, F Mugneret, G Lefort, L Faivre, P Callier.   

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Year:  2011        PMID： 21706508     DOI： 10.1002/pd.2793

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


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  9 in total

Review 1.  The influence of genetics in congenital diaphragmatic hernia.

Authors:  Lan Yu; Rebecca R Hernan; Julia Wynn; Wendy K Chung
Journal:  Semin Perinatol       Date:  2019-08-01       Impact factor: 3.300

2.  Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the Literature.

Authors:  Molka Kammoun; Wafa Slimani; Hanene Hannachi; Mohamed Bibi; Ali Saad; Soumaya Mougou-Zerelli
Journal:  J Pediatr Genet       Date:  2017-04-26

3.  Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks.

Authors:  Mauro Longoni; Kasper Lage; Meaghan K Russell; Maria Loscertales; Omar A Abdul-Rahman; Gareth Baynam; Steven B Bleyl; Paul D Brady; Jeroen Breckpot; Chih P Chen; Koenraad Devriendt; Gabriele Gillessen-Kaesbach; Arthur W Grix; Alan F Rope; Osamu Shimokawa; Bernarda Strauss; Dagmar Wieczorek; Elaine H Zackai; Caroline M Coletti; Faouzi I Maalouf; Kristin M Noonan; Ji H Park; Adam A Tracy; Charles Lee; Patricia K Donahoe; Barbara R Pober
Journal:  Am J Med Genet A       Date:  2012-11-19       Impact factor: 2.802

Review 4.  Genetic causes of congenital diaphragmatic hernia.

Authors:  Julia Wynn; Lan Yu; Wendy K Chung
Journal:  Semin Fetal Neonatal Med       Date:  2014-10-28       Impact factor: 3.926

5.  MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development.

Authors:  Seema R Lalani; Stephanie M Ware; Xueqing Wang; Gladys Zapata; Qi Tian; Luis M Franco; Zhengxin Jiang; Kristine Bucasas; Daryl A Scott; Philippe M Campeau; Neil Hanchard; Luis Umaña; Ashley Cast; Ankita Patel; Sau W Cheung; Kim L McBride; Molly Bray; A Craig Chinault; Barbara A Boggs; Miao Huang; Mariah R Baker; Susan Hamilton; Jeff Towbin; John L Jefferies; Susan D Fernbach; Lorraine Potocki; John W Belmont
Journal:  Hum Mol Genet       Date:  2013-06-16       Impact factor: 6.150

6.  De novo frameshift mutation in COUP-TFII (NR2F2) in human congenital diaphragmatic hernia.

Authors:  Frances A High; Pooja Bhayani; Jay M Wilson; Carol J Bult; Patricia K Donahoe; Mauro Longoni
Journal:  Am J Med Genet A       Date:  2016-07-01       Impact factor: 2.802

7.  Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities.

Authors:  Seema R Lalani; Chad Shaw; Xueqing Wang; Ankita Patel; Lance W Patterson; Katarzyna Kolodziejska; Przemyslaw Szafranski; Zhishuo Ou; Qi Tian; Sung-Hae L Kang; Amina Jinnah; Sophia Ali; Aamir Malik; Patricia Hixson; Lorraine Potocki; James R Lupski; Pawel Stankiewicz; Carlos A Bacino; Brian Dawson; Arthur L Beaudet; Fatima M Boricha; Runako Whittaker; Chumei Li; Stephanie M Ware; Sau Wai Cheung; Daniel J Penny; John Lynn Jefferies; John W Belmont
Journal:  Eur J Hum Genet       Date:  2012-08-29       Impact factor: 4.246

8.  Ultrasound, Echocardiography, MRI, and Genetic Analysis of a Fetus with Congenital Diaphragmatic Hernia and Partial 11q Trisomy.

Authors:  Yolanda Fernández-Perea; Lutgardo García-Díaz; Javier Sánchez; Guillermo Antiñolo; Salud Borrego
Journal:  Case Rep Obstet Gynecol       Date:  2017-03-02

Review 9.  The Role of De Novo Variants in Patients with Congenital Diaphragmatic Hernia.

Authors:  Charlotte Bendixen; Heiko Reutter
Journal:  Genes (Basel)       Date:  2021-09-11       Impact factor: 4.096
  9 in total

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