158 related articles for article (PubMed ID: 21085971)
1. Identification of TCTE3 as a gene responsible for congenital diaphragmatic hernia using a high-resolution single-nucleotide polymorphism array.
Teshiba R; Masumoto K; Esumi G; Nagata K; Kinoshita Y; Tajiri T; Taguchi T; Yamamoto K
Pediatr Surg Int; 2011 Feb; 27(2):193-8. PubMed ID: 21085971
[TBL] [Abstract][Full Text] [Related]
2. Systematic analysis of copy number variation associated with congenital diaphragmatic hernia.
Zhu Q; High FA; Zhang C; Cerveira E; Russell MK; Longoni M; Joy MP; Ryan M; Mil-Homens A; Bellfy L; Coletti CM; Bhayani P; Hila R; Wilson JM; Donahoe PK; Lee C
Proc Natl Acad Sci U S A; 2018 May; 115(20):5247-5252. PubMed ID: 29712845
[TBL] [Abstract][Full Text] [Related]
3. A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia.
Arrington CB; Bleyl SB; Matsunami N; Bowles NE; Leppert TI; Demarest BL; Osborne K; Yoder BA; Byrne JL; Schiffman JD; Null DM; DiGeronimo R; Rollins M; Faix R; Comstock J; Camp NJ; Leppert MF; Yost HJ; Brunelli L
Am J Med Genet A; 2012 Dec; 158A(12):3137-47. PubMed ID: 23165927
[TBL] [Abstract][Full Text] [Related]
4. Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia.
Wat MJ; Veenma D; Hogue J; Holder AM; Yu Z; Wat JJ; Hanchard N; Shchelochkov OA; Fernandes CJ; Johnson A; Lally KP; Slavotinek A; Danhaive O; Schaible T; Cheung SW; Rauen KA; Tonk VS; Tibboel D; de Klein A; Scott DA
J Med Genet; 2011 May; 48(5):299-307. PubMed ID: 21525063
[TBL] [Abstract][Full Text] [Related]
5. De novo copy number variants are associated with congenital diaphragmatic hernia.
Yu L; Wynn J; Ma L; Guha S; Mychaliska GB; Crombleholme TM; Azarow KS; Lim FY; Chung DH; Potoka D; Warner BW; Bucher B; LeDuc CA; Costa K; Stolar C; Aspelund G; Arkovitz MS; Chung WK
J Med Genet; 2012 Oct; 49(10):650-9. PubMed ID: 23054247
[TBL] [Abstract][Full Text] [Related]
6. Gene expression in the developing diaphragm: significance for congenital diaphragmatic hernia.
Clugston RD; Zhang W; Greer JJ
Am J Physiol Lung Cell Mol Physiol; 2008 Apr; 294(4):L665-75. PubMed ID: 18263670
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects.
Keitges EA; Pasion R; Burnside RD; Mason C; Gonzalez-Ruiz A; Dunn T; Masiello M; Gebbia JA; Fernandez CO; Risheg H
Am J Med Genet A; 2013 Jul; 161A(7):1755-8. PubMed ID: 23696316
[TBL] [Abstract][Full Text] [Related]
8. Identification of the human ortholog of the t-complex-encoded protein TCTE3 and evaluation as a candidate gene for primary ciliary dyskinesia.
Neesen J; Drenckhahn JD; Tiede S; Burfeind P; Grzmil M; Konietzko J; Dixkens C; Kreutzberger J; Laccone F; Omran H
Cytogenet Genome Res; 2002; 98(1):38-44. PubMed ID: 12584439
[TBL] [Abstract][Full Text] [Related]
9. Genome-wide oligonucleotide-based array comparative genome hybridization analysis of non-isolated congenital diaphragmatic hernia.
Scott DA; Klaassens M; Holder AM; Lally KP; Fernandes CJ; Galjaard RJ; Tibboel D; de Klein A; Lee B
Hum Mol Genet; 2007 Feb; 16(4):424-30. PubMed ID: 17210672
[TBL] [Abstract][Full Text] [Related]
10. The etiology of congenital diaphragmatic hernia: still largely unknown?
Klaassens M; de Klein A; Tibboel D
Eur J Med Genet; 2009; 52(5):281-6. PubMed ID: 19464395
[TBL] [Abstract][Full Text] [Related]
11. Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization.
Klaassens M; van Dooren M; Eussen HJ; Douben H; den Dekker AT; Lee C; Donahoe PK; Galjaard RJ; Goemaere N; de Krijger RR; Wouters C; Wauters J; Oostra BA; Tibboel D; de Klein A
Am J Hum Genet; 2005 May; 76(5):877-82. PubMed ID: 15750894
[TBL] [Abstract][Full Text] [Related]
12. Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: two patients and review of the literature.
Klaassens M; Galjaard RJ; Scott DA; Brüggenwirth HT; van Opstal D; Fox MV; Higgins RR; Cohen-Overbeek TE; Schoonderwaldt EM; Lee B; Tibboel D; de Klein A
Am J Med Genet A; 2007 Sep; 143A(18):2204-12. PubMed ID: 17702015
[TBL] [Abstract][Full Text] [Related]
13. Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2.
Slavotinek AM; Moshrefi A; Davis R; Leeth E; Schaeffer GB; Burchard GE; Shaw GM; James B; Ptacek L; Pennacchio LA
Eur J Hum Genet; 2006 Sep; 14(9):999-1008. PubMed ID: 16736036
[TBL] [Abstract][Full Text] [Related]
14. Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts.
Veenma D; Brosens E; de Jong E; van de Ven C; Meeussen C; Cohen-Overbeek T; Boter M; Eussen H; Douben H; Tibboel D; de Klein A
Eur J Hum Genet; 2012 Mar; 20(3):298-304. PubMed ID: 22071887
[TBL] [Abstract][Full Text] [Related]
15. Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1.
Wat MJ; Beck TF; Hernández-García A; Yu Z; Veenma D; Garcia M; Holder AM; Wat JJ; Chen Y; Mohila CA; Lally KP; Dickinson M; Tibboel D; de Klein A; Lee B; Scott DA
Hum Mol Genet; 2012 Sep; 21(18):4115-25. PubMed ID: 22723016
[TBL] [Abstract][Full Text] [Related]
16. Congenital diaphragmatic hernia in Smith-Magenis syndrome: a possible locus at chromosome 17p11.2.
Sanford EF; Bermudez-Wagner K; Jeng LJ; Rauen KA; Slavotinek AM
Am J Med Genet A; 2011 Nov; 155A(11):2816-20. PubMed ID: 21965155
[TBL] [Abstract][Full Text] [Related]
17. Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia.
Yu L; Wynn J; Cheung YH; Shen Y; Mychaliska GB; Crombleholme TM; Azarow KS; Lim FY; Chung DH; Potoka D; Warner BW; Bucher B; Stolar C; Aspelund G; Arkovitz MS; Chung WK
Hum Genet; 2013 Mar; 132(3):285-92. PubMed ID: 23138528
[TBL] [Abstract][Full Text] [Related]
18. Examination of FGFRL1 as a candidate gene for diaphragmatic defects at chromosome 4p16.3 shows that Fgfrl1 null mice have reduced expression of Tpm3, sarcomere genes and Lrtm1 in the diaphragm.
LopezJimenez N; Gerber S; Popovici V; Mirza S; Copren K; Ta L; Shaw GM; Trueb B; Slavotinek AM
Hum Genet; 2010 Mar; 127(3):325-36. PubMed ID: 20024584
[TBL] [Abstract][Full Text] [Related]
19. Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks.
Longoni M; Lage K; Russell MK; Loscertales M; Abdul-Rahman OA; Baynam G; Bleyl SB; Brady PD; Breckpot J; Chen CP; Devriendt K; Gillessen-Kaesbach G; Grix AW; Rope AF; Shimokawa O; Strauss B; Wieczorek D; Zackai EH; Coletti CM; Maalouf FI; Noonan KM; Park JH; Tracy AA; Lee C; Donahoe PK; Pober BR
Am J Med Genet A; 2012 Dec; 158A(12):3148-58. PubMed ID: 23165946
[TBL] [Abstract][Full Text] [Related]
20. Identification of dosage-sensitive genes in fetuses referred with severe isolated congenital diaphragmatic hernia.
Brady PD; DeKoninck P; Fryns JP; Devriendt K; Deprest JA; Vermeesch JR
Prenat Diagn; 2013 Dec; 33(13):1283-92. PubMed ID: 24122781
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
