213 related articles for article (PubMed ID: 29025761)
1. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the
Guo T; Repetto GM; McDonald McGinn DM; Chung JH; Nomaru H; Campbell CL; Blonska A; Bassett AS; Chow EWC; Mlynarski EE; Swillen A; Vermeesch J; Devriendt K; Gothelf D; Carmel M; Michaelovsky E; Schneider M; Eliez S; Antonarakis SE; Coleman K; Tomita-Mitchell A; Mitchell ME; Digilio MC; Dallapiccola B; Marino B; Philip N; Busa T; Kushan-Wells L; Bearden CE; Piotrowicz M; Hawuła W; Roberts AE; Tassone F; Simon TJ; van Duin EDA; van Amelsvoort TA; Kates WR; Zackai E; Johnston HR; Cutler DJ; Agopian AJ; Goldmuntz E; Mitchell LE; Wang T; Emanuel BS; Morrow BE;
Circ Cardiovasc Genet; 2017 Oct; 10(5):e001690. PubMed ID: 29025761
[TBL] [Abstract][Full Text] [Related]
2. 22q11.2 deletion syndrome is associated with increased mortality in adults with tetralogy of Fallot and pulmonary atresia with ventricular septal defect.
Kauw D; Woudstra OI; van Engelen K; Meijboom FJ; Mulder BJM; Schuuring MJ; Bouma BJ
Int J Cardiol; 2020 May; 306():56-60. PubMed ID: 32145937
[TBL] [Abstract][Full Text] [Related]
3. 22q11.2 Deletion syndrome is associated with perioperative outcome in tetralogy of Fallot.
Mercer-Rosa L; Pinto N; Yang W; Tanel R; Goldmuntz E
J Thorac Cardiovasc Surg; 2013 Oct; 146(4):868-73. PubMed ID: 23312975
[TBL] [Abstract][Full Text] [Related]
4. Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
Zhao Y; Diacou A; Johnston HR; Musfee FI; McDonald-McGinn DM; McGinn D; Crowley TB; Repetto GM; Swillen A; Breckpot J; Vermeesch JR; Kates WR; Digilio MC; Unolt M; Marino B; Pontillo M; Armando M; Di Fabio F; Vicari S; van den Bree M; Moss H; Owen MJ; Murphy KC; Murphy CM; Murphy D; Schoch K; Shashi V; Tassone F; Simon TJ; Shprintzen RJ; Campbell L; Philip N; Heine-Suñer D; García-Miñaúr S; Fernández L; ; Bearden CE; Vingerhoets C; van Amelsvoort T; Eliez S; Schneider M; Vorstman JAS; Gothelf D; Zackai E; Agopian AJ; Gur RE; Bassett AS; Emanuel BS; Goldmuntz E; Mitchell LE; Wang T; Morrow BE
Am J Hum Genet; 2020 Jan; 106(1):26-40. PubMed ID: 31870554
[TBL] [Abstract][Full Text] [Related]
5. 22q11.2 deletion detected by
Ramírez-Velazco A; Rivera H; Vásquez-Velázquez AI; Aguayo-Orozco TA; Delgadillo-Pérez S; Domínguez MG
Colomb Med (Cali); 2018 Sep; 49(3):219-222. PubMed ID: 30410196
[TBL] [Abstract][Full Text] [Related]
6. 22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia.
van Engelen K; Topf A; Keavney BD; Goodship JA; van der Velde ET; Baars MJ; Snijder S; Moorman AF; Postma AV; Mulder BJ
Heart; 2010 Apr; 96(8):621-4. PubMed ID: 20357389
[TBL] [Abstract][Full Text] [Related]
7. 22q11.2 Deletion Status Influences Resource Utilization in Infants Requiring Repair of Tetralogy of Fallot and Common Arterial Trunk.
Ghimire LV; Devoe C; Moon-Grady AJ
Pediatr Cardiol; 2020 Jun; 41(5):918-924. PubMed ID: 32112115
[TBL] [Abstract][Full Text] [Related]
8. Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.
Silversides CK; Lionel AC; Costain G; Merico D; Migita O; Liu B; Yuen T; Rickaby J; Thiruvahindrapuram B; Marshall CR; Scherer SW; Bassett AS
PLoS Genet; 2012; 8(8):e1002843. PubMed ID: 22912587
[TBL] [Abstract][Full Text] [Related]
9. The role of 22q11.2 deletion syndrome in the relationship between congenital heart disease and scoliosis.
Homans JF; de Reuver S; Heung T; Silversides CK; Oechslin EN; Houben ML; McDonald-McGinn DM; Kruyt MC; Castelein RM; Bassett AS
Spine J; 2020 Jun; 20(6):956-963. PubMed ID: 31958577
[TBL] [Abstract][Full Text] [Related]
10. Atypical microdeletion 22q11.2 in a patient with tetralogy of Fallot.
Carli D; Moroni A; Eleonora DG; Zonta A; Montin D; Licciardi F; Aidala E; Bordese R; Carlo PN; Brusco A; Giovanni Battista F; Mussa A
J Genet; 2021; 100():. PubMed ID: 33707356
[TBL] [Abstract][Full Text] [Related]
11. 22q11.2 Deletion Syndrome in Taiwan: Clinical Presentation and Immune System Status of Patients.
Lee CL; Lin SM; Chen MR; Chuang CK; Chiu HC; Tu YR; Lo YT; Chang YH; Lin HY; Lin SP
Int J Med Sci; 2023; 20(11):1377-1385. PubMed ID: 37790845
[No Abstract] [Full Text] [Related]
12. Impact of a 22q11.2 Microdeletion on Adult All-Cause Mortality in Tetralogy of Fallot Patients.
van Mil S; Heung T; Malecki S; Van L; Chang J; Breetvelt E; Wald R; Oechslin E; Silversides C; Bassett AS
Can J Cardiol; 2020 Jul; 36(7):1091-1097. PubMed ID: 32348848
[TBL] [Abstract][Full Text] [Related]
13. JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot.
Digilio MC; Luca AD; Lepri F; Guida V; Ferese R; Dentici ML; Angioni A; Marino B; Dallapiccola B
Am J Med Genet A; 2013 Dec; 161A(12):3133-6. PubMed ID: 23956173
[TBL] [Abstract][Full Text] [Related]
14. Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
Cordell HJ; Töpf A; Mamasoula C; Postma AV; Bentham J; Zelenika D; Heath S; Blue G; Cosgrove C; Granados Riveron J; Darlay R; Soemedi R; Wilson IJ; Ayers KL; Rahman TJ; Hall D; Mulder BJ; Zwinderman AH; van Engelen K; Brook JD; Setchfield K; Bu'Lock FA; Thornborough C; O'Sullivan J; Stuart AG; Parsons J; Bhattacharya S; Winlaw D; Mital S; Gewillig M; Breckpot J; Devriendt K; Moorman AF; Rauch A; Lathrop GM; Keavney BD; Goodship JA
Hum Mol Genet; 2013 Apr; 22(7):1473-81. PubMed ID: 23297363
[TBL] [Abstract][Full Text] [Related]
15. Whole-Genome Sequencing and Integrative Genomic Analysis Approach on Two 22q11.2 Deletion Syndrome Family Trios for Genotype to Phenotype Correlations.
Chung JH; Cai J; Suskin BG; Zhang Z; Coleman K; Morrow BE
Hum Mutat; 2015 Aug; 36(8):797-807. PubMed ID: 25981510
[TBL] [Abstract][Full Text] [Related]
16. Familial 22q11.2 deletion: an infant with interrupted aortic arch and DiGeorge syndrome delivered from by a mother with tetralogy of Fallot.
Ito T; Okubo T; Sato H
Eur J Pediatr; 2002 Mar; 161(3):173-4. PubMed ID: 11998920
[TBL] [Abstract][Full Text] [Related]
17. Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome.
Goldmuntz E; Driscoll DA; Emanuel BS; McDonald-McGinn D; Mei M; Zackai E; Mitchell LE
Birth Defects Res A Clin Mol Teratol; 2009 Feb; 85(2):125-9. PubMed ID: 18770859
[TBL] [Abstract][Full Text] [Related]
18. Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.
Xu YJ; Wang J; Xu R; Zhao PJ; Wang XK; Sun HJ; Bao LM; Shen J; Fu QH; Li F; Sun K
BMC Med Genet; 2011 Dec; 12():169. PubMed ID: 22185286
[TBL] [Abstract][Full Text] [Related]
19. Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients.
León LE; Benavides F; Espinoza K; Vial C; Alvarez P; Palomares M; Lay-Son G; Miranda M; Repetto GM
Sci Rep; 2017 May; 7(1):1795. PubMed ID: 28496102
[TBL] [Abstract][Full Text] [Related]
20. Molecular screening for 22Q11.2 deletion syndrome in patients with congenital heart disease.
Huber J; Peres VC; de Castro AL; dos Santos TJ; da Fontoura Beltrão L; de Baumont AC; Cossio SL; Dalberto TP; Riegel M; Cañedo AD; Schaan BD; Pellanda LC
Pediatr Cardiol; 2014 Dec; 35(8):1356-62. PubMed ID: 24880467
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
