130 related articles for article (PubMed ID: 38310401)
1. Young adults with a 22q11.2 microdeletion and the cost of aging with complexity in a population-based context.
Malecki SL; Heung T; Wodchis WP; Saskin R; Palma L; Verma AA; Bassett AS
Genet Med; 2024 May; 26(5):101088. PubMed ID: 38310401
[TBL] [Abstract][Full Text] [Related]
2. A genetic model for multimorbidity in young adults.
Malecki SL; Van Mil S; Graffi J; Breetvelt E; Corral M; Boot E; Chow EWC; Sanches M; Verma AA; Bassett AS
Genet Med; 2020 Jan; 22(1):132-141. PubMed ID: 31363180
[TBL] [Abstract][Full Text] [Related]
3. All-cause mortality and survival in adults with 22q11.2 deletion syndrome.
Van L; Heung T; Graffi J; Ng E; Malecki S; Van Mil S; Boot E; Corral M; Chow EWC; Hodgkinson KA; Silversides C; Bassett AS
Genet Med; 2019 Oct; 21(10):2328-2335. PubMed ID: 30948858
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Differences in speech and language abilities between children with 22q11.2 deletion syndrome and children with phenotypic features of 22q11.2 deletion syndrome but without microdeletion.
Rakonjac M; Cuturilo G; Stevanovic M; Jelicic L; Subotic M; Jovanovic I; Drakulic D
Res Dev Disabil; 2016 Aug; 55():322-9. PubMed ID: 27235769
[TBL] [Abstract][Full Text] [Related]
6. The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon.
Wonkam A; Toko R; Chelo D; Tekendo-Ngongang C; Kingue S; Dahoun S
Glob Heart; 2017 Jun; 12(2):115-120. PubMed ID: 28302550
[TBL] [Abstract][Full Text] [Related]
7. Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study.
Hoeffding LK; Trabjerg BB; Olsen L; Mazin W; Sparsø T; Vangkilde A; Mortensen PB; Pedersen CB; Werge T
JAMA Psychiatry; 2017 Mar; 74(3):282-290. PubMed ID: 28114601
[TBL] [Abstract][Full Text] [Related]
8. Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study.
Olsen L; Sparsø T; Weinsheimer SM; Dos Santos MBQ; Mazin W; Rosengren A; Sanchez XC; Hoeffding LK; Schmock H; Baekvad-Hansen M; Bybjerg-Grauholm J; Daly MJ; Neale BM; Pedersen MG; Agerbo E; Mors O; Børglum A; Nordentoft M; Hougaard DM; Mortensen PB; Geschwind DH; Pedersen C; Thompson WK; Werge T
Lancet Psychiatry; 2018 Jul; 5(7):573-580. PubMed ID: 29886042
[TBL] [Abstract][Full Text] [Related]
9. Consequences of 22q11.2 Microdeletion on the Genome, Individual and Population Levels.
Karbarz M
Genes (Basel); 2020 Aug; 11(9):. PubMed ID: 32842603
[TBL] [Abstract][Full Text] [Related]
10. Pediatric healthcare costs for patients with 22q11.2 deletion syndrome.
Benn P; Iyengar S; Crowley TB; Zackai EH; Burrows EK; Moshkevich S; McDonald-McGinn DM; Sullivan KE; Demko Z
Mol Genet Genomic Med; 2017 Nov; 5(6):631-638. PubMed ID: 29178641
[TBL] [Abstract][Full Text] [Related]
11. Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.
Brunet A; Gabau E; Perich RM; Valdesoiro L; Brun C; Caballín MR; Guitart M
Am J Med Genet A; 2006 Nov; 140(22):2426-32. PubMed ID: 17041934
[TBL] [Abstract][Full Text] [Related]
12. [Study on clinical features and fluorescence in situ hybridization detections of 22q11 microdeletion syndrome].
Qin YF; Yang JB; Xie CH; Shao J; Zhao ZY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):284-7. PubMed ID: 17557238
[TBL] [Abstract][Full Text] [Related]
13. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
Muñoz S; Garay F; Flores I; Heusser F; Talesnik E; Aracena M; Mellado C; Méndez C; Arnaiz P; Repetto G
Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533
[TBL] [Abstract][Full Text] [Related]
14. Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.
Bassett AS; Marshall CR; Lionel AC; Chow EW; Scherer SW
Hum Mol Genet; 2008 Dec; 17(24):4045-53. PubMed ID: 18806272
[TBL] [Abstract][Full Text] [Related]
15. [Microdeletion of 22q11, DiGeorge and velocardiofacial syndrome].
Hjalgrim H; Hahnemann JM; Timshel S; Brøndum-Nielsen K
Ugeskr Laeger; 2000 Jul; 162(31):4169-70. PubMed ID: 10962926
[No Abstract] [Full Text] [Related]
16. [Prenatal diagnosis of 22q11 microdeletion syndrome].
Cai M; Huang H; Lin N; Guo N; Wu X; Su L; Xu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):192-195. PubMed ID: 28397216
[TBL] [Abstract][Full Text] [Related]
17. Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architecture.
Tuţulan-Cuniţă AC; Budişteanu M; Papuc SM; Dupont JM; Blancho D; Lebbar A; Viot G; Lungeanu A; Arghir A
Psychiatry Res; 2012 May; 197(3):356-7. PubMed ID: 22365273
[TBL] [Abstract][Full Text] [Related]
18. [Diagnosis of 22q11.2 deletion syndrome in the context of newly developed psychosis].
Kaltenboeck A; Friedrich F; Hinterbuchinger B; Litvan Z; Mossaheb N
Neuropsychiatr; 2016 Dec; 30(4):223-226. PubMed ID: 27822729
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy.
Wither RG; Borlot F; MacDonald A; Butcher NJ; Chow EWC; Bassett AS; Andrade DM
Epilepsia; 2017 Jun; 58(6):1095-1101. PubMed ID: 28448680
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
