223 related articles for article (PubMed ID: 23517654)
1. Association of brain-derived neurotrophic factor (BDNF) haploinsufficiency with lower adaptive behaviour and reduced cognitive functioning in WAGR/11p13 deletion syndrome.
Han JC; Thurm A; Golden Williams C; Joseph LA; Zein WM; Brooks BP; Butman JA; Brady SM; Fuhr SR; Hicks MD; Huey AE; Hanish AE; Danley KM; Raygada MJ; Rennert OM; Martinowich K; Sharp SJ; Tsao JW; Swedo SE
Cortex; 2013; 49(10):2700-10. PubMed ID: 23517654
[TBL] [Abstract][Full Text] [Related]
2. Brain-derived neurotrophic factor and obesity in the WAGR syndrome.
Han JC; Liu QR; Jones M; Levinn RL; Menzie CM; Jefferson-George KS; Adler-Wailes DC; Sanford EL; Lacbawan FL; Uhl GR; Rennert OM; Yanovski JA
N Engl J Med; 2008 Aug; 359(9):918-27. PubMed ID: 18753648
[TBL] [Abstract][Full Text] [Related]
3. Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.
Xu S; Han JC; Morales A; Menzie CM; Williams K; Fan YS
Cytogenet Genome Res; 2008; 122(2):181-7. PubMed ID: 19096215
[TBL] [Abstract][Full Text] [Related]
4. Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including PAX6, WT1, and PRRG4.
Yamamoto T; Togawa M; Shimada S; Sangu N; Shimojima K; Okamoto N
Am J Med Genet A; 2014 Mar; 164A(3):634-8. PubMed ID: 24357251
[TBL] [Abstract][Full Text] [Related]
5. Aniridia as part of a WAGR syndrome in a girl whose brother presented hypospadias.
Lorda-Sanchez I; Sanz R; Diaz-Guillen MA; Fernandez-Toral J; Heine-Suñer D; Rodriguez De Alba M; Gonzalez-Gonzalez C; Trujillo MJ; Ramos C; Rodriguez De Cordoba S; Ayuso C
Genet Couns; 2002; 13(2):171-7. PubMed ID: 12150218
[TBL] [Abstract][Full Text] [Related]
6. The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome.
Rodríguez-López R; Pérez JM; Balsera AM; Rodríguez GG; Moreno TH; García de Cáceres M; Serrano MG; Freijo FC; Ruiz JR; Angueira FB; Pérez PM; Estévez MN; Gómez EG
Gene; 2013 Mar; 516(2):285-90. PubMed ID: 23266638
[TBL] [Abstract][Full Text] [Related]
7. Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGH.
Blanco-Kelly F; Palomares M; Vallespín E; Villaverde C; Martín-Arenas R; Vélez-Monsalve C; Lorda-Sánchez I; Nevado J; Trujillo-Tiebas MJ; Lapunzina P; Ayuso C; Corton M
PLoS One; 2017; 12(2):e0172363. PubMed ID: 28231309
[TBL] [Abstract][Full Text] [Related]
8. A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.
Crolla JA; Cawdery JE; Oley CA; Young ID; Gray J; Fantes J; van Heyningen V
J Med Genet; 1997 Mar; 34(3):207-12. PubMed ID: 9132491
[TBL] [Abstract][Full Text] [Related]
9. Sustained endocrine profiles of a girl with WAGR syndrome.
Takada Y; Sakai Y; Matsushita Y; Ohkubo K; Koga Y; Akamine S; Torio M; Ishizaki Y; Sanefuji M; Torisu H; Shaw CA; Kagami M; Hara T; Ohga S
BMC Med Genet; 2017 Oct; 18(1):117. PubMed ID: 29061165
[TBL] [Abstract][Full Text] [Related]
10. A 1.7-Mb YAC contig around the human BDNF gene (11p13): integration of the physical, genetic, and cytogenetic maps in relation to WAGR syndrome.
Rosier MF; Goguel AF; Martin A; Le Paslier D; Couillin P; Houlgatte R; Bernheim A; Auffray C; Devignes MD
Genomics; 1994 Nov; 24(1):69-77. PubMed ID: 7896291
[TBL] [Abstract][Full Text] [Related]
11. Congenital diaphragmatic hernia in WAGR syndrome.
Scott DA; Cooper ML; Stankiewicz P; Patel A; Potocki L; Cheung SW
Am J Med Genet A; 2005 May; 134(4):430-3. PubMed ID: 15779010
[TBL] [Abstract][Full Text] [Related]
12. Haploinsufficiency of the brain-derived neurotrophic factor gene is associated with reduced pain sensitivity.
Sapio MR; Iadarola MJ; LaPaglia DM; Lehky T; Thurm AE; Danley KM; Fuhr SR; Lee MD; Huey AE; Sharp SJ; Tsao JW; Yanovski JA; Mannes AJ; Han JC
Pain; 2019 May; 160(5):1070-1081. PubMed ID: 30855519
[TBL] [Abstract][Full Text] [Related]
13. WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH.
Lennon PA; Scott DA; Lonsdorf D; Wargowski DS; Kirkpatrick S; Patel A; Cheung SW
Am J Med Genet A; 2006 Jun; 140(11):1214-8. PubMed ID: 16646034
[TBL] [Abstract][Full Text] [Related]
14. LMO2 gene deletions significantly worsen the prognosis of Wilms' tumor development in patients with WAGR syndrome.
Marakhonov AV; Vasilyeva TA; Voskresenskaya AA; Sukhanova NV; Kadyshev VV; Kutsev SI; Zinchenko RA
Hum Mol Genet; 2019 Oct; 28(19):3323-3326. PubMed ID: 31304537
[TBL] [Abstract][Full Text] [Related]
15. WAGRO syndrome: a rare genetic condition associated with aniridia and additional ophthalmologic abnormalities.
Ferreira MAT; Almeida Júnior IG; Kuratani DK; Rosa RFM; Gonzales JFO; Telles LEB; Ferrão YA; Zen PRG
Arq Bras Oftalmol; 2019 May; 82(4):336-338. PubMed ID: 31116317
[TBL] [Abstract][Full Text] [Related]
16. [WAGR syndrome by heterozygous deletion of the WT1 gene. Pediatric case report].
Galvis-Blanco SJ; Arias-Flórez JS; Contreras-García GA
Arch Argent Pediatr; 2019 Oct; 117(5):e505-e508. PubMed ID: 31560501
[TBL] [Abstract][Full Text] [Related]
17. Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twins.
Brémond-Gignac D; Gérard-Blanluet M; Copin H; Bitoun P; Baumann C; Crolla JA; Benzacken B; Verloes A
Am J Med Genet A; 2005 May; 134(4):422-5. PubMed ID: 15779023
[TBL] [Abstract][Full Text] [Related]
18. Unusual Presentation in WAGR Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Diseases.
Wang Q; Zhang X; Qin T; Wang D; Lin X; Zhu Y; Tan H; Zhao L; Li J; Lin Z; Lin H; Chen W
Genes (Basel); 2022 Aug; 13(8):. PubMed ID: 36011342
[TBL] [Abstract][Full Text] [Related]
19. WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion.
Huynh MT; Boudry-Labis E; Duban B; Andrieux J; Tran CT; Tampere H; Ceraso D; Manouvrier S; Tachdjian G; Roche-Lestienne C; Vincent-Delorme C
Am J Med Genet A; 2017 Jun; 173(6):1690-1693. PubMed ID: 28398607
[TBL] [Abstract][Full Text] [Related]
20. Combination of WAGR and Potocki-Shaffer contiguous deletion syndromes in a patient with an 11p11.2-p14 deletion.
Brémond-Gignac D; Crolla JA; Copin H; Guichet A; Bonneau D; Taine L; Lacombe D; Baumann C; Benzacken B; Verloes A
Eur J Hum Genet; 2005 Apr; 13(4):409-13. PubMed ID: 15702131
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
