184 related articles for article (PubMed ID: 24308542)
1. Brain morphology in children with 47, XYY syndrome: a voxel- and surface-based morphometric study.
Lepage JF; Hong DS; Raman M; Marzelli M; Roeltgen DP; Lai S; Ross J; Reiss AL
Genes Brain Behav; 2014 Feb; 13(2):127-34. PubMed ID: 24308542
[TBL] [Abstract][Full Text] [Related]
2. Sex chromosomes and the brain: a study of neuroanatomy in XYY syndrome.
Bryant DM; Hoeft F; Lai S; Lackey J; Roeltgen D; Ross J; Reiss AL
Dev Med Child Neurol; 2012 Dec; 54(12):1149-56. PubMed ID: 23057627
[TBL] [Abstract][Full Text] [Related]
3. Characterization of autism spectrum disorder and neurodevelopmental profiles in youth with XYY syndrome.
Joseph L; Farmer C; Chlebowski C; Henry L; Fish A; Mankiw C; Xenophontos A; Clasen L; Sauls B; Seidlitz J; Blumenthal J; Torres E; Thurm A; Raznahan A
J Neurodev Disord; 2018 Oct; 10(1):30. PubMed ID: 30348076
[TBL] [Abstract][Full Text] [Related]
4. Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features.
Ross JL; Tartaglia N; Merry DE; Dalva M; Zinn AR
Genes Brain Behav; 2015 Feb; 14(2):137-44. PubMed ID: 25558953
[TBL] [Abstract][Full Text] [Related]
5. Testicular function in boys with 47,XYY and relationship to phenotype.
Davis SM; Bloy L; Roberts TPL; Kowal K; Alston A; Tahsin A; Truxon A; Ross JL
Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):371-385. PubMed ID: 32544298
[TBL] [Abstract][Full Text] [Related]
6. Posterior fossa malformations and sex chromosomes anomalies. Report of a case with XYY syndrome and overview of known associations.
Ulgiati F; Nicita F; Papetti L; Ursitti F; Di Maggio A; Tarani L; Spalice A
Eur J Pediatr; 2013 Sep; 172(9):1267-70. PubMed ID: 23695861
[TBL] [Abstract][Full Text] [Related]
7. Abnormal Auditory Mismatch Fields in Children and Adolescents with 47,XYY Syndrome.
Matsuzaki J; Bloy L; Blaskey L; Miller J; Kuschner ES; Ku M; Dipiero M; Airey M; Edgar JC; Embick D; Ross JL; Roberts TPL
Dev Neurosci; 2019; 41(1-2):123-131. PubMed ID: 31280271
[TBL] [Abstract][Full Text] [Related]
8. Cognitive Profile, Emotional-Behavioral Features, and Parental Stress in Boys With 47,XYY Syndrome.
Operto FF; Pastorino GMG; Amadori E; Mazza R; Bernardo P; Campanozzi S; Margari L; Coppola G
Cogn Behav Neurol; 2019 Jun; 32(2):87-94. PubMed ID: 31205122
[TBL] [Abstract][Full Text] [Related]
9. Decreased levels of γ-aminobutyric acid in temporal lobe of children with 47,XYY syndrome.
Roberts TPL; Bloy L; Miller JS; Blaskey L; Ross J
Neuroreport; 2021 May; 32(7):541-547. PubMed ID: 33850088
[TBL] [Abstract][Full Text] [Related]
10. Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior.
Lalatta F; Folliero E; Cavallari U; Di Segni M; Gentilin B; Fogliani R; Quagliarini D; Vizziello P; Monti F; Gargantini L
Ital J Pediatr; 2012 Oct; 38():52. PubMed ID: 23034220
[TBL] [Abstract][Full Text] [Related]
11. 47,XYY syndrome: clinical phenotype and timing of ascertainment.
Bardsley MZ; Kowal K; Levy C; Gosek A; Ayari N; Tartaglia N; Lahlou N; Winder B; Grimes S; Ross JL
J Pediatr; 2013 Oct; 163(4):1085-94. PubMed ID: 23810129
[TBL] [Abstract][Full Text] [Related]
12. Oral, physical, and behavioral aspects of patient with chromosome 47, XYY syndrome.
Scheidt L; Sanabe ME; Diniz MB
J Indian Soc Pedod Prev Dent; 2015; 33(4):347-50. PubMed ID: 26381641
[TBL] [Abstract][Full Text] [Related]
13. A patient with 46,XY/47,XYY karyotype and female phenotype: a case report.
Liu ZH; Zhou SC; Du JW; Zhang K; Wu T
BMC Endocr Disord; 2020 Mar; 20(1):42. PubMed ID: 32209072
[TBL] [Abstract][Full Text] [Related]
14. Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression.
Ross JL; Bloy L; Roberts TPL; Miller J; Xing C; Silverman LA; Zinn AR
Am J Med Genet B Neuropsychiatr Genet; 2019 Oct; 180(7):471-482. PubMed ID: 31161682
[TBL] [Abstract][Full Text] [Related]
15. Auditory evoked response delays in children with 47,XYY syndrome.
Bloy L; Ku M; Edgar JC; Miller JS; Blaskey L; Ross J; Roberts TPL
Neuroreport; 2019 May; 30(7):504-509. PubMed ID: 30896674
[TBL] [Abstract][Full Text] [Related]
16. White and Gray Matter Volume Changes and Correlation with Visual Evoked Potential in Patients with Optic Neuritis: A Voxel-Based Morphometry Study.
Huang X; Zhang Q; Hu PH; Zhong YL; Zhang Y; Wei R; Xu TT; Shao Y;
Med Sci Monit; 2016 Apr; 22():1115-23. PubMed ID: 27045330
[TBL] [Abstract][Full Text] [Related]
17. Modeling familial predictors of proband outcomes in neurogenetic disorders: initial application in XYY syndrome.
Wilson KE; Fish AM; Mankiw C; Xenophontos A; Warling A; Whitman E; Clasen L; Torres E; Blumenthal J; Raznahan A
J Neurodev Disord; 2021 Mar; 13(1):12. PubMed ID: 33752588
[TBL] [Abstract][Full Text] [Related]
18. Autism spectrum disorders in XYY syndrome: two new cases and systematic review of the literature.
Margari L; Lamanna AL; Craig F; Simone M; Gentile M
Eur J Pediatr; 2014 Mar; 173(3):277-83. PubMed ID: 24464091
[TBL] [Abstract][Full Text] [Related]
19. 47,XYY karyotypes and pervasive developmental disorders.
Nicolson R; Bhalerao S; Sloman L
Can J Psychiatry; 1998 Aug; 43(6):619-22. PubMed ID: 9729690
[TBL] [Abstract][Full Text] [Related]
20. Childhood acne in a boy with XYY syndrome.
Kasparis C; Loffeld A
BMJ Case Rep; 2014 Jan; 2014():. PubMed ID: 24395875
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
