284 related articles for article (PubMed ID: 25558953)
1. 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]
2. 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]
3. 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]
4. Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome.
Ross JL; Roeltgen DP; Kushner H; Zinn AR; Reiss A; Bardsley MZ; McCauley E; Tartaglia N
Pediatrics; 2012 Apr; 129(4):769-78. PubMed ID: 22412026
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Autism Spectrum Disorder in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, and XXYY.
Tartaglia NR; Wilson R; Miller JS; Rafalko J; Cordeiro L; Davis S; Hessl D; Ross J
J Dev Behav Pediatr; 2017 Apr; 38(3):197-207. PubMed ID: 28333849
[TBL] [Abstract][Full Text] [Related]
8. Overlap Between Autism Spectrum Disorders and Attention Deficit Hyperactivity Disorder: Searching for Distinctive/Common Clinical Features.
Craig F; Lamanna AL; Margari F; Matera E; Simone M; Margari L
Autism Res; 2015 Jun; 8(3):328-37. PubMed ID: 25604000
[TBL] [Abstract][Full Text] [Related]
9. Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation.
Farzin F; Perry H; Hessl D; Loesch D; Cohen J; Bacalman S; Gane L; Tassone F; Hagerman P; Hagerman R
J Dev Behav Pediatr; 2006 Apr; 27(2 Suppl):S137-44. PubMed ID: 16685180
[TBL] [Abstract][Full Text] [Related]
10. Social deficits in male children and adolescents with sex chromosome aneuploidy: a comparison of XXY, XYY, and XXYY syndromes.
Cordeiro L; Tartaglia N; Roeltgen D; Ross J
Res Dev Disabil; 2012; 33(4):1254-63. PubMed ID: 22502852
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The behavioral profile of children aged 1-5 years with sex chromosome trisomy (47,XXX, 47,XXY, 47,XYY).
Urbanus E; Swaab H; Tartaglia N; Cordeiro L; van Rijn S
Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):444-455. PubMed ID: 32432413
[TBL] [Abstract][Full Text] [Related]
13. The XYY syndrome: a follow-up study on 38 boys.
Geerts M; Steyaert J; Fryns JP
Genet Couns; 2003; 14(3):267-79. PubMed ID: 14577671
[TBL] [Abstract][Full Text] [Related]
14. X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits.
Kent L; Emerton J; Bhadravathi V; Weisblatt E; Pasco G; Willatt LR; McMahon R; Yates JR
J Med Genet; 2008 Aug; 45(8):519-24. PubMed ID: 18413370
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Gonosomal trisomy syndrome. Five case reports and review of literature].
Schwemmle C; Jungheim M; Ptok M
Laryngorhinootologie; 2013 Nov; 92(11):725-31. PubMed ID: 23929211
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. [Genetic analysis of a child with XYY syndrome mainly featuring mental retardation].
Liu Y; Dong R; Zhang K; Wang Y; Zhang H; Zhang Y; Zhao D; Gai Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):686-9. PubMed ID: 27577224
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]