(Q33518807)

27 July 2017

1 reference

title

Effects of sex chromosome aneuploidies on brain development: evidence from neuroimaging studies (English)

1 reference

27 July 2017

0 references

Nancy Raitano Lee

2

0 references

Jay N. Giedd

series ordinal

3

object named as

Jay N Giedd

1 reference

27 July 2017

Rhoshel K Lenroot

1

1 reference

27 July 2017

publication date

1 January 2009

1 reference

Developmental Disabilities Research Reviews

27 July 2017

published in

1 reference

27 July 2017

volume

15

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27 July 2017

issue

4

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27 July 2017

page(s)

318-327

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Fetal testosterone and autistic traits

27 July 2017

cites work

1 reference

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Brain magnetic resonance imaging findings in 49,XXXXY syndrome

21 June 2018

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A new look at XXYY syndrome: medical and psychological features

21 June 2018

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Effect of ascertainment and genetic features on the phenotype of Klinefelter syndrome.

21 June 2018

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Mapping Early Brain Development in Autism

21 June 2018

1 reference

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Abnormal sex chromosome constitution and longitudinal growth: serum levels of insulin-like growth factor (IGF)-I, IGF binding protein-3, luteinizing hormone, and testosterone in 109 males with 47,XXY, 47,XYY, or sex-determining region of the Y chrom

21 June 2018

1 reference

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High normal testosterone levels in infants with non-mosaic Klinefelter's syndrome

21 June 2018

1 reference

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Establishment of testicular endocrine function impairment during childhood and puberty in boys with Klinefelter syndrome.

21 June 2018

1 reference

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Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY

21 June 2018

1 reference

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Genetic features of the X chromosome affect pubertal development and testicular degeneration in adolescent boys with Klinefelter syndrome

21 June 2018

1 reference

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Cognition and the sex chromosomes: studies in Turner syndrome

21 June 2018

1 reference

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Natural history of seminiferous tubule degeneration in Klinefelter syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

The consequence of errors. From memory molecules to the criminal chromosome, erroneous conclusions continue to blight scientific research

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

X-linked genes and mental functioning

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

X-inactivation profile reveals extensive variability in X-linked gene expression in females

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Klinefelter's syndrome (XXY) as a genetic model for psychotic disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Sex chromosomes and brain gender

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Tall stature, insulin resistance, and disturbed behavior in a girl with the triple X syndrome harboring three SHOX genes: offspring of a father with mosaic Klinefelter syndrome but with two maternal X chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Gender-specific gene expression in post-mortem human brain: localization to sex chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Neurologic aspects of 49,XXXXY syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Automatic "pipeline" analysis of 3-D MRI data for clinical trials: application to multiple sclerosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Tetrasomy Y by structural rearrangement: clinical report

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalities

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Criminality and antisocial behaviour in unselected men with sex chromosome abnormalities

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Long-term outcome in children of sex chromosome abnormalities

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Volumetric magnetic resonance imaging study of the brain in subjects with sex chromosome aneuploidies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

An adult with 49,XYYYY karyotype: case report and endocrine studies.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Neuropsychological impairment in 42 adolescents with sex chromosome abnormalities

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Cancer incidence in men with Klinefelter syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Sex chromosome tetrasomy and pentasomy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Abnormal cerebral cortical convolutions in an XYY fetus.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

The development of four unselected 47,XYY boys.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Cognitive development of unselected girls with complete and partial X monosomy.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

A psychological study of the personalities of XYY- and XXY-men.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Behavioral implications of the human XYY genotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Neurodevelopmental and psychological aspects in a child with 49XYYYY karyotype.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Behavioral development of boys with X chromosome aneuploidy: impact of reactive style on the educational intervention for learning deficits.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

The positive and negative syndrome scale (PANSS) for schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

The Structured Interview for Schizotypy (SIS): a preliminary report

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Cognitive and behavioral factors in the learning disabilities of 47,XXY and 47,XYY boys

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Sex chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Edinburgh study of growth and development of children with sex chromosome abnormalities. IV.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

The SPQ: A Scale for the Assessment of Schizotypal Personality Based on DSM-III-R Criteria

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Hypoplasia of the corpus callosum and growth hormone deficiency in the XXXXY syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

A developmental study of girls with trisomy X

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Growth and development of children with X and Y chromosome aneuploidy: a prospective study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

The Edinburgh study of growth and development in children with sex chromosome abnormalities

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Transcriptome analysis of male-female differences in prefrontal cortical development.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Effects of an extra X chromosome on language lateralization: an fMRI study with Klinefelter men (47,XXY).

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Autism spectrum disorder and Klinefelter syndrome

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

XXY (Klinefelter syndrome): a pediatric quantitative brain magnetic resonance imaging case-control study.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Prevalence, incidence, diagnostic delay, and mortality in Turner syndrome.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

The structural brain correlates of cognitive deficits in adults with Klinefelter's syndrome

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Early androgen deficiency in infants and young boys with 47,XXY Klinefelter syndrome

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

X-linked mental retardation

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Cortical thickness analysis examined through power analysis and a population simulation

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

White matter alterations associated with chromosomal disorders.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Functional neuroimaging provides evidence of anomalous cerebral laterality in adults with Klinefelter's syndrome

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

The XYY syndrome: a follow-up study on 38 boys

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Clinical findings and phenotype in a toddler with 48,XXYY syndrome.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Brain anomalies associated with 47,XYY karyotypes detected on a prenatal scan.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Functional neuroanatomy of visuo-spatial working memory in Turner syndrome

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Psychosocial competence of unselected young adults with sex chromosome abnormalities.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

47,XYY karyotypes and pervasive developmental disorders.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Sexual dimorphism of the developing human brain.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Head circumference and IQ of children with sex chromosome abnormalities

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Verbal deficits in children with 47,XXY and 47,XXX karyotypes: a descriptive and experimental study.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Automated morphometric study of brain variation in XXY males

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2996824

Klinefelter's syndrome (karyotype 47,XXY) and schizophrenia-spectrum pathology

31 October 2018

1 reference

12 December 2020

Summary overview of behavioural development in individuals with neonatally identified X and Y aneuploidy

1 reference

12 December 2020

The influence of sex chromosome aneuploidy on brain asymmetry

1 reference

12 December 2020

Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients

1 reference

12 December 2020

Y chromosomal polysomy: a unique case of 49,XYYYY in amniotic fluid cells

1 reference

12 December 2020

Schizophrenia as the price that Homo sapiens pays for language: a resolution of the central paradox in the origin of the species

1 reference

12 December 2020

Brain morphology in Klinefelter syndrome: extra X chromosome and testosterone supplementation

1 reference

12 December 2020

1 reference

12 December 2020

The Edinburgh study of growth and development of children with sex chromosome abnormalities

1 reference

12 December 2020

'Double male'-a new chromosome constitution in the Klinefelter syndrome

1 reference

12 December 2020

Syndrome Characterized by Gynecomastia, Aspermatogenesis without A-Leydigism, and Increased Excretion of Follicle-Stimulating Hormone1

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FDDRR.86

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1002/DDRR.86

1 reference

27 July 2017

1 reference

27 July 2017

1 reference