The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review*
Open accessAbstract
Aim To review systematically the neurodevelopmental characteristics of individuals with sex chromosome trisomies (SCTs). Method A bibliographic search identified English‐language articles on SCTs. The focus was on studies unbiased by clinical referral, with power of at least 0.69 to detect an effect size of 1.0. Results We identified 35 articles on five neonatally identified samples that had adequate power for our review. An additional 11 studies were included where cases had been identified for reasons other than neurodevelopmental concerns. Individuals with an additional X chromosome had mean IQs that were within broadly normal limits but lower than the respective comparison groups, with verbal IQ most affected. Cognitive outcomes were poorest for females with XXX. Males with XYY had normal‐range IQs, but all three SCT groups (XXX, XXY, and XYY) had marked difficulties in speech and language, motor skills, and educational achievement. Nevertheless, most adults with SCTs lived independently. Less evidence was available for brain structure and for attention, social, and psychiatric outcomes. Within each group there was much variation. Interpretation Individuals with SCTs are at risk of cognitive and behavioural difficulties. However, the evidence base is slender, and further research is needed to ascertain the nature, severity, and causes of these difficulties in unselected samples.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Faul, F., Erdfelder, E., Lang, A.-G., & Buchner, A. (2007) · Behavior Research Methods · doi:10.3758/bf03193146 · Cited by 65,971
Diagnostic and Statistical Manual of Mental Disorders
&NA; (1988) · Alzheimer Disease & Associated Disorders · doi:10.1097/00002093-198802020-00022 · Cited by 12,526
A cytogenetic survey of 14,069 newborn infants: I. Incidence of chromosome abnormalities
Hamerton, J. L., Canning, N., Ray, M., & Smith, S. (1975) · Clinical Genetics · doi:10.1111/j.1399-0004.1975.tb01498.x · Cited by 565
A cytogenetic survey of 11,680 newborn infants
JACOBS, P. A., MELVILLE, M., RATCLIFFE, S., KEAY, A. J., & SYME, J. (1974) · Annals of Human Genetics · doi:10.1111/j.1469-1809.1974.tb01843.x · Cited by 430
Self-citationAggressive Behaviour, Mental Sub-normality and the XYY Male
Jacobs, P. A., BRUNTON, M., Melville, M. M., Brittain, R. P., & MCCLEMONT, W. F. (1965) · Nature · doi:10.1038/2081351a0 · Cited by 429
Self-citationLong term outcome in children of sex chromosome abnormalities
Ratcliffe, S. (1999) · Archives of Disease in Childhood · doi:10.1136/adc.80.2.192 · Cited by 334
Is the prevalence of Klinefelter syndrome increasing?
Morris, J. K., Alberman, E., Scott, C., & Jacobs, P. (2008) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201956 · Cited by 290
Self-citationIncidence of chromosome aberrations among 11 148 newborn children
Nielsen, J., & Sillesen, I. (1975) · Humangenetik · doi:10.1007/bf00273626 · Cited by 253
Witkin, H. A., Mednick, S. A., Schulsinger, F., Bakkestrøm, E., Christiansen, K. O., Goodenough, D. R., Hirschhorn, K., Lundsteen, C., Owen, D. R., Philip, J., et al. (1976) · Science · doi:10.1126/science.959813 · Cited by 240
Edinburgh study of growth and development of children with sex chromosome abnormalities. III.
Ratcliffe, S. G., Tierney, I., Nshaho, J., et al. (1979) · PubMed · Cited by 209
Cited by
An epigenetic framework for neurodevelopmental disorders: From pathogenesis to potential therapy
Millan, M. J. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.11.015 · Cited by 229
Behavioral and Social Phenotypes in Boys With 47,XYY Syndrome or 47,XXY Klinefelter Syndrome
Ross, J. L., Roeltgen, D. P., Kushner, H., Zinn, A. R., Reiss, A., Bardsley, M. Z., McCauley, E., & Tartaglia, N. (2012) · Pediatrics · doi:10.1542/peds.2011-0719 · Cited by 185
van Rijn, S. (2019) · Current Opinion in Psychiatry · doi:10.1097/yco.0000000000000471 · Cited by 89
Jaramillo, C., Nyquist, C., Riggan, K. A., Egginton, J., Phelan, S., & Allyse, M. (2019) · Clinical Pediatrics · doi:10.1177/0009922818817310 · Cited by 39
Patterns of psychopathology and cognition in sex chromosome aneuploidy
Rau, S., Whitman, E. T., Schauder, K., Gogate, N., Lee, N. R., Kenworthy, L., & Raznahan, A. (2021) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-021-09407-9 · Cited by 14
Metadata
- Authors
- LEGGETT, V., JACOBS, P., NATION, K., SCERIF, G., & BISHOP, D. V. M.
- Venue
- Developmental Medicine & Child Neurology
- Publisher
- Wiley
- Published
- 2010-01-15
- Volume
- 52
- Issue
- 2
- Pages
- 119-129
- ISSN
- 0012-1622 (ISSN-L)
- 1469-8749
- OpenAlex
- W1861196653
- Cited by
- 291
- References
- 42
- FWCI
- 2.11
- Type
- journal article
- Language
- en
- Open access
- bronze
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review*. https://app.cochat.ai/papers/10.1111/j.1469-8749.2009.03545.x
- The paper
- LEGGETT, V., JACOBS, P., NATION, K., SCERIF, G., & BISHOP, D. V. M. (2010). Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review*. Developmental Medicine & Child Neurology. https://doi.org/10.1111/j.1469-8749.2009.03545.x
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.