CoChat
Sign Up
Cited by 73

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Cognition in people with Prader-Willi syndrome: Insights into genetic influences on cognitive and social development

Whittington, Joyce, Holland, Anthony·2017·Neuroscience & Biobehavioral Reviews
DOI 10.1016/j.neubiorev.2016.09.013
Open this paper in CoChat — free account

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.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.neubiorev.2016.09.013

Cites

2 of 2 references verified0 citation errors · 0 not checkable

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.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

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

Research works printed but not linked: 48

  1. Bennet, 2015, Autism spectrum disorder in Prader-Willi syndrome: a systematic review, Am. J. Med. Genet. A, 167A, 2936, 10.1002/ajmg.a.37286 · DOI
  2. Bertella, 2005, Mathematical skills in Prader-Willi syndrome, J. Intellect. Disabil. Res., 49, 159, 10.1111/j.1365-2788.2004.00634.x · DOI
  3. Butler, 2004, Pediatrics, 113, 565, 10.1542/peds.113.3.565 · DOI · Paper page
  4. Chen, 2010, Developmental profiles and mentality in preschool children with Prader-Willi syndrome: a preliminary study, Chang Gung Med. J., 33, 436
  5. Chevalere, 2015, Executive functions and Prader-Willi syndrome: global deficit linked with intellectual level and syndrome-specific associations, Am. J. Intellect. Dev. Disabil., 120, 215, 10.1352/1944-7558-120.3.215 · DOI
  6. Copet, 2010, Cognitive profile in a large French cohort of adults with Prader-Willi syndrome: differences between genotypes, J. Intellect. Disabil. Res., 54, 204, 10.1111/j.1365-2788.2010.01251.x · DOI
  7. Curfs, 1991, Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome, Clin. Genet., 40, 430, 10.1111/j.1399-0004.1991.tb03114.x · DOI
  8. Dimitropoulos, 2013, Expressive and receptive language in Prader-Willi syndrome: report on genetic subtype differences, J. Commun. Disord., 46, 193, 10.1016/j.jcomdis.2012.12.001 · DOI
  9. Ding, 2008, SnoRNA Snord116 (Pwcr1/MBll-85) deletion causes growth deficiency and hyperphagia in mice, PLoS One, 3, e1709, 10.1371/journal.pone.0001709 · DOI
  10. Dombret, 2012, Loss of Maged1 results in obesity, deficits of social interactions, impaired sexual behavior and severe alteration of mature oxytocin production in the hypothalamus, Hum. Mol. Genet., 21, 4703, 10.1093/hmg/dds310 · DOI
  11. Dykens, 1992, Profiles, correlates, and trajectories of intelligence in Prader-Willi syndrome, J. Am. Acad. Child Adolesc. Psychiatry, 31, 1125, 10.1097/00004583-199211000-00022 · DOI
  12. Halit, 2008, Face and gaze processing in Prader-Willi syndrome, J. Neuropsychol., 2, 65, 10.1348/174866407X243305 · DOI
  13. Hashimoto, 1998, Proton magnetic resonance spectroscopy of the brain in patients with Prader-Willi syndrome, Pediatr. Neurol., 18, 30, 10.1016/S0887-8994(97)00139-2 · DOI
  14. Honea, 2012, The neuroanatomy of genetic subtype differences in Prader-Willi syndrome, Am. J. Med. Genet. B, 159B, 243, 10.1002/ajmg.b.32022 · DOI
  15. Jauregi, 2007, A neuropsychological assessment of frontal cognitive functions in Prader-Willi syndrome, J. Intellect. Disabil. Res., 51, 350, 10.1111/j.1365-2788.2006.00883.x · DOI
  16. Keverne, 1996, Genomic imprinting and the differential roles of parental genomes in brain development, Brain Res. Dev. Brain Res., 92, 91, 10.1016/0165-3806(95)00209-X · DOI
  17. Keverne, 2015, Genomic imprinting, action, and interaction of maternal and fetal genomes, Proc. Natl. Acad. Sci. U. S. A., 112, 6789, 10.1073/pnas.1501482112 · DOI
  18. Key, 2013, Social and emotional processing in Prader-Willi syndrome:genetic subtype differences, J. Neurodev. Disord., 5, 7, 10.1186/1866-1955-5-7 · DOI
  19. Koenig, 2004, Deficits in social attribution theory in Prader-Willi syndrome, J. Autism Dev. Dis., 34, 573, 10.1007/s10803-004-2551-z · DOI
  20. Lo, 2013, Impaired theory of mind and symptoms of Autism Spectrum Disorder in children with Prader-Willi syndrome, Res. Dev. Disabil., 34, 2764, 10.1016/j.ridd.2013.05.024 · DOI
  21. Lucignani, 2004, GABAA receptor abnormalities in Prader-Willi syndrome assessed with positron emission tomography and [11C] flumazenil, Neuroimage, 22, 22, 10.1016/j.neuroimage.2003.10.050 · DOI
  22. Lukoshe, 2014, Reduced cortical complexity in children with Prader-Willi syndrome and its association with cognitive impairment and developmental delay, PLoS One, 9, e107320, 10.1371/journal.pone.0107320 · DOI
  23. Malich, 2000, Phenotypic heterogeneity of growth and psychometric intelligence in Prader-Willi syndrome:variable expression of a contiguous gene syndrome or parent-child resemblance?, Am. J. Med. Genet., 31, 298, 10.1002/(SICI)1096-8628(20000410)91:4<298::AID-AJMG11>3.0.CO;2-G · DOI
  24. Manning, 2015, Puzzle pieces: neural structure and function in Prader-Willi syndrome, Diseases, 3, 382, 10.3390/diseases3040382 · DOI
  25. Meziane, 2015, An early postnatal oxytocin treatment prevents social and learning deficits in adult mice deficient for Magel2, a gene involved in Prader-Willi syndrome and autism, Biol. Psychiatry, 78, 85, 10.1016/j.biopsych.2014.11.010 · DOI
  26. Miller, 2006, Neurocognitive findings in Prader-Willi syndrome and early onset morbid obesity, J. Pediatr., 149, 192, 10.1016/j.jpeds.2006.04.013 · DOI
  27. Miller, 2007, Intracranial abnormalities detected by three-dimensional magnetic resonance imaging in Prader-Willi syndrome, Am. J. Med. Genet. A, 143A, 476, 10.1002/ajmg.a.31508 · DOI · Paper page
  28. Muscatelli, 2000, Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome, Hum. Mol. Genet., 9, 3101, 10.1093/hmg/9.20.3101 · DOI
  29. Ogata, 2014, Autism spectrum disorders and hyperactive/impulsive behaviors in Japanese patients with Prader-Willi syndrome: a comparison between maternal uniparental disomy and deletion cases, Am. J. Med. Genet. Part A, 164A, 2180, 10.1002/ajmg.a.36615 · DOI
  30. Paul, 1980, Sibling resemblance in mental ability: a review, Behav. Genet., 10, 277, 10.1007/BF01067773 · DOI
  31. Relkovic, 2010, Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome, Eur. J. Neurosci., 31, 156, 10.1111/j.1460-9568.2009.07048.x · DOI
  32. Relkovic, 2012, Enhanced appetitive learning and reversal learning in a mouse model for Prader-Willi syndrome, Behav. Neurosci., 126, 488, 10.1037/a0028155 · DOI
  33. Semenza, 2008, Genetics and mathematics: evidence from Prader-Willi syndrome, Neuropsychologia, 46, 206, 10.1016/j.neuropsychologia.2007.07.017 · DOI
  34. Stauder, 2002, Multi-modal P3 deflation of event-related brain activity in Prader-Willi syndrome, Neurosci. Lett., 327, 99, 10.1016/S0304-3940(02)00377-4 · DOI
  35. Stauder, 2005, Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader-Willi syndrome: an ERP study, Clin. Neurophysiol., 116, 1464, 10.1016/j.clinph.2005.02.019 · DOI
  36. Sullivan, 1999, Second-order belief attribution in Williams syndrome: intact or impaired?, Am. J. Ment. Retard., 104, 523, 10.1352/0895-8017(1999)104<0523:SBAIWS>2.0.CO;2 · DOI
  37. Tager-Flusberg, 2000, A componential view of theory of mind: evidence from Williams syndrome, Cognition, 76, 59, 10.1016/S0010-0277(00)00069-X · DOI
  38. Verdine, 2008, Strategies and correlates of jigsaw puzzle and visuospatial performance by persons with Prader-Willi syndrome, Am. J. Ment. Retard., 113, 343, 10.1352/2008.113:342-355 · DOI
  39. Walley, 2005, An investigation of executive function abilities in adults with Prader-Willi syndrome, J. Intellect. Disabil. Res., 49, 613, 10.1111/j.1365-2788.2005.00717.x · DOI
  40. Whittington, 2011, Recognition of emotion in facial expression by people with Prader-Willi syndrome, J. Intellect. Disabil. Res., 55, 75, 10.1111/j.1365-2788.2010.01348.x · DOI
  41. Whittington, 2002, Relationship between clinical and genetic diagnosis of Prader-Willi syndrome, J. Med. Genet., 39, 926, 10.1136/jmg.39.12.926 · DOI
  42. Whittington, 2004, Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome, J. Intellect. Disabil. Res., 48, 172, 10.1111/j.1365-2788.2004.00556.x · DOI
  43. Whittington, 2004, Underachievement in Prader-Willi syndrome, J. Intellect. Disabil. Res., 48, 188, 10.1111/j.1365-2788.2004.00473.x · DOI
  44. Whittington, 2009, Relationship between the IQ of people with Prader-Willi syndrome and that of their siblings: evidence for imprinted gene effects, J. Intellect. Disabil. Res., 53, 411, 10.1111/j.1365-2788.2009.01157.x · DOI
  45. Woodcock, 2009, Associations between repetitive questioning, resistance to change, temper outbursts and anxiety in Prader-Willi and Fragile-X syndromes, J. Intellect. Disabil. Res., 53, 265, 10.1111/j.1365-2788.2008.01122.x · DOI
  46. Woodcock, 2009, Task-switching deficits and repetitive behaviour in genetic neurodevelopmental disorders: data from children with Prader-Willi syndrome chromosome 15 q11-q13 deletion and boys with Fragile X syndrome, Cogn. Neuropsychol., 26, 172, 10.1080/02643290802685921 · DOI
  47. Woodcock, 2011, The relationship between specific cognitive impairment and behaviour in Prader-Willi syndrome, J. Intellect. Disabil. Res., 55, 152, 10.1111/j.1365-2788.2010.01368.x · DOI
  48. Yamada, 2006, Brain developmental abnormalities in Prader-Willi syndrome detected by diffusion tensor imaging, Pediatrics, 118, e442, 10.1542/peds.2006-0637 · DOI

Cited by

Sorted by citations

See all 73

Metadata

Authors
Whittington, J., & Holland, A.
Venue
Neuroscience & Biobehavioral Reviews
Publisher
Elsevier BV
Published
2017-01
Volume
72
Pages
153-167
ISSN
0149-7634
DOI
10.1016/j.neubiorev.2016.09.013
Cited by
73
References
2
Language
en
Licence
www.elsevier.com/tdm/userlicense/1.0/ (tdm)

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