Bolton PF - Search Results

1

An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder.

Curran S, Roberts S, Thomas S, Veltman M, Browne J, Medda E, Pickles A, Sham P, Bolton PF. Curran S, et al. Among authors: bolton pf. Am J Med Genet B Neuropsychiatr Genet. 2005 Aug 5;137B(1):25-8. doi: 10.1002/ajmg.b.30126. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15952184

2

Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.

Milner KM, Craig EE, Thompson RJ, Veltman MW, Thomas NS, Roberts S, Bellamy M, Curran SR, Sporikou CM, Bolton PF. Milner KM, et al. Among authors: bolton pf. J Child Psychol Psychiatry. 2005 Oct;46(10):1089-96. doi: 10.1111/j.1469-7610.2005.01520.x. J Child Psychol Psychiatry. 2005. PMID: 16178933

3

Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review.

Veltman MW, Craig EE, Bolton PF. Veltman MW, et al. Among authors: bolton pf. Psychiatr Genet. 2005 Dec;15(4):243-54. doi: 10.1097/00041444-200512000-00006. Psychiatr Genet. 2005. PMID: 16314754 Review.

4

Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders.

Bolton PF, Veltman MW, Weisblatt E, Holmes JR, Thomas NS, Youings SA, Thompson RJ, Roberts SE, Dennis NR, Browne CE, Goodson S, Moore V, Brown J. Bolton PF, et al. Psychiatr Genet. 2004 Sep;14(3):131-7. doi: 10.1097/00041444-200409000-00002. Psychiatr Genet. 2004. PMID: 15318025

5

A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study.

Veltman MW, Thompson RJ, Craig EE, Dennis NR, Roberts SE, Moore V, Brown JA, Bolton PF. Veltman MW, et al. Among authors: bolton pf. J Autism Dev Disord. 2005 Feb;35(1):117-27. doi: 10.1007/s10803-004-1039-1. J Autism Dev Disord. 2005. PMID: 15796127

6

Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders.

Veltman MW, Thompson RJ, Roberts SE, Thomas NS, Whittington J, Bolton PF. Veltman MW, et al. Among authors: bolton pf. Eur Child Adolesc Psychiatry. 2004 Feb;13(1):42-50. doi: 10.1007/s00787-004-0354-6. Eur Child Adolesc Psychiatry. 2004. PMID: 14991431

7

Neuro-epileptic determinants of autism spectrum disorders in tuberous sclerosis complex.

Bolton PF, Park RJ, Higgins JN, Griffiths PD, Pickles A. Bolton PF, et al. Brain. 2002 Jun;125(Pt 6):1247-55. doi: 10.1093/brain/awf124. Brain. 2002. PMID: 12023313

8

No major effect of twinning on autistic traits.

Curran S, Dworzynski K, Happé F, Ronald A, Allison C, Baron-Cohen S, Brayne C, Bolton PF. Curran S, et al. Among authors: bolton pf. Autism Res. 2011 Oct;4(5):377-82. doi: 10.1002/aur.207. Epub 2011 Jul 15. Autism Res. 2011. PMID: 21766464

9

Behavioral signatures related to genetic disorders in autism.

Bruining H, Eijkemans MJ, Kas MJ, Curran SR, Vorstman JA, Bolton PF. Bruining H, et al. Among authors: bolton pf. Mol Autism. 2014 Feb 11;5(1):11. doi: 10.1186/2040-2392-5-11. Mol Autism. 2014. PMID: 24517317 Free PMC article.

10

Rare deletions at the neurexin 3 locus in autism spectrum disorder.

Vaags AK, Lionel AC, Sato D, Goodenberger M, Stein QP, Curran S, Ogilvie C, Ahn JW, Drmic I, Senman L, Chrysler C, Thompson A, Russell C, Prasad A, Walker S, Pinto D, Marshall CR, Stavropoulos DJ, Zwaigenbaum L, Fernandez BA, Fombonne E, Bolton PF, Collier DA, Hodge JC, Roberts W, Szatmari P, Scherer SW. Vaags AK, et al. Among authors: bolton pf. Am J Hum Genet. 2012 Jan 13;90(1):133-41. doi: 10.1016/j.ajhg.2011.11.025. Epub 2011 Dec 29. Am J Hum Genet. 2012. PMID: 22209245 Free PMC article.

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