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Items: 18

1.

Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome.

Baker EK, Arpone M, Vera SA, Bretherton L, Ure A, Kraan CM, Bui M, Ling L, Francis D, Hunter MF, Elliott J, Rogers C, Field MJ, Cohen J, Maria LS, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende AM, Amor DJ, Godler DE.

J Neurodev Disord. 2019 Dec 26;11(1):41. doi: 10.1186/s11689-019-9288-7.

2.

Managed retreat through voluntary buyouts of flood-prone properties.

Mach KJ, Kraan CM, Hino M, Siders AR, Johnston EM, Field CB.

Sci Adv. 2019 Oct 9;5(10):eaax8995. doi: 10.1126/sciadv.aax8995. eCollection 2019 Oct.

3.

Climate as a risk factor for armed conflict.

Mach KJ, Kraan CM, Adger WN, Buhaug H, Burke M, Fearon JD, Field CB, Hendrix CS, Maystadt JF, O'Loughlin J, Roessler P, Scheffran J, Schultz KA, von Uexkull N.

Nature. 2019 Jul;571(7764):193-197. doi: 10.1038/s41586-019-1300-6. Epub 2019 Jun 12.

PMID:
31189956
4.

Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.

Baker EK, Arpone M, Aliaga SM, Bretherton L, Kraan CM, Bui M, Slater HR, Ling L, Francis D, Hunter MF, Elliott J, Rogers C, Field M, Cohen J, Cornish K, Santa Maria L, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende AM, Amor DJ, Godler DE.

Mol Autism. 2019 May 3;10:21. doi: 10.1186/s13229-019-0271-7. eCollection 2019.

5.

Epigenetics of fragile X syndrome and fragile X-related disorders.

Kraan CM, Godler DE, Amor DJ.

Dev Med Child Neurol. 2019 Feb;61(2):121-127. doi: 10.1111/dmcn.13985. Epub 2018 Aug 7. Review.

PMID:
30084485
6.

FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohorts.

Kraan CM, Bui QM, Field M, Archibald AD, Metcalfe SA, Christie LM, Bennetts BH, Oertel R, Smith MJ, du Sart D, Bruno D, Wotton TL, Amor DJ, Francis D, Godler DE.

Genet Med. 2018 Dec;20(12):1627-1634. doi: 10.1038/gim.2018.52. Epub 2018 Mar 29.

PMID:
29595813
7.

β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies.

Kraan CM, Cornish KM, Bui QM, Li X, Slater HR, Godler DE.

PLoS One. 2018 Feb 23;13(2):e0192151. doi: 10.1371/journal.pone.0192151. eCollection 2018.

8.

Brain structure and intragenic DNA methylation are correlated, and predict executive dysfunction in fragile X premutation females.

Shelton AL, Cornish KM, Kolbe S, Clough M, Slater HR, Li X, Kraan CM, Bui QM, Godler DE, Fielding J.

Transl Psychiatry. 2016 Dec 13;6(12):e984. doi: 10.1038/tp.2016.250.

9.

The developmental dynamics of gait maturation with a focus on spatiotemporal measures.

Kraan CM, Tan AHJ, Cornish KM.

Gait Posture. 2017 Jan;51:208-217. doi: 10.1016/j.gaitpost.2016.10.021. Epub 2016 Oct 29. Review.

PMID:
27816899
10.

β-glucuronidase mRNA levels are correlated with gait and working memory in premutation females: understanding the role of FMR1 premutation alleles.

Kraan CM, Cornish KM, Bui QM, Li X, Slater HR, Godler DE.

Sci Rep. 2016 Jul 8;6:29366. doi: 10.1038/srep29366.

11.

Executive Dysfunction in Female FMR1 Premutation Carriers.

Shelton AL, Cornish KM, Kraan CM, Lozano R, Bui M, Fielding J.

Cerebellum. 2016 Oct;15(5):565-9. doi: 10.1007/s12311-016-0782-0.

PMID:
27126308
12.

Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women.

Cornish KM, Kraan CM, Bui QM, Bellgrove MA, Metcalfe SA, Trollor JN, Hocking DR, Slater HR, Inaba Y, Li X, Archibald AD, Turbitt E, Cohen J, Godler DE.

Neurology. 2015 Apr 21;84(16):1631-8. doi: 10.1212/WNL.0000000000001496. Epub 2015 Mar 25.

13.

Evidence linking FMR1 mRNA and attentional demands of stepping and postural control in women with the premutation.

Hocking DR, Kraan CM, Godler DE, Bui QM, Li X, Bradshaw JL, Georgiou-Karistianis N, Metcalfe SA, Archibald AD, Turbitt E, Fielding J, Trollor J, Cohen J, Cornish KM.

Neurobiol Aging. 2015 Mar;36(3):1400-8. doi: 10.1016/j.neurobiolaging.2014.11.012. Epub 2014 Nov 26.

PMID:
25541421
14.

Age and CGG-repeat length are associated with neuromotor impairments in at-risk females with the FMR1 premutation.

Kraan CM, Hocking DR, Georgiou-Karistianis N, Metcalfe SA, Archibald AD, Fielding J, Trollor J, Bradshaw JL, Cohen J, Cornish KM.

Neurobiol Aging. 2014 Sep;35(9):2179.e7-13. doi: 10.1016/j.neurobiolaging.2014.03.018. Epub 2014 Mar 20.

PMID:
24814676
15.

Symbolic sequence learning is associated with cognitive-affective profiles in female FMR1 premutation carriers.

Kraan CM, Hocking DR, Bradshaw JL, Georgiou-Karistianis N, Metcalfe SA, Archibald AD, Fielding J, Trollor J, Cohen J, Cornish KM.

Genes Brain Behav. 2014 Apr;13(4):385-93. doi: 10.1111/gbb.12122. Epub 2014 Mar 11.

16.

Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers.

Kraan CM, Hocking DR, Georgiou-Karistianis N, Metcalfe SA, Archibald AD, Fielding J, Trollor J, Bradshaw JL, Cohen J, Cornish KM.

Am J Med Genet B Neuropsychiatr Genet. 2014 Jan;165B(1):41-51. doi: 10.1002/ajmg.b.32203. Epub 2013 Oct 26.

PMID:
24166828
17.

Cognitive-motor interference during postural control indicates at-risk cerebellar profiles in females with the FMR1 premutation.

Kraan CM, Hocking DR, Georgiou-Karistianis N, Metcalfe SA, Archibald AD, Fielding J, Trollor J, Bradshaw JL, Cohen J, Cornish KM.

Behav Brain Res. 2013 Sep 15;253:329-36. doi: 10.1016/j.bbr.2013.07.033. Epub 2013 Jul 27.

PMID:
23896050
18.

Neurobehavioural evidence for the involvement of the FMR1 gene in female carriers of fragile X syndrome.

Kraan CM, Hocking DR, Bradshaw JL, Fielding J, Cohen J, Georgiou-Karistianis N, Cornish KM.

Neurosci Biobehav Rev. 2013 Mar;37(3):522-47. doi: 10.1016/j.neubiorev.2013.01.010. Epub 2013 Jan 23. Review.

PMID:
23352653

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