Cornish, Kim M
Article
Article
Cvejic, Rachael C, Hocking, Darren ORCID: 0000-0003-1143-8190, Wen, Wei, Georgiou-Karistianis, N, Cornish, Kim M, Godler, David E, Rogers, Carolyn and Trollor, Julian N
ORCID: 0000-0002-7685-2977
(2018)
Reduced caudate volume and cognitive slowing in men at risk of fragile X-associated tremor ataxia syndrome.
Brain Imaging and Behavior, 13.
pp. 1128-1134.
ISSN 1931-7557
Birch, Rachael C, Hocking, Darren ORCID: 0000-0003-1143-8190, Cornish, Kim M, Menant, Jasmine, Lord, Stephen, Georgiou-Karistianis, N, Godler, David E, Wen, Wei, Rogers, Carolyn and Trollor, Julian N
ORCID: 0000-0002-7685-2977
(2017)
Selective subcortical contributions to gait impairments in males with the FMR1 premutation.
Journal of Neurology, Neurosurgery and Psychiatry, 88 (2).
pp. 188-190.
ISSN 0022-3050
Cornish, Kim M, Kraan, Claudine M, Bui, Quang M, Bellgrove, M, Metcalfe, Sylvia A, Trollor, Julian N ORCID: 0000-0002-7685-2977, Hocking, Darren
ORCID: 0000-0003-1143-8190, Slater, Howard R, Inaba, Yoshimi, Li, Xin, Archibald, Alison D, Turbitt, Erin, Cohen, Jonathan and Godler, David E
ORCID: 0000-0002-6405-269X
(2015)
Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women.
Neurology, 84 (16).
pp. 1631-1638.
ISSN 0028-3878
Birch, Rachael C ORCID: 0000-0001-8026-2155, Hocking, Darren
ORCID: 0000-0003-1143-8190, Cornish, Kim M, Menant, Jasmine C, Georgiou-Karistianis, N, Godler, David E
ORCID: 0000-0002-6405-269X, Wen, Wei, Hackett, Anna, Rogers, Carolyn and Trollor, Julian N
ORCID: 0000-0002-7685-2977
(2015)
Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males.
Genes, Brain and Behavior, 14 (3).
pp. 251-259.
ISSN 1601-1848
Hocking, Darren ORCID: 0000-0003-1143-8190, Kraan, Claudine M
ORCID: 0000-0003-1805-6339, Godler, David E
ORCID: 0000-0002-6405-269X, Bui, Quang M, Li, Xin, Bradshaw, John
ORCID: 0000-0002-8714-5231, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Archibald, Alison D, Turbitt, Erin
ORCID: 0000-0002-6650-9702, Fielding, Joanne
ORCID: 0000-0002-1131-0587, Trollor, Julian N
ORCID: 0000-0002-7685-2977, Cohen, Jonathan and Cornish, Kim M
ORCID: 0000-0003-2014-0193
(2014)
Evidence linking FMR1 mRNA and attentional demands of stepping and postural control in women with the premutation.
Neurobiology of Aging, 36 (3).
pp. 1400-1408.
ISSN 0197-4580
Grigsby, Jim, Cornish, Kim M ORCID: 0000-0003-2014-0193, Hocking, Darren
ORCID: 0000-0003-1143-8190, Kraan, Claudine M
ORCID: 0000-0003-1805-6339, Olichney, John M, Rivera, Susan M, Schneider, Andrea, Sherman, Stephanie, Wang, Jun Yi and Yang, Jin-Chen
(2014)
The cognitive neuropsychological phenotype of carriers of the FMR1 premutation.
Journal of Neurodevelopmental Disorders, 6.
ISSN 1866-1947
Birch, Rachael C ORCID: 0000-0001-8026-2155, Cornish, Kim M
ORCID: 0000-0003-2014-0193, Hocking, Darren
ORCID: 0000-0003-1143-8190 and Trollor, Julian N
ORCID: 0000-0002-7685-2977
(2014)
Understanding the neuropsychiatric phenotype of fragile X-associated tremor ataxia syndrome: a systematic review.
Neuropsychology Review, 24.
pp. 491-513.
ISSN 1040-7308
Kraan, Claudine M ORCID: 0000-0003-1805-6339, Hocking, Darren
ORCID: 0000-0003-1143-8190, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Archibald, Alison D, Fielding, Joanne
ORCID: 0000-0002-1131-0587, Trollor, Julian N
ORCID: 0000-0002-7685-2977, Bradshaw, John
ORCID: 0000-0002-8714-5231, Cohen, Jonathan and Cornish, Kim M
ORCID: 0000-0003-2014-0193
(2014)
Age and CGG-repeat length are associated with neuromotor impairments in at-risk females with the FMR1 premutation.
Neurobiology of Aging, 35 (9).
pp. 7-13.
ISSN 0197-4580
Kraan, Claudine M ORCID: 0000-0003-1805-6339, Hocking, Darren
ORCID: 0000-0003-1143-8190, Bradshaw, John
ORCID: 0000-0002-8714-5231, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Archibald, Alison D, Fielding, Joanne
ORCID: 0000-0002-1131-0587, Trollor, Julian N
ORCID: 0000-0002-7685-2977, Cohen, Jonathan and Cornish, Kim M
ORCID: 0000-0003-2014-0193
(2014)
Symbolic sequence learning is associated with cognitive-affective profiles in female FMR1 premutation carriers.
Genes, Brain and Behavior, 13 (4).
pp. 385-393.
ISSN 1601-1848
Shelton, Annie L, Cornish, Kim M ORCID: 0000-0003-2014-0193, Kraan, Claudine M
ORCID: 0000-0003-1805-6339, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Bradshaw, John
ORCID: 0000-0002-8714-5231, Hocking, Darren
ORCID: 0000-0003-1143-8190, Archibald, Alison D, Cohen, Jonathan, Trollor, Julian N
ORCID: 0000-0002-7685-2977 and Fielding, Joanne
ORCID: 0000-0002-1131-0587
(2014)
Exploring inhibitory deficits in female premutation carriers of fragile X syndrome: through eye movements.
Brain and Cognition, 85.
pp. 201-208.
ISSN 0278-2626
Riby, Deborah M, Hanley, Mary, Kirk, Hannah, Clark, Fiona, Little, Katie, Fleck, Ruth, Janes, Emily, Kelso, Linzi, O'Kane, Fionnuala, Cole-Fletcher, Rachel, Allday, Marianne Hvistendahl, Hocking, Darren ORCID: 0000-0003-1143-8190, Cornish, Kim M
ORCID: 0000-0003-2014-0193 and Rodgers, Jacqui
(2013)
The interplay between anxiety and social functioning in Williams syndrome.
Journal of Autism and Developmental Disorders, 44.
pp. 1220-1229.
ISSN 0162-3257
Kraan, Claudine M ORCID: 0000-0003-1805-6339, Hocking, Darren
ORCID: 0000-0003-1143-8190, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Archibald, Alison D, Fielding, Joanne
ORCID: 0000-0002-1131-0587, Trollor, Julian N
ORCID: 0000-0002-7685-2977, Bradshaw, John
ORCID: 0000-0002-8714-5231, Cohen, Jonathan and Cornish, Kim M
ORCID: 0000-0003-2014-0193
(2013)
Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers.
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 165 (1).
pp. 41-51.
ISSN 1552-4841
Kirk, Hannah, Hocking, Darren ORCID: 0000-0003-1143-8190, Riby, Deborah M and Cornish, Kim M
ORCID: 0000-0003-2014-0193
(2013)
Linking social behaviour and anxiety to attention to emotional faces in Williams syndrome.
Research in Developmental Disabilities, 34 (12).
pp. 4608-4616.
ISSN 0891-4222
Kraan, Claudine M ORCID: 0000-0003-1805-6339, Hocking, Darren
ORCID: 0000-0003-1143-8190, Georgiou-Karistianis, N, Metcalfe, Sylvia A, Archibald, Alison D, Fielding, Joanne
ORCID: 0000-0002-1131-0587, Trollor, Julian N
ORCID: 0000-0002-7685-2977, Bradshaw, John
ORCID: 0000-0002-8714-5231, Cohen, Jonathan and Cornish, Kim M
ORCID: 0000-0003-2014-0193
(2013)
Cognitive-motor interference during postural control indicates at-risk cerebellar profiles in females with the FMR1 premutation.
Behavioural Brain Research, 253.
pp. 329-336.
ISSN 0166-4328
Hocking, Darren ORCID: 0000-0003-1143-8190, Thomas, Daniel, Menant, Jasmine C, Porter, Melanie A, Smith, Stuart, Lord, Stephen R
ORCID: 0000-0002-7111-8802 and Cornish, Kim M
ORCID: 0000-0003-2014-0193
(2013)
The interplay between executive control and motor functioning in Williams syndrome.
Developmental Science, 16 (3).
pp. 428-442.
ISSN 1363-755X
Kraan, Claudine M ORCID: 0000-0003-1805-6339, Hocking, Darren
ORCID: 0000-0003-1143-8190, Bradshaw, John
ORCID: 0000-0002-8714-5231, Fielding, Joanne
ORCID: 0000-0002-1131-0587, Cohen, Jonathan, Georgiou-Karistianis, N and Cornish, Kim M
ORCID: 0000-0003-2014-0193
(2013)
Neurobehavioural evidence for the involvement of the FMR1 gene in female carriers of fragile X syndrome.
Neuroscience and Biobehavioral Reviews, 37 (3).
pp. 522-547.
ISSN 0149-7634
Hocking, Darren ORCID: 0000-0003-1143-8190, Kogan, Cary S and Cornish, Kim M
ORCID: 0000-0003-2014-0193
(2012)
Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation.
Brain and Cognition, 79 (1).
pp. 39-44.
ISSN 0278-2626
Cornish, Kim M ORCID: 0000-0003-2014-0193, Savage, Robert, Hocking, Darren
ORCID: 0000-0003-1143-8190 and Hollis, Chris P
ORCID: 0000-0003-1083-6744
(2011)
Association of the dat1 genotype with inattentive behavior is mediated by reading ability in a general population sample.
Brain and Cognition, 77 (3).
pp. 453-458.
ISSN 0278-2626
Cornish, Kim M ORCID: 0000-0003-2014-0193, Hocking, Darren
ORCID: 0000-0003-1143-8190, Moss, Simon and Kogan, Cary S
(2011)
Selective executive markers of at-risk profiles associated with the fragile X premutation.
Neurology, 77 (7).
pp. 618-622.
ISSN 0028-3878