Year |
Citation |
Score |
2020 |
Brkić D, Ng-Cordell E, O'Brien S, Scerif G, Astle D, Baker K. Gene functional networks and autism spectrum characteristics in young people with intellectual disability: a dimensional phenotyping study. Molecular Autism. 11: 98. PMID 33308299 DOI: 10.1186/s13229-020-00403-9 |
0.311 |
|
2020 |
John A, Ng-Cordell E, Hanna N, Brkic D, Baker K. The neurodevelopmental spectrum of synaptic vesicle cycling disorders. Journal of Neurochemistry. PMID 32738165 DOI: 10.1111/jnc.15135 |
0.32 |
|
2019 |
O'Brien S, Ng-Cordell E, Astle DE, Scerif G, Baker K. STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics. Journal of Neurodevelopmental Disorders. 11: 17. PMID 31387522 DOI: 10.1186/S11689-019-9278-9 |
0.428 |
|
2019 |
Baker K, Gordon SL, O'Brien S, Ng-Cordell E, Cousin MA, Raymond FL. Synaptic vesicle cycling disorders: is phenotype predicted by gene, mutation or physiology? F1000research. 8. DOI: 10.7490/F1000Research.1116497.1 |
0.348 |
|
2018 |
Baker K, Gordon SL, Melland H, Bumbak F, Scott DJ, Jiang TJ, Owen D, Turner BJ, Boyd SG, Rossi M, Al-Raqad M, Elpeleg O, Peck D, Mancini GMS, Wilke M, et al. SYT1-associated neurodevelopmental disorder: a case series. Brain : a Journal of Neurology. PMID 30107533 DOI: 10.1093/Brain/Awy209 |
0.386 |
|
2017 |
Suri M, Evers JMG, Laskowski RA, O'Brien S, Baker K, Clayton-Smith J, Dabir T, Josifova D, Joss S, Kerr B, Kraus A, McEntagart M, Morton J, Smith A, Splitt M, et al. Protein structure and phenotypic analysis of pathogenic and population missense variants in STXBP1. Molecular Genetics & Genomic Medicine. 5: 495-507. PMID 28944233 DOI: 10.1002/Mgg3.304 |
0.335 |
|
2017 |
Bathelt J, Barnes J, Raymond FL, Baker K, Astle D. Global and Local Connectivity Differences Converge With Gene Expression in a Neurodevelopmental Disorder of Known Genetic Origin. Cerebral Cortex (New York, N.Y. : 1991). 1-12. PMID 28168288 DOI: 10.1093/Cercor/Bhx027 |
0.614 |
|
2016 |
Bathelt J, Astle D, Barnes J, Raymond FL, Baker K. Structural brain abnormalities in a single gene disorder associated with epilepsy, language impairment and intellectual disability. Neuroimage. Clinical. 12: 655-665. PMID 27747153 DOI: 10.1016/J.Nicl.2016.07.016 |
0.599 |
|
2015 |
Baker K, Astle DE, Scerif G, Barnes J, Smith J, Moffat G, Gillard J, Baldeweg T, Raymond FL. Epilepsy, cognitive deficits and neuroanatomy in males with ZDHHC9 mutations. Annals of Clinical and Translational Neurology. 2: 559-69. PMID 26000327 DOI: 10.1002/Acn3.196 |
0.468 |
|
2015 |
Astle DE, Barnes JJ, Baker K, Colclough GL, Woolrich MW. Cognitive training enhances intrinsic brain connectivity in childhood. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 6277-83. PMID 25904781 DOI: 10.1523/Jneurosci.4517-14.2015 |
0.331 |
|
2015 |
Baker K, Scerif G, Astle DE, Fletcher PC, Raymond FL. Psychopathology and cognitive performance in individuals with membrane-associated guanylate kinase mutations: a functional network phenotyping study. Journal of Neurodevelopmental Disorders. 7: 8. PMID 25802558 DOI: 10.1186/S11689-015-9105-X |
0.413 |
|
2015 |
Barnes JJ, Woolrich MW, Baker K, Colclough GL, Astle DE. Electrophysiological measures of resting state functional connectivity and their relationship with working memory capacity in childhood. Developmental Science. PMID 25782537 DOI: 10.1111/Desc.12297 |
0.391 |
|
2015 |
Baker K, Gordon SL, Grozeva D, van Kogelenberg M, Roberts NY, Pike M, Blair E, Hurles ME, Chong WK, Baldeweg T, Kurian MA, Boyd SG, Cousin MA, Raymond FL. Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling. The Journal of Clinical Investigation. 125: 1670-8. PMID 25705886 DOI: 10.1172/Jci79765 |
0.378 |
|
2015 |
Scerif G, Baker K. Annual research review: Rare genotypes and childhood psychopathology--uncovering diverse developmental mechanisms of ADHD risk. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 56: 251-73. PMID 25494546 DOI: 10.1111/Jcpp.12374 |
0.452 |
|
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