Browse by UCL people
Group by: Type | Date
Number of items: 5.
Article
Al Eissa, MM;
Fiorentino, A;
Sharp, SI;
O'Brien, NL;
Wolfe, K;
Giaroli, G;
Curtis, D;
... McQuillin, A; + view all
(2018)
Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia.
Annals of human genetics
, 82
(2)
pp. 88-92.
10.1111/ahg.12226.
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Wolfe, K;
McQuillin, A;
Alesi, V;
Boudry Labis, E;
Cutajar, P;
Dallapiccola, B;
Dentici, ML;
... Bass, N; + view all
(2018)
Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.
American Journal of Medical Genetics: Part B Neuropsychiatric Genetics
, 177
(4)
pp. 397-405.
10.1002/ajmg.b.32627.
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Wolfe, K;
Strydom, A;
Morrogh, D;
Carter, J;
Cutajar, P;
Eyeoyibo, M;
Hassiotis, A;
... Bass, N; + view all
(2016)
Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders.
European Journal of Human Genetics
, 25
(1)
pp. 66-72.
10.1038/ejhg.2016.107.
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Wolfe, K;
Stueber, K;
McQuillin, A;
Jichi, F;
Patch, C;
Flinter, F;
Strydom, A;
(2017)
Genetic testing in intellectual disability psychiatry: Opinions and practices of UK child and intellectual disability psychiatrists.
J Appl Res Intellect Disabil
10.1111/jar.12391.
(In press).
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Thesis
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Wolfe, Kate Alexandra;
(2018)
Copy number variation in co-morbid neurodevelopmental disorders.
Doctoral thesis (Ph.D), UCL (University College London).
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