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Author Details

Sarah Curran
2000
57
34
PMIDPaper TitleJournal TitlePublished Year
33384013A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants.Am J Psychiatry2021
33939246Self-harm as the first presentation of attention deficit hyperactivity disorder in adolescents.Child and Adolescent Mental Health2021
27853387Treatment-resistant schizophrenia: current insights on the pharmacogenomics of antipsychotics.Pharmacogenomics and Personalized Medicine2016
27151072Immune signatures and disorder-specific patterns in a cross-disorder gene expression analysis.Br J Psychiatry2016
27073233Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions.J Med Genet2016
26174111Diagnosing autism spectrum disorder in community settings using the Development and Well-Being Assessment: validation in a UK population-based twin sample.J Child Psychol Psychiatry2016
26010655Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.Hum Mutat2015
25738232Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample.JAMA Psychiatry2015
24517317Behavioral signatures related to genetic disorders in autism.Molecular Autism2014
25363760Synaptic, transcriptional and chromatin genes disrupted in autism.Nature2014
23839283The utility of patient specific induced pluripotent stem cells for the modelling of Autistic Spectrum Disorders.Psychopharmacology (Berl)2014
23164818Common variant at 16p11.2 conferring risk of psychosis.Mol Psychiatry2014
23666566Plasma, oral fluid, and whole-blood distribution of antipsychotics and metabolites in clinical samples.Therapeutic Drug Monitoring2013
25408897NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series - further understanding of the relevance of NRXN1 to neurodevelopmental disorders.J Mol Psychiatry2013
24077841BBGRE: brain and body genetic resource exchange.Database (Oxford)2013
24386451Random or stochastic monoallelic expressed genes are enriched for neurodevelopmental disorder candidate genes.PLoS One2013
24236489Opening Pandora's box in the UK: a hypothetical pharmacogenetic test for clozapine.Pharmacogenomics2013
23637818Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.PLoS One2013
22209245Rare deletions at the neurexin 3 locus in autism spectrum disorder.Am J Hum Genet2012
22346768Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.PLoS Genet2012
21656903No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.Am J Med Genet B Neuropsychiatr Genet2011
23861644Aripiprazole: a review of its use in the treatment of irritability associated with autistic disorder patients aged 6-17.2011
21766464No major effect of twinning on autistic traits.Autism Research2011
19891805Clinical and anatomical heterogeneity in autistic spectrum disorder: a structural MRI study.Psychol Med2010
20952166Maturation of limbic regions in Asperger syndrome: a preliminary study using proton magnetic resonance spectroscopy and structural magnetic resonance imaging.Psychiatry Res2010
19841640The 8th annual pharmacogenetics in psychiatry meeting report.Pharmacogenomics J2009
19058789A common variant in DRD3 receptor is associated with autism spectrum disorder.Biol Psychiatry2009
18495494Altered cerebellar feedback projections in Asperger syndrome.Neuroimage2008
19125863Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism.Genes Brain Behav2008
17400195An event related functional magnetic resonance imaging study of facial emotion processing in Asperger syndrome.Biol Psychiatry2007
16648340Cortical serotonin 5-HT2A receptor binding and social communication in adults with Asperger's syndrome: an in vivo SPECT study.Am J Psychiatry2006
16868570An association analysis of candidate genes on chromosome 15 q11-13 and autism spectrum disorder.Mol Psychiatry2006
16684884Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.Proc Natl Acad Sci U S A2006
16389200A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy.Arch Gen Psychiatry2006
16178933Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.J Child Psychol Psychiatry2005
15719397The serotonin transporter gene as a QTL for ADHD.Am J Med Genet B Neuropsychiatr Genet2005
16059935Molecular and phenotypic characterization of ring chromosome 22.Am J Med Genet A2005
15685426Continuity and change in preschool ADHD symptoms: longitudinal genetic analysis with contrast effects.Behav Genet2005
15952184An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder.Am J Med Genet B Neuropsychiatr Genet2005
15578613Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B.Am J Med Genet B Neuropsychiatr Genet2005
15007392Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD.Mol Psychiatry2004
14755441Polymorphisms in the dopamine D5 receptor (DRD5) gene and ADHD.Am J Med Genet B Neuropsychiatr Genet2004
12707944CHIP: Defining a dimension of the vulnerability to attention deficit hyperactivity disorder (ADHD) using sibling and individual data of children in a community-based sample.Am J Med Genet B Neuropsychiatr Genet2003
12960764Polymorphisms in the dopamine D4 receptor gene and attention-deficit hyperactivity disorder.Neuroreport2003
12740596The dopamine transporter gene is associated with attention deficit hyperactivity disorder in a Taiwanese sample.Mol Psychiatry2003
11857575Association of DRD4 in children with ADHD and comorbid conduct problems.Am J Med Genet2002
12448880Validation of single nucleotide polymorphism quantification in pooled DNA samples with SNaPIT. A glycosylase-mediated methods for polymorphism detection method.Mol Biotechnol2002
12192616Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample.Molecular Psychiatry2002
11920846Association study of a SNAP-25 microsatellite and attention deficit hyperactivity disorder.Am J Med Genet2002
11483473Approaches to gene mapping in complex disorders and their application in child psychiatry and psychology.British Journal of Psychiatry2001
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Institute of Psychiatry, King's College London
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University of Exeter Medical School, University of Exeter.
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King's College London
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the University of Hong Kong
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Institute of Psychiatry, King's College London
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The Hospital for Sick Children
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Institute of Psychiatry, King's College London
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Institute of Psychiatry, King's College London
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Icahn School of Medicine at Mount Sinai
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University of Exeter
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Brigham and Women's Hospital
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Data Science Institute and Lancaster University Medical School
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at the University of Pennsylvania Perelman School of Medicine
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King's College of London, Institute of Psychiatry
Co-authored papers 2
INSERM U
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