S
Sarah Curran
Researcher at King's College London
Publications - 78
Citations - 7948
Sarah Curran is an academic researcher from King's College London. The author has contributed to research in topics: Autism & Attention deficit hyperactivity disorder. The author has an hindex of 36, co-authored 77 publications receiving 7179 citations. Previous affiliations of Sarah Curran include Sussex Partnership NHS Foundation Trust & Brighton and Sussex Medical School.
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Journal ArticleDOI
Molecular and phenotypic characterization of ring chromosome 22.
Aaron R. Jeffries,Sarah Curran,Frances Elmslie,Ajay Sharma,Sharon L. Wenger,Marybeth Hummel,John Powell +6 more
TL;DR: This study identifies a phenotypically normal r(22) individual whose ring chromosome does not disrupt SHANK3, and proposes it to be a candidate gene for autism or abnormal brain development.
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Association study of a SNAP-25 microsatellite and attention deficit hyperactivity disorder.
Jonathan Mill,Sarah Curran,Lindsey Kent,A Gould,Louise Huckett,S Richards,Eric Taylor,Philip Asherson +7 more
TL;DR: A novel microsatellite repeat is identified in SNAP-25 located between the 5'UTR and the first coding exon, and tested for association with ADHD, suggesting a role of this polymorphism in ADHD.
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The serotonin transporter gene as a QTL for ADHD
TL;DR: It is shown here that SLC6A4, which has a major influence on brain serotonin availability, may be a QTL for ADHD.
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Attention deficit hyperactivity disorder (ADHD) and the dopamine D4 receptor gene: evidence of association but no linkage in a UK sample.
Jonathan Mill,Sarah Curran,Lindsey Kent,S Richards,A Gould,V Virdee,L Huckett,J Sharp,C Batten,S Fernando,E Simanoff,M Thompson,J Zhao,PC Sham,Eric Taylor,Philip Asherson +15 more
TL;DR: It is concluded that the case-control findings are likely to be falsely positive, resulting from genetic stratification, and can not rule out alternative explanations of low statistical power and gene–environment correlation.
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A Common Variant in DRD3 Receptor Is Associated with Autism Spectrum Disorder
Mariken de Krom,Wouter G. Staal,Roel A. Ophoff,Judith Hendriks,Jan K. Buitelaar,Barbara Franke,Maretha de Jonge,Patrick Bolton,David A. Collier,Sarah Curran,Herman van Engeland,Jan M. van Ree +11 more
TL;DR: The DRD3 gene is related to stereotyped behavior, liability to side effects of antipsychotic medication, and movement disorders and may therefore have important clinical implications for ASD.