P
Philip Asherson
Researcher at King's College London
Publications - 455
Citations - 34889
Philip Asherson is an academic researcher from King's College London. The author has contributed to research in topics: Attention deficit hyperactivity disorder & Population. The author has an hindex of 91, co-authored 442 publications receiving 29480 citations. Previous affiliations of Philip Asherson include University of Cambridge & King's College.
Papers
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Journal ArticleDOI
Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies.
Richard Anney,Elaine Kenny,Colm O'Dushlaine,Jessica Lasky-Su,Barbara Franke,Derek W. Morris,Benjamin M. Neale,Benjamin M. Neale,Benjamin M. Neale,Philip Asherson,Stephen V. Faraone,Michael Gill +11 more
TL;DR: It is observed that missing genotypes are not randomly distributed throughout the homozygous and heterozygous groups and these findings have important implications to study design, quality‐control procedures and reporting of findings in GWAS.
Book
Handbook for attention deficit hyperactivity disorder in adults
Philip Asherson,Susan Young,Marios Adamou,Blanca Bolea,David Coghill,Gisli H. Gudjonsson,J Kustow,Ulrich Müller,Mark Pitts,Johannes Thome +9 more
TL;DR: In this paper, the authors address the treatment gap in recognizing, treating and managing Attention Deficit Hyperactivity Disorder (ADHD) in adults and advocate expanding ADHD treatment across all age ranges.
Journal ArticleDOI
High-density SNP screen of sodium channel genes by haplotype tagging and DNA pooling for association with idiopathic generalized epilepsy
Andrew Makoff,Teck Lai,Catherine Barratt,Antonio Valentin,Nick Moran,Nick Moran,Philip Asherson,Lina Nashef +7 more
TL;DR: Two SCN2A SNPs (rs3943809 and rs16850331) were associated by case–control with a subgroup with IGE and history of febrile seizures and also by transmission disequilibrium test (TDT) in parent–proband trios, but none are obvious functional variants.
Journal ArticleDOI
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes (vol 11, pg 934, 2006)
Keeley J. Brookes,Xiaohui Xu,Wei J. Chen,Kaixin Zhou,Benjamin M. Neale,N. Lowe,Richard Anney,Barbara Franke,Michael Gill,Richard P. Ebstein,Jan K. Buitelaar,Pak C. Sham,Desmond Campbell,Jo Knight,Penny Andreou,Marieke E. Altink,Raoul Arnold,Folkert Boer,Cathelijne J. M. Buschgens,Louise Butler,Hanna Christiansen,Leonard C. Feldman,K. Fleischman,Ellen A. Fliers,Raoul Howe-Forbes,A. Goldfarb,Alexander Heise,Isabel Gabriëls,Isabelle Korn-Lubetzki,Lena Johansson,Rafaela Marco,She'era Medad,Ruud B. Minderaa,Fernando Mulas,Ueli Mueller,Aisling Mulligan,K. Rabin,Nanda Rommelse,Vaheshta Sethna,J. Sorohan,Henrik Uebel,Lamprini Psychogiou,Anne Weeks,R. Barrett,Ian W. Craig,Tobias Banaschewski,Edmund J.S. Sonuga-Barke,Jacques Eisenberg,Jonna Kuntsi,Iris Manor,Peter McGuffin,Ana Miranda,Robert D. Oades,Robert Plomin,Herbert Roeyers,Aribert Rothenberger,Joseph A. Sergeant,H-C Steinhausen,Eric Taylor,Margaret Thompson,Stephen V. Faraone,Philip Asherson +61 more
TL;DR: Correction to: Molecular Psychiatry (2006) 11, 934–953; doi:10.1038/sj.mp4001869 Following publication of the above article, errors in the names and listing of the authors were noted.
Journal ArticleDOI
No Association of Single Nucleotide Polymorphisms in the μ-Opioid Receptor Subunit Gene with Idiopathic Generalized Epilepsy
Catherine Barratt,Teck Lai,Lina Nashef,Antonio Valentin,Leonora Fisniku,Nicholas Moran,Nicholas Moran,Philip Asherson,Andrew Makoff +8 more
TL;DR: The results provide no support for association of A118G with either IAE or IGE and also exclude association in the sample of a small‐to‐moderate gene effect with IGE from a large part of OPRM1.