L
Liam S. Carroll
Researcher at Southampton General Hospital
Publications - 23
Citations - 2354
Liam S. Carroll is an academic researcher from Southampton General Hospital. The author has contributed to research in topics: Single-nucleotide polymorphism & Genetic association. The author has an hindex of 17, co-authored 23 publications receiving 2146 citations. Previous affiliations of Liam S. Carroll include King's College London & Brighton and Sussex Medical School.
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Journal ArticleDOI
Identification of loci associated with schizophrenia by genome-wide association and follow-up
Michael Conlon O'Donovan,Nicholas John Craddock,Nadine Norton,Hywel Williams,T. Peirce,Valentina Moskvina,Ivan Nikolov,Marian L. Hamshere,Liam S. Carroll,Lyudmila Georgieva,Sarah Dwyer,Peter Holmans,Jonathan Marchini,Chris C. A. Spencer,Bryan Howie,H. T. Leung,Annette M. Hartmann,Hans-Jürgen Möller,Derek W. Morris,Yongyong Shi,Guo Yin Feng,Per Hoffmann,Peter Propping,Catalina Vasilescu,Wolfgang Maier,Marcella Rietschel,Stanley Zammit,Johannes Schumacher,Emma M. Quinn,Thomas G. Schulze,Nigel Williams,Ina Giegling,Nakao Iwata,Masashi Ikeda,Ariel Darvasi,Sagiv Shifman,Lin He,Jubao Duan,Alan R. Sanders,Douglas F. Levinson,Pablo V. Gejman,Nancy G. Buccola,Bryan J. Mowry,Robert Freedman,Farooq Amin,Donald W. Black,Jeremy M. Silverman,William Byerley,C. Robert Cloninger,Sven Cichon,Markus M. Nöthen,Michael Gill,Aiden Corvin,Dan Rujescu,George Kirov,Michael John Owen +55 more
TL;DR: Meta-analysis provided strongest evidence for association around ZNF804A and this strengthened when the affected phenotype including bipolar disorder included bipolar disorder and the overall pattern of replication was unlikely to occur by chance.
Journal ArticleDOI
Genetic overlap between autism, schizophrenia and bipolar disorder
TL;DR: It is shown that copy number variations are likely to be important risk factors for autism and schizophrenia, whereas common single-nucleotide polymorphism alleles have a role in all disorders, and some of the specific genetic loci implicated so far encode proteins that function in synaptic development and plasticity, and therefore may represent a common biological pathway for these disorders.
Journal ArticleDOI
Fine mapping of ZNF804A and genome wide significant evidence for its involvement in schizophrenia and bipolar disorder.
Hywel Williams,Nadine Norton,Sarah Dwyer,Valentina Moskvina,Ivan Nikolov,Liam S. Carroll,Lyudmila Georgieva,Nigel Williams,Derek W. Morris,Emma M. Quinn,Ina Giegling,Masashi Ikeda,Masashi Ikeda,Joel Wood,Todd Lencz,Todd Lencz,Christina M. Hultman,Paul Lichtenstein,Dawn L. Thiselton,Brion S. Maher,Anil K. Malhotra,Anil K. Malhotra,Brien P. Riley,Kenneth S. Kendler,Michael Gill,Patrick F. Sullivan,Pamela Sklar,Pamela Sklar,Shaun Purcell,Shaun Purcell,Vishwajit L. Nimgaonkar,George Kirov,Peter Holmans,Aiden Corvin,Dan Rujescu,N. Craddock,M. J. Owen,Michael Conlon O'Donovan +37 more
TL;DR: The allelic association at the ZNF804A locus is now one of the most compelling in schizophrenia to date, and supports the accumulating data suggesting overlapping genetic risk between schizophrenia and bipolar disorder.
Journal ArticleDOI
Immune or Genetic-Mediated Disruption of CASPR2 Causes Pain Hypersensitivity Due to Enhanced Primary Afferent Excitability.
John M. Dawes,Greg A. Weir,Steven J. Middleton,Ryan Patel,Kim I. Chisholm,Philippa Pettingill,Liam J Peck,Joseph Sheridan,Akila Shakir,Leslie Jacobson,Maria Gutierrez-Mecinas,Jorge Galino,Jan Walcher,Johannes Kühnemund,Hannah Kuehn,Maria D. Sanna,Bethan Lang,Alex J. Clark,Andreas C. Themistocleous,Noboru Iwagaki,Steven J. West,Karolina Werynska,Liam S. Carroll,Teodora Trendafilova,David A. Menassa,Maria Pia Giannoccaro,Ester Coutinho,Ilaria Cervellini,Damini Tewari,Camilla Buckley,M. Isabel Leite,Hendrik Wildner,Hanns Ulrich Zeilhofer,Hanns Ulrich Zeilhofer,Elior Peles,Andrew J. Todd,Stephen B. McMahon,Anthony H. Dickenson,Gary R. Lewin,Angela Vincent,David L.H. Bennett +40 more
TL;DR: This is the first example of passive transfer of an autoimmune peripheral neuropathic pain disorder and demonstrates that CASPR2 has a key role in regulating cell-intrinsic dorsal root ganglion (DRG) neuron excitability.
Journal ArticleDOI
Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene.
Joseph D. Buxbaum,Lyudmila Georgieva,James J. Young,C. Plescia,Yuji Kajiwara,Ying Jiang,Valentina Moskvina,Nadine Norton,T. Peirce,Hywel Williams,Nicholas John Craddock,Liam S. Carroll,Gabriel Corfas,Kenneth L. Davis,Michael John Owen,Sheila Harroch,Takeshi Sakurai,Michael Conlon O'Donovan +17 more
TL;DR: The yeast two-hybrid system is used to identify proteins that interact with ERBB4, to identify genes and pathways that might contribute to schizophrenia susceptibility and indicates a role for RPTPβ in the modulation of ER BB4 signaling that may in turn provide further support for an important role of neuregulin/ERBB4 signaling in the molecular basis of schizophrenia.