Publications by authors named "Alan Maclean"

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Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness.
Mandy Johnstone, Alan Maclean, Lien Heyrman, An-Sofie Lenaerts, Annelie Nordin

Mol Neuropsychiatry· October 2015

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Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trial.
Eric W F W Alton, David K Armstrong, Deborah Ashby, Katie J Bayfield, Diana Bilton, Alan W Maclean

Lancet Respir Med· September 2015

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A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.
Eske M Derks, Muhammad Ayub, Kimberly Chambert, Jurgen Del Favero, Mandy Johnstone, Alan Maclean

Am J Med Genet B Neuropsychiatr Genet· December 2013

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Homozygosity mapping of depressive disorder in a large family from Pakistan: significant linkage on chromosome 6 and 9.
Muhammad Ayub, Muhammad Irfan, Alan Maclean, Farooq Naeem, Douglas Blackwood

Am J Med Genet B Neuropsychiatr Genet· March 2013

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Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder.
René A W Frank, Allan F McRae, Andrew J Pocklington, Louie N van de Lagemaat, Pau Navarro, Alan W MacLean

PLoS One· April 2011

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Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder.
Rosie M Walker, Andrea Christoforou, Pippa A Thomson, Kevin A McGhee, Alan Maclean

Neurosci Lett· June 2010

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Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population.
Donald J Macintyre, Kevin A McGhee, Alan W Maclean, Maryam Afzal, Katy Briffa

Neurosci Lett· May 2010

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A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression.
Helen M Knight, Benjamin S Pickard, Alan Maclean, Mary P Malloy, Dinesh C Soares

Am J Hum Genet· December 2009

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Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencing.
Ravinesh A Kumar, Kevin A McGhee, Stephen Leach, Russell Bonaguro, Alan Maclean

Am J Med Genet B Neuropsychiatr Genet· September 2008

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Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.
Manuel A R Ferreira, Michael C O'Donovan, Yan A Meng, Ian R Jones, Douglas M Ruderfer, Alan W MacLean

Nat Genet· September 2008

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Linkage analysis in a large family from Pakistan with depression and a high incidence of consanguineous marriages.
Muhammad Ayub, Muhammad Irfan, Alan Maclean, Farooq Naeem, Stuart MacGregor

Hum Hered· August 2008

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Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment.
Helen M Knight, Alan Maclean, Muhammad Irfan, Farooq Naeem, Stephen Cass

Eur J Hum Genet· June 2008

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A genome-wide linkage study in families with major depression and co-morbid unexplained swelling.
Carl A Anderson, Alan Maclean, Matthew G Dunnigan, Anthony J Pelosi, Valerie Murray

Am J Med Genet B Neuropsychiatr Genet· April 2008

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ALG-2 interacting protein AIP1: a novel link between D1 and D3 signalling.
Lingping Zhan, Bigang Liu, Maria Jose-Lafuente, Margarita V Chibalina, Andrew Grierson, Alan Maclean

Eur J Neurosci· April 2008

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Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation.
Xinsheng Nan, Jianghui Hou, Alan Maclean, Jamal Nasir, Maria Jose Lafuente

Proc Natl Acad Sci U S A· February 2007

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Targeted disruption of Huntingtin-associated protein-1 (Hap1) results in postnatal death due to depressed feeding behavior.
Edmond Y W Chan, Jamal Nasir, Claire-Anne Gutekunst, Sarah Coleman, Alan Maclean

Hum Mol Genet· April 2002

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