A. Morris

发表

CAG repeat expansions and schizophrenia: association with disease in females and with early age-at-onset.

J. Mollon, P. McKenna, D. Hunt, 1995, Human molecular genetics.

Association studies indicate that protein disulfide isomerase is a risk factor in amyotrophic lateral sclerosis.

J. De Belleroche, C. Shaw, Bradley N Smith, 2013, Free radical biology & medicine.

Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma

S. Bhattacharya, T. Aung, R. Hitchings, 2002, Human Genetics.

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase

C. Shaw, C. Vance, M. Falchi, 2010, Proceedings of the National Academy of Sciences.

Sequestosome-1 (SQSTM1) sequence variants in ALS cases in the UK: prevalence and coexistence of SQSTM1 mutations in ALS kindred with PDB

J. Belleroche, A. Morris, C. Kwok, 2013, European Journal of Human Genetics.

A cluster of single nucleotide polymorphisms in the 5′-leader of the human dopamine D3 receptor gene (DRD3) and its relationship to schizophrenia

J. Mollon, P. McKenna, D. Hunt, 2000, Neuroscience Letters.

Early development and unstable genes in schizophrenia: preliminary results

A. Mortimer, D. Hunt, A. Morris, 2002, European Psychiatry.

Variants in the zinc transporter-3 encoding gene (SLC30A3) in schizophrenia and bipolar disorder: Effects on brain glutamate–A pilot study

A. Young, D. Lythgoe, L. Jelen, 2022, Frontiers in Psychiatry.

High Prevalence of Posterior Polymorphous Corneal Dystrophy in the Czech Republic; Linkage Disequilibrium Mapping and Dating an Ancestral Mutation

P. Deloukas, R. Gwilliam, S. Bhattacharya, 2012, PloS one.

Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies

D. Hunt, A. Bird, S. Bhattacharya, 2001, Journal of medical genetics.

The rhodopsin gene of the cuttlefish Sepia officinalis: sequence and spectral tuning.

D M Hunt, D. Hunt, J. Bellingham, 1998, The Journal of experimental biology.

The molecular basis of a spectral shift in the rhodopsins of two species of squid from different photic environments

J. Bowmaker, D. Hunt, A. Morris, 1993, Proceedings of the Royal Society of London. Series B: Biological Sciences.

A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect

T. Rosenberg, S. Bhattacharya, H. Eiberg, 2001, Human Genetics.

A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene

M. Krawczak, S. Bhattacharya, T. Aung, 2001, Human Genetics.

Thioredoxin reductase 1 haplotypes modify familial amyotrophic lateral sclerosis onset.

A. Morris, J. Mitchell, J. de Belleroche, 2009, Free radical biology & medicine.

VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK

J. Belleroche, C. Shaw, A. Morris, 2015, Journal of the Neurological Sciences.

Common variants in the chromosome 2p23 region containing the SLC30A3 (ZnT3) gene are associated with schizophrenia in female but not male individuals in a large collection of European samples

P. McKenna, P. McKenna, A. Mortimer, 2016, Psychiatry Research.

Allelic variants in the zinc transporter-3 gene, SLC30A3, a candidate gene identified from gene expression studies, show gender-specific association with schizophrenia

P. McKenna, A. Mortimer, A. Morris, 2014, European psychiatry.

Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7).

D. Hunt, S. Halford, A. Moore, 2003, Genomics.

Exclusion of CAG repeat expansion as the cause of disease in autosomal dominant retinitis pigmentosa families.

C. Inglehearn, A. Morris, T. Keen, 1997, Journal of medical genetics.

The number of triplet repeats in five brain-expressed loci with CAG repeats is not associated with schizophrenia

J. Mollon, P. McKenna, D. Hunt, 1997, Schizophrenia Research.

Sequence variation within the RPGR gene: Evidence for a founder complex allele

S. Bhattacharya, I. Winship, A. Morris, 2000, Human mutation.

Characterization of the Properties of a Novel Mutation in VAPB in Familial Amyotrophic Lateral Sclerosis

Han-Jou Chen, Andrea Chai, G. Pennetta, 2010, The Journal of Biological Chemistry.

Assessment of association of D3 dopamine receptor MscI polymorphism with schizophrenia: analysis of symptom ratings, family history, age at onset, and movement disorders.

J. Mollon, P. McKenna, D. Hunt, 1996, American journal of medical genetics.

Effect of dopamine D3 receptor gene polymorphisms and clozapine treatment response: exploratory analysis of nine polymorphisms and meta-analysis of the Ser9Gly variant

J. Lieberman, S. Potkin, P. McKenna, 2010, The Pharmacogenomics Journal.

The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder

Michelle K. Lupton, T. Hortobágyi, Robert H. Brown, 2012, European Journal of Human Genetics.

Reply to Millecamps et al.: Elucidating the role of D amino acid oxidase in familial amyotrophic lateral sclerosis

A. Morris, J. de Belleroche, 2010, Proceedings of the National Academy of Sciences.

Characterisation of the ultraviolet-sensitive opsin gene in the honey bee, Apis mellifera.

D M Hunt, J. Bowmaker, D. Hunt, 1997, European journal of biochemistry.

The rhodopsin gene of the cuttlefish, Sepia officinalis: cDNA sequence, gene structure and spectral tuning.

D. Hunt, J. Bellingham, A. Morris, 1998 .

Clustering and frequency of mutations in the retinal guanylate cyclase ( GUCY2D ) gene in patients with dominant cone-rod dystrophies

D. Hunt, A. Bird, S. Bhattacharya, 2001 .

Allelic variants in the zinc transporter-3 gene, SLC30A3, a candidate gene identified from gene expression studies, show gender-specific association with schizophrenia

P. McKenna, A. Mortimer, J. Belleroche, 2014, European psychiatry.