M. Davis

发表

The phenotypic manifestations of chromosome 17p11.2 duplication.

A. Harding, P. Thomas, W. Marques, 1997, Brain : a journal of neurology.

Positive and negative intronic regulatory elements control muscle-specific alternative exon splicing of Drosophila myosin heavy chain transcripts.

M. Davis, C. Emerson, M B Davis, 2001, Genetics.

Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study.

M. Farrer, S. Lincoln, D. Brooks, 2002, Brain : a journal of neurology.

PARK6 is a common cause of familial parkinsonism

A. Bentivoglio, A. Albanese, M. Breteler, 2002, Neurological Sciences.

Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis

D. Kullmann, G. Meola, S. Schorge, 2009, Neurology.

A cytochrome P‐450 gene family mapped to human chromosome 19

S. Povey, G. Kelsey, M. Davis, 1985, Annals of human genetics.

Spinocerebellar ataxia type 11.

J. Johnson, T. Révész, N. Wood, 2012, Handbook of clinical neurology.

Localization of an ovarian cancer tumor suppressor gene to a 0.5-cM region between D22S284 and CYP2D, on chromosome 22q.

W. Foulkes, I. Campbell, M. Davis, 1996, Cancer research.

Prenatal diagnosis of mitochondrial DNA8993 T----G disease.

A. Harding, M. Davis, M. Sweeney, 1992, American journal of human genetics.

Breakage on chromosome 2 brings the Ck gene to a region 3' of c-myc in a Burkitt's lymphoma line carrying a (2;8) translocation.

T. Rabbitts, M. Davis, S. Malcolm, 1985, Cytogenetics and cell genetics.

Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence

A. Bird, F. Fitzke, M. Michaelides, 2008, British Journal of Ophthalmology.

Paroxysmal dystonic choreoathetosis. Genetic linkage studies in a British family.

C. Marsden, P. Jarman, N. Wood, 1997, Brain : a journal of neurology.

Linkage analysis in British and French families with idiopathic torsion dystonia.

C. Marsden, A. Harding, M. Davis, 1993, Brain : a journal of neurology.

Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.

N W Wood, N. Wood, M. Davis, 1999, American journal of human genetics.

Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients

K P Bhatia, N W Wood, I Trender-Gerhard, 2008, Journal of Neurology, Neurosurgery, and Psychiatry.

Sequence ofthesuperoxide dismutase 1(SOD1) gene infamilial Parkinson's disease

C. Marsden, A. Harding, M. Davis, 1995 .

Sequence of the superoxide dismutase 1 (SOD 1) gene in familial Parkinson's disease.

C. Marsden, A. Harding, M. Davis, 1995, Journal of neurology, neurosurgery, and psychiatry.

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India

K. Bhatia, N. Wood, M. Davis, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Detailed haplotype analysis in Ashkenazi Jewish and non‐Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations

S. Povey, N. Wood, T. Warner, 1999, Annals of human genetics.

disease . polymorphism in familial Parkinson ' s Debrisoquine hydroxylase gene

C. Marsden, A. Harding, M. Davis, 2022 .

Evidence for locus heterogeneity in autosomal dominant torsion dystonia.

C. Marsden, A. Harding, M. Davis, 1993, Genomics.

The gene for human αaL‐lactalbumin is assigned to chromosome 12q13

S. Povey, M. Davis, R. Craig, 1987, Annals of human genetics.

The c-myc gene paradox in Burkitt's lymphoma chromosomal translocation.

T. Rabbitts, M. Davis, S. Malcolm, 1984, Current topics in microbiology and immunology.

Localization of PEPD to the long arm of chromosome 19

S. Povey, F. Oerlemans, B. Wieringa, 1987, Annals of human genetics.

Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort

M. Roberts, F. Muntoni, R. Horvath, 2012, Journal of Neurology.

Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy

D. Booth, A. Harding, P. Thomas, 1996, Neuromuscular Disorders.

GJB1 gene mutations in suspected inflammatory demyelinating neuropathies not responding to treatment

N. Wood, H. Houlden, M. Davis, 2009, Journal of Neurology, Neurosurgery, and Psychiatry.

Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases.

T. Crow, J. Collinge, A. Harding, 1991, American journal of human genetics.

MFN2 mutations cause severe phenotypes in most patients with CMT2A

M. Shy, M. Davis, S. Feely, 2011, Neurology.

What causes paramyotonia in the United Kingdom?

M. Davis, M. Sweeney, M. Hanna, 2008, Neurology.

Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing

D. Kullmann, S. Schorge, N. Tubridy, 2009, Journal of Medical Genetics.

The assignment of the human gene coding for complement C5 to chromosome 9q22‐9q33.

S. Povey, M. Davis, S. Jeremiah, 1988, Annals of human genetics.

Familial polyposis coli: growth characteristics of karyotypically variable cultured fibroblasts, response to epidermal growth factor and the tumour promoter 12-0-tetradecanoyl phorbol-13-acetate.

M. Davis, J. Delhanty, S. Rider, 1986, Journal of medical genetics.

Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations

H. Houlden, R. Sandford, D. Pareyson, 2011, Neurology.

Regional localization of a human cytochrome P‐450 (CYP1) to chromosome 19q 13.1–13.3

M. Davis, I. Phillips, L. West, 1986, Annals of human genetics.

Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77)

A. Harding, M. Davis, M. Reilly, 1995, Journal of Neurology.

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype

R. Griggs, M. Davis, M. Hanna, 2011, Neurology.

Refinement of two chromosome 11q regions of loss of heterozygosity in ovarian cancer.

W. Foulkes, I. Campbell, M. Davis, 1996, Cancer research.

Regional localization of carbonic anhydrase genesCA1 andCA3 on human chromosome 8

M. Davis, Y. Edwards, P. Butterworth, 1987, Somatic cell and molecular genetics.

Chloride channel myotonia: exon 8 hot-spot for dominant-negative interactions.

D. Kullmann, S. Schorge, M. Davis, 2007, Brain : a journal of neurology.

Gene for alpha-chain of human T-cell receptor: location on chromosome 14 region involved in T-cell neoplasms.

A. Palumbo, M. Isobe, C. Croce, 1985, Science.

Mutation analysis in patients with possible but apparently sporadic Huntington's disease

C. Marsden, N. Quinn, A. Harding, 1994, The Lancet.

Chromosome instability in lymphocytes, fibroblasts, and colon epithelial-like cells from patients with familial polyposis coli.

M. Davis, J. Delhanty, J. Wood, 1983, Cancer genetics and cytogenetics.

Multiple mitochondrial DNA deletions in monozygotic twins with OPMD

N. Wood, D. Healy, M. Davis, 2007, Journal of Neurology, Neurosurgery, and Psychiatry.

African-Ancestry Associated Gene Expression Signatures and Pathways in Triple Negative Breast Cancer, a Comparison Across Women of African Descent

O. Elemento, J. Carpten, A. Sboner, 2022, medRxiv.

Transposable element insertions respecify alternative exon splicing in three Drosophila myosin heavy chain mutants.

M. Davis, C. Emerson, D. Standiford, 1998, Genetics.

A gene from human chromosome region 3p21 with reduced expression in small cell lung cancer.

J. Osinga, R. Hofstra, K. Kok, 1992, Cancer research.

Splice-junction elements and intronic sequences regulate alternative splicing of the Drosophila myosin heavy chain gene transcript.

M. Davis, C. Emerson, M B Davis, 1997, Genetics.

Transthyretin gene mutations in British and French patients with amyloid neuropathy.

K. Bhatia, A. Harding, P. Thomas, 1993, Journal of neurology, neurosurgery, and psychiatry.

French patients with amyloid neuropathy . Transthyretin gene mutations in British and

A. Harding, P. Thomas, M. Davis, 2022 .

Linkage analysis in adenomatous polyposis coli: the use of four closely linked DNA probes in 20 UK families.

J. Attwood, J. Burn, M. Davis, 1991, Journal of medical genetics.

A novel point mutation in the mcleod syndrome gene in neuroacanthocytosis

A. Monaco, A. Harding, A. Harding, 1996, Annals of neurology.

REARRANGEMENTS OF THE C-MYC GENE IN BURKITTS-LYMPHOMA

T. Rabbitts, M. Davis, S. Malcolm, 1984 .

RFLP and mapping of human MOX-1 gene on chromosome 3.

D. Albertson, A. Barclay, M. Davis, 1988, Nucleic acids research.

Localisation of the human N‐ras oncogene to chromosome 1cen ‐ p21 by in situ hybridisation.

C. Marshall, A. Hall, M. Davis, 1983, The EMBO journal.

Myosin rod protein: a novel thick filament component of Drosophila muscle.

C. Franzini-armstrong, M. Davis, C. Emerson, 1997, Journal of molecular biology.

The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.

A. Federico, N. Wood, M. Davis, 1998, Brain : a journal of neurology.

Variable phenotypes are associated with PMP22 missense mutations

David L. Bennett, M. Russo, M. Laurá, 2011, Neuromuscular Disorders.

Loss of heterozygosity for DNA polymorphisms mapping to chromosomes 10 and 17 and prognosis in patients with gliomas.

D. Thomas, A. Harding, M. Davis, 1995, Journal of neurology, neurosurgery, and psychiatry.

Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease

D. Maraganore, A. Harding, M. Davis, 1994, Movement disorders : official journal of the Movement Disorder Society.

Cortical myoclonus in huntington's disease

C. Marsden, N. Quinn, K. Bhatia, 1994, Movement disorders : official journal of the Movement Disorder Society.

Linkage analysis with chromosome 9 markers in hereditary essential tremor

P. Thompson, C. Marsden, P. Bain, 1993, Movement disorders : official journal of the Movement Disorder Society.

The human homologue of the weaver mouse gene in familial and sporadic Parkinson's disease

N. Wood, M. Davis, O. Bandmann, 1996, Neuroscience.

Genetics of Parkinsonism: a review.

N. Wood, M. Davis, J. Vaughan, 2001, Annals of human genetics.

Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease.

C. Marsden, A. Harding, M. Davis, 1994, Journal of neurology, neurosurgery, and psychiatry.

Identification and sizing of the GAA trinucleotide repeat expansion of Friedreich's ataxia in 56 patients. Clinical and genetic correlates.

N. Wood, N. Wood, M. Davis, 1997, Brain : a journal of neurology.

Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.

N. Wood, A. Harding, M. Davis, 1996, American journal of human genetics.

Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity.

C. Marsden, P. Jarman, K. Bhatia, 1997, American journal of human genetics.

Creation of EcR isoform-specific mutations in Drosophila melanogaster via local P element transposition, imprecise P element excision, and male recombination

M. Davis, A. Robertson, G. E. Carney, 2004, Molecular Genetics and Genomics.

Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy.

A. Harding, M. Davis, M. Sweeney, 1992, American journal of human genetics.

Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset

A. Albanese, N. Wood, E. Valente, 2001, Neurological Sciences.

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.

K. Bhatia, N. Wood, E. Valente, 2000, Brain : a journal of neurology.

When genes go wild: highly variable internal transcibed spacer1 and conserved mitochondrial DNA haplotypes used to examine the genetic diversity and dispersal pathways of invasive Hylotrupes bajulus in Western Australia

R. J. Cunningham, M. Davis, D. Groth, 2013 .

A new explanation for recessive myotonia congenita

S. Schorge, M. Davis, M. Hanna, 2012, Neurology.

Episodic ataxia and hemiplegia caused by the 8993T→C mitochondrial DNA mutation

M. Davis, M. Sweeney, C. Woodward, 2007, Journal of Medical Genetics.

A model of the Drosophila melanogaster glycerol-3-phosphate oxidase-encoding gene.

M. Davis, J. Ross, S. McKechnie, 1994, Gene.

Irish (Donegal) amyloidosis is associated with the transthyretinALA60 (Appalachian) variant.

H. Staunton, A. Harding, M. Davis, 1991, Brain : a journal of neurology.