C. Russ

发表

Exome Sequencing Can Improve Diagnosis and Alter Patient Management

Vineet Bafna, Nitin Udpa, Carrie Sougnez, 2012, Science Translational Medicine.

Supporting Online Material Materials and Methods Figs. S1 to S7 Tables S1 to S4 References Mutations in the Fus/tls Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

J L Haines, M A Pericak-Vance, J. Haines, 2022 .

No association of the SOD1 locus and disease susceptibility or phenotype in sporadic ALS

J. Powell, A. Al-Chalabi, C. Shaw, 2004, Neurology.

CYP2D6 polymorphisms in Alzheimer’s disease, with and without extrapyramidal signs, showing no apolipoprotein E ε4 effect modification

S. Lovestone, J. Powell, C. Holmes, 1999, Biological Psychiatry.

50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis

Robert H. Brown, S. Purcell, J. Glass, 2008, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

The extended haplotype of the microtubule associated protein tau gene is not associated with Pick's disease

S. Lovestone, J. Powell, P. Andersen, 2001, Neuroscience Letters.

Apolipoprotein E: Depressive illness, depressive symptoms, and Alzheimer's disease

D. Collier, G. Kirov, S. Lovestone, 1998, Biological Psychiatry.

A Familial Form of Pallidoluysionigral Degeneration and Amyotrophic Lateral Sclerosis With Divergent Clinical Presentations

C. Portera-Cailliau, Robert H. Brown, J. Corbo, 2007, Journal of neuropathology and experimental neurology.

Genetics, molecular biology, neuropathology and phenotype of frontal lobe dementia: a case history.

P. Lantos, M. Philpot, S. Lovestone, 2002, The British journal of psychiatry : the journal of mental science.

De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly

S. Gabriel, V. Bafna, G. Mathern, 2012, Nature Genetics.

Systematic screening of the 14-3-3 eta (eta) chain gene for polymorphic variants and case-control analysis in schizophrenia.

D. Collier, R. Kerwin, J. Powell, 2000, American journal of medical genetics.

Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis.

A Al-Chalabi, J. Powell, A. Al-Chalabi, 1999, Human molecular genetics.

Novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene associated with bipolar affective disorder

T. G. Bruun, D. Collier, O. Mors, 2002, Molecular Psychiatry.

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis

S. Ennis, Robert H. Brown, P. Andersen, 2006, Nature Genetics.

Two novel variants in the DOPA decarboxylase gene: association with bipolar affective disorder

T. G. Bruun, D. Collier, G. Kirov, 1999, Molecular Psychiatry.

Evolutionarily Assembled cis-Regulatory Module at a Human Ciliopathy Locus

Colin A. Johnson, S. Gabriel, N. Katsanis, 2012, Science.

Functional effects of a tandem duplication polymorphism in the 5′flanking region of the DRD4 gene

I. Craig, P. McGuffin, J. Mill, 2004, Biological Psychiatry.

Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes

Colin A. Johnson, K. Cibulskis, S. Gabriel, 2010, Nature Genetics.

The association between APOE and dementia does not seem to be mediated by vascular factors

S. Lovestone, J. Powell, M. Prince, 2000, Neurology.

Association analysis of the glycogen synthase kinase-3β gene in bipolar disorder

D. Collier, D. Clair, G. Breen, 2006, Neuroscience Letters.

Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease

M. Owen, P. Holmans, N. Cairns, 1999, Nature Genetics.

S. Lovestone, M. Prince, J. Cervilla, 2004, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

Identification of sequence variants and analysis of the role of the glycogen synthase kinase 3 β gene and promoter in late onset Alzheimer's disease

S. Lovestone, J. Powell, C. Russ, 2001, Molecular Psychiatry.

unctional Effects of a Tandem Duplication olymorphism in the 5 = Flanking Region of he DRD 4 Gene

P. McGuffin, J. Mill, P. Asherson, 2004 .

Depression, APOE genotype and subjective memory impairment: a cross-sectional study in an African-Caribbean population

R. Stewart, S. Lovestone, C. Brayne, 2001, Psychological Medicine.

The microtubule associated protein Tau gene and Alzheimer's disease – an association study and meta-analysis

S. Lovestone, J. Powell, M. Cruts, 2001, Neuroscience Letters.

Rate of progression of cognitive decline in Alzheimer’s disease: effect of butyrylcholinesterase K gene variation

C. Morris, T. del Ser, S. Lovestone, 2005, Journal of Neurology, Neurosurgery & Psychiatry.

Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS

S. Ennis, Robert H. Brown, O. Hardiman, 2008, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains

Robert H. Brown, J. Growdon, B. Hyman, 2007, Acta Neuropathologica.

K variant of butyrycholinesterase and late-onset Alzheimer's disease

S. Lovestone, J. Powell, C. Russ, 1998, The Lancet.

No association of DYNC1H1 with sporadic ALS in a case‐control study of a northern European derived population: A tagging SNP approach

D. Goldstein, Robert H. Brown, K. Ahmadi, 2006, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

SOD1A4V-mediated ALS: Absence of a closely linked modifier gene and origination in Asia

A. Iafrate, A. Al-Chalabi, P. Sapp, 2008, Neuroscience Letters.

Identification of genomic organisation, sequence variants and analysis of the role of the human dishevelled 1 gene in late onset Alzheimer's disease

S. Lovestone, J. Powell, C. Russ, 2002, Molecular Psychiatry.

Variants in candidate ALS modifier genes linked to Cu/Zn superoxide dismutase do not explain divergent survival phenotypes

P. Andersen, P. Sapp, D. McKenna-Yasek, 2006, Neuroscience Letters.

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

J. Haines, M. Pericak-Vance, H. Horvitz, 2009, Science.

Apolipoprotein E Genotype, Vascular Risk and Early Cognitive Impairment in an African Caribbean Population

R. Stewart, S. Lovestone, C. Brayne, 2001, Dementia and Geriatric Cognitive Disorders.

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

M. Pericak-Vance, H. Horvitz, P. D. de Jong, 2009, Science.