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VariVis: a visualisation toolkit for variation databases

BMC bioinformatics, 2008-04, Vol.9 (1), p.206-206, Article 206

2008

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Collection of variation causing disease--the Human Variome Project

Human genomics, 2009-07, Vol.3 (4), p.301-303

Cotton, Richard G H

2009

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Response to Stenson et al. in human genomics vol. 4, No. 2, pp. 69-72: 'The human gene mutation database: providing a comprehensive central mutation database for molecular diagnostics and personalised genomics'

Human genomics, 2010-02, Vol.4 (3), p.145-146

Cotton, Richard G H

2010

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Difficulties in finding DNA mutations and associated phenotypic data in web resources using simple, uncomplicated search terms, and a suggested solution

Human genomics, 2011-03, Vol.5 (3), p.141-155, Article 141

2011

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Tetrahydrobiopterin, its Mode of Action on Phenylalanine Hydroxylase, and Importance of Genotypes for Pharmacological Therapy of Phenylketonuria

Human mutation, 2013-07, Vol.34 (7), p.927-936

2013

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Guidelines for establishing locus specific databases

Human mutation, 2012-02, Vol.33 (2), p.298-305

2012

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DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome

Pediatric nephrology (Berlin, West), 2014-06, Vol.29 (6), p.971-977

2014

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Coping with esophageal cancer approaches worldwide

Annals of the New York Academy of Sciences, 2014-09, Vol.1325 (1), p.138-158

2014

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Capture of Somatic mtDNA Point Mutations with Severe Effects on Oxidative Phosphorylation in Synaptosome Cybrid Clones from Human Brain

Human mutation, 2014-12, Vol.35 (12), p.1476-1484

2014

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The Human Variome Project: ensuring the quality of DNA variant databases in inherited renal disease

Pediatric Nephrology, 2015-11, Vol.30 (11), p.1893-1901

2015

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Practical guidelines addressing ethical issues pertaining to the curation of human locus‐specific variation databases (LSDBs)

Human mutation, 2010-11, Vol.31 (11), p.1179-1184

2010

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Letter to the Editor: Personalized medicine in the era of the personal genome

Personalized medicine, 2010-05, Vol.7 (3), p.243-243

Cotton, Richard Gh

2010

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Recommendations of the 2006 Human Variome Project meeting

Nature genetics, 2007-04, Vol.39 (4), p.433-436

Cotton, Richard G.H

2007

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A Foundation for a Community Consortium in an Inherited Disease and Complete Mutation Collection

Human mutation, 2010-12, Vol.31 (12), p.V-V

Cotton, Richard G.H.

2010

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Database overkill

Human mutation, 2010-01, Vol.31 (1), p.1-1

Cotton, Richard G.H.

2010

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Initiating a Human Variome Project Country Node

Human mutation, 2011-05, Vol.32 (5), p.501-506

2011

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Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection

Human mutation, 2011-01, Vol.32 (1), p.2-9

2011

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The Mutome and the 100,000 Mutation Milestone

Human mutation, 2010-06, Vol.31 (6), p.v-v

Cotton, Richard G.H.

2010

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Human Variome Project: an international collaboration to catalogue human genetic variation

Pharmacogenomics, 2006-10, Vol.7 (7), p.969-972

2006

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The value of countrywide mutation reporting

Human mutation, 2010-05, Vol.31 (5), p.v-v

Cotton, Richard G.H.

2010

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Letter to the Editor

Personalized medicine, 2010-05, Vol.7 (3), p.243-243

Cotton, Richard GH

2010

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Early hippocampal oxidative stress is a direct consequence of seizures in the rapid electrical amygdala kindling model

Epilepsy research, 2010-08, Vol.90 (3), p.285-294

2010

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"Mutation in brief" online articles discontinued-introducing "brief reports"

Human mutation, 2011-01, Vol.32 (1), p.1-1

2011

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On genomic DNA paradigms, research publications, and scholarly inquiry

Human mutation, 2010-10, Vol.31 (10), p.1089-1089

2010

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The Human Variome Project (HVP) 2009 Forum "Towards Establishing Standards"

Human Mutation, 2010-03, Vol.31 (3), p.366-367

2010

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VariVis: a visualisation toolkit for variation databases

Collection of variation causing disease--the Human Variome Project

Response to Stenson et al. in human genomics vol. 4, No. 2, pp. 69-72: 'The human gene mutation database: providing a comprehensive central mutation database for molecular diagnostics and personalised genomics'

Difficulties in finding DNA mutations and associated phenotypic data in web resources using simple, uncomplicated search terms, and a suggested solution

Tetrahydrobiopterin, its Mode of Action on Phenylalanine Hydroxylase, and Importance of Genotypes for Pharmacological Therapy of Phenylketonuria

Guidelines for establishing locus specific databases

DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome

Coping with esophageal cancer approaches worldwide

Capture of Somatic mtDNA Point Mutations with Severe Effects on Oxidative Phosphorylation in Synaptosome Cybrid Clones from Human Brain

The Human Variome Project: ensuring the quality of DNA variant databases in inherited renal disease

Practical guidelines addressing ethical issues pertaining to the curation of human locus‐specific variation databases (LSDBs)

Letter to the Editor: Personalized medicine in the era of the personal genome

Recommendations of the 2006 Human Variome Project meeting

A Foundation for a Community Consortium in an Inherited Disease and Complete Mutation Collection

Database overkill

Initiating a Human Variome Project Country Node

Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection

The Mutome and the 100,000 Mutation Milestone

Human Variome Project: an international collaboration to catalogue human genetic variation

The value of countrywide mutation reporting

Letter to the Editor

Early hippocampal oxidative stress is a direct consequence of seizures in the rapid electrical amygdala kindling model

"Mutation in brief" online articles discontinued-introducing "brief reports"

On genomic DNA paradigms, research publications, and scholarly inquiry

The Human Variome Project (HVP) 2009 Forum "Towards Establishing Standards"

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