VariVis: a visualisation toolkit for variation databases von Smith, Timothy D, Cotton, Richard G H

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Collection of variation causing disease--the Human Variome Project von Cotton, Richard G H

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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 diagnost... von Cotton, Richard G H

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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 von Webb, Elizabeth A, Smith, Timothy D, Cotton, Richard G H

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Tetrahydrobiopterin, its Mode of Action on Phenylalanine Hydroxylase, and Importance of Genotypes for Pharmacological Therapy of Phenylketonuria von Heintz, Caroline, Cotton, Richard G.H., Blau, Nenad

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Guidelines for establishing locus specific databases von Vihinen, Mauno, den Dunnen, Johan T., Dalgleish, Raymond, Cotton, Richard G. H.

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Coping with esophageal cancer approaches worldwide von Cotton, Richard G.H., Langer, Rupert, Leong, Trevor, Martinek, Jan, Sewram, Vikash, Smithers, Mark, Swanson, Paul E., Qiao, You-Lin, Udagawa, Harushi, Ueno, Masaki, Wang, Meng, Wei, Wen-Qiang, White, Russell E.

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DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome von Savige, Judy, Ars, Elisabet, Cotton, Richard G. H., Crockett, David, Dagher, Hayat, Deltas, Constantinos, Ding, Jie, Flinter, Frances, Pont-Kingdon, Genevieve, Smaoui, Nizar, Torra, Roser, Storey, Helen

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Capture of Somatic mtDNA Point Mutations with Severe Effects on Oxidative Phosphorylation in Synaptosome Cybrid Clones from Human Brain von McKenzie, Matthew, Chiotis, Maria, Hroudová, Jana, Lopez Sanchez, Maria I.G., Lim, Sze Chern, Cook, Mark J., McKelvie, Penny, Cotton, Richard G. H., Murphy, Michael, St John, Justin C., Trounce, Ian A.

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The Human Variome Project: ensuring the quality of DNA variant databases in inherited renal disease von Savige, Judy, Dalgleish, Raymond, Cotton, Richard GH, den Dunnen, Johan T, Macrae, Finlay, Povey, Sue

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Practical guidelines addressing ethical issues pertaining to the curation of human locus‐specific variation databases (LSDBs) von Povey, Sue, Al Aqeel, Aida I, Cambon‐Thomsen, Anne, Dalgleish, Raymond, den Dunnen, Johan T, Firth, Helen V, Greenblatt, Marc S, Barash, Carol Isaacson, Parker, Michael, Patrinos, George P, Savige, Judith, Sobrido, Maria‐Jesus, Winship, Ingrid, Cotton, Richard G.H

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Recommendations of the 2006 Human Variome Project meeting von Cotton, Richard G.H

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A Foundation for a Community Consortium in an Inherited Disease and Complete Mutation Collection von Cotton, Richard G.H.

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Database overkill von Cotton, Richard G.H.

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Initiating a Human Variome Project Country Node von AlAama, Jumana, Smith, Timothy D., Lo, Alan, Howard, Heather, Kline, Alexandria A., Lange, Matthew, Kaput, Jim, Cotton, Richard G.H.

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Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection von Patrinos, George P., Al Aama, Jumana, Al Aqeel, Aida, Al-Mulla, Fahd, Borg, Joseph, Devereux, Andrew, Felice, Alex E., Macrae, Finlay, Marafie, Makia J., Petersen, Michael B., Qi, Ming, Ramesar, Rajkumar S., Zlotogora, Joel, Cotton, Richard G.H.

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The Mutome and the 100,000 Mutation Milestone von Cotton, Richard G.H.

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The value of countrywide mutation reporting von Cotton, Richard G.H.

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Early hippocampal oxidative stress is a direct consequence of seizures in the rapid electrical amygdala kindling model von Sashindranath, Maithili, McLean, Karen J, Trounce, Ian A, Cotton, Richard G.H, Cook, Mark J

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"Mutation in brief" online articles discontinued-introducing "brief reports" von Paalman, Mark H., Cutting, Garry R., Cotton, Richard G.H.

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