Publications by authors named "SA Forbes"

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COSMIC: the Catalogue Of Somatic Mutations In Cancer.
John G Tate, Sally Bamford, Harry C Jubb, Zbyslaw Sondka, David M Beare, Simon A Forbes

Nucleic Acids Res· January 2019

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The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers.
Zbyslaw Sondka, Sally Bamford, Charlotte G Cole, Sari A Ward, Ian Dunham, Simon A Forbes

Nat Rev Cancer· November 2018

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COSMIC-3D provides structural perspectives on cancer genetics for drug discovery.
Harry C Jubb, Harpreet K Saini, Marcel L Verdonk, Simon A Forbes

Nat Genet· September 2018

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COSMIC: somatic cancer genetics at high-resolution.
Simon A Forbes, David Beare, Harry Boutselakis, Sally Bamford, Nidhi Bindal

Nucleic Acids Res· January 2017

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COSMIC: High-Resolution Cancer Genetics Using the Catalogue of Somatic Mutations in Cancer.
S A Forbes, D Beare, N Bindal, S Bamford, S Ward

Curr Protoc Hum Genet· October 2016

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COSMIC: exploring the world's knowledge of somatic mutations in human cancer.
Simon A Forbes, David Beare, Prasad Gunasekaran, Kenric Leung, Nidhi Bindal

Nucleic Acids Res· January 2015

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Clinical and biological implications of driver mutations in myelodysplastic syndromes.
Elli Papaemmanuil, Moritz Gerstung, Luca Malcovati, Sudhir Tauro, Gunes Gundem, Simon A Forbes

Blood· November 2013

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Data mining using the Catalogue of Somatic Mutations in Cancer BioMart.
Rebecca Shepherd, Simon A Forbes, David Beare, S Bamford, Charlotte G Cole

Database (Oxford)· September 2011

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COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer.
Simon A Forbes, Nidhi Bindal, Sally Bamford, Charlotte Cole, Chai Yin Kok

Nucleic Acids Res· January 2011

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A detailed feeding algorithm improves delivery of nutrition support in an intensive care unit.
Michaela E Clifford, Merrilyn D Banks, Lynda J Ross, Natalie A Obersky, Sharon A Forbes

Crit Care Resusc· September 2010

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COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer.
Simon A Forbes, Gurpreet Tang, Nidhi Bindal, Sally Bamford, Elisabeth Dawson

Nucleic Acids Res· January 2010

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The Catalogue of Somatic Mutations in Cancer (COSMIC).
S A Forbes, G Bhamra, S Bamford, E Dawson, C Kok

Curr Protoc Hum Genet· April 2008

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Quality of life in hospice patients with terminal illness.
Woung-Ru Tang, Lauren S Aaronson, Sarah A Forbes

West J Nurs Res· February 2004

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Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism.
A A J Pannett, A M Kennedy, J J O Turner, S A Forbes, B M Cavaco

Clin Endocrinol (Oxf)· May 2003

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Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1.
Jeremy J O Turner, Poloko D Leotlela, Anna A J Pannett, Simon A Forbes, J H Duncan Bassett

J Clin Endocrinol Metab· June 2002

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MHC-linked olfactory receptor loci exhibit polymorphism and contribute to extended HLA/OR-haplotypes.
A Ehlers, S Beck, S A Forbes, J Trowsdale, A Volz

Genome Res· December 2000

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The MHC quarterly report.
S A Forbes, J Trowsdale

Immunogenetics· November 1999

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Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1.
J H Bassett, P Rashbass, B Harding, S A Forbes, A A Pannett

J Bone Miner Res· January 1999

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Decision making by high functional status elders regarding nursing home placement.
S A Forbes, N Hoffart, L J Redford

J Case Manag· December 1998

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A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1.
J W Höppener, M J De Wit, A Y Simarro-Doorten, J F Roijers, H M van Herrewaarden, S A Forbes

Genomics· June 1998

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Control over nursing practice: a construct coming of age.
S A Forbes, M J Bott, R L Taunton

J Nurs Meas· April 1998

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Characterization of mutations in patients with multiple endocrine neoplasia type 1.
J H Bassett, S A Forbes, A A Pannett, S E Lloyd, P T Christie

Am J Hum Genet· February 1998

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Review criteria for stroke rehabilitation outcomes.
S A Forbes, P W Duncan, M K Zimmerman

Arch Phys Med Rehabil· October 1997

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Estimation of the age of the ancestral arginine3500-->glutamine mutation in human apoB-100.
N B Myant, S A Forbes, I N Day, J Gallagher

Genomics· October 1997

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Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).
S A Forbes, A A Pannett, J H Bassett, B Harding, C Wooding

Hum Genet· September 1997

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