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A Model of Prostate-Specific Antigen Screening Outcomes for Low- to High-Risk Men: Information to Support Informed ChoicesHOWARD, Kirsten; BARRATT, Alex; MANN, Graham J et al.Archives of internal medicine (1960). 2009, Vol 169, Num 17, pp 1603-1610, issn 0003-9926, 8 p.Article

Prognostic and Clinicopathologic Associations of Oncogenic BRAF in Metastatic MelanomaLONG, Georgina V; MENZIES, Alexander M; NAGRIAL, Adnan M et al.Journal of clinical oncology. 2011, Vol 29, Num 10, pp 1239-1246, issn 0732-183X, 8 p.Article

Selection criteria for genetic assessment of patients with familial melanomaLEACHMAN, Sancy A; CARUCCI, John; CURIEL-LEWANDROWSKI, Clara et al.Journal of the American Academy of Dermatology. 2009, Vol 61, Num 4, pp 677-684, issn 0190-9622, 8 p.Article

Frequent loss of heterozygosity targeting the inactive X chromosome in melanomaINDSTO, James O; NASSIF, Najah T; KEFFORD, Richard F et al.Clinical cancer research. 2003, Vol 9, Num 17, pp 6476-6482, issn 1078-0432, 7 p.Article

Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UKCUST, Anne E; HARLAND, Mark; CHANG, Yu-Mei et al.Journal of medical genetics. 2011, Vol 48, Num 4, pp 266-272, issn 0022-2593, 7 p.Article

Genome-wide association study identifies novel loci predisposing to cutaneous melanomaAMOS, Christopher I; WANG, Li-E; SCHACHERER, Christopher W et al.Human molecular genetics (Print). 2011, Vol 20, Num 24, pp 5012-5023, issn 0964-6906, 12 p.Article

Localization of a novel melanoma susceptibility locus to 1p22GILLANDERS, Elizabeth; JUO, Suh-Hang Hank; KEFFORD, Richard F et al.American journal of human genetics. 2003, Vol 73, Num 2, pp 301-313, issn 0002-9297, 13 p.Article

Online Prostate Cancer Screening Decision Aid for At-Risk Men: A Randomized TrialWATTS, Kaaren J; MEISER, Bettina; BARRATT, Alexandra L et al.Health psychology (Hillsdale, N.J.). 2014, Vol 33, Num 9, pp 986-997, issn 0278-6133, 12 p.Article

The melanoma-associated 24 base pair duplication in p16INK4a is functionally impairedBECKER, Therese M; AYUB, Ana L; KEFFORD, Richard F et al.International journal of cancer. 2005, Vol 117, Num 4, pp 569-573, issn 0020-7136, 5 p.Article

EDD, the human orthologue of the hyperplastic discs tumour suppressor gene, is amplified and overexpressed in cancerCLANCY, Jennifer L; HENDERSON, Michelle J; BRADY, Ged et al.Oncogene (Basingstoke). 2003, Vol 22, Num 32, pp 5070-5081, issn 0950-9232, 12 p.Article

Dominant negative ATM mutations in breast cancer familiesCHENEVIX-TRENCH, Georgia; SPURDLE, Amanda B; SCOTT, Clare et al.Journal of the National Cancer Institute. 2002, Vol 94, Num 3, pp 205-215, issn 0027-8874Article

BRAF/NRAS Wild-Type Melanomas Have a High Mutation Load Correlating with Histologic and Molecular Signatures of UV DamageMAR, Victoria J; WONG, Stephen Q; BEHREN, Andreas et al.Clinical cancer research (Print). 2013, Vol 19, Num 17, pp 4589-4598, issn 1078-0432, 10 p.Article

Common sequence variants on 20qll.22 confer melanoma susceptibilityBROWN, Kevin M; MACGREGOR, Stuart; THOMAS, Shane et al.Nature genetics. 2008, Vol 40, Num 7, pp 838-840, issn 1061-4036, 3 p.Article

Functional impairment of Melanoma-associated p16INK4a mutants in melanoma cells despite retention of cyclin-dependent kinase 4 bindingBECKER, Therese M; RIZOS, Helen; KEFFORD, Richard F et al.Clinical cancer research. 2001, Vol 7, Num 10, pp 3282-3288, issn 1078-0432Article

CDKN2A mutation and deletion status in thin and thick primary melanomaCACHIA, Adrian R; INDSTO, James O; MCLAREN, Kathryn M et al.Clinical cancer research. 2000, Vol 6, Num 9, pp 3511-3515, issn 1078-0432Article

The Effect on Melanoma Risk of Genes Previously Associated With Telomere LengthILES, Mark M; BISHOP, D. Timothy; ANDRESEN, Per A et al.Journal of the National Cancer Institute. 2014, Vol 106, Num 10, issn 0027-8874, 267.1-267.5Article

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3MACGREGOR, Stuart; MONTGOMERY, Grant W; PAINTER, Jodie N et al.Nature genetics. 2011, Vol 43, Num 11, pp 1114-1118, issn 1061-4036, 5 p.Article

A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL)HARLAND, Mark; GOLDSTEIN, Alisa M; HAYWARD, Nicholas K et al.European journal of cancer (1990). 2008, Vol 44, Num 9, pp 1269-1274, issn 0959-8049, 6 p.Article

Low prevalence of RAS-RAF-activating mutations in Spitz melanocytic nevi compared with other melanocytic lesionsINDSTO, James O; KUMAR, Swapna; LIXIANG WANG et al.Journal of cutaneous pathology. 2007, Vol 34, Num 6, pp 448-455, issn 0303-6987, 8 p.Article

High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMELGOLDSTEIN, Alisa M; CHAN, May; BRUNO, William et al.Cancer research (Baltimore). 2006, Vol 66, Num 20, pp 9818-9828, issn 0008-5472, 11 p.Article

X inactivation, DNA deletion, and microsatellite instability in common acquired melanocytic neviINDSTO, James O; CACHIA, Adrian R; KEFFORD, Richard F et al.Clinical cancer research. 2001, Vol 7, Num 12, pp 4054-4059, issn 1078-0432Article

Meta-Analysis Combining New and Existing Data Sets Confirms that the TERT-CLPTM1L Locus Influences Melanoma RiskLAW, Matthew H; MONTGOMERY, Grant W; BROWN, Kevin M et al.Journal of investigative dermatology. 2012, Vol 132, Num 2, pp 485-487, issn 0022-202X, 3 p.Article

Review and Cross-Validation of Gene Expression Signatures and Melanoma PrognosisSCHRAMM, Sarah-Jane; CAMPAIN, Anna E; SCOLYER, Richard A et al.Journal of investigative dermatology. 2012, Vol 132, Num 2, pp 274-283, issn 0022-202X, 10 p.Article

Sunbed use during adolescence and early adulthood is associated with increased risk of early-onset melanomaCUST, Anne E; ARMSTRONG, Bruce K; GOUMAS, Chris et al.International journal of cancer (Print). 2011, Vol 128, Num 10, pp 2425-2435, issn 0020-7136, 11 p.Article

A novel recurrent mutation in MITF predisposes to familial and sporadic melanomaYOKOYAMA, Satoru; WOODS, Susan L; TAYLOR, John C et al.Nature (London). 2011, Vol 480, Num 7375, pp 99-103, issn 0028-0836, 5 p.Article

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