Items where authors include "Robles-Espinoza, CD"

Article

Birkeälv, S, Harland, M, Matsuyama, LSAS et al. (15 more authors) (2023) Mutually exclusive genetic interactions and gene essentiality shape the genomic landscape of primary melanoma. Journal of Pathology, 259 (1). pp. 56-68. ISSN 0022-3417

Simonin-Wilmer, I, Ossio, R, Leddin, EM et al. (14 more authors) (2022) Population-based analysis of POT1 variants in a cutaneous melanoma case–control cohort. Journal of Medical Genetics (JMG). ISSN 0022-2593

Castaneda-Garcia, C, Iyer, V, Nsengimana, J et al. (11 more authors) (2022) Defining novel causal SNPs and linked phenotypes at melanoma-associated loci. Human Molecular Genetics, 31 (17). pp. 2845-2856. ISSN 0964-6906

Simonin-Wilmer, I, Orozco-del-Pino, P, Bishop, DT orcid.org/0000-0002-8752-8785 et al. (2 more authors) (2021) An Overview of Strategies for Detecting Genotype-Phenotype Associations Across Ancestrally Diverse Populations. Frontiers in Genetics, 12. 703901. ISSN 1664-8021

Adams, DJ, Bishop, DT orcid.org/0000-0002-8752-8785 and Robles-Espinoza, CD (2020) Melanoma predisposition—A limited role for germline BRCA1 and BRCA2 variants. Pigment Cell & Melanoma Research, 33 (1). pp. 6-7. ISSN 1755-1471

Wong, K, Robles-Espinoza, CD, Rodriguez, D et al. (22 more authors) (2019) Association of the POT1 Germline Missense Variant p.I78T With Familial Melanoma. JAMA dermatology, 155 (5). pp. 604-609. ISSN 2168-6068

Robles-Espinoza, CD, Roberts, ND, Chen, S et al. (8 more authors) (2016) Germline MC1R status influences somatic mutation burden in melanoma. Nature Communications, 7. 12064.

Harland, M, Petljak, M, Robles-Espinoza, CD et al. (13 more authors) (2016) Germline TERT promoter mutations are rare in familial melanoma. Familial Cancer, 15 (1). pp. 139-144. ISSN 1389-9600