Publicaciones
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Martínez-Barrios E, César-Díaz S, Cruzalegui JC, Hernandez C, Arbelo E, Fiol JV, Brugada-Terradellas J, Brugada R, Campuzano O and Sarquella-Brugada G.
Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population
Biomedicines . 10(1): . Nº de citas: 17
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Martins da Silva V, Martínez-Barrios E, Tell-Martí G, Dabad M, Carrera C, Aguilera P, Daniel Antoni Brualla Palazón, Esteve-Codina A, Vicente-Villa MA, Puig S, Puig-Butillé JA and Malvehy J.
Genetic Abnormalities in Large to Giant Congenital Nevi: Beyond NRAS Mutations
JOURNAL OF INVESTIGATIVE DERMATOLOGY . 139(4): 900-908. Nº de citas: 90
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Mademont-Soler I, Morales C, Soler A, Clusellas N, Margarit E, Martínez-Barrios E, Martínez JM and Sánchez A.
MLPA: A prenatal diagnostic tool for the study of congenital heart defects?
GENE . 500(1): 151-154. Nº de citas: 10
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Schoof, N, Iles, MM, Bishop, DT, Newton-Bishop, JA, Barrett, JH and Martínez-Barrios E.
Pathway-Based Analysis of a Melanoma Genome-Wide Association Study: Analysis of Genes Related to Tumour-Immunosuppression
PLoS One . 6(12): . Nº de citas: 17
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Amos, CI, Wang, LE, Lee, JE, Gershenwald, JE, Chen, WV, Fang, SY, Kosoy, R, Zhang, MF, Qureshi, AA, Vattathil, S, Schacherer, CW, Gardner, JM, Wang, YL, Bishop, DT, Barrett, JH, MacGregor, S, Hayward, NK, Martin, NG, Duffy, DL, Mann, GJ, Cust, A, Hopper, J, Brown, KM, Grimm, EA, Xu, YJ, Han, YH, Jing, KY, McHugh, C, Laurie, CC, Doheny, KF, Pugh, EW, Seldin, MF, Han, JL, Wei, QY and Martínez-Barrios E.
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma
HUMAN MOLECULAR GENETICS . 20(24): 5012-5023. Nº de citas: 171
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Costantino A, Campuzano O, Vaiano F, Nardi E, Dimitrova A, Greco A, Martínez-Barrios E, Arena V, Jarvis H, Sarquella-Brugada G, Brugada R, Oliva A and Grassi S.
Multidisciplinary and Personalized Molecular Diagnosis to Solving Sudden Death During Sport.
Molecular Diagnosis & Therapy . : .