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Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.
Landi MT, Bishop DT, MacGregor S, Machiela MJ, Stratigos AJ, Ghiorzo P, Brossard M, Calista D, Choi J, Fargnoli MC, Zhang T, Rodolfo M, Trower AJ, Menin C, Martinez J, Hadjisavvas A, Song L, Stefanaki I, Scolyer R, Yang R, Goldstein AM, Potrony M, Kypreou KP, Pastorino L, Queirolo P, Pellegrini C, Cattaneo L, Zawistowski M, Gimenez-Xavier P, Rodriguez A, Elefanti L, Manoukian S, Rivoltini L, Smith BH, Loizidou MA, Del Regno L, Massi D, Mandala M, Khosrotehrani K, Akslen LA, Amos CI, Andresen PA, Avril MF, Azizi E, Soyer HP, Bataille V, Dalmasso B, Bowdler LM, Burdon KP, Chen WV, Codd V, Craig JE, Dębniak T, Falchi M, Fang S, Friedman E, Simi S, Galan P, Garcia-Casado Z, Gillanders EM, Gordon S, Green A, Gruis NA, Hansson J, Harland M, Harris J, Helsing P, Henders A, Hočevar M, Höiom V, Hunter D, Ingvar C, Kumar R, Lang J, Lathrop GM, Lee JE, Li X, Lubiński J, Mackie RM, Malt M, Malvehy J, McAloney K, Mohamdi H, Molven A, Moses EK, Neale RE, Novaković S, Nyholt DR, Olsson H, Orr N, Fritsche LG, Puig-Butille JA, Qureshi AA, Radford-Smith GL, Randerson-Moor J, Requena C, Rowe C, Samani NJ, Sanna M, Schadendorf D, Schulze HJ, Simms LA, Smithers M, Song F, Swerdlow AJ, van der S… See abstract for full author list ➔ Landi MT, et al. Among authors: martinez j. Nat Genet. 2020 May;52(5):494-504. doi: 10.1038/s41588-020-0611-8. Epub 2020 Apr 27. Nat Genet. 2020. PMID: 32341527 Free PMC article.
Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats.
Gennarelli M, Novelli G, Andreasi Bassi F, Martorell L, Cornet M, Menegazzo E, Mostacciuolo ML, Martinez JM, Angelini C, Pizzuti A, Baiget M, Dallapiccola B. Gennarelli M, et al. Among authors: martinez jm. Am J Med Genet. 1996 Nov 11;65(4):342-7. doi: 10.1002/(SICI)1096-8628(19961111)65:4<342::AID-AJMG18>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8923947
Clinical and genetic factors involved in Porto-sinusoidal vascular disorder after oxaliplatin exposure.
Puente A, Fortea JI, Del Pozo C, Serrano M, Alonso-Peña M, Giráldez A, Tellez L, Martinez J, Magaz M, Ibañez L, Garcia J, Llop E, Alvarez-Navascues C, Romero M, Rodriguez E, Arias Loste MT, Antón A, Echavarria V, López C, Albillos A, Hernández-Gea V, Garcia-Pagán JC, Bañares R, Crespo J; by REHEVASC group. Puente A, et al. Among authors: martinez j. Dig Liver Dis. 2024 May 7:S1590-8658(24)00711-4. doi: 10.1016/j.dld.2024.04.010. Online ahead of print. Dig Liver Dis. 2024. PMID: 38719628
Clinical impact of remote heart failure management using the multiparameter ICD HeartLogic alert.
Bagudá JJ, León RC, Gómez JJG, Pachón M, Artaza JG, Mateo VM, Pérez VE, Manjavacas ÁMI, Gándara NR, Álvarez-García J, Ramos JGS, Agudo CA, Manuel Rubín López J, Gallego AM, Fernández SL, Torres LG, Martínez JG, Negrín NM, Maqueda JR, Ramos MC, María Medina Gil J, Rus CD, Jiménez FJB, Madrazo I, Molina BD, Marcos MC, Duthil ADR, Cordero D, Fernández ABM, Conde LP, Torres MFA, Castellano NP, Arias MA, Bolao IG, Infante ED, Campari M, Ynsaurriaga FA, Jiménez JFD, Valsecchi S, Bodes RS. Bagudá JJ, et al. Among authors: martinez jg. Rev Esp Cardiol (Engl Ed). 2024 Apr 30:S1885-5857(24)00148-8. doi: 10.1016/j.rec.2024.04.006. Online ahead of print. Rev Esp Cardiol (Engl Ed). 2024. PMID: 38697283 English, Spanish.
Strategies to promote language inclusion at 17 CTSA hubs.
Sprague Martinez L, Araujo Brinkerhoff C, Howard RC, Feldman JA, Kobetz E, White JT, Tumiel Berhalter L, Bilheimer A, Hoffman M, Isasi CR, Killough C, Martinez J, Chesley J, Baig AA, Foy C, Islam N, Petruse A, Rosales C, Kipke MD, Baezconde-Garbanati L, Battaglia TA, Lobb R. Sprague Martinez L, et al. Among authors: martinez j. J Clin Transl Sci. 2024 Mar 25;8(1):e67. doi: 10.1017/cts.2024.13. eCollection 2024. J Clin Transl Sci. 2024. PMID: 38690228 Free PMC article.
8,958 results