Bernués M - Search Results

1

t(10;12)(q24;q15): A new cytogenetic marker in hematological malignancies.

Bernués M, González T, Corchete LA, Santos S, Durán MA, López-Andrade B, Riso LL, Martínez-Serra J, Ramos R, Iglesias J, Royo I, Rosell J. Bernués M, et al. Cancer Genet. 2022 Jun;264-265:60-65. doi: 10.1016/j.cancergen.2022.03.004. Epub 2022 Mar 26. Cancer Genet. 2022. PMID: 35397254 Review.

2

dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in myelodysplastic syndromes.

Alfaro R, Pérez-Granero A, Durán MA, Besalduch J, Rosell J, Bernués M. Alfaro R, et al. Among authors: bernues m. Leuk Res. 2008 Jan;32(1):159-61. doi: 10.1016/j.leukres.2007.03.033. Epub 2007 May 16. Leuk Res. 2008. PMID: 17509681

3

Structural rearrangements of trisomies are a risk marker of clinical progression in hyperdiploid multiple myeloma.

Alfaro R, Rosell J, Durán MA, Puget G, Besalduch J, Galán P, Vallés A, Bernués M. Alfaro R, et al. Among authors: bernues m. Anticancer Res. 2011 May;31(5):1599-602. Anticancer Res. 2011. PMID: 21617215

4

Genetics of lymphocytes influences the emergence of second cancer in chronic lymphocytic leukemia.

Bernués M, Durán MA, Puget G, Iglesias J, Galán P, Vercher FJ, Besalduch J, Rosell J. Bernués M, et al. Anticancer Res. 2014 May;34(5):2311-4. Anticancer Res. 2014. PMID: 24778036

5

Acute lymphoblastic leukemia with e1a3 BCR/ABL fusion protein. A report of two cases.

López-Andrade B, Sartori F, Gutiérrez A, García L, Cunill V, Durán MA, Sampol A, Bernués M, Iglesias J, Ramos R, Lladó J, Sánchez M, Amat JC, Martínez-Serra J. López-Andrade B, et al. Among authors: bernues m. Exp Hematol Oncol. 2016 Jul 29;5:21. doi: 10.1186/s40164-016-0049-y. eCollection 2015. Exp Hematol Oncol. 2016. PMID: 27478684 Free PMC article.

6

Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation.

Torres-Juan L, Rosell J, Morla M, Vidal-Pou C, García-Algas F, de la Fuente MA, Juan M, Tubau A, Bachiller D, Bernues M, Perez-Granero A, Govea N, Busquets X, Heine-Suñer D. Torres-Juan L, et al. Among authors: bernues m. Eur J Hum Genet. 2007 Jun;15(6):658-63. doi: 10.1038/sj.ejhg.5201819. Epub 2007 Mar 21. Eur J Hum Genet. 2007. PMID: 17377518

7

Fragile-X syndrome and skewed X-chromosome inactivation within a family: a female member with complete inactivation of the functional X chromosome.

Heine-Suñer D, Torres-Juan L, Morlà M, Busquets X, Barceló F, Picó G, Bonilla L, Govea N, Bernués M, Rosell J. Heine-Suñer D, et al. Among authors: bernues m. Am J Med Genet A. 2003 Oct 1;122A(2):108-14. doi: 10.1002/ajmg.a.20160. Am J Med Genet A. 2003. PMID: 12955761

8

Cytogenetic characterization of a familial papillary renal cell carcinoma.

Bernués M, Casadevall C, Miró R, Caballín MR, Villavicencio H, Salvador J, Zamarrón A, Egozcue J. Bernués M, et al. Cancer Genet Cytogenet. 1995 Oct 15;84(2):123-7. doi: 10.1016/0165-4608(95)00044-5. Cancer Genet Cytogenet. 1995. PMID: 8536226

9

Analysis of kidney tumors by comparative genomic hybridization and conventional cytogenetics.

Rigola MA, Casadevall C, Bernués M, Caballín MR, Fuster C, Gelabert A, Egozcue J, Miró R. Rigola MA, et al. Among authors: bernues m. Cancer Genet Cytogenet. 2002 Aug;137(1):49-53. doi: 10.1016/s0165-4608(02)00544-7. Cancer Genet Cytogenet. 2002. PMID: 12377413

10

Comparative genomic hybridization analysis of transitional cell carcinomas of the renal pelvis.

Rigola MA, Fuster C, Casadevall C, Bernués M, Caballín MR, Gelabert A, Egozcue J, Miró R. Rigola MA, et al. Among authors: bernues m. Cancer Genet Cytogenet. 2001 May;127(1):59-63. doi: 10.1016/s0165-4608(00)00426-x. Cancer Genet Cytogenet. 2001. PMID: 11408067

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