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Items: 1 to 50 of 329

1.

SPARC gene variants predict clinical outcome in locally advanced and metastatic pancreatic cancer patients.

Arqueros C, Salazar J, Arranz MJ, Sebio A, Mora J, Sullivan I, Tobeña M, Martín-Richard M, Barnadas A, Baiget M, Páez D.

Med Oncol. 2017 Aug;34(8):136. doi: 10.1007/s12032-017-0993-3. Epub 2017 Jul 7.

PMID:
28687963
2.

KRAS genetic variant as a prognostic factor for recurrence in resectable non-small cell lung cancer.

Sullivan I, Salazar J, Arqueros C, Andrés M, Sebio A, Majem M, Szafranska J, Martínez E, Páez D, López-Pousa A, Baiget M, Barnadas A.

Clin Transl Oncol. 2017 Jul;19(7):884-890. doi: 10.1007/s12094-017-1620-7. Epub 2017 Feb 1.

PMID:
28150169
3.

Methotrexate pharmacokinetic genetic variants are associated with outcome in rheumatoid arthritis patients.

Moya P, Salazar J, Arranz MJ, Díaz-Torné C, del Río E, Casademont J, Corominas H, Baiget M.

Pharmacogenomics. 2016;17(1):25-9. doi: 10.2217/pgs.15.150. Epub 2015 Dec 14.

PMID:
26652611
4.

DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype Correlations.

Juan-Mateu J, Gonzalez-Quereda L, Rodriguez MJ, Baena M, Verdura E, Nascimento A, Ortez C, Baiget M, Gallano P.

PLoS One. 2015 Aug 18;10(8):e0135189. doi: 10.1371/journal.pone.0135189. eCollection 2015.

5.

Genetic variations in the VEGF pathway as prognostic factors in metastatic colorectal cancer patients treated with oxaliplatin-based chemotherapy.

Paré-Brunet L, Sebio A, Salazar J, Berenguer-Llergo A, Río E, Barnadas A, Baiget M, Páez D.

Pharmacogenomics J. 2015 Oct;15(5):397-404. doi: 10.1038/tpj.2015.1. Epub 2015 Feb 24.

PMID:
25707392
6.

Consensus on the use of methotrexate beyond the clinical recommendation: Adjusted dose and pharmacogenetics.

Moya P, Corominas H, Salazar J, Baiget M.

Reumatol Clin. 2015 Jul-Aug;11(4):261-2. doi: 10.1016/j.reuma.2014.12.010. Epub 2015 Jan 24. English, Spanish. No abstract available.

7.

Polymorphisms in genes involved in the mechanism of action of methotrexate: are they associated with outcome in rheumatoid arthritis patients?

Salazar J, Moya P, Altés A, Díaz-Torné C, Casademont J, Cerdà-Gabaroi D, Corominas H, Baiget M.

Pharmacogenomics. 2014 Jun;15(8):1079-90. doi: 10.2217/pgs.14.67.

PMID:
25084201
8.

Pharmacogenetics of the DNA repair pathways in advanced non-small cell lung cancer patients treated with platinum-based chemotherapy.

Sullivan I, Salazar J, Majem M, Pallarés C, Del Río E, Páez D, Baiget M, Barnadas A.

Cancer Lett. 2014 Oct 28;353(2):160-6. doi: 10.1016/j.canlet.2014.07.023. Epub 2014 Jul 25.

PMID:
25069034
9.

EGFR ligands and DNA repair genes: genomic predictors of complete response after capecitabine-based chemoradiotherapy in locally advanced rectal cancer.

Sebio A, Salazar J, Páez D, Berenguer-Llergo A, Del Río E, Tobeña M, Martín-Richard M, Sullivan I, Targarona E, Balart J, Baiget M, Barnadas A.

Pharmacogenomics J. 2015 Feb;15(1):77-83. doi: 10.1038/tpj.2014.33. Epub 2014 Jul 15.

PMID:
25026457
10.

Analysis of the C9orf72 gene in spinal muscular atrophy patients.

Alías L, Bernal S, Barceló MJ, Martínez-Hernández R, Martínez E, Baiget M, Tizzano EF.

Amyotroph Lateral Scler Frontotemporal Degener. 2014 Dec;15(7-8):563-8. doi: 10.3109/21678421.2014.929148. Epub 2014 Jul 7.

PMID:
24998634
11.

Overview of Bardet-Biedl syndrome in Spain: identification of novel mutations in BBS1, BBS10 and BBS12 genes.

Álvarez-Satta M, Castro-Sánchez S, Pereiro I, Piñeiro-Gallego T, Baiget M, Ayuso C, Valverde D.

Clin Genet. 2014 Dec;86(6):601-2. doi: 10.1111/cge.12334. Epub 2014 Jan 26. No abstract available.

PMID:
24611592
12.

Assessment of primary healthcare professionals' management of hypertensive patients with riser pattern.

Sagarra-Tió M, Félez-Carrobé E, Baiget M, Félez J.

Eur J Cardiovasc Nurs. 2015 Feb;14(1):73-8. doi: 10.1177/1474515113518856. Epub 2014 Jan 6.

PMID:
24396114
13.

A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer.

Fernandez-Rozadilla C, Cazier JB, Tomlinson I, Brea-Fernández A, Lamas MJ, Baiget M, López-Fernández LA, Clofent J, Bujanda L, Gonzalez D, de Castro L; EPICOLON Consortium, Hemminki K, Bessa X, Andreu M, Jover R, Xicola R, Llor X, Moreno V, Castells A, Castellví-Bel S, Carracedo A, Ruiz-Ponte C.

Hum Genet. 2014 May;133(5):525-34. doi: 10.1007/s00439-013-1390-4. Epub 2013 Nov 12.

PMID:
24218287
14.

Molecular detection of peripheral blood breast cancer mRNA transcripts as a surrogate biomarker for circulating tumor cells.

Lasa A, Garcia A, Alonso C, Millet P, Cornet M, Ramón y Cajal T, Baiget M, Barnadas A.

PLoS One. 2013 Sep 18;8(9):e74079. doi: 10.1371/journal.pone.0074079. eCollection 2013.

15.

Intergenic polymorphisms in the amphiregulin gene region as biomarkers in metastatic colorectal cancer patients treated with anti-EGFR plus irinotecan.

Sebio A, Páez D, Salazar J, Berenguer-Llergo A, Paré-Brunet L, Lasa A, Del Río E, Tobeña M, Martín-Richard M, Baiget M, Barnadas A.

Pharmacogenomics J. 2014 Jun;14(3):256-62. doi: 10.1038/tpj.2013.29. Epub 2013 Aug 20.

PMID:
23959273
16.

Polymorphisms of Pyrimidine Pathway Enzymes Encoding Genes and HLA-B*40∶01 Carriage in Stavudine-Associated Lipodystrophy in HIV-Infected Patients.

Domingo P, Mateo MG, Pruvost A, Torres F, Salazar J, Gutierrez Mdel M; Ma Carmen Cabeza, Domingo JC, Fernandez I, Villarroya F, Vidal F, Baiget M, de la Calle-Martín O.

PLoS One. 2013 Jun 26;8(6):e67035. doi: 10.1371/journal.pone.0067035. Print 2013.

17.

Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene.

Alías L, Barceló MJ, Bernal S, Martínez-Hernández R, Also-Rallo E, Vázquez C, Santana A, Millán JM, Baiget M, Tizzano EF.

Clin Genet. 2014 May;85(5):470-5. doi: 10.1111/cge.12222. Epub 2013 Jul 16.

PMID:
23799925
18.

Nurse-driven training courses: impact on implementation of ambulatory blood pressure monitoring.

Félez-Carrobé E, Sagarra-Tió M, Romero A, Rubio M, Planas L, Pérez-Lucena MJ, Baiget M, Cabistañ C, Félez J.

Open Nurs J. 2013 Apr 5;7:35-40. doi: 10.2174/1874434601307010035. Print 2013.

19.

Uranium removal from a contaminated effluent using a combined microbial and nanoparticle system.

Baiget M, Constantí M, López MT, Medina F.

N Biotechnol. 2013 Sep 25;30(6):788-92. doi: 10.1016/j.nbt.2013.05.003. Epub 2013 May 17.

PMID:
23689043
20.

Interplay between DMD point mutations and splicing signals in Dystrophinopathy phenotypes.

Juan-Mateu J, González-Quereda L, Rodríguez MJ, Verdura E, Lázaro K, Jou C, Nascimento A, Jiménez-Mallebrera C, Colomer J, Monges S, Lubieniecki F, Foncuberta ME, Pascual-Pascual SI, Molano J, Baiget M, Gallano P.

PLoS One. 2013;8(3):e59916. doi: 10.1371/journal.pone.0059916. Epub 2013 Mar 25.

21.

Association of thymidylate synthase polymorphisms with acute pancreatitis and/or peripheral neuropathy in HIV-infected patients on stavudine-based therapy.

Domingo P, Cabeza Mdel C, Torres F, Salazar J, Gutierrez Mdel M, Mateo MG, Martínez E, Domingo JC, Fernandez I, Villarroya F, Ribera E, Vidal F, Baiget M.

PLoS One. 2013;8(2):e57347. doi: 10.1371/journal.pone.0057347. Epub 2013 Feb 28.

22.

High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish population.

Corton M, Tatu SD, Avila-Fernandez A, Vallespín E, Tapias I, Cantalapiedra D, Blanco-Kelly F, Riveiro-Alvarez R, Bernal S, García-Sandoval B, Baiget M, Ayuso C.

Orphanet J Rare Dis. 2013 Feb 5;8:20. doi: 10.1186/1750-1172-8-20.

23.

A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.

Fernandez-Rozadilla C, Cazier JB, Tomlinson IP, Carvajal-Carmona LG, Palles C, Lamas MJ, Baiget M, López-Fernández LA, Brea-Fernández A, Abulí A, Bujanda L, Clofent J, Gonzalez D, Xicola R, Andreu M, Bessa X, Jover R, Llor X; EPICOLON Consortium, Moreno V, Castells A, Carracedo Á, Castellvi-Bel S, Ruiz-Ponte C.

BMC Genomics. 2013 Jan 26;14:55. doi: 10.1186/1471-2164-14-55.

24.

The LCS6 polymorphism in the binding site of let-7 microRNA to the KRAS 3'-untranslated region: its role in the efficacy of anti-EGFR-based therapy in metastatic colorectal cancer patients.

Sebio A, Paré L, Páez D, Salazar J, González A, Sala N, del Río E, Martín-Richard M, Tobeña M, Barnadas A, Baiget M.

Pharmacogenet Genomics. 2013 Mar;23(3):142-7. doi: 10.1097/FPC.0b013e32835d9b0b.

PMID:
23324806
25.

Pharmacogenetic analysis in the treatment of Hodgkin lymphoma.

Altés A, Paré L, Esquirol A, Xicoy B, Rámila E, Vicente L, López R, Orriols J, Vall-llovera F, Sánchez-González B, del Río E, Sureda A, Páez D, Baiget M.

Leuk Lymphoma. 2013 Aug;54(8):1706-12. doi: 10.3109/10428194.2012.752080. Epub 2013 Feb 1.

PMID:
23323945
26.

BMP2/BMP4 colorectal cancer susceptibility loci in northern and southern European populations.

Fernandez-Rozadilla C, Palles C, Carvajal-Carmona L, Peterlongo P, Nici C, Veneroni S, Pinheiro M, Teixeira MR, Moreno V, Lamas MJ, Baiget M, Lopez-Fernandez LA, Gonzalez D, Brea-Fernandez A, Clofent J, Bujanda L, Bessa X, Andreu M, Xicola R, Llor X, Jover R; EPICOLON Consortium, Castells A, Castellvi-Bel S, Carracedo A, Tomlinson I, Ruiz-Ponte C.

Carcinogenesis. 2013 Feb;34(2):314-8. doi: 10.1093/carcin/bgs357. Epub 2012 Nov 16. Erratum in: Carcinogenesis. 2013 Jul;34(7):1697.

PMID:
23161572
27.

Genome-wide DNA methylation profiling predicts relapse in childhood B-cell acute lymphoblastic leukaemia.

Sandoval J, Heyn H, Méndez-González J, Gomez A, Moran S, Baiget M, Melo M, Badell I, Nomdedéu JF, Esteller M.

Br J Haematol. 2013 Feb;160(3):406-9. doi: 10.1111/bjh.12113. Epub 2012 Oct 30. No abstract available.

28.

Study of three families with Hb Agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the Spanish population: three homozygous cases.

de la Fuente-Gonzalo F, Baiget M, Badell I, Ricard P, Vinuesa L, Martínez-Nieto J, Ropero P, Villegas A, González FA, Díaz-Mediavilla J, Erythropathology Spanish Group.

Hemoglobin. 2012;36(6):526-32. doi: 10.3109/03630269.2012.733988. Epub 2012 Oct 24.

PMID:
23094635
29.

Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy.

Juan-Mateu J, Rodríguez MJ, Nascimento A, Jiménez-Mallebrera C, González-Quereda L, Rivas E, Paradas C, Madruga M, Sánchez-Ayaso P, Jou C, González-Mera L, Munell F, Roig-Quilis M, Rabasa M, Hernández-Lain A, Díaz-Manera J, Gallardo E, Pascual J, Verdura E, Colomer J, Baiget M, Olivé M, Gallano P.

Orphanet J Rare Dis. 2012 Oct 23;7:82. doi: 10.1186/1750-1172-7-82.

30.

Molecular approach in the study of Alström syndrome: analysis of ten Spanish families.

Piñeiro-Gallego T, Cortón M, Ayuso C, Baiget M, Valverde D.

Mol Vis. 2012;18:1794-802. Epub 2012 Jul 3.

31.

UGT1A1 genotype in a white boy with Crigler-Najjar syndrome type 2.

Peña L, Pico M, Rosatelli C, Meloni A, Del Río E, Tizzano EF, Baiget M.

J Pediatr Gastroenterol Nutr. 2012 Nov;55(5):e136-7. doi: 10.1097/MPG.0b013e318234ecd9. No abstract available.

PMID:
22722682
32.

F8 gene dosage defects in atypical patients with severe haemophilia A.

Venceslá Á, Baena M, Garrido RP, Núñez R, Velasco F, Rosell J, Villar A, Jiménez-Yuste V, Baiget M, Tizzano EF.

Haemophilia. 2012 Sep;18(5):708-13. doi: 10.1111/j.1365-2516.2012.02818.x. Epub 2012 May 23.

PMID:
22621702
33.

Association of ITPA gene polymorphisms and the risk of ribavirin-induced anemia in HIV/hepatitis C virus (HCV)-coinfected patients receiving HCV combination therapy.

Domingo P, Guardiola JM, Salazar J, Torres F, Mateo MG, Pacho C, Del Mar Gutierrez M, Lamarca K, Fontanet A, Martin J, Muñoz J, Vidal F, Baiget M.

Antimicrob Agents Chemother. 2012 Jun;56(6):2987-93. doi: 10.1128/AAC.06473-11. Epub 2012 Mar 19.

34.

Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration.

Fernandez-Rozadilla C, Cazier JB, Moreno V, Crous-Bou M, Guinó E, Durán G, Lamas MJ, López R, Candamio S, Gallardo E, Paré L, Baiget M, Páez D, López-Fernández LA, Cortejoso L, García MI, Bujanda L, González D, Gonzalo V, Rodrigo L, Reñé JM, Jover R, Brea-Fernández A, Andreu M, Bessa X, Llor X, Xicola R, Palles C, Tomlinson I, Castellví-Bel S, Castells A, Ruiz-Ponte C, Carracedo A; EPICOLON Consortium.

Pharmacogenomics J. 2013 Jun;13(3):209-17. doi: 10.1038/tpj.2012.2. Epub 2012 Feb 7.

PMID:
22310351
35.

Isolated cardiomyopathy caused by a DMD nonsense mutation in somatic mosaicism: genetic normalization in skeletal muscle.

Juan-Mateu J, Paradas C, Olivé M, Verdura E, Rivas E, González-Quereda L, Rodríguez MJ, Baiget M, Gallano P.

Clin Genet. 2012 Dec;82(6):574-8. doi: 10.1111/j.1399-0004.2011.01814.x. Epub 2011 Dec 13.

PMID:
22092019
36.

Evaluation of fetal nuchal translucency in 98 pregnancies at risk for severe spinal muscular atrophy: possible relevance of the SMN2 copy number.

Parra J, Alias L, Also-Rallo E, Martínez-Hernández R, Senosiain R, Medina C, Alejos O, Rams N, Amenedo M, Ormo F, Jesús Barceló M, Calaf J, Baiget M, Bernal S, Tizzano EF.

J Matern Fetal Neonatal Med. 2012 Aug;25(8):1246-9. doi: 10.3109/14767058.2011.636101. Epub 2011 Nov 30.

PMID:
22082206
37.

Mutational screening of the USH2A gene in Spanish USH patients reveals 23 novel pathogenic mutations.

Garcia-Garcia G, Aparisi MJ, Jaijo T, Rodrigo R, Leon AM, Avila-Fernandez A, Blanco-Kelly F, Bernal S, Navarro R, Diaz-Llopis M, Baiget M, Ayuso C, Millan JM, Aller E.

Orphanet J Rare Dis. 2011 Oct 17;6:65. doi: 10.1186/1750-1172-6-65.

38.

LMNA mutation in progeroid syndrome in association with strokes.

Gonzalez-Quereda L, Delgadillo V, Juan-Mateu J, Verdura E, Rodriguez MJ, Baiget M, Pineda M, Gallano P.

Eur J Med Genet. 2011 Nov-Dec;54(6):e576-9. doi: 10.1016/j.ejmg.2011.06.012. Epub 2011 Jul 18.

PMID:
21791255
39.

Methotrexate consolidation treatment according to pharmacogenetics of MTHFR ameliorates event-free survival in childhood acute lymphoblastic leukaemia.

Salazar J, Altés A, del Río E, Estella J, Rives S, Tasso M, Navajas A, Molina J, Villa M, Vivanco JL, Torrent M, Baiget M, Badell I.

Pharmacogenomics J. 2012 Oct;12(5):379-85. doi: 10.1038/tpj.2011.25. Epub 2011 Jul 12.

PMID:
21747412
40.

A genotype-directed phase I-IV dose-finding study of irinotecan in combination with fluorouracil/leucovorin as first-line treatment in advanced colorectal cancer.

Marcuello E, Páez D, Paré L, Salazar J, Sebio A, del Rio E, Baiget M.

Br J Cancer. 2011 Jun 28;105(1):53-7. doi: 10.1038/bjc.2011.206. Epub 2011 Jun 7.

41.

Treatment of spinal muscular atrophy cells with drugs that upregulate SMN expression reveals inter- and intra-patient variability.

Also-Rallo E, Alías L, Martínez-Hernández R, Caselles L, Barceló MJ, Baiget M, Bernal S, Tizzano EF.

Eur J Hum Genet. 2011 Oct;19(10):1059-65. doi: 10.1038/ejhg.2011.89. Epub 2011 May 25.

42.

Pharmacogenetic study in rectal cancer patients treated with preoperative chemoradiotherapy: polymorphisms in thymidylate synthase, epidermal growth factor receptor, GSTP1, and DNA repair genes.

Páez D, Salazar J, Paré L, Pertriz L, Targarona E, del Rio E, Barnadas A, Marcuello E, Baiget M.

Int J Radiat Oncol Biol Phys. 2011 Dec 1;81(5):1319-27. doi: 10.1016/j.ijrobp.2011.01.025. Epub 2011 May 11.

PMID:
21570215
43.

Accuracy of marker analysis, quantitative real-time polymerase chain reaction, and multiple ligation-dependent probe amplification to determine SMN2 copy number in patients with spinal muscular atrophy.

Alías L, Bernal S, Barceló MJ, Also-Rallo E, Martínez-Hernández R, Rodríguez-Alvarez FJ, Hernández-Chico C, Baiget M, Tizzano EF.

Genet Test Mol Biomarkers. 2011 Sep;15(9):587-94. doi: 10.1089/gtmb.2010.0253. Epub 2011 May 6.

PMID:
21548796
44.

Plastin 3 expression in discordant spinal muscular atrophy (SMA) siblings.

Bernal S, Also-Rallo E, Martínez-Hernández R, Alías L, Rodríguez-Alvarez FJ, Millán JM, Hernández-Chico C, Baiget M, Tizzano EF.

Neuromuscul Disord. 2011 Jun;21(6):413-9. doi: 10.1016/j.nmd.2011.03.009. Epub 2011 May 4.

PMID:
21546251
45.

Copy-number variations in EYS: a significant event in the appearance of arRP.

Pieras JI, Barragán I, Borrego S, Audo I, González-Del Pozo M, Bernal S, Baiget M, Zeitz C, Bhattacharya SS, Antiñolo G.

Invest Ophthalmol Vis Sci. 2011 Jul 29;52(8):5625-31. doi: 10.1167/iovs.11-7292.

PMID:
21519034
46.

Diagnosis of CADASIL disease in normotensive and non-diabetics with lacunar infarct.

Cocho D, Martí-Fàbregas J, Baiget M, Gallardo E, Rio E, Arboix A, Ruscalleda J, Martí-Vilalta JL.

Neurologia. 2011 Jul-Aug;26(6):325-30. doi: 10.1016/j.nrl.2010.12.004. Epub 2011 Feb 22. English, Spanish.

47.

Association of thymidylate synthase gene polymorphisms with stavudine triphosphate intracellular levels and lipodystrophy.

Domingo P, Cabeza MC, Pruvost A, Torres F, Salazar J, del Mar Gutierrez M, Mateo MG, Fontanet A, Fernandez I, Domingo JC, Villarroya F, Vidal F, Baiget M.

Antimicrob Agents Chemother. 2011 Apr;55(4):1428-35. doi: 10.1128/AAC.01589-10. Epub 2011 Jan 31.

48.

Novel mutations in the USH1C gene in Usher syndrome patients.

Aparisi MJ, García-García G, Jaijo T, Rodrigo R, Graziano C, Seri M, Simsek T, Simsek E, Bernal S, Baiget M, Pérez-Garrigues H, Aller E, Millán JM.

Mol Vis. 2010 Dec 31;16:2948-54.

49.

Ultrasound evaluation of fetal movements in pregnancies at risk for severe spinal muscular atrophy.

Parra J, Martínez-Hernández R, Also-Rallo E, Alias L, Barceló MJ, Amenedo M, Medina C, Senosiain R, Calaf J, Baiget M, Bernal S, Tizzano EF.

Neuromuscul Disord. 2011 Feb;21(2):97-101. doi: 10.1016/j.nmd.2010.09.010. Epub 2010 Dec 30.

PMID:
21194946
50.

Pharmacogenetic studies on the antipsychotic treatment. Current status and perspectives.

Gesteira A, Barros F, Martín A, Pérez V, Cortés A, Baiget M, Carracedo A.

Actas Esp Psiquiatr. 2010 Sep-Oct;38(5):301-16. Epub 2010 Sep 1. Review. English, Spanish.

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